Expression of human multidrug resistance genes and improved selection of cells transduced with such genes

This invention relates to the transduction of cells with human multidrug resistance (mdr) genes and the expression thereof, as well as the selection or identification of cells transduced with such genes. More particularly, this invention relates to the enhanced expression of mdr genes by transduced cells, and an improved method of selecting or identifying cells transduced with mdr genes.
Genes for multidrug resistance such as, for example, mdr1 and mutated forms thereof, encode proteins of a class known as p-glycoprotein, that confer resistance to a range of cytotoxic drugs used in the treatment of human malignancies. The introduction and expression of the mdr1 gene in human cells may serve several useful purposes in the treatment of diseases. For example, the mdr1 gene can function as a dominant selectable marker that will allow for positive selection of cells transduced by an expression vehicle, such as, for example, a retroviral vector, ex vivo or in vivo. Used in this manner, expression of the mdr1 gene in normal human cells may be useful in increasing the proportion of a target cell population that has been transformed by an expression vehicle, such as a retroviral particle. Also, expression of the mdr1 gene in normal human cells may permit more intensive use of chemotherapeutic drugs in the treatment of cancer. For example, expression of the mdr1 gene in human bone marrow cells could reduce the severity and duration of cytopenias following chemotherapy, which may facilitate dose intensification while reducing morbidity and mortality.
In accordance with an aspect of the present invention, there is provided human mdr1 DNA or RNA which encodes p-glycoprotein or an analogue or fragment of such DNA or RNA which encodes an iso-form of p-glycoprotein which confers multidrug resistance. The DNA or RNA includes at least one splice site, and at least one base in the splice site has been changed to a different base which thereby inactivates the splice site. Preferably, the DNA or RNA is a DNA or RNA sequence for human mdr1 which encodes p-glycoprotein wherein at least one base in a splice site of said DNA encoding p-glycoprotein is changed.
The natural human mdr1 gene contains at least one functional splice donor site and splice acceptor site. This invention provides a modification of the mdr1 gene whereby at least one base in a splice site has been changed to a different base which thereby inactivates the splice site.
The term "human mdr1 gene" as used herein means the wild type human mdr1 gene, which encodes p-glycoprotein, as well as mutated human mdr1 genes which encode what are known as iso-forms of p-glycoprotein. Such mutated genes include a mutation in which the human mdr1 DNA encodes a p-glycoprotein in which the first 23 pk amino acids at the N-terminal are deleted (Currier, et al., J. Biol. Chem., Vol. 264, pgs. 14376-14381 (1989)); insertional mutation(s) in the human mdr1 DNA in which amino acids have been inserted into ATP binding or utilization sites (Currier, et al; 1989); a complementary human mdr1 DNA sequence (cDNA sequence) in which codon 185, which encodes Gly 185, has been changed from GGT to GTT to encode Val 185. (PCT Application No. W087/05943; Choi, et al., Cell, Vol. 53, pgs. 519-529 (1988); Safa, et al., Proc.Nat.Acad.Sci., Vol. 87, pgs. 7225-7229 (1990)); and a chimeric gene encoding a protein having adenosine deaminase added to the N-terminal of p-glycoprotein (Germann, et al., J. Biol. Chem., Vol. 264, pgs. 7418-7424 (1989)).
Although the scope of this aspect of the present invention is not to be limited to any theoretical reasoning, Applicants have found that aberrant splicing of the mdr1 gene may occur within the coding sequence for p-glycoprotein. Such splicing, which uses cryptic splice donor and splice acceptor sites, results in the production of expression vehicles (such as, for example, recombinant retroviruses) that contain a truncated mdr1 gene, which encodes a truncated and non-functional p-glycoprotein.
Applicants have found a cryptic splice donor site having a length of 9 bases from nucleotide 760 to nucleotide 768 of the human mdr1 gene, and which has the following sequence:
CAGGTATGC (SEQ ID NO:1)
A cryptic splice acceptor site was also found, which has a length of 16 bases from nucleotide 2729 to nucleotide 2744 of the human mdr1 gene; and which has the following sequence:
ACATTTTTCCTTCAGG (SEQ ID NO:2)
Applicants have found that, by changing at least one base of the cryptic splice donor and/or acceptor sites, one may suppress aberrant splicing of the mdr1 gene and maximize the transfer of DNA encoding functional p-glycoprotein into desired cells.
In one embodiment, at least one base which is changed is in a splice donor site. In another embodiment, the at least one base which is changed is in a splice acceptor site. In yet another embodiment, at least one base is changed in a splice donor site and at least one base is changed in a splice acceptor site.
In a preferred embodiment, at least one base in a splice site which is changed is in the splice donor site and is at least one of guanine (G) or thymine (T) contained in the splice donor site wherein G and T are adjacent.
In another preferred embodiment, at least one base in a splice site which is changed is in the splice acceptor site and is at least one of adenine (A) or guanine (G) contained in the splice acceptor site wherein A and G are adjacent.
In a more preferred embodiment, at least one base is changed in the splice donor site wherein the at least one base is at least one of G or T contained in the splice donor site wherein G and T are adjacent; and at least one base is changed in the splice acceptor site wherein the at least one base is at least one of A or G contained in the splice acceptor site wherein A and G are adjacent.
In another embodiment, at least one base in a splice site is changed such that a codon encoding an amino acid is changed to a different codon encoding the same amino acid. Preferably, the at least one base is the third, or "wobble" base in the codon.
In one embodiment, codon 113, located in the splice donor site, and which encodes Arg, is changed from AGG to AGA, which also encodes Arg. In another embodiment, codon 773, located in the splice acceptor site, and which encodes Gln, is changed from CAG to CAA, which also encodes Gln. It is also contemplated that in yet another embodiment, both codon 113 of the mdr1 gene is changed from AGG to AGA, and codon 773 of the mdr1 gene is changed from CAG to CAA.
In one embodiment, the DNA sequence is further mutated such that at least a portion of the 5' untranslated region of the DNA has been removed.
In another embodiment, the DNA sequence may be further mutated such that at least a portion of the 3' untranslated region of the DNA has been removed. In yet another embodiment, the DNA sequence is further mutated such that at least a portion of the 5' untranslated region of the DNA and at least a portion of the 3' untranslated region of the DNA have been removed. Although Applicants do not intend to be limited thereby, the DNA of the human mdr1 gene is quite large and contains extended 5' and 3' untranslated regions. Such extended regions may result in the generation of a reduced titer of viral vector particles, such as retroviral vector particles, which may be engineered with such DNA. Thus, removal of at least a portion(s) of the 5' and/or 3' untranslated regions may enable one to insert such DNA into a viral vector, such as a retroviral vector, whereby one generates an increased titer of retroviral particles. Within the scope of the present invention, up to the entire 5' untranslated region and/or up to the entire 3' untranslated region may be removed.
In accordance with another aspect of the present invention, there is provided DNA (or RNA) encoding a protein which provides for multidrug resistance, wherein the DNA includes the following sequence:
CAGGTATGC (SEQ ID NO:1)
At least one base is changed to a different base. Preferably at least one base of the GT doublet is changed.
In accordance with yet another aspect of the present invention, there is provided DNA (or RNA) encoding a protein which provides for multidrug resistance, wherein the DNA includes the following sequence:
ACATTTTTCCTTCAGG (SEQ ID NO:2)
At least one base is changed to a different base. Preferably, at least one base of the AG doublet is changed.
In one embodiment, the DNA encoding a protein which provides for multidrug resistance includes a first sequence.
CAGGTATGC, (SEQ ID NO:1) and a second sequence:
ACATTTTTCCTTCAGG (SEQ ID NO:2)
At least one base in the first sequence, and at least one base in the second sequence is changed to a different base. Preferably, at least one base of the GT doublet of the first sequence is changed, and at least one base of the AG doublet of the second sequence is changed.
The changed DNA or RNA sequence for a human mdr1 gene, or the changed DNA or RNA encoding a protein which provides for multidrug resistance, of the present invention may be cloned into any of a variety of expression vectors by genetic engineering techniques known to those skilled in the art. Such expression vectors include, but are not limited to, prokaryotic vectors, including bacterial vectors; eukaryotic vectors, such as, for example, yeast vectors and fungal vectors, and viral vectors, such as, but not limited to, retroviral vectors, and non-retroviral vectors such as, but not limited to, adenoviral vectors, adeno-associated viral vectors, and Herpes virus vectors. In one embodiment, the changed DNA (or RNA) is cloned into a retroviral expression vector. It is also contemplated that the changed DNA or RNA may be introduced into cells by means of non-viral systems and non-plasmid-based systems. Such systems include, but are not limited to, the injection of the naked changed DNA or RNA into a desired cell, liposomes which encapsulate such DNA or RNA, and which deliver such DNA or RNA to a cell, and the coupling of the DNA or RNA to a protein or other agent which binds to a cellular receptor.
Retroviral vectors which may be employed include those derived from Moloney Murine Leukemia Virus, Moloney Murine Sarcoma Virus, Rous Sarcoma Virus, Harvey Sarcoma Virus, and Spleen Necrosis Virus. In one embodiment, the retroviral vector may be derived from Moloney Murine Leukemia Virus and is one of the LN series of vectors, as described in Miller, et al., Biotechniques, Vol. 7, pgs. 980-990 (1989). Such vectors have a portion of the packaging signal derived from a mouse sarcoma virus, and a mutated gag initiation codon.
In another embodiment, the retroviral vector may include at least four cloning, or restriction enzyme recognition sites, wherein at least two of the sites have an average frequency of appearance in eukaryotic genes of less than once in 10,000 base pairs; i.e., the restriction product has an average DNA size of at least 10,000 base pairs. Preferred cloning sites are selected from the group consisting of NotI, SnaBI, SalI, and XhoI. In a preferred embodiment, the retroviral vector includes each of these cloning sites.
When a retroviral vector including such cloning sites is employed, there may also be provided a shuttle cloning vector which includes at least two cloning sites which are compatible with at least two cloning sites selected from the group consisting of NotI, SnaBI, SalI, and XhoI located on the retroviral vector. The shuttle cloning vector also includes at least one desired gene which is capable of being transferred from the shuttle cloning vector to the retroviral vector.
The shuttle cloning vector may be constructed from a basic "backbone" vector or fragment to which are ligated one or more linkers which include cloning or restriction enzyme recognition sites. Included in the cloning sites are the compatible, or complementary cloning sites hereinabove described. Genes and/or promoters having ends corresponding to the restriction sites of the shuttle vector may be ligated into the shuttle vector through techniques known in the art.
The shuttle cloning vector can be employed to amplify DNA sequences in prokaryotic systems. The shuttle cloning vector may be prepared from plasmids generally used in prokaryotic systems and in particular in bacteria. Thus, for example, the shuttle cloning vector may be derived from plasmids such as pBR322; pUC 18; etc.
Examples of retroviral vectors having at least two restriction enzyme recognition sites having an average frequency of appearance in eukaryotic genes of less than once in 10,000 base pairs, and of the shuttle cloning vectors employed in transfering genes to such vectors are further described in PCT Application No. W091/10728.
The vectors also include one or more promoters. Suitable promoters which may be employed include, but are not limited to, the retroviral LTR; the SV40 promoter; and the human cytomegalovirus (CMV) promoter described in Miller, et al., Biotechniques, Vol. 7, No. 9, pgs. 980-990 (1989), or any other promoter (e.g., cellular promoter such as eukaryotic cellular promoters including, but not limited to, the histone, pol III, and .beta.-actin promoters). Other viral promoters which may be employed include, but are not limited to, adenovirus promoters, TK promoters, and B19 parvovirus promoters. The selection of a suitable promoter will be apparent to those skilled in the art from the teachings contained herein.
The vector may also further include a heterologous or foreign gene.
Heterologous or foreign genes which may be placed into the vectors of the present invention include, but are not limited to genes which encode cytokines or cellular growth factors, such as lymphokines, which are growth factors for lymphocytes. Other examples of foreign genes include, but are not limited to, genes encoding soluble CD4, Factor VIII, Factor IX, ADA, the LDL receptor, ApoI, tumor necrosis factors (TNF's) and ApoC.
Suitable promoters which may control the foreign genes include those hereinabove described.
The vector including the DNA of the present invention may be transduced into a suitable packaging cell line. Examples of suitable packaging cell lines include the PA317 cell line and the PE501 cell line (Miller, et al., 1989), and the PAT 2.4 cell line (U.S. application Ser. No. 792,281, filed Nov. 14, 1991.) Transduction of the packaging cell line may be accomplished by standard techniques such as electroporation or CaPO.sub.4 precipitation. Vector particles generated from such producer cells may then be employed to generate a producer cell line, and to transduce cells (eg., eukaryotic cells such as mammalian cells), which may be administered to a host as part of a gene therapy procedure. Examples of cells which may be transduced include, but are not limited to, primary human cells such as primary human nucleated blood cells (such as leukocytes, and lymphocytes such as TIL cells, T-lymphocytes, and .beta.-lymphocytes), tumor cells, endothelial cells, epithelial cells, keratinocytes, stem cells, bone marrow cells, hepatocytes, connective tissue cells, fibroblasts, mesenchymal cells, mesothelial cells, and parenchymal cells.
Upon transfection or transduction of a packaging cell line with a retroviral vector, it is essential that the producer cell line generate a sufficient titer of vector particles for gene therapy protocols. Selection for growth of such packaging or producer cells in the presence of colchicine has resulted in the isolation of producer clones with viral titers below what is currently adequate for clinical gene therapy protocols.
It is therefore another object of the present invention to provide a method of selecting producer cells which generate an acceptable titer of retroviral particles including a human mdr1 gene, and in particular for generating an adequate titer of retroviral particles suitable for inserting and expressing the mdr1 gene in primate cells, particularly in primate repopulating hematopoietic stem cells.
In accordance with an aspect of the present invention, there is provided a method of identifying cells which overexpress a gene encoding multidrug resistance (preferably such gene is the human mdr1 gene) in a cell population transduced with an expression vehicle including a gene which encodes a protein which provides for multidrug resistance (preferably such gene is the human mdr1 gene). The method comprises contacting the cell population with a staining material, and identifying the cells which overexpress the gene encoding a protein which provides for multidrug resistance (preferably the human mdr1 gene) based on differentiation of color among the cells of the cell population.
Such differentiation in color may be based on differences in color intensity between cells which overexpress the human mdr1 gene and cells which do not overexpress the human mdr1 gene (for example, cells which contain vectors including the human mdr1 gene, whereby such cells overexpress the human mdr1 gene, may be brighter or duller than those cells which do not contain vectors including the human mdr1 gene, whereby such cells which express the human mdr1 gene at normal levels or do not express the gene); or differences in color or shades of color between cells which contain vectors including the human mdr1 gene, and thereby overexpress the human mdr1 gene, and cells which do not contain vectors including the human mdr1 gene, and thereby express the human mdr1 gene at normal levels or do not express the human mdr1 gene. Alternatively, cells which contain vectors including the human mdr1 gene, and thereby overexpress the human mdr1 gene may change color after staining, while cells which do not contain vectors which include the human mdr1 gene do not change color after staining.
The term "overexpress" as used herein, means that the gene encoding multidrug resistance is expressed at a level above that which is expressed by a normal human cell. In normal human cells, the mdr1 gene is expressed at low levels or is not expressed. In cells transduced with an expression vehicle including the mdr1 gene, the expression level of the mdr1 gene is considerably increased, and thus, the mdr1 gene is "overexpressed."
Applicants have found that, by identifying cells which overexpress the human mdr1 gene in a cell population transduced with infectious viral particles which include the human mdr1 gene, in accordance with the method of the present invention, Applicants have been able to isolate clones which produce higher viral titers than clones selected with drugs such as colchicine, for example.
In one embodiment, the staining material is a fluorescent dye. Fluorescent dyes which may be employed include, but are not limited to, rhodamine 123, 3,3'-diethyloxacarbocyanine iodide (DiOC.sub.2), and 3,3'-diethyloxadicarbocyanine iodide (DODC iodide).
In one embodiment, the fluorescent dye is rhodamine 123. Rhodamine 123 ordinarily concentrates within the mitochondria of cells, but can be effluxed from the cell by p-glycoprotein. Cells stained with rhodamine 123 that do not express p-glycoprotein or express p-glycoprotein at normal or lower than normal levels appear "bright" by fluorescence microscopy or by FACS analysis, whereas cells that overexpress p-glycoprotein appear "dull," even if small quantities of p-glycoprotein are expressed. (Chaudhary, et al., Cell, Vol. 66, pgs. 85-94 (Jul. 12, 1991)). Thus, producer cells or other cells which have incorporated and express a functional human mdr1 gene may be distinguished from non-transformed cells on the basis of this "dull" staining phenotype.
Such a method may also be employed to determine viral titer of human mdr1 retrovirus producer cell lines. In one embodiment, a defined number of target cells are exposed to serial dilutions of a viral supernatant produced by a defined number of producer cells. After infection (eg., at about 48 hrs. after infection), the cells are stained with rhodamine 123 and allowed to efflux the dye. The proportion of "dull" cells can be visually estimated by fluorescence microscopy, or accurately quantitated by scoring a defined number of individual cells by FACS analysis. Because the proportion of cells overexpressing p-glycoprotein is known, it is possible to calculate accurately the minimum number of infectious viral particles present in a known volume of viral supernatant.
Although it has been demonstrated that retroviral vectors may be used to transfer and express the mdr1 gene in cultured cells (Proc.Nat.Acad.Sci., Vol. 85, pgs. 1595-1596 (1988)); in murine repopulating hematopoietic stem cells (Sorrentino, et al., Science, (in press)), and in murine hematopoietic progenitors in vitro (McLachlin, et al., J.Nat.Canc.Inst., Vol. 82, pgs. 1260-1263 (1990)), there has been no demonstration of transfer and expression of the mdr1 gene in primate cells, and in particular in primate stem cells capable of reconstituting transplant recipients.
Thus, in accordance with an aspect of the present invention, there is provided a primate cell which is genetically engineered with DNA (RNA) which encodes a protein which provides multidrug resistance. The DNA (RNA) may be any DNA (RNA) which encodes a protein which provides multidrug reistance or the changed DNA or RNA sequences which are hereinabove described.
Applicants have discovered that by selecting for cells transduced with a gene encoding multidrug resistance in accordance with the selection method hereinabove described, one is able to obtain producer cells which generate a sufficient titer of infectious viral particles which provide for the transfer and expression of multidrug resistance genes in primate cells, in particular in primate repopulating hematopoietic stem cells.
Primate cells which may be genetically engineered with such DNA (RNA) include, but are not limited to, primate bone marrow cells, preferably enriched primate bone marrow cells, and hematopoietic progenitor (CD34+) cells or hematopoietic stem cells (in particular, primate repopulating hematopoietic stem cells), and human primary cells. The hematopoietic stem cells may also be CD33.sup.- and HLA-DR.sup.low. (Chaudhary, et al., 1991) The primate cells may be obtained from humans or other primates, such as monkeys, for example.
This aspect of the present invention is particularly applicable to the use of primate repopulating hematopoietic stem cells which are genetically engineered with DNA (RNA) which encodes a protein which provides multidrug resistance. Such stem cells give rise to bone marrow cells and may be administered, for example, to a patient who has undergone chemotherapy and/or radiation treatment in order to regenerate healthy bone marrow cells in the patient. Thus Applicants have devised a system for identifying producer cells which generate a sufficient titer of viral particles including a gene encoding multidrug resistance, whereby such viral particles may be used to infect primate repopulating hematopoietic stem cells, which may then be administered to a patient in order to regenerate bone marrow in said patient, wherein such regenerated bone marrow is resistant to the toxic effects of chemotherapy.
In one embodiment, bone marrow cells are harvested by needle aspiration from a primate, and purified by positive selection for cells expressing the CD34 antigen. CD34 selected cells are enriched 50-100 fold in clonogenic hematopoietic progenitors and contain all of the repopulating stem cells. Alternatively, the bone marrow cells may be purified in accordance with the procedures described in U.S. Pat. No. 5,061,620.
The CD34+ cells are incubated in vitro in the presence of stimulatory hematopoietic growth factors and in the presence of retroviral supernatant containing infectious viral particles which include a multidrug resistance gene. The viral particles are generated from a producer cell line selected in accordance with the selection procedure hereinabove described. After incubation, the cells are transplanted into recipients suitably treated to receive a bone marrow transplant. After transplantation, bone marrow cells, peripheral blood leukocytes, purified granulocytes, and T-lymphocytes are assayed for presence and expression of the introduced mdr1 gene.
The invention will be described with respect to the following examples; however, the scope of the present invention is not intended to be limited thereby.

BRIEF DESCRIPTION OF THE DRAWINGS
The invention now will be described with respect to the drawings, wherein:
FIG. 1 is a schematic of the construction strategy for pG1;
FIG. 2 is a DNA sequence of the multiple cloning site in pG1;
FIG. 3 is a plasmid map of pG1;
FIG. 4 is the cDNA sequence of the human mdr1 gene;
FIG. 5 is a plasmid map of pGEM-2;
FIG. 6 is a restriction map of pMDR 2000XS;
FIG. 7 is a plasmid map of pG1MD1; and
FIGS. 8A and 8B are measures of the results of rhodamine titering assays for the presence of the human mdr1 gene in viral producer cells.

EXAMPLE 1
A. Construction of plasmid pG1
Plasmid pG1 was constructed from pLNSX (Palmer et al., Blood, 73:438-445; 1989). The construction strategy for plasmid pG1 is shown in FIG. 1. The 1.6 kb EcoRI fragment, containing the 5' Moloney Sarcoma Virus (MoMuSV) LTR, and the 3.0 kb EcoRI/ClaI fragment, containing the 3' LTR, the bacterial origin of replication and the ampicillin resistance gene, were isolated separately. A linker containing seven unique cloning sites was then used to close the EcoRI/ClaI fragment on itself, thus generating the plasmid pG0. The plasmid pG0 was used to generate the vector plasmid pG1 by the insertion of the 1.6 kb EcoRI fragment containing the 5' LTR into the unique EcoRI site of pG0. Thus, pG1 (FIG. 3). consists of a retroviral vector backbone composed of a 5' portion dervied from MoMuSV, a short portion of gag in which the authentic ATG start codon has been mutated to TAG (Bender et al. 1987), a 54 base pair multiple cloning site (MCS) containing from 5' to 3' the sites EcoRI, NotI, SnaBI, SalI, BamHI, XhoI, HindIII, ApaI, and ClaI, and a 3' portion of MoMuLV from base pairs 7764 to 7813 numbered as described in (Van Beveren et al., Cold Spring Harbor, Vol. 2, pg. 567, 1985). (FIG. 2). The MCS was designed to generate a maximum number of unique insertion sites, based on a screen of non-cutting restriction enzymes of the pG1 plasmid, the neo.sup.R gene, the .beta.-galactosidase gene, the hygromycin.sup.R gene, and the SV40 promoter.
B. Construction of pG1MD1
pMDR2000 (Ueda, et al., PNAS, Vol. 84, pgs. 3004-3008 (May 1987)), which contains an mdr1 cDNA sequence (SEQ ID NO:18) (FIG. 4) described in PCT application number W087/05943, wherein the first 282 bp of the untranslated 5' region and the last 23 bp of the untranslated 3' region of the cDNA sequence have been removed, was cut with SacI and EcoRI, and was inserted into a multiple cloning site of SacI and EcoRI digested pGEM2 (FIG. 5.) (Promega, Madison, Wis.) to form pGEM2MDR. pGEM2MDR was then cut with Smal at the 5' end of the multiple cloning site and a SacII linker having a length of 8 bp was inserted. At the 3' end of the plasmid, the plasmid was cut with EcoRI and a 12 bp XhoI linker was inserted. The resulting plasmid was pMDR2000XS. (FIG. 6.)
Plasmid pMDR2000XS was then cut at the 5' end of the cDNA sequence for mdr1 with HhaI, and at the 3' end of the cDNA sequence for mdr1 with HaeII, and a 3,845 bp fragment was removed. Such cutting removed an additional 131 bp from the 5' end, and an additional 384 bp from the 3' end of the cDNA. A linker was then added to the 3' sequence to reconstitute the amino acids that were cut off by cutting with HaeII and to add the TGA stop (or termination) codon back into the sequence. The linker has four restriction enzyme sites, HpaI, XhoI, BglII, and ClaI, and has the following sequence:
5'-A G T G A A C T C T G G T T A A C T C C
10 20
A C T C G A G C A C A G A T C T G G A
30
C A T C G A T A C T C (SEQ ID NO:3)
40 50
Bases 12-17 are recognized by HpaI, bases 22-27 are recognized by XhoI, bases 31-36 are recognized by Bg1II, and bases 41-46 are recognized by C1aI.
pG1 was then cut with SnaBI and C1aI, and the mdr1 fragment containing the added linker was cut with C1aI and inserted into the SnaBI and C1aI digested pG1 to form pG1MD1 (FIG. 7.)
C. Changing codons 113,185, and 773 of the mdr1 gene
Changing the mdr1 gene in pG1MD1 such that codon 113 is changed from AGG to AGA, codon 185 is changed from GTT to GGT (whereby Val is changed to Gly in the resulting expressed p-glycoprotein), and codon 773 is changed from CAG to CAA may be accomplished by either of the following strategies.
1. Introduction of point mutations into G1MD1 by site-directed mutagenesis
pG1MD1 is digested with NotI and XhoI, and a NotI-XhoI fragment is cloned into the phagemid pBluescriptSK+(Stratagene). The resulting subclone is transformed into E. coli strain CJ236 (Biorad). A 5 ml culture is grown at 37.degree. C. overnight in LB broth with 200 .mu.g/ml ampicillin and 30 .mu.g/ml chloramphenicol. 2.5 ml of this culture is then added to 25 ml of fresh media with the same antibiotics, and grown at 37.degree. C. until the O.D.600 of the culture reaches 0.3. Helper phage R408 (Stratagene) is then added at a multiplicity of infection of 20 to the culture. The culture is then incubated by vigorous shaking for 8 hours. The culture is then harvested by centrifugation at 17,000.times. g for 15 minutes at 4.degree. C. The supernatant fluid is harvested and spun again at 17,000.times. g for 15 minutes at 4.degree. C. The supernatant is then harvested and measured for volume.
A 1/4 volume of a solution containing 3.5M ammonium acetate and 20% polyethylene glycol is then added to the supernatant to precipitate the phage. The solution and supernatant mixture is incubated at room temperature for 15 minutes. The precipitate is then centrifuged at 11,000.times. g for 15 minutes at 4.degree. C. The resulting pellet is suspended in 400 .mu.lTE (10 mM Tris, 1 mM EDTA) and extracted with phenol/chloroform until the interphase is clear. The DNA (phage/template) is then ethanol precipitated by standard procedures.
2 ng of the following antisense oligonucleotides:
(a) 5'-T C T G T A C T G G T C T A T A C G G A T A A T
10 20
A A T G T C-3'(SEQ ID NO:4)
30
wherein the TCT sequence (nucleotides 11-13) will provide for a change of codon 139 from AGG to AGA;
(b) 5'-C T A A T T A C T T C C A T A A C C A C T G T T
10 20
T T A A C C-3'(SEQ ID NO:5)
30
wherein the CCA sequence (nucleotides 11-13) will provide for a change of codon 185 from GTT to GGT (whereby Val 185 is changed to Gly 185); and
(c) 5'-G T A A A A A G G A A G T T C C A A A G T G T A
10 20
A A C C G T-3'(SEQ ID NO:6)
30
wherein the GTT sequence (nucleotides 12-14) will provide for a change of codon 733 from CAG to CAA, and 200 ng of the phage/template DNA are then mixed in 10 .mu.l of TE. The mixture is heated to 70.degree. C., and then allowed to cool slowly to room temperature in order to anneal the oligonucleotides to the template. Deoxynucleotide triphosphates are then added to the mixture, followed by T4 DNA polymerase, T4 ligase, 10.times. synthesis buffer, and water to make the volume 20 .mu.l. The mixture is then placed on ice for 5 minutes, then at 25.degree. C. for 5 minutes, and then at 37.degree. C. for 90 minutes.
At the end of the 90 minute incubation, 90 .mu.l of TE is added and 5 .mu.l of the resulting mixture is used to transform E. coli strain DH5.alpha..
Mutagenized clones are then identified by colony hybridization with the oligonucleotides (a), (b), and (c) hereinabove described. The identified and changed mdr1 gene is then cut out of pBluescript with NotI and XhoI and cloned into pG1 cut with NotI and XhoI to form pG1MD3.
2. Introduction of Point Mutations into G1MD1 by PCR Based Strategy
The cryptic splice donor site and the Gly to Val point mutation in codon 185 are contained within a NotI to Apal restriction fragment of pG1MD1. This NotI to ApaI fragment can be excised, purified, and subcloned into a pUC based cloning vector called pUC007 (Sorrentino, et al., Nucleic Acids Research, Vol. 18, No. 9, pgs. 2721-2731 (1990)) that contains a synthetic polylinker multiple cloning site. The vector is prepared by partial digestion of pUC007 with EspI, and complete digestion with ApaI. The insert is prepared by digesting with NotI, blunting the NotI digested end with Klenow, and then digesting with ApaI. Following ligation, the abutment of the blunt FspI site with the blunted NotI site will recreate a NotI site that can be used to excise a NotI to ApaI fragment.
Following subcloning of the NotI to ApaI fragment into pUC007 (to form pMD1NA), the cryptic splice donor site and the codon 185 point mutation will be contained within a unique BstXI to MscI fragment. A strategy of overlapping or "recombinant" PCR to introduce point mutations into this BstXI to MscI fragment is employed. (Higuchi, PCR Protocols: A Guide to Methods and Applications, Innis, et al., eds, San Diego, Academic Press, pgs. 177-183 (1990)). Three sets of PCR primers are made. One set of complementary primers (SD-A and SD-B), which have the following sequences:
SD-A:GGAAGACATGACCAGATATGCCTATTATTACAG (SEQ ID NO:7)
SD-B:CTGTAATAATAGGCATATCTGGTCATGTCTTCC (SEQ ID NO:10)
are centered around the cryptic splice donor site, and differ from the sequence of G1MD1 at only one base, located in codon 139 of the mdr1 gene, wherein AGG is changed to AGA. This difference inactivates the splice donor site, although the amino acid is not changed. The second set of primers (C185-A and C185-B), which have the following sequences:
C185-A:CTCTAAGATTAATGAAGGTATTGGTGACAAAATTG (SEQ ID NO:9)
C185-B:CAATTTTGTCACCAATACCTTCATTAATCTTAGAG (SEQ ID NO:10)
are centered at the codon 185 mutation of the mdr1 gene and will differ from the sequence of G1MD1 only at the point mutation wherein codon 185 is changed from GTT to GGT. This difference corrects the point mutation in the cDNA sequence (FIG. 7) and encodes Gly in the final construction. The third set of primers flank the BstXI and MscI restriction sites. These primers (5'Bst and 3'Msc), which have the following sequences:
5'Bst:ATCGCGGATCCATGGTGGTGGGAACTTTGGC (SEQ ID NO:11)
3'Msc:CATCCGGAATTCAGCTGACAGTCCAAGAACAGGACTGATG (SEQ ID NO:12)
overlap the BstXI and MscI sites, respectively, and also incorporate another flanking restriction site that will allow the PCR fragment to be conveniently subcloned. Using the technique of "recombinant" PCR, three separate PCR reactions will be initiated, using MD1NA as the template DNA. In these reactions, a "proofreading" thermostable DNA polymerase, such as Vent polymerase marketed by New England BioLabs, is used to avoid misincorporation of nucleotides, as can occur with high frequency when Taq polymerase is used. In the first PCR reaction, the two primers are 5'Bst and SD-B, and amplify the sequence from the BstXI site to the cryptic splice donor site. In the second PCR reaction, the two primers are SD-A and C185-B, and amplify the sequence from the splice donor to the codon 185 mutation. In the third PCR reaction, the primers are C185-A and 3'Msc, and amplify the sequence from the codon 185 mutation to the MscI site. Following ten cycles of amplification, the product of these three reactions is purified away from unused primers, nucleotides, and buffer. The purified PCR products are mixed together, and then amplified for an additional 10 to 20 cycles with a "proofreading" polymerase such as Vent polymerase, using the 5'Bst and 3'Msc primers. This final PCR reaction results in an amplified PCR product that extends from the BstXI site to the MscI site, and has introduced point mutations into the cryptic splice donor site and the mutant codon 185. Using the flanking restriction sites, the PCR product is digested with BamHI and EcoRI and is subcloned into a pUC based vector prepared by digestion with BamHI and EcoRI using inactivation of the lacZ gene to identify vectors that have incorporated the insert. This construct is referred to as pMD1BM and is used to transform bacteria. Bacteria that contain the plasmid carrying the desired point mutations will be identified by hybridization to allele specific oligonucleotides. MD1BM plasmid DNA isolated from these subclones is then sequenced, using standard M13 sequence primers, to confirm that the desired mutations have been introduced, and that no additional mutations have been created.
After sequencing, a BstXI to MscI fragment is excised from MD1BM and subcloned into a vector prepared by digestion of MD1NA with BstXI and MscI. This plasmid is referred to as MD1NA-C. A NotI to ApaI fragment is excised from MD1NA-C and inserted into a vector prepard by digestion of G1MD1 with NotI and ApaI. The resulting plasmid is referred to as pG1MD1A, and contains a cDNA for a human mdr1 gene that has a conservative point mutation inactivating a cryptic splice donor site, as well as another point mutation that causes a reversion in the amino acid sequence at codon 185 to the wild type sequence.
The cryptic splice acceptor site can be corrected using a similar PCR based strategy. A HindIII to XhoI fragment containing the cryptic splice acceptor can be subcloned directly into the HindIII and XhoI sites of pUC007 (This plasmid is designated pMD1HX). The cryptic splice acceptor is contained within an XmnI to KpnI fragment. Recombinant PCR is then used to introduce a point mutation into the cryptic splice acceptor site. One primer set is required. The first primer (5'Xmn) having the following sequence:
5'Xmn:
ATCGCGGATCCGGAATTATTTCTTTTATTACATTTTTCCTTCAAGGTTTCACATTTGG (SEQ ID NO:13)
overlaps the XmnI site and extends past the cryptic splice acceptor. This primer will be identical to the sequence in G1MD1 except at one base in codon 773 wherein codon 773 is changed from CAG to CAA, which inactivates the splice acceptor site. The amino acid encoded by codon 773, however, is unchanged. This primer also incorporates a flanking BamHI site to facilitate subcloning of the PCR product. The second primer (3'Kpn), having the following sequence:
3'Kpn:
CTCAAAGAGTTTCTGTATGGTACC (SEQ ID NO:14)
overlaps the KpnI site. These primers are used to amplify a fragment of DNA from pMD1HX with a proofreading polymerase such as Vent polymerase. This PCR product is digested with BamHI and KpnI and subcloned into the BamHI and KpnI sites of a cloning vector such as pUC19 (This plasmid is designated pMD1XK). This plasmid is used to transform bacteria. Subclones containing the "corrected" sequence are identified by allele specific oligonucleotide hybridization and sequencing as described above. Subsequently, an XmnI to KpnI fragment from pMD1XK is subcloned into the XmnI and KpnI sites of pMD1HX (The resulting plasmid is designated pMD1HX-C). Finally, a HindIII to XhoI fragment from MD1HX-C is subcloned into the HindIII and XhoI sites of pG1MD1 to form pG1MD1B, which contains a cDNA for the mdr1 gene that has a conservative point mutation inactivating a cryptic splice acceptor site.
In order to construct a plasmid that contains a cDNA for an mdr1 gene with mutations introduced into the cryptic splice donor site, codon 185, and the cryptic splice acceptor site, a HindIII to XhoI fragment is excised from pG1MD1B. This fragment is then subcloned into a vector prepared by digesting pG1MD1A with HindIII and XhoI. The resulting plasmid is referred to as pG1MD1AB.
D. Generation of producer cell lines from pG1MD3 and pG1MD1AB
The vectors pG1MD3 and pG1MD1AB, described in Example 1, which contain the changes in codon 1113 (in the splice donor site), in codon 773 (in the splice acceptor site), and in codon 185 (wherein Val 185 is changed to Gly 185), may be placed into a packaging cell line to generate vector particles, and to generate producer cell lines.
Vector producer cell lines are prepared using established protocols. The packaging cell line PE501 (Miller and Rosman, Biotechniques 7:980-990 (1989)) or cell line GP+E86 is plated at a density of 5.times.10.sup.5 cells per 100 mm plate and the following day purified vector DNA is introduced using standard CaPO.sub.4 precipitation (Wigler et al., Cell 14725-731 (1978)). For each plate of cells to be transfected, 20-40 .mu.g of vector DNA is prepared with a co-precipitate consisting of 0.25M CaCl.sub.2 /1 mM Hepes (pH 7.2) and 140 mM NaCl, 0.75 mM Na.sub.2 HPO.sub.4, 25 mM Hepes (pH 7.2). The DNA/precipitate is allowed to sit at room temperature for 30 min and then added (1 ml/plate) to the cells in tissue culture medium (DMEM+10% fetal Bovine serum) for an overnight incubation. The medium is changed to fresh DMEM+serum the following morning. The transfected cells are allowed to grow to near confluence for the next 48 hours, at which point virus supernatant is collected to infect a separate population of PA317 or GP+AM12 vector packaging cell lines at a density of 1.times.10.sup.5 cells per 100 mm plate seeded 24 hours prior to infection. The standard infection conditions include undiluted virus supernatant, filtered through a 0.2 uM membrane, to which 8 ug/ml polybrene is added. After overnight incubation for 16 hours, the medium is changed to DMEM and 10% Fetal Bovine Serum, and grown until such cells are selected with rhodamine 123. The polyclonal population of GP+Am12 or PA 317 cells are incubated with rhodamine 123 at a concentration of 1 microgram per ml at 37.degree. C. for 30 minutes. Following staining, the cells are allowed to efflux the dye for two hours in medium that did not contain rhodamine. The cells are then trypsinized, and 5.times.10.sup.6 cells are sorted on a Coulter EPICS Elite FACS machine, with excitation at 480 nm and fluorescence measured at 525 nm. The bright cells, which did not express p-glycoprotein, are discarded. Cells that are "dull" following rhodamine staining express p-glycoprotein and are collected for further processing.
Example 2
Selection of producer cells generating high titers of viral particles including an mdr1 gene
PA317 (amphotropic) packaging cells were transfected by the CaPO.sub.4 method with pG1MD1. 48 hours later, supernatant from the transfected PA317 cells (Miller, et al., 1989) was filtered and added to GP+E86 (ecotropic) packaging cells in the presence of 6 micrograms per ml of polybrene. 24 hours following infection with this transient supernatant, drug selection with colchicine at a concentration of 60 ng/ml was applied. Afte two weeks of drug selection, individual drug resistant GP+E86 clones were isolated and characterized for production of recombinant retrovirus using an RNA slot blot technique (Bodine, et al., Proc. Nat. Acad. Sci., Vol. 87, pgs. 3738-3742 (May 1990)). The ecotropic MDR producer clone with the highest apparent titer, referred to as E4, was used in the subsequent experiments.
Filtered viral supernatant from the ecotropic E4 producer cell line was used to infect the amphotropic packaging cell line GP+Am12 (Markowitz, et al., Virology, Vol. 167, pgs. 400-406 (1988), Markowitz, et al., J. Virol., Vol. 62, pgs. 1120-1124 (1988)) In this particular experiment, the GP+Am12 line was exposed to a total of 6 viral supernatants over the course of one week. Following infection, GP+Am12 cells that had been transduced with the MDR virus and expressed p-glycoprotein were selected by FACS using rhodamine 123 staining to identify transduced cells. The polyclonal population of GP+Am12 cells was incubated with rhodamine 123 at a concentration of 1 microgram/ml at 37 degrees C. for 30 minutes. Following staining, the cells were allowed to efflux the dye for two hours in medium that did not contain rhodamine. The cells were then trypsinized, and 5.times.10.sup.6 cells were sorted on a Coulter EPICS Elite FACS machine, with excitation at 480 nm and fluorescence measured at 525 nm. The bright cells, that did not express p-glycoprotein, were discarded. Cells that were "dull" following rhodamine staining express p-glycoprotein and were collected for further processing. In this particular experiment, the "dull" population was further subdivided into three groups ("A", "B", and "C") based on the degree of "dullness." These dull cells were plated at limiting dilution. A total of 1500 wells were plated at two concentrations of one cell per two wells and one cell per five wells. Following two weeks in culture, individual subclones were expanded and characterized for estimated viral titer using the RNA slot blot technique on filtered viral supernatant. Ten clones were identified with the highest production of packaged and secreted viral RNA. These clones were subsequently characterized for viral titer using the rhodamine titering protocol. In this protocol, 10 ml of media is conditioned by 5.times.10.sup.6 producer cells for 24 hours. The supernatant is filtered, and dilutions of the filtered supernatant are used to infect a target cell population, in this case 3T3 cells. To infect 3T3 cells a total of 10 ml of media containing viral supernatant and 6 micrograms per ml of polybrene (or 5 micrograms per ml of protamine sulfate) is added to 10.sup.6 target cells on a 10 cm plate for a period of 48 to 72 hours. The plate of infected 3T3 cells is then stained with rhodamine 123 at 1 microgram/ml at 37 degrees for 30 minutes, and then destained for two hours in media without rhodamine. The plate is then trypsinized and analyzed by FACS to quantitate the proportion of cells that express the "dull" phenotype. Alternatively, the plate of cells can be directly examined by fluorescence microscopy. This information is then used to calculate viral titer. For example, if 0.1 ml of viral supernatant is able to confer the "dull" phenotype to 10 percent of 10.sup.6 cells, then 0.1 ml of viral supernatant contains a minimum of 1.times.10.sup.5 viral particles, and 1 ml of viral supernatant contains a minimum of 1.times.10.sup.6 viral particles. As shown in FIG. 8A, as the volume of viral supernatant from producer clone G1MD1 A1.2 which contacts the 3T3 cells increases from 0.025 ml to 0.1 ml, and then to 1.0 ml, the height of the left peak, which corresponds to the number of cells having the "dull" phenotype, and which therefore have a lower fluorescence intensity, increases, while there is a decrease in the number of cells having the "bright" phenotype (such cells have a higher fluorescence intensity) as evidenced by the decrease in the size of the right peak. Using this assay, a identified GP+Am clone with a titer of 4.times.10.sup.6 viral particles per ml was identified. This producer clone was designated G1MD1 A1.2.
Example 3
PA317 cells (Miller, et al., 1989), obtained from the ATCC and selected in HMT medium (following the protocol suggested by the ATCC) were transduced with viral supernatant from the ecotropic E4 producer cell line obtained as hereinabove described in Example 2. The PA317 packaging cell line was serially infected with E4 viral supernatant over the course of 10 days until 100% of the cells in the population expressed the rhodamine "dull" phenotype. The phenotype was evaluated by fluorescence microscopy and FACS analysis on aliquots of the population. A total of 13 exposures to viral supernatants were used. The population of infected PA317 cells were directly plated at limiting dulution. A total of 1,500 wells were plated at dilutions of 1:3 and 1:5 cells per well. Individual clones were isolated and subsequently scored for viral RNA production using the slot blot assay. The subclones with the highest production of viral RNA were then analyzed by the rhodamine titering assay hereinabove described in Example 2. As shown in FIG. 8B, as the volume of viral supernatant from producer clone PA15 which contacts the 3T3 cells increases from 0.025 ml to 0.1 ml and then to 1.0 ml, the height of the left peak, which corresponds to the number of cells having the "dull" phenotype, and which therefore have a lower fluorescence intensity, increases, while there is a decrease in the number of cells having the "bright" phenotype (such cells have a higher fluorescence intensity) as evidenced by the decrease in the size of the right peak. One subclone, PA15, was identified which had a titer of 5.times.10.sup.6 viral particles per ml.
Example 4
Bone marrow cells were harvested from the posterior iliac crests and femurs of 3-4 kg juvenile rhesus monkeys (Proc. Natl. Acad. Sci. USA, Vol. 87, pgs. 3738-3742 (1990)). The cells are aspirated into Dulbecco's Modified Eagle's Medium (DMEM) containing 2% fetal calf serum and 10 units of heparin/ml. Five days before the bone marrow harvest, the animals receive 5-fluorouracil (70 mg/kg) as a single intravenous bolus. During the bone marrow harvest procedure, the animal receives 100 ml of autologous red cells to replace the volume of blood that is removed. Prior to the bone marrow harvest, an in-dwelling central venous catheter is established by standard surgical techniques.
After harvest, the bone marrow was diluted with Hank's Buffered Saline Solution (HBSS) and passed through wire mesh to remove clumps of cells. Mononuclear cells were isolated by density gradient centrifugation using Ficoll-Paque. Cells expressing the CD34 antigen are isolated by immunoselection (Science, Vol. 242, pgs. 919-922 (1988)) using the magnetic bead technology. 2-4.times.10.sup.9 total bone marrow cells are recovered by the harvest procedure. Approximately 20% of these cells are recovered as the mononuclear cell preparation and 2-3% of these cells are recovered by immunoselection. Thus a total of 2-4.times.10.sup.7 CD34 cells are obtained at the time of bone marrow harvest. These were incubated at an initial concentration of 5.times.10.sup.5 cells/ml for 36 hours in DMEM, 15% fetal calf serum, penicillin-streptomycin, and 2.times. glutamine. The following hematopoietic growth factors were added: Stem Cell Factor (100 ng/ml), interleukin-3(50 ng/ml) and interleukin-6 (50 ng/ml). After 36 hours, the cells were recovered by centrifugation and resuspended at 5.times.10.sup.5 cells/ml in fresh medium conditioned by the retroviral producer clone G1MD1 A1.2 prepared as described in Example 2. This medium includes hematopoietic growth factors as specified above plus protamine sulfate at a concentration of 5 ug/ml. Every twelve hours the cells were recovered by centrifugation and resuspended in fresh virus conditioned medium with growth factors and protamine. After 72 hours of incubation in the presence of retroviral vector particles, the cells were recovered by centrifugation, resuspended in DMEM or HBSS containing 2% fetal calf serum and 10 units of heparin per ml, and reinfused into the transplant recipient. During the in vitro culture, the cells expand approximately 10 fold so that 2-4.times.10.sup.6 cells are returned to the animal.
Initially, cells were analyzed after in vitro incubation for evidence of gene transfer and expression. DNA was recovered and subjected to analysis by the polymerase chain reaction methodology using primers (MDR Primer 7, which has the sequence 5'-GCCCACATCATCATGATC-3'p0 (SEQ ID NO:15) and MDR Primer 8, which has the sequence 5'-GTCTCCTACTTTAGTGCT-3' (SEQ ID NO:16)) specific for the human mdr1 coding sequences. Based on comparison to signal intensity obtained with a retorviral producer clone containing a single copy of the retroviral genome, we concluded that 10% of the cells had undergone transduction. The Rhodamine efflux assay hereinabove described was performed confirming that, when compared to a mock infected control sample, 10% of the CD34 selected, transduced cells expressed the mdr1 gene product.
The transplant recipients received daily intravenous fluids, broad spectrum antibiotics, antifungal agents, hyperalimentation solution and blood products as needed to maintain an optimal physiological condition. Daily blood counts and blood chemistries were obtained to monitor recovery. On day 1 following transplantation, granulocyte colony-stimulating factor was given at a dose of 5 ug/kg/day by continuous intravenous infusion. When recovery to a leukocyte count of 1,000-3,000/mm.sup.3 occurs (day 14-22), blood samples are obtained for detection of the mdr1 gene and its expression.
DNA was purified from the total population of blood leukocytes after lysis of the red cells, and isolation of nuclei from leukocytes. This DNA was analyzed by the polymerase chain reaction methodology using the P7 and P8 primers described above. In the first animal transplanted, approximately 1% of the cells contained the retroviral genome whereas in the second animal 8% of the cells contained the transferred sequences.
It is to be understood, however, that the scope of the present invention is not to be limited to the specific embodiments described above. The invention may be practiced other than as particularly described and still be within the scope of the accompanying claims.
__________________________________________________________________________SEQUENCE LISTING(1) GENERAL INFORMATION:(iii) NUMBER OF SEQUENCES: 19(2) INFORMATION FOR SEQ ID NO:1:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 9 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:CAGGTATGC9(2) INFORMATION FOR SEQ ID NO:2:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 16 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:ACATTTTTCCTTCAGG16(2) INFORMATION FOR SEQ ID NO:3:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 50 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:AGTGAACTCTGGTTAACTCCACTCGAGCACAGATCTGGACATCGATACTC50(2) INFORMATION FOR SEQ ID NO:4:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 30 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:4:TCTGTACTGGTCTATACGGATAATAATGTC30(2) INFORMATION FOR SEQ ID NO:5:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 30 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:5:CTAATTACTTCCATAACCACTGTTTTAACC30(2) INFORMATION FOR SEQ ID NO:6:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 30 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:6:GTAAAAAGGAAGTTCCAAAGTGTAAACCGT30(2) INFORMATION FOR SEQ ID NO:7:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:7:GGAAGACATGACCAGATATGCCTATTATTACAG33(2) INFORMATION FOR SEQ ID NO:8:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 33 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:8:CTGTAATAATAGGCATATCTGGTCATGTCTTCC33(2) INFORMATION FOR SEQ ID NO:9:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 35 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:9:CTCTAAGATTAATGAAGGTATTGGTGACAAAATTG35(2) INFORMATION FOR SEQ ID NO:10:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 35 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:10:CAATTTTGTCACCAATACCTTCATTAATCTTAGAG35(2) INFORMATION FOR SEQ ID NO:11:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 31 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:11:ATCGCGGATCCATGGTGGTGGGAACTTTGGC31(2) INFORMATION FOR SEQ ID NO:12:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 40 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:12:CATCCGGAATTCAGCTGACAGTCCAAGAACAGGACTGATG40(2) INFORMATION FOR SEQ ID NO:13:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 58 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:13:ATCGCGGATCCGGAATTATTTCTTTTATTACATTTTTCCTTCAAGGTTTCACATTTGG58(2) INFORMATION FOR SEQ ID NO:14:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 24 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:14:CTCAAAGAGTTTCTGTATGGTACC24(2) INFORMATION FOR SEQ ID NO:15:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 18 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:15:GCCCACATCATCATGATC18(2) INFORMATION FOR SEQ ID NO:16:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 18 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: DNA primer(xi) SEQUENCE DESCRIPTION: SEQ ID NO:16:GTCTCCTACTTTAGTGCT18(2) INFORMATION FOR SEQ ID NO:17:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 51 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: single(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Plasmid DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:17:AATTCGCGGCCGCTACGTAGTCGACGGATCCCTCGAGAAGCTTGGGCCCAT51(2) INFORMATION FOR SEQ ID NO:18:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 4669 bases(B) TYPE: nucleic acid(C) STRANDEDNESS: singular(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: Genomic DNA(xi) SEQUENCE DESCRIPTION: SEQ ID NO:18:CCTACTCTATTCAGATATTCTCCAGATTCCTAAAGATTAGAGATCATTTCTCATTCTCCT60AGGAGTACTCACTTCAGGAAGCAACCAGATAAAAGAGAGGTGCAACGGAAGCCAGAACAT120TCCTCCTGGAAATTCAACCTGTTTCGCAGTTTCTCGAGGAATCAGCATTCAGTCAATCCG180GGCCGGGACCAGTCATCTGTGGTGAGGCTGATTGGCTGGGCAGGAACAGCGCCGGGGCGT240GGGCTGAGCACAGCGCTTCGCTCTCTTTGCCACAGGAAGCCTGAGCTCATTCGAGTAGCG300GCTCTTCCAAGCTCAAAGAAGCAGAGGCCGCTGTTCGTTTCCTTTAGGTCTTTCCACTAA360AGTCGGAGTATCTTCTTCCAAGATTTCACGTCTTGGTGGCCGTTCCAAGGAGCGCGAGGT420CGGGATGGATCTTGAAGGGGACCGCAATGGAGGAGCAAAGAAGAAGAACTTTTTTAAACT480GAACAATAAAAGTGAAAAAGATAAGAAGGAAAAGAAACCAACTGTCAGTGTATTTTCAAT540GTTTCGCTATTCAAATTGGCTTGACAAGTTGTATATGGTGGTGGGAACTTTGGCTGCCAT600CATCCATGGGGCTGGACTTCCTCTCATGATGCTGGTGTTTGGAGAAATGACAGATATCTT660TGCAAATGCAGGAAATTTAGAAGATCTGATGTCAAACATCACTAATAGAAGTGATATCAA720TGATACAGGGTTCTTCATGAATCTGGAGGAAGACATGACCAGGTATGCCTATTATTACAG780TGGAATTGGTGCTGGGGTGCTGGTTGCTGCTTACATTCAGGTTTCATTTTGGTGCCTGGC840AGCTGGAAGACAAATACACAAAATTAGAAAACAGTTTTTTCATGCTATAATGCGACAGGA900GATAGGCTGGTTTGATGTGCACGATGTTGGGCAGCTTAACACCCGACTTACAGATGATGT960CTCTAAGATTAATGAACTTATTGGTGACAAAATTGGAATGTTCTTTCAGTCAATGGCAAC1020ATTTTTCACTGGGTTTATAGTAGGATTTACACGTGGTTGGAAGCTAACCCTTGTGATTTT1080GGCCATCAGTCCTGTTCTTGGACTGTCAGCTGCTGTCTGGGCAAAGATACTATCTTCATT1140TACTGATAAAGAACTCTTAGCGTATGCAAAAGCTGGAGCAGTAGCTGAAGAGGTCTTGGC1200AGCAATTAGAACTGTGATTGCATTTGGAGGACAAAAGAAAGAACTTGAAAGGTACAACAA1260AAATTTAGAAGAAGCTAAAAGAATTGGGATAAAGAAAGCTATTACAGCCAATATTTCTAT1320AGGTGCTGCTTTCCTGCTGATCTATGCATCTTATGCTCTGGCCTTCTGGTATGGGACCAC1380CTTGGTCCTCTCAGGGGAATATTCTATTGGACAAGTACTCACTGTATTCTTTTCTGTATT1440AATTGGGGCTTTTAGTGTTGGACAGGCATCTCCAAGCATTGAAGCATTTGCAAATGCAAG1500AGGAGCAGCTTATGAAATCTTCAAGATAATTGATAATAAGCCAAGTATTGACAGCTATTC1560GAAGAGTGGGCACAAACCAGATAATATTAAGGGAAATTTGGAATTCAGAAATGTTCACTT1620CAGTTACCCATCTCGAAAAGAAGTTAAGATCTTGAAGGGCCTGAACCTGAAGGTGCAGAG1680TGGGCAGACGGTCCCCCTGGTTGGAAACAGTGGCTGTGGGAAGAGCACAACAGTCCAGCT1740GATGCAGAGGCTCTATGACCCCACAGAGGGGATGGTCAGTGTTCATGGACAGGATATTAG1800GACCATAAATGTAAGGTTTCTACGGGAAATCATTGGTGTGGTGAGTCAGGAACCTGTATT1860GTTTGCCACCACGATAGCTGAAAACATTCGCTATGGCCGTGAAAATGTCACCATGGATGA1920GATTGAGAAAGCTGTCAAGGAAGCCAATGCCTATGACTTTATCATGAAACTGCCTCATAA1980ATTTGACACCCTGGTTGGAGAGAGAGGGCCCCAGTTGAGTGGTGGGCAGAAGCAGAGGAT2040CGCCATTGCACGTGCCCTGGTTCGCAACCCCAAGATCCTCCTGCTGGATGAGGCCACGTC2100AGCCTTGGACACAGAAAGCGAAGCAGTGGTTCAGGTGGCTCTGGATAAGGCCAGAAAAGG2160TCGGACCACCATTGTGATAGCTCATCGTTTGTCTACAGTTCGTAATGCTGACGTCATCGC2220TGGTTTCGATGATGGAGTCATTGTGGAGAAAGGAAATCATGATGAACTCATGAAAGAGAA2280AGGCATTTACTTCAAACTTGTCACAATGCAGACAGCAGGAAATGAAGTTGAATTAGAAAA2340TGCAGCTGATGAATCCAAAAGTGAAATTGATGCCTTGGAAATGTCTTCAAATGATTCAAG2400ATCACGTCTAATAAGAAAAAGATCAACTCGTAGGAGTGTCCGTGGATCACAACCCCAAGA2460CAGAAAGCTTAGTACCAAAGAGGCTCTGGATGAAAGTATACCTCCAGTTTCCTTTTGGAG2520GATTATGAAGCTAAATTTAACTGAATGGCCTTATTTTGTTGTTGGTGTATTTTGTGCCAT2580TATAAATGGAGGCCTGCAACCAGCATTTGCAATAATATTTTCAAAGATTATAGGGGTTTT2640TACAAGAATTGATGATCCTGAAACAAAACGACAGAATACTAACTTGTTTTCACTATTGTT2700TCTAGCCCTTGGAATTATTTCTTTTATTACATTTTTCCTTCAGGGTTTCACATTTGGCAA2760AGCTGGAGAGATCCTCACCAAGCGGCTCCGATACATGGTTTTCCGATCCATGCTCAGACA2820GGATGTGAGTTGGTTTGATGACCCTAAAAACACCACTGGAGCATTGACTACCAGGCTCGC2880CAATGATGCTGCTCAAGTTAAAGGGGCTATAGGTTCCAGGCTTGCTGTAATTACCCAGAA2940TATAGCAATTCTTGGGACAGGAATAATTATATCCTTCATCTATGGTTGGCAACTAACACT3000GTTACTCTTAGCAATTGTACCCATCATTGCAATAGCAGGAGTTGTTGAAATGAAAATGTT3060GTCTGGACAAGCACTGAAAGATAAGAAAGAACTAGAAGGTGCTGGGAAGATCGCTACTGA3120AGCAATAGAAAACTTCCGAACCGTTGTTTCTTTGACTCAGGAGCAGAAGTTTGAACATAT3180GTATGCTCAGAGTTTGCAGGTACCATACAGAAACTCTTTGAGGAAAGCACACATCTTTGG3240AATTACATTTTCCTTCACCCAGGCAATGATGTATTTTTCCTATGCTGGATGTTTCCGGTT3300TGGAGCCTACTTGGTGGCACATAAACTAATGAGCTTTGAGGATGTTCTGTTAGTATTTTC3360AGCTGTTGTCTTTGGTGCCATGGCCGTGGGGCAAGTGAGTTCATTTGCTCCTGACTATGC3420CAAAGCCAAAATATCAGCAGCCCACATCATCATGATCATTGAAAAAACCCCTTTGATTGA3480CAGCTACAGCACGGAAGGCCTAATGCCGAACACATTGGAAGGAAATGTCACATTTGGTGA3540AGTTGTATTCAACTATCCCACCCGACCGGACATCCCAGTCCTTCAGGGACTGAGCCTGGA3600GGTGAAGAAGGGCCAGACGCTGGCTCTGGTGGGCAGCAGTGGCTGTGGGAAGAGCACAGT3660GGTCCAGCTCCTGGAGCGGTTCTACGACCCCTTGGCAGGGAAAGTGCTGCTTGATGGCAA3720AGAAATAAAGCGACTGAATGTTCAGTGGCTCCGAGCACACCTGGGCATCGTGTCCCAGGA3780GCCCATCCTGTTTGACTGCAGCATTGCTGAGAACATTGCCTATGGACACAACAGCCGGGT3840GGTGTCACAGGAAGAGATCGTGAGGGCAGCAAAGGAGGCCAACATACATGCCTTCATCGA3900GTCACTGCCTAATAAATATAGCACTAAAGTAGGAGACAAAGGAACTCAGCTCTCTGGTGG3960CCAGAAACAACGCATTGCCATAGCTCGTGCCCTTGTTAGACAGCCTCATATTTTGCTTTT4020GGATGAAGCCACGTCAGCTCTGGATACAGAAAGTGAAAAGGTTGTCCAAGAAGCCCTGGA4080CAAACCCAGAGAAGGCCGCACCTGCATTGTGATTGCTCACCGCCTGTCCACCATCCAGAA4140TGCAGACTTAATAGTGGTGTTTCAGAATGGCAGAGTCAAGCAGCATGGCACGCATCAGCA4200GCTGCTGGCACAGAAAGGCATCTATTTTTCAATGGTCAGTGTCCAGCCTGGAACAAAGCG4260CCAGTGAACTCTGACTGTATGAGATGTTAAATACTTTTTAATATTTGTTTAGATATGACA4320TTTATTCAAAGTTAAAAGCAAACACTTACAGAATTATGAAGAGGTATCTGTTTAACATTT4380CCTCACTCAACTTCAGAGTCTTCAGAGACTTCGTAATTAAAGGAACAGAGTGAGAGACAT4440CATCAAGTGGAGAGAAATCATAGTTTAAACTGCATTATAAATTTTATAACAGAATTAAAG4500TAGATTTTAAAAGATAAAATGTGTAATTTTGTTTATATTTTCCCATTTGGACTGTAACTG4560ACTGCCTTGCTAAAAGATTATAGAAGTAGCAAAAAGTATTGAAATGTTTGCATAAAGTGT4620CTATAATAAAACTAAACTTTCATGTGAAAAAAAAAAAAAAAAAAAAAAA4669(2) INFORMATION FOR SEQ ID NO:19:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 1280 amino acids(B) TYPE: amino acid(C) STRANDEDNESS:(D) TOPOLOGY: linear(ii) MOLECULE TYPE:(A) DESCRIPTION: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:19:MetAspLeuGluGlyAspArgAsnGlyGlyAlaLysLysLysAsn51015PhePheLysLeuAsnAsnLysSerGluLysAspLysLysGluLys202530LysProThrValSerValPheSerMetPheArgTyrSerAsnTrp354045LeuAspLysLeuTyrMetValValGlyThrLeuAlaAlaIleIle505560HisGlyAlaGlyLeuProLeuMetMetLeuValPheGlyGluMet657075ThrAspIlePheAlaAsnAlaGlyAsnLeuGluAspLeuMetSer808590AsnIleThrAsnArgSerAspIleAsnAspThrGlyPhePheMet95100105AsnLeuGluGluAspMetThrArgTyrAlaTyrTyrTyrSerGly110115120IleGlyAlaGlyValLeuValAlaAlaTyrIleGlnValSerPhe125130135TrpCysLeuAlaAlaGlyArgGlnIleHisLysIleArgLysGln140145150PhePheHisAlaIleMetArgGlnGluIleGlyTrpPheAspVal155160165HisAspValGlyGluLeuAsnThrArgLeuThrAspAspValSer170175180LysIleAsnGluValIleGlyAspLysIleGlyMetPhePheGln185190195SerMetAlaThrPhePheThrGlyPheIleValGlyPheThrArg200205210GlyTrpLysLeuThrLeuValIleLeuAlaIleSerProValLeu215220225GlyLeuSerAlaAlaValTrpAlaLysIleLeuSerSerPheThr230235240AspLysGluLeuLeuAlaTyrAlaLysAlaGlyAlaValAlaGlu245250255GluValLeuAlaAlaIleArgThrValIleAlaPheGlyGlyGln260265270LysLysGluLeuGluArgTyrAsnLysAsnLeuGluGluAlaLys275280285ArgIleGlyIleLysLysAlaIleThrAlaAsnIleSerIleGly290295300AlaAlaPheLeuLeuIleTyrAlaSerTyrAlaLeuAlaPheTrp305310315TyrGlyThrThrLeuValLeuSerGlyGluTyrSerIleGlyGln320325330ValLeuThrValPhePheSerValLeuIleGlyAlaPheSerVal335340345GlyGlnAlaSerProSerIleGluAlaPheAlaAsnAlaArgGly350355360AlaAlaTyrGluIlePheLysIleIleAspAsnLysProSerIle365370375AspSerTyrSerLysSerGlyHisLysProAspAsnIleLysGly380385390AsnLeuGluPheArgAsnValHisPheSerTyrProSerArgLys395400405GluValLysIleLeuLysGlyLeuAsnLeuLysValGlnSerGly410415420GlnThrValAlaLeuValGlyAsnSerGlyCysGlyLysSerThr425430435ThrValGlnLeuMetGlnArgLeuTyrAspProThrGluGlyMet440445450ValSerValAspGlyGlnAspIleArgThrIleAsnValArgPhe455460465LeuArgGluIleIleGlyValValSerGlnGluProValLeuPhe470475480AlaThrThrIleAlaGluAsnIleArgTyrGlyArgGlnAsnVal485490495ThrMetAspGluIleGluLysAlaValLysGluAlaAsnAlaTyr500505510AspPheIleMetLysLeuProHisLysPheAspThrLeuValGly515520525GluArgGlyAlaGlnLeuSerGlyGlyGlnLysGlnArgIleAla530535540IleAlaArgAlaLeuValArgAsnProLysIleLeuLeuLeuAsp545550555GluAlaThrSerAlaLeuAspThrGluSerGluAlaValValGln560565570ValAlaLeuAspLysAlaArgLysGlyArgThrThrIleValIle575580585AlaHisArgLeuSerThrValArgAsnAlaAspValIleAlaGly590595600PheAspAspGlyValIleValGluLysGlyAsnHisAspGluLeu605610615MetLysGluLysGlyIleTyrPheLysLeuValThrMetGlnThr620625630AlaGlyAsnGluValGluLeuGluAsnAlaAlaAspGluSerLys635640645SerGluIleAspAlaLeuGluMetSerSerAsnAspSerArgSer650655660SerLeuIleArgLysArgSerThrArgArgSerValArgGlySer665670675GlnAlaGlnAspArgLysLeuSerThrLysGluAlaLeuAspGlu680685690SerIleProProValSerPheTrpArgIleMetLysLeuAsnLeu695700705ThrGluTrpProTyrPheValValGlyValPheCysAlaIleIle710715720AsnGlyGlyLeuGlnProAlaPheAlaIleIlePheSerLysIle725730735IleGlyValPheThrArgIleAspAspProGluThrLysArgGln740745750AsnSerAsnLeuPheSerLeuLeuPheLeuAlaLeuGlyIleIle755760765SerPheIleThrPhePheLeuGlnGlyPheThrPheGlyLysAla770775780GlyGluIleLeuThrLysArgLeuArgTyrMetValPheArgSer785790795MetLeuArgGlnAspValSerTrpPheAspAspProLysAsnThr800805810ThrGlyAlaLeuThrThrArgLeuAlaAsnAspAlaAlaGlnVal815820825LysGlyAlaIleGlySerArgLeuAlaValIleThrGlnAsnIle830835840AlaAsnLeuGlyThrGlyIleIleIleSerPheIleTyrGlyTrp845850855GlnLeuThrLeuLeuLeuLeuAlaIleValProIleIleAlaIle860865870AlaGlyValValGluMetLysMetLeuSerGlyGlnAlaLeuLys875880885AspLysLysGluLeuGluGlyAlaGlyLysIleAlaThrGluAla890895900IleGluAsnPheArgThrValValSerLeuThrGlnGluGlnLys905910915PheGluHisMetTyrAlaGlnSerLeuGlnValProTyrArgAsn920925930SerLeuArgLysAlaHisIlePheGlyIleThrPheSerPheThr935940945GlnAlaMetMetTyrPheSerTyrAlaGlyCysPheArgPheGly950955960AlaTyrLeuValAlaHisLysLeuMetSerPheGluAspValLeu965970975LeuValPheSerAlaValValPheGlyAlaMetAlaValGlyGln980985990ValSerSerPheAlaProAspTyrAlaLysAlaLysIleSerAla99510001005AlaHisIleIleMetIleIleGluLysThrProLeuIleAspSer101010151020TyrSerThrGluGlyLeuMetProAsnThrLeuGluGlyAsnVal102510301035ThrPheGlyGluValValPheAsnTyrProThrArgProAspIle104010451050ProValLeuGlnGlyLeuSerLeuGluValLysLysGlyGlnThr105510601065LeuAlaLeuValGlySerSerGlyCysGlyLysSerThrValVal107010751080GlnLeuLeuGluArgPheTyrAspProLeuAlaGlyLysValLeu108510901095LeuAspGlyLysGluIleLysArgLeuAsnValGlnTrpLeuArg110011051110AlaHisLeuGlyIleValSerGlnGluProIleLeuPheAspCys111511201125SerIleAlaGluAsnIleAlaTyrGlyAspAsnSerArgValVal113011351140SerGlnGluGluIleValArgAlaAlaLysGluAlaAsnIleHis114511501155AlaPheIleGluSerLeuProAsnLysTyrSerThrLysValGly116011651170AspLysGlyThrGlnLeuSerGlyGlyGlnLysGlnArgIleAla117511801185IleAlaArgAlaLeuValArgGlnProHisIleLeuLeuLeuAsp119011951200GluAlaThrSerAlaLeuAspThrGluSerGluLysValValGln120512101215GluAlaLeuAspLysAlaArgGluGlyArgThrCysIleValIle122012251230AlaHisArgLeuSerThrIleGlnAsnAlaAspLeuIleValVal123512401245PheGlnAsnGlyArgValLysGluHisGlyThrHisGlnGlnLeu125012551260LeuAlaGlnLysGlyIleTyrPheSerMetValSerValGlnAla126512701275GlyThrLysArgGln1280__________________________________________________________________________

Number	Name	Date
4912039	Riordan	Mar 1990
5166059	Pastan et al.	Nov 1992
5175099	Wills	Dec 1992
5192553	Boyse et al.	Mar 1993
5198344	Croop et al.	Mar 1993
5206352	Roninson et al.	Apr 1993

	Number	Date	Country
Parent	332444	Oct 1994
Parent	887712	May 1992

Expression of human multidrug resistance genes and improved selection of cells transduced with such genes

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Parent Case Info

US Referenced Citations (6)

Foreign Referenced Citations (1)

Non-Patent Literature Citations (11)

Continuations (2)

Entry
Safa, et al., Proc. Nat. Acad. Sci., vol. 87, pp. 7225-7229 (1990).
Weinstein, et al. "Multidrug Resistance Gene Product (P-Glycoprotein) in Normal Tissue and Tumors," Advances in Pathology and Laboratory Medicine, Mosby Yearbook, Inc. (1991).
Schinkel, et al., Cancer Research, vol. 51, pp. 2628-2635 (May 15, 1991).
Devine, et al., Proc. Nat. Acad. Sci., vol. 89, pp. 4565-4568 (May 1992).
Pastan, et al., FASEB J., vol. 5, pp. 2523-2528 (1991).
Chaudhary, et al., Cell, vol. 68, pp. 85-94 (Jul. 12, 1991).
Devine et al. Mar. 5, 1991. J. Biol. Chem. 266(7):4545-4555.
Chaudhary et al. 1991. Cell 66:85-94.
Pastan et al. 1991. The FASEB J. 5:2523-2528.
Aebi et al. 1986. Cell 47:555-565.
Ohshima et al. 1987. J. Mol. Biol. 195:247-259.