CAPON: a protein associated with neuronal nitric oxide synthase

TECHNICAL AREA OF THE INVENTION
The invention relates to the area of neurotransmitter regulation. More particularly, the invention relates to the regulation of neuronal nitric oxide synthase.
BACKGROUND OF THE INVENTION
Studies of neuronally-derived nitric oxide (NO) have revealed many roles for this gaseous messenger molecule (Moncada, 1994; Yun et al., 1996). In the peripheral nervous system, NO mediates nonadrenergic, noncholinergic neurotransmission, serving as an effector of autonomic neurons on smooth muscle. NO has been implicated in several forms of neuronal plasticity, such as LTP (for a review see Huang, 1997). Studies in mice with a targeted genomic deletion of the NO biosynthetic enzyme, neuronal NO synthase (nNOS), have shown that NO mediates a substantial portion of the neurotoxicity associated with stroke (Huang et al., 1994). In the brain, NO and citrulline are produced from arginine predominantly by a neuronal isoform of NOS (nNOS) (Huang et al., 1993), although endothelial NOS (eNOS) may also occur in neurons (Dinerman et al., 1994; O'Dell et al., 1994). Most neurotransmitters are stored in synaptic vesicles and neurotransmitter effects are elicited following the exocytosis of transmitter into the synaptic space. For an evanescent transmitter such as NO there is no storage pool and newly synthesized NO is used as it is made. NO synthesis is triggered by the influx of calcium, which, when complexed with calmodulin, activates the biosynthetic activity of NOS (Bredt and Snyder, 1990).
Because NO lacks vesicular storage and depends on new synthesis for its release, nNOS must be associated with the plasma membrane. Subcellular fractionation indicates that roughly half of brain nNOS is soluble and half particulate (Bredt, 1996; Hecker et al., 1994). Recently, Bredt and associates showed that nNOS is targeted to membranes by binding to syntrophin, PSD95/SAP90, or PSD93 (Brenman et al., 1996; Brenman et al., 1996). These proteins are enriched in synaptic densities and interact with nNOS through PDZ domains, consensus sequences of about 100 amino acids that are found in proteins which tend to be associated with cell-cell junctions (Ponting and Phillips, 1995). The nNOS/PSD95 interaction involves a portion of nNOS which includes its sole PDZ domain and the second PDZ domain of PSD95. PSD95 was first isolated from postsynaptic densities (Cho et al., 1992) but also occurs in presynaptic nerve terminals (Kistner et al., 1993) and clusters neurotransmitter receptors and ion channels at synaptic sites (Kornau et al., 1997). For instance, the NMDA receptor and several potassium channels are associated with PSD95 at synapses (Kornau et al., 1995). The linking of NMDA receptors to nNOS by PSD95 may explain why calcium influx following NMDA receptor activation leads to a tightly coupled nNOS activation (Brenman et al., 1996). Indeed, the effects of NO appear to be intimately tied to the NMDA receptor. For example, NMDA receptor-mediated neurotoxicity (Dawson and Dawson, 1996), neurotransmitter release (Schuman and Madison, 1994), and cGMP elevations (Bredt and Snyder, 1989; Garthwaite et al., 1989) each require nNOS and are blocked by nNOS-specific inhibitors. Moreover, NO can directly modulate NMDA receptors (Lipton and Stamler, 1994).
There is a continuing need in the art of neurotransmitter regulation for methods of affecting the activity of neuronal NOS, so that one can manipulate NO levels when required for therapeutic effect in such disorders.
SUMMARY OF THE INVENTION
It is an object of the invention to provide an isolated mammalian Capon (Carboxy-terminal PDZ ligand of nNOS) protein.
It is another object of the invention to provide a fusion protein comprising at least eight contiguous amino acids selected from the Capon amino acid sequence shown in SEQ ID NO:2.
It is yet another object of the invention to provide an isolated polypeptide consisting of at least eight contiguous amino acids of Capon as shown in SEQ ID NO:2 and capable of binding an nNOS PDZ domain.
It is still another object of the invention to provide a preparation of antibodies which specifically bind to a Capon protein as shown in SEQ ID NO:2 or 4.
It is even another object of the invention to provide a subgenomic polynucleotide which encodes a Capon protein as shown in SEQ ID NO:2 or 4.
It is yet another object of the invention to provide a recombinant DNA construct for expressing Capon antisense nucleic acids.
It is still another object of the invention to provide a method of inhibiting a mammalian neuronal nitric oxide synthase (nNOS).
It is even another object of the invention to provide methods of screening test compounds for the ability to decrease or augment the activity of nNOS.
These and other objects of the invention are provided by one or more of the embodiments described below. One embodiment of the invention provides an isolated mammalian Capon protein which has the sequence shown in SEQ ID NO:2 or 4, and naturally occurring biologically active variants thereof.
Another embodiment of the invention provides a mammalian Capon fusion protein which comprises two protein segments fused to each other by means of a peptide bond, wherein one of the protein segments consists of at least eight contiguous amino acids selected from the amino acid sequence shown in SEQ ID NO:2 or 4.
Yet another embodiment of the invention provides an isolated polypeptide which consists of at least eight contiguous amino acids of Capon as shown in SEQ ID NO:2 or 4, wherein the polypeptide binds to an nNOS PDZ domain.
Still another embodiment of the invention provides a preparation of antibodies which specifically bind to a mammalian Capon protein as shown in SEQ ID NO:2 or 4.
Even another embodiment of the invention provides a subgenomic polynucleotide which encodes a Capon protein as shown in SEQ ID NO:2 or 4.
Yet another embodiment of the invention provides a recombinant DNA construct for expressing Capon antisense nucleic acids, comprising a promoter and a coding sequence for Capon consisting of at least 12 contiguous base pairs selected from SEQ ID NO:1 or 3, wherein the coding sequence is in an inverted orientation with respect to the promoter, such that upon transcription from the promoter an RNA is produced that is complementary to native mRNA encoding Capon.
Still another embodiment of the invention provides a method of decreasing a mammalian nNOS activity, comprising the step of contacting a nNOS with a Capon protein having an amino acid sequence as shown in SEQ ID NO:2 or 4.
Even another embodiment of the invention provides a method of screening test compounds for the ability to decrease or augment nNOS activity. The method comprises the steps of: (a) contacting a test compound with a mixture of a mammalian Capon protein and a polypeptide comprising an nNOS PDZ domain; and (b) measuring the amount of Capon or the polypeptide that is bound or unbound in the presence of the test compound, a test compound that decreases the amount of bound Capon or the polypeptide being a potential drug for increasing nNOS activity, and a test compound that increases the amount of the polypeptide or Capon that are bound being a potential drug for decreasing nNOS activity.
Yet another embodiment of the invention provides a method of screening test compounds for the ability to decrease or augment nNOS activity comprising the steps of: (a) contacting a cell with a test compound, wherein the cell comprises: i) a first fusion protein comprising (1) a DNA binding domain or a transcriptional activation domain, and (2) all or a portion of a mammalian Capon protein, wherein the portion consists of a contiguous sequence of amino acids selected from the amino acid sequence shown in SEQ ID NO:2 or 4, wherein the portion is capable of binding to nNOS; ii) a second fusion protein comprising (1) a transcriptional activation domain or a DNA binding domain and (2) all or a portion of nNOS, wherein the portion comprises a PDZ domain, or a naturally occurring biologically active variant thereof, wherein the interaction of the portion of the Capon protein with the portion of nNOS reconstitutes a sequence-specific transcriptional activating factor, wherein when the first fusion protein comprises a DNA binding domain the second fusion protein comprises a transcriptional activation domain and when the first fusion protein comprises a transcriptional activation domain the second fusion protein comprises a DNA binding domain; and iii) a reporter gene comprising a DNA sequence to which the DNA binding domain of the first fusion protein specifically binds; and (b) measuring the expression of the reporter gene, a test compound that increases the expression of the reporter gene being a potential drug for decreasing nNOS activity, and a test compound that decreases the expression of the reporter gene being a potential drug for augmenting nNOS activity.
Even another embodiment of the invention provides a method of screening test compounds for the ability to decrease or augment nNOS activity comprising the steps of: (a) contacting a cell with a test compound, wherein the cell comprises: (i) a first expression vector comprising a subgenomic polynucleotide encoding at least the PDZ domain of nNOS or a naturally occurring biologically active variant thereof; (ii) a second expression vector comprising a subgenomic polynucleotide encoding at least the portion of Capon or a naturally occurring biologically active variant thereof, wherein the portion of Capon is capable of binding to nNOS; and (b) measuring the amount of cGMP, NO, or citrulline in the cell, a test compound that increases the amount of cGMP, NO, or citrulline being a potential drug for augmenting nNOS activity, and a test compound that decreases the amount of cGMP being a potential drug for decreasing nNOS activity.
According to still another embodiment a method is provided for diagnosing a neurological disease or a propensity for a neurological disease, comprising: determining number of glutamine repeats present in a Capon protein of a patient wherein a number greater than 6 indicates a neurologic disease or a propensity therefor.
According to still another embodiment a method is provided for diagnosing a nuerological disease or a propensity for a neurological disease, comprising: determining number of CAG repeats in a Capon gene of a patient, wherein a number greater than 6 indicates a neurologic disease or a propensity therefor.
Another aspect of the invention is a cell comprising one or more recombinant nucleic acid molecules. The cell comprises: (i) a first expression vector comprising a subgenomic polynucleotide encoding at least the PDZ domain of nNOS or a naturally occurring biologically active variant thereof; and (ii) a second expression vector comprising a subgenomic polynucleotide encoding at least a portion of Capon or a naturally occurring biologically active variant thereof, wherein the portion of Capon is capable of binding to nNOS.
Another aspect of the invention is a cell comprising one or more recombinant nucleic acid molecules. The cell comprises: i) a nucleotide construct encoding a first fusion protein comprising (1) a DNA binding domain or a transcriptional activation domain, and (2) all or a portion of a mammalian Capon protein, wherein the portion consists of a contiguous sequence of amino acids selected from the amino acid sequence shown in SEQ ID NO:2 or 4, wherein the portion is capable of binding to nNOS; ii) a nucleotide construct encoding a second fusion protein comprising (1) a transcriptional activation domain or a DNA binding domain and (2) all or a portion of nNOS, wherein the portion comprises a PDZ domain, or a naturally occurring biologically active variant thereof, wherein the interaction of the portion of the Capon protein with the portion of nNOS reconstitutes a sequence-specific transcriptional activating factor, wherein when the first fusion protein comprises a DNA binding domain the second fusion protein comprises a transcriptional activation domain, and when the first fusion protein comprises a transcriptional activation domain the second fusion protein comprises a DNA binding domain; and iii) a reporter gene comprising a DNA sequence to which the DNA binding domain of the first fusion protein specifically binds, wherein upon reconstitution of the sequence specific transactivating factor, expression of the reporter gene is increased.
The present invention thus provides the art with the information that Capon, a heretofore unknown protein, regulates the activity of neuronal nitric oxide synthase. Capon can be used, inter alia, in assays to screen for substances which have the ability to decrease or augment neuronal nitric oxide synthase activity.

BRIEF DESCRIPTION OF THE DRAWINGS
The file of this patent contains at least one drawing executed in color. Copies of this patent with color drawings will be provided by the Patent and Trademark Office upon request and payment of the necessary fee.
FIGS. 1A-1C. Cloning of the CAPON cDNA and distribution of CAPON mRNA. (FIG. 1A) CAPON specifically interacts with nNOS in the yeast two-hybrid system. Yeast were transformed with the indicated Gal4 activation domain (AD) and Gal4 DNA-binding domain (BD) plasmids and grown on plates containing histidine. A typical filter lift is shown in which b-galactosidase activity was detected by the appearance of a blue precipitate. pAD-CAPON1, comprising the last 125 amino acids of CAPON, activates lacZ transcription in the presence of pBD-nNOS (2-377) but not with plasmids the first three PDZ domains of PSD95 (amino acids 20-364) or the second PDZ domain of PSD93 (amino acids 116-421).
(FIG. 1B) Amino acid sequence of rat CAPON and alignment with a partial human sequence. The underlined sequence corresponds to the putative PTB domain. The bracketed sequence is encoded by a CAG repeat. A human expressed sequence tag (EST) (accession number R19867 SEQ ID NO:3) obtained from a library derived from infant brain contains a 459 bp open reading frame with homology to the C-terminus of the CAPON cDNA (p=5.1.times.10.sup.-17). The conceptual translation of this clone reveals a protein with 92% amino acid identity with the rat protein.
(FIG. 1C) CAPON is enriched in neuronal structures. Northern (RNA) blot analysis reveals that several CAPON transcripts are present, and these transcripts are enriched in neuronal tissues.
FIGS. 2A-2E. Interaction of CAPON and nNOS.
(FIG. 2A) CAPON binds to nNOS, but not eNOS or iNOS. Bacterially expressed GST, GST-PIN, and GST-CAPON were bound to glutathione agarose and then incubated with lysates of HEK293 cells transfected with expression plasmids for the indicated isoforms of NOS. After extensive washing of the resins, bound NOS was detected with isoform specific antibodies. While nNOS binds to both GST-PIN and GST-CAPON, neither eNOS or iNOS bind to either protein. Input=10% of starting material applied to each resin.
(FIG. 2B) A GST-NOS fusion protein specifically binds to rat brain CAPON. A fusion protein consisting of GST and amino acids 1-100 of nNOS was bound to glutathione agarose and then incubated with cerebellar supernatants. After extensive washing, CAPON is detected on the NOS resin but not on the control GST resin. A second .about.48 kD band is also detected with this antibody, but fails to interact with nNOS. This band may represent a cross-reactive protein, an alternatively spliced isoform of CAPON, or a degradation product.
(FIG. 2C) CAPON interacts with nNOS directly. HEK293 lysates transfected with a expression plasmid containing the nNOS cDNA or empty vector were resolved by electrophoresis, transferred to nitrocellulose, and probed with radiolabeled CAPON (see Methods). Purified nNOS is recognized with this probe, along with a comigrating band detected in NOS-transfected but not mock-transfected cells.
(FIG. 2D) CAPON and nNOS complexes are detectable in cerebellar lysates (I). Cerebellar supernatants were prepared from wild-type (+/+) and nNOS knockout (-/-) mice and incubated with the 2', 5', ADP-sepharose, an nNOS-affinity resin. Only CAPON derived from supernatants of wild-type and not knockout animals was capable of binding the resin indicating that the presence of nNOS is required for CAPON to bind to the resin. CAPON levels were decreased in knockout animals, presumably due to decreased stability in the absence of the nNOS binding partner. A lower molecular weight band (arrowhead), frequently detected with the anti-CAPON antibody, bound weakly to the resin in an nNOS-specific manner as well. Input=20% of lysate used for binding.
(FIG. 2E) CAPON and nNOS complexes are detectable in cerebellar lysates (II). An antibody to CAPON (5 mg) specifically coprecipitates nNOS, while comprable amounts of antibody to the G-protein subunit bl, cyclin-dependent kinase 2, and preimmune serum fail to coprecipitate nNOS. Enrichment of nNOS in CAPON immunoprecipitates was specific as a control protein, protein kinase C- b I/II did not display similar enrichment. Input=10% of lysate used for immunoprecipitation.
FIGS. 3A and 3B. Immunohistochemical localization of nNOS and CAPON.
(FIG. 3A) Comparison of nNOS-IR (immunoreactivity), CAPON-IR, and CAPON in situ hybridization patterns in sagittal sections of adult rat. Islands of Calleja (solid arrowhead); supraoptic nucleus (open arrowhead); AOB, accessory olfactory bulb; C, colliculi; Cb, cerebellum; Cx, cerebral cortex; OB, olfactory bulb. Immunohistochemical nonspecific labelling ("Block") was determined using a CAPON antibody pre-absorbed with the antigenic peptide. Nonspecific hybridization ("Sense") was detected using a sense probe.
(FIG. 3B) Comparison of cellular localization of nNOS-IR and CAPON-IR in adult rat brain. CAPON-IR (a) and nNOS-IR (b) hypothalamic neurons, solid arrowheads indicate IR dendritic processes. CAPON-IR (c) and nNOS-IR (d) of the supraoptic nucleus. CAPON-IR (e) and nNOS-IR (f) cell bodies of the nucleus of the trapezoid body separated by unreactive fascicles of nerve fibers. Adjacent is the pontine nucleus (Pn) which exhibits both CAPON and nNOS-IR (e,f). CAPON-IR (g) and nNOS-IR (h) in the cerebellum. Molecular cell layer (Mol); granular cell layer (Gr). Micrographs e,f, (100.times.); c, d, g, h, (200.times.); a, b (400.times.).
FIGS. 4A-4C. The PDZ domain of nNOS interacts with the C-terminus of CAPON.
(FIG. 4A) The PDZ domain of nNOS (amino acids 20-100) is sufficient for binding to CAPON. Truncations of nNOS were subcloned into the Gal4 BD vector and nNOS/CAPON interactions were detected by b-galactosidase assays.
(FIG. 4B) The C-terminal 13 amino acids of CAPON are sufficient for binding to nNOS. Various GST-CAPON fusion proteins were incubated with HEK293 lysates containing nNOS. A CAPON fusion protein comprising the last 100 amino acids binds nNOS, as do fusion proteins comprising the last 13 or 20 amino acids of CAPON. A CAPON fusion protein with the last 20 amino acids deleted no longer binds nNOS. Neither of the control proteins, GST or GST-14-3-3, are able to bind nNOS.
(FIG. 4C) Amino acid substitutions in the C-terminus of CAPON prevent it from interacting with nNOS. His.sub.6 -fusion proteins of the last 100 amino acids of CAPON were generated and incubated with GST-NOS (1-100) immobilized on glutathione agarose. While the unmutagenized sequence binds (last four amino acids EIAV), mutation of the terminal valine (EIAA) or the penultimate alanine (EIDV) prevents binding. Serine or alanine mutations are tolerated at the n-2 position (ESAV and EAAV), but truncation of the C-terminal 13 amino acids blocks binding altogether.
FIGS. 5A and 5B. CAPON and PSD95 compete for binding to nNOS.
(FIG. 5A) His.sub.6 -CAPON fusion proteins specifically block the nNOS/PSD95 interaction in vitro. The C-terminal 100 amino acids were fused to a His6 tag and added to HEK293 lysates transfected with nNOS expression plasmids at the indicated fusion protein concentration. This mixture was added to GST-PSD95 (amino acids 20-364) or GST-PSD93 (116-421), the regions of these proteins previously shown to interact with nNOS (Brenrman et al., 1996). The disruption of the nNOS/PSD95 interaction required the C-terminal 13 amino acids, as this fusion protein (DC20) fails to block the interaction even at 5 mM. Other control proteins such as His.sub.6 -PIN or His.sub.6 -FKBP do not disrupt the nNOS-PSD95 interaction.
(FIG. 5B) Quantification of CAPON inhibition of the nNOS/PSD95 interaction. HEK293 cells were transfected with nNOS expression plasmids and then metabolically labeled with [.sup.35 S] methionine. Radiolabeled nNOS was purified and mixed with His.sub.6 -CAPON as in (A), above. Bound nNOS was resolved by electrophoresis and counts were determined on a Phospholmager.
FIG. 6. CAPON expression prevents the interaction of PSD95 and nNOS. HEK293 cells were transfected with various combinations of expression plasmids for HA-tagged nNOS (HA-NOS), myc-tagged PSD95, or CAPON. Following transfection, the lysates were immunoprecipitated with an anti-HA antibody and bound proteins were detected with the appropriate antibodies. Following cotransfection of HA-NOS and myc-PSD95, myc-PSD95 is detected in anti-HA immunoprecipitates. Cotransfection of a full-length CAPON expression plasmid substantially reduces the amount of myc-PSD95 in anti-HA precipitates. In the absence of HA-nNOS transfection, neither myc-PSD95 or CAPON is immunoprecipitated by anti-HA antibodies.
FIG. 7. Model of PSD95/nNOS regulation by CAPON.
NMDA receptors are coupled to nNOS through a PSD95 multimer. These interactions are mediated by PDZ domains. In this complex, nNOS is situated close to NMDA receptor-modulated calcium influx (left). Binding of CAPON (right) results in a reduction of NMDA receptor/PSD95/nNOS complexes, leading to decreased access to NMDA receptor-gated calcium influx and a catalytically inactive enzyme.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
We conducted a yeast two-hybrid screen in which we have identified a novel protein which we designate CAPON (Carboxyl-terminal PDZ ligand of nNOS). CAPON is a cytoplasmic protein whose carboxyl terminus binds to the PDZ domain of nNOS. CAPON competes with PSD95 and PSD93 for binding to nNOS and thus may participate in the translocation and impede the activation of this enzyme.
It is a discovery of the present invention that the mammalian protein Capon (Carboxy-terminal PDZ ligand of nNOS) physically interacts with and inhibits the activity of neuronal nitric oxide synthase (nNOS). Although it was known that nNOS regulates the release of its product, the messenger molecule nitric oxide, all of the proteins involved in its cellular localization were previously unknown.
Mammalian Capon protein has the sequence disclosed in SEQ ID NO:2 or 4, or other sequences which are at least about 80, 85, 87, 89, or 90% identical. Any biologically active variants of this sequence that may occur in mammalian tissues are within the scope of this invention. Biologically active variants bind to and inhibit nNOS binding to PSD95 and PSD93. Mammalian Capon proteins may comprise amino acids 1-503 as shown in SEQ ID NO:2 or 1-156 as shown in SEQ ID NO: 4. Fragments of a mammalian Capon protein, comprising at least eight, nine, ten, twelve, thirteen, or sixteen consecutive amino acids selected from the sequence shown in SEQ ID NO:2 or 4, may also be used. Such fragments may be useful, for example, in various assays, as immunogens, or in therapeutic compositions. They may also be used as preparative reagents for purifying nNOS. A fusion protein may also be used for many of these purposes, including as a reagent and as an immunogen.
A fusion protein consists of a full length mammalian Capon protein or a Capon protein fragment fused to a second protein or protein fragment by means of a peptide bond. The second protein or protein fragment may be, for example, a ligand for yet a third molecule. The second protein or protein fragment may be labeled with a detectable marker or may be an enzyme that will generate a detectable product. A fusion protein may be useful, for example, to target full-length Capon protein or a Capon fragment comprising one or more specific domains, to a specific location in a cell or tissue.
Any of these Capon-related proteins may be produced by expressing Capon cDNA sequences in prokaryotic or eukaryotic host cells, using known expression vectors. Synthetic chemistry methods can also be used to synthesize Capon protein, fusion protein, or fragments. Alternatively, Capon protein can be extracted, using standard biochemical methods, from Capon-producing mammalian cells, such as brain cells. The source of the cells may be any mammalian tissue that produces Capon protein including human, rat, or mouse. Methods of protein purification, such as size exclusion chromatography, ammonium sulfate fractionation, ion exchange chromatography, affinity chromatography, or preparative gel electrophoresis, are well known in the art. Given the sequences disclosed in SEQ ID NO:2 and 4, an ordinary artisan can readily select appropriate methods to obtain a preparation of mammalian Capon protein that is substantially free from other mammalian proteins. An isolated Capon protein is purified from other compounds that may normally associate with Capon protein in a cell, such as certain proteins, carbohydrates, lipids, or subcellular organelles.
The present invention also provides a preparation of antibodies that specifically bind to mammalian Capon protein. The antibodies may be polyclonal or monoclonal and may be raised against biochemically isolated, chemically synthesized, or recombinantly produced full-length Capon protein, Capon protein fragments, or Capon fusion proteins. Techniques for raising antibodies directed against intracellular proteins such as mammalian Capon are well known in the art. The antibodies bind specifically to Capon epitopes, preferably epitopes not present on other mammalian proteins. Antibodies that bind specifically to Capon proteins include those that bind to full-length Capon protein, Capon fragments or degradation products, as weak as to alternatively spliced forms of Capon proteins, or to Capon fusion proteins. In preferred embodiments of the invention the antibodies prevent Capon binding to nNOS, immunoprecipitate Capon protein from solution, and react with Capon protein on Western blots of polyacrylamide gels. Preferably the antibodies do not exhibit nonspecific cross-reactivity with other mammalian proteins on Western blots or in immunocytochemical assays. Techniques for purifying Capon antibodies are those which are available in the art. In a more preferred embodiment, antibodies are affinity purified by passing antiserum over a support column to which Capon protein is bound and then eluting the bound antibody, for example with high salt concentrations. Any such techniques may be chosen to achieve the preparation of the invention.
The polynucleotides of the present invention encode Capon protein. These polynucleotides may be isolated and purified free from other nucleotide sequences by standard purification techniques, using restriction enzymes to isolate fragments comprising the Capon encoding sequences. The polynucleotide molecules are preferably intron-free and have the sequence shown in SEQ ID NO:1 or 3. Such Capon cDNA molecules can be made inter alia by using reverse transcriptase with Capon mRNA as a template. The polynucleotide molecules of the invention can also be made using the techniques of synthetic chemistry given the sequence disclosed herein. The degeneracy of the genetic code permits alternate nucleotide sequences to be synthesized that will encode the Capon amino acid sequence shown in SEQ ID NO:2 or 4. All such nucleotide sequences are within the scope of the present invention, as well as those which are at least 70, 75, 80, 85, or 90% identical. The Capon polynucleotide molecules can be propagated in vectors and cell lines as is known in the art. The constructs may be on linear or circular molecules. They may be on autonomously replicating molecules or on molecules without replication sequences. Recombinant host cells can be formed by introducing the genetic constructs of the present invention into cells. Any of those techniques which are available in the art can be used to introduce genetic constructs into the cells. These include, but are not limited to, transfection with naked or encapsulated nucleic acids, cellular fusion, protoplast fusion, viral infection, and electroporation. Introduction of genetic constructs may be carried out in vitro or in vivo.
The invention also provides a recombinant DNA construct for expressing Capon antisense nucleic acids. The construct contains a promoter and a coding sequence for Capon consisting of at least 12 and preferably at least 15 or 20 contiguous base pairs selected from SEQ ID NO:1 or 3. The Capon coding sequence is in an inverted orientation with respect to the promoter, so that when the sequence is transcribed from the promoter, an RNA complementary to native Capon-encoding mRNA is produced. The construct may also include a terminator at the 3' end of the inverted Capon coding sequence. The antisense molecules produced using the DNA construct of the invention may be used to decrease or prevent the transcription of Capon mRNA. The antisense molecules may be used in vitro or in vivo, as pharmacological agents for the purpose of influencing nNOS activity.
According to the present invention, nNOS is inhibited by mammalian Capon protein, which competes with PSD95 and PSD93 for binding to nNOS, thereby inhibiting nNOS activity. Suitable inhibitory concentrations range from 1 nM to 1 mM. In a preferred embodiment the concentration of Capon protein is at least 250 nM. In a more preferred embodiment the concentration of Capon protein is at least 1 .mu.M. Greater concentrations of Capon protein may also be used. nNOS activity may be measured, for example, by assaying nitric oxide-dependent cGMP formation in HEK 293 cells cotransfected with DNA encoding Capon and nNOS. Other cell lines, such as mouse N1E-115 neuroblastoma cells, may be used as well. Formation of cGMP may be measured, for example, by radioimmunoassay or by spectrophotometry. nNOS activity may be measured in intact cells or in cell lysates. Other assays for measuring nNOS activity may also be used. NO or citrulline can also be measured.
The present invention also provides methods of screening test compounds for the ability to decrease or augment nNOS activity. The test compounds may be pharmacologic agents already known in the art or may be compounds previously unknown to have any pharmacological activity. The compounds may be naturally occurring or designed in the laboratory. They may be isolated from microorganisms, animals, or plants, and may be produced recombinantly, or synthesized by chemical methods known in the art. A test compound can be contacted with a mixture of mammalian Capon protein (or the NOS-binding portion thereof) and a polypeptide containing an nNOS PDZ domain which is a contiguous sequence selected from the N-terminal about 100 amino acids of nNOS amino acid sequences as shown in SEQ ID NO:5 and 6. Analogous domains in other mammalian nNOS proteins can also be used. These are referred to as biologically active, naturally occurring variants of the rat or human protein. These molecules may be produced recombinantly or may be synthesized using standard chemical methods. The nNOS or Capon binding partner may consist of less than the entire nNOS. The two binding partners may be prebound prior to the step of contacting with the test compound. Alternatively, the test compound may contact one of the binding partners before the second binding partner is added. The PDZ domain-containing molecule may be in solution or may be bound to a solid support. These molecules may be unlabeled or labeled, for example, with a radioactive, fluorescent, or other detectable marker. They may be fusion proteins comprising a nNOS PDZ domain and another protein with or without a detectable enzymatic activity. The amount of at least one of the two binding partners that is bound or unbound in the presence of the test compound is then measured. A number of methods may be used to measure the amount of bound molecules. For example, the relative concentration of bound to unbound may be detected by examining the apparent molecular masses of the molecules by size exclusion chromatography or by polyacrylamide gel electrophoresis under non-reducing conditions. Other methods of measuring binding or dissociation of the molecules will readily occur to those of ordinary skill in the art and can be used. A test compound that decreases the amount of the polypeptide and Capon that are bound is a potential drug for increasing nNOS activity. A test compound that increases the amount of the polypeptide and Capon that are bound is a potential drug for decreasing nNOS activity.
According to the present invention a method is also provided of using the yeast two-hybrid technique to screen for test compounds that decrease or augment nNOS activity. The yeast two-hybrid technique is generically taught in Fields, S. and Song, O., Nature 340, 245-46, 1989. In a preferred embodiment, a cell is contacted with a test compound. The cell comprises a first fusion protein comprising a DNA binding domain and all or a portion of a mammalian Capon protein consisting of a contiguous sequence of amino acids selected from the amino acid sequence shown in SEQ ID NO:2 and capable of binding to nNOS (this typically requires the 13 carboxy terminal amino acids). The cell also comprises a second fusion protein comprising a transcriptional activating domain and all or a portion of nNOS, wherein the portion comprises a contiguous sequence of amino acids selected from amino acids 14-89 as shown in SEQ ID NO:5 or 6 or naturally occurring biologically active variants thereof. Alternatively, the DNA binding domain and the transcriptional activating domains can be paired with the opposite proteins. The interaction of the portion of the Capon protein with the portion of nNOS reconstitutes a sequence specific transcriptional activating factor. A reporter gene is also present in the cell. The reporter gene comprises a DNA sequence to which the DNA binding domain of the first fusion protein specifically binds. When the Capon and nNOS regions are bound together, the DNA binding domain and the transcriptional activating domain will be in close enough proximity to reconstitute a transcriptional activator capable of initiating transcription of a detectable reporter gene in the cell. The expression of the reporter gene in the presence of the test compound is then measured. A test compound that increases the expression of the reporter gene is a potential drug for decreasing nNOS activity. A test compound that decreases the expression of the reporter gene is a potential drug for augmenting nNOS activity. Test compounds which increase nNOS activity are potential drugs for modulating aggressive behaviour, particularly aggressive sexual behavior. Test compounds which decrease nNOS activity are potential drugs for treating stroke patients and other neuronal degeneration which is mediated by NO.
Many DNA binding domains and transcriptional activating domains can be used in this system, including the DNA binding domains of GAL4, LexA, and the human estrogen receptor paired with the acidic transcriptional activating domains of GAL4 or the herpes virus simplex protein VP16 (See, e.g., G. J. Hannon et al., Genes Dev. 7, 2378, 1993; A. S. Zervos et al., Cell 72, 223, 1993; A. B. Votjet et al., Cell 74, 205, 1993; J. W. Harper et al., Cell 75, 805, 1993; B. Le Douarin et al., Nucl. Acids Res. 23, 876, 1995). A number of plasmids known in the art can be constructed to contain the coding sequences for the fusion proteins using standard laboratory techniques for manipulating DNA (see, e.g., Example 1, below). Suitable detectable reporter genes include the E. coli lacZ gene, whose expression may be measured colorimetrically (see, e.g., Fields and Song, supra), and yeast selectable genes such as HIS3 (Harper et al., supra; Votjet et al., supra; Hannon et aL, supra) or URA3 (Le Douarin et al., supra). Methods for transforming cells are also well known in the art. See, e.g., A. Hinnen et al., Proc. Natl. Acad. Sci. U.S.A. 75, 1929-1933, 1978. The test compound may comprise part of the cell culture medium or it may be added separately. The tester cell need not be a yeast cell, but may be a bacterial, other fungal, or mammalian cell.
In another embodiment, a cell is contacted with a test compound. In this embodiment, the cell comprises (i) a first expression vector comprising a subgenomic polynucleotide encoding nNOS or a naturally occurring biologically active variant thereof, and (ii) a second expression vector comprising a subgenomic polynucleotide encoding a portion of Capon or a naturally occurring biologically active variant thereof The portion of Capon is capable of binding to nNOS. NO production by the cell is then measured, for example by radioimmunoassay or by spectrophotometry. A test compound that increases the amount of NO produced by the cell is a potential drug for augmenting nNOS activity. A test compound that decreases the amount of NO in the cell is a potential drug for decreasing nNOS activity. NO production may be determined by assaying for cGMP or citrulline as well. A test compound which binds to nNOS at the Capon binding site may either inhibit Capon binding, thus favoring the interaction of nNOS and PSD95 or mimic Capon thus inhibiting the interaction of nNOS and PSD95.
Because expansion of glutamine repeats has been shown to be associated with neurodegenerative and other neurological diseases, the glutamine repeat in Capon is believed to be relevant to pathogenesis. Thus either the Capon protein or the gene encoding it can be examined for the number of glutamine residues in the glutamine repeat region, or the number of glutamine codons (CAG) in the CAG repeat region of the gene. Expansion to a number greater than 6 indicates a propensity for or the presence of a neurological disease, likely a neurodegenerative disease. As in other examples where this mechanism has been demonstrated, the degree of expansion is associated with the severity of disease. It is likely that the glutamine repeat region interacts with a binding partner, and the avidity of the inteaction is governed by the degree of expansion of the glutamine repeats. Any means for determining the sequence of a gene or protein may be used, including but not limited to direct sequencing, hybridization with allele-specific probes, binding to antibodies, size determination on gel electrophoresis.
The main finding of this study is the identification of a novel protein, CAPON, which interacts selectively with nNOS. The interaction of CAPON with nNOS is highly specific and has been verified by several methods of monitoring protein-protein interactions. The similarities in neuronal localizations of CAPON and nNOS imply that these proteins interact physiologically and that the principal biological function of CAPON may be to interact with nNOS. The apparent selectivity of this interaction contrasts with other nNOS binding proteins such as PSD95, PIN and calmodulin, each of which bind to multiple other proteins.
The competitive binding for nNOS by CAPON and PSD95 suggests a model for regulating the translocation of nNOS between cytoplasm and synaptic structures (FIG. 7). Presumably, NO release into the synaptic space must be preceded by its translocation to synaptic structures by binding to PSD95. We propose that this process can be blocked by CAPONs removal of nNOS from PSD95, and translocating nNOS into the cytoplasm, or some other cellular compartment. In this manner CAPON could lead to effective nNOS inhibition. Although CAPON does not inhibit nNOS catalytic activity directly (data not shown), CAPON would reduce the accessibility of nNOS to NMDA receptor-mediated calcium influx, thus diminishing the capacity of nNOS to exert its physiologic or pathologic effects. Small molecules which specifically bind to nNOS in a manner similar to that of CAPON are useful for blocking NO-mediated neuronal degeneration.
We have explored potential mechanisms that might regulate the nNOS/CAPON interaction. For instance, we phosphorylated nNOS in transfected HEK 293 cells by treatment with forskolin, phorbol esters, dibutyryl cyclic AMP and 8-bromo-cyclic GMP and in vitro or with purified nNOS protein utilizing protein kinase C, protein kinase A and calcium calmodulin dependent protein kinase using methods described previously (Bredt et al., 1992). We have been unable to alter CAPON-nNOS interactions by any of these treatments.
Conceivably, phosphorylation of CAPON regulates its interactions with nNOS. Recently some of us showed that phosphorylation of the n-2 serine in the potassium channel BIRK-2 regulates its binding to a PDZ domain in PSD95 (Cohen et al., 1996). CAPON, and several other PDZ-domain ligands (Songyang et al., 1997), lack a serine in this position and so must be regulated in some other manner. One possible mechanism may be a regulation of the ligand's C-terminal secondary structure. A recent crystallographic study of a PDZ domain complexed with a short cognate peptide shows that the peptide binds in an antiparallel beta-sheet conformation, with characteristic beta-sheet contacts between the peptide and a strand of a beta-sheet within the PDZ domain (see Doyle et al., 1996). In a physiologic setting, the unbound cognate sequence may constitutively adopt a beta-sheet conformation, with the other beta-strands coming from other, possibly distant, residues within the ligand protein's sequence. This beta-sheet might constitute an endogenous high-affinity ligand. This notion is supported by our observation that short, presumably unfolded, peptides comprising the C-terminal nine residues of CAPON bind nNOS weakly, while 16-residue peptides are more potent competitors (IC.sub.50 =10 mM), although both are much less effective than 100 amino acid fusion proteins which are active in the nanomolar range (see FIG. 5). Peptide competitors that interact with other PDZ domains have also been utilized at 10 and 500 mM concentrations (see Brenman et al., 1996; Kornau et al., 1995). Conceivably, the nNOS-CAPON interaction would be disrupted simply by disrupting the beta-sheet conformation of the C-terminus, which might be achieved by phosphorylation at a distance.
The nNOS PDZ domain is the first example of a PDZ domain which binds to other PDZ domains. The region of nNOS which possesses this property is the PDZ domain plus the adjacent .about.50 amino acids on the carboxyl-side of the PDZ domain (residues 1-150) (Brenman et al., 1996). The additional amino acids in this super-sized PDZ domain may by required to accomodate larger ligands such as other PDZ domains. The finding in this report of another physiologic ligand for the PDZ domain, namely, the C-terminal region of CAPON, raises the question of whether the same or different portions of the nNOS PDZ domain account for the binding to two seemingly different ligands. Because these interactions are mutually exclusive, it is likely that the ligand-binding cleft in the PDZ domain mediates both interactions. Previously identified proteins which contain C-terminal PDZ-binding sequences have been membrane associated. By contrast, CAPON is soluble. This demonstrates that PDZ domains may mediate purely cytosolic protein-protein interactions.
Stricker et al. (1997) recently characterized the specificity of the nNOS PDZ-binding domain. These researchers used a phage display method to identify NOS-binding peptides. Peptides ending in the sequence aspartate-X-valine were found to be high affinity ligands. Interestingly, unlike CAPON, these peptides did not bind the canonical nNOS PDZ domain (amino acids 13.about.89) but bound the extended PDZ domain only (amino acids 1-150). This extended domain is the minimal sequence which mediates PDZ-PDZ interactions. Presumably the differences in the binding sites in nNOS for the phage display peptide and CAPON account for the differences between the sequence specificity requirements for PDZ-PDZ interactions and PDZ-CAPON interactions.
The following are provided for exemplification purposes only and are not intended to limit the scope of the invention which has been described in broad terms above.
EXAMPLE 1.
Identification and Cloning of CAPON
We conducted a yeast two-hybrid screen employing the first 377 amino acids of nNOS, a region which includes the PDZ domain that comprises the first 100 amino acids of nNOS. Screening of six million clones resulted in the identification of three distinct cDNA inserts, one of which, PIN, has been previously reported (Jaffrey and Snyder, 1996) while the other two are overlapping cDNAs derived from a gene which is designated CAPON. The CAPON two-hybrid clones share a common carboxyl terminus and are predicted to translate into 125 and 327 amino acid peptides followed by a stop codon. The 125 amino acid C-terminal fragment of CAPON specifically interacts with nNOS in the two-hybrid system as is evident from the failure of CAPON to interact with fragments of PSD93 and PSD95 containing PDZ domains (FIG. 1A). Moreover, nNOS fails to interact with another control protein, c-fos. To obtain a full-length CAPON cDNA, we screened a rat brain cDNA library with the larger two-hybrid clone and isolated a 2100 bp cDNA which overlapped with the two-hybrid clone and was used to assemble a final 2820 bp cDNA (see Methods). The conceptual translation of this cDNA produces a 503 amino acid protein (FIG. 1B SEQ ID NO:4). The first ATG in the cDNA was 393 bp from the 5' end of the cDNA and was situated in a context that conformed to the Kozak consensus sequence for an initiator methionine (Kozak, 1991).
CAPON displays no significant homology to any other known class of protein except for an N-terminal 145 amino acid stretch of amino acids which has residues suggestive of a phosphotyrosine-binding (PTB) domain (Zhou et al., 1995). CAPON's PTB domain most closely resembles the mouse numb protein's PTB domain (Zhong et al., 1996) with nearly 28% sequence identity on this region. The similarity between CAPON and numb are limited to this domain. PTB domains are targetted to phosphotyrosine containing proteins such as growth factor receptors (reviewed in van der Geer and Pawson, 1995).
Outside of the PTB domain, CAPON lacks any well known consensus sequences except for an 18 nucleotide stretch of CAG repeats that corresponds to six glutamines. Glutamine repeats occur in proteins whose expansion results in neurodegenerative diseases as exemplified by huntingtin, the protein which is altered in Huntington's disease (Ross, 1995). A BLAST search (Altschul et al., 1990) of an expressed sequence-tag database, dBEST, reveals a human brain-derived EST with .about.75% nucleotide identity to CAPON. The cDNA insert was 1.4 kb and corresponds to the C-terminal 156 amino acids of CAPON plus one kb of 3' UTR. The conceptual translation of this portion of human CAPON has 92% amino acid identity with the rat protein (FIG. 1B).
Northern (RNA) blotting reveals a predominant 7.5 kb transcript which is detected only in brain regions with no expression evident in adrenal, bladder, heart, kidney, lung and skeletal muscle (FIG. 1C). Marked regional variations occur in the brain with highest densities in the cerebral cortex and medulla-oblongata and lowest levels in the hippocampus.
To assess the specificity of interactions between CAPON and nNOS, we evaluated the binding of a GST-CAPON fusion protein, consisting of C-terminal 125 amino acids of CAPON, with nNOS, eNOS and inducible NOS (iNOS) (FIG. 2A). Lysates of HEK-293 cells transfected with expression plasmids for each of the three forms of NOS were incubated with GST-CAPON. After extensive washing of the resin, bound nNOS was detected by Western blotting with the appropriate isoform-specific antibody. nNOS interacts strongly with GST-CAPON, while eNOS and iNOS do not interact. No interactions are evident with the GST control.
We also examined interactions of CAPON and nNOS by utilizing a GST-fusion protein of the NH.sub.3 -terminal 100 amino acids of nNOS, the PDZ domain. Following incubation with cerebellar lysates the washed GST-nNOS resin was subjected to SDS-PAGE and Western blotted with a purified antibody directed against the C-terminal 125 amino acids of CAPON. A single band corresponding to CAPON is detected, while no CAPON is bound to the GST control. A lower molecular weight band in homogenates is occasionally detected using our anti-CAPON antibodies. This protein fails to interact with GST-nNOS fusion proteins (FIG. 2B) and may represent an unrelated cross-reactive protein, or the product of an alternatively spliced CAPON mRNA which fails to bind nNOS.
The protein-protein interactions we detected with cell lysates and GST-fusion proteins might have reflected a tertiary interaction between nNOS, an unidentified protein and CAPON. To determine if CAPON directly binds to nNOS, we conducted blot overlay experiments (FIG. 2C). Lysates of HEK 293 cells transfected with nNOS were resolved on a polyacrylamide gel, transferred to nitrocellulose and then probed with [.sup.32 P]GST-CAPON. The radiolabeled CAPON probe binds to a single 160 kD band comigrating with a nNOS standard, while no binding is evident in mock transfected cells, demonstrating that CAPON physically interacts in a direct manner with nNOS.
To ascertain if complexes of CAPON and nNOS exist physiologically, we used two approaches. Our first approach took advantage of a NOS-affinity resin consisting of 2', 5'-ADP ribose crosslinked to an agarose matrix. This resin has been used previously to purify nNOS from cerebellar supernatants (Bredt and Snyder, 1990). Following incubation with cerebellar supernatants, the resin and washed extensively. As expected, a significant portion of the nNOS found in the starting material was bound to the resin (FIG. 2D). To determine if nNOS and CAPON were physiologically associated, we next assayed for CAPON bound to the resin. Like nNOS, CAPON was substantially enriched in the bound fraction. As a control we assayed for the resin-binding ability of CAPON from supernatants derived from mice with a genomic deletion of nNOS. These mice express a truncated version of nNOS which lacks the PDZ domain and is unable to bind CAPON. Substantially less CAPON in these supernatants bound to the 2', 5'-ADP ribose resin indicating that CAPON has negligible intrinsic affinity for the resin and that CAPON-binding in wild-type supernatants was due to nNOS. The smaller cross-reactive band was also enriched on this resin, supporting the notion that it is in some manner related to CAPON by alternative splicing or proteolytic degradation. Interestingly, the total level of CAPON in knockout supernatants was approximately one half that in wild-type mice, possibly due to the absence of a stabilizing effect of nNOS.
As a second approach, we immunoprecipitated CAPON from cerebellar supernatants and assayed for nNOS by Western blot (FIG. 2E). nNOS coprecipitates with anti-CAPON antibodies but is not detected in immunoprecipitates generated using preimmune serume, an antibody to the G-protein subunit .beta.1, or with an antibody to cyclin-dependent kinase 2. To determine if the enrichment observed in anti-CAPON immunoprecipitates was specific, we asked if a control protein, protein kinase C-.beta. I/II, was similarly enriched in these fractions, We found that this protein was absent in all of the precipitates (FIG. 2E) indicating that the coprecipitation of nNOS with CAPON was specific. These two approaches support the notion that CAPON and NOS exist as a complex in the rat cerebellum.
In other experiments we metabolically labeled N1E-115 mouse neuroblastoma cells with [.sup.35 S] methionine and examined for the presence of proteins that would bind to GST-CAPON. The only protein that specifically interacted with CAPON is a 160 kD) protein that comigrates with an nNOS standard (unpublished observations), suggesting that nNOS is the most abundant CAPON-binding protein in these cells.
General Methods and Materials
Molecular biology reagents were from New England Biolabs (Beverly, Mass.) and all other reagents were from Sigma (St. Louis, Mo.) except as indicated. Protein concentrations were determined by Bradford assay.
Yeast Two-Hybrid Methods
Two-hybrid screens and the construction of the parent vectors pPC86, containing the GAL4-activation domain, and pPC97, containing the GAL4-DNA binding domain, have been described (Jaffrey and Snyder, 1996). Plasmid pBD-NOS(2-377) was prepared by the insertion of an nNOS PCR product corresponding to amino acids 2-377 of rat nNOS into the Sal I and Bgl II sites of pPC97, resulting in an open reading frame encoding a GAL4 BD-NOS fusion protein (Jaffrey and Snyder, 1996). The nNOS fragment was constructed by PCR using the following primers: 5'-GACTAGTCGACTGAAGAGAACACGTTTGGG-3' (coding strand, SEQ ID NO: 7) and 5'-TCTGCAGATCTCAGTGGGCCTTGGAGCCAAA-3' (noncoding strand. SEQ ID NO: 8).
A rat hippocampal cDNA library in pPC86 (Li et al., 1995) was amplified once in DH10B (Gibco BRL) as described (Jaffrey and Snyder, 1996) and transformed into yeast containing the pBD-NOS(2-377) plasmid. pAD-CAPON1 and pAD-CAPON2 were identified as 0.8 kb and 1.9 kB clones, respectively, that activated lacZ transcription and conferred histidine prototrophy in the presence of pBD-NOS(2-377). Plasmids were sequenced by automated fluorescent sequencing of both strands. Yeast two-hybrid vectors containing the second PDZ domain of PSD93 (amino acids 116-421) and the three PDZ domains of PSD95 (amino acids 20-364) have been described previously (Brenman et al., 1996).
Truncated NOS fragments comprising amino acids 2-165 and 2-284 were generated by restriction of the initial NOS (2-377) PCR fragment with Nco I and Ava I, respectively followed by Klenow-filling in of that end and ligation into pPC97. Other truncated NOS fragments were prepared by PCR and have been described (Jaffrey and Snyder, 1996).
cDNA cloning of CAPON
A CAPON DNA probe was generated by the random hexamer method using the pAD-CAPON2 cDNA as a template. This probe was used to screen a rat brain lamdaZAP II cDNA library (Stratagene) using methods described by the manufacturer. A 2.1 kb cDNA was isolated which overlapped with the pAD-CAPON2 clone. The cDNAs were ligated at an overlapping Xba I site to produce the full-length 2,812 bp cDNA and subcloned into pCMV for eukaryotic expression. The human CAPON EST was the sole CAPON homolog identified in a BLAST seacrh (Altschul et al., 1990). I.M.A.G.E. consortium (http://www-bio.llnl.gov/bbrp/image/image.html/) clone 34183 (Lennon et al., 1996) was purchased from Research Genetics (Huntsville, AL.).
RNA (Northern) Blotting
Thirty micrograms of whole RNA were isolated from rat tissues using the Triazol reagent (Gibco BRL) and separated on agarose-formaldehyde gels. RNA was transferred to Hybond N+membranes (Amersham) and a DNA probe, generated using the random hexamer method with the two-hybrid CAPON cDNA as a template, was hybridized in Rapid-hyb buffer (Amersham) overnight at 65.degree. C. The blots were subsequently washed sequentially in 2.times.SSC with 0.1% SDS, once at room temperature for 15 min, 1.times.SSC with 1% SDS twice at 65.degree. C., 0.1.times.SSC with 1% SDS twice at 65.degree. C., and then with 0.1.times.SSC with 5% SDS twice at 65.degree. C. The blot was apposed to film for 4 days at -80.degree. C. to visualize the bands.
GST-Fusion Protein Binding Assays
GST-fusion proteins were prepared in BL21(DE3) Escherichia coli (Novagen) with glutathione agarose as an affinity resin for purification (Smith and Johnson, 1988), except that bacterial pellets were sonicated in lysis buffer (50 mM Tris-HCl (pH 7.7), 100 mM NaCl, and 2 mM EDTA), supernatants were adjusted to 1% Triton X-100, washes were done in 50 mM Tris-HCl (pH 7.7), 500 mM NaCl, 2 mM EDTA, and 1% Triton X-100, and protein was purified with elution buffer (50 mM tris-HCl (pH 7.7), 100 mM NaCl, 10 mM reduced glutathione, and 2 mM EDTA).
Transfections were performed with 10 .mu.g of each plasmid using the calcium phosphate method. Following transfection, cells were sonicated in buffer A [50 mM Tris-HCl (pH 7.7), 100 mM NaCl, 2 mM EDTA, and 1% Triton X-100] and cleared by centrifugation. This cellular lysate was incubated with GST-fusion protein immobilized on glutathione-agarose for one hour at 4.degree. C. and washed extensively in HNTG buffer [20 mM Hepes (pH 7.4), 500 mM NaCl, 10% glycerol, and 0.1% Triton X-100] five times, for ten minutes per wash at room temperature. A GST-CAPON fusion protein consisting of amino acids 379-503 was used for binding assays because it was was more soluble when expressed in bacteria than larger CAPON fusion proteins.
For quantitative binding experiments, transfected cells were metabolically labeled overnight with 200 mci [.sup.35 S] methionine and nNOS was purified by NADPH elution of 2', 5' ADP ribose as described previously (Bredt and Snyder, 1990).
The material remaining on the resin was eluted with SDS-PAGE sample buffer and nNOS was detected by immunoblot using antibodies specific to each NOS isoform (Transduction Labs). A polyclonal antiserum to CAPON was generated in rabbits by using a His.sub.6 -tagged CAPON fusion protein. GST-CAPON was crosslinked to glutathione agarose with dimethylpimelimidate and this resin was used to purify CAPON antibody. To confirm the specificity of the antibody, immune serum was incubated with His.sub.6 -CAPON which results in the abolishment of the signal. Incubation with His.sub.6 -FKBP has no effect on the signal (data not shown).
For blot-overlay analysis, CAPON was inserted into pGEX-4T2, a derivative of PGEX4T2 in which two cyclic AMP-dependent protein kinase (PKA) sites were inserted between the GST moiety and the multiple cloning site (Jaffrey and Snyder, 1996). Kinase reactions and blot overlays were performed as described (Kavanaugh and Williams, 1994).
EXAMPLE 2.
The C-terminus of CAPON Binds to the PDZ Domain of nNOS
To examine the region of nNOS that binds to CAPON, we conducted yeast two-hybrid experiments with various truncations of nNOS (FIG. 4A). As little as the first 100 amino acids of nNOS binds to the C-terminal 125 amino acids of CAPON. This portion of nNOS contains the full PDZ domain as defined by MacKinnon and associates (Doyle et al., 1996) who identified the PDZ consensus domain in nNOS as amino acids 14-89. Deletion of the first 20 amino acids of nNOS, which includes the first seven amino acids of the PDZ domain, does not abolish binding, but larger NH.sub.3 -terminal deletions abolish binding, presumably because they result in a loss of important structural components of the PDZ domain. The nNOS construct comprising amino acids 163-245, which represents the PIN-binding domain of nNOS (Jaffrey and Snyder, 1996), shows no interaction with CAPON.
PDZ domains typically interact with a characteristic C-terminal motif in other proteins (Songyang et al., 1997). By contrast, the nNOS PDZ domain binds directly to other PDZ domains, such as those in PSD95, but has not previously been reported to interact with any known physiological C-terminal peptide motifs. Since we could not detect any PDZ domain motifs in the CAPON sequence we sought to determine the region in CAPON which accounted for nNOS binding. We investigated the domain of CAPON that interacts with nNOS using GST-CAPON fusion proteins containing various deletions at the C-terminus FIG. 4B). Immobilized fusion proteins were incubated with HEK 293 lysates containing nNOS. Bound nNOS was detected by Western blot. Robust interactions with nNOS are evident with constructs containing as little as the C-terminal thirteen amino acids of CAPON. Deleting the C-terminal 20 amino acids of CAPON abolishes its interactions with nNOS. These data show that the C-terminal portion of CAPON is necessary and sufficient for nNOS binding.
Recently Cantley and associates (Songyang et al., 1997) identified consensus sequences for binding to several PDZ domains. Binding of PDZ ligands involves the C-terminus of proteins, with determinants of specificity lying within the eight or fewer C-terminal amino acids. A consistent requirement among all the PDZ domain ligands is a hydrophobic residue, such as valine or leucine, as the final amino acid. To determine if the binding of CAPON to nNOS exhibits similar sequence-specificity, we examined the binding of mutagenized His.sub.6 -CAPON fusion proteins to immobilized GST-nNOS PDZ domain fusion proteins (FIG. 4C). The C-terminal residue of CAPON is a valine, and conversion of this residue to alanine abolishes binding. Binding is also greatly reduced by changing the penultimate amino acid from alanine to aspartate. However, changing the n-2 amino acid from isoleucine to serine or alanine does not alter binding. These experiments indicate that the nNOS-CAPON interaction resembles those of other PDZ-C-terminal peptide ligand interactions. Specifically, C-terminal residues of CAPON are important for the specificity in CAPON binding to nNOS.
EXAMPLE 3.
CAPON and PSD95 Compete for Binding to nNOS
Since the nNOS PDZ domain is capable of both PDZ-PDZ interactions and PDZ-C-terminal peptide interactions we wondered whether CAPON and PSD95 can bind simultaneously to nNOS or whether their interactions with nNOS are mutually exclusive. To answer this question we incubated lysates of HEK-293 cells containing nNOS with various concentrations of a His.sub.6 -CAPON fusion protein, comprising the last 125 amino acids of CAPON, and then added these lysates to GST-PSD95 immobilized on glutathione agarose resin (FIG. 5A). After extensive washing of the resin, we assayed for nNOS bound to PSD95 by Western blot. As little as 5 nM His.sub.6 -CAPON causes a substantial reduction of nNOS binding to GST-PSD95. Half maximal reduction of binding is evident between 5 and 50 nM His.sub.6 -CAPON (FIG. 5B). Deletion of the C-terminal 20 amino acids of CAPON abolishes its ability to serve as a competitor for nNOS binding to GST-PSD95. As controls, we examined the effects of 5 .mu.M His.sub.6 -PIN or 5 mM His.sub.6 -FK506 binding protein-12 kD (FKBP). Neither of these proteins compete for binding to nTNOS. nNOS also binds to the second PDZ domain of PSD93, a protein which is highly homologous to PSD95 (Brenman et al., 1996). His.sub.6 -CAPON is an effective competitor for nNOS binding to immobilized GST-PSD93 as well (FIG. 5A, B). These effects of CAPON likely reflect its binding to nNOS rather than to the PDZ domains of either PSD95 or PSD93 because CAPON fails to interact with either PSD93 or PSD95 using (i) a two-hybrid assay (see FIG. 1A) and (ii) in vitro experiments utilizing immobilized GST-PSD95 and purified recombinant CAPON (data not shown).
We wanted to determine if CAPON and PSD95 compete for binding to nNOS in intact cells. Accordingly, we transfected HEK-293 cells with various mixtures of expression plasmids containing cDNAs of hemagglutinin antigen (HA)-tagged nNOS, myc-tagged PSD95 and/or full-length CAPON. Following immunoprecipitation with antibodies to HA, we examined which proteins coprecipitated. In cells expressing HA-nNOS and myc-PSD95, antibodies to HA coprecipitate myc-PSD95 (FIG. 6). When various amounts of CAPON cDNA containing expression plasmids are also transfected, HA-immunoprecipitates contain CAPON but substantially less PSD95.
Immunoprecipitations
Immunoprecipitations were performed by homogenizing one rat cerebellum in 3 ml lysis buffer followed by centrifugation at 100,000.times.g for 30 min at 4.degree. C. Two hundred microliters of the supernatant was incubated with 40 ml of protein A-agarose (Oncogene Sciences, Cambridge, Mass.) and 5 mg of the indicated antibody for 60 min at 4.degree. C. The resins were then washed with IP wash buffer (50 mM Tris-HCl (pH 7.7), 400 mM NaCl, and 2 mM EDTA) six times and eluted in 60 ul of 1.times.SDS-PAGE sample buffer by boiling. Western blots were performed using an nNOS-specific monoclonal antibody (Transduction Labs) or a PKC- b I/II monoclonal antibody (Santa Cruz Biotechnology, Inc., Santa Cruz, Calif.). The immunoprecipitating antibodies used as controls were from Santa Cruz Biotechnology, Inc.
For experiments utilizing 2', 5', ADP sepharose (Pharmacia), tissues were prepared identically as for immunoprecipitations except mouse cerebella were used and the homogenization volume was 400 ml per cerebellum. Supernatants were incubated with 100 ul of affinity resin. Incubations and washes were performed identically as for immunoprecipitations. The generation of mice with a targetted deletion of nNOS has been described previously (Huang et al., 1993).
Immunohistochemistry
Adult Sprague-Dawley rats (200-250 gm) were obtained from Charles River and housed at the Johns Hopkins Animal Care Facility. A polyclonal antiserum to the C-terminal region of human nNOS (residues 1419-1433) was kindly provided by J. Spangenberg (IncStar, Stillwater, MN). The peroxidase Elite staining kit was from Vector Laboratories.
Anesthetized rats were perfused through the left ventricle with 50 ml of 0.9% NaCl followed by 500 ml 4% paraformaldehyde in 0.1 M phosphate buffer (PB), pH 7.4. The brains were removed, cut into saggital blocks, and postfixed in 4% paraformaldehyde in 0.1 M PB for 4 h at room temperature. Blocks were cryoprotected for 2 days at 4.degree. C. in 50 mM sodium phosphate, pH 7.4/0.1 M NaCl/20% (vol./vol.) glycerol. Brain sections, 40 mm thick, were cut on a sliding microtome. Free-floating sections were incubated in PBS (10 mM, pH 7.4/0.19 M NaCl), containing 4% normal goat serum (Jackson Labs), and 0.2% Triton X-100 for 45 min, and then incubated overnight at 4.degree. C. with the primary antiserum diluted 1:500 (CAPON) or 1:15,000 (nNOS) in phosphate buffered saline (PBS) containing 2% goat serum and 0.1% Triton X-100. Immunoreactivity was visualized with the Vectastain ABC Elite kit following the nickel-enhanced diaminobenzidine procedure. To test immunohistochemical specificity of the CAPON antiserum, the antiserum was incubated overnight with 13.5 mg/ml of the antigenic fusion protein before incubation with brain sections.
In Situ Hybridization
In situ hybridization used DNA oligonucleotide probes corresponding to amino acids 478-503. Probes were end-labelled with [a-.sup.32 P] dATP and terminal deoxynucleotidyl transferase to a specific activity of 800 mCi/mg and in situ hybridization was performed as described previously (Jaffrey et al., 1994). Non-specific hybridization was determined using the corresponding sense probe.
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SEQUENCE LISTING SUMMARY
SEQ ID NO: 1. Rat capon cDNA
SEQ ID NO: 2. Rat capon amino acids
SEQ ID NO: 3. Human capon cDNA
SEQ ID NO: 4. Human capon amino acids
SEQ ID NO: 5. Rat nNOS amino acids
SEQ ID NO: 6. Human nNOS amino acids
SEQ ID NO: 7. nNOS probe
SEQ ID NO: 8. nNOS probe
__________________________________________________________________________# SEQUENCE LISTING - - - - (1) GENERAL INFORMATION: - - (iii) NUMBER OF SEQUENCES: 8 - - - - (2) INFORMATION FOR SEQ ID NO:1: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 2826 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:1: - - GAATTCGGCA CGAGCCGGGT CGTGCGCGCC GAGCTCGGGA TCCGGCTCCC AG -#TCTAGCCC 60 - - CGCTTCGGGC CGTGCGCCCT TTGCTCGGCG TCCGGCTCCG GGGCTCCGCG CC -#ACCCGCTC 120 - - CCGCCTGCCC GGCCGCCTGG CCGCCTCCCC GTAGTCAGAG CGCGGCCACC GA -#GCTGCTCG 180 - - CGCCAGCCGC ATCCGCGCCG CCCCTGCCGA TCGGCCCTCC GGAGGCACCG CT -#CCGGGTCC 240 - - CCCCCGCCAC TGCCTGGCAC CCAGGCTGCC CACCTCGCGA CCCGGGTCCT CG -#CTGCCGCC 300 - - TCGCCCGGCC CCACTGTTCT CTCCACGGGG TCTCGCCAGC TCTTTCTCGT CG -#CCGCCACC 360 - - GCCGCCCCCT TGGAGCAGCG GGTCCGCCGC GGGTCACCAT GCCCAGCAAA AC -#CAAGTACA 420 - - ACCTTGTGGA CGATGGGCAC GACTTACGGA TCCCTTTGCA CAACGAGGAC GC -#CTTCCAGC 480 - - ACGGCATCTC TTTTGAGGCC AAGTACGTGG GAAGCCTGGA TGTGCCCAGA CC -#CAACAGCA 540 - - GGGTTGAGAT CGTGGCTGCC ATGCGCAGAA TCCGGTATGA GTTTAAAGCC AA -#GAATATCA 600 - - AGAAGAAGAA AGTAAGCATC ATGGTCTCCG TGGACGGTGT CAAAGTGATT CT -#GAAGAAGA 660 - - AGAAAAAGAA AAAGGAGTGG ACGTGGGATG AGAGCAAGAT GCTGGTGATG CA -#GGACCCTA 720 - - TCTACAGGAT CTTCTATGTC TCTCATGACT CCCAAGACTT GAAAATCTTC AG -#CTATATCG 780 - - CTCGAGATGG TGCCAGCAAT ATCTTCAGAT GCAATGTCTT TAAATCCAAG AA -#GAAGAGCC 840 - - AAGCTATGAG AATCGTACGG ACAGTGGGAC AGGCCTTTGA GGTCTGCCAC AA -#GCTGAGCC 900 - - TGCAGCACAC ACAGCAGAAT GCAGATGGCC AGGAAGATGG AGAGAGCGAG AG -#GAACAGCG 960 - - ATGGCTCAGG AGACCCAGGC CGCCAGCTCA CTGGAGCTGA GAGGGTCTCC AC -#AGCCACCG 1020 - - CAGAGGAGAC CGACATTGAC GCTGTGGAGG TCCCACTCCC CGGGAATGAC AT -#TCTAGAAT 1080 - - TCAGCCGAGG TGTGACTGAC CTGGATGCTA TTGGGAAGGA CGGAGGCTCC CA -#CATAGACA 1140 - - CGACGGTCTC ACCCCATCCA CAGGAGCCCA TGCTGGCAGC CTCCCCTCGC AT -#GCTGCTCC 1200 - - CTTCTTCTTC TTCCTCGAAG CCACCGGGCT TGGGCACTGG GACGCCCCTG TC -#CACTCACC 1260 - - ACCAGATGCA GCTCCTCCAG CAGCTCCTCC AGCAGCAGCA GCAGCAGACA CA -#AGTGGCTG 1320 - - TGGCTCAGGT TCACTTGCTG AAGGATCAGT TGGCTGCTGA GGCTGCGGCA CG -#GCTGGAGG 1380 - - CCCAGGCACG AGTGCACCAG CTCCTGCTAC AGAACAAAGA CATGCTTCAG CA -#CATCTCTC 1440 - - TGCTGGTTAA GCAGGTGCAG GAGCTGGAAC TGAAGCTGTC AGGACAGAGC AC -#CATGGGCT 1500 - - CCCAGGACAG CTTGCTGGAG ATCACCTTCC GTTCAGGTGC CCTGCCTGTG CT -#CTGTGAAT 1560 - - CCACCACTCC TAAGCCAGAG GACCTACACT CACCACTGCT GGGCGCTGGC TT -#GGCTGACT 1620 - - TTGCCCACCC AGTGGGCAGC CCCTTAGGTA GGCGTGACTG CTTGGTGAAG CT -#GGAGTGCT 1680 - - TTCGTTTCCT CCCAGCCGAG GATAACCAGC CGATGGCACA GGGTGAGCCG CT -#CCTAGGTG 1740 - - GCCTGGAGCT CATCAAGTTC CGAGAGTCAG GCATCGCCTC AGAGTATGAG TC -#CAACACAG 1800 - - ACGAAAGCGA GGAGCGTGAC TCGTGGTCGC AGGAAGAGCT GCCACGCCTG CT -#CAATGTCC 1860 - - TACAGCGGCA GGAGTTGGGT GACAGTTTGG ATGATGAGAT CGCCGTGTAG GT -#GCAGGGCA 1920 - - AGGAGCTGGT GAAGGTGGCA GCATGATGCC AAGGGGGTCA AGTCTGCCTG TC -#CCCGGCTG 1980 - - GGGAAGCCCA GGGGAAAGCA CCGCTGAGAA AAACACCCAG GGCTGAGAGT GT -#AGGGTTTC 2040 - - AGAAGAGGGT TGGGATTTTG CTTTGGAAGG TAAAGCAGGG AAGAAAATGG AT -#TCCTAGAC 2100 - - ACAGGAATCA GCACCTGTAT TCTGCTAATG ACTGAATGGG ACGGAAGCAG GG -#CTTTCCAG 2160 - - AACCCAGGAC CTTGGGATGG GTCCGCCTTC AAGAATCACA GTTCTGGAAG GC -#CTGTTGCT 2220 - - CCCACCGTTA TAGTCAGGTT CTACTCAATC TGTCCGTGAT GTCTCAGTGG CC -#TACACTCT 2280 - - CCTGTCTCTG TGGTGCAGAT CATAAATGGA AGCCATTGAT ACCGTCTCAC GT -#ACTTTGTT 2340 - - TTGGATATCA GGATGCTACA AGTTGCCTAA CCCTCCCTTA AGCTGTAGGA GA -#ATTCCTTC 2400 - - CCCAGGCCCT GGCTGAGATC AGAGAGGTTG GAGGATTTCC CTCACTGCTG GG -#AAATTGAG 2460 - - ACTCTGCCAT TCAGTGAGCA TGGAGGTGAC AGCAGTCACA AGTCACAGTG AA -#TAAACTAG 2520 - - GAATTTACTC TAAGTGGGGT GTTGGATGTT GCTTCTGAGG AAGCTAGGAG TA -#TGAATAGG 2580 - - ATTGAGGACC CTGCAGGGAG AGCCTGGGGA GGGTTAGCCT AGGGGAGGGT TA -#GCCTAGAG 2640 - - AAGGGTTAGC CTAGGAGTGC TGATGACAGT TGTGGCAGCT CATGTAGGTG TG -#ATTCTTCA 2700 - - GTTTGGAAAC CATGCCCCTT ACCCATCTCC TGCCTGCAAC CCAGCTCATA TA -#AACGAGGC 2760 - - TAAGAACTAT CATAATATCC CCTTTTCTTG CCTCAGGGGC TGTGCCTGCC TA -#ATGAGTGC 2820 - - GGCCGC - # - # -# 2826 - - - - (2) INFORMATION FOR SEQ ID NO:2: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 503 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: None - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:2: - - Met Pro Ser Lys Thr Lys Tyr Asn Leu Val As - #p Asp Gly His Asp Leu 1 5 - # 10 - # 15 - - Arg Ile Pro Leu His Asn Glu Asp Ala Phe Gl - #n His Gly Ile Ser Phe 20 - # 25 - # 30 - - Glu Ala Lys Tyr Val Gly Ser Leu Asp Val Pr - #o Arg Pro Asn Ser Arg 35 - # 40 - # 45 - - Val Glu Ile Val Ala Ala Met Arg Arg Ile Ar - #g Tyr Glu Phe Lys Ala 50 - # 55 - # 60 - - Lys Asn Ile Lys Lys Lys Lys Val Ser Ile Me - #t Val Ser Val Asp Gly 65 - #70 - #75 - #80 - - Val Lys Val Ile Leu Lys Lys Lys Lys Lys Ly - #s Lys Glu Trp Thr Trp 85 - # 90 - # 95 - - Asp Glu Ser Lys Met Leu Val Met Gln Asp Pr - #o Ile Tyr Arg Ile Phe 100 - # 105 - # 110 - - Tyr Val Ser His Asp Ser Gln Asp Leu Lys Il - #e Phe Ser Tyr Ile Ala 115 - # 120 - # 125 - - Arg Asp Gly Ala Ser Asn Ile Phe Arg Cys As - #n Val Phe Lys Ser Lys 130 - # 135 - # 140 - - Lys Lys Ser Gln Ala Met Arg Ile Val Arg Th - #r Val Gly Gln Ala Phe 145 1 - #50 1 - #55 1 -#60 - - Glu Val Cys His Lys Leu Ser Leu Gln His Th - #r Gln Gln Asn AlaAsp 165 - # 170 - # 175 - - Gly Gln Glu Asp Gly Glu Ser Glu Arg Asn Se - #r Asp Gly Ser Gly Asp 180 - # 185 - # 190 - - Pro Gly Arg Gln Leu Thr Gly Ala Glu Arg Va - #l Ser Thr Ala Thr Ala 195 - # 200 - # 205 - - Glu Glu Thr Asp Ile Asp Ala Val Glu Val Pr - #o Leu Pro Gly Asn Asp 210 - # 215 - # 220 - - Ile Leu Glu Phe Ser Arg Gly Val Thr Asp Le - #u Asp Ala Ile Gly Lys 225 2 - #30 2 - #35 2 -#40 - - Asp Gly Gly Ser His Ile Asp Thr Thr Val Se - #r Pro His Pro GlnGlu 245 - # 250 - # 255 - - Pro Met Leu Ala Ala Ser Pro Arg Met Leu Le - #u Pro Ser Ser Ser Ser 260 - # 265 - # 270 - - Ser Lys Pro Pro Gly Leu Gly Thr Gly Thr Pr - #o Leu Ser Thr His His 275 - # 280 - # 285 - - Gln Met Gln Leu Leu Gln Gln Leu Leu Gln Gl - #n Gln Gln Gln Gln Thr 290 - # 295 - # 300 - - Gln Val Ala Val Ala Gln Val His Leu Leu Ly - #s Asp Gln Leu Ala Ala 305 3 - #10 3 - #15 3 -#20 - - Glu Ala Ala Ala Arg Leu Glu Ala Gln Ala Ar - #g Val His Gln LeuLeu 325 - # 330 - # 335 - - Leu Gln Asn Lys Asp Met Leu Gln His Ile Se - #r Leu Leu Val Lys Gln 340 - # 345 - # 350 - - Val Gln Glu Leu Glu Leu Lys Leu Ser Gly Gl - #n Ser Thr Met Gly Ser 355 - # 360 - # 365 - - Gln Asp Ser Leu Leu Glu Ile Thr Phe Arg Se - #r Gly Ala Leu Pro Val 370 - # 375 - # 380 - - Leu Cys Glu Ser Thr Thr Pro Lys Pro Glu As - #p Leu His Ser Pro Leu 385 3 - #90 3 - #95 4 -#00 - - Leu Gly Ala Gly Leu Ala Asp Phe Ala His Pr - #o Val Gly Ser ProLeu 405 - # 410 - # 415 - - Gly Arg Arg Asp Cys Leu Val Lys Leu Glu Cy - #s Phe Arg Phe Leu Pro 420 - # 425 - # 430 - - Ala Glu Asp Asn Gln Pro Met Ala Gln Gly Gl - #u Pro Leu Leu Gly Gly 435 - # 440 - # 445 - - Leu Glu Leu Ile Lys Phe Arg Glu Ser Gly Il - #e Ala Ser Glu Tyr Glu 450 - # 455 - # 460 - - Ser Asn Thr Asp Glu Ser Glu Glu Arg Asp Se - #r Trp Ser Gln Glu Glu 465 4 - #70 4 - #75 4 -#80 - - Leu Pro Arg Leu Leu Asn Val Leu Gln Arg Gl - #n Glu Leu Gly AspSer 485 - # 490 - # 495 - - Leu Asp Asp Glu Ile Ala Val 500 - - - - (2) INFORMATION FOR SEQ ID NO:3: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1504 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: double (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:3: - - AAGCTTGGCA CGAGGTCAAG CAGGTGCAAG AGCTGGAACT GAAGCTGTCA GG -#ACAGAACG 60 - - CCATGGGCTC CCAGGACAGC TTGCTGGAGA TCACCTTCCG CTCCGGAGCC CT -#GCCCGTGC 120 - - TCTGTGACCC CACGACCCCT AAGCCAGAGG ACCTGCATTC GCCGCCGCTG GG -#CGCGGGCT 180 - - TGGCTGACTT TGCCCACCCT GCGGGCAGCC CCTTAGGTAG GCGCGACTGC TT -#GGTGAAGC 240 - - TGGAGTGCTT TCGCTTTCTT CCGCCCGAGG ACACCCCGCC CCCAGCGCAG GG -#CGAGGCGC 300 - - TCCTGGGCGG TCTGGAGCTC ATCAAGTTCC GAGAGTCAGG CATCGCCTCG GA -#GTACGAGT 360 - - CCAACACGGA CGAGAGCGAG GAGCGCGACT CGTGGTCCCA GGAGGAGCTG CC -#GCGCCTGC 420 - - TGAATGTCCT GCAGAGGCAG GAACTGGGCG ACGGCCTGGA TGATGAGATC GC -#CGTGTAGG 480 - - TGCCGAGGGC GAGGAGATGG AGGCGGCGGC GTGGCTGGAG GGGCCGTGTC TG -#GCTGCTGC 540 - - CCGGGTAGGG GATGCCCAGT GAATGTGCAC TGCCGAGGAG AATGCCAGCC AG -#GGCCCGGG 600 - - AGAGTGTGAG GTTTCAGGAA AGTATTGAGA TTCTGCTTTG GAGGGTAAAG TG -#GGGAAGAA 660 - - ATCGGATTCC CAGAGGTGAA TCAGCTCCTC TCCTACTTGT GACTAGAGGG TG -#GTGGAGGT 720 - - AAGGCCTTCC AGAGCCCATG GCTTCAGGAG AGGGTCTCTC TCCAGGACTG CC -#AGGCTGCT 780 - - GGAGGACCTG CCCCTACCTG CTGCATCGTC AGGCTCCCAC GCTTTGTCCG TG -#ATGCCCCC 840 - - CTACCCCCTC ACTCTCCCCG TCTCCATGGT CCCGACCAGG AAGGGAAGCC AT -#CGGTACCT 900 - - TCTCAGGTAC TTTGTTTCTG GATATCACGA TGCTGCGAGT TGCCTAACCC TC -#CCCCTACC 960 - - TTTATGAGAG GAATTCCTTC TCCAGGCCCT TGCTGAGATT GTAGAGATTG AG -#TGCTCTGG 1020 - - ACCGCAAAAG CCAGGCTAGT CCTTGTAGGG TGAGCATGGA ATTGGAATGT GT -#CACAGTGG 1080 - - ATAAGCTTTT AGAGGAACTG AATCCAAACA TTTTCTCCAG CCGGACATTG AA -#TGTTGCTA 1140 - - CAAAGGGAGC CTTGAAGCTT TAACATGGTT CAGGCCCTTG GTGTGAGAGC CC -#AGGGGGAG 1200 - - GACAGCTTGT CTGCTGCTCC AAATCACTTA GATCTGATTC CTGTTTTGAA AG -#TCCTGCCC 1260 - - TGCCTTCCTC CTGCCTGTAG CCCAGCCCAT CTAAATGGAA GCTGGGAATT GC -#CCCTCACC 1320 - - TCCCCTGTGT CCTGTCCAGC TGAAGCTTTT GCAGCACTTT ACCTCTCTGA AA -#GCCCCAGA 1380 - - GGACCAGAGC CCCCAGCCTT ACCTCTCAAC CTGTCCCCTC CACTGGGCAG TG -#GTGGTCAG 1440 - - TTTTTACTGC AAAAAAAAAA AAAAAGAAAA AAGAGAAAAA AAAAAAAAAA AT -#TCCTGCGG 1500 - - CCGC - # - # - # 1504 - - - - (2) INFORMATION FOR SEQ ID NO:4: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 153 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: None - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:4: - - Lys Gln Val Gln Glu Leu Glu Leu Lys Leu Se - #r Gly Gln Asn Ala Met 1 5 - # 10 - # 15 - - Gly Ser Gln Asp Ser Leu Leu Glu Ile Thr Ph - #e Arg Ser Gly Ala Leu 20 - # 25 - # 30 - - Pro Val Leu Cys Asp Pro Thr Thr Pro Lys Pr - #o Glu Asp Leu His Ser 35 - # 40 - # 45 - - Pro Pro Leu Gly Ala Gly Leu Ala Asp Phe Al - #a His Pro Ala Gly Ser 50 - # 55 - # 60 - - Pro Leu Gly Arg Arg Asp Cys Leu Val Lys Le - #u Glu Cys Phe Arg Phe 65 - #70 - #75 - #80 - - Leu Pro Pro Glu Asp Thr Pro Pro Pro Ala Gl - #n Gly Glu Ala Leu Leu 85 - # 90 - # 95 - - Gly Gly Leu Glu Leu Ile Lys Phe Arg Glu Se - #r Gly Ile Ala Ser Glu 100 - # 105 - # 110 - - Tyr Glu Ser Asn Thr Asp Glu Ser Glu Glu Ar - #g Asp Ser Trp Ser Gln 115 - # 120 - # 125 - - Glu Glu Leu Pro Arg Leu Leu Asn Val Leu Gl - #n Arg Gln Glu Leu Gly 130 - # 135 - # 140 - - Asp Gly Leu Asp Asp Glu Ile Ala Val 145 1 - #50 - - - - (2) INFORMATION FOR SEQ ID NO:5: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1430 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: None - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:5: - - Met Glu Glu Asn Thr Phe Gly Val Gln Gln Il - #e Gln Pro Asn Val Ile 1 5 - # 10 - # 15 - - Ser Val Arg Leu Phe Lys Arg Lys Val Gly Gl - #y Leu Gly Phe Leu Val 20 - # 25 - # 30 - - Lys Glu Arg Val Ser Lys Pro Pro Val Ile Il - #e Ser Asp Leu Ile Arg 35 - # 40 - # 45 - - Gly Gly Ala Ala Glu Gln Ser Gly Leu Ile Gl - #n Ala Gly Asp Ile Ile 50 - # 55 - # 60 - - Leu Ala Val Asn Asp Arg Pro Leu Val Asp Le - #u Ser Tyr Asp Ser Ala 65 - #70 - #75 - #80 - - Leu Glu Val Leu Arg Gly Ile Ala Ser Glu Th - #r His Val Val Leu Ile 85 - # 90 - # 95 - - Leu Arg Gly Pro Glu Gly Phe Thr Thr His Le - #u Glu Thr Thr Phe Thr 100 - # 105 - # 110 - - Gly Asp Gly Thr Pro Lys Thr Ile Arg Val Th - #r Gln Pro Leu Gly Pro 115 - # 120 - # 125 - - Pro Thr Lys Ala Val Asp Leu Ser His Gln Pr - #o Ser Ala Ser Lys Asp 130 - # 135 - # 140 - - Gln Ser Leu Ala Val Asp Arg Val Thr Gly Le - #u Gly Asn Gly Pro Gln 145 1 - #50 1 - #55 1 -#60 - - His Ala Gln Gly His Gly Gln Gly Ala Gly Se - #r Val Ser Gln AlaAsn 165 - # 170 - # 175 - - Gly Val Ala Ile Asp Pro Thr Met Lys Ser Th - #r Lys Ala Asn Leu Gln 180 - # 185 - # 190 - - Asp Ile Gly Glu His Asp Glu Leu Leu Lys Gl - #u Ile Glu Pro Val Leu 195 - # 200 - # 205 - - Ser Ile Leu Asn Ser Gly Ser Lys Ala Thr As - #n Arg Gly Gly Pro Ala 210 - # 215 - # 220 - - Lys Ala Glu Met Lys Asp Thr Gly Ile Gln Va - #l Asp Arg Asp Leu Asp 225 2 - #30 2 - #35 2 -#40 - - Gly Lys Ser His Lys Ala Pro Pro Leu Gly Gl - #y Asp Asn Asp ArgVal 245 - # 250 - # 255 - - Phe Asn Asp Leu Trp Gly Lys Asp Asn Val Pr - #o Val Ile Leu Asn Asn 260 - # 265 - # 270 - - Pro Tyr Ser Glu Lys Glu Gln Ser Pro Thr Se - #r Gly Lys Gln Ser Pro 275 - # 280 - # 285 - - Thr Lys Asn Gly Ser Pro Ser Arg Cys Pro Ar - #g Phe Leu Lys Val Lys 290 - # 295 - # 300 - - Asn Trp Glu Thr Asp Val Val Leu Thr Asp Th - #r Leu His Leu Lys Ser 305 3 - #10 3 - #15 3 -#20 - - Thr Leu Glu Thr Gly Cys Thr Glu His Ile Cy - #s Met Gly Ser IleMet 325 - # 330 - # 335 - - Leu Pro Ser Gln His Thr Arg Lys Pro Glu As - #p Val Arg Thr Lys Asp 340 - # 345 - # 350 - - Gln Leu Phe Pro Leu Ala Lys Glu Phe Leu As - #p Gln Tyr Tyr Ser Ser 355 - # 360 - # 365 - - Ile Lys Arg Phe Gly Ser Lys Ala His Met As - #p Arg Leu Glu Glu Val 370 - # 375 - # 380 - - Asn Lys Glu Ile Glu Ser Thr Ser Thr Tyr Gl - #n Leu Lys Asp Thr Glu 385 3 - #90 3 - #95 4 -#00 - - Leu Ile Tyr Gly Ala Lys His Ala Trp Arg As - #n Ala Ser Arg CysVal 405 - # 410 - # 415 - - Gly Arg Ile Gln Trp Ser Lys Leu Gln Val Ph - #e Asp Ala Arg Asp Cys 420 - # 425 - # 430 - - Thr Thr Ala His Gly Met Phe Asn Tyr Ile Cy - #s Asn His Val Lys Tyr 435 - # 440 - # 445 - - Ala Thr Asn Lys Gly Asn Leu Arg Ser Ala Il - #e Thr Ile Phe Pro Gln 450 - # 455 - # 460 - - Arg Thr Asp Gly Lys His Asp Phe Arg Val Tr - #p Asn Ser Gln Leu Ile 465 4 - #70 4 - #75 4 -#80 - - Arg Tyr Ala Gly Tyr Lys Gln Pro Asp Gly Se - #r Thr Leu Gly AspPro 485 - # 490 - # 495 - - Ala Asn Val Gln Phe Thr Glu Ile Cys Ile Gl - #n Gln Gly Trp Lys Ala 500 - # 505 - # 510 - - Pro Arg Gly Arg Phe Asp Val Leu Pro Leu Le - #u Leu Gln Ala Asn Gly 515 - # 520 - # 525 - - Asn Asp Pro Glu Leu Phe Gln Ile Pro Pro Gl - #u Leu Val Leu Glu Val 530 - # 535 - # 540 - - Pro Ile Arg His Pro Lys Phe Asp Trp Phe Ly - #s Asp Leu Gly Leu Lys 545 5 - #50 5 - #55 5 -#60 - - Trp Tyr Gly Leu Pro Ala Val Ser Asn Met Le - #u Leu Glu Ile GlyGly 565 - # 570 - # 575 - - Leu Glu Phe Ser Ala Cys Pro Phe Ser Gly Tr - #p Tyr Met Gly Thr Glu 580 - # 585 - # 590 - - Ile Gly Val Arg Asp Tyr Cys Asp Asn Ser Ar - #g Tyr Asn Ile Leu Glu 595 - # 600 - # 605 - - Glu Val Ala Lys Lys Met Asp Leu Asp Met Ar - #g Lys Thr Ser Ser Leu 610 - # 615 - # 620 - - Trp Lys Asp Gln Ala Leu Val Glu Ile Asn Il - #e Ala Val Leu Tyr Ser 625 6 - #30 6 - #35 6 -#40 - - Phe Gln Ser Asp Lys Val Thr Ile Val Asp Hi - #s His Ser Ala ThrGlu 645 - # 650 - # 655 - - Ser Phe Ile Lys His Met Glu Asn Glu Tyr Ar - #g Cys Arg Gly Gly Cys 660 - # 665 - # 670 - - Pro Ala Asp Trp Val Trp Ile Val Pro Pro Me - #t Ser Gly Ser Ile Thr 675 - # 680 - # 685 - - Pro Val Phe His Gln Glu Met Leu Asn Tyr Ar - #g Leu Thr Pro Ser Phe 690 - # 695 - # 700 - - Glu Tyr Gln Pro Asp Pro Trp Asn Thr His Va - #l Trp Lys Gly Thr Asn 705 7 - #10 7 - #15 7 -#20 - - Gly Thr Pro Thr Lys Arg Arg Ala Ile Gly Ph - #e Lys Lys Leu AlaGlu 725 - # 730 - # 735 - - Ala Val Lys Phe Ser Ala Lys Leu Met Gly Gl - #n Ala Met Ala Lys Arg 740 - # 745 - # 750 - - Val Lys Ala Thr Ile Leu Tyr Ala Thr Glu Th - #r Gly Lys Ser Gln Ala 755 - # 760 - # 765 - - Tyr Ala Lys Thr Leu Cys Glu Ile Phe Lys Hi - #s Ala Phe Asp Ala Lys 770 - # 775 - # 780 - - Ala Met Ser Met Glu Glu Tyr Asp Ile Val Hi - #s Leu Glu His Glu Ala 785 7 - #90 7 - #95 8 -#00 - - Leu Val Leu Val Val Thr Ser Thr Phe Gly As - #n Gly Asp Pro ProGlu 805 - # 810 - # 815 - - Asn Gly Glu Lys Phe Gly Cys Ala Leu Met Gl - #u Met Arg His Pro Asn 820 - # 825 - # 830 - - Ser Val Gln Glu Glu Arg Lys Ser Tyr Lys Va - #l Arg Phe Asn Ser Val 835 - # 840 - # 845 - - Ser Ser Tyr Ser Asp Ser Arg Lys Ser Ser Gl - #y Asp Gly Pro Asp Leu 850 - # 855 - # 860 - - Arg Asp Asn Phe Glu Ser Thr Gly Pro Leu Al - #a Asn Val Arg Phe Ser 865 8 - #70 8 - #75 8 -#80 - - Val Phe Gly Leu Gly Ser Arg Ala Tyr Pro Hi - #s Phe Cys Ala PheGly 885 - # 890 - # 895 - - His Ala Val Asp Thr Leu Leu Glu Glu Leu Gl - #y Gly Glu Arg Ile Leu 900 - # 905 - # 910 - - Lys Met Arg Glu Gly Asp Glu Leu Cys Gly Gl - #n Glu Glu Ala Phe Arg 915 - # 920 - # 925 - - Thr Trp Ala Lys Lys Val Phe Lys Ala Ala Cy - #s Asp Val Phe Cys Val 930 - # 935 - # 940 - - Gly Asp Asp Val Asn Ile Glu Lys Pro Asn As - #n Ser Leu Ile Ser Asn 945 9 - #50 9 - #55 9 -#60 - - Asp Arg Ser Trp Lys Arg Asn Lys Phe Arg Le - #u Thr Tyr Val AlaGlu 965 - # 970 - # 975 - - Ala Pro Asp Leu Thr Gln Gly Leu Ser Asn Va - #l His Lys Lys Arg Val 980 - # 985 - # 990 - - Ser Ala Ala Arg Leu Leu Ser Arg Gln Asn Le - #u Gln Ser Pro Lys Phe 995 - # 1000 - # 1005 - - Ser Arg Ser Thr Ile Phe Val Arg Leu His Th - #r Asn Gly Asn Gln Glu 1010 - # 1015 - # 1020 - - Leu Gln Tyr Gln Pro Gly Asp His Leu Gly Va - #l Phe Pro Gly Asn His 025 1030 - # 1035 - # 1040 - - Glu Asp Leu Val Asn Ala Leu Ile Glu Arg Le - #u Glu Asp Ala Pro Pro 1045 - # 1050 - # 1055 - - Ala Asn His Val Val Lys Val Glu Met Leu Gl - #u Glu Arg Asn Thr Ala 1060 - # 1065 - # 1070 - - Leu Gly Val Ile Ser Asn Trp Lys Asp Glu Se - #r Arg Leu Pro Pro Cys 1075 - # 1080 - # 1085 - - Thr Ile Phe Gln Ala Phe Lys Tyr Tyr Leu As - #p Ile Thr Thr Pro Pro 1090 - # 1095 - # 1100 - - Thr Pro Leu Gln Leu Gln Gln Phe Ala Ser Le - #u Ala Thr Asn Glu Lys 105 1110 - # 1115 - # 1120 - - Glu Lys Gln Arg Leu Leu Val Leu Ser Lys Gl - #y Leu Gln Glu Tyr Glu 1125 - # 1130 - # 1135 - - Glu Trp Lys Trp Gly Lys Asn Pro Thr Met Va - #l Glu Val Leu Glu Glu 1140 - # 1145 - # 1150 - - Phe Pro Ser Ile Gln Met Pro Ala Thr Leu Le - #u Leu Thr Gln Leu Ser 1155 - # 1160 - # 1165 - - Leu Leu Gln Pro Arg Tyr Tyr Ser Ile Ser Se - #r Ser Pro Asp Met Tyr 1170 - # 1175 - # 1180 - - Pro Asp Glu Val His Leu Thr Val Ala Ile Va - #l Ser Tyr His Thr Arg 185 1190 - # 1195 - # 1200 - - Asp Gly Glu Gly Pro Val His His Gly Val Cy - #s Ser Ser Trp Leu Asn 1205 - # 1210 - # 1215 - - Arg Ile Gln Ala Asp Asp Val Val Pro Cys Ph - #e Val Arg Gly Ala Pro 1220 - # 1225 - # 1230 - - Ser Phe His Leu Pro Arg Asn Pro Gln Val Pr - #o Cys Ile Leu Val Gly 1235 - # 1240 - # 1245 - - Pro Gly Thr Gly Ile Ala Pro Phe Arg Ser Ph - #e Trp Gln Gln Arg Gln 1250 - # 1255 - # 1260 - - Phe Asp Ile Gln His Lys Gly Met Asn Pro Cy - #s Pro Met Val Leu Val 265 1270 - # 1275 - # 1280 - - Phe Gly Cys Arg Gln Ser Lys Ile Asp His Il - #e Tyr Arg Glu Glu Thr 1285 - # 1290 - # 1295 - - Leu Gln Ala Lys Asn Lys Gly Val Phe Arg Gl - #u Leu Tyr Thr Ala Tyr 1300 - # 1305 - # 1310 - - Ser Arg Glu Pro Asp Arg Pro Lys Lys Tyr Va - #l Gln Asp Val Leu Gln 1315 - # 1320 - # 1325 - - Glu Gln Leu Ala Glu Ser Val Tyr Arg Ala Le - #u Lys Glu Gln Gly Gly 1330 - # 1335 - # 1340 - - His Ile Tyr Val Cys Gly Asp Val Thr Met Al - #a Ala Asp Val Leu Lys 345 1350 - # 1355 - # 1360 - - Ala Ile Gln Arg Ile Met Thr Gln Gln Gly Ly - #s Leu Ser Glu Glu Asp 1365 - # 1370 - # 1375 - - Ala Gly Val Phe Ile Ser Arg Leu Arg Asp As - #p Asn Arg Tyr His Glu 1380 - # 1385 - # 1390 - - Asp Ile Phe Gly Val Thr Leu Arg Thr Tyr Gl - #u Val Thr Asn Arg Leu 1395 - # 1400 - # 1405 - - Arg Ser Glu Ser Ile Ala Phe Ile Glu Glu Se - #r Lys Lys Asp Ala Asp 1410 - # 1415 - # 1420 - - Glu Val Phe Ser Ser Pro 425 1430 - - - - (2) INFORMATION FOR SEQ ID NO:6: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 1554 amino - #acids (B) TYPE: amino acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: None - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:6: - - Met Glu Asp His Met Phe Gly Val Gln Gln Il - #e Gln Pro Asn Val Ile 1 5 - # 10 - # 15 - - Ser Val Arg Leu Phe Lys Arg Lys Val Gly Gl - #y Leu Gly Phe Leu Val 20 - # 25 - # 30 - - Lys Glu Arg Val Ser Lys Pro Pro Val Ile Il - #e Ser Asp Leu Ile Arg 35 - # 40 - # 45 - - Gly Gly Ala Ala Glu Gln Ser Gly Leu Ile Gl - #n Ala Gly Asp Ile Ile 50 - # 55 - # 60 - - Leu Ala Val Asn Gly Arg Pro Leu Val Asp Le - #u Ser Tyr Asp Ser Ala 65 - #70 - #75 - #80 - - Leu Glu Val Leu Arg Gly Ile Ala Ser Glu Th - #r His Val Val Leu Ile 85 - # 90 - # 95 - - Leu Arg Gly Pro Glu Gly Phe Thr Thr His Le - #u Glu Thr Thr Phe Thr 100 - # 105 - # 110 - - Gly Asp Gly Thr Pro Lys Thr Ile Arg Val Th - #r Gln Pro Leu Gly Pro 115 - # 120 - # 125 - - Pro Thr Lys Ala Val Asp Leu Ser His Gln Pr - #o Pro Ala Gly Lys Glu 130 - # 135 - # 140 - - Gln Pro Leu Ala Val Asp Gly Ala Ser Gly Pr - #o Gly Asn Gly Pro Gln 145 1 - #50 1 - #55 1 -#60 - - His Ala Tyr Asp Asp Gly Gln Glu Ala Gly Se - #r Leu Pro His AlaAsn 165 - # 170 - # 175 - - Gly Leu Ala Pro Arg Pro Pro Gly Gln Asp Pr - #o Ala Lys Lys Ala Thr 180 - # 185 - # 190 - - Arg Val Ser Leu Gln Gly Arg Gly Glu Asn As - #n Glu Leu Leu Lys Glu 195 - # 200 - # 205 - - Ile Glu Pro Val Leu Ser Leu Leu Thr Ser Gl - #y Ser Arg Gly Val Lys 210 - # 215 - # 220 - - Gly Gly Ala Pro Ala Lys Ala Glu Met Lys As - #p Met Gly Ile Gln Val 225 2 - #30 2 - #35 2 -#40 - - Asp Arg Asp Leu Asp Gly Lys Ser His Lys Pr - #o Leu Pro Leu GlyVal 245 - # 250 - # 255 - - Glu Asn Asp Arg Val Phe Asn Asp Leu Trp Gl - #y Lys Gly Asn Val Pro 260 - # 265 - # 270 - - Val Val Leu Asn Asn Pro Tyr Ser Glu Lys Gl - #u Gln Pro Pro Thr Ser 275 - # 280 - # 285 - - Gly Lys Gln Ser Pro Thr Lys Asn Gly Ser Pr - #o Ser Lys Cys Pro Arg 290 - # 295 - # 300 - - Phe Leu Lys Val Lys Asn Trp Glu Thr Glu Va - #l Val Leu Thr Asp Thr 305 3 - #10 3 - #15 3 -#20 - - Leu His Leu Lys Ser Thr Leu Glu Thr Gly Cy - #s Thr Glu Tyr IleCys 325 - # 330 - # 335 - - Met Gly Ser Ile Met His Pro Ser Gln His Al - #a Arg Arg Pro Glu Asp 340 - # 345 - # 350 - - Val Arg Thr Lys Gly Gln Leu Phe Pro Leu Al - #a Lys Glu Phe Ile Asp 355 - # 360 - # 365 - - Gln Tyr Tyr Ser Ser Ile Lys Arg Phe Gly Se - #r Lys Ala His Met Glu 370 - # 375 - # 380 - - Arg Leu Glu Glu Val Asn Lys Glu Ile Asp Th - #r Thr Ser Thr Tyr Gln 385 3 - #90 3 - #95 4 -#00 - - Leu Lys Asp Thr Glu Leu Ile Tyr Gly Ala Ly - #s His Ala Trp ArgAsn 405 - # 410 - # 415 - - Ala Ser Arg Cys Val Gly Arg Ile Gln Trp Se - #r Lys Leu Gln Val Phe 420 - # 425 - # 430 - - Asp Ala Arg Asp Cys Thr Thr Ala His Gly Me - #t Phe Asn Tyr Ile Cys 435 - # 440 - # 445 - - Asn His Val Lys Tyr Ala Thr Asn Lys Gly As - #n Leu Arg Ser Ala Ile 450 - # 455 - # 460 - - Thr Ile Phe Pro Gln Arg Thr Asp Gly Lys Hi - #s Asp Phe Arg Val Trp 465 4 - #70 4 - #75 4 -#80 - - Asn Ser Gln Leu Ile Arg Tyr Ala Gly Tyr Ly - #s Gln Pro Asp GlySer 485 - # 490 - # 495 - - Thr Leu Gly Asp Pro Ala Asn Val Gln Phe Th - #r Glu Ile Cys Ile Gln 500 - # 505 - # 510 - - Gln Gly Trp Lys Pro Pro Arg Gly Arg Phe As - #p Val Leu Pro Leu Leu 515 - # 520 - # 525 - - Leu Gln Ala Asn Gly Asn Asp Pro Glu Leu Ph - #e Gln Ile Pro Pro Glu 530 - # 535 - # 540 - - Leu Val Leu Glu Val Pro Ile Arg His Pro Ly - #s Phe Glu Trp Phe Lys 545 5 - #50 5 - #55 5 -#60 - - Asp Leu Gly Leu Lys Trp Tyr Gly Leu Pro Al - #a Val Ser Asn MetLeu 565 - # 570 - # 575 - - Leu Glu Ile Gly Gly Leu Glu Phe Ser Ala Cy - #s Pro Phe Ser Gly Trp 580 - # 585 - # 590 - - Tyr Met Gly Thr Glu Ile Gly Val Arg Asp Ty - #r Cys Asp Asn Ser Arg 595 - # 600 - # 605 - - Tyr Asn Ile Leu Glu Glu Val Ala Lys Lys Me - #t Asn Leu Asp Met Arg 610 - # 615 - # 620 - - Lys Thr Ser Ser Leu Trp Lys Asp Gln Ala Le - #u Val Glu Ile Asn Ile 625 6 - #30 6 - #35 6 -#40 - - Ala Val Leu Tyr Ser Phe Gln Ser Asp Lys Va - #l Thr Ile Val AspHis 645 - # 650 - # 655 - - His Ser Ala Thr Glu Ser Phe Ile Lys His Me - #t Glu Asn Glu Tyr Arg 660 - # 665 - # 670 - - Cys Arg Gly Gly Cys Pro Ala Asp Trp Val Tr - #p Ile Val Pro Pro Met 675 - # 680 - # 685 - - Ser Gly Ser Ile Thr Pro Val Phe His Gln Gl - #u Met Leu Asn Tyr Arg 690 - # 695 - # 700 - - Leu Thr Pro Ser Phe Glu Tyr Gln Pro Asp Pr - #o Trp Asn Thr His Val 705 7 - #10 7 - #15 7 -#20 - - Trp Lys Gly Thr Asn Gly Thr Pro Thr Lys Ar - #g Arg Ala Ile GlyPhe 725 - # 730 - # 735 - - Lys Lys Leu Ala Glu Ala Val Lys Phe Ser Al - #a Lys Leu Met Gly Gln 740 - # 745 - # 750 - - Ala Met Ala Lys Arg Val Lys Ala Thr Ile Le - #u Tyr Ala Thr Glu Thr 755 - # 760 - # 765 - - Gly Lys Ser Gln Ala Tyr Ala Lys Thr Leu Cy - #s Glu Ile Phe Lys His 770 - # 775 - # 780 - - Ala Phe Asp Ala Lys Val Met Ser Met Glu Gl - #u Tyr Asp Ile Val His 785 7 - #90 7 - #95 8 -#00 - - Leu Glu His Glu Thr Leu Val Leu Val Val Th - #r Ser Thr Phe GlyAsn 805 - # 810 - # 815 - - Gly Asp Pro Pro Glu Asn Gly Glu Lys Phe Gl - #y Cys Ala Leu Met Glu 820 - # 825 - # 830 - - Met Arg His Pro Asn Ser Val Gln Glu Glu Ar - #g Lys Ser Tyr Lys Val 835 - # 840 - # 845 - - Arg Phe Asn Ser Val Ser Ser Tyr Ser Asp Se - #r Gln Lys Ser Ser Gly 850 - # 855 - # 860 - - Asp Gly Pro Asp Leu Arg Asp Asn Phe Glu Se - #r Ala Gly Pro Leu Ala 865 8 - #70 8 - #75 8 -#80 - - Asn Val Arg Phe Ser Val Phe Gly Leu Gly Se - #r Arg Ala Tyr ProHis 885 - # 890 - # 895 - - Phe Cys Ala Phe Gly His Ala Val Asp Thr Le - #u Leu Glu Glu Leu Gly 900 - # 905 - # 910 - - Gly Glu Arg Ile Leu Lys Met Arg Glu Gly As - #p Glu Leu Cys Gly Gln 915 - # 920 - # 925 - - Glu Glu Ala Phe Arg Thr Trp Ala Lys Lys Va - #l Phe Lys Ala Ala Cys 930 - # 935 - # 940 - - Asp Val Phe Cys Val Gly Asp Asp Val Asn Il - #e Glu Lys Ala Asn Asn 945 9 - #50 9 - #55 9 -#60 - - Ser Leu Ile Ser Asn Asp Arg Ser Trp Lys Ar - #g Asn Lys Phe ArgLeu 965 - # 970 - # 975 - - Thr Phe Val Ala Glu Ala Pro Glu Leu Thr Gl - #n Gly Leu Ser Asn Val 980 - # 985 - # 990 - - His Lys Lys Arg Val Ser Ala Ala Arg Leu Le - #u Ser Arg Gln Asn Leu 995 - # 1000 - # 1005 - - Gln Ser Pro Lys Ser Ser Arg Ser Thr Ile Ph - #e Val Arg Leu His Thr 1010 - # 1015 - # 1020 - - Asn Gly Ser Gln Glu Leu Gln Tyr Gln Pro Gl - #y Asp His Leu Gly Val 025 1030 - # 1035 - # 1040 - - Phe Pro Gly Asn His Glu Asp Leu Val Asn Al - #a Leu Ile Glu Arg Leu 1045 - # 1050 - # 1055 - - Glu Asp Ala Pro Pro Val Asn Gln Met Val Ly - #s Val Glu Leu Leu Glu 1060 - # 1065 - # 1070 - - Glu Arg Asn Thr Ala Leu Gly Val Ile Ser As - #n Trp Thr Asp Glu Leu 1075 - # 1080 - # 1085 - - Arg Leu Pro Pro Cys Thr Ile Phe Gln Ala Ph - #e Lys Tyr Tyr Leu Asp 1090 - # 1095 - # 1100 - - Ile Thr Thr Pro Pro Thr Pro Leu Gln Leu Gl - #n Gln Phe Ala Ser Leu 105 1110 - # 1115 - # 1120 - - Ala Thr Ser Glu Lys Glu Lys Gln Arg Leu Le - #u Val Leu Ser Lys Gly 1125 - # 1130 - # 1135 - - Leu Gln Glu Tyr Glu Glu Trp Lys Trp Gly Ly - #s Asn Pro Thr Ile Val 1140 - # 1145 - # 1150 - - Glu Val Leu Glu Glu Phe Pro Ser Ile Gln Me - #t Pro Ala Thr Leu Leu 1155 - # 1160 - # 1165 - - Leu Thr Gln Leu Ser Leu Leu Gln Pro Arg Ty - #r Tyr Ser Ile Ser Ser 1170 - # 1175 - # 1180 - - Ser Pro Asp Met Tyr Pro Asp Glu Val His Le - #u Thr Val Ala Ile Val 185 1190 - # 1195 - # 1200 - - Ser Tyr Arg Thr Arg Asp Gly Glu Gly Pro Il - #e His His Gly Val Cys 1205 - # 1210 - # 1215 - - Ser Ser Trp Leu Asn Arg Ile Gln Ala Asp Gl - #u Leu Val Pro Cys Phe 1220 - # 1225 - # 1230 - - Val Arg Gly Ala Pro Ser Phe His Leu Pro Ar - #g Asn Pro Gln Val Pro 1235 - # 1240 - # 1245 - - Cys Ile Leu Val Gly Pro Gly Thr Gly Ile Al - #a Pro Phe Arg Ser Phe 1250 - # 1255 - # 1260 - - Trp Gln Gln Arg Gln Phe Asp Ile Gln His Ly - #s Gly Met Asn Pro Cys 265 1270 - # 1275 - # 1280 - - Pro Met Val Leu Val Phe Gly Cys Arg Gln Se - #r Lys Ile Asp His Ile 1285 - # 1290 - # 1295 - - Tyr Arg Glu Glu Thr Leu Gln Ala Lys Asn Ly - #s Gly Val Phe Arg Glu 1300 - # 1305 - # 1310 - - Leu Tyr Thr Ala Tyr Ser Arg Glu Pro Asp Ly - #s Pro Lys Lys Tyr Val 1315 - # 1320 - # 1325 - - Gln Asp Ile Leu Gln Glu Gln Leu Ala Glu Se - #r Val Tyr Arg Ala Leu 1330 - # 1335 - # 1340 - - Lys Glu Gln Gly Gly His Ile Tyr Val Cys Gl - #y Asp Val Thr Met Ala 345 1350 - # 1355 - # 1360 - - Ala Asp Val Leu Lys Ala Ile Gln Arg Ile Me - #t Thr Gln Gln Gly Lys 1365 - # 1370 - # 1375 - - Leu Ser Ala Glu Asp Ala Gly Val Phe Ile Se - #r Arg Met Arg Asp Asp 1380 - # 1385 - # 1390 - - Asn Arg Tyr His Glu Asp Ile Phe Gly Val Th - #r Leu Arg Thr Tyr Glu 1395 - # 1400 - # 1405 - - Val Thr Asn Arg Leu Arg Ser Glu Ser Ile Al - #a Phe Ile Glu Glu Ser 1410 - # 1415 - # 1420 - - Lys Lys Asp Thr Asp Glu Gly Phe Gln Leu Le - #u Thr Gly Pro Ser Cys 425 1430 - # 1435 - # 1440 - - Pro Ala Gly Cys Lys Phe Cys Lys Arg Gly Gl - #n Thr Leu Leu Asn Leu 1445 - # 1450 - # 1455 - - Ser Ser Gly Thr Pro Cys Gly Pro Arg Ser Al - #a Ser Cys Pro Cys Arg 1460 - # 1465 - # 1470 - - Cys Ala Leu Val Ser Leu Leu Gly Leu Leu Al - #a Pro Gln Trp Phe Pro 1475 - # 1480 - # 1485 - - Arg Pro Ser Trp Val Tyr Ser Leu Ser Phe Pr - #o Ala Ala Met Gln Cys 1490 - # 1495 - # 1500 - - Phe Ser Asn Leu Gln Trp Leu Leu Gln Asn Se - #r Val Pro Thr Pro Ser 505 1510 - # 1515 - # 1520 - - Leu Ala Asp Lys Gly Asn Ser Arg Val His Gl - #u Thr Thr Gly Thr Trp 1525 - # 1530 - # 1535 - - Pro Ser Leu Trp Gly Phe Phe Ser Leu Gly Ph - #e Pro Trp Lys Gly Cys 1540 - # 1545 - # 1550 - - Arg Asn - - - - (2) INFORMATION FOR SEQ ID NO:7: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 30 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:7: - - GACTAGTCGA CTGAAGAGAA CACGTTTGGG - # - # 30 - - - - (2) INFORMATION FOR SEQ ID NO:8: - - (i) SEQUENCE CHARACTERISTICS: (A) LENGTH: 31 base - #pairs (B) TYPE: nucleic acid (C) STRANDEDNESS: single (D) TOPOLOGY: linear - - (ii) MOLECULE TYPE: cDNA - - (xi) SEQUENCE DESCRIPTION: SEQ ID NO:8: - - TCTGCAGATC TCAGTGGGCC TTGGAGCCAA A - # - # 31__________________________________________________________________________

CAPON: a protein associated with neuronal nitric oxide synthase

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Non-Patent Literature Citations (3)

Entry
Jaffrey et al. "PIN: An Associated Protein Inhibitor of Neuronal Nitric Oxide Synthase" Science vol. 274, Nov. 1, 1996, pp. 774-777.
Brenman et al. "Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alphal-syntrophin mediated ny PDZ domains" Cell, vol. 84, Mar. 8, 1996, pp. 757-767.
Samie R. Jaffrey et al. "CAPON: A Protein Asociated with Neuronal Nitric Oxide Synthase that Regulates its Interactions with PSD95" Neuron, vol. 20, 115-124 Jan. 1998.