Calcium channel compositions and methods of use thereof

Abstract

The present invention relates to calcium channel compositions and methods of making and using same. In particular, the invention relates to calcium channel alpha2delta (α2δ) subunits and nucleic acid sequences encoding them. These compositions are useful in methods for identifying compounds that modulate the activity of calcium channels and for identifying compounds as therapeutic for disease.

Description

FIELD OF THE INVENTION

The present invention relates to calcium channel compositions and methods of making and using same. In particular, the invention relates to calcium channel alpha2delta (α 2 δ) subunits and nucleic acid sequences encoding them. These compositions are useful in methods for identifying compounds that modulate the activity of calcium channels and for identifying compounds as therapeutic for disease.

BACKGROUND OF THE INVENTION

Calcium channels are present in various tissues, have a central role in regulating intracellular calcium ion concentrations, and are implicated in several vital processes in animals (e.g., neurotransmitter release, muscle contraction, pacemaker activity, secretion of hormones and other substances, etc.). Thus, changes in calcium influx into cells which are mediated through calcium channels have been implicated in various human diseases such as disorders of the central nervous system and cardiovascular disease.

For example, changes to calcium influx into neuronal cells may be implicated in conditions such as epilepsy, stroke, brain trauma, Alzheimer's disease, multiinfarct dementia, other classes of dementia, Korsakoff's disease, neuropathy caused by a viral infection of the brain or spinal cord (e.g., human immunodeficiency viruses, etc.), amyotrophic lateral sclerosis, convulsions, seizures, Huntington's disease, amnesia, or damage to the nervous system resulting from reduced oxygen supply, poison or other toxic substances (See e.g., Goldin et al., U.S. Pat. No. 5,312,928).

Additionally, changes to calcium influx into cardiovascular cells may be implicated in conditions such as cardiac arrhythmia, angina pectoris, hypoxic damage to the cardiovascular system, ischemic damage to the cardiovascular system, myocardial infarction, and congestive heart failure (Goldin et al., supra). Other pathological conditions associated with elevated intracellular free calcium levels include muscular dystrophy and hypertension (Steinhardt et al., U.S. Pat. No. 5,559,004). While there has been limited success in expressing DNA encoding rabbit and rat calcium channel subunits, little is known about human calcium channel structure, function and gene expression. Additionally, there is limited knowledge in the art of the role of calcium channel types in cell growth control and abnormalities of calcium channels leading to cancer development.

In addition to the implication of calcium channels in animal (including human) diseases, a number of compounds which are currently used for treating various cardiovascular diseases in animals (including humans) are believed to exert their beneficial effects by modulating the functions of voltage-dependent calcium channels present in cells, such as cardiac cells and vascular smooth muscle cells. Nonetheless, there is a paucity of understanding of the pharmacology of compounds which interact with calcium channels. This paucity of understanding, together with the limited knowledge in the art of the human calcium channel types, the molecular nature of the human calcium channel subtypes, and the limited availability of pure preparations of specific calcium channel subtypes to use for evaluating the efficacy of calcium channel-modulating compounds has hampered the rational testing and screening of compounds that interact with the specific subtypes of human calcium channels to have desired therapeutic effects.

SUMMARY OF THE INVENTION

The invention provides calcium channel alpha2delta (α 2 δ) subunits, as well as amino and nucleic acids encoding them. In one embodiment, the invention provides a substantially purified nucleic acid sequence consisting of at least a portion of a nucleotide sequence selected from the group consisting of (a) SEQ ID NO:1, the complement thereof, variants thereof, and homologs thereof, (b) SEQ ID NO:3, the complement thereof, variants thereof, and homologs thereof, and (c) SEQ ID NO:5, the complement thereof, variants thereof, and homologs thereof. In a preferred embodiment, the nucleic acid sequence encodes at least a portion of the amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof. In a more preferred embodiment, the nucleic acid sequence is double-stranded. In an alternative more preferred embodiment, the nucleic acid sequence is single-stranded.

Without intending to limit the nucleic acid sequences of the invention to any particular type of encoded protein, in an alternative preferred embodiment, the nucleic acid sequence encodes a fusion protein. While it is not contemplated that the invention be limited to the type or nature of fusion partner in the fusion protein, in a more preferred embodiment, the fusion protein comprises a polypeptide selected from the group consisting of chloramphenicol acetyltransferase, luciferase, beta-galactosidase, green fluorescent protein, Myc protein, protein A, glutathione-S-transferase, FLAG tag, and polyhistidine.

In another alternative preferred embodiment, the nucleic acid sequence is contained on a recombinant expression vector. In a more preferred embodiment, the expression vector is contained within a host cell. While it is not contemplated that the invention be limited to the type of host cell, in a yet more preferred embodiment, the host cell is eukaryotic. In an even more preferred embodiment, the eukaryotic cell is selected from the group consisting of cancer cells and amphibian oocytes.

Also provided by the invention is a substantially purified amino acid sequence comprising at least a portion of an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof. In a preferred embodiment, the portion is part of a fusion protein. While not intending to limit the invention to any particular type or nature of fusion protein, in a more preferred embodiment, the fusion protein comprises a polypeptide selected from the group consisting of chloramphenicol acetyltransferase, luciferase, beta-galactosidase, protein A, glutathione-S-transferase, FlAG tag, and polyhistidine.

The invention further provides substantially purified amino acid sequences encoded by at least a portion of a nucleotide sequence selected from the group consisting of (a) SEQ ID NO: 1, the complement thereof, variants thereof, and homologs thereof, (b) SEQ ID NO:3, the complement thereof, variants thereof, and homologs thereof, and (c) SEQ ID NO:5, the complement thereof, variants thereof, and homologs thereof.

The invention additionally provides methods for detecting presence of a nucleic acid sequence encoding at least a portion of a calcium channel protein, comprising: a) providing: i) a sample suspected of containing the nucleic acid sequence; and ii) at least a portion of a nucleotide sequence selected from the group consisting of (1) SEQ ID NO: 1, the complement thereof, variants thereof, and homologs thereof, (2) SEQ ID NO:3, the complement thereof, variants thereof, and homologs thereof, and (3) SEQ ID NO:5, the complement thereof, variants thereof, and homologs thereof, b) combining the sample with at least a portion of the nucleotide sequence under conditions such that the nucleic acid hybridizes with at least a portion of the nucleotide sequence; and c) detecting the hybridization. Although it is not contemplated that the invention be limited to the level of stringency of hybridization, in one preferred embodiment, the hybridization is under conditions of low stringency. In another preferred embodiment, the hybridization is under conditions of high stringency. Furthermore, it is contemplated that the invention will also be used in various assays to detect mRNA using these sequences (i.e., SEQ ID NOS:1, 3, and 5) including, but not limited to microassays.

The invention also provides methods for producing at least a portion of a calcium channel protein, comprising: a) providing: i) a recombinant expression vector comprising a nucleic acid sequence encoding at least a portion of an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof, and ii) a host cell; and b) introducing the vector into the host cell under conditions such that the host cell expresses the portion of the amino acid sequence. In one preferred embodiment, the method further comprises step c) recovering the expressed amino acid sequence (or portion thereof). While not intending to limit the invention to the type or nature of host cell, in an alternative preferred embodiment, the host cell is eukaryotic. In a more preferred embodiment, the eukaryotic host cell is selected from the group consisting of cancer cells and amphibian oocytes.

The invention also provides methods for screening test compounds for modulating calcium channel activity, comprising: a) providing: i) the test compound; ii) a calcium channel selective ion; iii) a control cell; and iv) a host cell comprising a cell membrane and expressing heterologous nucleic acid sequences encoding: 1) calcium channel α 1 subunit; and 2) at least a portion of an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof; b) contacting the host cell with the test compound and with the molecule to produce a treated host cell; c) depolarizing the cell membrane of the treated host cell under conditions such that the molecule enters the cell through a functional calcium channel; and d) detecting a difference between current flowing into the treated host cell and current flowing into a control cell, thereby identifying the test compound as a compound capable of modulating calcium channel activity. In one preferred embodiment, the method further comprises, prior to the depolarizing, maintaining the treated host cell at a holding potential that substantially inactivates endogenous calcium channels. In another preferred embodiment, the method further comprises, prior to or simultaneously with the step of contacting the host cell with the test compound, contacting the host cell with a calcium channel agonist, wherein the test compound is tested for activity as an antagonist. In yet another preferred embodiment, the host cell further expresses calcium channel beta (β) subunit. In another preferred embodiment, the host cell further expresses calcium channel beta (β) subunit and gamma (γ) subunit. Without intending to limit the type or source of host cell, in yet another preferred embodiment, the host cell is eukaryotic. In a more preferred embodiment, the eukaryotic host cell is selected from the group consisting of cancer cells and amphibian oocytes.

Also provided herein is a method of generating antibodies directed against at least a portion of a calcium channel protein, comprising: a) providing: i) at least a portion of an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof; and ii) a host; b) immunizing the host with at least a portion of the amino acid sequence so as to generate an antibody; and c) collecting the antibody from the host. In one preferred embodiment, the method further comprises step d) purifying the antibody. Without limiting the type of host cell, in another preferred embodiment, the host is a mammal. In yet another preferred embodiment, the mammal is a mouse.

The invention further provides an antibody raised according to the method described in the preceding paragraph, i.e., by a) providing: i) at least a portion of an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof; and ii) a host; b) immunizing the host with at least a portion of the amino acid sequence so as to generate antibody; and c) collecting the antibody from the host. In one preferred embodiment, the antibody is monoclonal. In another preferred embodiment, the antibody is polyclonal. In still further embodiments, the present invention provides methods and compositions for genetic immunization for the production of antibodies (e.g., by injecting expression plasmid into an animal).

Also provided herein is an antibody which specifically binds to an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof. In a preferred embodiment, the antibody is monoclonal. In another preferred embodiment, the antibody is polyclonal.

The invention also provides a method of detecting expression of at least a portion of a calcium channel protein, comprising: a) providing: i) a sample suspected of expressing the calcium channel protein; and ii) an antibody raised according to the above-described method (i.e., by a) providing: i) at least a portion of an amino acid sequence selected from the group consisting of SEQ ID NO:2 and variants thereof, SEQ ID NO:4 and variants thereof, and SEQ ID NO:6 and variants thereof; and ii) a host; b) immunizing the host with at least a portion of the amino acid sequence so as to generate an antibody; and c) collecting the antibody from the host); b) combining the sample and the antibody under conditions such that the antibody binds to the calcium channel protein; and c) detecting the binding between the antibody and the calcium channel protein in the sample.

The present invention additionally provides methods for producing transgenic non-human animals, wherein the animal expresses a reduced level of calcium channel α 2 δ subunit relative to a corresponding wild-type animal, comprising: a) providing: i) an embryonic stem cell comprising wild-type calcium channel α 2 δ-subunit genes; ii) a blastocyst of a non-human animal; iii) a pseudopregnant non-human animal; and iv) an oligonucleotide sequence comprising at least a portion of a non-human nucleotide sequence homologous to a nucleic acid sequence selected from the group consisting of (1) SEQ ID NO:1, complements thereof and variants thereof, (2) SEQ ID NO:3, complements thereof and variants thereof, and (3) SEQ ID NO:5, complements thereof and variants thereof; b) introducing the oligonucleotide sequence into the embryonic stem cell under conditions such that the oligonucleotide sequence is homologously recombined into at least one of the wild-type calcium channel α 2 δ-subunit genes in the genome of the embryonic stem cell to produce a treated embryonic stem cell; c) injecting the treated embryonic stem cell into the blastocyst to produce an injected blastocyst; d) introducing the injected blastocyst into the pseudopregnant non-human animal; and e) permitting the pseudopregnant animal to deliver progeny comprising the homologously recombined oligonucleotide, wherein the progeny express a reduced level of calcium channel α 2 δ-subunit relative to a corresponding wild-type animal. In one preferred embodiment, the transgenic non-human animal is selected from the order Rodentia. In a more preferred embodiment, the transgenic non-human animal is a mouse.

The invention also provides methods for producing transgenic non-human animals, wherein the animal expresses reduced activity of calcium channel α 2 δ subunit relative to a corresponding wild-type animal, comprising: a) providing: i) an embryonic stem cell comprising wild-type calcium channel α 2 δ-subunit genes; ii) a blastocyst of a non-human animal; iii) a pseudopregnant non-human animal; and iv) an oligonucleotide sequence comprising at least a portion of a non-human nucleotide sequence homologous to a nucleic acid sequence selected from the group consisting of (1) SEQ ID NO:1, complements thereof and variants thereof, (2) SEQ ID NO:3, complement thereof and variants thereof, and (3) SEQ ID NO:5, complements thereof and variants thereof, wherein at least portion of the nucleotide sequence comprises one or more mutations selected from the group consisting of deletion, insertion and point mutation(s); b) introducing the oligonucleotide sequence into the embryonic stem cell under conditions such that the oligonucleotide sequence is homologously recombined into at least one of the wild-type calcium channel α 2 δ-subunit genes in the genome of the embryonic stem cell to produce a treated embryonic stem cell; c) injecting the treated embryonic stem cell into the blastocyst to produce an injected blastocyst; d) introducing the injected blastocyst into the pseudopregnant non-human animal; and e) permitting the pseudopregnant animal to deliver progeny comprising the homologously recombined oligonucleotide, wherein the progeny express reduced activity of calcium channel α 2 δ-subunit relative to a corresponding wild-type animal. In one preferred embodiment, the transgenic non-human animal is selected from the order Rodentia. In a more preferred embodiment, the transgenic non-human animal is a mouse.

Additionally provided herein is a method for identifying a therapeutic compound, comprising: a) providing: i) a transgenic non-human animal produced by the method described in either of the previous two paragraphs; and ii) a composition comprising the compound; and b) administering the compound to the transgenic non-human animal to produce a treated animal. While it is not intended that the transgenic animal be limited to a particular type, in one preferred embodiment, the transgenic animal has cancer. In a more preferred embodiment, the cancer is selected from the group consisting of lung cancer, breast cancer, nasopharyngeal cancer, cervical cancer, head cancer and neck cancer. In yet a more preferred embodiment, the lung cancer is selected from the group consisting of small cell carcinoma and non small cell carcinoma. In another preferred embodiment, the transgenic animal has a neurological disease selected from the group consisting of epilepsy, stroke, brain trauma, Alzheimer's disease, multiinfarct dementia, amyotrophic lateral sclerosis, convulsions, seizures, Huntington's disease, and amnesia. In yet another preferred embodiment, the transgenic animal has a cardiovascular disease selected from the group consisting of cardiac arrhythmia, angina pectoris, hypoxic damage to the cardiovascular system, ischemic damage to the cardiovascular system, myocardial infarction, and congestive heart failure. In a further preferred embodiment, the transgenic animal has Lambert-Eton myasthenic syndrome.

In still further embodiments, the present invention provides methods for treatment of human tumors in non-human animals. For example, it is contemplated that the methods for identifying therapeutic compounds as described herein will find use in the treatment of human tumors in immunodeficient mice (e.g., nude and/or SCID [severe combined immunodeficiency] mice) or other animals.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 (A-B) provides a schematic outline of the positional cloning of the α 2 δ gene in lung cancer critical region on the short arm of human chromosome region 3p21.3.

FIG. 2 (A-B) shows polyA+ multiple tissue Northern blots (ClonTech) probed for α 2 δ expression. The tissue sources of the RNA are shown above each lane. Panel A shows a multiple tissue Northern blot with spleen, thymus, prostate, testis, ovary, small intestine, colon, and peripheral blood lymphocyte (PBL) samples, while Panel B shows a multiple tissue Northern blot with heart, brain, placenta, lung, liver, skeletal muscle, kidney, and pancreas.

FIG. 3 (A-C) provides Western blot data from transcription and translation experiments. Panel A provides results from in vitro transcription and translation of α 2 δ in expression vector pcDNA3.1 and a control sample. Panel B provides results for transfection of NCI-H1299 cells with α 2 δ-2 and a control.

FIG. 4 (A-G) provides data obtained from Xenopus oocyte expression system tests. Panel A provides representative records of barium currents evoked by step depolarization from −120 to 0 mV and +20 mV, for oocytes injected with cRNA encoding α 1 B+β3, while Panel B provides results for oocytes injected with cRNA encoding α 1 B+β3+α2δ-1, and Panel C provides results for oocytes injected with cRNA encoding α 1 B+β3+α 2 δ-2. Panel D provides mean current-voltage curves from two independent injections (mean±EM), with α 1 B+β3 (open circles), α 1 B+β3+α2δ-1 (filled triangles), and α 1 B+β3+α 2 δ-2 (filled circle) combinations. Panel E provides current-voltage relationships of α1C alone (filled circles) and α1C/α2δ-2 (circles) induced currents. Panel F provides current-voltage relationships of α1G (filled squares) and α1G/α2δ-2 (squares) induced currents. Panel G provides the average stimulation of α1C and α1G currents by co-expression with α 2 δ-2.

DEFINITIONS

To facilitate an understanding of the invention, a number of terms are defined below.

As used herein the term “portion” when made in reference to a nucleic acid sequence refers to a fragment of that sequence. The fragment may range in size from five (5) contiguous nucleotide residues to the entire nucleic acid sequence minus one nucleic acid residue. Thus, “a nucleic acid sequence comprising at least a portion of a nucleotide sequence” comprises from (5) contiguous nucleotide residues of the nucleotide sequence to the entire nucleotide sequence.

The term “portion” when used in reference to a protein (as in a “portion of a given protein”) refers to fragments of that protein. The fragments may range in size from four (4) contiguous amino acid residues to the entire amino acid sequence minus one amino acid residue. Thus, a polypeptide sequence comprising “at least a portion of an amino acid sequence” comprises from four (4) contiguous amino acid residues of the amino acid sequence to the entire amino acid sequence.

As used herein, the term “purified” or “to purify” refers to the removal of undesired components from a sample. For example, where recombinant α 2 δ polypeptides are expressed in eukaryotic host cells, the α 2 δ polypeptides are purified by the removal of host cell proteins thereby increasing the percent of recombinant α 2 δ polypeptides in the sample.

As used herein, the term “substantially purified” refers to molecules, either nucleic or amino acid sequences, that are removed from their natural environment such that they are at least 60% free, preferably 75% free, and more preferably 90% free from other components with which they are naturally associated.

The term “recombinant DNA molecule” as used herein refers to a DNA molecule which is comprised of segments of DNA joined together by means of molecular biological techniques. The term “recombinant protein” or “recombinant polypeptide” as used herein refers to a protein molecule which is expressed using a recombinant DNA molecule. A “recombinant calcium channel” protein refers to a calcium channel that contains one or more recombinant calcium channel subunits or one or more recombinant portions of at least one calcium channel subunit.

The term “oligonucleotide” as used herein is defined as a molecule containing from two (2) to one hundred (100), preferably from ten (10) to fifty (50), and more preferably from twenty (20) to thirty (30) deoxyribonucleotides or ribonucleotides. Oligonucleotides may be generated by several methods known in the art including, but not limited to, chemical synthesis, DNA replication, reverse transcription, restriction digestion, polymerase chain reaction, and the like.

The term “transfection” as used herein refers to the introduction of a transgene into a cell. The term “transgene” as used herein refers to any nucleic acid sequence which is introduced into the genome of a cell by experimental manipulations (e.g., using methods including, but not limited to recombinant cloning). A transgene may be an “endogenous DNA sequence,” or a “heterologous DNA sequence” (i.e., “foreign DNA”). The term “endogenous DNA sequence” refers to a nucleotide sequence which is naturally found in the cell into which it is introduced so long as it does not contain some modification (e.g., a point mutation, the presence of a selectable marker gene, etc.) relative to the naturally-occurring sequence. The term “heterologous DNA sequence” refers to a nucleotide sequence which is ligated to, or is manipulated to become ligated to, a nucleic acid sequence to which it is not ligated in nature, or to which it is ligated at a different location in nature. Heterologous DNA is not endogenous to the cell into which it is introduced, but has been obtained from another cell. Heterologous DNA also includes an endogenous DNA sequence which contains some modification. Generally, although not necessarily, heterologous DNA encodes RNA and proteins that are not normally produced by the cell into which it is expressed. Examples of heterologous DNA include reporter genes, transcriptional and translational regulatory sequences, selectable marker proteins (e.g., proteins which confer drug resistance), etc.

Transfection may be stable or transient. The term “stable transfection” or “stably transfected” refers to the introduction and integration of a transgene into the genome of the transfected cell. The term “stable transfectant” refers to a cell which has stably integrated one or more transgenes into the genomic DNA. The term “transient transfection” or “transiently transfected” refers to the introduction of one or more transgenes into a transfected cell in the absence of integration of the transgene into the host cell's genome. The term “transient transfectant” refers to a cell which has transiently integrated one or more transgenes.

The term “foreign gene” refers to any nucleic acid (e.g., gene sequence) which is introduced into the genome of an animal by experimental manipulations and may include gene sequences found in that animal so long as the introduced gene contains some modification (e.g., a point mutation, the presence of a selectable marker gene, etc.) relative to the naturally-occurring gene.

The term “gene” refers to a DNA sequence that comprises control and coding sequences necessary for the production of RNA or a polypeptide. The polypeptide can be encoded by a full length coding sequence or by any portion of the coding sequence.

The term “wild-type” refers to a gene or gene product which has the characteristics of that gene or gene product when isolated from a naturally occurring source. A wild-type gene is that which is most frequently observed in a population and is thus arbitrarily designated the “normal” or “wild-type” form of the gene. In contrast, the term “modified” or “mutant” refers to a gene or gene product which displays modifications in sequence and or functional properties (i.e., altered characteristics) when compared to the wild-type gene or gene product. It is noted that naturally-occurring mutants can be isolated; these are identified by the fact that they have altered characteristics when compared to the wild-type gene or gene product.

A “variant” of a nucleic acid sequence is defined as a nucleotide sequence which differs from the nucleic acid sequence (e.g., by having deletions, insertions, and substitutions) that may be detected using hybridization assays or sequencing.

A “variant” of a polypeptide sequence is defined as an amino acid sequence which differs by one or more amino acids from the polypeptide sequence. The variant may have “conservative” changes, wherein a substituted amino acid has similar structural or chemical properties (e.g., replacement of leucine with isoleucine). More rarely, a variant may have “non-conservative” changes (e.g., replacement of a glycine with a tryptophan). Similar minor variations may also include amino acid deletions or insertions (i.e., additions), or both. Guidance in determining which and how many amino acid residues may be substituted, inserted or deleted without abolishing biological or immunological activity may be found using computer programs well known in the art, for example, DNAStar software.

A nucleic acid sequence which is a “homolog” of a α 2 δ nucleic acids sequence (e.g., SEQ ID NOs: 1, 3, and 5) is defined herein as a nucleic acid sequence which exhibits more than 56%, more preferably at least 70%, and most preferably at least 95% identity to the α 2 δ nucleic acid sequence. Alternatively, a homolog of a α 2 δ nucleic acid sequence (e.g., SEQ ID NOs: 1, 3, and 5) is defined as a nucleic acid sequence which encodes a biologically active α 2 δ subunit polypeptide.

The term “substantially homologous” when used in reference to a double-stranded nucleic acid sequence such as a cDNA or genomic clone refers to any nucleic acid sequence which is capable of hybridizing to either or both strands of the double-stranded nucleic acid sequence of interest under conditions of low stringency.

Low stringency conditions when used in reference to nucleic acid hybridization comprise conditions equivalent to binding or hybridization at 42° C. in a solution consisting of 5×SSPE (43.8 g/l NaCl, 6.9 g/l NaH 2 PO 4 .H 2 O and 1.85 g/l EDTA, pH adjusted to 7.4 with NaOH), 0.1% SDS, 5×Denhardt's reagent [50×Denhardt's contains the following per 500 ml: 5 g Ficoll (Type 400, Pharmacia), 5 g BSA (Fraction V; Sigma)] and 100 μg/ml denatured salmon sperm DNA followed by washing in a solution comprising 5×SSPE, 0.1% SDS at 42° C. when a probe of about 500 nucleotides in length is employed.

High stringency conditions when used in reference to nucleic acid hybridization comprise conditions equivalent to binding or hybridization at 42° C. in a solution consisting of 5×SSPE (43.8 g/l NaCl, 6.9 g/l NaH 2 PO 4 .H 2 O and 1.85 g/l EDTA, pH adjusted to 7.4 with NaOH), 0.5% SDS, 5×Denhardt's reagent and 100 μg/ml denatured salmon sperm DNA followed by washing in a solution comprising 0.1×SSPE, 1.0% SDS at 42° C. when a probe of about 500 nucleotides in length is employed.

The term “equivalent” when made in reference to a hybridization condition as it relates to a hybridization condition of interest means that the hybridization condition and the hybridization condition of interest result in hybridization of nucleic acid sequences which have the same range of percent (%) homology. For example, if a hybridization condition of interest results in hybridization of a first nucleic acid sequence with other nucleic acid sequences that have from 50% to 70% homology to the first nucleic acid sequence, then another hybridization condition is the to be equivalent to the hybridization condition of interest if this other hybridization condition also results in hybridization of the first nucleic acid sequence with the other nucleic acid sequences that have from 50% to 70% homology to the first nucleic acid sequence.

When used in reference to nucleic acid hybridization the art knows well that numerous equivalent conditions may be employed to comprise either low or high stringency conditions; factors such as the length and nature (DNA, RNA, base composition) of the probe and nature of the target (DNA, RNA, base composition, present in solution or immobilized, etc.) and the concentration of the salts and other components (e.g., the presence or absence of formamide, dextran sulfate, polyethylene glycol) are considered and the hybridization solution may be varied to generate conditions of either low or high stringency hybridization different from, but equivalent to, the above listed conditions.

The term “hybridization” as used herein includes “any process by which a strand of nucleic acid joins with a complementary strand through base pairing.” (See e.g., J. Coombs, Dictionary of Biotechnology, Stockton Press, New York N.Y. [1994]). Hybridization and the strength of hybridization (i.e., the strength of the association between the nucleic acids) is impacted by such factors as the degree of complementarity between the nucleic acids, stringency of the conditions involved, the T m of the formed hybrid, and the G:C ratio within the nucleic acids.

The terms “alpha2delta,” “α 2 δ,” “alpha2delta subunit,” “α 2 δ subunit” when made in reference to a polypeptide sequence are used interchangeably to refer to a calcium channel subunit type. The α 2 δ subunit type comprises subunit subtypes, also referred to as subunit isoforms (e.g., isoforms I and II disclosed herein), which arise as a result of translation of splice variants of the primary transcript of the α 2 δ gene.

As used herein, a “splice variant” refers to an RNA sequence produced by processing of a primary transcript (i.e., pre-mRNA) of a genomic DNA sequence. Pre-mRNAs (also referred to as heterogenous nuclear RNA or hnRNA) in higher eukaryotes contain multiple introns which must be precisely excised by RNA splicing prior to transport over the nuclear membranae into the cytoplasm for translation. Differential processing of the primary transcript results in more than one RNA sequence, wherein each RNA sequence is referred to as a splice variant of the primary DNA transcript. Splice variants may occur within a single tissue type or among different tissues (e.g., neuronal tissue, muscle tissue, etc.) Splice variants which occur among different tissues are referred to as “tissue specific variants.”

The term “calcium channel selective ion” is an ion that is capable of entering, or of being blocked from entering, a cell through a calcium channel which spans a cellular membrane under conditions which would permit or block the entry of calcium ions (Ca ++ ) into the cell. Calcium channel selective ions are exemplified, but not limited to, Ca ++ (calcium ions) and Ba ++ (barium ions).

A “calcium channel” as used herein refers to a peptide sequence comprising at least alpha 1 (α 1 ) subunit. More preferably, a calcium channel further comprises alpha 2 (α 2 ), beta (β), gamma (γ) and delta (δ) subunits. The nucleic acid and amino acid sequences of calcium channel subunits in different organisms (e.g., human, rabbit, and rat) and in different tissues of the same organism (e.g., neuronal tissue, cardiovascular tissue) are known in the art (See e.g., Ellis et al., Science 241(4873):1661-4 [1988]; Williams et al., Neuron 8(1):71-84 [1992]; Ellis et al. U.S. Pat. No. 5,686,241 hereby incorporated by reference; and Harpold et al., U.S. Pat. No. 5,792,846 hereby incorporated by reference).

The terms “functional calcium channel” and “biologically active calcium channel” interchangeably refer to a calcium channel which allows entry into a cell of a calcium channel selective ion in response to a stimulus. Such entry may be determined by measuring the amount of current which flows through the calcium channel in response to the stimulus. Alternatively, a functional calcium channel refers to a calcium channel which binds ligands that have affinity for a calcium channel. For ligand binding assays of a recombinant calcium channel, it is preferred that the host cell which is used for testing the function of the recombinant calcium channel not produce endogenous calcium channel subunits that are of a type or in an amount that interferes with the detection of the recombinant calcium channel. Methods for determining the function of a calcium channel are known in the art, such as those described in Harpold et al., supra.

The terms “functional calcium channel subunit” and “biologically active calcium channel subunit” are equivalent terms which refer to a calcium channel subunit which is capable of associating with at least one other calcium channel subunit to form a functional calcium channel.

The term “compound that modulates calcium channel activity” and grammatical equivalents thereof refers to a compound that alters (i.e., reduces or increases) the ability of a calcium channel to pass calcium channel selective ions as measured by, for example, the current flowing through the calcium channel. Such compounds include, but are not limited to, calcium channel agonists (e.g., Goldin et al., U.S. Pat. No. 5,312,928, herein incorporated by reference) and antagonists, and compounds that exert their effect on the activity of the calcium channel directly or indirectly.

The term “agonist” refers to a molecule which, when interacting with a biologically active molecule, causes an enhancement in the activity of the biologically active molecule. Agonists may include proteins, nucleic acids, carbohydrates, or any other molecules which bind and/or interact with biologically active molecules. For example, an agonist can alter the activity of gene transcription by interacting with RNA polymerase directly, or through a transcription factor.

The terms “antagonist” or “inhibitor” refer to molecules which, when interacting with a biologically active molecule, block or inhibit the biological activity of the biologically active molecule. Antagonists and inhibitors may include proteins, nucleic acids, carbohydrates, or any other molecules which bind and/or interact with biologically active molecules. Inhibitors and antagonists can affect the biology of entire cells, organs, or organisms (e.g., an inhibitor that slows tumor growth).

The term “modulate” refers to a change or an alteration in the biological activity of a biologically active molecule. Modulation may be an increase or a decrease in activity, a change in binding characteristics, or any other change in the biological, functional, and/or immunological properties of biologically active molecules.

The term “biologically active” refers to molecules, compounds, etc., with structural, regulatory, and/or biochemical functions in an organism, cell, and/or organ.

A “non-human animal” refers to any animal which is not a human and includes vertebrates such as rodents, non-human primates, ovines, bovines, ruminants, lagomorphs, porcines, caprines, equines, canines, felines, aves, etc. Preferred non-human animals are selected from the order Rodentia.

The term “order Rodentia” refers to rodents (i.e., placental mammals in the Class Euthria, which also include the family Muridae (e.g., rats and mice)), most preferably mice.

A “transgenic animal” as used herein refers to an animal that includes a transgene which is inserted into an embryonal cell and which becomes integrated into the genome either of somatic and/or germ line cells of the animal which develops from that embryonal cell, or of an offspring of such an animal.

As used herein, the term “therapeutic” when made in reference to a compound refers to a compound which is capable of reducing, delaying, or eliminating one or more undesirable pathologic effects in a subject.

DESCRIPTION OF THE INVENTION

The invention provides nucleic acid sequences encoding calcium channel α 2 δ subunits. In particular, the invention provides cDNA sequences which are derived from splice variants of the calcium channel α 2 δ gene and which encode α 2 δ protein isoforms (e.g., isoforms I and II). Also provided herein are polypeptide sequences of calcium channel α 2 δ subunit isoforms. The compositions of the invention are useful in the detection, prevention and treatment of diseases such as cancer, autoimmune, cardiovascular, and neurological diseases. The compositions provided herein are also useful for the generation of in vitro and in vivo animal models for diseases (e.g., cancer, autoimmune, cardiovascular and neurological diseases) which in turn may be used to screen compounds for their therapeutic effects on these diseases.

The nucleic acids of the invention were discovered during a search by the inventors for a lung cancer and breast cancer tumor suppressor gene in the chromosome region 3p21.3, which the inventors considered to be one of the earliest regions undergoing genetic change in the smoking damaged bronchial epithelium and to thus to be associated with the development of lung and breast cancers. Furthermore, frequent allele loss and occasional homozygous deletions have been found in lung, breast, other human tumors (Wei et al., Cancer Res., 56(7):1487-1992 [1996]). As the lung cancer epidemic kills annually 150,000 victims in the USA, more deaths than due to colon, prostate, and breast cancer combined, much research has been conducted in the area of lung cancer diagnosis, prognosis, treatment, and prevention. The magnitude of this epidemic has heightened efforts to discover the genetic origin of lung cancer. While tobacco smoking is a well-established environmental trigger in lung carcinogenesis, the art's understanding of the genetic etiology of lung cancer is still incomplete.

Based on evidence from genetic mapping studies including overlapping homozygous deletions, it was the inventors' consideration that a tumor suppressor gene was located in the chromosome 3p21.3 band. To this end, the present inventors constructed a ˜700 kb long clone contig (i.e., a continuous sequence of DNA that has been assembled from overlapping cloned DNA fragments) covering the lung cancer region in 3p21.3 and isolated a number of genes residing on the contig (Wei et al., Cancer Res., 6(7):1487-92 [1996]). This 700 kb segment has been sequenced jointly by the Washington University Sequencing Center (Saint Louis, Mo.) and the Sanger Sequencing Centre (Hixton, UK) (See, web sites: http://www.sanger.ac.uk/ and http://genome.wustl.edu/gsc/gschmpg.html). The inventors used this sequence as a tool to detect and clone more genes from the region by in silico initiated methods. In addition, by discovering and mapping a new overlapping homozygous deletion in the region, the inventors narrowed the critical area to approximately 120 kb, thus limiting the search for the lung and breast cancer gene to a set of eight resident genes. One of these genes was identified by the inventors using bioinformatics methods as a new calcium channel α 2 δ subunit gene. It was surprising that the new calcium channel α 2 δ subunit gene was identified by the inventors to be located in a region of this contig that was different from the region which was reported in the art to contain the sought-after lung cancer tumor suppressor gene.

Importantly, the present inventors also discovered that expression of the α 2 δ subunit was shut off in a majority of lung cancer cells. This indicated to the inventors that an alteration in calcium homeostasis in cancer cells leads to malignancy. Sequence analysis of the α 2 δ gene and deduced protein identified this gene as a new calcium channel α 2 δ subunit gene.

The α 2 δ subunit gene disclosed herein is located in the lung cancer critical region on 3p21.3, is about 140 kb long, contains at least 37 exons, and encodes at least three differentially spliced mRNA isoforms of about 5.3-5.5 kb in length differing at their 5′ ends. Data disclosed herein reveals that, by Northern analysis, the α 2 δ subunits are highly expressed in lung and testis, moderately expressed in brain, heart, skeletal muscle, pancreas, small intestine, ovary, and spleen, with low levels of expression in kidney, and undetectable levels of expression in liver, thymus, and colon.

The tissue distribution of mRNA for the three α 2 δ subunits is very different (Klugbauer et al., J. Neurosci., 19(2):684-691 [1999]; and Angelotti and Hofmann, supra). All three genes are expressed in brain, which is the only tissue that expresses α 2 δ-3. The α 2 δ-1 gene is highly expressed in skeletal muscle, where little or no expression of α 2 δ-2 was found. Both α 2 δ-1 and -2 are expressed in heart. The α 2 δ-2 gene is highly expressed in lung where the expression of α 2 δ-1 is low. It is contemplated that the present invention will be used to determine which cells in the lung express α 2 δ-2. In fact, the present inventors have shown that several lung cancers representing different lung epithelial types can express α 2 δ-2. Thus, it is contemplated that some normal lung epithelial cells also express α 2 δ-2. In this regard, it is also interesting to note that α1C was cloned from lung cDNA libraries (Biel et al., FEBS Lett., 269(2):409-412 [1990]), and L-type currents have been characterized from tracheal smooth muscle (Welling et al,. Am. J. Physiol., 262(3 Pt 1):L351-359 [1992]). The only β subunit detected in lung mRNA is β 2 (Castellano and Perez-Reyes, Biochem. Soc. Trans., 22(2):483-488 [1994]). Therefore, the minimum subunit composition of lung L-type channels can be deduced as α1Cα 2 δ-2β 2 .

It was noted that the results obtained during the development of the present invention do not agree with those of Klugbauer et al. (Klugbauer et al., supra), who found abundant cross-reactive material from what they reported to be α 2 δ-2, in mRNA from skeletal muscle, pancreas, and heart, with hardly any signal from lung (Klugbauer et al., supra). It is believed that the expression pattern described herein is the correct one for α 2 δ-2, since the probes used for Northern blotting were derived from the whole coding region of α 2 δ-2, while authors of the Klugbauer report used only a 356 nucleotide probe from the coding region. In addition, the results of tissue expression pattern in independent Northern blot experiments were confirmed using two additional different short CACNA2D2 probes. The result of the cDNA screening also supports the high expression of α 2 δ-2 in lung, as 120 α 2 δ-2 clones were obtained from a screening of 1 million clones of a lung cDNA library. A possible explanation for the discrepancy could be that Klugbauer et al.'s probe cross-reacted with α 2 δ-1, since it has an expression pattern very similar to what they reported for α 2 δ-2 (Angelotti and Hofmann, FEBS Lett., 397(2-3):331-337 [1996]). Furthermore, it is unlikely that α 2 δ -2 is highly expressed in skeletal muscle, because α 2 δ proteins were purified from that tissue and only the sequence of α 2 δ-1 was detected (Ellis et al., Science 214(4873):1661-1663 [1988]).

The function of the gene product of the new α 2 δ-2 gene was tested in Xenopus oocytes by co-expressing α 2 δ-2 cRNAs along with a representative member of the three families of calcium subunit α1 subunits. In these experiments, three α1 subunits were investigated for their effect on currents. The α1 subunits were chosen to represent each of the three subfamilies of Ca 2+ channels: Ca v 1.2 or α1C, Ca v 2.2 or α1B, and an LVA channel Ca v 3.1 or α1G. In each case, α 2 δ-2 was able to stimulate functional expression. No effect was observed on the biophysical properties of the current, suggesting that α 2 δ-2 simply increased the number of functional channels at the plasma membrane. Similar results were obtained with α 2 δ-1 on the expression of α1G in both COS cells and Xenopus oocytes (Dolphin et al., J. Physiol., 519.1:35-45 [1999]). Surprisingly, a pattern of expression was identified that was different from the other α 2 δ subunit, and α 2 δ-2 was found to enhance the activity of the calcium α1 subunits.

Co-expression studies of α 2 δ-2 plus α1B also included the β 3 subunit. In these experiments, the largest stimulatory effect on expression was observed. Some studies have reported a synergistic action of α 2 and β on α1B expression (See e.g., Brust et al., Neuropharmacol., 32(11:1089-1102 [1993]). The experiments with α1C did not include a β subunit because they stimulate current so much already that it has been difficult to see any effect of α 2 δ at the whole cell level (Wei et al., J. Biol. Chem., 270(45):27106-27111 [1995]).

The invention discloses that the α 2 δ subunit gene is a candidate tumor suppressor gene which is involved in the origin of cancers (e.g., lung cancer, breast cancer, etc.). Indeed, interest in the physiological roles of Ca 2+ channels has increased, due to finding that mutations in their genes can lead to human diseases (Lehmann-Horn and Jurkatt-Roth, Physiol. Rev., 79:1317-1372 [1997]). In addition to potential role(s) in cancer pathogenesis, defects in the auxiliary subunits of Ca 2+ channels have been described in mouse models of absence epilepsy. These include mouse strains that have lost the expression of β 4 , and the recently discovered γ 2 subunit (Letts et al., Nat. Genet., 19:340-347 [1998]; and Burgess et al., Cell 88:385-392 [1997]). In this regard after CACNA2D2 was cloned, it was noted with great interest that the syntenic region in the mouse (mouse chromosome 9, 59.0-60.0 cM, http://www.informatics.jax.org/) contains the mouse mutant ducky and also 5 other flanking genes (CISH, GNAI2, GNAT, and HYAL1) that were identified in the ˜600 kb region (Wei et al., Cancer Res., 56(7):1487-1492 [1996]; and GenBank deposits AF132297 for CISH and U03056 for HYAL1). The partial mouse cDNA sequence was found to be 92% identical to the human α 2 δ-2 sequence (GenBank #AF169633.1). Indeed, preliminary evidence suggests that loss of α 2 δ-2 expression leads to the epileptic phenotype, ducky (Barclay et al., Epilepsia 40(Suppl. 2):137 [1990]). Histological examination of mouse ducky mutants reveals atrophy of the cerebellum, medulla oblongata, and spinal cord (Meier, Acta Neurol., 11:15-28 [1968]). These mice develop a spike-and-wave phenotype in the electroencephalogram, which is similar to that observed in absence epilepsy patients. Thus, it is contemplated that the present invention will find use in the development of methods to identify and test for the presence of inherited defects in CACNA2D2 in other species, including humans. It is also contemplated that the present invention will find use in assessing calcium channel defects associated with epileptic and other pathological phenotypes.

The invention further discloses that biallelic inactivation (i.e., inactivation of two alleles leading to complete loss-of-function) or monoallelic inactivation (i.e., inactivation of one allele leading to haploinsufficiency) of the α 2 δ subunit gene represents the critical rate-limiting step in the development of cancer. Thus, it is clear that the present inventors' discovery of a novel α 2 δ subunit of calcium channels provides compositions which are useful in the detection, prevention and treatment of cancer, as well as other diseases (e.g., epilepsy, migraine, episodic ataxia, stroke, brain trauma, Alzheimer's disease, multiinfarct dementia, Korsakoff's disease, amyotrophic lateral sclerosis, convulsions, seizures, Huntington's disease, amnesia, cardiac arrhythmia, angina pectoris, hypoxic damage to the cardiovascular system, ischemic damage to the cardiovascular system, myocardial infarction, congestive heart failure, muscular dystrophy, hypertension, etc.) which implicate calcium channels.

In addition, the present inventors have also discovered that the α 2 δ subunit gene is involved in lung carcinogenesis based on their observation of reduced levels of expression of the α 2 δ subunit gene in lung cancer (e.g., small cell lung cancer and non-small cell lung cancer) cell lines as compared to normal lung cells. The present inventors have also discovered that the α 2 δ subunit gene is implicated in breast carcinogenesis based on a homozygous deletion of the gene in a breast cancer cell line and in its primary tumor.

Furthermore, a clinical connection between voltage dependent calcium channels and lung cancer is well established by the Lambert-Eaton myasthenic syndrome (LEMS) seen in some small cell lung cancer patients (Takamori, Intern. Med., 38(2):86-96 [1999]). LEMS is a human autoimmune disorder that impairs neuromuscular transmission such that patients with this syndrome have a defect in the Ca 2+ dependent quantal release of acetylcholine from motor nerve terminals (O'Neill et all., Brain 111(Pt. 3):577-596 [1988]). In this syndrome, patients develop antibodies (presumably initiated by expression of the channel proteins in their small cell lung cancer) that react with voltage-gated calcium channel polypeptides which block depolarization-induced Ca 2+ influx leading to the myasthenia (Lennon et al., New Engl. J. Med., 332(22):146701474 [1995]; Raymond et al., Neurosci., 90(1):269-277 [1999]; and Voltz et al., Muscle Nerve 22(l):119-122 [1999]). During the development of the present invention the ability of α 2 δ-2 to functionally interact with the T-type channel subunit α1G was observed. In addition, Toyota et al. reported that CACNA1G encoding this subunit could have its expression inactivated by aberrant methylation of its 5′ CpG island in human tumors such as colorectal cancers, gastric cancers, and acute myelogenous leukemias (Toyota et al., Cancer Res., 59(18):4535-4541 [1999]). CACNA1G maps to chromosome region 17q21 another site of frequent allele loss in human cancer. Such acquired CpG island methylation in promoter regions of cancer cells as an acquired abnormality silencing genes such as tumor suppressor genes has been described (Baylin et al., Adv. Cancer Res., 72:141-196 [1998]; and Schmutte and Jones, Biol. Chem., 379(4-5):377-388 [1998]).

Furthermore, calcium influx via voltage-gated calcium channels including T-type channels and intracellular calcium signaling plays a role in apoptosis (Berridge et al., Nature 395(6703):645-648 [1998]). In addition, platelet derived growth factor stimulated calcium influx changed during transformation of mouse C3H 10T1/2 fibroblasts accompanied by a marked reduction in expression of T-type calcium channels (Estacion and Mordan, Cell Signal 9(5):363-366 [1997]). Thus, it is contemplated that the present invention will find use in investigations regarding the inactivation of voltage gated calcium channel subunits such as CACNA2D2 and CACNA1G by any of several means (e.g., in investigations pertaining to such areas as cancer pathogenesis)..

The invention is further described under (A) Calcium channel types and subtypes, (B) Using probes to identify and isolate DNA encoding α 2 δ calcium channel peptides, (C) Using primers to amplify splice variant RNAs encoding α 2 δ calcium channel peptides, (D) Using nucleic acid sequences for gene therapy, (E) Generation of calcium channel α 2 δ subunit peptides, (F) Generation of antibodies directed to α 2 δ calcium channel peptides, (G) Screening compounds that modulate the activity of α 2 δ calcium channel peptides, (H) in vitro and in vivo suppression of tumor cell growth, and (I) Generating transgenic animals expressing reduced levels of α 2 δ calcium channel peptides.

A. Calcium Channel Types and Subtypes

Living cells of all biological orders are uniquely equipped with an impressive number and variety of calcium channels and pumps that are involved in maintaining calcium homeostasis within cells, tissues, and whole organisms (McEnery (Ed) J. Bioenerg. Biomembr., 30(4): 297-418 [1998]). Changes in the concentration of intracellular calcium is the central focus of many signaling networks within cells that converge to bring about changes in gene expression in response to cellular and extracellular cues to control a diverse range of cell functions (McEnery, supra; and Walker and De Waard, Trends Neurosci., 21(4):148-54 [1998]). The transduction of these stimuli results in oscillations in the intracellular concentration of calcium ions assuming the form of spikes and waves that encode signal information in their frequency and amplitude (De Koninck and Schulman, Science 279(5348):227-30 [1998]). The passage of calcium ions across the plasma membrane generating these calcium fluxes is governed by a diverse group of calcium channels encoded by separate gene families (McEnery, supra; and Walker and De Waard, supra). These calcium channels have a very wide distribution of expression throughout brain, muscle and the endocrine system, as well as other tissues (McEnery, supra; Walker and De Waard, supra; De Koninck and Schulman, supra; Gurnett et al. Neuron 16(2):431-40 [1996]; and Miller, Trends Neurosci., 20(5):189-92 [1997]).

These channels are formed by heteromultimeric complexes of α1, α 2 δ, β, and γ subunits. Electrophysiological and molecular cloning studies have revealed an incredible diversity of voltage-gated calcium channels. Physically, the voltage-gated calcium channels are composed of five subunits each encoded by separate distinct gene families (Walker and De Waard, supra). The major alpha 1 (α 1 ) subunit which is encoded by at least 6 different genes is the pore-forming protein which interacts with other auxiliary subunits (i.e., alpha2 (α 2 ), beta (β), gamma (γ), and delta (δ)) to produce fully functional channels composed by unique combinations of distinct gene products. The auxiliary subunits (i.e., α 2 , β, γ and δ) with the exception of the gamma subunit significantly increase the functional expression of calcium currents. Like the alpha 1 subunit, the beta and gamma subunits are encoded by several genes; the beta subunit is encoded by 4 genes, while the gamma subunit is encoded by two genes.

The α1 subunits contain the channel pore, voltage sensors, and the receptors for various classes of drugs and toxins (Perez-Reyes and Schneider, Kidney Int'l., 48:1111-1124 [1995]). There are three families of α1 subunits: the L-type (or C v 1 family), composed of α1S, α1 C, (Ca v 1.2), α1D, and α1F; the non-L-type high voltage-activated (Ca v 2) family composed of P/Q-types encoded by α 1 A, the N-type is encoded by α1B (Ca v 2.2), and R-types encoded by α1E; and the T-type family (Ca v 3), encoded by α1G (Ca v 3.1), α1H, and α1I. Klugbauer et al. (Klugbauer et al., supra) cloned another related α 2 δ subunit (i.e., a subunit that is different from the present invention), then proposed the following nomenclature: α 2 δ-1, for the original α 2 δ cloned from skeletal muscle; α 2 δ-2 for the protein described herein, and α 2 δ-3 for their novel sequence. Similarly the genes may be referred to as CACNA2D1, CACNA2D2, and CACNA2D3, respectively (Lory et al., Hum. Genet., 100(2):149-150 [1997]). An α 2 δ-2 clone (KIAA0558, GenBank # AB011130, NP 006021.1) was recently independently isolated by the Kazusa DNA Research Institute from human brain as part of large scale anonymous cDNA sequencing efforts (Nagase et al., DNA Res., 5(1):31-39 [1998]).

Co-expression studies have established two physiological roles for β subunits in high voltage-activated (HVA) Ca 2+ channels, by dramatically increasing α1 expression at the plasma membrane and altering the biophysical properties of the channel currents. In general, β subunits have little effect on the expression of low voltage-activated (LVA) currents (See, Dolphin et al., J. Physiol., 519.1:35-45 [1999]). Although only one γ and α 2 δ subunit have been biochemically characterized, there is recent evidence to suggest that there may be additional members of these gene families (See e.g., Letts et al., Nature Genet., 19:340-347 [1998]; Black, Mayo Clin. Proc. 74(4):357-361 [1999]; and Klugbauer et al., supra). The γ1 subunit was shown to be part of the skeletal muscle L-type channel (Sharp and Campbell, J. Biol. Chem., 264(5):2816-2825 [1989]). In addition, co-expression studies have indicated that this subunit aids in the formation of L-type channels (assayed by dihydropyridine binding (Suh-Kim et al., Recept. Channels 4(4):217-225 [1996]), and may play a role in channel inactivation (Singer et al., Science 253(5027):1553-1557 [1991]).

The α 2 δ subunit (α 2 δ-1) was first identified in biochemical studies of skeletal muscle L-type Ca 2+ channels (See, Perez-Reyes and Schneider, Kidney Intl., 48:1111-1124 [1995]). Through the use of antibodies, it has also been shown to be part of the cardiac L-type and neuronal N-type channels (See, Schmid et al., Biochem., 25(12):3492-3495 [1986]; and McEnery et al., Proc. Natl. Acad. Sci. USA 88(24):11095-11099 [1991]). α 2 δ-1 cDNA has been cloned from skeletal muscle and brain cDNA libraries (Ellis et al., Science 241(4873):1661-1664 [1988]; De Jongh et al., J. Biol. Chem., 265(25):14738-14741 [1990]; and Williams et al., Neuron 8(1):71-84 [1992]). The 175 kDa protein product is post-translationally cleaved to form disulfide-linked α2 and δ peptides, both of which are heavily glycosylated. Biochemical and mutation analysis supports a single transmembrane domain in the δ subunit that anchors the α 2 δ protein to the membrane (Brown and Gee, J. Biol. Chem., 273(39):25458-25468 [1998]). Co-expression of α 2 δ-1 with both HVA and LVA α1 subunits facilitates the assembly of channels in the plasma membrane (Dolphin et al., J. Physiol., 519.1:35-45 [1999]; Suh-Kim et al., Recept. Channels 4(4):217-225 [1996]; and Burst et al., Neuropharmacol., 32(11):1089-1102 [1993]). Co-expression studies also indicate that α 2 δ-1 can alter the pharmacological properties of L-type channels. In contrast to the β subunits that have a dramatic effect on gating of all HVA channel in many expression systems, the effects of α 2 δ-1 are more controversial, perhaps depending on the α1 subunit used or the expression system. For example, α 2 δ-1 has little or no effect on either L-type (Wei et al., J. Biol. Chem., 279(45):27106-27111 [1995]; and Biel et al., FEBS Lett., 269(2):409-412 [1990]) or N-type currents expressed in Xenopus oocytes (Brust et al, Neuropharmacol., 32(110):1089-1102 [1993]), but appears to affect inactivation of L-type channels expressed in mammalian cells (Shirokov et al., J. Gen. Physiol., 111(6):807-823 [1998]; and Bangalore et al., Am. J. Physiol., 270(5 Pt. 2):H1521-1528 [1996]). The opposite result occurred in studies on α1E-mediated currents, where no effect was observed in mammalian cells (Jones et al., J. Gen. Physiol., 112(2):125-143 [1998]), ) and effects on channel inactivation were observed in Xenopus oocytes (Qin et al., J. Gen. Physiol., 274(5 Pt. 1 ):C1324-1331 [1998]). The α 2 δ-1 subunit has a high affinity binding site for the anti-epileptic drug gabapentin (Brown and Gee, J. Biol. Chem., 273(39):25458-25465 [1998]). Gabapentin has been shown to modestly inhibit (˜30%) neuronal Ca 2+ currents, although it is unclear if this is its mechanism of action (Stefani et al., Neuropharmacol., 37(1):83-91 [1998]). Nonetheless, it is not necessary to understand the mechanisms involved with calcium channels in order to use the present invention.

Recent studies that demonstrated the association of mutations in calcium channel genes (α1 and β genes) with inherited and acquired diseases further underlined the importance of calcium channels and have created a new field of research aimed at understanding and controlling these “channelopathies” (Miller, supra). Thus, efforts were made to obtain sequences of calcium channel subunit genes, such as the human (alpha 2 )-subunit gene (Ellis et al., Science 241(4873):1661-[1988]; Williams et al., Neuron, 8(1):71-84 [1992]; Ellis et al. U.S. Pat. No. 5,686,241; and Harpold et al., U.S. Pat. No. 5,792,846), and its murine (GenBank Accession ## U73483-U73487), rat (GenBank Accession # M86621), porcine (GenBank Accession # M21948), and rabbit orthologs (GenBank Accession # AF077665). The regulatory α 2 δ subunit (exemplified by the sequences disclosed herein) is of special importance since it plays a dual function in both current stimulation and subunit interaction by changing microscopic channel properties (Gurnett et al., supra).

B. Using Probes to Identify and Isolate DNA Encoding α 2 δ Calcium Channel Peptides

The present invention contemplates using a portion of the nucleic acid sequences set forth as SEQ ID NOs: 1, 3 and 5 as probes. As used herein, the term “probe” refers to an oligonucleotide, whether occurring naturally as in a purified restriction digest or produced synthetically, recombinantly or by PCR amplification, which is capable of hybridizing to another oligonucleotide of interest. A probe may be single-stranded or double-stranded. It is contemplated that any probe used in the present invention will be labelled with any “reporter molecule,” so that it is detectable in any detection system including, but not limited to enzyme (e.g., ELISA, as well as enzyme-based histochemical assays), fluorescent, radioactive, colorimetric, gravimetric, magnetic, and luminescent systems. It is not intended that the present invention be limited to any particular detection system or label.

The probes provided herein are useful in the detection, identification and isolation of, for example, α 2 δ subunit sequences such as those listed as SEQ ID NOs:1, 3 and 5 as well as of homologs thereof. Preferred probes are of sufficient length (e.g., from about 9 nucleotides to about 20 nucleotides or more in length) such that high stringency hybridization may be employed.

The probes provided herein are also useful in the detection, diagnosis and typing of preneoplasias and cancers. This utility is based on the inventors' observation that genetic disruption of the 3p21.3 region (in which the α 2 δ gene is located) is common in cancer (e.g., lung cancer and breast cancer) and preneoplastic lesion (e.g., hyperplasia, dysplasia, carcinoma in situ). This observation was based on the inventors' results using cells which represent clones of cells that contained 3p21.3 genetic lesions (compare Wistuba et al., J. Natl. Cancer Instit., 89:1366-1377 [1997]). It is also the inventors' consideration that genetic disruption of 3p21.3 which is associated with mutation or strand break of the α 2 δ gene leads to reduced expression of the α 2 δ gene and/or inactivation of the expressed α 2 δ subunit peptides. Furthermore, the present invention also contemplates methylation of the promoter region to inactivate its expression.

As used herein, the term “mutation” refers to a deletion, insertion, or substitution. A “deletion” is defined as a change in a nucleic acid sequence in which one or more nucleotides is absent. An “insertion” or “addition” is that change in a nucleic acid sequence which has resulted in the addition of one or more nucleotides. A “substitution” results from the replacement of one or more nucleotides by a molecule which is different molecule from the replaced one or more nucleotides. For example, a nucleic acid may be replaced by a different nucleic acid as exemplified by replacement of a thymine by a cytosine, adenine, guanine, or uridine. Alternatively, a nucleic acid may be replaced by a modified nucleic acid as exemplified by replacement of a thymine by thymine glycol. The term “strand break” when made in reference to a double stranded nucleic acid sequence includes a single-strand break and/or a double-strand break. A single-strand break refers to an interruption in one of the two strands of the double stranded nucleic acid sequence. This is in contrast to a double-strand break which refers to an interruption in both strands of the double stranded nucleic acid sequence.

Diagnosis and detection of cancer and/or preneoplastic lesions using the invention's probes involves the use of nucleic acid probes which hybridize with α 2 δ nucleotide sequences that are associated with cancer and/or preneoplastic lesion. These probes are used in hybridization assays (e.g., in situ hybridization) with nucleic acid sequences from cells suspected of cancerous and/or preneoplastic. Hybridization of the nucleic acid sequences with these probes indicates that the cells are cancerous and/or preneoplastic.

C. Using Primers to Amplify Splice Variant RNAs Encoding α 2 δ Calcium Channel Peptides

The invention also specifically contemplates using a portion of the nucleic acid sequences set forth as SEQ ID NOs:1, 3 and 5 as primers for the amplification of nucleic acid sequences by, for example, polymerase chain reactions (PCR) or reverse transcription-polymerase chain reactions (RT-PCR). Exemplary primers which are used to amplify exon sequences of the α 2 δ gene are illustrated in Tables 1 and 2 (Example 7, infra). The term “amplification” is defined as the production of additional copies of a nucleic acid sequence and is generally carried out using polymerase chain reaction technologies well known in the art (Dieffenbach and Dveksler, PCR Primer, a Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y. [1995]). As used herein, the term “polymerase chain reaction” (“PCR”) refers to the method of K. B. Mullis disclosed in U.S. Pat. Nos. 4,683,195, 4,683,202 and 4,965,188, all of which are hereby incorporated by reference, which describe a method for increasing the concentration of a segment of a target sequence in a mixture of genomic DNA without cloning or purification. This process for amplifying the target sequence consists of introducing a large excess of two oligonucleotide primers to the DNA mixture containing the desired target sequence, followed by a precise sequence of thermal cycling in the presence of a DNA polymerase. The two primers are complementary to their respective strands of the double stranded target sequence. To effect amplification, the mixture is denatured and the primers then annealed to their complementary sequences within the target molecule. Following annealing, the primers are extended with a polymerase so as to form a new pair of complementary strands. The steps of denaturation, primer annealing and polymerase extension can be repeated many times (i.e., denaturation, annealing and extension constitute one “cycle”; there can be numerous “cycles”) to obtain a high concentration of an amplified segment of the desired target sequence. The length of the amplified segment of the desired target sequence is determined by the relative positions of the primers with respect to each other, and therefore, this length is a controllable parameter. By virtue of the repeating aspect of the process, the method is referred to as the “polymerase chain reaction” (hereinafter “PCR”). Because the desired amplified segments of the target sequence become the predominant sequences (in terms of concentration) in the mixture, they are the to be “PCR amplified.”

With PCR, it is possible to amplify a single copy of a specific target sequence in genomic DNA to a level detectable by several different methodologies (e.g., hybridization with a labeled probe; incorporation of biotinylated primers followed by avidin-enzyme conjugate detection; and/or incorporation of 32 P-labeled deoxyribonucleotide triphosphates, such as dCTP or dATP, into the amplified segment). In addition to genomic DNA, any oligonucleotide sequence can be amplified with the appropriate set of primer molecules. In particular, the amplified segments created by the PCR process itself are, themselves, efficient templates for subsequent PCR amplifications. Amplified target sequences may be used to obtain segments of DNA (e.g., genes) for the construction of targeting vectors, transgenes, etc.

As used herein, the term “primer” refers to an oligonucleotide, whether occurring naturally as in a purified restriction digest or produced synthetically, which is capable of acting as a point of initiation of synthesis when placed under conditions in which synthesis of a primer extension product which is complementary to a nucleic acid strand is induced, (i.e., in the presence of nucleotides and an inducing agent such as DNA polymerase and at a suitable temperature and pH). The primer is preferably single stranded for maximum efficiency in amplification, but may alternatively be double stranded. If double stranded, the primer is first treated to separate its strands before being used to prepare extension products. Preferably, the primer is an oligodeoxyribonucleotide. The primer must be sufficiently long (e.g., from about 9 nucleotides to about 20 nucleotides or more in length) to prime the synthesis of extension products in the presence of the inducing agent. Suitable lengths of the primers may be empirically determined and depend on factors such as temperature, source of primer and the use of the method.

The primers contemplated by the invention are useful in, for example, identifying sequences which are homologous to the α 2 δ sequences in humans and in other species.

D. Using Nucleic Acid Sequences for Gene Therapy

The α 2 δ nucleic acid sequences provided herein may be used for gene therapy applications in both non-human animals as well as in humans.

Viral vectors commonly used for in vivo or ex vivo targeting and therapy procedures are DNA-based vectors and retroviral vectors. Methods for constructing and using viral vectors are known in the art (See e.g., Miller and Rosman, BioTechn., 7:980-990 [1992]). Preferably, the viral vectors are replication defective, that is, they are unable to replicate autonomously in the target cell. In general, the genome of the replication defective viral vectors that are used within the scope of the present invention lack at least one region that is necessary for the replication of the virus in the infected cell. These regions can either be eliminated (in whole or in part), be rendered non-functional by any technique known to a person skilled in the art. These techniques include the total removal, substitution (by other sequences, in particular by the inserted nucleic acid), partial deletion or addition of one or more bases to an essential (for replication) region. Such techniques may be performed in vitro (i.e., on the isolated DNA) or in situ, using the techniques of genetic manipulation or by treatment with mutagenic agents.

Preferably, the replication defective virus retains the sequences of its genome that are necessary for encapsidating the viral particles. DNA viral vectors include an attenuated or defective DNA virus, including, but not limited to, herpes simplex virus (HSV), papillomavirus, Epstein Barr virus (EBV), adenovirus, adeno-associated virus (AAV), and the like. Defective viruses, that entirely or almost entirely lack viral genes, are preferred, as defective virus is not infective after introduction into a cell. Use of defective viral vectors allows for administration to cells in a specific, localized area, without concern that the vector can infect other cells. Thus, a specific tissue can be specifically targeted. Examples of particular vectors include, but are not limited to, a defective herpes virus 1 (HSV1) vector (Kaplitt et al., Mol. Cell. Neurosci., 2:320-330 [1991]), defective herpes virus vector lacking a glycoprotein L gene (See e.g., Patent Publication RD 371005 A), or other defective herpes virus vectors (See e.g., WO 94/21807; and WO 92/05263); an attenuated adenovirus vector, such as the vector described by Stratford-Perricaudet et al. (Stratford-Perricaudet et al., J. Clin. Invest., 90:626-630 [1992]; See also, La Salle et al., Science 259:988-990 [1993]); and a defective adeno-associated virus vector (Samulski et al., J. Virol., 61:3096-3101 [1987]; Samulski et al., J. Virol. 63:3822-3828 [1989]; and Lebkowski et al., Mol. Cell. Biol., 8:3988-3996 [1988]).

Preferably, for in vivo administration, an appropriate immunosuppressive treatment is employed in conjunction with the viral vector (e.g., adenovirus vector), to avoid immunodeactivation of the viral vector and transfected cells. For example, immunosuppressive cytokines, such as interleukin- 12 (IL-12),interferon-gamma (IFN-γ), or anti-CD4 antibody, can be administered to block humoral or cellular immune responses to the viral vectors. In addition, it is advantageous to employ a viral vector that is engineered to express a minimal number of antigens. Other molecules are also useful for facilitating transfection of a nucleic acid in vivo, such as a cationic oligopeptide (e.g., WO95/21931), peptides derived from DNA binding proteins (e.g., WO96/25508), or a cationic polymer (e.g., WO95/21931).

It is also possible to introduce the vector in vivo as a naked DNA plasmid. Methods for formulating and administering naked DNA to mammalian muscle tissue are disclosed in U.S. Pat. Nos. 5,580,859 and 5,589,466, both of which are herein incorporated by reference.

DNA vectors for gene therapy can be introduced into the desired host cells by methods known in the art, including but not limited to transfection, electroporation, microinjection, transduction, cell fusion, DEAE dextran, calcium phosphate precipitation, use of a gene gun, or use of a DNA vector transporter (See e.g., Wu et al., J. Biol. Chem., 267:963-967 [1992]; Wu and Wu, J. Biol. Chem., 263:14621-14624 [1988]; and Williams et al., Proc. Natl. Acad. Sci. U.S.A., 88:2726-2730 [1991]). Receptor-mediated DNA delivery approaches can also be used (Curiel et al., Hum. Gene Ther., 3:147-154 [1992]; and Wu and Wu, J. Biol. Chem., 262:4429-4432 [1987]).

For example, the nucleic acids provided herein may be introduced into cancer or preneoplastic cells using an expression vector which encodes a α 2 δ subunit protein using a variety of means known in the art to be useful both for delivery in vivo and ex vivo, including (1) retroviral transduction, (2) recombinant adenoviral vectors, (3) recombinant adeno-associated vectors, (4) targeted cationic liposomes, and (5) gene transfer using biolistics, as described in the following sections.

1. Retroviral Transduction

In one embodiment, the gene can be introduced in a retroviral vector (e.g., as described in U.S. Pat. Nos. 5,399,346, 4,650,764, 4,980,289 and 5,124,263; all of which are herein incorporated by reference; Mann et al., Cell 33:153 [1983]; Markowitz et al., J. Virol., 62:1120 [1988]; PCT/US95/14575; EP 453242; EP178220; Bernstein et al. Genet. Eng., 7:235 [1985]; McCormick, BioTechnol., 3:689 [1985]; WO 95/07358; and Kuo et al., Blood 82:845 [1993]). The retroviruses are integrating viruses that infect dividing cells. The retrovirus genome includes two LTRs, an encapsidation sequence and three coding regions (gag, pol and env). In recombinant retroviral vectors, the gag, pol and env genes are generally deleted, in whole or in part, and replaced with a heterologous nucleic acid sequence of interest. These vectors can be constructed from different types of retrovirus, such as, HIV, MoMuLV (“murine Moloney leukaemia virus” MSV (“murine Moloney sarcoma virus”), HaSV (“Harvey sarcoma virus”); SNV (“spleen necrosis virus”); RSV (“Rous sarcoma virus”) and Friend virus. Defective retroviral vectors are disclosed in WO95/02697.

In general, in order to construct recombinant retroviruses containing a nucleic acid sequence, a plasmid is constructed that contains the LTRs, the encapsidation sequence and the coding sequence. This construct is used to transfect a packaging cell line, which cell line is able to supply in trans the retroviral functions that are deficient in the plasmid. In general, the packaging cell lines are thus able to express the gag, pol and env genes. Such packaging cell lines have been described in the prior art, in particular the cell line PA317 (U.S. Pat. No. 4,861,719, herein incorporated by reference); the PsiCRIP cell line (See, WO90/02806), and the GP+envAm-12 cell line (See, WO89/07150). In addition, the recombinant retroviral vectors can contain modifications within the LTRs for suppressing transcriptional activity as well as extensive encapsidation sequences that may include a part of the gag gene (Bender et al., J. Virol., 61:1639 [1987]). Recombinant retroviral vectors are purified by standard techniques known to those having ordinary skill in the art.

Retroviral vectors encoding α 2 δ subunit proteins may be used for the expression of α 2 δ subunit proteins in established or primary tumor cells. The transfer of α 2 δ genes encoding subunit proteins using retroviruses may be made more efficient by increasing the titer of the virus encoding the α 2 δ subunit proteins and increasing the transduction efficiency. To increase the virus titer, the retroviral construct may be designed to include a selectable marker (e.g., neo gene), and cells harboring the retroviral construct are selected by growth in the presence of a suitable selective agent (e.g., G418) followed by expansion of clones producing the highest titers of virus. To improve the transduction efficiency, retrovirus are used in combination with liposomes or poly-L-ornithine or polylysine to enhance virus uptake.

Another way to improve gene transfer efficiency using retroviruses is to increase the targeting efficiency. Many tumor cells including glioblastomas and melanomas express excess levels of the transferrin receptor. Transferrin has been used to increase the transduction efficiency of adenovirus in combination with polylysine. Several recent reports demonstrated that replacing the SU (surface) domain of the env gene of a retrovirus can increase receptor-mediated transduction efficiency. The human transferrin gene is 2097 bp long and its insertion into the SU domain of the env gene of MLV vector may not produce a stable Env product. However, since earlier studies have suggested that the modified Env fusion protein requires the native Env for stable assembly and efficient entry, co-transfection of the transferrin-env fusion gene with the native env gene may be used to produce retrovirus particles bearing a mixture of wild type and recombinant Env. The gene transfer efficiency of the new vector may be examined by transducing tumor cells expressing high levels of transferrin receptor.

2. Recombinant Adenoviral Vectors

In an alternative embodiment, the vector is an adenovirus vector. Adenoviruses are eukaryotic DNA viruses that can be modified to efficiently deliver a nucleic acid of the invention to a variety of cell types. Various serotypes of adenovirus exist. Of these serotypes, preference is given in one alternative embodiment, within the scope of the present invention, to type 2 or type 5 human adenoviruses (Ad 2 or Ad 5), or adenoviruses of animal origin (See, WO94/26914). Those adenoviruses of animal origin that can be used within the scope of the present invention include adenoviruses of canine, bovine, murine (e.g., Mavl, Beard et al., Virol., 75-81 [1990]), ovine, porcine, avian, and simian (e.g., SAV) origin. Preferably, the adenovirus of animal origin is a canine adenovirus, more preferably a CAV2 adenovirus (e.g. Manhattan or A26/61 strain (ATCC VR-800)). Recombinant adenoviruses can accommodate relatively large segments of foreign DNA (˜7 kb), and have the advantage of a broad host cell range and high titer virus production. Adenoviruses have been used in vivo in rats to efficiently deliver genes to the liver and the pancreatic islets (reviewed in Becker et al., In Protein Expression in Animal Cells, Roth et al. (eds.) [1994]) and to the central nervous system (Davidson et al., Nature Genet., 3:219 [1993]). Rat livers have also been efficiently transduced ex vivo and then re-implanted (Shaked et al., Transplant., 57:1508 [1994]).

Preferably, the replication defective adenoviral vectors of the invention comprise the ITRs, an encapsidation sequence and the nucleic acid of interest. Still more preferably, at least the El region of the adenoviral vector is non-functional. The deletion in the El region preferably extends from nucleotides 455 to 3329 in the sequence of the Ad5 adenovirus (PvuII-BglII fragment) or 382 to 3446 (HinfII-Sau3A fragment). Other regions may also be modified, in particular the E3 region (e.g., WO95/02697), the E2 region (e.g., WO94/28938), the E4 region (e.g., WO94/28152, WO94/12649 and WO95/02697), or in any of the late genes L1-L5.

In a preferred embodiment, the adenoviral vector has a deletion in the E1 region (Ad 1.0). The replication defective recombinant adenoviruses are preferably employed; in some embodiments, these viruses contain a deletion of the key immediate early genes E1a and E1b. To generate and propagate recombinant viruses, a packaging cell line such as 293 cells which supply the E1a and E2a proteins in trans is employed. Examples of E1-deleted adenoviruses are disclosed in EP 185,573, the contents of which are incorporated herein by reference. In another preferred embodiment, the adenoviral vector has a deletion in the E1 and E4 regions (Ad 3.0). Examples of E1/E4-deleted adenoviruses are disclosed in WO95/02697 and WO96/22378. In still another preferred embodiment, the adenoviral vector has a deletion in the E1 region into which the E4 region and the nucleic acid sequence are inserted.

The replication defective recombinant adenoviruses according to the invention can be prepared by any technique known to the person skilled in the art (See e.g., Levrero et al., Gene 101:195 [1991]; EP 185 573; and Graham, EMBO J., 3:2917 [1984]). In particular, they can be prepared by homologous recombination between an adenovirus and a plasmid which carries, inter alia, the DNA sequence of interest. The homologous recombination is effected following co-transfection of the adenovirus and plasmid into an appropriate cell line. The cell line that is employed should preferably (i) be transformable by the elements, and (ii) contain the sequences that are able to complement the part of the genome of the replication defective adenovirus, preferably in integrated form in order to avoid the risks of recombination. Examples of cell lines that may be used are the human embryonic kidney cell line 293 (Graham et al., J. Gen. Virol., 36:59 [1977]), which contains the left-hand portion of the genome of an Ad5 adenovirus (12%) integrated into its genome, and cell lines that are able to complement the E1 and E4 functions, as described in applications WO94/26914 and WO95/02697. Recombinant adenoviruses are recovered and purified using standard molecular biological techniques, that are well known to one of ordinary skill in the art.

In particular, recombinant adenoviruses are created by making use of intracellular recombination between a much larger plasmid encoding most of the viral genome and a small plasmid containing the gene of interest (i.e., a gene encoding a α 2 δ subunit protein) flanked by regions of homology with the viral integration site. Standard methods may be used to construct the recombinant adenoviruses (Graham and Prevec, Meth. Mol. Biol., 7:109-128 [1991]; and Becker et al., supra). Briefly, each plasmid is co-transfected together with pJM17 (Microbix Systems, Toronto) into sub-confluent monolayers of 293 cells (ATCC CRL 1573) using calcium phosphate precipitation and a glycerol shock. Initial recombinant viral stocks are titered on monolayers of 293 cells, and isolated single plaques are obtained and tested for α 2 δ subunit protein expression using ELISA. Viral stocks are amplified and titered on 293 cells, and stored in aliquots at −70° C.; if necessary, stocks are concentrated by centrifugation on density gradients. To infect tumor cells with recombinant adenoviruses, freshly isolated tumor cells are mixed with adenoviral stocks in a minimal volume. Titers of stocks are typically 10 5 -10 8 /ml. Medium is replaced after several hours and the cells are followed for expression of the recombinant adenoviral-encoded α 2 δ subunit proteins and/or reporter genes.

A potential drawback of using an adenoviral delivery system is that the transduced cells may retain or express small quantities of adenoviral antigens on their surface. “Second generation” adenoviral vectors which contain deletions in the E2a gene are available and are associated with less inflammation in the recipient and a longer period of expression of the gene of interest (Engelhardt et al., Proc. Natl. Acad. Sci. USA 91:6196 [1994]). If necessary, nucleic acid sequences encoding α 2 δ subunit proteins are inserted into second generation adenoviral vectors.

3. Adeno-Associated Viral Vectors

In a further alternative embodiment, the vector is an adeno-associated virus (AAV) vector. The adeno-associated viruses (AAV) are DNA viruses of relatively small size that can integrate, in a stable and site-specific manner, into the genome of the cells that they infect. They are able to infect a wide spectrum of cells without inducing any effects on cellular growth, morphology or differentiation, and they do not appear to be involved in human pathologies. The AAV genome has been cloned, sequenced and characterized. It encompasses approximately 4700 bases and contains an inverted terminal repeat (ITR) region of approximately 145 bases at each end, which serves as an origin of replication for the virus. The remainder of the genome is divided into two essential regions that carry the encapsidation functions: the left-hand part of the genome, that contains the rep gene involved in viral replication and expression of the viral genes; and the right-hand part of the genome, that contains the cap gene encoding the capsid proteins of the virus.

The use of vectors derived from the AAVs for transferring genes in vitro and in vivo has been described (See e.g., WO 91/18088; WO 93/09239; U.S. Pat. Nos. 4,797,368; 5,139,941; 5,843,742; and EP 488 528; See also, Hermonat et al., Proc. Natl. Acad. Sci. USA 81:6466-6470 [1984]; Chiorini et al., J. Virol., 71:6823-6833 [1997]; and Chorini et al., J. Virol., 73:1309-1319 [1999]; each of which is incorporated by reference). These publications describe various AAV-derived constructs in which the rep and/or cap genes are deleted and replaced by a gene of interest, and the use of these constructs for transferring the gene of interest in vitro (into cultured cells) or in vivo, (directly into an organism). The replication defective recombinant AAVs according to the invention can be prepared by co-transfecting a plasmid containing the nucleic acid sequence of interest flanked by two AAV inverted terminal repeat (ITR) regions, and a plasmid carrying the AAV encapsidation genes (rep and cap genes), into a cell line that is infected with a human helper virus (for example an adenovirus). The AAV recombinants that are produced are then purified by standard techniques.

4. Targeted Cationic Liposomes

Alternatively, the vector can be introduced in vivo by lipofection. For the past decade, there has been increasing use of liposomes for encapsulation and transfection of nucleic acids in vitro. Furthermore, synthetic cationic lipids designed to limit the difficulties and dangers encountered with liposome mediated transfection can be used to prepare liposomes for in vivo transfection of a gene encoding a marker (Felgner et. al., Proc. Natl. Acad. Sci. U.S.A., 84:7413-7417 [1987]; See also, Mackey, et al., Proc. Natl. Acad. Sci. U.S.A., 85:8027-8031 [1988]; and Ulmer et al., Science 259:1745-1748 [1993]). The use of cationic lipids may promote encapsulation of negatively charged nucleic acids, and also promote fusion with negatively charged cell membranes (Felgner and Ringold, Science 337:387-388 [1989]). Particularly useful lipid compounds and compositions for transfer of nucleic acids are described in WO95/18863 and WO96/17823, and in U.S. Pat. No. 5,459,127, herein incorporated by reference.

Cationic liposomes have proven to be a safe and effective means for inducing the transient expression of DNA in target cells [Ledley, Hum. Gene Ther., 6:1129 [1995]; Felgner, Adv. Drug Del. Rev., 5:167 [1990]; Felgner et al. Proc. Natl. Acad. Sci. USA 84:7413 [1987]; and Smith et al., Biochim. Biophys. Acta 1154:327 [1993]). Clinical trials are underway using cationic liposomes to introduce the CFTR gene into the lungs of cystic fibrosis patients (Caplen et al., Gene Ther. 1:139 [1994]; and Alton et al., Nature Genet., 5:135 [1993]) or to introduce, by direct intra-tumor injection, the T cell costimulator B7-1 into malignant melanoma lesions in order to induce a cell-mediated immune response (Nabel et al., Proc. Natl. Acad. Sci. USA 90:11307 [1993]).

Cationic liposomes (e.g., DOTAP/DOPE) and ligand-targeted cationic liposomes may be employed for the delivery of α 2 δ subunit proteins to tumor cells. Ligand-targeted liposomes are made by covalently attaching ligands or antibodies to the surface of the cationic liposome. For example, when glioblastoma cells are to be targeted, transferrin is used as the ligand as glioblastoma cells express high levels of the transferrin receptor on their surface. When melanoma cells are to be targeted, internalizing receptors, monoclonal antibodies directed against melanoma-specific surface antigens (e.g., mAb HMSA5) may be employed as the ligand.

Plasmid DNA encoding α 2 δ subunit proteins is formed into a complex with preformed cationic liposomes using standard methodology or alternatively the DNA is encapsulated into the liposome interior. The DNA-containing liposomes are then used to transfer the DNA to tumor cells in vivo by direct intra-tumor injection or in vitro (using freshly explanted tumor cells) followed by return of the transduced cells to the recipient (e.g., a human patient or non-human animal).

5. Gene Transfer Using Biolistics

Biolistics (microballistics) is a method of delivering DNA into cells by projection of DNA-coated particles into cells or tissues. DNA is coated onto the surface of gold or tungsten microparticles (˜1-3 μm diameter) and these particles are accelerated to high velocity and are impacted onto the target cells. The particles burst through the cell membrane and lodge within the target cell. The cell membrane quickly reseals and the passenger DNA elutes off of the particle and is expressed. The biolistic method has been used to transfect mammalian cells (Williams et al., Proc. Natl. Acad. Sci. USA 88:2726 [1991]; Tang et al., Nature 356:152 [1992]; and Sanford et al., Meth. Enzymol., 217:483 [1993]).

A hand-held biolistic apparatus (BioRad) is used to transfer DNA into tumor cells or isolated tumor fragments. This device uses compressed helium to drive a disc-shaped macroprojectile which carries on its surface microparticles (1-5 μm) of gold which have been coated with purified plasmid DNA (coprecipitated with spermine) (Williams et al., supra). This apparatus has been used to successfully transfect primary tissues.

Plasmid DNA encoding the α 2 δ subunit proteins may be coated onto the surface of gold microparticles according to the manufacturer's instructions (BioRad) and the biolistic apparatus is used to transfer the DNA into freshly explanted tumor cells or directly into exposed tumors (e.g., metastatic nodules on the surface of the liver, melanoma lesions on the skin).

Regardless of the method of delivery of the expression vector into a cell, it is preferred, though not required, that the expression vector contain a selection marker (e.g., neo gene) to facilitate selection of transfected cells. Transfected cells are selected by growth in the presence of G418 (e.g., 200 μg/ml), followed by culture in growth medium containing reduced concentrations of G418 (e.g., 100 μg/ml) and growth to confluence. Expression of the α 2 δ subunit protein is evaluated using, for example, immunoblot analysis or flow cytometry using monoclonal antibodies which are specific for the α 2 δ subunit protein. It is preferred, though not necessary, that expression of the α 2 δ subunit protein in the transfected tumor cells is both constitutive and stable. Constitutive expression refers to expression in the absence of a triggering event or condition, and can be achieved by the selection of a promoter which drives expression of the nucleic acid sequence encoding the α 2 δ subunit protein. Examples of promoters which drive constitutive expression of a structural nucleic acid sequence which is operably linked to the promoter include the SRα promoter, CMV promoter, and HIV promoter.

Regardless of the type of expression vector used for delivery of the α 2 δ nucleic acid sequences into a cell, the expression vector may be introduced to the cell by direct injection into tumor and/or preneoplastic tissue, systemic (e.g., intravenous) administration, aerosol administration (e.g., for delivery to the bronchial tree and other lung tissues), injection into breast ducts (e.g., for delivery to breast tissue), topical administration (e.g., for delivery to cervical tissue). It is expected that the α 2 δ nucleic acids of the invention would function as a tumor suppressor. Tumor suppressor function may be determined by (for example) reduction in the size of tumors which are detectable at the time of administration of the expression vectors containing α 2 δ nucleic acid sequences as compared to the size of the tumors prior to such administration. Alternatively, where the expression vectors containing α 2 δ nucleic acid sequences are introduced to preneoplastic cells, tumor suppressor function may be determined by lack of progression of the preneoplastic cells to cancer cells over time.

E. Generation of Calcium Channel α 2 δ Subunit Peptides

The present invention provides the polypeptide sequences of isoform I (SEQ ID NOs:2 and 4) and isoform II (SEQ ID NO:6) of the human calcium channel α 2 δ subunit and specifically contemplates portions and variants thereof. For example, α 2 δ subunit variants included within the scope of this invention include α 2 δ subunit polypeptide sequences containing deletions, insertions or substitutions of amino acid residues which result in a polypeptide that is functionally equivalent to the α 2 δ subunit polypeptide isoforms. By the term “functionally equivalent to the α 2 δ subunit polypeptide isoforms” is meant that a polypeptide is capable of associating with at least an α 1 subunit (preferably with α 1 and β subunits, and more preferably with α 1 , β and γ subunits) to produce a functional calcium channel. For example, amino acids may be substituted for other amino acids having similar characteristics of polarity, charge, solubility, hydrophobicity, hydrophilicity and/or amphipathic nature. Alternatively, substitution of amino acids with other amino acids having one or more different characteristic may be desirable for the purpose of producing a polypeptide which is secreted from the cell in order to, for example, simplify purification of the polypeptide.

The α 2 δ subunit isoform I and II polypeptide sequences and their functional variants may be made using chemical synthesis. For example, peptide synthesis of the α 2 δ subunit polypeptide, in whole or in part, can be performed using solid-phase techniques well known in the art. Synthesized polypeptides can be substantially purified by high performance liquid chromatography (HPLC) techniques, and the composition of the purified polypeptide confirmed by amino acid sequencing. One skilled in the art would recognize that variants of the α 2 δ subunit isoform I and II polypeptides can be produced by manipulating the polypeptide sequence during and/or after its synthesis.

The α 2 δ subunit and its functional variants can also be produced by an expression system. Expression of α 2 δ subunit isoform I and II polypeptides may be accomplished by inserting nucleotide sequences which encode these polypeptides (or variants, portions, or homologs of the nucleotide sequences) into appropriate vectors to create expression vectors, and transfecting the expression vectors into host cells. The term “expression vector” as used herein refers to a recombinant DNA molecule containing a desired coding sequence and appropriate nucleic acid sequences necessary for the expression of the operably linked coding sequence in a particular host organism. Nucleic acid sequences necessary for expression in prokaryotes include a promoter, optionally an operator sequence, a ribosome binding site and possibly other sequences. Eukaryotic cells are known to utilize promoters, enhancers, and termination and polyadenylation signals. Expression in insect cells (e.g., Spodoptera) using insect vectors (e.g., baculovirus) is also contemplated to be within the scope of the invention.

The scope of this invention further encompasses amino acid sequences of the α 2 δ polypeptides ligated to one or more amino acid sequences as part of a fusion protein. Such fusion proteins may be desirable, for example, to detect expression of the α 2 δ polypeptides. Examples of amino acid sequences which may be used as fusion partners include β-galactosidase, luciferase, green fluorescent protein, Myc protein tags, FLAG tags, and chloramphenicol acetyltransferase. Fusion proteins may also be desirable to facilitate purification of the expressed α 2 δ polypeptides. For example, the heterologous sequence of protein A allows purification of the fusion protein on immobilized immunoglobulin. Other affinity traps are well known in the art and can be utilized to advantage in purifying the expressed fusion protein. For example, pGEX vectors (Promega, Madison Wis.) may be used to express the α 2 δ polypeptides as a fusion protein with glutathione S-transferase (GST). In general, such fusion proteins are soluble and can easily be purified from lysed cells by adsorption to glutathione-agarose beads followed by elution in the presence of free glutathione. Proteins made in such systems are designed to include heparin, thrombin or factor XA protease cleavage sites so that the cloned polypeptide of interest can be released from the GST moiety at will.

While the invention discloses cloning of the sequences of the invention in the CMV expression vector pcDNA3.1 His C (Invitrogen), the adenovirus shuttle vector pLJ17 (pAdE1/CMV), and the retrovirus tetracycline regulatable vectors pRev-TRE vector (Clontech) (Example 8), and in the pETE vector (Example 9), other expression vectors are expressly contemplated to be within the scope of the invention. Expression vectors are exemplified by plasmids, recombinant bacteriophage, cosmid DNA vectors, viruses and the like. Expression vectors can be constructed using techniques well known in the art (Sambrook et al., Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Press, Plainview N.Y. [1989]; and Ausubel et al., Current Protocols in Molecular Biology, John Wiley & Sons, New York N.Y. [1989]). Briefly, the nucleic acid sequence of interest is placed in operable combination with transcription and translation regulatory sequences. The term “in operable combination” as used herein refers to the linkage of nucleic acid sequences in such a manner that a nucleic acid molecule capable of directing the transcription of a given gene and/or the synthesis of a desired protein molecule is produced. The term also refers to the linkage of amino acid sequences in such a manner so that a functional protein is produced. Regulatory sequences include initiation signals such as start (i.e., ATG) and stop codons, promoters which may be constitutive (i.e., continuously active) or inducible, as well as enhancers to increase the efficiency of expression, and transcription termination signals. Transcription termination signals must be provided downstream from the structural gene if the termination signals of the structural gene are not included in the expression vector. Expression vectors may become integrated into the genome of the host cell into which they are introduced, or are present as unintegrated episomal vectors. Typically, unintegrated nonepisomal vectors are transiently expressed and regulated for several hours (e.g., 72 hours) after transfection.

The choice of promoter is governed by the type of host cell to be transfected with the expression vector. Host cells include, but are not limited to eukaryotic cells, prokaryotic cells, insect cells, etc. In one embodiment the cell is eukaryotic. In a more preferred embodiment, the eukaryotic cell is a cancer cell. Other eukaryotic cells are expressly contemplated (e.g., COS cells, mouse L cells, Chinese hamster ovary cells, human embryonic kidney cells, and African green monkey cells). In an alternative preferred embodiment, the eukaryotic cell is an amphibian oocyte. In a more preferred embodiment, the amphibian oocyte is a frog oocyte.

Transfected cells may be identified by any of a number of marker genes. These include antibiotic (e.g., neomycin, puromycin, hygromycin for eukaryotic cells, and gentamicin, penicillin, and kanamycin for prokaryotic cells) resistance genes as well as marker or reporter genes (e.g., β-galactosidase, luciferase, green fluorescent protein, and Myc protein tags) which catalyze the synthesis of a visible reaction product.

Vectors may be introduced into a host cell using a number of standard and routine methods known to those skilled in the art (See e.g., Sambrook, et al., supra) including, but not limited to, microinjection, DEAE-dextran, calcium phosphate co-precipitation, cell fusion, electroporation, biolistics, lipofection, DNA viruses, and RNA viruses, or retrovirus-mediated transduction.

Expression of the α 2 δ nucleic acid sequences provided herein by transfected cells may be detected either indirectly using reporter genes, or directly by detecting mRNA or protein encoded by the α 2 δ nucleic acid sequences. Indirect detection of expression may be achieved by placing a reporter gene in tandem with the nucleic acid sequence encoding α 2 δ subunits under the control of a single promoter. Expression of the reporter gene indicates expression of the tandem α 2 δ subunit nucleic acid sequence. It is preferred that the reporter gene either have a visible reaction product or have a “tag” which may be detected by antibodies to give such a product. For example, cells expressing the reporter gene β-galactosidase produce a blue color when grown in the presence of X-Gal; cells grown in medium containing luciferin will fluoresce when expressing the reporter gene luciferase; cells containing green fluorescent protein spontaneously fluoresce when exposed to appropriate light wavelengths; cells expressing Myc, FLAG or His tags are detectable using commercially available anti-Myc, anti-FLAG or anti-His antibodies which are themselves coupled to a reporter molecule (e.g., enzyme or fluorescent compound).

Direct detection of expression of α 2 δ polypeptides can be achieved using methods well known to those skilled in the art. For example, mRNA isolated from transfected cells can be hybridized to labelled oligonucleotide probes and the hybridization detected. Alternatively, polyclonal or monoclonal antibodies specific for α 2 δ polypeptides can be used to detect expression of the recombinant α 2 δ polypeptide using enzyme-linked immunosorbent assay (ELISA), radioimmunoassay (RIA), fluorescent activated cell sorting (FACS) and immunohistochemical assays (e.g., enzyme-linked and fluorescent assays). Those skilled in the art recognize that, for example, immunohistochemical assays are useful in diagnostic test to identify individual cells which express α 2 δ polypeptides.

Recombinant α 2 δ polypeptides and their variants which are expressed by the host cell can be purified either from the culture medium, if the expression construct directs secretion into culture medium, or from the host cell lysate using purification techniques known in the art. For example, α 2 δ polypeptides may be expressed as a fusion protein with heterologous metal chelating peptides (i.e., polyhistidine tracts) or with protein A domains, and purified on commercially available immobilized metals or immunoglobulins, respectively.

The polypeptides of the invention are also useful in treating patients with Lambert-Eaton myasthenic syndrome (LEMS). LEMS is an autoimmune disease characterized by an insufficient release of acetylcholine from motor nerve terminals which normally are responsive to nerve impulses. Immunoglobulins (IgG) from LEMS patients block voltage-dependent calcium channels and thus inhibit calcium channel activity. Treatment of LEMS patients may be achieved by using a recombinant α 2 δ protein to clear patients' blood of the damaging autoantibodies.

The polypeptides of the invention are additionally useful for reconstituting a fully functional channel (e.g., on the cell membrane of frog eggs) by, for example, introducing into a cell expression vectors which encode the α1 subunit [Harpold et al. supra] as well as the α 2 δ subunits of the invention, and optionally the β-subunit and/or γ-subunit (Harpold et al., supra).

Additionally, those skilled in the art recognize that the α 2 δ subunit polypeptide sequences of the present invention are useful in generating antibodies as further described below.

F. Generation of Antibodies Directed to Calcium Channel α 2 δ Peptides

Antibodies (polyclonal and monoclonal) which are specific for at least a portion of the α 2 δ subunit isotype I and II provided herein may be generated using methods known in the art (see Example 8). The term “antibody” refers to immunoglobulin evoked in animals by an immunogen (antigen). It is desired that the antibody demonstrates specificity to epitopes contained in the immunogen. The term “polyclonal antibody” refers to immunoglobulin produced from more than a single clone of plasma cells; in contrast “monoclonal antibody” refers to immunoglobulin produced from a single clone of plasma cells. The terms “specific binding,” “specifically binding” and grammatical equivalents thereof when used in reference to the interaction of an antibody and a protein or peptide mean that the interaction is dependent upon the presence of a particular structure (i.e., the antigenic determinant or epitope) on the protein; in other words the antibody is recognizing and binding to a specific protein structure rather than to proteins in general. For example, if an antibody is specific for epitope “A”, the presence of a protein containing epitope A (or free, unlabelled A) in a reaction containing labelled “A” and the antibody will reduce the amount of labelled A bound to the antibody.

Those skilled in the art know how to make polyclonal and monoclonal antibodies which are specific to a desirable polypeptide. These include but are not limited to the hybridoma technique originally developed by Köhler and Milstein (Köhler and Milstein, Nature 256:495-497 [1975]), as well as the trioma technique, the human B-cell hybridoma technique (See e.g., Kozbor et al. Immunol. Today 4:72 [1983]), and the EBV-hybridoma technique to produce human monoclonal antibodies (Cole et al., in Monoclonal Antibodies and Cancer Therapy, Alan R. Liss, Inc., pp. 77-96 [1985]). For example, as described further below, monoclonal antibodies may be generated by immunizing an animal (e.g., mouse, rabbit, etc.) with a desired antigen and the spleen cells from the immunized animal are immortalized, commonly by fusion with a myeloma cell. Furthermore, the present invention encompasses antibodies produced using genetic immunization (e.g., immunization of an animal with a recombinant construct that provokes an immune response against the construct by the animal).

In an additional embodiment of the invention, monoclonal antibodies can be produced in germ-free animals utilizing relatively recent technology (See e.g., PCT/US90/02545). Also according to the invention, human antibodies may be used and can be obtained by using human hybridomas (Cote et al., Proc. Natl. Acad. Sci. U.S.A.80:2026-2030 [1983]).

According to the invention, techniques described for the production of single chain antibodies (U.S. Pat. No. 4,946,778; herein incorporated by reference) can be adapted to produce α 2 δ single chain antibodies. An additional embodiment of the invention utilizes the techniques described for the construction of Fab expression libraries (Huse et al., Science 246:1275-1281 [1989]) to allow rapid and easy identification of monoclonal Fab fragments with the desired specificity for α 2 δ.

Antibody fragments which contain the idiotype (antigen binding region) of the antibody molecule can be generated by known techniques. For example, such fragments include but are not limited to: the F(ab′)2 fragment which can be produced by pepsin digestion of the antibody molecule; the Fab′ fragments which can be generated by reducing the disulfide bridges of the F(ab′)2 fragment, and the Fab fragments which can be generated by treating the antibody molecule with papain and a reducing agent.

For monoclonal antibody production, immunization with antigen may be accomplished in the presence or absence of an adjuvant (e.g., Freund's adjuvant). Typically, for a mouse, 10 μg antigen in 50-200 μl adjuvant or aqueous solution is administered per mouse by subcutaneous, intraperitoneal or intramuscular routes. Booster immunization may be given at intervals, e.g., 2-8 weeks. The final boost is given approximately 2-4 days prior to fusion and is generally given in aqueous form rather than in adjuvant.

Spleen cells from the immunized animals may be prepared by teasing the spleen through a sterile sieve into culture medium at room temperature, or by gently releasing the spleen cells into medium by pressure between the frosted ends of two sterile glass microscope slides. The cells are harvested by centrifugation (400×g for 5 min.), washed and counted. Spleen cells are fused with myeloma cells to generate hybridoma cell lines. Several mouse myeloma cell lines which have been selected for sensitivity to hypoxanthine-aminopterin-thymidine (HAT) are commercially available and may be grown in, for example, Dulbecco's modified Eagle's medium (DMEM) (Gibco BRL) containing 10-15% fetal calf serum. Fusion of myeloma cells and spleen cells may be accomplished using polyethylene glycol (PEG) or by electrofusion using protocols which are routine in the art. Fused cells are distributed into 96-well plates followed by selection of fused cells by culture for 1-2 weeks in 0.1 ml DMEM containing 10-15% fetal calf serum and HAT. The supernatants are screened for antibody production using methods well known in the art. Hybridoma clones from wells containing cells which produce antibody are obtained (e.g., by limiting dilution). Cloned hybridoma cells (4-5×10 6 ) are implanted intraperitoneally in recipient mice, preferably of a BALB/c genetic background. Sera and ascites fluids are collected from mice after 10-14 days.

The invention also contemplates humanized antibodies which are specific for at least a portion of the α 2 δ subunit isotype I and II provided herein. Humanized antibodies may be generated using methods known in the art, such as those described in U.S. Pat. Nos. 5,545,806; 5,569,825 and 5,625,126, the entire contents of each of which are incorporated by reference. Such methods include, for example, generation of transgenic non-human animals which contain human immunoglobulin chain genes and which are capable of expressing these genes to produce a repertoire of antibodies of various isotypes encoded by the human immunoglobulin genes.

The antibodies of the invention which are directed against α 2 δ polypeptides may be used for the detection of expression of the α 2 δ proteins in cells. This may be desirable to, for example, use changes in the levels of expression of the cell's α 2 δ subunit proteins as a prognostic marker for the development of disease (e.g., cancer, neurological, autoimmune, and cardiovascular diseases) as well as for monitoring the efficacy of compounds in the prevention and treatment of these diseases. Thus, antibodies specific for α 2 δ polypeptides may be used to identify cells in clinically relevant samples from patients who have lost expression of the α 2 δ polypeptides.

Additionally, the antibodies provided herein may be used in the detection, diagnosis and typing of preneoplasias and cancers. For example, differences in the level of expression of the α 2 δ gene in preneoplastic and cancer cells as compared to normal cells may be used to detect and diagnose the presence of preneoplastic and cancer cells as well as to type such cells using methods known in the art, e.g., immunohistochemical assays including, but not limited to, enzyme-linked and fluorescent assays.

In the production of antibodies, screening for the desired antibody can be accomplished by techniques known in the art (e.g., radioimmunoassay, ELISA [enzyme-linked immunosorbant assay], “sandwich” immunoassays, immunoradiometric assays, gel diffusion precipitin reactions, immunodiffusion assays, in situ immunoassays [using colloidal gold, enzyme or radioisotope labels, for example], Western Blots, precipitation reactions, agglutination assays (e.g., gel agglutination assays, hemagglutination assays, etc.), complement fixation assays, immunofluorescence assays, protein A assays, and immunoelectrophoresis assays, etc. In addition, it is contemplated that phage display technology as known in the art will find use in conjunction with the present invention to detect the CACNA2D2 subunit in samples of interest.

G. Screening Compounds that Modulate the Activity of α 2 δ Calcium Channel Peptides

The invention provides methods for identifying compounds (e.g., calcium channel agonists and antagonists) that modulate the activity of calcium channels. These methods involve contacting cells which have been transfected with an expression vector that contains α 2 δ nucleic acid sequences provided herein, and which express α 2 δ polypeptides, with a test compound as well as with a calcium channel selective ion (e.g., calcium ion, barium ion, etc.). This is followed by measuring the ability of the compound to alter the activity of the calcium channel in the transfected cell which expresses the heterologous α 2 δ polypeptides as compared to that in a control cell which does not express the heterologous α 2 δ polypeptides. The cell is maintained in a solution having a concentration of calcium channel selective ions which is sufficient to provide an inward current when the channels open. Methods which are similar to those of the instant invention but which utilize calcium channel subunits other than the invention's α 2 δ subunit are known in the art such as those described by Ellis et al, U.S. Pat. No. 5,407,820; Harpold et al., U.S. Pat. No. 5,429,921; and Harpold et al., U.S. Pat. No. 5,792,846, the entire contents of each of which are incorporated by reference.

The activity of the calcium channel is determined by measuring the magnitude and duration of the inward current caused by flow of calcium channel selective ions. The amount of current which flows through the recombinant calcium channel of the cell may be determined directly (e.g., physiologically) as described, for example, by Harpold et al., U.S. Pat. No. 5,792,846. Alternatively, the amount of current may be determined indirectly by monitoring an independent reaction which occurs intracellularly and which is directly influenced in a calcium (or other) ion dependent manner. For example, the cell expresses a heterologous α 2 δ subunit and also contains a transcriptional control element which is responsive to a calcium channel selective ion and which is operatively linked to a structural gene that encodes an indicator protein.

The assays of the invention may be used in conjunction with methods of rational drug design to select among compounds that modulate the activity of calcium channels. Such compounds may then be tested for their activity in the treatment of channelopathies (e.g., migraine, epilepsy, and episodic ataxia, cardiovascular diseases, LEMS, cancer, etc.) in model animals as well as human subjects.

H. In Vitro and In Vivo Suppression of Tumor Cell Growth

The function of the invention's α 2 δ nucleic acid sequences, portions and homologs thereof in suppression of tumor cell growth in vitro and in vivo may be ascertained using the following guidelines. The nucleic acid sequence of interest is cloned into a vector to generate an expression vector as described supra. The expression vectors are transfected into cancer cells which are then used for the determination of the effect of expression of the nucleic acid sequence of interest on cell growth both in vitro and in vivo. The cancer cells into which the expression vectors are transfected may be engineered to express only a heterologous functional α 2 δ subunit. This may be desirable where, for example, the transfected cancer cell expresses functional endogenous calcium channel subunits but lacks expression of a functional endogenous α 2 δ subunit. Alternatively, the cancer cells into which the expression vectors are transfected may be engineered to express α 2 δ subunits as well as calcium channel subunits other than the α 2 δ subunit, such as the human calcium channel alpha 1, beta, and gamma subunits disclosed in the art (Ellis et al. [1988] supra; Williams et al. [1992] supra; Ellis et al. U.S. Pat. No. 5,686,241; and Harpold et al., U.S. Pat. No. 5,792,846).

For example, transfected tumor cells which express the α 2 δ nucleic acid sequence as well as control cells (i.e., corresponding tumor cells which have not been transfected with the expression vector) are cultured in vitro under conditions which result in growth of the control cells as determined by, for example, an increase in cell number over a period of time. Growth of the control and transfected cells is then compared. Detection of a growth level which is statistically lower in the transfected cells as compared to the control cells indicates that the nucleic acid sequence of interest functions as a tumor suppressor.

It is also contemplated that the present invention encompass methods that include the measurement of apoptosis (i.e., programmed cell death) either by itself or after other treatment (e.g., drugs). An increase in apoptosis could be viewed as a consequence of a normal function of the calcium channel gene product under certain conditions.

The tumor suppressor function of the sequence of interest may also be determined in vivo. This may be accomplished by introducing (e.g., by injection) transfected and control tumor cells into a host animal (e.g., mouse, etc.) and observing the growth of the introduced tumor cells as determined, for example, by the number of tumors, time at which tumors are first detected, and/or change in the diameter of a tumor over a period of time. One of skill in the art knows that immunological rejection of the tumor cells by the host animal is undesirable and may be avoided by, for example, introducing tumor cells which are derived from one species into a host of the same species (e.g., mouse tumor cells into a mouse host). Alternatively, tumor cells from one species may be introduced into an immunocompromised host animal of another species (e.g., human tumor cells into a nude (nu/nu) SCID mouse host). Detection of a growth level which is statistically lower in the transfected tumor cells as compared to the control tumor cells indicates that the nucleic acid sequence of interest functions as a tumor suppressor. Other measurements can also be used to assess the efficacy of treatment, including but not limited to determining whether there is a decrease in metastatic behavior of the tumor, an increase in apoptosis, a decrease in tumor angiogenesis, the complete absence of tumors, an increase in animal survival, and/or an increase in cure rates of animals.

I. Generating Transgenic Animals Expressing Reduced Levels of α 2 δ Calcium Channel Peptides

In addition to animals which express increased levels of calcium channel α 2 δ polypeptides relative to a corresponding wild-type animal, the present invention provides transgenic non-human animals which express reduced levels of calcium channel α 2 δ polypeptides relative to a corresponding wild-type animal. The present invention also provides transgenic non-human animals which express reduced activity of calcium channel α 2 δ polypeptides relative to a corresponding wild-type animal.

The transgenic animals of the present invention are generated by introducing a targeting vector into a host cell. It is contemplated that the targeting vector contains the α 2 δ subunit nucleic acid sequences disclosed herein (e.g., SEQ ID NOs:1, 3, and 5). Additionally, the targeting vector may contain the α 2 δ subunit nucleic acid sequences which have been modified by, for example, an insertion, deletion, or substitution of one or more nucleotide sequences into the α 2 δ subunit nucleic acid sequence.

A. Transgenic Animal Production In General

For example, the present invention provides a method for gene recombination in post-mitotic cells, comprising: providing a gene transfer system comprising a DNA sequence encoding a Cre recombinase and post-mitotic target tissue comprising target nucleic acid, wherein the target nucleic acid comprises one or more site-specific recombination target sequences; and introducing the gene transfer system to the target tissue, whereby recombination occurs at the one or more site-specific recombination target sequences. In one embodiment of the present invention, the DNA sequence encoding a Cre recombinase further comprises a tissue-specific promoter sequence.

In some preferred embodiments, the gene transfer system comprises a viral gene transfer system. In particularly preferred embodiments, the viral gene transfer system comprises an adenoviral gene transfer system.

In certain embodiments of the present invention, the post-mitotic target tissue comprises cardiac, skeletal muscle, brain, lung, testis, pancreas, small intestine, ovary, spleen, or kidney, although the methods of the present invention are applicable to any post-mitotic target tissue. In other embodiments, the target nucleic acid comprises a gene. In yet other embodiments, the one or more site-specific recombination target sequences comprises one or more loxP target sequences, although other site-specific recombination target sequences are contemplated by the present invention, including, but not limited to, loxP2, loxP3, loxP23, loxP511, loxB, loxC2, loxL, loxR, loxΔ86, loxΔ117, frt, dif flp, and att target sequences.

In certain embodiments of the present invention, the introducing of the gene transfer system to the target tissue, comprises injecting the gene transfer system into the target tissue.

The present invention further provides a method for gene recombination in a tissue of interest (e.g., cardiac, skeletal muscle, brain, lung testis, pancreas, small intestine, ovary, spleen, or kidney), comprising: providing a viral gene transfer system comprising a DNA sequence encoding a Cre recombinase and a tissue of interest comprising target nucleic acid, wherein the target nucleic acid comprises one or more site-specific recombination target sequences; and introducing the viral gene transfer system to the tissue of interest, whereby recombination occurs at the one or more site-specific recombination target sequences. In some embodiments of the present invention, the tissue of interest comprises post-mitotic cardiac tissue. In other embodiments, the DNA sequence encoding a Cre recombinase further comprises a tissue-specific promoter sequence. In yet other embodiments, the introducing of the viral gene transfer system to the tissue of interest, comprises injecting the viral gene transfer system into the tissue.

The present invention further provides a method for tissue-restricted gene recombination, comprising: providing a viral gene transfer system comprising a DNA sequence encoding a Cre recombinase and a tissue-specific promoter sequence and post-mitotic cardiac tissue comprising target nucleic acid, wherein the target nucleic acid comprises one or more site-specific recombination target sequences; and introducing the viral gene transfer system to the post-mitotic tissue, whereby recombination occurs at the one or more site-specific recombination target sequences. In some embodiments, the introducing of the viral gene transfer system to the post-mitotic cardiac tissue comprises injecting the viral gene transfer system into the post-mitotic tissue. In certain embodiments, the tissue-specific promoter sequence comprises an α-myosin heavy chain promoter sequence.

The present invention further provides a non-human mammal, wherein one or more tissues of the non-human mammal comprise tissue prepared according to the methods described above. In preferred embodiments, the non-human mammal is selected from the order Rodentia. In particularly preferred embodiments, the non-human mammal is selected from the group consisting of mice and rats.

The present invention further provides a non-human mammal having post-mitotic tissue comprising an altered genotype as compared to wild-type post-mitotic tissue, wherein the altered genotype is the result of tissue-specific recombination. In preferred embodiments the post-mitotic tissue comprises cardiac, skeletal muscle, brain, lung testis, pancreas, small intestine, ovary, spleen, or kidney tissue, although the present invention contemplates all other post-mitotic tissues. In some embodiments, the altered genotype comprises a gene knockout.

In addition, the present invention provides a method for screening compounds for their effect on a transgenic animal, comprising: providing a transgenic animal, wherein the transgenic animal is the non-human mammal described above and a composition comprising a test compound in a form suitable for administration to the non-human mammal; and administering the test compound to the non-human mammal. In some embodiments, the method further comprises the step of detecting a response of the non-human mammal to the test compound.

B. Transgenic Knockout Animals

This section provides descriptions of various means to produce transgenic knockout animals of the present invention. The transgenic α 2 δ-knockout (α 2 δ-KO) animals of the present invention may be produced by a variety of means. Where the transgenic animal is a mouse, any targeting vector containing at least a portion of α 2 δ nucleic acid sequences of the invention which is capable of homologously recombining into the mouse α 2 δ subunit gene in a manner that disrupts the mouse α 2 δ gene (e.g., deletion, introduction of a frameshift, premature stop codon, missense mutation, etc.) may be employed. The targeting vector may be of the replacement- or insertion-type. Replacement-type vectors contain two regions of homology with the targeted gene flanking a selectable marker and result in the insertion of the selectable marker which thereby disrupts the targeted gene. Insertion-type vectors contain a single region of homology with the targeted gene and result in the insertion of the entire targeting vector into the targeted gene.

Positive selection markers include, but are not limited to, the neo gene, the hyg gene and gpt gene, may also be used so long as the selection marker permits detection of the disruption of the wild-type α 2 δ subunit gene with the vector sequence. Negative selectable markers are exemplified by the dt gene, and the HSV-tk gene.

It is not necessary that the targeting vector contain a selectable marker gene as discussed above, although the use of a selectable marker is preferred. Further, it is not necessary that, if a selectable marker is employed, the targeting vector employ both a positive (e.g., neo) and a negative (e.g., dt) selectable marker gene.

The targeting vector may be introduced into a variety of host cells, e.g., oocytes, zygotes and embryonic stem (ES) cells. In a preferred embodiment, the host cell is an embryonal stem (ES) cell. Another method of introducing the vector into the animal's germ line involves using embryonic stem (ES) cells as recipients of the expression vector. ES cells are pluripotent cells directly derived from the inner cell mass of blastocysts. Vectors can be introduced into ES cells using any method which is suitable for gene transfer into cells (e.g., by transfection, cell fusion, electroporation, microinjection, DNA viruses, and RNA viruses). Once the expression vector has been introduced into an ES cell, the modified ES cell is then introduced back into the embryonic environment for expression and subsequent transmission to progeny animals. The most commonly used method is the injection of several ES cells into the blastocoel cavity of intact blastocysts. Alternatively, a clump of ES cells may be sandwiched between two eight-cell embryos. Both methods result in germ line transmission at high frequency.

Transgenes may also be introduced into ES cells by retrovirus-mediated transduction or by micro-injection. Transfected ES cells which contain the transgene may be subjected to various selection protocols to enrich for ES cells which have integrated the transgene assuming that the transgene provides a means for such selection. Alternatively, the polymerase chain reaction may be used to screen for ES cells which have integrated the transgene. This technique obviates the need for growth of the transfected ES cells under appropriate selective conditions prior to transfer into the blastocoel.

Transfected ES cells can thereafter colonize an embryo following their introduction into the blastocoel of a blastocyst-stage embryo and contribute to the germ line of the resulting chimeric animal.

The generation of transgenic α 2 δ-KO mice need not employ ES cells. For example, embryonal cells at various developmental stages can be used to introduce transgenes for the production of transgenic animals. Different methods are used depending on the stage of development of the embryonal cell. The zygote is the best target for micro-injection. In the mouse, the male pronucleus reaches the size of approximately 20 micrometers in diameter which allows reproducible injection of 1-2 picoliters (pl) of DNA solution. The use of zygotes as a target for gene transfer has a major advantage in that in most cases the injected DNA will be incorporated into the host genome before the first cleavage. As a consequence, all cells of the transgenic non-human animal will carry the incorporated transgene. This will, in general, also be reflected in the efficient transmission of the transgene to offspring of the founder since 50% of the germ cells will harbor the transgene. Micro-injection of zygotes is the preferred method for incorporating transgenes in practicing the invention.

Alternatively, targeting vectors or transgenes may be microinjected into mouse oocytes to generate mice containing a disrupted α 2 δ subunit gene. PCR can be employed to screen the targeted cells to identify cells containing a disrupted α 2 δ gene without the need to use a selectable marker and to subject the targeted cells to growth in selective medium. In addition, chimeric RNA-DNA oligonucleotides containing modified RNA residues (2′-O-methyl modification of the ribose) can be used to target mutations (e.g., the introduction of a frameshift, premature stop codon, etc.) into the α 2 δ gene using ES cells or oocytes to create transgenic α 2 δ-KO mice.

Once the expression vector has been injected into the fertilized egg cell, the cell is implanted into the uterus of a pseudopregnant female and allowed to develop into an animal. Heterozygous and homozygous animals can then be produced by interbreeding founder transgenics. This method has been successful in producing transgenic mice, sheep, pigs, rabbits and cattle.

Retroviral infection can also be used to introduce transgenes into a non-human animal. The developing non-human embryo can be cultured in vitro to the blastocyst stage. During this time, the blastomeres can be targets for retroviral infection. Efficient infection of the blastomeres is obtained by enzymatic treatment to remove the zona pellucida. The viral vector system used to introduce the transgene is typically a replication-defective retrovirus carrying the transgene. Transfection is easily and efficiently obtained by culturing the blastomeres on a monolayer of virus-producing cells.

Alternatively, infection can be performed at a later stage. Virus or virus-producing cells can be injected into the blastocoele. Most of the founders will be mosaic for the transgene since incorporation occurs only in a subset of cells which form the transgenic animal. Further, the founder may contain various retroviral insertions of the transgene at different positions in the genome which generally will segregate in the offspring. In addition, it is also possible to introduce transgenes into the germline, albeit with low efficiency, by intrauterine retroviral infection of the mid-gestation embryo. Additional means of using retroviruses or retroviral vectors to create transgenic animals known to the art involves the micro-injection of retroviral particles or mitomycin C-treated cells producing retrovirus into the perivitelline space of fertilized eggs or early embryos.

A transgenic animal of the invention which “expresses a reduced level of calcium channel α 2 δ subunit relative to a corresponding wild-type animal” is a transgenic animal which contains a quantity of at least one isoform of α 2 δ subunit that is less than, preferably 50% less than, and more preferably 90% less than, the quantity of a corresponding isoform of α 2 δ subunit in an isogeneic animal which contains a wild-type α 2 δ gene. Most preferably, the transgenic animals of the invention contain a quantity of at least one isoform of α 2 δ subunit which is at the background level of, or is undetectable by, an Enzyme Linked Immunosorbent Assay (ELISA).

A transgenic animal of the invention which “expresses a reduced activity of calcium channel α 2 δ subunit relative to a corresponding wild-type animal” is a transgenic animal which contains at least one isoform of α 2 δ subunit that exhibits less than, preferably 50% less than, and more preferably 90% less than, the biological activity of a corresponding isoform of α 2 δ subunit in an isogeneic animal which contains a wild-type α 2 δ gene. The biological activity of α 2 δ subunit may be determined by methods known in the art (e.g., oocyte injection assay disclosed by Ellis et al., U.S. Pat. No. 5,407,820; Harpold et al., U.S. Pat. No. 5,429,921; and Harpold et al., U.S. Pat. No. 5,792,846, the contents of each of which are incorporated by reference). Most preferably, the transgenic animals of the invention contain at least one isoform of α 2 δ subunit whose activity is undetectable by an oocyte injection assay.

The transgenic α 2 δ-KO animals provided by the present invention find several uses. For example, these animals (including heterozygous (α 2 δ +/−) mice which contain only one copy of the gene, as well as homozygous (α 2 δ +/−) mice which lack both copies of the gene) may be used as murine models of cancer (e.g., lung cancer, breast cancer, etc.), human neurological diseases (e.g., epilepsy, migraine, episodic ataxia, etc.), human cardiovascular diseases (e.g., cardiac arrhythmia, angina pectoris, etc.), and human autoimmune disease (e.g., LEMS).

Experimental

The following examples serve to illustrate certain preferred embodiments and aspects of the present invention and are not to be construed as limiting the scope thereof. Unless otherwise mentioned, all molecular manipulations (e.g., DNA and RNA isolation, screening cDNA libraries, Northern and Southern blot analyses, PCR, etc.) were performed using standard methods (See e.g., Sambrook et al. [1989], supra).

In the experimental disclosure which follows, the following abbreviations apply: ° C. (degrees Centigrade); rpm (revolutions per minute); IM (intramuscular); IP (intraperitoneal); IV (intravenous or intravascular); SC (subcutaneous); H 2 O (water); aa (amino acid); bp (base pair); kb (kilobase pair); kD (kilodaltons); gm (grams); μg (micrograms); mg (milligrams); ng (nanograms); μl (microliters); ml (milliliters); mm (millimeters); nm (nanometers); μm (micrometer); M (molar); mM (millimolar); μM (micromolar); nM (nanomolar); U (units); V (volts); MW (molecular weight); μCi (microcurrie); sec (seconds); min(s) (minute/minutes); hr(s) (hour/hours); ab (antibody); HCl (hydrochloric acid); MgCl 2 (magnesium chloride); KCl (potassium chloride); NaCl (sodium chloride); OD 280 (optical density at 280 nm); PAGE (polyacrylamide gel electrophoresis); PCR (polymerase chain reaction); RT-PCR (reverse transcription PCR); SDS (sodium dodecyl sulfate); Tris (tris(hydroxymethyl)aminomethane); EDTA (ethylenediaminetetraacetic acid); w/v (weight to volume); v/v (volume to volume); SSCP (single strand conformation polymorphism analysis); ATCC (American Type Culture Collection, Manassas, Va.); Bio-Rad (BioRad, Richmond, Calif.); Sigma (Sigma Chemical Co., St. Louis, Mo.); Boehringer-Mannheim, (Boehringer-Mannheim, Indianapolis, Ind.); Scan Analytics (Scan Analytics Corp., Vienna, Va.); Oncor (Oncor, Gaithersburg, Md.); Applied Biosystems (Applied Biosystems, Foster City, Calif.); Clontech (Clontech, Palo Alto, Calif.); Gibco-BRL (Gibco-BRL, Gaithersburg, Md.); Amersham (Amersham Life Sciences, Arlington Heights, Ill.); BioServe (BioServe Ltd, Laurel Md); FMC (FMC BioProducts, Rockland Me.); Invitrogen (Invitrogen, Carlsbad Calif.); Kodak (Kodak, Rochester, N.Y.); Life Technologies (Life Technologies, Rockville, Md.); DNAStar (DNAStar Inc., Madison, Wis.); Bio 101 (Bio 101, Inc., Vista, Calif.); Ambion (Ambion, Austin, Tex.); and Axon Instruments (Axon Instruments, Foster City, Calif.).

EXAMPLE 1

Positional Cloning of the α 2 δ Subunit Gene

A ˜700 kb clone contig was constructed covering the tumor suppressor gene region on human chromosome 3p21.3 defined by extensive allelotyping (Wei et al., supra] and overlapping homozygous deletions in lung and breast cancers (Wei et al. supra; Sekido et al., Oncogene 16(24):3151-7 [1998]). This cloned DNA was used to isolate 17 resident genes by conventional laboratory techniques (Wei et al., supra). The 700 kb clone contig was sequenced by The WU Sequencing Center (St Louis, Mo., USA) and The Sanger Sequencing Centre (Hixton, UK) ( FIG. 1 provides the GenBank accession numbers of sequences). The ˜700 kb sequence and in silico methods were used to detect and isolate additional 9 genes residing in the ˜700 kb sequence bringing the total number of cloned genes to 26. Eight of these genes were encoded in the critical 120 kb region defined by the recently discovered small nesting homozygous deletion in breast cancer cell line and primary tumor HCC1500 (Sekido et al., supra). The most centromeric of these genes (the α 2 δ gene) was interrupted by the centromeric breakpoint of the homozygous nested deletion (Sekido et al., supra), and spanned about 140 kb of genomic DNA (FIG. 1 ).

A cosmid probe (LUCA8; GenBank accession # Z84495) representing a large intron of the gene also included the chromosome 3 framework genetic marker, D3S1568 (also called LUCA8.2, D354614), allocated at a 68 cM distance from the telomere of the short arm on the chromosome 3 genetic map corresponding to the 3p21.3 band (FIG. 1 ).

The eight critical genes were extensively analyzed by bioinformatics methods and the interrupted large gene was identified as encoding at least two splice isoforms of a new calcium channel α 2 δ gene (FIG. 1 ).

Fluorescent in situ hybridization (FISH) was used to determine whether the α 2 δ subunit gene was indeed located in the 3p21.3 region as follows. Metaphase spreads derived from 5-bromodeoxyuridine synchronized normal peripheral lymphocytes were used as a template. Probes containing LUCA8 cosmid DNA were labeled with digoxigenin 11-dUTP by nick-translation and hybridization signals were detected with rhodamine-conjugated anti-digoxigenin antibodies (Boehringer-Mannheim). The conditions of hybridization, detection of hybridization signals, and digital-image acquisition, processing and analyses were performed as previously described (Ivanov et al., Proc. Natl. Acad. Sci USA 95(21):12596-601 [1998]). Chromosomes were identified by converting DAPI-banding into G-simulated banding using the IP Lab Image Software (Scan Analytics). Rehybridization with alpha-satellite centromeric probes (Oncor) was performed to confirm chromosomal localization. FISH analysis confirmed that the α 2 δ gene was located in the 3p21.3 region of chromosome 3.

EXAMPLE 2

Isolation of Full-Length cDNAs Encoded by the α 2 δ Subunit Gene

An EST (GenBank Accession #N53512) was first detected by BLAST homology searches in the databases using the genomic sequences of contig (Wei et al., supra) cosmid LUCA11 (GenBank accession # Z84492). This EST clone was found to contain a portion of the 3′ end as well as putative exons of α 2 δ-2. Further Southern blot analysis showed that various exons of the α 2 δ-2 gene are located on cosmid LUCA6 (GenBank Accession #Z84493), LUCA7 (GenBank Accession #Z84494, LUCA8 (GenBank Accession #Z84495), LUCA9 (GenBank Accession #Z75743), LUCA10 (GenBank Accession #Z75742), and LUCA11 (GenBank Accession #Z84495). Based on GENSCAN predictions, a primer set of LUCA11r5 (5′-CTGAGAGTGAGGATGTGGAA-3′ (sense primer)(SEQ ID NO:12)), and LUCA11pr18, 5′-GTGCATCCTCATACACGTTG-3′ (anti-sense primer)(SEQ ID NO: 13), was used for RT-PCR amplification for normal lung cDNA template and a 960 bp product was successfully amplified. The 1.5 kb NotI/HindIII fragment of the EST clone N53512, and the 960 bp product were used as probes on human multiple tissue Northern blots (Clontech). The screening of a million clones from a lung cDNA library (Clontech) with the 960 bp RT-PCR product yielded 120 positive clones, which were also screened by probing clone N53512 to obtain the clones with long inserts. Five clones randomly selected as single positives for the 960 bp probe, and 5 clones double positive for both probes were subcloned and sequenced. All of the 10 clones had the sequence of α 2 δ-2, suggesting that all of the 120 clones were α 2 δ-2. Two clones (pY720c21 and pY724c95) that covered the longest sequence were assembled and further inserted into a plasmid expression vector pcDNA3.1 (Invitrogen) by standard methods (See below for additional details).

The EST was sequenced using methods known in the art. Briefly, cDNA clones were sequenced on an Applied Biosystems 373 and 377 DNA sequencers (Stretch) using Taq Dyedeoxy Terminator Cycle Sequence kits (Applied Biosystems) with either vector or clone-specific walking primers. This EST was first used as probe on commercial multiple tissues RNA Northern blots to estimate the size(s) of the mRNA(s) and to identify tissues with high expression.

For mRNA expression analyses, Northern blot hybridization was performed with α 2 δ cDNA probes using commercial MTN polyA RNA blots (Clontech) from a variety of adult human tissues and tumor cell lines and polyA+RNA or total RNA (JM lab) prepared from lung cancer cell lines. In these experiments, a 5.7 kb mRNA was found. In addition, the presence of the α 2 δ transcripts was monitored in silico by BLAST homology searches (Altschul et al., J. Mol. Biol., 215:403-410 [1990]; and Altschul et al., Nucl. Acids Res., 25:3389-3402 [1997]) in public EST databases.

Since high expression levels were detected in adult lung, testis, and brain ( FIG. 2 ) several commercial cDNA libraries made from mRNAs of these tissues were screened to isolate overlapping cDNA clones. More than two hundred (200) cDNA clones were sequenced and shown to represent at least three distinct splice isoforms differing at the 5′ end. Full-length cDNA clones for each of the three splice isoforms were then constructed and completely sequenced. In addition, cDNA clones from a commercial normal lung cDNA library (Clontech) were isolated, sequenced and shown to contain the entire open reading frame (3,435 nucleotides encoding 1,145 amino acids) of the α 2 δ gene protein isoform I. The molecular weight of the deduced amino acid sequence was determined to be approximately 129 kDa. As indicated below, BLAST searches and homology alignment revealed that the predicted protein shares 56% amino acid sequence identity with the human auxiliary α-δ-1 subunit (GenBank Accession #M76559) of voltage-gated Ca 2+ channels.

World Wide Web based servers were used to analyze the cDNAs and deduced protein sequences. Global sequence alignments were done using BLAST and Advanced BLAST programs (Altschul et al. (1990), supra; and Altschul et al. (1997), supra), as provided by NCBI (http://www.ncbi.nlm.nih.gov/), and BLAST2/WU Blast, provided by EMBL (http://dove.embl-heidelberg.de/Blast2/). Multiple sequence alignments, global and local, were done using the CLUSTAL version W program as provided by EMBL (http://www.bork.embl-heidelberg.de/Alignment/) and Baylor Computing Center (http://dot.imgen.bcm.tmc.edu:9331/seq-search/alignment.html).

Protein domains were discovered on the Pfam (Sonnhammer et al., Nucl. Acids Res., 26:320-322 [1998]; Sonnhammer et al., Proteins 28:405-420 [1997]) server, and membrane topology on the PSORT (Nakai and Kanehisa, Genomics 14:897-911 [1992]; http://www.imcb.osaka-u.ac.jp/nakai/psort.html; SPLIT (Juretic and Lucin, J. Chem. Inf. Comput. Sci., 38(4): 575-585 [1998]; http://drava.etfos.hr/˜zucic/split.html); and TMHMM (http://www.cbs.dtu.dk/services/TMHMM-1.0/) servers.

The nucleic acid sequence of splice isoform 1 (SEQ ID NO:1) (GenBank accession #AF042792) of human α 2 δ subunit cDNA and its encoded amino acid sequence (SEQ ID NO:2) are provided herein. The nucleic acid sequence of splice isoform 2 (SEQ ID NO:3) (GenBank Accession #AF040709) of human α 2 δ subunit cDNA and its encoded amino acid sequence (SEQ ID NO:4) are also provided herein. The nucleic acid sequence of splice isoform 3 (SEQ ID NO:5) (GenBank Accession #AF042793) of human α 2 δ subunit cDNA and its encoded amino acid sequence (SEQ ID NO:6) are also provided herein.

Two of the cDNA clones (i.e., splice isoforms 1 and 2) predicted the same amino acid sequence (SEQ ID NOs:2 and 4) and the third clone (i.e., splice isoform 3) encoded a shorter amino acid sequence (SEQ ID NO:6) in which the first coding exon was spliced out. The longer insert sizes of 5,463 bp (splice isoform 1) and 5,482 bp (splice isoform 2) correspond to the roughly estimated major mRNA species of 5.5-5.7 kb. Splice isoform 1 and 2 cDNAs encode identical amino acid sequences (SEQ ID NOs:2 and 4) referred to as isoform I and differ only in their 5′UTRs that are followed by identical ORFs and identical 3′UTRs. The smaller cDNA of 5,279 bp (splice isoform 3) encodes a shorter amino acid sequence (SEQ ID NO:6) referred to as isoform II. The amino acid sequence of isoform II is identical to that of isoform I but is missing the first 69 amino acids. The isoform I protein is composed of 1145 amino acids predicting a theoretical pI/Mw of 5.5/129 kD; the isoform II protein comprises 1076 amino acids predicting a pI/Mw values of 5.22/122 kD. Both isoform I and II proteins are of high complexity and are not biased against any amino acids.

EXAMPLE 3

Genomic Structure and Bioinformatics Analysis of the α 2 δ Gene

The exon-intron structure of the α 2 δ gene was obtained by pairwise alignments of the cDNAs and genomic sequences of overlapping cosmids, LUCA 6-11 (FIG. 1 ). So far, 37 exons ( FIG. 1 ) were detected bounded by consensus splice sites. In addition, exon trapping technology identified several more exons in the genomic sequence that were not present in the cDNAs. This indicates the possible existence of other isoforms generated by alternative splicing. The putative promoter of the α 2 δ gene was identified by the PromoterScan program (Prestridge, J. Mol. Biol., 249:923-932 [1995]; http://www.crc.nus.sg:80/bio/proscan/proscan.html) in the upstream sequence on LUCA6 and verified by cloning and sequencing (GenBank Accession #AF042794). Thus, there are two sequences relevant to the LUCA6 cosmid. The first is “LU6 Z84493” or LUCA6” and the second is “LU6Pr ZF042794” or “LUCA6 promoter region.” It is contemplated that Z94493 is inclusive of the entire sequence.

A number of bioinformatics web based servers were used to analyze the cDNAs and the predicted protein sequences. A global BLAST (Altschul et al. [1990], supra; and Altschul et al. [1997], supra) analysis of the cDNAs and deduced protein sequences employing NCBI (http://www.ncbi.nlm.nih.gov) and EMBL (http://www.bork.embl-heidelberg) servers was carried out to compare the inventions' α 2 δ isoforms I and II with the (alpha) 2 -subunit protein (1091 amino acids predicting a pI/Mw values of 5.10/123 kD) which is encoded by the previously reported human (alpha) 2 -subunit isoform A gene (Ellis et al., Science 241(4873):1661-4 [1988]; Williams et al., Neuron, 8(1):71-84 [1992]; Ellis et al. U.S. Pat. No. 5,686,241; and Harpold et al., U.S. Pat. No. 5,792,846). Protein and cDNA alignments of the invention's α 2 δ isoforms I and II with the art's (alpha) 2 -subunit sequences show 55% identity and 65% similarity on the protein level and overall 56% identity on cDNA level. It appears that α 2 δ-2 and α 2 δ-1 share similar overall secondary structure, as 17 out of 22 cysteines are conserved between these proteins. In addition, as with α 2 δ-1, α 2 δ-2 contains multiple putative N-glycosylation sites and is likely to be glycosylated. Without intending to limit the invention to any particular theory or mechanism, this degree of homology suggests that the gene encoding the art's (alpha) 2 -subunit cDNA and the gene encoding the invention's α 2 δ subunit cDNA splice isoforms 1, 2 and 3 may be different members of a new gene family.

To further characterize the α 2 δ subunit gene, the predicted post-translational biochemical modifications, secondary structures, and membrane topologies of protein isoforms I and II which are encoded by the α 2 δ gene were compared. The complexity of interactions involving the five calcium channel subunits comprising a fully functional channel is influenced by distinct post-translational biochemical modifications that include O-glycosylation, amidation, myristoylation, and, most importantly, phosphorylation of specific conserved tyrosine and serine residues. The ScanProsite server (http://expasy.hcuge.ch/sprot/scnpsite.html) revealed similar distributions of potential N-glycosylation, O-glycosylation, N-myristoylation, and amidation sites in both isoform I and II proteins. The distribution of potential cAMP/cGMP-dependent protein kinase phosphorylation sites, CK2 and PKC phosphorylation sites, and tyrosine kinase phosphorylation sites was also similar among both isoform I and II proteins. Without limiting the invention to any particular mechanism, these potential post-translational modifications of the α 2 δ proteins may add more complexity and flexibility to the variety of functions attributed to these proteins. Three putative transmembrane helices were predicted in both protein isoforms of the α 2 δ gene with the SPLIT 35 software (Juretic and Lucin [1998], supra; and http://drava.etfos.hr/˜zucic/ split.html). Interestingly, isoform I of the α 2 δ gene has an additional membrane helix at the very amino terminus. Using the TMHMM server (http://www.cbs.dtu. dk/services/TMHMM-1.0/) isoform I protein was predicted to span the membrane only once at the amino terminus while isoform II was predicted to span the membrane once at the carboxy terminus. Without intending to limit the invention to any particular mechanism, this favors the single-transmembrane model for the α 2 δ subunit proteins. In addition, the protein binding von Willebrand factor type A domain (VWA-like domain) (Bork et al., Biochem. J., 279 ( Pt 3):908-10 [1991]) was discovered by the Pfam (Sonnhammer et al. [1998], supra; and Sonnhammer et al. [1997], supra) server (http://www.sanger.ac.uk/Pfam/) in the extracellular region at similar positions in both isoform I and II proteins (residues: 291-469, and 222-400 for α 2 δ isoforms I and II respectively). While not limiting the invention to any particular theory or mechanism, the VWA-like domain may facilitate the binding of the α 2 δ complex with the alpha 1 pore forming subunit (Walker and De Waard [1998] supra).

EXAMPLE 4

Chromosomal Mapping of the α 2 δ Gene Locus

The chromosomal location of the α 2 δ gene locus was determined by FISH as described above (Example 1) using the cosmid LUCA8 ( FIG. 1 ) probe which represents a large intron of the gene. The α 2 δ gene was localized as a single locus on 3p21.3 confirming the mapping of the microsatellite marker, D3S1568, that is located in LUCA8 sequence. This region of chromosome 3p21.3 is syntenic with mouse chromosome 9 region at position 60-70 cM (homology group #25) that harbors mouse loci implicated in epilepsy, namely, Ell, ducky, and tippy indicating that the α 2 δ gene may be responsible for these neurological phenotypes.

EXAMPLE 5

Detection of Mouse Orthologous cDNA Sequences

BLAST searches in the mouse EST database maintained by NCBI detected two different non-overlapping ESTs (GenBank Accession ## AA000341 and AA08996) which showed 91% and 85% identity with the invention's α 2 δ DNA (residues 2925-3421, and 4989-5391 of splice isoform 1) respectively. These ESTs showed only limited homologies (about 50%) to the murine (alpha 2 )-subunit genes suggesting that they represent true orthologous sequences (i.e., homologous sequences present in different organisms) of the human α 2 δ gene. This was further corroborated by protein alignment of the 86 amino acid ORF encoded by the EST, # AA000341 which was 96% identical to the invention's α 2 δ isoform I protein (residues 922-1005 of isoform I). The second EST (# AA008996) represents the 3′ UTR of the mouse α 2 δ gene and therefore has no ORF.

EXAMPLE 6

Expression Analysis of the α 2 δ Gene

The expression patterns of the α 2 δ gene were analyzed by Northern blot hybridization of human adult tissues and tumor cell lines and by monitoring EST databases. Probes for Northern analysis were labeled with a 32 P-dCTP using a random primer labelling kit (Gibco-BRL). RNA was prepared from cell lines by standard techniques (See e.g., Sambrook et al., supra). Ten micrograms of total RNA (or 2 μg of poly A+ RNA) from cell lines were electrophoresed in formaldehyde-1% agarose gel and transferred to Hybond N (Amersham), and membrane preparation, hybridization, and washing were performed as described using standard techniques (Sambrook et al. [1989] supra; Sekido et al., Cancer Res., 55:1227-31 [1995]; Sekido et al., Proc. Natl. Acad. Sci USA 93:4120-4125 [1996]; and Ivanov et al. [1998], supra). Human multiple tissue Northern blots I and II and human brain blot III all made with poly A+ RNA were purchased from Clontech and handled as the tumor cell line Northerns. The DNA probes used for the α 2 δ gene were: the 1.5 kb fragment (Solution # Y612) NotI/HindIII fragment of EST clone N53512 for the tumor cell line Northerns and the Multiple Tissue Blot Northerns; and for other Multiple Tissue Blot Northerns 308 bp Probe A (Solution #Y614) (LUCA 11 pr1/pr2) and 291 bp Probe B (Solution # Y615) (LUCA 11 pr3/pr4); (LUCA11pr1: CTCTACAACCCAATTCACCAT (SEQ ID NO:8); LUCA 11pr2: TAGATGGCACTGGCCTTCT (SEQ ID NO:9); LUCA11pr3: ACTCACCACCCTACTGTTC (SEQ ID NO:10); LUCA11pr4: AGCTGCCTGTTTGGTGCTA (SEQ ID NO:11)). Northern Blots were exposed first for 1 or 4 days and then for ˜30 days.

A. Expression in Normal Tissues

A predominant 5.7 kb α 2 δ mRNA was seen in all normal tissues expressing the calcium channel gene and in some cases minor larger and smaller species. The highest level of α 2 δ expression in normal adult human tissues was found in lung and testis, with some expression also seen in heart, brain, skeletal muscle, pancreas, spleen, prostate, ovary, small intestine, and peripheral blood lymphocytes. Northern blot results from various tissue sources are shown in FIG. 2 . In this Figure, Panel A shows the results for samples from spleen, thymus, prostate, testis, ovary, small intestine, colon, and peripheral blood lymphocytes (PBL), while Panel B shows the results for samples from heart, brain, placenta, lung, liver, skeletal muscle, kidney, and pancreas. The calcium channel α 2 δ gene was also expressed extensively in all different areas of the brain tested in an additional multiple tissue Northern blot (e.g., thalamus, subthalamic nucleus, substantia nigra, whole brain, hippocampus, corpus callosum, caudate nucleus, and amygdala samples; results not shown).

B. Expression in Lung Cancers

A predominant 5.7 kb mRNA was also seen in lung cancer cell lines that expressed the α 2 δ calcium channel gene. Various cell lines were used in these experiments, including a B lymphoblastoid cell line, and lung cancer cell lines designated as NCI lines (e.g., NCI-H82). The histologies of the lines tested included small cell lung cancer (SCLC), NCI-H82 (SCLC) , H146 (SCLC), H249 (SCLC), H524 (SCLC), H740 (SCLC), H1514 (SCLC), H1618 (SCLC), H2141 (SCLC), H2171 (SCLC), H2227 (SCLC), H187, H209, H345, H378, H524, H526, H865, H889, H1045, H1092, H1105, H1238, H1514, H1618, H1672, H1963, H2141, H2171; non-small cell lung cancers (NSCLC), H358 (NSCLC, adeno/bronchoalveolar), H838 (NSCLC, adeno), H1792 (NSCLC, adeno), H2077 (NSCLC, adeno), H460 (NSCLC, large cell), H1155 (NSCLC, large cell), H1299 (NSCLC, large cell), H720 (carcinoma); H28 (mesothelioma); H290 (mesothelioma), H2052 (mesothelioma), H23 (adeno), H322 (adeno), H1437 (adeno), H1666 (adeno), H2009 (adeno), H661 (large cell), H2106 (large cell), and NCI-H460 (NSCLC, large cell). These lines have been deposited with the American Type Culture Collection (ATCC).

After exposure for 1 day for poly A + RNA blots, or 4 days for total RNA blots, only a few tumor cell lines showed detectable signals. After prolonged 30 days' exposure some additional tumor lines showed expression. Overall, α 2 δ expression was found in 41 lung cancer samples as follows: 19 expressed the gene and 22 had no, or very weak, expression. As a function of histologic type: Small cell lung cancers: 15 expressed, 8 had no, or very weak, expression; Non-small cell lung cancers: 4 expressed, 10 had no, or very weak, expression; mesotheliomas: all 3 had no, or very weak, expression; carcinoid: 1 had no expression.

In an additional set of experiments using polyA+RNA prepared from 14 SCLC lines and 11 NSCLC lines, only about 35% of the cell lines tested showed low levels of expression and the rest no expression at all. These results collectively suggest that the α 2 δ gene is silenced during lung carcinogenesis.

C. EST Database Analysis

The EST matches were mostly in the testis, lung, and brain libraries (85%). Several ESTs were detected in libraries made from tumor tissues, namely, prostate, lung, and ovarian carcinomas. (NCBI, dBEST, NCI CGAP database, http://www.ncbi.nlm.nih.gov/ncicgap/). These combined results suggest that the α 2 δ gene is expressed in several normal tissues and that its expression is particularly high in lung and testis (as compared to other normal tissues tested). However, the dramatic reduction in the levels of expression of the α 2 δ subunit gene in lung cancer cell lines as compared to the levels of expression in normal lung cells suggests that the α 2 δ subunit gene is involved in carcinogenesis.

EXAMPLE 7

Mutation Analysis of α 2 δ Subunit Gene

Mutations in the α 2 δ subunit gene were analyzed in lung and breast cancer cell lines using Southern blot analysis, exon-PCR using intronic primers, reverse transcription polymerase chain reaction (RT-PCR) and single strand conformation polymorphism analysis (SSCP) followed by sequencing as described below.

A. Southern Blot Analysis

For Southern blot analysis, probes were labeled with a 32 P-dCTP using a random primer labelling kit (Gibco-BRL). Restricted DNAs (5 or 10 μg) were run on a 0.8% agarose gel, transferred and UV cross linked to Hybond N+ membranes (Amersham). Hybridization was performed at 65° C. overnight, and the filters were washed and subjected to autoradiography. Southern blot analysis with an α 2 δ gene probe was performed on >100 lung cancer cell line and 26 breast cancer cell line cDNAs. This led to the discovery of another homozygous nesting deletion involving α 2 δ in a breast cancer cell line HCC1500 (Sekido et al., Oncogene 16:3151-3157 [1998]).

B. Exon-PCR-SSCP

To perform Single Strand Polymorphism Analysis (SSCP), PCR primer pairs (Table 1) were designed to amplify α 2 δ gene sequences which range in size between 80 and 298 pb. In this Table, “LU11” refers to Z84492, or LUCA 11, while “LU9” refers to Z75743 or LUCA9, “LU7” refers to Z74484 or LUCA7, and “LU6 (5′UTR)” refers to Z84493 or LUCA6.

TABLE 1
Primer Pairs for SSCP Analysis of α 2 δ Gene
Primer Name	Primer Scquence	size (bp)	Cosmid	SNP
c16E3 F	GAC AAG CCA CCC CTT ACC TAC
	(SEQ ID NO:14)
c16E3 R	GCA GAG CCC AGT TCT GGC TG	228	LU11
	(SEQ ID NO:15)
c16E4 F	CCA GCA TAG AGT GGT CAG TG
	(SEQ ID NO:16)
c16E4 R	AGT ACC CTG TCC ATT GCC TG	210	LU11
	(SEQ ID NO:17)
c16E5 F	GGC AGG TAG CAC TGA TGG TC
	(SEQ ID NO:18)
c16E5 R	TTG GAG CCA CTG AGT GGA AG	217	LU11
	(SEQ ID NO:19)
c16E6 F	GTG GCT TAC GGT CCT CAC TC
	(SEQ ID NO:20)
c16E6 R	TGT GCT GGG AGT CGC GGC TG	169	LU11
	(SEQ ID NO:21)
c16F7 F	ACC ACT GGA CTG CCT GCG GTG
	(SEQ ID NO:22)
c16E7 R	CAG GGC TGG CAG TGC TAC AC	226	LU11
	(SEQ ID NO:23)
c16E8F	ACT GCC AGC CCT GTG ACC ATG
	(SEQ ID NO:24)
c16E8R	CCA TCT CCA GTC CAG GCA TC	229	LU11	yes
	(SEQ ID NO:25)
MJE2F	TTC GAC AGG ACA CAG CCC AG
	(SEQ ID NO:26)
MJE2R	TGC TGG GTA GAC AGG GGA CAG	221	LU11
	(SEQ ID NO:27)
MJE3F	AGC CCA GTC GCC TCT GCA AG
	(SEQ ID NO:28)
MJE3R	TGG ATA CAG CTG GCT GCG CC	235	LU11
	(SEQ ID NO:29)
MJE4F	CCT TAC CCT AAC AGA GGC ATC
	(SEQ ID NO:30)
MJE4R	AAC CTC ACG TGT TCT CCT GC	189	LU11
	(SEQ ID NO:31)
MJE5F	TGG GCA GGA GAA CAC GTG AG
	(SEQ ID NO:32)
MJE5R	CTG GTG ATG GTC ACA GGA GC	236	LU11
	(SEQ ID NO:33)
MJE6F	AGG CCA CTC ACC ACC CTA CTG
	(SEQ ID NO:34)
MJE6R	TCC TGG GTA CAC CAA GCC AG	259	LU11
	(SEQ ID NO:35)
MJE7F	GGA GGG CTG AGA GCT GCC TG
	(SEQ ID NO:36)
MJE7R	TTG AGG TTA CTG CTG TGG CCA C	235	LU11
	(SEQ ID NO:37)
MJE8F	CTG GTG GCC ACA GCA GTC AC
	(SEQ ID NO:38)
MJE8R	GGA TGG CCA GTT GAA CAT ACG	183	LU11
	(SEQ ID NO:39)
g26MJ2FA	TTC GAC AGG ACA CAG CCC AG
	(SEQ ID NO:40)
g26MJ2RA	GTG CTG GGT AGA CAG GGG ACA GG	222	LU11	yes
	(SEQ ID NO:41)
g26MJ5F	TGG GCA GGA GAA CAC GTG AG
	(SEQ ID NO:42)
g26MJ5RA	CTG GTG ATG GTC ACA GGA GC	235	LU11
	(SEQ ID NO:43)
LU9 F	ACC CCT GGC TTC TGC TTC CTT
	(SEQ ID NO:44)
LU9 R	ACA CTG CCC TCA TGG TAC AG	221	LU9	yes
	(SEQ ID NO:45)
LU10-1 F	ACC TCC CTG TGC TCT GTC CCT CA
	(SEQ ID NO:46)
LU10-1 R	AAT CCA CGC ATG GAT GGG CA	150	LU9
	(SEQ ID NO:47)
LU10-2 F	TGA GCA GCT AGT GCT GAG GCC TCT
	(SEQ ID NO:48)
LU10-2 R	CAG CAA GGA GGT GTG GCT CAG GA	117	LU9
	(SEQ ID NO:49)
gene X 1F	ACT CCA AGC AGT GTG AGT GC
	(SEQ ID NO:50)
gene X 1R	GAA GGA AGT TGT TGC CTG GAA	261	LU9
	(SEQ ID NO:51)
gene X 2F	CAG GTG TGG AAA TAA GCA GG
	(SEQ ID NO:52)
gene X 2R	CAT CTT CTT GCA GCT CCT TG	124	LU9
	(SEQ ID NO:53)
gx LU 9 4F	TGC CCT TGT TAC AGT CAT CTC CA		LU9
	(SEQ ID NO:54)
gx LU 9 3F	TAA GAT GAA AAG CCA GCC AGC TG		LU9
	(SEQ ID NO:55)
genx LU9 2F	GTC TCC TCT TTG GAC AGA TTC TG
	(SEQ ID NO:56)
genx LU9 2R	TGG AGA TGA CTG TAA CAA GGG CAC	115	LU9
	(SEQ ID NO:57)
gx LU9 3R	AAG AGG AGA CTT CCC AGT CTC TTG		LU9
	(SEQ ID NO:58)
g26 Ef	CTG CAT ACA GGA TGC AGC ACT G
	(SEQ ID NO:59)
g26 Er	GCT CAC CTC ACG GAG CTG CTG CGA	88	LU7	yes
	(SEQ ID NO:60)
GX H f	TGT TCA GCC CAG GGA AGC GAA GC
	(SEQ ID NO:61)
GX H r	ACT TAC AGC CCC CGT GGC TCT AG	197	LU6 (5′UTR)
	(SEQ ID NO:62)
−1 ex 1F	CCT GGC TCT GGA AGA ATC TA
	(SEQ ID NO:63)
−1 ex 1R	CAG AAA AGG AGG CAT GCT GA	298	LU6 (5′UTR)
	(SEQ ID NO:64)
−1 ex 2F	AAG CGA GTG GCT GCA GAG
	(SEQ ID NO:65)
−1 ex 2R	CTA AGC GGA AAC CTG GGC A	80	LU6 (5′UTR)
	(SEQ ID NO:66)

Each pair of primers (prepared by Gibco-BRL; BioServe; see Table) was tested for the optimal cycling conditions by running the product on a 4% 3:1 Nu-Sieve agarose gel (FMC). A typical cycling program included: 3 minutes at 95° C., 35 cycles of 1 minute at 95° C., 1 minute at the optimal annealing temperature, 1 minute at 72° C. followed by 7 minutes at 72° C. CEPH family-heads DNA was used as positive control; homozygously deleted cell line DNAs was used as negative control. PCR products were eventually cloned by means of TA Cloning Kit (Invitrogen). The radioactive reaction was performed in a total reaction volume of 12.5 μl containing 100 ng of genomic DNA, 12.5 pmol of each primer, 200 μM dNTPs, 1.5 mM MgCl 2 , 1.25 nCi 35 S-dATP. After heat denaturation (8 min at 90° C.) in formamide buffer (Stop Solution, Amersham), PCR products were run overnight in a 0.5×MDE gel (FMC), 0.6×TBE, at room temperature, 8 W constant power; blotted, dried and exposed to autoradiography film (X-OMAT AR, Kodak).

C. RT-PCR and SSCP

PCR amplified exons or RT-PCR amplified mRNA fragments were subjected to SSCP analyses followed by sequencing when gel shifts were evident as follows. Random-primed, first-strand cDNAs were synthesized from total RNA (1-3 μg/20 μl reaction) using Superscript II (Life Technologies) according to the manufacturer's instructions. All of these samples were shown to successfully amplify for glyceraldehyde 3-phosphate dehydrogenase (GAPDH) cDNA as a control test of the quality of the random primed cDNA. One μl of the random-primed cDNA was subjected to non-nested PCR in a volume of 20 μl containing 1 μM of each primer; 250 mM of dGTP, dATP, and dTTP; 25 mM of “cold” dCTP; 0.05 μl of 3000 mCi/mmol [32P]dCTP (Amersham); 1×reaction buffer (Life Technologies); 2.0 mM MgCL; 5% DMSO; and 1.25 of Taq polymerase in a Perkin-Elmer 9600 thermocycler, using 23 primer sets amplifying the Calcium Channel gene (CACNA2D2) open reading frame exons provided coverage for mutation scanning from nt 164 to 3679 of the AF040709 sequence, as shown in Table 2.

TABLE 2
Primers Used for Single Strand Conformation Polymorphism (SSCP) and RT/PCR cDNA Analysis of
a2d-2 Gene (Nucleotides refer to the AF040709 sequence location)
						Pro-
Forward		Nucle-	Reverse		Nucle-	duct
Primers	5′---> 3′	otides	Primers	5′ ---> 3′	otides	Size
g97F	GCA TCT TGA ATG GAA ACA TGG C	164-185	16GR	TCG ACC TCC TGC TCC AGA	408-425	262
	(SEQ ID NO:67)			(SEQ ID NO:68)
I5GF	AGC ACA CGA TGC AGC ACT G	380-398	15GR	CTT CTC CAC CAA CTT CTG AG	515-534	155
	(SEQ ID NO:69)			(SEQ ID NO:70)
LO9s12075	ACA ACC GGA ACC TGT TCG A	479-497	e80R	CGT CAT AGT ACA CGA TGT CTT C	649-670	192
	(SEQ ID NO:71)			(SEQ ID NO:72)
e79F	ATG CTG CAG AGA ACT TCC AG	596-615	L11pr42	TGA AGT TTG GGT CCT CGA TG	753-772	177
	(SEQ ID NO:73)			(SEQ ID NO:74)
pr5	CTG AGA GTG AGG ATG TGG AA	698-718	pr44	AAG ACC TGC CAC AGC AGT G	911-929	232
	(SEQ ID NO:75)			(SEQ ID NO:76)
pr51	GTG TTC ATG GAA AAC CGC AG	880-899	pr52	CCA CTC ACA TCC ACG ATG ATG	1059-1079	200
	(SEQ ID NO:77)			(SEQ ID NO:78)
pr53	CTG TAC GAT GTC CGA AGG AGA C	997-1018	pr54	TGT GAA GCA TGA CAC AGG CTG	1189-1209	213
	(SEQ ID NO:79)			(SEQ ID NO:80)
pr55	ATC TGT CTG CGA GAT GCT GG	1116-1135	pr16	TTC TGC AGC TGG TCA AAG GG	1313-1331	216
	(SEQ ID NO:81)			(SEQ ID NO:82)
pr57	CGC AAC AAG AAG GTG TTC AAG	1231-1251	pr58	GCC CCA CGG AGA AAG TAA AC	1449-1468	238
	(SEQ ID NO:83)			(SEQ ID NO:84)
pr59	TGT TCA CGG ATG GTG GTG AG	1373-1392	pr60	TTC CTG TGT GTT GAT GCG G	1554-1572	200
	(SEQ ID NO:85)			(SEQ ID NO:86)
g81F	TTG AGA TCC CTT CCA TCG G	1529-1547	g82R	GCT GGT TCT TCT TTT CCC CAG	1718-1738	210
	(SEQ ID NO:87)			(SEQ ID NO:88)
g83F	GTG GTA ACA GGG ACC CTC CCT	1672-1692	g84R	AGA TTG GGG TGC AGC AAC AC	1852-1871	200
	(SEQ ID NO:89)			(SEQ ID NO:90)
g85F	GCT ATG TGT TTG CCA TTG ACC	1820-1840	g86R	CTA TGT ACC TCT CAT CCA GGG AC	2013-2038	219
	(SEQ ID NO:91)			(SEQ ID NO:92)
g87F	CAT GAT TGA TGG CAA CAA GG	1965-1984	g88R	GGG GAG CAG GAA CTC AAA ATA C	2163-2184	220
	(SEQ ID NO:93)			(SEQ ID NO:94)
g89F	GCC AAT CTC AGT GAC CAG ATC C	2131-2152	g90R	AGG TTG TGC AGA AGG AAG TTG	2328-2348	218
	(SEQ ID NO:95)			(SEQ ID NO:96)
g9lF	AGA AAG TGA CTC CAG ACT CCA AG	2297-2319	g92R	TTG AAG GGC TCA GGG TTC TC	2497-2516	220
	(SEQ ID NO:97)			(SEQ ID NO:98)
pr6l	GGA TCT CAA CAC GTA CAG CCT AC	2403-2425	pr62	GGA TGC CCA CAG TGT CAT TC	2607-2626	224
	(SEQ ID NO:99)			(SEQ ID NO:100)
pr63	CCC TTC AAT GCC AGC TTC TAC	2508-2529	pr64	AAC TTC TCA GCC CAA GCC TC	2704-2723	216
	(SEQ ID NO:101)			(SEQ ID NO:102)
pr65	AAT GAC ACT GTG GGC ATC CTC	2608-2629	pr66	TTA ACC TCG CAG TCC ATC TCA C	2789-2810	203
	(SEQ ID NO:103)			(SEQ ID NO:104)
pr67	ACC AAG ACC AGC CTC AGA AGT G	2750-2771	pr68	ATA GGA CTC CTT GCG GGT GTA G	2952-2973	224
	(SEQ ID NO:105)			(SEQ ID NO:106)
pr69	AGG TGG ATG CCA ACC TGA TG	2908-2928	pr70	CGT AGA GAA GCT GCT GGA ACA G	3100-3122	215
	(SEQ ID NO:107)			(SEQ ID NO:108)
pr7l	CAC CGT TGC AGA TTT CCT TAA C	3045-3066	pr72	AGT TTC CGC AGT CGA TGA TG	3252-3272	228
	(SEQ ID NO:109)			(SEQ ID NO:110)
pr73	GAA ACA GAC CCA GTA CTA CTT C	3204-3225	pr74	GCG TTG TAG TCG AAG CAG AT	3454-3473	270
	(SEQ ID NO:111)			(SEQ ID NO:112)
pr75	AGC AGT GTG AGC TAG TGC AG	3407-3426	pr76	AGG GTG GGA AAG GCG AAG A	3661-3679	273
	(SEQ ID NO:113)			(SEQ ID NO:114)

Most of these primer sets amplified fragments of <225 bp of cDNA while two amplified 270 bp of cDNA for optimal mutation detection. A modified touch-down PCR (initial denaturation at 94° C. for 2.5 min, followed by 5 cycles of 30 s at 94° C., 30 s at 68° C., 30 s at 72° C., and then 30 cycles of 30 s at 94° C., 30 s at at 72° C., and a final extension for 10 min at 72° C.) was used. The samples were heat denatured, snap chilled, and run on 0.5×Mutation Detection Enhancement (MDE) gels (FMC) with and without 10% glycerol at 5 W overnight, and subjected to autoradiography for 24 h. Shifted SSCP bands were excised from the MDE gels, and the DNA was eluted with distilled water and re-amplified using the original PCR primers. The PCR product was run on a 2% agarose gel and purified by GeneClean (Bio 101). Automated bi-directional sequencing was performed by ABI 377 Dye Terminator cycle sequencing. Sequences were analyzed and compared to wild-type Calcium channel gene (CACNA2D2) sequences with DNAStar software.

Fifty-nine lung cancer cell line samples (33 small cell lung cancer and 26 non-small cell lung cancers) were tested for mutations by this SSCP method and no amino acid altering mutations were found. As a control normal lung cDNA was also run. In the course of cDNA and SSCP sequencing, at least four (4) single nucleotide polymorphisms (SNPs) were recorded. The previously known microsatellite polymorphic locus, D3S1568, was detected in the sequence of a large intron of the α 2 δ gene.

However, 19 (19/59, i.e., 32%) of the lung cancer cDNA samples gave a blank signal on repeated testing of their cDNAs for several of the primer sets. Without limiting the invention to any particular theory or mechanism, these results indicate either extremely low levels of expression of the gene in lung cancer cell lines and/or modifications in the cDNA which disrupt the open reading frame.

EXAMPLE 8

Generation of Polyclonal Antibodies Against α 2 δ Subunit Isoform I and Expression of α 2 δ in Lung Cancer Cells

The coding region of the cDNA splice isoform 2 (SEQ ID NO:3) (3,442 bp, nt 175 to nt 3,616) was cloned into each of the following three expression vectors: pcDNA3.1 His C (Invitrogen) at the BamHI/NotI site (CMV expression vector), pLJ17 (pAdE1/CMV) at the BamHI/NotI site (adenovirus shuttle vector), and pRev-TRE vector (ClonTech) at the BamHl/SalI site (retrovirus tetracycline regulatable vector). The 3,442 bp construct was subjected to in vitro translation giving a product of ˜130 Kd which compares well to the calculated molecular weight of 129,268 Daltons.

NCI-H1299 non-small cell lung cancer cells were transfected with plasmid pcDNA3.1(α 2 δ) (i.e., the above-described pcDNA3.1 plHisC plasmid into which the cDNA splice isoform 2 was cloned) and tested in in vitro translation experiments using 35 S-methionine in an in vitro transcription/translation system (TNT Coupled Reticulocyte Systems, Promega). For transfection experiments, NCI-H1299 cells (3×10 5 ) were seeded in 3.5 cm culture dishes for 24 h in RPMI 1640 containing 5% fetal bovine serum. Then, 1 μg of cloned DNA was introduced into the cells using the lipofectamine reagent (Gibco-BRL). For protein expression after transfection, cells were harvested 48 hrs later and lysed in 80 μl of sample buffer (50 mM Tris, pH 6.8; 1% SDS, 10% glycerol and 0.3M of β-mercaptoethanol). NCI-H1299 cells were used for these studies because they do not express endogenous α 2 δ-2 mRNA or protein, and are homozygous for multiple polymorphic markers in the 600 kb homozygous deletion region, and thus have undergone loss of heterozygosity for this region.

After transient expression, Western blot analysis using affinity purified rabbit polyclonal anti-peptide antibody which was raised against α 2 δ subunit amino acids 161-181 (peptide A) of SEQ ID NO:4 was used to detect the expressed protein. Western blots showed a band at ˜150 Kd and also at ˜300 Kd area in a non-reduced 4-15% gradient PAGE using the polyclonal antibody against peptide A. It is possible that the increase in the apparent molecular weight (i.e., approximately 129 to 150 kDa) compared to the conceptually translated protein and the in vitro translated protein is the result of N′-glycosylation, in agreement with multiple putative N-glycosylation sites in the α 2 δ-sequence which represent known properties of the α 2 δ-1 protein (Gurnett et al., Neuron 16(2):431-440 [1996]). Endogenous α 2 δ-2 protein of 150 kDa was also detected in some lung tumor cell lines using the same antibody, further confirming that the conceptual translation and anti-peptide antibody preparation were correct.

After reducing the protein with beta-mercaptoethanol only a single band was observed at ˜150 Kd. This is in contrast to the result with the previously reported (alpha 2 )-subunit gene (Ellis et al. [1988], supra; Williams et al. [1992], supra; Ellis et al., U.S. Pat. No. 5,686,241; and Harpold et al., U.S. Pat. No. 5,792,846) which showed a reduction in size after treatment with a reducing agent. While not intending to limit the invention to any particular mechanism, these results demonstrate that while the previously reported human (alpha 2 )-subunit gene is processed into two subunits, the α 2 δ subunit gene of the invention may be processed in a similar or different manner.

FIG. 3 provides Western blot data showing the results of in vitro transcription and translation of α 2 δ-2 experiments. In Panel A, lane 1 contains the products of in vitro transcription and translation of α 2 δ-2 in expression vector pcDNA3.1. In lane 2, no DNA was added in the same reaction. The arrow indicates the expected approximately 130 kd product. In Panel B, results from Western blot analysis of transfection of NCI-H1299 cells with α 2 δ-2 are shown. Lane 1 shows the results for NCI-H1299 cells with α 2 δ-2 in expression vector pcDNA3.1. Lane 2 shows the results for NCI-H1299 cells transfected with pcDNA3.1 vector alone. In these Westerns, affinity-purified anti-α 2 δ-2 peptide antibody was used to detect the protein product. The arrow in the Figure indicates the expected protein product. Sizes of the prestained protein molecular weight markers are indicated on the right. In Panel C results are shown for protein from tumor lysates (loaded at 40 μg per lane). Lane 1 contains protein lysate from NCI-H2077 cells (adenocarcinoma), lane 2 contains lysate from NCI-H383 cells (adenocarcinoma), lane 3 contains lysate from NCI-H2106 cells (large cell neuroendocrine carcinoma), and lane 4 contains lysate from NCI-H1299 cells (large cell carcinoma). As indicated above, the results shown in Panel C indicate that endogenous α 2 δ-2 protein of 150 kDa was detected in some lung tumor cell lines (using the same antibody as with other preparations), further confirming that the conceptual translation and anti-peptide antibody preparation were correct.

EXAMPLE 9

Regulation of Calcium Ion Flux In Vitro by the α 2 δ Subunit Through Cancer Cells and Oocytes

The bioinformatics analysis of the α 2 δ subunit gene and its isoforms clearly demonstrated that this is a new human gene coding for at least two α 2 δ subunits of the voltage-gated plasma membrane calcium channels. It is the inventors' consideration that the single polypeptide products of the gene are post-translationally cleaved into the α 2 and δ polypeptide subunits which, after extensive biochemical modifications, form the α 2 δ protein complex that is necessary to assemble a fully functional plasma membrane calcium channel(s).

Two series of experiments are conducted to ascertain the subunit function of the gene products in regulating calcium ion flux in vitro across cell membranes. First, cDNA sequences (which correspond to ORFs of GenBank Accession ## AF040709, AF042792 and AF042793) and which code for both isoform I and isoform II variants respectively were inserted into the tetracycline controlled episomal expression vectors Tet OFF (Clontech) or pETE. In the Clontech Tet OFF system the gene is not expressed (or expressed at very low levels) in the presence of doxycycline and expressed at very high levels in the absence of doxycycline. The pETE vector is derived from the commercially available Tet OFF vector (Clontech) by inserting an EBNA-1 element to confer an episomal property on the vector. The pETE vectors were then transfected into lung cancer (e.g., NSCLC NCI-H1299, H1607, and A549) and nasopharyngeal cancer cells (HONE-1) which were specifically engineered to constitutively express the tetracycline-controlled transcription activator (TA) by infecting the tumor cells with a retrovirus expressing TA. In this system the transfected genes were highly-to-moderately expressed (as determined by Northern analysis) in the absence of tetracycline and not expressed at all in the presence of tetracycline or its analog, doxycycline. These results demonstrate high level expression in vitro in cancer cells of each of isoforms I and II of the α 2 δ subunit protein.

Clonal NCI-H1299 cell lines constitutively expressing high levels of the α 2 δ subunit polypeptide have already been developed. Clonal cell lines which express high levels of the transfected α 2 δ subunit proteins in a tetracycline controlled fashion are developed by selecting and clonally expanding only transfected cell which express high levels of the subunit. These clonal cell lines are used to measure calcium ion fluxes in the presence and absence of tetracycline or doxycycline special fluorescent staining as previously described (McEnery [1998], supra). Voltage dependent calcium channels:structural insights into channel function, pharmacology, and assembly in health and disease (McEnery [1998], supra). In this setting, it may be established whether the expression of the α 2 δ subunit gene products in cells which otherwise lack expression of endogenous α 2 δ subunit gene would increase calcium entry into the cells as compared to control cells (i.e., a corresponding cell which has not been transfected with the expression vector that encodes the α 2 δ subunit).

Secondly, frog oocytes expressing calcium channels that do not contain α 2 δ subunits may be prepared using methods known in the art (See e.g., Ellis et al. U.S. Pat. No. 5,686,241, and Harpold et al., U.S. Pat. No. 5,792,846, the contents of both of which are herein incorporated by reference). These oocytes are used to test whether a fully functional calcium channel may be reconstituted. This is achieved by introducing recombinant plasmids expressing α 2 δ subunit proteins into these frog oocytes and by measuring calcium fluxes in the transfected cells as compared to control cells. Controls include oocytes which express calcium channels that do not contain α 2 δ subunits and which are not transfected with recombinant plasmids that express α 2 δ subunit proteins. Another control includes oocytes which express a calcium channel that contains α 2 δ subunits and which are not transfected with the recombinant plasmids that express α 2 δ subunit proteins.

EXAMPLE 10

Electrophysiologic Studies

In these experiments, co-expression of α1B and β3 subunits was investigated. Complementary RNA (cRNA) encoding human brain α1B, rabbit skeletal muscle α 2 δ-1, rabbit β 3 , and α 2 δ-2 subunits were synthesized in vitro using T7 RNA polymerase, resuspended in water at a final concentration of ˜1 mg/ml and stored at −80° C. until injection. Xenopus oocytes harvested by standard methods known in the art were injected with a mixtures of the following transcripts: α1B+β 3 , α1B+β 3 +α 2 δ-1, α1B+β 3 +α 2 δ-2 or α 2 δ-2 alone (approximately 50 ng total cRNA/oocyte). Two days later, the oocytes were analyzed using standard two-electrode voltage-clamp technique with 5 mM Ba 2+ as a charge carrier, as known in the art. The holding potential was −120 mV. Currents were recorded in response to test potentials ranging from −110 to +100 mV, filtered at 200 Hz, then analyzed using pClamp 6.04 (Axon Instruments) and Origin (Microcal) software. Leak and capacitance currents were subtracted on-line with a P/4 protocol.

For the studies of coexpression with α1C and α1G subunits, cRNA of either α1C, α1G, or α 2 δ-2 cDNA was synthesized using Ambion Megascript Kit according to the supplier's protocol (Ambion). Due to low expression of wild-type α1C, the modified cDNA, ΔN60, which is truncated by 60 amino acids at the N-terminal end of the rabbit cardiac α1 subunit was used. The rat brain α1G cDNA was contained in the vector pGEM-HE. Fifty nl of cRNA (5 ng for α1C; 5 ng for α1G; and 2.5 ng for α 2 δ-2) of either α1C alone, α1C plus α 2 δ-2, α1G alone, or α1G plus α 2 δ-2, were injected into each oocyte using a Drummond Nanoject pipette injector (Parkway, Pa.). Expression of injected cRNA was measured from the 4th day after injection for α1C alone or α1C plus α 2 δ-2, and the 6-7th day after injection for α1G alone, or α1G plus α 2 δ-2 using the two-electrode voltage clamp method known in the art. Currents were measured in either 40 mM Ba 2+ solution (40 mM Ba(OH) 2 , 50 mM NaOH, 1 mM KOH, and 5 mM HEPES, adjusted to pH 7.4 with methanesulfonic acid) for L-type currents, or 10 mM Ba 2+ solution (10 mM Ba(OH) 2 , 80 mM NaOH, 1 mM KOH, and 5 mM HEPES, adjusted to pH 7.4 with methanesulfonic acid) for T-type currents. Data were sampled at either 2 KHz for L-type currents, or 5 KHz for T-type currents using the pClamp 6 system via a Digidata 1200 A/D converter (Axon Instrument). Leak currents were subtracted using a P/+4 for L-type currents or a P/−6 for T-type currents.

Injection of oocytes with cRNA encoding the pore-forming human α1B subunit together with an auxiliary β 3 subunit resulted in expression of functional N-type calcium channels in oocyte plasma membranes with a peak current of 1.0±0.1 μA (n=4) (See, FIG. 4 A). Channel activity was indicated as representative inward barium currents observed in response to 0 mV and +20 mV test potentials. The magnitude of N-type currents was increased 9 fold to 9.1±1.4 μA (n=10) when α1B and β 3 were co-expressed with the rabbit skeletal muscle α 2 δ-1 subunit (See, FIG. 4 B). When co-expressed with α1B and β 3 subunits, the α 2 δ-2 subunit exerted a similar effect on N-type channel expression, increasing peak current size to 7.6±0.6 μA (n=10)(See, FIG. 4 C). No channel activity was observed after injection of α 2 δ-2 cRNA alone (data not shown). By varying the test potential in the range from −100 mV to +100 mV it was established that the shape and position of current-voltage (IV) relationships were similar for all 3 subunit combinations, with the maximum current at 0 mV test potential and reversal potential at +50 mV (See, FIG. 4 D).

Stimulation of N-type current expression by α2δ-1 and α 2 δ-2 subunits ( FIGS. 4A-C ) is similar to the previously described effect of α2δ-1 on P/Q-type Ca 2+ channels formed by α1A and β subunits (De Waard and Campbell, Neuron 16(2):431-400 [1996]; and Walker and De Waard, Trends Neurosci., 21(4):148-154 [1998]), which has been shown to depend on α2δ-1 subunit glycosylation (Gurnett et al., supra). Thus, it is likely that α 2 δ-2 subunit is glycosylated when expressed in Xenopus oocytes, as is expected from biochemical and sequence analysis. Noticeably, the α 2 δ-1, but not the α 2 δ-2 subunit was able to hasten N-type Ca 2+ channel inactivation. Indeed, at the end of a 50 ms test pulse to +20 mV, the size of the current was reduced to 33±10% (n=8) of the peak current for α1B+β 3 +α 2 δ-1, to 59±5% (n=24) of the peak current for α1B+β 3 +α 2 δ-2 and to 51±4% (n=15) of the peak current for α1B+β 3 subunit combinations.

To test for an α 2 δ-2 effect on L-type channels, either α1C cRNA alone, or α1C plus α 2 δ-2 cRNA were injected into oocytes. Peak currents measured during a series of test potentials were averaged (See, FIG. 4 E). The results shown in Panel E correspond to experiments in which currents were evoked by a series of test pulses of −50 mV to +70 mV from a holding potential of −70 mV in 40 mM Ba 2+ solution. Average α1C currents were collected from 33 oocytes, α1C/α2δ-2 currents were from 31 oocytes isolated from three different frogs. Data represent mean±SEM. The results shown in Panel F correspond to experiments in which currents were elicited by test pulses of −70 mV to +50 mV from a holding potential of −90 mV in 10 mM Ba 2+ solution. Average α1G currents were collected from 33 oocytes, α1G/α2δ-2 currents were from 32 oocytes isolated from four frogs. Panel G provides the average stimulation of α1C and α1G currents by co-expression with α 2 δ-2. When peak current amplitudes measured at +30 mV were compared, α1C/α 2 δ-2 currents were significantly larger than α1C by 201% (t-test, P<0.001). However, there were no significant differences in the position of the IV curves, which peaked at ˜+35 mV. Similar to the α 2 δ-2 effect on α1C channels, co-injection of α 2 δ-2 cRNA with α1G cRNA increased T-type current amplitudes by 176% (t-test, P<0.05), compared to α1G alone.

There were no significant differences in their biophysical properties including activation threshold, position of their IV curves, reversal potentials, and activation and inactivation kinetics. Based upon these experiments, it appears that the cloned α 2 δ-2 protein is able to function as an auxiliary subunit of all three subfamilies of voltage-gated Ca 2+ channels. Since expression of the cloned T-type channels was found to be highly variable between batches of oocytes, each batch was injected with both α1 and α1α2δ-2. Stimulation by α2δ-2 was measured for each batch, then averaged.

EXAMPLE 11

In Vitro and In Vivo Growth Suppression of Tumor Cell Growth

It is the inventors' consideration that the α 2 δ gene by virtue of its location in the critical cancer region on human chromosome 3p21.3 and its association with small cell lung carcinoma in patients with Lambert-Eton syndrome is a strong candidate tumor suppressor gene that is involved in the causation of lung cancer and in the development of several common human malignancies including, but not limited to, lung, breast, cervical, head and neck carcinomas. The tumor growth suppression function of the α 2 δ subunit is analyzed using either constitutively expressed α 2 δ subunit or tet-controlled expression vectors which contain DNA sequences that encode at least a portion of isoform I or isoform II and which express the DNA sequences in the presence of tetracycline, as described supra (Example 9). The constitutively expressing vectors or tet-controlled vectors are transfected into lung cancer and nasopharyngeal carcinoma cells (Example 9) and the transfected cells are used to determine the effect of expression of α 2 δ subunits on growth of the transformed tumor cells both in vitro and in vivo.

The effect on tumor cell growth of the constitutively expressing vectors or in the presence and absence of tetracycline is assessed in vitro under cell culture conditions and in vivo by measuring tumor formation and/or growth rate in nude or SCID mice. The function of the α 2 δ gene as a tumor suppressor gene is determined by observing an increased rate of cell growth of transfected cancer cells in vitro in the presence either of a control vector transfected cell or of tetracycline as compared to the rate of cell growth in the absence of tetracycline. The tumor suppressor function of the α 2 δ gene is also confirmed in vivo by the observation that the number and/or rate of tumor formation by the transfected tumor cells in nude mice is increased in the presence or absence of tetracycline as compared to that in the presence or absence of tetracycline for tumor cells transfected with the Tet regulatable system. In the constitutively expressing system, the tumor growth rate or number is compared for tumors arising from tumor cells transfected with either the control vector or the control vector which contains a specifically constructed inactive mutant form of the α 2 δ gene.

EXAMPLE 12

Generation of Knockout Mice by Targeted Inactivation of the α 2 δ Subunit Gene

Knockout mice which do not contain a functional murine orthologous α 2 δ gene are generated as follows. The mouse ESTs (GenBank Accession ## AA000341 and AA08996) which the inventors identified as representing sequences of the murine orthologous α 2 δ gene were used to screen a phage genomic library made from mouse stem cells (ES). An overlapping phage contig (about 25 kb in size) containing several exons from the carboxy terminus of the mouse gene and part of the 3′ UTR was assembled and used in the construction work. Using methods known in the art, a targeting vector containing this portion of the murine ortholog of the human α 2 δ gene interrupted by a neo positive selection cassette is constructed. This vector is electroporated into mouse 129SVJ embryonic stem cells and the targeted DNA is integrated in a site-specific manner by homologous recombination. The targeted ES cells are injected into mouse blastocysts and placed into a pseudopregnant female for production of heterozygous mice. These mice are used for production of homozygous null mice by interbreeding and screening the progeny for the presence of the α 2 δ gene. Heterozygous and homozygous transgenic knockout mice are used in carcinogenesis studies (e.g., to determine whether there is a change in tumor incidence and/or growth rate compared to wild-type mice). Tumor development in multiple tissues is monitored and animals are sacrificed to remove and evaluate tumors for size, location and histology. The heterozygous and homozygous transgenic knockout mice are also used to evaluate development of neurological and cardiovascular pathology using methods well known in the art.

From the above, it is clear that the invention provides calcium channel alpha2delta (α 2 δ) subunits and nucleic acid sequences encoding them. These compositions are useful in methods for identifying compounds that modulate the activity of calcium channels and for identifying compounds as therapeutic for disease.

All publications and patents mentioned in the above specification are herein incorporated by reference. Various modifications and variations of the described method and system of the invention will be apparent to those skilled in the art without departing from the scope and spirit of the invention. Although the invention has been described in connection with specific preferred embodiments, it should be understood that the invention as claimed should not be unduly limited to such specific embodiments. Indeed, various modifications of the described modes for carrying out the invention which are obvious to those skilled in the art and in fields related thereto are intended to be within the scope of the invention.

114 1 5463 DNA Homo sapiens CDS (162)..(3599) 1gccagcgctg cagggagata gcagcgcgca gcccgcagag gcgctgcggc ccgtgcagcc 60ccggaggccc ctcgcggaga aggcggcggc ggaggagagg ccgagttacc gcccgccgcc 120cgcgcccccc ctccccgcgg cgccgcatct tgaatggaaa c atg gcg gtg ccg gct 176 Met Ala Val Pro Ala 1 5cgg acc tgc ggc gcc tct cgg ccc ggc cca gcg cgg act gcg cgc ccc 224Arg Thr Cys Gly Ala Ser Arg Pro Gly Pro Ala Arg Thr Ala Arg Pro 10 15 20tgg ccc ggc tgc ggc ccc cac cct ggc ccc ggc acc cgg cgc ccg acg 272Trp Pro Gly Cys Gly Pro His Pro Gly Pro Gly Thr Arg Arg Pro Thr 25 30 35tcc ggg ccc ccg cgc ccg ctg tgg ctg ctg ctg ccg ctt cta ccg ctg 320Ser Gly Pro Pro Arg Pro Leu Trp Leu Leu Leu Pro Leu Leu Pro Leu 40 45 50ctc gcc gcc ccc ggc gcc tct gcc tac agc ttc ccc cag cag cac acg 368Leu Ala Ala Pro Gly Ala Ser Ala Tyr Ser Phe Pro Gln Gln His Thr 55 60 65atg cag cac tgg gcc cgg cgt ctg gag cag gag gtc gac ggc gtg atg 416Met Gln His Trp Ala Arg Arg Leu Glu Gln Glu Val Asp Gly Val Met 70 75 80 85cgg att ttt gga ggc gtc cag cag ctc cgt gag att tac aag gac aac 464Arg Ile Phe Gly Gly Val Gln Gln Leu Arg Glu Ile Tyr Lys Asp Asn 90 95 100cgg aac ctg ttc gag gta cag gag aat gag cct cag aag ttg gtg gag 512Arg Asn Leu Phe Glu Val Gln Glu Asn Glu Pro Gln Lys Leu Val Glu 105 110 115aag gtg gca ggg gac att gag agc ctt ctg gac agg aag gtg cag gcc 560Lys Val Ala Gly Asp Ile Glu Ser Leu Leu Asp Arg Lys Val Gln Ala 120 125 130ctg aag aga ctg gct gat gct gca gag aac ttc cag aaa gca cac cgc 608Leu Lys Arg Leu Ala Asp Ala Ala Glu Asn Phe Gln Lys Ala His Arg 135 140 145tgg cag gac aac atc aag gag gaa gac atc gtg tac tat gac gcc aag 656Trp Gln Asp Asn Ile Lys Glu Glu Asp Ile Val Tyr Tyr Asp Ala Lys150 155 160 165gct gac gct gag ctg gac gac cct gag agt gag gat gtg gaa agg ggg 704Ala Asp Ala Glu Leu Asp Asp Pro Glu Ser Glu Asp Val Glu Arg Gly 170 175 180tct aag gcc agc acc cta agg ctg gac ttc atc gag gac cca aac ttc 752Ser Lys Ala Ser Thr Leu Arg Leu Asp Phe Ile Glu Asp Pro Asn Phe 185 190 195aag aac aag gtc aac tat tca tac gcg gct gta cag atc cct acg gac 800Lys Asn Lys Val Asn Tyr Ser Tyr Ala Ala Val Gln Ile Pro Thr Asp 200 205 210atc tac aaa ggc tcc act gtc atc ctc aat gag ctc aac tgg aca gag 848Ile Tyr Lys Gly Ser Thr Val Ile Leu Asn Glu Leu Asn Trp Thr Glu 215 220 225gcc ctg gag aat gtg ttc atg gaa aac cgc aga caa gac ccc aca ctg 896Ala Leu Glu Asn Val Phe Met Glu Asn Arg Arg Gln Asp Pro Thr Leu230 235 240 245ctg tgg cag gtc ttc ggc agc gcc aca gga gtc act cgc tac tac ccg 944Leu Trp Gln Val Phe Gly Ser Ala Thr Gly Val Thr Arg Tyr Tyr Pro 250 255 260gcc acc ccg tgg cga gcc ccc aag aag atc gac ctg tac gat gtc cga 992Ala Thr Pro Trp Arg Ala Pro Lys Lys Ile Asp Leu Tyr Asp Val Arg 265 270 275agg aga ccc tgg tat atc cag ggg gcc tcg tca ccc aaa gac atg gtc 1040Arg Arg Pro Trp Tyr Ile Gln Gly Ala Ser Ser Pro Lys Asp Met Val 280 285 290atc atc gtg gat gtg agt ggc agt gtg agc ggc ctg acc ctg aag ctg 1088Ile Ile Val Asp Val Ser Gly Ser Val Ser Gly Leu Thr Leu Lys Leu 295 300 305atg aag aca tct gtc tgc gag atg ctg gac acg ctg tct gat gat gac 1136Met Lys Thr Ser Val Cys Glu Met Leu Asp Thr Leu Ser Asp Asp Asp310 315 320 325tat gtg aat gtg gcc tcg ttc aac gag aag gca cag cct gtg tca tgc 1184Tyr Val Asn Val Ala Ser Phe Asn Glu Lys Ala Gln Pro Val Ser Cys 330 335 340ttc aca cac ctg gtg cag gcc aat gtg cgc aac aag aag gtg ttc aag 1232Phe Thr His Leu Val Gln Ala Asn Val Arg Asn Lys Lys Val Phe Lys 345 350 355gaa gct gtg cag ggc atg gtg gcc aag ggc acc aca ggc tac aag gcc 1280Glu Ala Val Gln Gly Met Val Ala Lys Gly Thr Thr Gly Tyr Lys Ala 360 365 370ggc ttt gag tat gcc ttt gac cag ctg cag aac tcc aac atc act cgg 1328Gly Phe Glu Tyr Ala Phe Asp Gln Leu Gln Asn Ser Asn Ile Thr Arg 375 380 385gcc aac tgc aac aag atg atc atg atg ttc acg gat ggt ggt gag gac 1376Ala Asn Cys Asn Lys Met Ile Met Met Phe Thr Asp Gly Gly Glu Asp390 395 400 405cgc gtg cag gac gtc ttt gag aag tac aat tgg cca aac cgg acg gtg 1424Arg Val Gln Asp Val Phe Glu Lys Tyr Asn Trp Pro Asn Arg Thr Val 410 415 420cgc gtg ttt act ttc tcc gtg ggg cag cat aac tat gac gtc aca ccg 1472Arg Val Phe Thr Phe Ser Val Gly Gln His Asn Tyr Asp Val Thr Pro 425 430 435ctg cag tgg atg gcc tgt gcc aac aaa ggc tac tat ttt gag atc cct 1520Leu Gln Trp Met Ala Cys Ala Asn Lys Gly Tyr Tyr Phe Glu Ile Pro 440 445 450tcc atc gga gcc atc cgc atc aac aca cag gaa tat cta gat gtg ttg 1568Ser Ile Gly Ala Ile Arg Ile Asn Thr Gln Glu Tyr Leu Asp Val Leu 455 460 465ggc agg ccc atg gtg ctg gca ggc aag gag gcc aag cag gtt cag tgg 1616Gly Arg Pro Met Val Leu Ala Gly Lys Glu Ala Lys Gln Val Gln Trp470 475 480 485acc aac gtg tat gag gat gca ctg gga ctg ggg ttg gtg gta aca ggg 1664Thr Asn Val Tyr Glu Asp Ala Leu Gly Leu Gly Leu Val Val Thr Gly 490 495 500acc ctc cct gtt ttc aac ctg aca cag gat ggc cct ggg gaa aag aag 1712Thr Leu Pro Val Phe Asn Leu Thr Gln Asp Gly Pro Gly Glu Lys Lys 505 510 515aac cag ctg atc ctg ggc gtg atg ggc att gac gtg gct ctg aat gac 1760Asn Gln Leu Ile Leu Gly Val Met Gly Ile Asp Val Ala Leu Asn Asp 520 525 530atc aag agg ctg acc ccc aac tac acg ctt gga gcc aac ggc tat gtg 1808Ile Lys Arg Leu Thr Pro Asn Tyr Thr Leu Gly Ala Asn Gly Tyr Val 535 540 545ttt gcc att gac ctg aac ggc tac gtg ttg ctg cac ccc aat ctc aag 1856Phe Ala Ile Asp Leu Asn Gly Tyr Val Leu Leu His Pro Asn Leu Lys550 555 560 565ccc cag acc acc aac ttc cgg gag cct gtg act ctg gac ttc ctg gat 1904Pro Gln Thr Thr Asn Phe Arg Glu Pro Val Thr Leu Asp Phe Leu Asp 570 575 580gcg gag cta gag gat gag aac aag gaa gag atc cgt cgg agc atg att 1952Ala Glu Leu Glu Asp Glu Asn Lys Glu Glu Ile Arg Arg Ser Met Ile 585 590 595gat ggc aac aag ggc cac aag cag atc aga acg ttg gtc aag tcc ctg 2000Asp Gly Asn Lys Gly His Lys Gln Ile Arg Thr Leu Val Lys Ser Leu 600 605 610gat gag agg tac ata gat gag gtg aca cgg aac tac acc tgg gtg cct 2048Asp Glu Arg Tyr Ile Asp Glu Val Thr Arg Asn Tyr Thr Trp Val Pro 615 620 625ata agg agc act aac tac agc ctg ggg ctg gtg ctc cca ccc tac agc 2096Ile Arg Ser Thr Asn Tyr Ser Leu Gly Leu Val Leu Pro Pro Tyr Ser630 635 640 645acc ttc tac ctc caa gcc aat ctc agt gac cag atc ctg cag gtc aag 2144Thr Phe Tyr Leu Gln Ala Asn Leu Ser Asp Gln Ile Leu Gln Val Lys 650 655 660tat ttt gag ttc ctg ctc ccc agc agc ttt gag tct gaa gga cac gtt 2192Tyr Phe Glu Phe Leu Leu Pro Ser Ser Phe Glu Ser Glu Gly His Val 665 670 675ttc att gct ccc aga gag tac tgc aag gac ctg aat gcc tca gac aac 2240Phe Ile Ala Pro Arg Glu Tyr Cys Lys Asp Leu Asn Ala Ser Asp Asn 680 685 690aac acc gag ttc ctg aaa aac ttt att gag ctc atg gag aaa gtg act 2288Asn Thr Glu Phe Leu Lys Asn Phe Ile Glu Leu Met Glu Lys Val Thr 695 700 705cca gac tcc aag cag tgc aac aac ttc ctt ctg cac aac ctg atc ttg 2336Pro Asp Ser Lys Gln Cys Asn Asn Phe Leu Leu His Asn Leu Ile Leu710 715 720 725gac acg ggc atc acg cag cag ctg gta gag cgt gtg tgg agg gac cag 2384Asp Thr Gly Ile Thr Gln Gln Leu Val Glu Arg Val Trp Arg Asp Gln 730 735 740gat ctc aac acg tac agc cta ctg gcc gtg ttc gct gcc aca gac ggt 2432Asp Leu Asn Thr Tyr Ser Leu Leu Ala Val Phe Ala Ala Thr Asp Gly 745 750 755ggc atc acc cga gtc ttc ccc aac aag gca gct gag gac tgg aca gag 2480Gly Ile Thr Arg Val Phe Pro Asn Lys Ala Ala Glu Asp Trp Thr Glu 760 765 770aac cct gag ccc ttc aat gcc agc ttc tac cgc cgc agc ctg gat aac 2528Asn Pro Glu Pro Phe Asn Ala Ser Phe Tyr Arg Arg Ser Leu Asp Asn 775 780 785cac ggt tat gtc ttc aag ccc cca cac cag gat gcc ctg tta agg ccg 2576His Gly Tyr Val Phe Lys Pro Pro His Gln Asp Ala Leu Leu Arg Pro790 795 800 805ctg gag ctg gag aat gac act gtg ggc atc ctc gtc agc aca gct gtg 2624Leu Glu Leu Glu Asn Asp Thr Val Gly Ile Leu Val Ser Thr Ala Val 810 815 820gag ctc agc cta ggc agg cgc aca ctg agg cca gca gtg gtg ggc gtc 2672Glu Leu Ser Leu Gly Arg Arg Thr Leu Arg Pro Ala Val Val Gly Val 825 830 835aag ctg gac cta gag gct tgg gct gag aag ttc aag gtg cta gcc agc 2720Lys Leu Asp Leu Glu Ala Trp Ala Glu Lys Phe Lys Val Leu Ala Ser 840 845 850aac cgt acc cac caa gac cag cct cag aag tgc ggc ccc aac agc cac 2768Asn Arg Thr His Gln Asp Gln Pro Gln Lys Cys Gly Pro Asn Ser His 855 860 865tgt gag atg gac tgc gag gtt aac aat gag gac tta ctc tgt gtc ctc 2816Cys Glu Met Asp Cys Glu Val Asn Asn Glu Asp Leu Leu Cys Val Leu870 875 880 885att gat gat gga gga ttc ctg gtg ctg tca aac cag aac cat cag tgg 2864Ile Asp Asp Gly Gly Phe Leu Val Leu Ser Asn Gln Asn His Gln Trp 890 895 900gac cag gtg ggc agg ttc ttc agt gag gtg gat gcc aac ctg atg ctg 2912Asp Gln Val Gly Arg Phe Phe Ser Glu Val Asp Ala Asn Leu Met Leu 905 910 915gca ctc tac aat aac tcc ttc tac acc cgc aag gag tcc tat gac tat 2960Ala Leu Tyr Asn Asn Ser Phe Tyr Thr Arg Lys Glu Ser Tyr Asp Tyr 920 925 930cag gca gcc tgt gcc cct cag ccc cct ggc aac ctg ggt gct gca ccc 3008Gln Ala Ala Cys Ala Pro Gln Pro Pro Gly Asn Leu Gly Ala Ala Pro 935 940 945cgg ggt gtc ttt gtg ccc acc gtt gca gat ttc ctt aac ctg gcc tgg 3056Arg Gly Val Phe Val Pro Thr Val Ala Asp Phe Leu Asn Leu Ala Trp950 955 960 965tgg acc tct gct gcc gcc tgg tcc ctg ttc cag cag ctt ctc tac ggc 3104Trp Thr Ser Ala Ala Ala Trp Ser Leu Phe Gln Gln Leu Leu Tyr Gly 970 975 980ctc atc tac cac agc tgg ttc caa gca gac ccc gcg gag gcc gag ggg 3152Leu Ile Tyr His Ser Trp Phe Gln Ala Asp Pro Ala Glu Ala Glu Gly 985 990 995agc ccc gag acg cgc gag agc agc tgc gtc atg aaa cag acc cag tac 3200Ser Pro Glu Thr Arg Glu Ser Ser Cys Val Met Lys Gln Thr Gln Tyr 1000 1005 1010tac ttc ggc tcg gta aac gcc tcc tac aac gcc atc atc gac tgc gga 3248Tyr Phe Gly Ser Val Asn Ala Ser Tyr Asn Ala Ile Ile Asp Cys Gly 1015 1020 1025aac tgc tcc agg ctg ttc cac gcg cag aga ctg acc aac acc aat ctt 3296Asn Cys Ser Arg Leu Phe His Ala Gln Arg Leu Thr Asn Thr Asn Leu1030 1035 1040 1045ctc ttt gtg gtg gcc gag aag ccg ctg tgc agc cag tgc gag gct ggc 3344Leu Phe Val Val Ala Glu Lys Pro Leu Cys Ser Gln Cys Glu Ala Gly 1050 1055 1060cgg ctg ctg cag aag gag acg cac tgc cca gcg gac ggc ccg gag cag 3392Arg Leu Leu Gln Lys Glu Thr His Cys Pro Ala Asp Gly Pro Glu Gln 1065 1070 1075tgt gag cta gtg cag aga ccg cga tac cgg aga ggc ccg cac atc tgc 3440Cys Glu Leu Val Gln Arg Pro Arg Tyr Arg Arg Gly Pro His Ile Cys 1080 1085 1090ttc gac tac aac gcg aca gaa gat acc tca gac tgt ggc cgc ggg gcc 3488Phe Asp Tyr Asn Ala Thr Glu Asp Thr Ser Asp Cys Gly Arg Gly Ala 1095 1100 1105tcc ttc ccg ccg tcg ctg ggc gtc ctg gtc tcc ctg caa ctg ctg ctc 3536Ser Phe Pro Pro Ser Leu Gly Val Leu Val Ser Leu Gln Leu Leu Leu1110 1115 1120 1125ctc ctg ggc ctg ccg ccc cgg ccg cag cct caa gtc ctc gtc cac gcc 3584Leu Leu Gly Leu Pro Pro Arg Pro Gln Pro Gln Val Leu Val His Ala 1130 1135 1140tct cgc cgc ctc tga gcaccctgcc ccaccccacc tccactccca cctcacccgg 3639Ser Arg Arg Leu 1145cctcttcgcc tttcccaccc tcctgcccca cactccccgc cttagagcct cgtccctccc 3699tcactgaagg acctgagctg gccaggccct gagagtctgg tctgcgcctt gggatgggga 3759gtcccaaagc gggacgccgc aggtgtttgg cacccaaatc acatctcacc tccgaactgt 3819tcaagtgtcc ccagaccctt cttgcctgct gggctccccc cagtgggatg ggacagggag 3879gccacacgca ctggtgccaa aaccaggcct ctgctgccgc ccttcctgga ggctgcctat 3939gttggggggg accctgcctc agctgacccg gcctctctgc cccacccaag cccaaacttg 3999gtttctgtga gaatagtgga ggaaggtgag atggccagtt tgaagcctgt gcctcccagc 4059ttaaatccta gcaggagaga ggctctgggg cagcccccat gggctcctgc ccctttcagg 4119cctacagcca catccccaag cccaccaggt gtcaggatag tcacagtgat accagttcag 4179acactacccc atatacacct ggaacattga ggatggaaac tggactcaca ttcgacatac 4239cccactgggc acacgcacaa acacacacac tatggggtgg ggtgggtgta ggggcttaca 4299aagccttaca cagggcgagg ggttggtggg agggttggca cctgcacact ccatctcctg 4359ctcaccacct gcctctaatc tgagctgcag cctggctggt cctcccattt ctaaagctga 4419atgtcaaaca gtgccaaatg ctggggcagg gggtgaagaa ccctctgtcc cacccctagc 4479caccagtgtc ctccaagtgc cccctcacct ctccaggtgc tcattgtaac catttctcac 4539tagtgtcagg cccccagtgg gaccacatgc cactgcctgc acctttcggc agaggaaccc 4599ccaccagaca tcaccctttg ccttagcagg ggtgactttg tctctcctgg ctgggccatc 4659cttccgccaa tctggccctt acacactcag gcctgtgccc actccctatc tccttcccac 4719ccctacacac acactccctg cttgcaggag gccaaactgt ccctcccttg ctgaacacac 4779acacacacac acacacacag gtggggactg ggcacagctc ttcacaccat tcattctggt 4839catttccccc aaaggcatcc cagcctgggg gccagtgggg aactgagggc aaggggatat 4899agtgatgggg ctcagatgga ctgggaggag ggggagggtg atgcattaat taatggcttc 4959gttaattaat gtcatgttgc ttgtcgcttt ctcagtgtgt gtgtgtggtc catgcccact 5019gctggtgcca gggtgggtgt ccatgtgcac ccggcctgga tgccagctgt gtccttcggg 5079ggcgtgcgtg taactgtagt gtagtcaggt gctcaatgga gaatataaac atatacagaa 5139aaatatatat tttaagttta aaaaacagaa aaacagacaa aacaatcccc atcaggtagc 5199tgtctaaccc ccagctgggt ctaatccttc tcattaccca cccgacctgg ctgcccctca 5259ccttgggctg ggggactggg gggccatttc cttttctctg cccttttttt gttgttctat 5319tttgtacaga caagttggaa aaacaacagc gacaaaaaag tcaagaaact ttgtaaaata 5379tcgtgtgtgt gattccttgt aaaatatttt caaatggttt attacagaag atcagttatt 5439aaataatgtt catattttca cttc 5463 2 1145 PRT Homo sapiens 2Met Ala Val Pro Ala Arg Thr Cys Gly Ala Ser Arg Pro Gly Pro Ala 1 5 10 15Arg Thr Ala Arg Pro Trp Pro Gly Cys Gly Pro His Pro Gly Pro Gly 20 25 30Thr Arg Arg Pro Thr Ser Gly Pro Pro Arg Pro Leu Trp Leu Leu Leu 35 40 45Pro Leu Leu Pro Leu Leu Ala Ala Pro Gly Ala Ser Ala Tyr Ser Phe 50 55 60Pro Gln Gln His Thr Met Gln His Trp Ala Arg Arg Leu Glu Gln Glu 65 70 75 80Val Asp Gly Val Met Arg Ile Phe Gly Gly Val Gln Gln Leu Arg Glu 85 90 95Ile Tyr Lys Asp Asn Arg Asn Leu Phe Glu Val Gln Glu Asn Glu Pro 100 105 110Gln Lys Leu Val Glu Lys Val Ala Gly Asp Ile Glu Ser Leu Leu Asp 115 120 125Arg Lys Val Gln Ala Leu Lys Arg Leu Ala Asp Ala Ala Glu Asn Phe 130 135 140Gln Lys Ala His Arg Trp Gln Asp Asn Ile Lys Glu Glu Asp Ile Val145 150 155 160Tyr Tyr Asp Ala Lys Ala Asp Ala Glu Leu Asp Asp Pro Glu Ser Glu 165 170 175Asp Val Glu Arg Gly Ser Lys Ala Ser Thr Leu Arg Leu Asp Phe Ile 180 185 190Glu Asp Pro Asn Phe Lys Asn Lys Val Asn Tyr Ser Tyr Ala Ala Val 195 200 205Gln Ile Pro Thr Asp Ile Tyr Lys Gly Ser Thr Val Ile Leu Asn Glu 210 215 220Leu Asn Trp Thr Glu Ala Leu Glu Asn Val Phe Met Glu Asn Arg Arg225 230 235 240Gln Asp Pro Thr Leu Leu Trp Gln Val Phe Gly Ser Ala Thr Gly Val 245 250 255Thr Arg Tyr Tyr Pro Ala Thr Pro Trp Arg Ala Pro Lys Lys Ile Asp 260 265 270Leu Tyr Asp Val Arg Arg Arg Pro Trp Tyr Ile Gln Gly Ala Ser Ser 275 280 285Pro Lys Asp Met Val Ile Ile Val Asp Val Ser Gly Ser Val Ser Gly 290 295 300Leu Thr Leu Lys Leu Met Lys Thr Ser Val Cys Glu Met Leu Asp Thr305 310 315 320Leu Ser Asp Asp Asp Tyr Val Asn Val Ala Ser Phe Asn Glu Lys Ala 325 330 335Gln Pro Val Ser Cys Phe Thr His Leu Val Gln Ala Asn Val Arg Asn 340 345 350Lys Lys Val Phe Lys Glu Ala Val Gln Gly Met Val Ala Lys Gly Thr 355 360 365Thr Gly Tyr Lys Ala Gly Phe Glu Tyr Ala Phe Asp Gln Leu Gln Asn 370 375 380Ser Asn Ile Thr Arg Ala Asn Cys Asn Lys Met Ile Met Met Phe Thr385 390 395 400Asp Gly Gly Glu Asp Arg Val Gln Asp Val Phe Glu Lys Tyr Asn Trp 405 410 415Pro Asn Arg Thr Val Arg Val Phe Thr Phe Ser Val Gly Gln His Asn 420 425 430Tyr Asp Val Thr Pro Leu Gln Trp Met Ala Cys Ala Asn Lys Gly Tyr 435 440 445Tyr Phe Glu Ile Pro Ser Ile Gly Ala Ile Arg Ile Asn Thr Gln Glu 450 455 460Tyr Leu Asp Val Leu Gly Arg Pro Met Val Leu Ala Gly Lys Glu Ala465 470 475 480Lys Gln Val Gln Trp Thr Asn Val Tyr Glu Asp Ala Leu Gly Leu Gly 485 490 495Leu Val Val Thr Gly Thr Leu Pro Val Phe Asn Leu Thr Gln Asp Gly 500 505 510Pro Gly Glu Lys Lys Asn Gln Leu Ile Leu Gly Val Met Gly Ile Asp 515 520 525Val Ala Leu Asn Asp Ile Lys Arg Leu Thr Pro Asn Tyr Thr Leu Gly 530 535 540Ala Asn Gly Tyr Val Phe Ala Ile Asp Leu Asn Gly Tyr Val Leu Leu545 550 555 560His Pro Asn Leu Lys Pro Gln Thr Thr Asn Phe Arg Glu Pro Val Thr 565 570 575Leu Asp Phe Leu Asp Ala Glu Leu Glu Asp Glu Asn Lys Glu Glu Ile 580 585 590Arg Arg Ser Met Ile Asp Gly Asn Lys Gly His Lys Gln Ile Arg Thr 595 600 605Leu Val Lys Ser Leu Asp Glu Arg Tyr Ile Asp Glu Val Thr Arg Asn 610 615 620Tyr Thr Trp Val Pro Ile Arg Ser Thr Asn Tyr Ser Leu Gly Leu Val625 630 635 640Leu Pro Pro Tyr Ser Thr Phe Tyr Leu Gln Ala Asn Leu Ser Asp Gln 645 650 655Ile Leu Gln Val Lys Tyr Phe Glu Phe Leu Leu Pro Ser Ser Phe Glu 660 665 670Ser Glu Gly His Val Phe Ile Ala Pro Arg Glu Tyr Cys Lys Asp Leu 675 680 685Asn Ala Ser Asp Asn Asn Thr Glu Phe Leu Lys Asn Phe Ile Glu Leu 690 695 700Met Glu Lys Val Thr Pro Asp Ser Lys Gln Cys Asn Asn Phe Leu Leu705 710 715 720His Asn Leu Ile Leu Asp Thr Gly Ile Thr Gln Gln Leu Val Glu Arg 725 730 735Val Trp Arg Asp Gln Asp Leu Asn Thr Tyr Ser Leu Leu Ala Val Phe 740 745 750Ala Ala Thr Asp Gly Gly Ile Thr Arg Val Phe Pro Asn Lys Ala Ala 755 760 765Glu Asp Trp Thr Glu Asn Pro Glu Pro Phe Asn Ala Ser Phe Tyr Arg 770 775 780Arg Ser Leu Asp Asn His Gly Tyr Val Phe Lys Pro Pro His Gln Asp785 790 795 800Ala Leu Leu Arg Pro Leu Glu Leu Glu Asn Asp Thr Val Gly Ile Leu 805 810 815Val Ser Thr Ala Val Glu Leu Ser Leu Gly Arg Arg Thr Leu Arg Pro 820 825 830Ala Val Val Gly Val Lys Leu Asp Leu Glu Ala Trp Ala Glu Lys Phe 835 840 845Lys Val Leu Ala Ser Asn Arg Thr His Gln Asp Gln Pro Gln Lys Cys 850 855 860Gly Pro Asn Ser His Cys Glu Met Asp Cys Glu Val Asn Asn Glu Asp865 870 875 880Leu Leu Cys Val Leu Ile Asp Asp Gly Gly Phe Leu Val Leu Ser Asn 885 890 895Gln Asn His Gln Trp Asp Gln Val Gly Arg Phe Phe Ser Glu Val Asp 900 905 910Ala Asn Leu Met Leu Ala Leu Tyr Asn Asn Ser Phe Tyr Thr Arg Lys 915 920 925Glu Ser Tyr Asp Tyr Gln Ala Ala Cys Ala Pro Gln Pro Pro Gly Asn 930 935 940Leu Gly Ala Ala Pro Arg Gly Val Phe Val Pro Thr Val Ala Asp Phe945 950 955 960Leu Asn Leu Ala Trp Trp Thr Ser Ala Ala Ala Trp Ser Leu Phe Gln 965 970 975Gln Leu Leu Tyr Gly Leu Ile Tyr His Ser Trp Phe Gln Ala Asp Pro 980 985 990Ala Glu Ala Glu Gly Ser Pro Glu Thr Arg Glu Ser Ser Cys Val Met 995 1000 1005Lys Gln Thr Gln Tyr Tyr Phe Gly Ser Val Asn Ala Ser Tyr Asn Ala 1010 1015 1020Ile Ile Asp Cys Gly Asn Cys Ser Arg Leu Phe His Ala Gln Arg Leu1025 1030 1035 1040Thr Asn Thr Asn Leu Leu Phe Val Val Ala Glu Lys Pro Leu Cys Ser 1045 1050 1055Gln Cys Glu Ala Gly Arg Leu Leu Gln Lys Glu Thr His Cys Pro Ala 1060 1065 1070Asp Gly Pro Glu Gln Cys Glu Leu Val Gln Arg Pro Arg Tyr Arg Arg 1075 1080 1085Gly Pro His Ile Cys Phe Asp Tyr Asn Ala Thr Glu Asp Thr Ser Asp 1090 1095 1100Cys Gly Arg Gly Ala Ser Phe Pro Pro Ser Leu Gly Val Leu Val Ser1105 1110 1115 1120Leu Gln Leu Leu Leu Leu Leu Gly Leu Pro Pro Arg Pro Gln Pro Gln 1125 1130 1135Val Leu Val His Ala Ser Arg Arg Leu 1140 1145 3 5482 DNA Homo sapiens CDS (181)..(3618) 3cgggcagcgc agcccgcaga ggcgctgcgg cccgtgcagc cccggaggcc cctcgcggag 60aaggcggcgg cggaggagag gccgagttac cgcccgccgc ccgcgccccc ccaaccccgc 120cgccgccgcc gccgccgcca ctgccccccc tccccgcggc gccgcatctt gaatggaaac 180atg gcg gtg ccg gct cgg acc tgc ggc gcc tct cgg ccc ggc cca gcg 228Met Ala Val Pro Ala Arg Thr Cys Gly Ala Ser Arg Pro Gly Pro Ala 1 5 10 15cgg act gcg cgc ccc tgg ccc ggc tgc ggc ccc cac cct ggc ccc ggc 276Arg Thr Ala Arg Pro Trp Pro Gly Cys Gly Pro His Pro Gly Pro Gly 20 25 30acc cgg cgc ccg acg tcc ggg ccc ccg cgc ccg ctg tgg ctg ctg ctg 324Thr Arg Arg Pro Thr Ser Gly Pro Pro Arg Pro Leu Trp Leu Leu Leu 35 40 45ccg ctt cta ccg ctg ctc gcc gcc ccc ggc gcc tct gcc tac agc ttc 372Pro Leu Leu Pro Leu Leu Ala Ala Pro Gly Ala Ser Ala Tyr Ser Phe 50 55 60ccc cag cag cac acg atg cag cac tgg gcc cgg cgt ctg gag cag gag 420Pro Gln Gln His Thr Met Gln His Trp Ala Arg Arg Leu Glu Gln Glu 65 70 75 80gtc gac ggc gtg atg cgg att ttt gga ggc gtc cag cag ctc cgt gag 468Val Asp Gly Val Met Arg Ile Phe Gly Gly Val Gln Gln Leu Arg Glu 85 90 95att tac aag gac aac cgg aac ctg ttc gag gta cag gag aat gag cct 516Ile Tyr Lys Asp Asn Arg Asn Leu Phe Glu Val Gln Glu Asn Glu Pro 100 105 110cag aag ttg gtg gag aag gtg gca ggg gac att gag agc ctt ctg gac 564Gln Lys Leu Val Glu Lys Val Ala Gly Asp Ile Glu Ser Leu Leu Asp 115 120 125agg aag gtg cag gcc ctg aag aga ctg gct gat gct gca gag aac ttc 612Arg Lys Val Gln Ala Leu Lys Arg Leu Ala Asp Ala Ala Glu Asn Phe 130 135 140cag aaa gca cac cgc tgg cag gac aac atc aag gag gaa gac atc gtg 660Gln Lys Ala His Arg Trp Gln Asp Asn Ile Lys Glu Glu Asp Ile Val145 150 155 160tac tat gac gcc aag gct gac gct gag ctg gac gac cct gag agt gag 708Tyr Tyr Asp Ala Lys Ala Asp Ala Glu Leu Asp Asp Pro Glu Ser Glu 165 170 175gat gtg gaa agg ggg tct aag gcc agc acc cta agg ctg gac ttc atc 756Asp Val Glu Arg Gly Ser Lys Ala Ser Thr Leu Arg Leu Asp Phe Ile 180 185 190gag gac cca aac ttc aag aac aag gtc aac tat tca tac gcg gct gta 804Glu Asp Pro Asn Phe Lys Asn Lys Val Asn Tyr Ser Tyr Ala Ala Val 195 200 205cag atc cct acg gac atc tac aaa ggc tcc act gtc atc ctc aat gag 852Gln Ile Pro Thr Asp Ile Tyr Lys Gly Ser Thr Val Ile Leu Asn Glu 210 215 220ctc aac tgg aca gag gcc ctg gag aat gtg ttc atg gaa aac cgc aga 900Leu Asn Trp Thr Glu Ala Leu Glu Asn Val Phe Met Glu Asn Arg Arg225 230 235 240caa gac ccc aca ctg ctg tgg cag gtc ttc ggc agc gcc aca gga gtc 948Gln Asp Pro Thr Leu Leu Trp Gln Val Phe Gly Ser Ala Thr Gly Val 245 250 255act cgc tac tac ccg gcc acc ccg tgg cga gcc ccc aag aag atc gac 996Thr Arg Tyr Tyr Pro Ala Thr Pro Trp Arg Ala Pro Lys Lys Ile Asp 260 265 270ctg tac gat gtc cga agg aga ccc tgg tat atc cag ggg gcc tcg tca 1044Leu Tyr Asp Val Arg Arg Arg Pro Trp Tyr Ile Gln Gly Ala Ser Ser 275 280 285ccc aaa gac atg gtc atc atc gtg gat gtg agt ggc agt gtg agc ggc 1092Pro Lys Asp Met Val Ile Ile Val Asp Val Ser Gly Ser Val Ser Gly 290 295 300ctg acc ctg aag ctg atg aag aca tct gtc tgc gag atg ctg gac acg 1140Leu Thr Leu Lys Leu Met Lys Thr Ser Val Cys Glu Met Leu Asp Thr305 310 315 320ctg tct gat gat gac tat gtg aat gtg gcc tcg ttc aac gag aag gca 1188Leu Ser Asp Asp Asp Tyr Val Asn Val Ala Ser Phe Asn Glu Lys Ala 325 330 335cag cct gtg tca tgc ttc aca cac ctg gtg cag gcc aat gtg cgc aac 1236Gln Pro Val Ser Cys Phe Thr His Leu Val Gln Ala Asn Val Arg Asn 340 345 350aag aag gtg ttc aag gaa gct gtg cag ggc atg gtg gcc aag ggc acc 1284Lys Lys Val Phe Lys Glu Ala Val Gln Gly Met Val Ala Lys Gly Thr 355 360 365aca ggc tac aag gcc ggc ttt gag tat gcc ttt gac cag ctg cag aac 1332Thr Gly Tyr Lys Ala Gly Phe Glu Tyr Ala Phe Asp Gln Leu Gln Asn 370 375 380tcc aac atc act cgg gcc aac tgc aac aag atg atc atg atg ttc acg 1380Ser Asn Ile Thr Arg Ala Asn Cys Asn Lys Met Ile Met Met Phe Thr385 390 395 400gat ggt ggt gag gac cgc gtg cag gac gtc ttt gag aag tac aat tgg 1428Asp Gly Gly Glu Asp Arg Val Gln Asp Val Phe Glu Lys Tyr Asn Trp 405 410 415cca aac cgg acg gtg cgc gtg ttt act ttc tcc gtg ggg cag cat aac 1476Pro Asn Arg Thr Val Arg Val Phe Thr Phe Ser Val Gly Gln His Asn 420 425 430tat gac gtc aca ccg ctg cag tgg atg gcc tgt gcc aac aaa ggc tac 1524Tyr Asp Val Thr Pro Leu Gln Trp Met Ala Cys Ala Asn Lys Gly Tyr 435 440 445tat ttt gag atc cct tcc atc gga gcc atc cgc atc aac aca cag gaa 1572Tyr Phe Glu Ile Pro Ser Ile Gly Ala Ile Arg Ile Asn Thr Gln Glu 450 455 460tat cta gat gtg ttg ggc agg ccc atg gtg ctg gca ggc aag gag gcc 1620Tyr Leu Asp Val Leu Gly Arg Pro Met Val Leu Ala Gly Lys Glu Ala465 470 475 480aag cag gtt cag tgg acc aac gtg tat gag gat gca ctg gga ctg ggg 1668Lys Gln Val Gln Trp Thr Asn Val Tyr Glu Asp Ala Leu Gly Leu Gly 485 490 495ttg gtg gta aca ggg acc ctc cct gtt ttc aac ctg aca cag gat ggc 1716Leu Val Val Thr Gly Thr Leu Pro Val Phe Asn Leu Thr Gln Asp Gly 500 505 510cct ggg gaa aag aag aac cag ctg atc ctg ggc gtg atg ggc att gac 1764Pro Gly Glu Lys Lys Asn Gln Leu Ile Leu Gly Val Met Gly Ile Asp 515 520 525gtg gct ctg aat gac atc aag agg ctg acc ccc aac tac acg ctt gga 1812Val Ala Leu Asn Asp Ile Lys Arg Leu Thr Pro Asn Tyr Thr Leu Gly 530 535 540gcc aac ggc tat gtg ttt gcc att gac ctg aac ggc tac gtg ttg ctg 1860Ala Asn Gly Tyr Val Phe Ala Ile Asp Leu Asn Gly Tyr Val Leu Leu545 550 555 560cac ccc aat ctc aag ccc cag acc acc aac ttc cgg gag cct gtg act 1908His Pro Asn Leu Lys Pro Gln Thr Thr Asn Phe Arg Glu Pro Val Thr 565 570 575ctg gac ttc ctg gat gcg gag cta gag gat gag aac aag gaa gag atc 1956Leu Asp Phe Leu Asp Ala Glu Leu Glu Asp Glu Asn Lys Glu Glu Ile 580 585 590cgt cgg agc atg att gat ggc aac aag ggc cac aag cag atc aga acg 2004Arg Arg Ser Met Ile Asp Gly Asn Lys Gly His Lys Gln Ile Arg Thr 595 600 605ttg gtc aag tcc ctg gat gag agg tac ata gat gag gtg aca cgg aac 2052Leu Val Lys Ser Leu Asp Glu Arg Tyr Ile Asp Glu Val Thr Arg Asn 610 615 620tac acc tgg gtg cct ata agg agc act aac tac agc ctg ggg ctg gtg 2100Tyr Thr Trp Val Pro Ile Arg Ser Thr Asn Tyr Ser Leu Gly Leu Val625 630 635 640ctc cca ccc tac agc acc ttc tac ctc caa gcc aat ctc agt gac cag 2148Leu Pro Pro Tyr Ser Thr Phe Tyr Leu Gln Ala Asn Leu Ser Asp Gln 645 650 655atc ctg cag gtc aag tat ttt gag ttc ctg ctc ccc agc agc ttt gag 2196Ile Leu Gln Val Lys Tyr Phe Glu Phe Leu Leu Pro Ser Ser Phe Glu 660 665 670tct gaa gga cac gtt ttc att gct ccc aga gag tac tgc aag gac ctg 2244Ser Glu Gly His Val Phe Ile Ala Pro Arg Glu Tyr Cys Lys Asp Leu 675 680 685aat gcc tca gac aac aac acc gag ttc ctg aaa aac ttt att gag ctc 2292Asn Ala Ser Asp Asn Asn Thr Glu Phe Leu Lys Asn Phe Ile Glu Leu 690 695 700atg gag aaa gtg act cca gac tcc aag cag tgc aac aac ttc ctt ctg 2340Met Glu Lys Val Thr Pro Asp Ser Lys Gln Cys Asn Asn Phe Leu Leu705 710 715 720cac aac ctg atc ttg gac acg ggc atc acg cag cag ctg gta gag cgt 2388His Asn Leu Ile Leu Asp Thr Gly Ile Thr Gln Gln Leu Val Glu Arg 725 730 735gtg tgg agg gac cag gat ctc aac acg tac agc cta ctg gcc gtg ttc 2436Val Trp Arg Asp Gln Asp Leu Asn Thr Tyr Ser Leu Leu Ala Val Phe 740 745 750gct gcc aca gac ggt ggc atc acc cga gtc ttc ccc aac aag gca gct 2484Ala Ala Thr Asp Gly Gly Ile Thr Arg Val Phe Pro Asn Lys Ala Ala 755 760 765gag gac tgg aca gag aac cct gag ccc ttc aat gcc agc ttc tac cgc 2532Glu Asp Trp Thr Glu Asn Pro Glu Pro Phe Asn Ala Ser Phe Tyr Arg 770 775 780cgc agc ctg gat aac cac ggt tat gtc ttc aag ccc cca cac cag gat 2580Arg Ser Leu Asp Asn His Gly Tyr Val Phe Lys Pro Pro His Gln Asp785 790 795 800gcc ctg tta agg ccg ctg gag ctg gag aat gac act gtg ggc atc ctc 2628Ala Leu Leu Arg Pro Leu Glu Leu Glu Asn Asp Thr Val Gly Ile Leu 805 810 815gtc agc aca gct gtg gag ctc agc cta ggc agg cgc aca ctg agg cca 2676Val Ser Thr Ala Val Glu Leu Ser Leu Gly Arg Arg Thr Leu Arg Pro 820 825 830gca gtg gtg ggc gtc aag ctg gac cta gag gct tgg gct gag aag ttc 2724Ala Val Val Gly Val Lys Leu Asp Leu Glu Ala Trp Ala Glu Lys Phe 835 840 845aag gtg cta gcc agc aac cgt acc cac caa gac cag cct cag aag tgc 2772Lys Val Leu Ala Ser Asn Arg Thr His Gln Asp Gln Pro Gln Lys Cys 850 855 860ggc ccc aac agc cac tgt gag atg gac tgc gag gtt aac aat gag gac 2820Gly Pro Asn Ser His Cys Glu Met Asp Cys Glu Val Asn Asn Glu Asp865 870 875 880tta ctc tgt gtc ctc att gat gat gga gga ttc ctg gtg ctg tca aac 2868Leu Leu Cys Val Leu Ile Asp Asp Gly Gly Phe Leu Val Leu Ser Asn 885 890 895cag aac cat cag tgg gac cag gtg ggc agg ttc ttc agt gag gtg gat 2916Gln Asn His Gln Trp Asp Gln Val Gly Arg Phe Phe Ser Glu Val Asp 900 905 910gcc aac ctg atg ctg gca ctc tac aat aac tcc ttc tac acc cgc aag 2964Ala Asn Leu Met Leu Ala Leu Tyr Asn Asn Ser Phe Tyr Thr Arg Lys 915 920 925gag tcc tat gac tat cag gca gcc tgt gcc cct cag ccc cct ggc aac 3012Glu Ser Tyr Asp Tyr Gln Ala Ala Cys Ala Pro Gln Pro Pro Gly Asn 930 935 940ctg ggt gct gca ccc cgg ggt gtc ttt gtg ccc acc gtt gca gat ttc 3060Leu Gly Ala Ala Pro Arg Gly Val Phe Val Pro Thr Val Ala Asp Phe945 950 955 960ctt aac ctg gcc tgg tgg acc tct gct gcc gcc tgg tcc ctg ttc cag 3108Leu Asn Leu Ala Trp Trp Thr Ser Ala Ala Ala Trp Ser Leu Phe Gln 965 970 975cag ctt ctc tac ggc ctc atc tac cac agc tgg ttc caa gca gac ccc 3156Gln Leu Leu Tyr Gly Leu Ile Tyr His Ser Trp Phe Gln Ala Asp Pro 980 985 990gcg gag gcc gag ggg agc ccc gag acg cgc gag agc agc tgc gtc atg 3204Ala Glu Ala Glu Gly Ser Pro Glu Thr Arg Glu Ser Ser Cys Val Met 995 1000 1005aaa cag acc cag tac tac ttc ggc tcg gta aac gcc tcc tac aac gcc 3252Lys Gln Thr Gln Tyr Tyr Phe Gly Ser Val Asn Ala Ser Tyr Asn Ala 1010 1015 1020atc atc gac tgc gga aac tgc tcc agg ctg ttc cac gcg cag aga ctg 3300Ile Ile Asp Cys Gly Asn Cys Ser Arg Leu Phe His Ala Gln Arg Leu1025 1030 1035 1040acc aac acc aat ctt ctc ttt gtg gtg gcc gag aag ccg ctg tgc agc 3348Thr Asn Thr Asn Leu Leu Phe Val Val Ala Glu Lys Pro Leu Cys Ser 1045 1050 1055cag tgc gag gct ggc cgg ctg ctg cag aag gag acg cac tgc cca gcg 3396Gln Cys Glu Ala Gly Arg Leu Leu Gln Lys Glu Thr His Cys Pro Ala 1060 1065 1070gac ggc ccg gag cag tgt gag cta gtg cag aga ccg cga tac cgg aga 3444Asp Gly Pro Glu Gln Cys Glu Leu Val Gln Arg Pro Arg Tyr Arg Arg 1075 1080 1085ggc ccg cac atc tgc ttc gac tac aac gcg aca gaa gat acc tca gac 3492Gly Pro His Ile Cys Phe Asp Tyr Asn Ala Thr Glu Asp Thr Ser Asp 1090 1095 1100tgt ggc cgc ggg gcc tcc ttc ccg ccg tcg ctg ggc gtc ctg gtc tcc 3540Cys Gly Arg Gly Ala Ser Phe Pro Pro Ser Leu Gly Val Leu Val Ser1105 1110 1115 1120ctg caa ctg ctg ctc ctc ctg ggc ctg ccg ccc cgg ccg cag cct caa 3588Leu Gln Leu Leu Leu Leu Leu Gly Leu Pro Pro Arg Pro Gln Pro Gln 1125 1130 1135gtc ctc gtc cac gcc tct cgc cgc ctc tga gcaccctgcc ccaccccacc 3638Val Leu Val His Ala Ser Arg Arg Leu 1140 1145tccactccca cctcacccgg cctcttcgcc tttcccaccc tcctgcccca cactccccgc 3698cttagagcct cgtccctccc tcactgaagg acctgagctg gccaggccct gagagtctgg 3758tctgcgcctt gggatgggga gtcccaaagc gggacgccgc aggtgtttgg cacccaaatc 3818acatctcacc tccgaactgt tcaagtgtcc ccagaccctt cttgcctgct gggctccccc 3878cagtgggatg ggacagggag gccacacgca ctggtgccaa aaccaggcct ctgctgccgc 3938ccttcctgga ggctgcctat gttggggggg accctgcctc agctgacccg gcctctctgc 3998cccacccaag cccaaacttg gtttctgtga gaatagtgga ggaaggtgag atggccagtt 4058tgaagcctgt gcctcccagc ttaaatccta gcaggagaga ggctctgggg cagcccccat 4118gggctcctgc ccctttcagg cctacagcca catccccaag cccaccaggt gtcaggatag 4178tcacagtgat accagttcag acactacccc atatacacct ggaacattga ggatggaaac 4238tggactcaca ttcgacatac cccactgggc acacgcacaa acacacacac tatggggtgg 4298ggtgggtgta ggggcttaca aagccttaca cagggcgagg ggttggtggg agggttggca 4358cctgcacact ccatctcctg ctcaccacct gcctctaatc tgagctgcag cctggctggt 4418cctcccattt ctaaagctga atgtcaaaca gtgccaaatg ctggggcagg gggtgaagaa 4478ccctctgtcc cacccctagc caccagtgtc ctccaagtgc cccctcacct ctccaggtgc 4538tcattgtaac catttctcac tagtgtcagg cccccagtgg gaccacatgc cactgcctgc 4598acctttcggc agaggaaccc ccaccagaca tcaccctttg ccttagcagg ggtgactttg 4658tctctcctgg ctgggccatc cttccgccaa tctggccctt acacactcag gcctgtgccc 4718actccctatc tccttcccac ccctacacac acactccctg cttgcaggag gccaaactgt 4778ccctcccttg ctgaacacac acacacacac acacacacag gtggggactg ggcacagctc 4838ttcacaccat tcattctggt catttccccc aaaggcatcc cagcctgggg gccagtgggg 4898aactgagggc aaggggatat agtgatgggg ctcagatgga ctgggaggag ggggagggtg 4958atgcattaat taatggcttc gttaattaat gtcatgttgc ttgtcgcttt ctcagtgtgt 5018gtgtgtggtc catgcccact gctggtgcca gggtgggtgt ccatgtgcac ccggcctgga 5078tgccagctgt gtccttcggg ggcgtgcgtg taactgtagt gtagtcaggt gctcaatgga 5138gaatataaac atatacagaa aaatatatat tttaagttta aaaaacagaa aaacagacaa 5198aacaatcccc atcaggtagc tgtctaaccc ccagctgggt ctaatccttc tcattaccca 5258cccgacctgg ctgcccctca ccttgggctg ggggactggg gggccatttc cttttctctg 5318cccttttttt gttgttctat tttgtacaga caagttggaa aaacaacagc gacaaaaaag 5378tcaagaaact ttgtaaaata tcgtgtgtgt gattccttgt aaaatatttt caaatggttt 5438attacagaag atcagttatt aaataatgtt catattttca cttc 5482 4 1145 PRT Homo sapiens 4Met Ala Val Pro Ala Arg Thr Cys Gly Ala Ser Arg Pro Gly Pro Ala 1 5 10 15Arg Thr Ala Arg Pro Trp Pro Gly Cys Gly Pro His Pro Gly Pro Gly 20 25 30Thr Arg Arg Pro Thr Ser Gly Pro Pro Arg Pro Leu Trp Leu Leu Leu 35 40 45Pro Leu Leu Pro Leu Leu Ala Ala Pro Gly Ala Ser Ala Tyr Ser Phe 50 55 60Pro Gln Gln His Thr Met Gln His Trp Ala Arg Arg Leu Glu Gln Glu 65 70 75 80Val Asp Gly Val Met Arg Ile Phe Gly Gly Val Gln Gln Leu Arg Glu 85 90 95Ile Tyr Lys Asp Asn Arg Asn Leu Phe Glu Val Gln Glu Asn Glu Pro 100 105 110Gln Lys Leu Val Glu Lys Val Ala Gly Asp Ile Glu Ser Leu Leu Asp 115 120 125Arg Lys Val Gln Ala Leu Lys Arg Leu Ala Asp Ala Ala Glu Asn Phe 130 135 140Gln Lys Ala His Arg Trp Gln Asp Asn Ile Lys Glu Glu Asp Ile Val145 150 155 160Tyr Tyr Asp Ala Lys Ala Asp Ala Glu Leu Asp Asp Pro Glu Ser Glu 165 170 175Asp Val Glu Arg Gly Ser Lys Ala Ser Thr Leu Arg Leu Asp Phe Ile 180 185 190Glu Asp Pro Asn Phe Lys Asn Lys Val Asn Tyr Ser Tyr Ala Ala Val 195 200 205Gln Ile Pro Thr Asp Ile Tyr Lys Gly Ser Thr Val Ile Leu Asn Glu 210 215 220Leu Asn Trp Thr Glu Ala Leu Glu Asn Val Phe Met Glu Asn Arg Arg225 230 235 240Gln Asp Pro Thr Leu Leu Trp Gln Val Phe Gly Ser Ala Thr Gly Val 245 250 255Thr Arg Tyr Tyr Pro Ala Thr Pro Trp Arg Ala Pro Lys Lys Ile Asp 260 265 270Leu Tyr Asp Val Arg Arg Arg Pro Trp Tyr Ile Gln Gly Ala Ser Ser 275 280 285Pro Lys Asp Met Val Ile Ile Val Asp Val Ser Gly Ser Val Ser Gly 290 295 300Leu Thr Leu Lys Leu Met Lys Thr Ser Val Cys Glu Met Leu Asp Thr305 310 315 320Leu Ser Asp Asp Asp Tyr Val Asn Val Ala Ser Phe Asn Glu Lys Ala 325 330 335Gln Pro Val Ser Cys Phe Thr His Leu Val Gln Ala Asn Val Arg Asn 340 345 350Lys Lys Val Phe Lys Glu Ala Val Gln Gly Met Val Ala Lys Gly Thr 355 360 365Thr Gly Tyr Lys Ala Gly Phe Glu Tyr Ala Phe Asp Gln Leu Gln Asn 370 375 380Ser Asn Ile Thr Arg Ala Asn Cys Asn Lys Met Ile Met Met Phe Thr385 390 395 400Asp Gly Gly Glu Asp Arg Val Gln Asp Val Phe Glu Lys Tyr Asn Trp 405 410 415Pro Asn Arg Thr Val Arg Val Phe Thr Phe Ser Val Gly Gln His Asn 420 425 430Tyr Asp Val Thr Pro Leu Gln Trp Met Ala Cys Ala Asn Lys Gly Tyr 435 440 445Tyr Phe Glu Ile Pro Ser Ile Gly Ala Ile Arg Ile Asn Thr Gln Glu 450 455 460Tyr Leu Asp Val Leu Gly Arg Pro Met Val Leu Ala Gly Lys Glu Ala465 470 475 480Lys Gln Val Gln Trp Thr Asn Val Tyr Glu Asp Ala Leu Gly Leu Gly 485 490 495Leu Val Val Thr Gly Thr Leu Pro Val Phe Asn Leu Thr Gln Asp Gly 500 505 510Pro Gly Glu Lys Lys Asn Gln Leu Ile Leu Gly Val Met Gly Ile Asp 515 520 525Val Ala Leu Asn Asp Ile Lys Arg Leu Thr Pro Asn Tyr Thr Leu Gly 530 535 540Ala Asn Gly Tyr Val Phe Ala Ile Asp Leu Asn Gly Tyr Val Leu Leu545 550 555 560His Pro Asn Leu Lys Pro Gln Thr Thr Asn Phe Arg Glu Pro Val Thr 565 570 575Leu Asp Phe Leu Asp Ala Glu Leu Glu Asp Glu Asn Lys Glu Glu Ile 580 585 590Arg Arg Ser Met Ile Asp Gly Asn Lys Gly His Lys Gln Ile Arg Thr 595 600 605Leu Val Lys Ser Leu Asp Glu Arg Tyr Ile Asp Glu Val Thr Arg Asn 610 615 620Tyr Thr Trp Val Pro Ile Arg Ser Thr Asn Tyr Ser Leu Gly Leu Val625 630 635 640Leu Pro Pro Tyr Ser Thr Phe Tyr Leu Gln Ala Asn Leu Ser Asp Gln 645 650 655Ile Leu Gln Val Lys Tyr Phe Glu Phe Leu Leu Pro Ser Ser Phe Glu 660 665 670Ser Glu Gly His Val Phe Ile Ala Pro Arg Glu Tyr Cys Lys Asp Leu 675 680 685Asn Ala Ser Asp Asn Asn Thr Glu Phe Leu Lys Asn Phe Ile Glu Leu 690 695 700Met Glu Lys Val Thr Pro Asp Ser Lys Gln Cys Asn Asn Phe Leu Leu705 710 715 720His Asn Leu Ile Leu Asp Thr Gly Ile Thr Gln Gln Leu Val Glu Arg 725 730 735Val Trp Arg Asp Gln Asp Leu Asn Thr Tyr Ser Leu Leu Ala Val Phe 740 745 750Ala Ala Thr Asp Gly Gly Ile Thr Arg Val Phe Pro Asn Lys Ala Ala 755 760 765Glu Asp Trp Thr Glu Asn Pro Glu Pro Phe Asn Ala Ser Phe Tyr Arg 770 775 780Arg Ser Leu Asp Asn His Gly Tyr Val Phe Lys Pro Pro His Gln Asp785 790 795 800Ala Leu Leu Arg Pro Leu Glu Leu Glu Asn Asp Thr Val Gly Ile Leu 805 810 815Val Ser Thr Ala Val Glu Leu Ser Leu Gly Arg Arg Thr Leu Arg Pro 820 825 830Ala Val Val Gly Val Lys Leu Asp Leu Glu Ala Trp Ala Glu Lys Phe 835 840 845Lys Val Leu Ala Ser Asn Arg Thr His Gln Asp Gln Pro Gln Lys Cys 850 855 860Gly Pro Asn Ser His Cys Glu Met Asp Cys Glu Val Asn Asn Glu Asp865 870 875 880Leu Leu Cys Val Leu Ile Asp Asp Gly Gly Phe Leu Val Leu Ser Asn 885 890 895Gln Asn His Gln Trp Asp Gln Val Gly Arg Phe Phe Ser Glu Val Asp 900 905 910Ala Asn Leu Met Leu Ala Leu Tyr Asn Asn Ser Phe Tyr Thr Arg Lys 915 920 925Glu Ser Tyr Asp Tyr Gln Ala Ala Cys Ala Pro Gln Pro Pro Gly Asn 930 935 940Leu Gly Ala Ala Pro Arg Gly Val Phe Val Pro Thr Val Ala Asp Phe945 950 955 960Leu Asn Leu Ala Trp Trp Thr Ser Ala Ala Ala Trp Ser Leu Phe Gln 965 970 975Gln Leu Leu Tyr Gly Leu Ile Tyr His Ser Trp Phe Gln Ala Asp Pro 980 985 990Ala Glu Ala Glu Gly Ser Pro Glu Thr Arg Glu Ser Ser Cys Val Met 995 1000 1005Lys Gln Thr Gln Tyr Tyr Phe Gly Ser Val Asn Ala Ser Tyr Asn Ala 1010 1015 1020Ile Ile Asp Cys Gly Asn Cys Ser Arg Leu Phe His Ala Gln Arg Leu1025 1030 1035 1040Thr Asn Thr Asn Leu Leu Phe Val Val Ala Glu Lys Pro Leu Cys Ser 1045 1050 1055Gln Cys Glu Ala Gly Arg Leu Leu Gln Lys Glu Thr His Cys Pro Ala 1060 1065 1070Asp Gly Pro Glu Gln Cys Glu Leu Val Gln Arg Pro Arg Tyr Arg Arg 1075 1080 1085Gly Pro His Ile Cys Phe Asp Tyr Asn Ala Thr Glu Asp Thr Ser Asp 1090 1095 1100Cys Gly Arg Gly Ala Ser Phe Pro Pro Ser Leu Gly Val Leu Val Ser1105 1110 1115 1120Leu Gln Leu Leu Leu Leu Leu Gly Leu Pro Pro Arg Pro Gln Pro Gln 1125 1130 1135Val Leu Val His Ala Ser Arg Arg Leu 1140 1145 5 5279 DNA Homo sapiens CDS (185)..(3415) 5atccgcggcg aagcgagtgg ctgcagaggg ctgcatcctg ccgtccccag ccccccacaa 60ccgtacagcc gtgcccaggt ttccgcttag ggaaccagga ggtccaggcc ctttctgcca 120gcagccgggc gtgcaagccc ccgacagaga gaaatcttaa agatagctag agccacgggg 180gctg atg cag cac tgg gcc cgg cgt ctg gag cag gag gtc gac ggc gtg 229 Met Gln His Trp Ala Arg Arg Leu Glu Gln Glu Val Asp Gly Val 1 5 10 15atg cgg att ttt gga ggc gtc cag cag ctc cgt gag att tac aag gac 277Met Arg Ile Phe Gly Gly Val Gln Gln Leu Arg Glu Ile Tyr Lys Asp 20 25 30aac cgg aac ctg ttc gag gta cag gag aat gag cct cag aag ttg gtg 325Asn Arg Asn Leu Phe Glu Val Gln Glu Asn Glu Pro Gln Lys Leu Val 35 40 45gag aag gtg gca ggg gac att gag agc ctt ctg gac agg aag gtg cag 373Glu Lys Val Ala Gly Asp Ile Glu Ser Leu Leu Asp Arg Lys Val Gln 50 55 60gcc ctg aag aga ctg gct gat gct gca gag aac ttc cag aaa gca cac 421Ala Leu Lys Arg Leu Ala Asp Ala Ala Glu Asn Phe Gln Lys Ala His 65 70 75cgc tgg cag gac aac atc aag gag gaa gac atc gtg tac tat gac gcc 469Arg Trp Gln Asp Asn Ile Lys Glu Glu Asp Ile Val Tyr Tyr Asp Ala 80 85 90 95aag gct gac gct gag ctg gac gac cct gag agt gag gat gtg gaa agg 517Lys Ala Asp Ala Glu Leu Asp Asp Pro Glu Ser Glu Asp Val Glu Arg 100 105 110ggg tct aag gcc agc acc cta agg ctg gac ttc atc gag gac cca aac 565Gly Ser Lys Ala Ser Thr Leu Arg Leu Asp Phe Ile Glu Asp Pro Asn 115 120 125ttc aag aac aag gtc aac tat tca tac gcg gct gta cag atc cct acg 613Phe Lys Asn Lys Val Asn Tyr Ser Tyr Ala Ala Val Gln Ile Pro Thr 130 135 140gac atc tac aaa ggc tcc act gtc atc ctc aat gag ctc aac tgg aca 661Asp Ile Tyr Lys Gly Ser Thr Val Ile Leu Asn Glu Leu Asn Trp Thr 145 150 155gag gcc ctg gag aat gtg ttc atg gaa aac cgc aga caa gac ccc aca 709Glu Ala Leu Glu Asn Val Phe Met Glu Asn Arg Arg Gln Asp Pro Thr160 165 170 175ctg ctg tgg cag gtc ttc ggc agc gcc aca gga gtc act cgc tac tac 757Leu Leu Trp Gln Val Phe Gly Ser Ala Thr Gly Val Thr Arg Tyr Tyr 180 185 190ccg gcc acc ccg tgg cga gcc ccc aag aag atc gac ctg tac gat gtc 805Pro Ala Thr Pro Trp Arg Ala Pro Lys Lys Ile Asp Leu Tyr Asp Val 195 200 205cga agg aga ccc tgg tat atc cag ggg gcc tcg tca ccc aaa gac atg 853Arg Arg Arg Pro Trp Tyr Ile Gln Gly Ala Ser Ser Pro Lys Asp Met 210 215 220gtc atc atc gtg gat gtg agt ggc agt gtg agc ggc ctg acc ctg aag 901Val Ile Ile Val Asp Val Ser Gly Ser Val Ser Gly Leu Thr Leu Lys 225 230 235ctg atg aag aca tct gtc tgc gag atg ctg gac acg ctg tct gat gat 949Leu Met Lys Thr Ser Val Cys Glu Met Leu Asp Thr Leu Ser Asp Asp240 245 250 255gac tat gtg aat gtg gcc tcg ttc aac gag aag gca cag cct gtg tca 997Asp Tyr Val Asn Val Ala Ser Phe Asn Glu Lys Ala Gln Pro Val Ser 260 265 270tgc ttc aca cac ctg gtg cag gcc aat gtg cgc aac aag aag gtg ttc 1045Cys Phe Thr His Leu Val Gln Ala Asn Val Arg Asn Lys Lys Val Phe 275 280 285aag gaa gct gtg cag ggc atg gtg gcc aag ggc acc aca ggc tac aag 1093Lys Glu Ala Val Gln Gly Met Val Ala Lys Gly Thr Thr Gly Tyr Lys 290 295 300gcc ggc ttt gag tat gcc ttt gac cag ctg cag aac tcc aac atc act 1141Ala Gly Phe Glu Tyr Ala Phe Asp Gln Leu Gln Asn Ser Asn Ile Thr 305 310 315cgg gcc aac tgc aac aag atg atc atg atg ttc acg gat ggt ggt gag 1189Arg Ala Asn Cys Asn Lys Met Ile Met Met Phe Thr Asp Gly Gly Glu320 325 330 335gac cgc gtg cag gac gtc ttt gag aag tac aat tgg cca aac cgg acg 1237Asp Arg Val Gln Asp Val Phe Glu Lys Tyr Asn Trp Pro Asn Arg Thr 340 345 350gtg cgc gtg ttt act ttc tcc gtg ggg cag cat aac tat gac gtc aca 1285Val Arg Val Phe Thr Phe Ser Val Gly Gln His Asn Tyr Asp Val Thr 355 360 365ccg ctg cag tgg atg gcc tgt gcc aac aaa ggc tac tat ttt gag atc 1333Pro Leu Gln Trp Met Ala Cys Ala Asn Lys Gly Tyr Tyr Phe Glu Ile 370 375 380cct tcc atc gga gcc atc cgc atc aac aca cag gaa tat cta gat gtg 1381Pro Ser Ile Gly Ala Ile Arg Ile Asn Thr Gln Glu Tyr Leu Asp Val 385 390 395ttg ggc agg ccc atg gtg ctg gca ggc aag gag gcc aag cag gtt cag 1429Leu Gly Arg Pro Met Val Leu Ala Gly Lys Glu Ala Lys Gln Val Gln400 405 410 415tgg acc aac gtg tat gag gat gca ctg gga ctg ggg ttg gtg gta aca 1477Trp Thr Asn Val Tyr Glu Asp Ala Leu Gly Leu Gly Leu Val Val Thr 420 425 430ggg acc ctc cct gtt ttc aac ctg aca cag gat ggc cct ggg gaa aag 1525Gly Thr Leu Pro Val Phe Asn Leu Thr Gln Asp Gly Pro Gly Glu Lys 435 440 445aag aac cag ctg atc ctg ggc gtg atg ggc att gac gtg gct ctg aat 1573Lys Asn Gln Leu Ile Leu Gly Val Met Gly Ile Asp Val Ala Leu Asn 450 455 460gac atc aag agg ctg acc ccc aac tac acg ctt gga gcc aac ggc tat 1621Asp Ile Lys Arg Leu Thr Pro Asn Tyr Thr Leu Gly Ala Asn Gly Tyr 465 470 475gtg ttt gcc att gac ctg aac ggc tac gtg ttg ctg cac ccc aat ctc 1669Val Phe Ala Ile Asp Leu Asn Gly Tyr Val Leu Leu His Pro Asn Leu480 485 490 495aag ccc cag acc acc aac ttc cgg gag cct gtg act ctg gac ttc ctg 1717Lys Pro Gln Thr Thr Asn Phe Arg Glu Pro Val Thr Leu Asp Phe Leu 500 505 510gat gcg gag cta gag gat gag aac aag gaa gag atc cgt cgg agc atg 1765Asp Ala Glu Leu Glu Asp Glu Asn Lys Glu Glu Ile Arg Arg Ser Met 515 520 525att gat ggc aac aag ggc cac aag cag atc aga acg ttg gtc aag tcc 1813Ile Asp Gly Asn Lys Gly His Lys Gln Ile Arg Thr Leu Val Lys Ser 530 535 540ctg gat gag agg tac ata gat gag gtg aca cgg aac tac acc tgg gtg 1861Leu Asp Glu Arg Tyr Ile Asp Glu Val Thr Arg Asn Tyr Thr Trp Val 545 550 555cct ata agg agc act aac tac agc ctg ggg ctg gtg ctc cca ccc tac 1909Pro Ile Arg Ser Thr Asn Tyr Ser Leu Gly Leu Val Leu Pro Pro Tyr560 565 570 575agc acc ttc tac ctc caa gcc aat ctc agt gac cag atc ctg cag gtc 1957Ser Thr Phe Tyr Leu Gln Ala Asn Leu Ser Asp Gln Ile Leu Gln Val 580 585 590aag tat ttt gag ttc ctg ctc ccc agc agc ttt gag tct gaa gga cac 2005Lys Tyr Phe Glu Phe Leu Leu Pro Ser Ser Phe Glu Ser Glu Gly His 595 600 605gtt ttc att gct ccc aga gag tac tgc aag gac ctg aat gcc tca gac 2053Val Phe Ile Ala Pro Arg Glu Tyr Cys Lys Asp Leu Asn Ala Ser Asp 610 615 620aac aac acc gag ttc ctg aaa aac ttt att gag ctc atg gag aaa gtg 2101Asn Asn Thr Glu Phe Leu Lys Asn Phe Ile Glu Leu Met Glu Lys Val 625 630 635act cca gac tcc aag cag tgc aac aac ttc ctt ctg cac aac ctg atc 2149Thr Pro Asp Ser Lys Gln Cys Asn Asn Phe Leu Leu His Asn Leu Ile640 645 650 655ttg gac acg ggc atc acg cag cag ctg gta gag cgt gtg tgg agg gac 2197Leu Asp Thr Gly Ile Thr Gln Gln Leu Val Glu Arg Val Trp Arg Asp 660 665 670cag gat ctc aac acg tac agc cta ctg gcc gtg ttc gct gcc aca gac 2245Gln Asp Leu Asn Thr Tyr Ser Leu Leu Ala Val Phe Ala Ala Thr Asp 675 680 685ggt ggc atc acc cga gtc ttc ccc aac aag gca gct gag gac tgg aca 2293Gly Gly Ile Thr Arg Val Phe Pro Asn Lys Ala Ala Glu Asp Trp Thr 690 695 700gag aac cct gag ccc ttc aat gcc agc ttc tac cgc cgc agc ctg gat 2341Glu Asn Pro Glu Pro Phe Asn Ala Ser Phe Tyr Arg Arg Ser Leu Asp 705 710 715aac cac ggt tat gtc ttc aag ccc cca cac cag gat gcc ctg tta agg 2389Asn His Gly Tyr Val Phe Lys Pro Pro His Gln Asp Ala Leu Leu Arg720 725 730 735ccg ctg gag ctg gag aat gac act gtg ggc atc ctc gtc agc aca gct 2437Pro Leu Glu Leu Glu Asn Asp Thr Val Gly Ile Leu Val Ser Thr Ala 740 745 750gtg gag ctc agc cta ggc agg cgc aca ctg agg cca gca gtg gtg ggc 2485Val Glu Leu Ser Leu Gly Arg Arg Thr Leu Arg Pro Ala Val Val Gly 755 760 765gtc aag ctg gac cta gag gct tgg gct gag aag ttc aag gtg cta gcc 2533Val Lys Leu Asp Leu Glu Ala Trp Ala Glu Lys Phe Lys Val Leu Ala 770 775 780agc aac cgt acc cac caa gac cag cct cag aag tgc ggc ccc aac agc 2581Ser Asn Arg Thr His Gln Asp Gln Pro Gln Lys Cys Gly Pro Asn Ser 785 790 795cac tgt gag atg gac tgc gag gtt aac aat gag gac tta ctc tgt gtc 2629His Cys Glu Met Asp Cys Glu Val Asn Asn Glu Asp Leu Leu Cys Val800 805 810 815ctc att gat gat gga gga ttc ctg gtg ctg tca aac cag aac cat cag 2677Leu Ile Asp Asp Gly Gly Phe Leu Val Leu Ser Asn Gln Asn His Gln 820 825 830tgg gac cag gtg ggc agg ttc ttc agt gag gtg gat gcc aac ctg atg 2725Trp Asp Gln Val Gly Arg Phe Phe Ser Glu Val Asp Ala Asn Leu Met 835 840 845ctg gca ctc tac aat aac tcc ttc tac acc cgc aag gag tcc tat gac 2773Leu Ala Leu Tyr Asn Asn Ser Phe Tyr Thr Arg Lys Glu Ser Tyr Asp 850 855 860tat cag gca gcc tgt gcc cct cag ccc cct ggc aac ctg ggt gct gca 2821Tyr Gln Ala Ala Cys Ala Pro Gln Pro Pro Gly Asn Leu Gly Ala Ala 865 870 875ccc cgg ggt gtc ttt gtg ccc acc gtt gca gat ttc ctt aac ctg gcc 2869Pro Arg Gly Val Phe Val Pro Thr Val Ala Asp Phe Leu Asn Leu Ala880 885 890 895tgg tgg acc tct gct gcc gcc tgg tcc ctg ttc cag cag ctt ctc tac 2917Trp Trp Thr Ser Ala Ala Ala Trp Ser Leu Phe Gln Gln Leu Leu Tyr 900 905 910ggc ctc atc tac cac agc tgg ttc caa gca gac ccc gcg gag gcc gag 2965Gly Leu Ile Tyr His Ser Trp Phe Gln Ala Asp Pro Ala Glu Ala Glu 915 920 925ggg agc ccc gag acg cgc gag agc agc tgc gtc atg aaa cag acc cag 3013Gly Ser Pro Glu Thr Arg Glu Ser Ser Cys Val Met Lys Gln Thr Gln 930 935 940tac tac ttc ggc tcg gta aac gcc tcc tac aac gcc atc atc gac tgc 3061Tyr Tyr Phe Gly Ser Val Asn Ala Ser Tyr Asn Ala Ile Ile Asp Cys 945 950 955gga aac tgc tcc agg ctg ttc cac gcg cag aga ctg acc aac acc aat 3109Gly Asn Cys Ser Arg Leu Phe His Ala Gln Arg Leu Thr Asn Thr Asn960 965 970 975ctt ctc ttt gtg gtg gcc gag aag ccg ctg tgc agc cag tgc gag gct 3157Leu Leu Phe Val Val Ala Glu Lys Pro Leu Cys Ser Gln Cys Glu Ala 980 985 990ggc cgg ctg ctg cag aag gag acg cac tgc cca gcg gac ggc ccg gag 3205Gly Arg Leu Leu Gln Lys Glu Thr His Cys Pro Ala Asp Gly Pro Glu 995 1000 1005cag tgt gag cta gtg cag aga ccg cga tac cgg aga ggc ccg cac atc 3253Gln Cys Glu Leu Val Gln Arg Pro Arg Tyr Arg Arg Gly Pro His Ile 1010 1015 1020tgc ttc gac tac aac gcg aca gaa gat acc tca gac tgt ggc cgc ggg 3301Cys Phe Asp Tyr Asn Ala Thr Glu Asp Thr Ser Asp Cys Gly Arg Gly 1025 1030 1035gcc tcc ttc ccg ccg tcg ctg ggc gtc ctg gtc tcc ctg caa ctg ctg 3349Ala Ser Phe Pro Pro Ser Leu Gly Val Leu Val Ser Leu Gln Leu Leu1040 1045 1050 1055ctc ctc ctg ggc ctg ccg ccc cgg ccg cag cct caa gtc ctc gtc cac 3397Leu Leu Leu Gly Leu Pro Pro Arg Pro Gln Pro Gln Val Leu Val His 1060 1065 1070gcc tct cgc cgc ctc tga gcaccctgcc ccaccccacc tccactccca 3445Ala Ser Arg Arg Leu 1075cctcacccgg cctcttcgcc tttcccaccc tcctgcccca cactccccgc cttagagcct 3505cgtccctccc tcactgaagg acctgagctg gccaggccct gagagtctgg tctgcgcctt 3565gggatgggga gtcccaaagc gggacgccgc aggtgtttgg cacccaaatc acatctcacc 3625tccgaactgt tcaagtgtcc ccagaccctt cttgcctgct gggctccccc cagtgggatg 3685ggacagggag gccacacgca ctggtgccaa aaccaggcct ctgctgccgc ccttcctgga 3745ggctgcctat gttggggggg accctgcctc agctgacccg gcctctctgc cccacccaag 3805cccaaacttg gtttctgtga gaatagtgga ggaaggtgag atggccagtt tgaagcctgt 3865gcctcccagc ttaaatccta gcaggagaga ggctctgggg cagcccccat gggctcctgc 3925ccctttcagg cctacagcca catccccaag cccaccaggt gtcaggatag tcacagtgat 3985accagttcag acactacccc atatacacct ggaacattga ggatggaaac tggactcaca 4045ttcgacatac cccactgggc acacgcacaa acacacacac tatggggtgg ggtgggtgta 4105ggggcttaca aagccttaca cagggcgagg ggttggtggg agggttggca cctgcacact 4165ccatctcctg ctcaccacct gcctctaatc tgagctgcag cctggctggt cctcccattt 4225ctaaagctga atgtcaaaca gtgccaaatg ctggggcagg gggtgaagaa ccctctgtcc 4285cacccctagc caccagtgtc ctccaagtgc cccctcacct ctccaggtgc tcattgtaac 4345catttctcac tagtgtcagg cccccagtgg gaccacatgc cactgcctgc acctttcggc 4405agaggaaccc ccaccagaca tcaccctttg ccttagcagg ggtgactttg tctctcctgg 4465ctgggccatc cttccgccaa tctggccctt acacactcag gcctgtgccc actccctatc 4525tccttcccac ccctacacac acactccctg cttgcaggag gccaaactgt ccctcccttg 4585ctgaacacac acacacacac acacacacag gtggggactg ggcacagctc ttcacaccat 4645tcattctggt catttccccc aaaggcatcc cagcctgggg gccagtgggg aactgagggc 4705aaggggatat agtgatgggg ctcagatgga ctgggaggag ggggagggtg atgcattaat 4765taatggcttc gttaattaat gtcatgttgc ttgtcgcttt ctcagtgtgt gtgtgtggtc 4825catgcccact gctggtgcca gggtgggtgt ccatgtgcac ccggcctgga tgccagctgt 4885gtccttcggg ggcgtgcgtg taactgtagt gtagtcaggt gctcaatgga gaatataaac 4945atatacagaa aaatatatat tttaagttta aaaaacagaa aaacagacaa aacaatcccc 5005atcaggtagc tgtctaaccc ccagctgggt ctaatccttc tcattaccca cccgacctgg 5065ctgcccctca ccttgggctg ggggactggg gggccatttc cttttctctg cccttttttt 5125gttgttctat tttgtacaga caagttggaa aaacaacagc gacaaaaaag tcaagaaact 5185ttgtaaaata tcgtgtgtgt gattccttgt aaaatatttt caaatggttt attacagaag 5245atcagttatt aaataatgtt catattttca cttc 5279 6 1076 PRT Homo sapiens 6Met Gln His Trp Ala Arg Arg Leu Glu Gln Glu Val Asp Gly Val Met 1 5 10 15Arg Ile Phe Gly Gly Val Gln Gln Leu Arg Glu Ile Tyr Lys Asp Asn 20 25 30Arg Asn Leu Phe Glu Val Gln Glu Asn Glu Pro Gln Lys Leu Val Glu 35 40 45Lys Val Ala Gly Asp Ile Glu Ser Leu Leu Asp Arg Lys Val Gln Ala 50 55 60Leu Lys Arg Leu Ala Asp Ala Ala Glu Asn Phe Gln Lys Ala His Arg 65 70 75 80Trp Gln Asp Asn Ile Lys Glu Glu Asp Ile Val Tyr Tyr Asp Ala Lys 85 90 95Ala Asp Ala Glu Leu Asp Asp Pro Glu Ser Glu Asp Val Glu Arg Gly 100 105 110Ser Lys Ala Ser Thr Leu Arg Leu Asp Phe Ile Glu Asp Pro Asn Phe 115 120 125Lys Asn Lys Val Asn Tyr Ser Tyr Ala Ala Val Gln Ile Pro Thr Asp 130 135 140Ile Tyr Lys Gly Ser Thr Val Ile Leu Asn Glu Leu Asn Trp Thr Glu145 150 155 160Ala Leu Glu Asn Val Phe Met Glu Asn Arg Arg Gln Asp Pro Thr Leu 165 170 175Leu Trp Gln Val Phe Gly Ser Ala Thr Gly Val Thr Arg Tyr Tyr Pro 180 185 190Ala Thr Pro Trp Arg Ala Pro Lys Lys Ile Asp Leu Tyr Asp Val Arg 195 200 205Arg Arg Pro Trp Tyr Ile Gln Gly Ala Ser Ser Pro Lys Asp Met Val 210 215 220Ile Ile Val Asp Val Ser Gly Ser Val Ser Gly Leu Thr Leu Lys Leu225 230 235 240Met Lys Thr Ser Val Cys Glu Met Leu Asp Thr Leu Ser Asp Asp Asp 245 250 255Tyr Val Asn Val Ala Ser Phe Asn Glu Lys Ala Gln Pro Val Ser Cys 260 265 270Phe Thr His Leu Val Gln Ala Asn Val Arg Asn Lys Lys Val Phe Lys 275 280 285Glu Ala Val Gln Gly Met Val Ala Lys Gly Thr Thr Gly Tyr Lys Ala 290 295 300Gly Phe Glu Tyr Ala Phe Asp Gln Leu Gln Asn Ser Asn Ile Thr Arg305 310 315 320Ala Asn Cys Asn Lys Met Ile Met Met Phe Thr Asp Gly Gly Glu Asp 325 330 335Arg Val Gln Asp Val Phe Glu Lys Tyr Asn Trp Pro Asn Arg Thr Val 340 345 350Arg Val Phe Thr Phe Ser Val Gly Gln His Asn Tyr Asp Val Thr Pro 355 360 365Leu Gln Trp Met Ala Cys Ala Asn Lys Gly Tyr Tyr Phe Glu Ile Pro 370 375 380Ser Ile Gly Ala Ile Arg Ile Asn Thr Gln Glu Tyr Leu Asp Val Leu385 390 395 400Gly Arg Pro Met Val Leu Ala Gly Lys Glu Ala Lys Gln Val Gln Trp 405 410 415Thr Asn Val Tyr Glu Asp Ala Leu Gly Leu Gly Leu Val Val Thr Gly 420 425 430Thr Leu Pro Val Phe Asn Leu Thr Gln Asp Gly Pro Gly Glu Lys Lys 435 440 445Asn Gln Leu Ile Leu Gly Val Met Gly Ile Asp Val Ala Leu Asn Asp 450 455 460Ile Lys Arg Leu Thr Pro Asn Tyr Thr Leu Gly Ala Asn Gly Tyr Val465 470 475 480Phe Ala Ile Asp Leu Asn Gly Tyr Val Leu Leu His Pro Asn Leu Lys 485 490 495Pro Gln Thr Thr Asn Phe Arg Glu Pro Val Thr Leu Asp Phe Leu Asp 500 505 510Ala Glu Leu Glu Asp Glu Asn Lys Glu Glu Ile Arg Arg Ser Met Ile 515 520 525Asp Gly Asn Lys Gly His Lys Gln Ile Arg Thr Leu Val Lys Ser Leu 530 535 540Asp Glu Arg Tyr Ile Asp Glu Val Thr Arg Asn Tyr Thr Trp Val Pro545 550 555 560Ile Arg Ser Thr Asn Tyr Ser Leu Gly Leu Val Leu Pro Pro Tyr Ser 565 570 575Thr Phe Tyr Leu Gln Ala Asn Leu Ser Asp Gln Ile Leu Gln Val Lys 580 585 590Tyr Phe Glu Phe Leu Leu Pro Ser Ser Phe Glu Ser Glu Gly His Val 595 600 605Phe Ile Ala Pro Arg Glu Tyr Cys Lys Asp Leu Asn Ala Ser Asp Asn 610 615 620Asn Thr Glu Phe Leu Lys Asn Phe Ile Glu Leu Met Glu Lys Val Thr625 630 635 640Pro Asp Ser Lys Gln Cys Asn Asn Phe Leu Leu His Asn Leu Ile Leu 645 650 655Asp Thr Gly Ile Thr Gln Gln Leu Val Glu Arg Val Trp Arg Asp Gln 660 665 670Asp Leu Asn Thr Tyr Ser Leu Leu Ala Val Phe Ala Ala Thr Asp Gly 675 680 685Gly Ile Thr Arg Val Phe Pro Asn Lys Ala Ala Glu Asp Trp Thr Glu 690 695 700Asn Pro Glu Pro Phe Asn Ala Ser Phe Tyr Arg Arg Ser Leu Asp Asn705 710 715 720His Gly Tyr Val Phe Lys Pro Pro His Gln Asp Ala Leu Leu Arg Pro 725 730 735Leu Glu Leu Glu Asn Asp Thr Val Gly Ile Leu Val Ser Thr Ala Val 740 745 750Glu Leu Ser Leu Gly Arg Arg Thr Leu Arg Pro Ala Val Val Gly Val 755 760 765Lys Leu Asp Leu Glu Ala Trp Ala Glu Lys Phe Lys Val Leu Ala Ser 770 775 780Asn Arg Thr His Gln Asp Gln Pro Gln Lys Cys Gly Pro Asn Ser His785 790 795 800Cys Glu Met Asp Cys Glu Val Asn Asn Glu Asp Leu Leu Cys Val Leu 805 810 815Ile Asp Asp Gly Gly Phe Leu Val Leu Ser Asn Gln Asn His Gln Trp 820 825 830Asp Gln Val Gly Arg Phe Phe Ser Glu Val Asp Ala Asn Leu Met Leu 835 840 845Ala Leu Tyr Asn Asn Ser Phe Tyr Thr Arg Lys Glu Ser Tyr Asp Tyr 850 855 860Gln Ala Ala Cys Ala Pro Gln Pro Pro Gly Asn Leu Gly Ala Ala Pro865 870 875 880Arg Gly Val Phe Val Pro Thr Val Ala Asp Phe Leu Asn Leu Ala Trp 885 890 895Trp Thr Ser Ala Ala Ala Trp Ser Leu Phe Gln Gln Leu Leu Tyr Gly 900 905 910Leu Ile Tyr His Ser Trp Phe Gln Ala Asp Pro Ala Glu Ala Glu Gly 915 920 925Ser Pro Glu Thr Arg Glu Ser Ser Cys Val Met Lys Gln Thr Gln Tyr 930 935 940Tyr Phe Gly Ser Val Asn Ala Ser Tyr Asn Ala Ile Ile Asp Cys Gly945 950 955 960Asn Cys Ser Arg Leu Phe His Ala Gln Arg Leu Thr Asn Thr Asn Leu 965 970 975Leu Phe Val Val Ala Glu Lys Pro Leu Cys Ser Gln Cys Glu Ala Gly 980 985 990Arg Leu Leu Gln Lys Glu Thr His Cys Pro Ala Asp Gly Pro Glu Gln 995 1000 1005Cys Glu Leu Val Gln Arg Pro Arg Tyr Arg Arg Gly Pro His Ile Cys 1010 1015 1020Phe Asp Tyr Asn Ala Thr Glu Asp Thr Ser Asp Cys Gly Arg Gly Ala1025 1030 1035 1040Ser Phe Pro Pro Ser Leu Gly Val Leu Val Ser Leu Gln Leu Leu Leu 1045 1050 1055Leu Leu Gly Leu Pro Pro Arg Pro Gln Pro Gln Val Leu Val His Ala 1060 1065 1070Ser Arg Arg Leu 1075 7 1070 DNA Homo sapiens 7cttaaagata gctagagcca cgggggctgt aagttcagca tgcctccttt tctggtctcc 60gctgaagctg tcactccacc attaaacctg tgactctagg ccttaagcct gttgaaggtc 120gagcccccaa aagggtcaca tatgctcctg ccttgggccg cggggcccgg gactcttccc 180gcgggtgggg tggggaggag cggcagggtc tgaggtgtgg gggcgggggc gcacccgggg 240cgctcgggta gcagctgggg cgcaggacgc ccgagccagt agggcaggat tcgggctgcg 300cggggacgag aggcgcgcgg gcacgggtgg gcgcgtggcc gcggcggggg cgcgcggggg 360cgggccagcc cgggaagaga gagggaggga gggagagaag agggcggtgc cggcaggttg 420gcggcggctg ctatttgagc gcaggtcccg ggccgggcgc tcagagcgct tggagccagc 480gctgcaggga gatagcagcg cgcagcccgc agaggcgctg cggcccgtgc agccccggag 540gcccctcgcg gagaaggcgg cggcggagga gaggccgagt taccgcccgc cgcccgcgcc 600cccccaaccc cgccgccgcc gccgccgccg ccactgcccc ccctccccgc ggcgccgcat 660cttgaatgga aacatggcgg tgccggctcg gacctgcggc gcctctcggc ccggcccagc 720gcggactgcg cgcccctggc ccggctgcgg cccccaccct ggccccggca cccggcgccc 780gacgtccggg cccccgcgcc cgctgtggct gctgctgccg cttctaccgc tgctcgccgc 840ccccggcgcc tctgcctaca gcttccccca gcagcacacg taagtggcct cggccggccg 900cgagaccccg gccgagcctt gcgccccgct ctgcccccgg tccgcgctac tccttccctg 960cgctccgcgc cagggcagag gcgctgggtc cggctgcccg ctgcgcccgg gggcgacggc 1020cccaagcccc gaaggctggc agccgcggtc ccggcgctct ggctgcgtca 1070 8 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 8ctctacaacc caattcacca t 21 9 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 9tagatggcac tggccttct 19 10 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 10actcaccacc ctactgttc 19 11 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 11agctgcctgt ttggtgcta 19 12 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 12ctgagagtga ggatgtggaa 20 13 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 13gtgcatcctc atacacgttg 20 14 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 14gacaagccac cccttaccta c 21 15 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 15gcagagccca gttctggctg 20 16 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 16ccagcataga gtggtcagtg 20 17 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 17agtaccctgt ccattgcctg 20 18 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 18ggcaggtagc actgatggtc 20 19 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 19ttggagccac tgagtggaag 20 20 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 20gtggcttacg gtcctcactc 20 21 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 21tgtgctggga gtcgcggctg 20 22 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 22accactggac tgcctgcggt g 21 23 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 23cagggctggc agtgctacac 20 24 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 24actgccagcc ctgtgaccat g 21 25 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 25ccatctccag tccaggcatc 20 26 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 26ttcgacagga cacagcccag 20 27 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 27tgctgggtag acaggggaca g 21 28 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 28agcccagtcg cctctgcaag 20 29 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 29tggatacagc tggctgcgcc 20 30 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 30ccttacccta acagaggcat c 21 31 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 31aacctcacgt gttctcctgc 20 32 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 32tgggcaggag aacacgtgag 20 33 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 33ctggtgatgg tcacaggagc 20 34 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 34aggccactca ccaccctact g 21 35 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 35tcctgggtac accaagccag 20 36 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 36ggagggctga gagctgcctg 20 37 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 37ttgaggttac tgctgtggcc ac 22 38 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 38ctggtggcca cagcagtcac 20 39 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 39ggatggccag ttgaacatac g 21 40 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 40ttcgacagga cacagcccag 20 41 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 41gtgctgggta gacaggggac agg 23 42 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 42tgggcaggag aacacgtgag 20 43 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 43ctggtgatgg tcacaggagc 20 44 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 44acccctggct tctgcttcct t 21 45 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 45acactgccct catggtacag 20 46 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 46acctccctgt gctctgtccc tca 23 47 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 47aatccacgca tggatgggca 20 48 24 DNA Artificial Sequence Description of Artificial Sequence Synthetic 48tgagcagcta gtgctgaggc ctct 24 49 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 49cagcaaggag gtgtggctca gga 23 50 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 50actccaagca gtgtgagtgc 20 51 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 51gaaggaagtt gttgcctgga a 21 52 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 52caggtgtgga aataagcagg 20 53 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 53catcttcttg cagctccttg 20 54 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 54tgcccttgtt acagtcatct cca 23 55 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 55taagatgaaa agccagccag ctg 23 56 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 56gtctcctctt tggacagatt ctg 23 57 24 DNA Artificial Sequence Description of Artificial Sequence Synthetic 57tggagatgac tgtaacaagg gcac 24 58 24 DNA Artificial Sequence Description of Artificial Sequence Synthetic 58aagaggagac ttcccagtct cttg 24 59 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 59ctgcatacag gatgcagcac tg 22 60 24 DNA Artificial Sequence Description of Artificial Sequence Synthetic 60gctcacctca cggagctgct gcga 24 61 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 61tgttcagccc agggaagcga agc 23 62 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 62acttacagcc cccgtggctc tag 23 63 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 63cctggctctg gaagaatcta 20 64 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 64cagaaaagga ggcatgctga 20 65 18 DNA Artificial Sequence Description of Artificial Sequence Synthetic 65aagcgagtgg ctgcagag 18 66 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 66ctaagcggaa acctgggca 19 67 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 67gcatcttgaa tggaaacatg gc 22 68 18 DNA Artificial Sequence Description of Artificial Sequence Synthetic 68tcgacctcct gctccaga 18 69 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 69agcacacgat gcagcactg 19 70 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 70cttctccacc aacttctgag 20 71 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 71acaaccggaa cctgttcga 19 72 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 72cgtcatagta cacgatgtct tc 22 73 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 73atgctgcaga gaacttccag 20 74 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 74tgaagtttgg gtcctcgatg 20 75 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 75ctgagagtga ggatgtggaa 20 76 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 76aagacctgcc acagcagtg 19 77 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 77gtgttcatgg aaaaccgcag 20 78 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 78ccactcacat ccacgatgat g 21 79 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 79ctgtacgatg tccgaaggag ac 22 80 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 80tgtgaagcat gacacaggct g 21 81 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 81atctgtctgc gagatgctgg 20 82 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 82ttctgcagct ggtcaaagg 19 83 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 83cgcaacaaga aggtgttcaa g 21 84 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 84gccccacgga gaaagtaaac 20 85 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 85tgttcacgga tggtggtgag 20 86 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 86ttcctgtgtg ttgatgcgg 19 87 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 87ttgagatccc ttccatcgg 19 88 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 88gctggttctt cttttcccca g 21 89 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 89gtggtaacag ggaccctccc t 21 90 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 90agattggggt gcagcaacac 20 91 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 91gctatgtgtt tgccattgac c 21 92 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 92ctatgtacct ctcatccagg gac 23 93 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 93catgattgat ggcaacaagg 20 94 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 94ggggagcagg aactcaaaat ac 22 95 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 95gccaatctca gtgaccagat cc 22 96 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 96aggttgtgca gaaggaagtt g 21 97 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 97agaaagtgac tccagactcc aag 23 98 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 98ttgaagggct cagggttctc 20 99 23 DNA Artificial Sequence Description of Artificial Sequence Synthetic 99ggatctcaac acgtacagcc tac 23 100 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 100ggatgcccac agtgtcattc 20 101 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 101cccttcaatg ccagcttcta c 21 102 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 102aacttctcag cccaagcctc 20 103 21 DNA Artificial Sequence Description of Artificial Sequence Synthetic 103aatgacactg tgggcatcct c 21 104 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 104ttaacctcgc agtccatctc ac 22 105 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 105accaagacca gcctcagaag tg 22 106 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 106ataggactcc ttgcgggtgt ag 22 107 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 107aggtggatgc caacctgatg 20 108 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 108cgtagagaag ctgctggaac ag 22 109 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 109caccgttgca gatttcctta ac 22 110 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 110agtttccgca gtcgatgatg 20 111 22 DNA Artificial Sequence Description of Artificial Sequence Synthetic 111gaaacagacc cagtactact tc 22 112 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 112gcgttgtagt cgaagcagat 20 113 20 DNA Artificial Sequence Description of Artificial Sequence Synthetic 113agcagtgtga gctagtgcag 20 114 19 DNA Artificial Sequence Description of Artificial Sequence Synthetic 114agggtgggaa aggcgaaga 19

Claims

1. A purified nucleic acid sequence comprising a nucleotide sequence selected from the group consisting of (a) SEQ ID NO:1 and the complement thereof, (b) SEQ ID NO:3 and the complement thereof, and (c) SEQ ID NO:5 and the complement thereof.

2. The nucleic acid of claim 1, wherein said nucleic acid sequence encodes the amino acid sequence selected from the group consisting of SEQ ID NO:2, SEQ ID NO:4, and SEQ ID NO:6.

3. The nucleic acid sequence of claim 2, wherein said nucleic acid sequence is double-stranded.

4. The nucleic acid sequence of claim 2, wherein said nucleic acid sequence is single-stranded.

5. The nucleic acid sequence of claim 1, wherein said nucleic acid sequence encodes a fusion protein.

6. The nucleic acid sequence of claim 5, wherein said fusion protein comprises a polypeptide selected from the group consisting of chloramphenicol acetyltransferase, luciferase, beta-galactosidase, green fluorescent protein, Myc protein, protein A, glutathione-S-transferase, and polyhistidine.

7. The nucleic acid sequence of claim 1, wherein said nucleic acid sequence is inserted into a recombinant expression vector.

8. The nucleic acid sequence of claim 7, wherein said expression vector is contained within a cultured host cell.

9. The nucleic acid sequence of claim 8, wherein said host cell is a eukaryotic cell.

10. The nucleic acid sequence of claim 9, wherein said eukaryotic cell is selected from the group consisting of cancer cells and amphibian oocytes.

11. A method for producing a calcium channel protein, comprising:a) providing: i) a recombinant expression vector comprising a nucleic acid sequence encoding an amino acid sequence selected from the group consisting of SEQ ID NOs: 2, 4, and 6; and ii) a cultured host cell; and b) introducing said vector into said host cell under conditions such that said host cell expresses said amino acid sequences, wherein said sequence encodes a calcium channel protein.

12. The method of claim 11, wherein said expressed amino acid sequence is recovered.

13. The method of claim 11, wherein said host cell is a eukaryotic cell.

14. The method of claim 13, wherein said eukaryotic host cell is selected from the group consisting of cancer cells and amphibian oocytes.

15. A method for coexpressing a plurality of calcium channel proteins, comprising:a) providing: i) one or more recombinant expression vectors comprising one or more nucleic acid sequences encoding amino acid sequences selected from the group consisting of SEQ ID NOs: 2, 4, and 6; and ii) a cultured host cell; and b) introducing said vectors into said host cell under conditions such that said host cell coexpresses said one or more amino acid sequences, wherein said amino acid sequences encode calcium channel proteins.

16. The method of claim 15, wherein said expressed amino acid sequence is recovered.

17. The method of claim 15, wherein said host cell is a eukaryotic cell.

18. The method of claim 17, wherein said eukaryotic host cell is selected from the group consisting of cancer cells and amphibian oocytes.