WO2002002600A2 - HUMAN G PROTEIN-COUPLED RECEPTOR IGPcR27, AND USES THEROF - Google Patents

Abstract

A novel human G protein-coupled receptor (GPcR) protein, IGPcR27, is identified and characterized. IGPcR27-encoding nucleotides, IGPcR27 proteins and fusion proteins, antibodies to the receptor, host cell expression systems, animal models in which the IGPcR27 gene is mutated, recombinant knock-out animals that do not express IGPcR27 and transgenic animals that express an IGPcR27 transgene are encompassed by the invention, as are compounds that modulate gene expression or receptor activity of IGPcR27 and their use for drug screening, and diagnosis or treatment of diseases and disorders, particularly central nervous system disorders.

Description

Human G protein-coupled receptor IGPcR27, and uses thereof

Field of the Invention

The present invention relates to the field of cellular and molecular biology, protein biochemistry, and pharmacology. The invention relates particularly to the identification of the polynucleotide sequence of a novel G protein-coupled receptor (GPcR) and the characterization of nucleic acids that encode this G protein-coupled receptor, which is referred to herein as IGPcR27. The invention further relates to animal orthologs of the human gene encoding IGPcR27, to expression of both human and animal proteins, to the function of the gene product and to uses for the receptor, and its ligands in drug screening and in diagnosing, preventing and treating disease, particularly dysfunctions associated with signal processing in the central nervous system (CNS). Animal models of such diseases and dysfunctions, in which the IGPcR27 gene is mutated, knocked-out or present in the form of a transgene, are also incorporated within the invention.

Background of the Invention

It is well established that many medically significant biological processes are mediated by proteins that participate in signal transduction pathways involving G proteins and second messengers; e.g. cAMP, diacylglycerol and inositol phosphates (Lefkowitz, 1991, Nature, 351:353-354). Herein these proteins are referred to as proteins participating in pathways with G protein-coupled receptors, either as the receptors themselves, such as those for adrenergic agents and dopamine (Kobilka,

BK, et al, 1987, P.N.A.S., USA, 84:46-50; Kobilka BK et al, 1987, Science, 238:650-656; Bunzow JR, et al, 1988, Nature, 336:783-787), or as the G proteins to which the receptors are coupled, or as effector proteins, e.g. adenylate cyclase, protein kinase A and protein kinase C (Simon MI, et al., 1991, Science, 252:802- 808).

Upon hormone binding to a GPcR the receptor interacts with the heterotrimeric G protein and induces the dissociation of GDP from the guanine nucleotide-binding site. At normal cellular concentrations of guanine nucleotides, GTP fills the site immediately. Binding of GTP to the alpha subunit of the G protein causes the dissociation of the G protein from the receptor and the dissociation of the G protein into alpha and beta-gamma subunits. The GTP -carrying form then binds to the generator of an intracellular second messenger: in one common form of signal transduction, activated adenylate cyclase. Hydrolysis of GTP to GDP, catalyzed by the intrinsic GTPase activity of the G protein alpha subunit, returns the G protein to its basal, inactive form. The GTPase activity of the alpha subunit determines the time period during which the G protein is active. The GDP-bound form of the alpha subunit (alpha. GDP) has high affinity for the beta- gamma subunit complex and subsequent re-association of G protein subunits alpha.GDP with beta-gamma returns the G protein to the basal state. Thus the G-protein serves a dual role: as an intermediate that relays the signal from receptor to effector (in this example adenylate cyclase), and as a timer that controls the duration of the signal.

Examples of members of the G protein-coupled receptor family gene family include acetylcholine, adenosine, adrenergic, bradykinin, cAMP, calcitonin, capsaicic, CCK, CGRP, CRF, cytomegalovirus, dopamine, endothelial differentiation gene-1, endothelin, FSH, galanin, histamine, kinin, motilin, muscarinic, neurokinin, neuropeptideY, neurotensin, nociceptin, odorant, opsin, rhodopsin, serotonin, somatostatin, thrombin, TSH and VIP receptors. Alteration of GPcR genes and gene products can cause medical disorders, dysfunctions, or diseases hereafter generally referred to as "diseases". The mechanism of disease may be due to a loss of receptor function or by constitutive receptor activation (reviewed by Coughlin et al, 1994,

Curr. Opin. Cell Biol., 6:191-197). For example, activating mutations of rhodopsin receptor have been found in retinitis pigmentosa and congenital night blindness (Rao et al, 1994, Nature 367:639-642); mutations of TSH receptor have been detected in sporadic and inherited hyperthyroidism (Parma et al, 1993, Nature 365:649-651) and nephrogenic diabetes insipidus (Holtzman et al, 1993, Hum. Mol. Genet. 2:1201- 1204); mis-sense mutations in the luteinizing hormone receptor (LHR) gene, leading to constitutive activation of the LHR, have been shown to be associated with a condition in boys called familial male-limited precocious puberty (Cocco et al, 1996, Hum. Mut, 7:164-166; Kosugi et al, 1995, Hum. Mol. Genet, 4:183-188). Moreover, dopamine receptors are known to bind neuroieptic drugs used for treating CNS disorders.

As a characteristic feature, G protein-coupled receptors exhibit seven transmembrane domains which are connected by three hydrophilic extracellular loops alternating with three intracellular loops. Most G protein-coupled receptors have single conserved cysteine residues in each of the first two extracellular loops which form disulfide bonds that are believed to stabilize functional protein structure. The seven transmembrane domains or regions are designated as TM1, TM2, TM3, TM4, TM5, TM6 and TM7. The cytoplasmic loop which connects TM5 and TM6 may be a mayor component of the G protein binding domain.

Most G protein-coupled receptors contain potential phosphorylation sites within the third cytoplasmic loop and/or the carboxyl terminus. For several GPcRs, such as the beta-adrenergic receptor, phosphorylation by protein kinase A and/or specific receptor kinases mediates receptor desensitization.

It has also been shown that certain G protein-coupled receptors, e.g. the calcitonin receptor-like receptor, might interact with small single pass membrane proteins called receptor-activity-modifying-proteins (RAMPs). This interaction of the GPcR with a certain RAMP determines which natural ligands have relevant affinity for the GPcR-RAMP combination and regulate the functional signaling activity of the complex (McLathie LM, etal, 1998, Nature, 393:333-339). For some receptors, the ligand binding sites of the G protein-coupled receptors are believed to comprise hydrophilic sockets formed by several GPcR transmembrane domains, said sockets being surrounded by hydrophobic residues of the G protein- coupled receptors. The hydrophilic side of each GPcR transmembrane helix is thought to face inward and form a polar ligand-binding site. TM3 has been implicated in several G protein-coupled receptors as having a ligand-binding site, such as the TM3 aspartate residues. TM5 serine residues, and TM6 asparagine and TM6 or TM7 phenylalanine or tyrosine residues are also implicated in ligand binding. G-protein coupled receptors bind to a variety of ligands ranging from small biogens to peptides, small proteins and large glycoproteins (Strader CD, et al , 1994, Annu. Rev. Biochem., 63:101-132).

G protein-coupled receptors can be coupled intracellulularly by heterotrimeric G proteins to various intracellular enzymes, ion channels and transporters (see Johnson et al, 1989, Endoc. Rev., 10:317-331). Different G protein alpha-subunits preferentially stimulate particular effectors to modulate various biological functions in a cell. Phosphorylation of cytoplasmic residues of G protein-coupled receptors has been identified as an important mechanism for the regulation of G protein coupling of some G protein-coupled receptors. G protein-coupled receptors are found in numerous sites within animal, and particularly mammalian hosts.

Evolutionary analyses suggest that the ancestor of G protein-coupled receptors originally developed in concert with complex body plans and nervous systems. With the exception of the visual opsins, the genes for the GPcR family have, in most instances, been characterized by a lack of introns within their coding sequences thus precluding the generation of receptor diversity through alternative splicing. Recent data support the idea that dimerization of G protein-coupled receptors is important in different aspects of receptor biogenesis and function. When considering, for example, the nervous system, the existence of homodimers and heterodimers of neurotransmitter G protein-coupled receptors offers an attractive explanation of the great diversity and plasticity that is characteristic of such a highly organized and complex system (see Bouvier M, 2001, Nature Rev. Neuroscience, 2:274-286).

In order to understand the role of particular G protein-coupled receptors in normal physiology and disease, knock-out mice have been generated in which the endogenous genes encoding these receptors have been individually targeted. Studies of mas-protooncogene knock-out mice indicate that this GPcR is a determinant of heart rate and blood pressure variability (Walther et al, 2000, Braz J, Med. Biol. Res., 33:1-9). Male mice showed increased anxiety, indicating a function for mas, which is an angiotensin receptor acting in the central nervous system (CNS) (Walther et al, 1998, J. Biol. Chem., 273:11867-11873). Incerti et al, (2000, Hum. Molec. Genet., 9:2871-2788) generated and characterized mice deficient in Oal (ocular albinism)-deficient mice by gene targeting. Ophthalmologic examination showed hypo-pigmentation of the ocular fundus in mutant animals compared with wildtype. Also demonstrated was a misrouting of the optic fibers at the chiasm and the presence of giant melanosomes in retinal pigment epithelium, as observed in OA1 patients. Prostaglandin E2 receptor knockout mice show a mild change in renal water handling, while EP2 receptor knock-out mice display salt-sensitive hypertension (Breyer et al, 2000, Curr. Opin. Nephrol. Hypertens., 9:23-29).

Based on malfunctions discovered in signaling pathways several drugs have been developed, for example, a compound that blocks the farnesylation of ras as a tumor inhibitor, a JAK-2 blocker as an inhibitor of recurrent pre-B cell acute lymphoblastic leukemia, and a platelet-derived growth factor receptor kinase as a blocker of restenosis (Reviewed in Levitzki A, 1996, Curr. Opin. Cell Biol, 8:239-244). G protein-coupled receptors have been identified and successfully used as targets for several existing drugs; for example, dopamine and serotonin G protein-coupled receptors have been targeted for CNS diseases, angiotensin, muscarinic and adrenergic receptor G protein-coupled receptors have been targeted for cardiovascular diseases, mstaminic G protein-coupled receptors have been targeted for respiratory diseases, the prostaglandin GPcR has been targeted for opthalmic purposes, and calcitonin and estrogen for treatment of arthritis.

On May 08, 2001 a GPR61 mRNA sequence was released from NCBI (Accession No. NM_031936; 1254bp mRNA), exhibiting high homology to human IGPcR27. The gene is described by Lee DK et al. (2001, Molecular Brain Research, 86: 13-22) indicating expression in brain. This published cDNA sequence of 1254bp, listed at NCBI, only partially describes the full-length cDNA, for a frameshift in the published sequence at coding position 1242 creates a premature stop codon, compared to the 1353bp IGPcR27 full-length cDNA, which was confirmed during the course of defining the present invention by several sequencing approaches of isolated genomic DNA and cDNA created in our laboratory. In addition, several base exchanges have been recognized in the cDNA sequences published by NCBI and by Lee et al. In the NCBI nucleotide database, a reference to human genomic sequence AF317652 is given, showing 100% identity between the 1254bp GPR61 mRNA and AF317652 sequences, including position 1242 of the potential open reading frame. This 1254bp sequence stretch within the AF317652 genomic DNA sequence is not confirmed by other, overlapping genomic sequences, as represented in AC01 1780 and AL355145. In contrast, both, AC01 1780 and AL355145, exhibit 100% sequence identity to the 1353 bp full-length cDNA of IGPcR27, described herein, delivering evidence for a 1353bp full-length cDNA encoding a particular human GPcR, described herein the first time. We note that errors in the AF317652 sequence were repeated in the results published for GPR61, including the premature stop codon and truncation of the corresponding peptide sequence.

The following information relating to CNS function is provided in relation to the particular human G protein-coupled receptor, and its animal orthologs, that are disclosed by the present invention. The cerebral cortex of the brain is divided into four distinct sections, the lobes, which are associated with distinct functions: the frontal lobe includes the motor area and is also connected to thinking, planning and spoken language. The parietal lobe includes the somatosensory area. The temporal lobe is active in the processes involved in understanding language and it contains the auditory area. The occipital lobe includes the area responsible for vision. It is not known how the cerebral cortex processes or stores the innumerable sensory stimuli and perceptions that it receives and is able to mark them as memories that can subsequently be recalled from storage, but it is generally agreed that the large association areas of the cerebral cortex are the location of stored memories (reviewed by Duus P, 1998, "Topical Diagnosis in Neurology", 3^rd edition, Thieme).

Because of the vital role of G protein-coupled receptors in the communication between cells and their environment, such receptors are attractive targets for therapeutic intervention. G protein-coupled receptors have led to more than half of the currently known drugs (Drews, Nature Biotechnology, 1996, 14: 1516). Mechanistically, approximately 50%o to 60%> of all clinically relevant drugs act by modulating the functions of various G protein-coupled receptors, as either agonist (activating activity) or antagonist (blocking activity) of a GPcR (Cudermann et al. , 1995, J. Mol. Med., 73:51-63). This indicates that these receptors have an established, proven history as therapeutic targets.

In consequence, there is a continuing medical need for identification and characterization of further receptors that can play a role in diagnosis, preventing, ameliorating or correcting dysfunctions, disorders, and diseases. Included among such diseases are a broad range of psychiatric and CNS disorders, including learning and memory dysfunctions.

Summary of the Invention

The G protein-coupled receptor of the present invention, IGPcR27, is especially useful for diagnosis, prevention, amelioration or correction of diseases associated with signal processing in the central nervous system (CNS). In particular, IGPcR27 satisfies a need in the art for identification and characterization of further receptors that can play an important role in diagnosis, prevention, amelioration or correction of psychiatric and central nervous system dysfunctions, diseases and disorders, especially movement dysfunctions, disorders or diseases, such as tics, tremor, Tourette's syndrome, Parkinson's disease, Huntington's disease, dyskinesias, dystonia, pain and spasms.

Embodiments of the invention include an isolated nucleic acid molecule, wherein said nucleic acid molecule comprises the nucleotide sequence of SEQ ID NO:l, or any unique fragment thereof, particularly wherein the nucleotide sequence of the fragment is greater than ten base pairs in length. Embodiments also include an isolated polynucleotide which encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:2, or any unique fragment thereof, particularly wherein the amino acid sequence of the fragment is greater than ten amino acids in length. Embodiments of the invention include any isolated nucleic acid molecule or polynucleotide comprising an allelic variant of a nucleotide sequence or polynucleotide which encodes a polypeptide comprising the amino acid sequence of

SEQ ID NO:2, wherein said allelic variant retains at least 70% nucleic acid homology, or in increasing preference at least 80%, 85%, 90%, 95% or 98% nucleic acid homology and hybridizes to the complement of SEQ ID NO:l under stringent conditions (Ausubel FM et al, eds., 1989, Current Protocols in Molecular Biology, Vol. I, Green Publishing Associates, Inc., and John Wiley & sons, Inc., New York): also included are such isolated nucleic acid molecules or polynucleotides that comprise a nucleotide sequence which encodes at least one of the group of polypeptides, peptides and fusion proteins, comprising an amino acid sequence at least 70%) similar, or in increasing preference at least 75%, 80%>, 85%), 90%, 95% or 98% similar, to SEQ ID NO:2.

Vectors comprising an isolated nucleic acid molecule or polynucleotide of the invention as previously described are a further embodiment of the invention.

Additional embodiments include host cells genetically engineered to contain such a vector or genetically engineered to contain such a nucleic acid molecule or polynucleotide of the invention as described above, and particularly wherein the nucleic acid molecule or polynucleotide of the invention is operatively linked with a nucleotide regulatory sequence that controls expression of said nucleic acid molecule or polynucleotide in the host cell. Also included are host cells which are drawn from prokaryotic bacterial cells, or from eukaryotic cells, particularly or yeast, insect or mammalian cells, preferred embodiments employing a mammalian host cell being those in which the host cell is a CHO, BHK, COS, CV1, 293, fibroblast or VERO cell. Embryonic stem cells containing a disrupted endogenous IGPcR27 gene are also preferred embodiments of the invention, the most preferred embryonic stem cells being derived from mice.

Preferred embodiments of the invention include antibodies to the IGPcR27 protein, polypeptides, peptides, isolated domains and fusion proteins.

Agonists and antagonists of IGPcR27 are preferred embodiments of the invention, including: (a) 'small molecules' of molecular mass less than 6 kDa; (b) molecules of intermediate size, having molecular mass between 5 kDa to 15 kDa; and (c) large molecules of molecular mass greater than 12 kDa; the latter including mutant natural IGPcR27 ligand proteins that compete with native natural !GPcR27 ligand and which modulate lGPcR27 gene expression or gene product activity. Preferred embodiments of the invention are those wherein such molecules bind specifically to the IGPcR27 receptor or to the IGPcR27 gene. Further embodiments are methods of identifying such compounds which modulate the activity of the IGPcR27 receptor or of IGPcR27 gene expression, such as anti-sense and ribozyme molecules that can be used to inhibit IGPcR27 gene expression, or expression constructs that are capable of enhancing IGPcR27 gene expression.

The non-human animal orthologs of the human sequence in SEQ ID NO.T are preferred embodiments of the invention, particularly ungulate and rodent sequences, and especially those of rat and mouse, and also polynucleotides comprising these sequences or homologous or partially homologous sequences as indicated for the human nucleic acid and polynucleotide. Preferred embodiments include polynucleotides of such non-human animal orthologs comprising a nucleotide sequence which encodes a polypeptide comprising an amino acid sequence at least 70% similar, or in increasing preference at least 75%, 80%, 85%, 90%, 95% or 98% similar, to SEQ ID NO:2; or being at least ten amino acid residues in length and bearing the stated similarity to a unique part of SEQ ID NO:2.

Embodiments of the invention include knock-out animals which are non-human animals and which do not express IGPcR27. Preferred embodiments are those wherein the endogenous animal ortholog is functionally disrupted by homologous recombination methods such as conditional knock-out and/or null allele knock-out of the IGPcR27 gene. Mutated animals that express a non-functional or partially functional form of IGPcR27 are further embodiments of the invention. Embodiments of the invention also include progeny of the non-human animals described as being embodiments of the invention, the term 'progeny' including both heterozygous and homozygous offspring. Further embodiments are non-human transgenic animal models expressing the human IGPcR27 cDNA sequence as shown in SEQ ID NO:l or a modification thereof as described above, operatively linked to a nucleotide regulatory sequence that controls expression of the nucleic acid molecule in the host animal. Particularly preferred embodiments are those non-human animals

(also termed animal models) in which the human IGPcR27 is encoded by a nucleic acid sequence which is homozygous in the animal model. In each embodiment of the invention comprising a non-human animal, preferable embodiments are those wherein the non-human animal is a mammal, particularly ungulate or rodent, and preferably wherein the non-human animal is from a genus selected from the group consisting of Mus (e.g., mice), Rattus (e.g., rats), Oryctologus (e.g., rabbits) and Mesocricetus (e.g., hamsters), mouse being the most preferable of this group.

Embodiments of the invention include primary cells and cell lines derived from any of the non-human animals of the invention, particularly the non-human transgenic animal models of the invention. Further embodiments include the amino acid sequence of those non-human animal orthologs of IGPcR27 that comprise an amino acid sequence at least 70% similar, or in increasing preference at least 75%, 80%, 85%, 90%, 95% or 98% similar, to the sequence of the mouse ortholog provided (SEQ ID NO:8); or a part of said non-human animal sequence which is at least ten amino acid residues in length and bears the stated similarity to a unique part of SEQ

ID NO:8.

The use of the non-human animal or animal model of the invention, as described above, for the dissection of the molecular mechanisms of the IGPcR27 pathway, for the identification and cloning of genes able to modify, reduce or inhibit the phenotype associated with IGPcR27 activity or deficiency, constitutes a further embodiment of the invention, as does the use of such non-human animal or animal model for the identification of gene and protein diagnostic markers for diseases, for the identification and testing of compounds useful in the prevention or treatment of symptoms associated with IGPcR27 activity or deficiency, in particular but not limited to central nervous system disorders, including neurologic, psychiatric and behavioral disorders, metabolic disorders, visual and olfactory disorders, and especially in the case of IGPcR27, movement dysfunctions, disorders or diseases, such as tics, tremor, Tourette's syndrome, Parkinson's disease, Huntington's disease, dyskinesias, dystonia, pain and spasms.

Additional embodiments of the invention include methods of identifying compounds suitable for modulating the activity of the protein or polypeptide of the invention, as described above, for treatment of diseases characterized by aberrant expression or activity of IGPcR27. Preferred embodiments include methods of prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27, by the administration of compounds that bind specifically to the IGPcR27 gene or protein and/or which modulate IGPcR27 expression or IGPcR27 activity; the compounds that that bind specifically to the IGPcR27 gene or protein and/or which modulate IGPcR27 expression or IGPcR27 activity for the prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27; and the use of compounds that that bind specifically to the IGPcR27 gene or protein and/or which modulate IGPcR27 expression or IGPcR27 activity for prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27. Further preferred embodiments are gene therapy methods of prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27, by the administration of vectors and/or host cells containing nucleotide sequences according to any of claims 1 to 7, that modulate IGPcR27 expression or IGPcR27 activity; the vectors and or host cells containing nucleotide sequences according to any of claims 1 to 7 which modulate IGPcR27 expression or IGPcR27 activity for the prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27 and the use of vectors and/or host cells containing nucleotide sequences according to any of claims 1 to 7 which modulate IGPcR27 expression or IGPcR27 activity for prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27.

Brief Description of the Figures

Figure 1 : Fig. 1 depicts the full-length coding DNA (cDNA) sequence of the human IGPcR27 gene (SEQ ID NO: 1).

Figure 2: Fig. 2 depicts the amino acid sequence of the human IGPcR27 protein (SEQ ID NO:2).

Figure 3: Fig. 3 depicts the full-length coding DNA (cDNA) sequence of the mouse IGPcR27 gene (SEQ ID NO:5)

Figure 4: Fig. 4 depicts the amino acid sequence of the mouse IGPcR27 protein (SEQ ID NO:6)

Figure 5: Fig. 5 depicts a comparison of the amino acid sequences of the human IGPcR27 protein and the Medaka fish p47MNR protein.

Figure 6: Fig. 6 depicts hydropathy plots comparing the IGPcR27 protein and the Medaka fish p47MNR protein.

Figure 7: Fig. 7 depicts a comparison of the amino acid sequence of the mouse IGPcR27 protein and the amino acid sequence of the human IGPcR27 protein.

Figure 8: Fig. 8 depicts hydropathy plots comparing the mouse IGPcR27 protein and the human IGPcR27 protein.

Figure 9: Fig. 9 depicts autoradiograms of human Multi-Tissue Northern Blots hybridized with a human IGPcR27 probe.

Figure 10: Fig. 10 depicts an autoradiogram of a mouse Multi-Tissue Northern Blot hybridized with a mouse IGPcR27 probe.

Figure 11 : Fig. 11 schematically outlines the construction of a mouse IGPcR27 targeting vector based on the method described by Wattler S & Nehls M,

German patent application DE 100 16 523.0, "Klonierungssystem zur

Konstruktion von homologen Rekombiationsvektoren", filed April 03, 2000, the major aspects of which are incorporated as Example 9.

Detailed Description of the Invention

The present invention relates to the discovery, identification and characterization of nucleic acids that encode IGPcR27, a novel G protein-coupled receptor protein that contains regions of homology to the Medaka fish p47MNR receptor. The invention encompasses nucleotide sequences encoding mammalian forms of IGPcR27, including human IGPcR27, nucleotides that encode some or all of its functional domains, such as extracellular domains (ECDs), the transmembrane domains (TMs), and the cytoplasmic domains (CDs); mutants of the IGPcR27 sequences, and fusion proteins of IGPcR27. The invention also encompasses host cell expression systems expressing such nucleotides, the host cells and expression products. The invention further encompasses IGPcR27 proteins, fusion proteins, antibodies to the receptor, antagonists and agonists of the receptor, transgenic animals that express an IGPcR27 transgene, recombinant knock-out animals that do not express the IGPcR27, and animal models in which the IGPcR27 gene is mutated. The invention also encompasses compounds that modulate IGPcR27 gene expression or IGPcR27 receptor activity that can be used for drug screening, or for diagnosis, monitoring, preventing or treating CNS diseases associated with signal processing, particularly movement dysfunctions, disorders or diseases, such as tics, tremor, Tourette's syndrome, Parkinson's disease, Huntington's disease, dyskinesias, dystonia, pain and spasms.

The invention further encompasses the use of IGPcR27 nucleotides, IGPcR27 proteins and peptides, as well as antibodies to IGPcR27, antagonists that inhibit ligand binding, receptor activity or expression, or agonists that increase ligand . binding, activate receptor activity, or increase its expression, for the diagnosis and treatment of disorders, including, but not limited to treatment of central nervous system disorders. In addition, IGPcR27 nucleotides and proteins are useful for the diagnosis of an IGPcR27 or pathway abnormality, and for the identification of compounds effective in the treatment of disorders based on the aberrant expression or activity of IGPcR27. The invention also relates to host cells and animals genetically engineered to express the human IGPcR27 (or mutants thereof) or to inhibit or knock-out expression of the animal's endogenous IGPcR27 gene.

IGPcR27, as a new G protein-coupled receptor, can play a role in diagnosis, preventing, ameliorating and correcting diseases. These diseases include, but are not limited to, psychiatric and CNS disorders, including learning and memory dysfunctions, schizophrenia, episodic paroxysmal anxiety (EPA) disorders such as obsessive compulsive disorder (COD), post traumatic stress disorders (PTSD), phobia and panic, major depressive disorder, bipolar disorder, Parkinson's disease, general anxiety disorder, autism, delirium, multiple sclerosis, Alzheimer disease/dementia and other neurodegenerative diseases, severe mental retardation, dyskinesias, Huntington's disease, Gille de la Tourette's syndrome, tics, tremor, dystonia, spasms, anorexia, bulimia, stroke, addiction/dependency/craving, sleep disorders, epilepsy, migraine, attention deficit/hyperactivity disorder (ADHD), cardiovascular diseases, angina pectoris, including heart failure, angina pectoris, arrythmias, myocardial infarction, cardiac hypertrophy, hypertension, thrombosis, arteriosclerosis, cerebral vasospasm, subarachnoid hemorrhage, cerebral ischenia, thrombosis, arteriosclerosis, peripheral vascular disease, Raynaud's disease, kidney disease - e.g. renal failure; dyslipidemias, obesity, emesis, gastrointestinal disorders, including irritable bowel syndrome (IBS), inflammatory bowel syndrome (IBD), diarrhoea, gastresophagal reflux disease (GERD), motility disorders and conditions of delayed gastric emptying, such as post operative or diabetic gastroparesis, and diabetis ulcers; other diseases including osteoporosis; inflammations; infections such as bacterial, fungal, protozoan and viral infections, particularly infections caused by

HIV-1 or HIV-2; pain; cancers; chemotherapy induced injury; tumor invasion; immune disorders; autoimmune diseases; urinary retention; asthma, allergies; arthritis; benign prostatic hypertrophy; endotoxin shock; sepsis; complication of diabetis mellitus; and gynaecological disorders.

In particular the new GPcR IGPcR27 satisfies a need in the art for identification and characterization of further receptors that can play an important role in diagnosis, preventing, ameliorating or correcting of diseases associated with signal processing in the CNS, particularly diseases relating to movement dysfunctions, disorders or diseases, such as tics, tremor, Tourette's syndrome, Parkinson's disease,

Huntington's disease, dyskinesias, dystonia, pain and spasms. Definitions

As used herein, the following terms, whether used in the singular or plural, have the meanings indicated.

IGPcR27 nucleotides, sequence or coding sequences - encompass DNA, including genomic DNA (e.g. the IGPcR27 gene), cDNA, RNA and include nucleotide sequences encoding IGPcR27 protein, peptide fragments, or fusion proteins.

IGPcR27 - means natural, or mature, IGPcR27 receptor protein. Polypeptides or peptide fragments of IGPCR27 protein are referred to as IGPcR27 polypeptides or IGPcR27 peptides. Fusions of IGPcR27, or IGPcR27 polypeptides or peptide fragments to an unrelated protein are referred to herein as IGPcR27 fusion proteins.

ECD - means "extracellular domain" of the receptor protein; TM - means "transmembrane domain" and CD - means "cytoplasmic domain". A functional IGPcR27 refers to a protein which binds natural IGPcR27 ligand with high affinity and specificity in vivo or in vitro.

Ligand - a molecule that selectively binds to a receptor.

Receptor - a plasma membrane protein which binds one or more appropriate ligands and propagates their regulatory signals to target cells, either by direct intracellular effects, or by promoting the synthesis and/or release of another regulatory molecule known as a second messenger.

Agonist - a molecule, being a ligand and/or drug, that acts on one or more physiological receptors and mimics the effects of the endogenous regulatory compounds; generally these are compounds that activate the receptor. Antagonist - a molecule, being a ligand and/or drug that inhibits a receptor, most acting by inhibiting the action of an agonist, for example by competing for agonist binding sites on a receptor. These are generally themselves devoid of intrinsic regulatory activity, but act to block receptor activation.

Transgenic animal - a non-human animal containing one or more additional, often foreign genes or "transgenes", integrated into its genome, that can be used as model systems to determine the phenotypic effects of expressing those genes.

Knock-out or knock-out animal - a non-human animal wherein a transgene is inserted into the genome to create a partial or complete loss-of-function mutation of an endogenous gene. Endogenous genes are inactivated usually by homologous recombination, using replacement or insertion-type gene targeting vectors.

Gene

Novel GPcR genes may be isolateά using expression cloning, by synthesizing specific oligonucleotides based on the sequence of purified proteins, using low stringency hybridization (Ausubel FM et al, eds., 1989, Current Protocols in Molecular Biology, Vol. I, Green Publishing Associates, Inc., and John Wiley & sons, Inc., New York) and by degenerate PCR using known receptor sequences. GPcR genes may also be identified by large scale sequencing, as in the Human Genome Project, followed by analysis of expressed sequence tags (ESTs), or complete sequences present in databases. Known GPcR sequences or conserved regions thereof may be employed as query sequences to extract novel GPcR sequences from these databases.

The present invention provides IGPcR27, a novel G protein-coupled receptor protein described for the first time herein, and characterized as having seven hydrophobic domains which span the plasma membrane and which are connected by alternating extracellular and intracellular hydrophilic loops. The IGPcR27 sequences encode a protein of 451 amino acids (see Fig. 2; SEQ ID NO:2. Human IGPcR27 has 41%> amino acid sequence identity and 60% sequence similarity to a GPcR of Medaka fish (Oryzais latipes), named p47MNR, of 428 amino acids in size. This 7TM receptor is related to human catecholamine, histamine, and serotonin receptors. The gene was isolated from a fish genomic DNA library using consensus sequences from the sixth transmembrane domain of human adrenergic receptor proteins (Yasuoka et al, 1995, Biochim. Biophys. Acta, 1235:467-469) (see Fig. 2; SEQ ID NO:2).

The adrenergic receptors mediate their action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. For example, the α 1 -adrenergic receptors mediate smooth muscle contraction in the prostate, and selected subtypes may be good targets for intervention in symptomatic benign prostatic hyperplasia (Forray et al, 1994, Mol. Pharmacol. 45:703-708). A similar adrenoreceptor has been isolated from the Medaka fish, with 61% similarity to αlA- AR (Yasuoka et al, 1995, Eur. J. Biochem., 235:501-507). Histamine receptors such as the HI receptor function in peripheral tissues, mediating smooth muscle contraction, increasing capillary permeability, and mediating neurotransmission in the CNS (Inoue et al, 1996, Genomics 36:178-181). There are several types of serotonin receptors: the 5HAT-2 type receptors for example, mediate their action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system. These receptors are involved in tracheal smooth muscle contraction, broncho-constriction and control of aldosterone production (Liu et al , 1991 , Genomics, 11:231-234).

In particular, the invention encompasses sequences coding for IGPcR27 polypeptides, or functional domains of the IGPcR27, mutated, truncated or deleted IGPcR27, and IGPcR27 fusion proteins. The invention also encompasses nucleotide constructs that inhibit expression of the !GPcR27 gene, such as anti-sense and ribozyme constructs, or enhance expression of IGPcR27 in combination with regulatory sequences like promoters, enhancers.

The cDNA sequence (SEQ ID NO:l) and deduced amino acid sequence (SEQ ID NO:2) of human IGPcR27 of this invention are shown in Fig. 1 and Fig. 2. The IGPcR27 nucleotide sequences of the invention include the DNA sequence shown in

Fig. 1, nucleotide sequences that encode the amino acid sequence shown in Fig. 2 and any nucleotide sequence that hybridizes to the complement of the DNA sequence shown in Fig. 1 under highly stringent conditions (Ausubel FM et al, eds., 1989, Current Protocols in Molecular Biology, Vol. I, Green Publishing Associates, Inc., and John Wiley & sons, Inc., New York). Functional equivalents of the IGPcR27 gene product include naturally occurring IGPcR27, mutant and degenerate variants present in humans and other species. Preferred IGPcR27 nucleic acids encode polypeptides that are at least 55% identical or similar to the amino acid sequence shown in Fig. 2. Nucleic acids which encode polypeptides which are at least 70%, and even more preferably, in increasing order of preference, at least 80%, 85%, 90%,

95%, or 98%o identical or similar. In a particularly preferred embodiment, the nucleic acid of the present invention encodes a polypeptide having an overall amino acid sequence homology or identity of, in increasing order of preference, at least 70%, 80%, 85%, 90%, 95%, 98%, or at least 99% with the amino acid sequence shown in Fig. 2.

The invention also provides DNA molecules that are the complements of the nucleotide sequences described above and which may act as IGPCR27 anti-sense molecules useful in IGPcR27 gene regulation. Orthologs of the human IGPCR27 gene present in other species can be identified and readily isolated. They can be useful for developing cell and animal model systems for purposes of drug discovery. For example, cDNA or genomic DNA libraries derived from the organism of interest can be screened by hybridization using the nucleotides described above, or by performing PCR using degenerate oligonucleotide primers. (See Sambrook et al, 1989, ''Molecular Cloning, A Laboratory Manual", Cold Spring Harbor Press, New

York, USA; and Ausubel FM et al, eds., 1989, Current Protocols in Molecular Biology, Vol. I, Green Publishing Associates, Inc., and John Wiley & Sons, Inc., New York). Additionally, expression libraries can be screened using standard antibody screening techniques or by doing database searches for homologues and then cloning them based on the sequence. The identified sequences may be sub- cloned and sequenced. The IGPcR27 gene sequences may additionally be used to isolate mutant IGPcR27 gene alleles, or to detect defects in the regulatory sequences of the IGPcR27 using DNA obtained from an individual suspected of or known to carry the mutant IGPcR27 allele. Mutant alleles may be isolated from individuals either known or proposed to have a genotype which contributes to the symptoms of disorders arising from the aberrant expression or activity of the IGPcR27 protein.

The isolation of human genomic clones is helpful for designing diagnostic tests and therapeutics. For example, sequences derived from the human gene can be used to design primers for use in PCR assays to detect mutations for diagnostics.

The nucleotides of this invention are also preferred for use^' in mapping the location of the gene to the chromosome, in a process termed chromosomal mapping. Various techniques known to those skilled in the art, including but not limited to in situ hybridization of labeled probes to flow-sorted chromosomes, fluorescence in situ hybridization (FISH) and PCR mapping of somatic cell hybrids may be employed. This allows the physical location of gene regions to be associated with genetic diseases, based on a genetic map. Genetic linkage analysis can then be used to identify the relationship between genes and diseases (see Egeland et al, 1987, Nature, 325:783-787). Preferred uses of this map include diagnostic tests and reagents, in pharmacogenetics studies and in monitoring patient responses to drugs in clinical trials.

Proteins and polypeptides

Fig. 2 shows the amino acid sequence of the human IGPcR27 protein. The amino acid sequence of IGPcR27 contains hydrophilic domains located between the transmembrane domains, arranging an alternating location of the hydrophilic domains inside and outside the cell membrane. Polypeptides which are at least 70%, and even more preferably at least 80%, 85%, 90%, 95%, 98% or 99% identical or similar to the amino acid sequence represented by Fig. 2 are encompassed by this invention.

In particular, the invention encompasses IGPcR27 polypeptides, or functional domains of the IGPcR27, mutated, truncated or deleted IGPcR27, and host cell expression systems that can produce such IGPcR27 products. IGPcR27 proteins, polypeptides and peptides, can be prepared for the generation of antibodies, as reagents in diagnostic assays, in the identification of other cellular gene products involved in regulating IGPcR27, as reagents for screening for compounds that can be used in the treatment of conditions involving IGPcR27, and as pharmaceutical reagents useful in the treatment of related disorders.

The invention also encompasses proteins that are functionally equivalent to the

IGPcR27 encoded by the nucleotide sequences, as defined by the ability to bind natural IGPcR27 ligand, the resulting biological effect of natural lGPcR27 ligand binding, e.g., signal transduction, a change in cellular metabolism or change in phenotype. Such functionally equivalent IGPcR27 proteins include but are not limited to additions or substitutions of amino acid residues, which result in a silent change. Also preferred in this invention are mutant IGPcR27 proteins with increased function, and/or greater signaling capacity; or decreased function, and/or decreased signal transduction capacity which may be generated by random mutagenesis techniques and site-directed mutagenesis techniques well known to those skilled in the art. The same strategy can also be used to design mutant forms of IGPcR27 based on the alignment of human IGPcR27 and IGPcR27 orthologs from other species. Highly preferred are other mutations to the IGPcR27 coding sequence that can be made to generate IGPcR27 constructs that are better suited for expression, scale up, etc. in the host cells chosen. Host cells may be chosen depending on their varying capacity to modify synthesized proteins. Peptides corresponding to one or more domains of the IGPcR27 (e.g., ECD, TM or CD), truncated or deleted forms of IGPcR27, as well as fusion proteins are also within the scope of the invention and can be designed on the basis of the IGPcR27 nucleotide and IGPcR27 amino acid sequences disclosed above. Such IGPcR27 polypeptides, peptides and fusion proteins can be produced using techniques well known in the art for expressing protein encoding IGPcR27 sequences. These methods include, for example, in vitro recombinant DNA techniques, synthetic techniques, and in vivo genetic recombination. (See Sambrook et al, 1989, ''Molecular Cloning, A Laboratory Manual", Cold Spring Harbor Press, N.Y.; and Ausubel FM et al, eds., 1989, Current Protocols in Molecular Biology, Vol. I, Green

Publishing Associates, Inc., and John Wiley & Sons, Inc., New York.). A variety of host-expression vector systems may be utilized to express the IGPcR27 nucleotide sequences of the invention. The IGPcR27 peptide or polypeptide may be anchored in the cell membrane and purified or enriched from such expression systems using appropriate detergents and lipid micelles, and methods well known to those skilled in the art. Or, where the IGPcR27 peptide or polypeptide is secreted by the cells, it may be isolated from the culture media. Such host cells themselves may be used to assess biological activity, e.g., in drug screening assays.

The expression systems that may be used for purposes of the invention include, but are not limited to microorganisms such as bacteria (e.g., E. coli, B. subtilis); yeast (e.g., Saccharomyces sp., Pichia sp.); insect cell systems infected with recombinant virus expression vectors (e.g., baculoviras); plant cell systems infected with recombinant viral or plasmid expression vectors; or mammalian cell systems (e.g., COS, CHO, BHK, 293, 3T3) harboring recombinant expression constructs containing mammalian promoters. Lower amounts of functional protein are expressible in E. coli and yeast, particularly as E. coli do not contain G proteins or effectors. G proteins may be added to E.coli expressing G protein-coupled receptors in cell membrane, in the cell-based assays. Yeast cells may be humanized by co- transfixing human G proteins. The yeast Pichia pastoris is preferred over

Saccharomyces cerevisiae for purification of G protein-coupled receptors for structural studies. The most preferred systems for expression are the baculovirus/insect cell and mammalian cell systems, as they can produce the largest quantities of G protein-coupled receptors in functional form for analysis. Mammalian cells are preferred because they express the necessary G proteins, and vaccinia and Semliki Forest virus are preferred as vectors. (See Tate et al, 1996,

Tibtech 14:426-430).

Diagnostic and therapeutic reagents and kits

In one embodiment of the invention, the invention encompasses antibodies directed against IGPcR27 proteins or peptides, or IGPcR27 fusion proteins, as described above. Such antibodies include but are not limited to polyclonal antibodies, monoclonal antibodies (mAbs), humanized or chimeric antibodies, single chain antibodies, anti-idiotypic (anti-Id) antibodies, including Fab fragments. The antibodies may be generated and purified, or conjugated according to methods well known in the art. See for example Harlow E and Lane D, 1988, "Antibodies: A Laboratory Manual", Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, which is incorporated herein by reference in its entirety.

In another embodiment, the antibodies of the invention may be used, for example, as part of a diagnostic or a prognostic, and as a part of compound screening schemes, for the evaluation of the effect of test compounds on expression and/or activity of the IGPcR27 gene product. Preferably, antibodies may be used in therapeutic regimes as a method for the inhibition of abnormal IGPcR27 activity. Also preferred are antibodies directed against wild type or mutant IGPcR27 gene products or conserved variants or peptide fragments thereof to detect the pattern and level of expression, as well as distribution in tissues, of the IGPcR27 in the body, also by in situ detection. The antibodies may be employed as part of an enzyme immunoassay (EIA), a radioimmunoassay, or as an antibody labeled with a chemiluminescent or a fluorescent compound. In yet another embodiment of the invention, the IGPCR27 proteins or peptides, IGPcR27 fusion proteins, IGPcR27 nucleotide sequences, antibodies, antagonists and agonists can be useful for the detection of mutant forms of IGPcR27 or inappropriately expressed forms of IGPcR27, for the diagnosis of disorders including but not limited to central nervous system disorders, neurologic, psychiatric and behavioral disorders, metabolic disorders, visual and olfactory disorders, immune, neuroirnmune, neuroendocrine and inflammatory disorders and diseases. DNA encoding IGPcR27 or parts thereof may be used in hybridization or amplification assays of biological samples to detect abnormalities involving IGPcR27 gene structure, including point mutations, insertions, deletions and chromosomal rearrangements. Such genotyping assays may include, but are not limited to Southern analyses, single stranded conformational polymorphism analyses (SSCP), and PCR analyses (See Mullis KB, U.S. Pat. No. 4,683,202), the use of restriction fragment length polymorphisms (RFLPs), of variable numbers of short, tandemly repeated DNA sequences between the restriction enzyme sites (see Weber, U.S. Pat.

No. 5,075,217), and by detecting and measuring IGPcR27 transcription.

Also within the scope of the invention are the IGPcR27 proteins or peptides, IGPcR27 fusion proteins, IGPcR27 nucleotide sequences, host cell expression systems, antibodies, antagonists, agonists and genetically engineered cells and animals. These can be used for screening for drugs effective in the treatment of disorders. The use of engineered host cells and/or animals may offer an advantage in that both compounds that bind to the ECD of the IGPcR27 and compounds that affect the signal transduced by the activated IGPcR27 may be identified.

Screening for receptor modulating agents

In another embodiment of the invention, the invention encompasses the pharmacological testing wherein the cloned IGPcR27 genes are expressed in yeast, insect or mammalian cells and screened for a response to cognate or surrogate agonists. The agonists may be present in, but are not limited to, biological extracts, peptide libraries and/or complex compound collections. The invention provides for screening which may utilize libraries of known compounds, including natural products or synthetic chemicals, and biologically active materials, including proteins, for compounds which are inhibitors or activators. Candidate test compounds include all kinds of combinatorial chemistry derived molecular libraries of amino acids, peptides, soluble peptides, modified peptides, antibodies, small organic and inorganic molecules.

In a further embodiment of the invention, a labeled test compound can be incubated with the receptor to determine whether one binds to the other. Functional assays including fϊbroblast and BM transformation assays, cell cycle analysis can be performed; as well as responses using signal transduction assays, including protein phosphorylation, guanylate cyclase activity, ion fluxes (e.g. calcium) and pH changes can be measured. High throughput drug screening systems are most preferred and may use assays including, but not limited to, the production of intracellular second messengers, such as cAMP, diacyiglycerol and inositol phosphates; the activation of reporter gene transcription, such as luciferase and beta-galactosidase under for example the cAMP-responsive element; receptor-mediated actions on adenylyl cyclase and phospholipase C leading also for example to dispersion or aggregation of frog melanophores. (Reviewed in Tate et al, 1996, Tibtech 14:426-430; included in entirety herein).

In a highly preferred embodiment, a functional genomics approach for protein- protein interaction screening may be employed wherein the GPcR is produced in "humanized yeast cells": expression in yeast along with endogenous or promiscuous mammalian or human G-alpha proteins. Transient expression of cDNA can also be carried out using mammalian CHO, HEK-293 cells or COS-7 cells and receptors can be analyzed for ligand binding and drug interactions (for example as described in Fraser et al, 1995, J. Nucl. Med., 36:17S-21S). Also preferred is site-directed mutagenesis to define regions of IGPcR27 that have functional importance. Site- directed mutagenesis may be used to map ligand-binding pockets and to identify residues important for receptor interaction and activation. Compounds that can be generated using modeling methods to bind these residues are also within the scope of this invention. For example, receptor down-regulation and the development of drag tolerance, such as seen in asthma patients who use bronchial dilators which are beta- adrenergic agonists leading to tachyphylaxis, can be studied in these cell systems.

The expression of both intact and hybrid receptors is preferred. The number of receptors, as well as mRNA levels can be measured. Agents for radionuclide imaging to monitor level changes can be developed.

\ Some of the known receptors and their ligands defined by above techniques are shown below.

Ligand screening

The invention encompasses antagonists and agonists of IGPcR27, as well as compounds or nucleotide constructs that inhibit expression of the IGPcR27 gene (anti-sense and ribozyme molecules), or promote expression of IGPcR27 (wherein IGPcR27 coding sequences are operatively associated with promoters, enhancers, etc.). Highly preferred are the IGPcR27 protein products (especially soluble derivatives of IGPcR27, or truncated polypeptides lacking the TM or CD domains) and fusion protein products, antibodies and anti-idiotypic antibodies, antagonists or agonists (including compounds that modulate signal transduction which may act on downstream targets in the IGPcR27 signal transduction pathway) that can be used for therapy of such diseases, by inhibiting receptor activity.

Nucleotide constructs encoding functional forms of IGPcR27 and mutant forms of IGPcR27 are preferred embodiments of the invention, as their uses include employment in the genetic engineering of host cells. Other preferred embodiments of the invention are anti-sense and ribozyme molecules, preferred for use in "gene therapy" approaches in the treatment of disorders or diseases arising from the aberrant or altered activity of IGPcR27. The gene therapy vector alone or when incorporated into recombinant cells, may be administered in a suitable formulation for intravenous, intra-muscular, intra-peritoneal delivery, or may be incorporated into a timed release delivery matrix.

Transgenic and knock-out animal models

The animal-based and cell-based models can be used to identify drugs, biologicals, therapies and interventions which can be effective in treating disorders with aberrant expression or activity. IGPcR27 sequences can be introduced into, and over- expressed and/or can be disrupted in order to under-express or inactivate IGPcR27 gene expression.

In one embodiment of the invention, the IGPcR27 gene products can also be expressed in transgenic animals. ^"Non-human animals of any species, including, but not limited to, mice, rats, rabbits, guinea pigs, sheep, cows, goats, may be used to generate IGPcR27 transgenic animals. The present invention provides for transgenic animals that carry the IGPcR27 transgene in all their cells, as well as animals which carry the transgene in some, but not all their cells, i.e., mosaic animals. The transgene may be expressed in all tissues of the animal, or may be limited to specific tissues. Any technique known in the art may be used to introduce the IGPcR27 transgene into animals to produce the founder lines of transgenic animals. Such techniques include, but are not limited to pronuclear microinjection (Hoppe PC and

Wagner TE, U.S. Patent No. 4,873,191); retrovirus mediated gene transfer into germ lines (Van der Putten et al, 1985, Proc. Natl. Acad. Sci., USA 82:6148-6152); gene targeting in embryonic stem cells (Thompson et al , 1989, Cell 56:313-321); electroporation of embryos (Lo, 1983, Mol. Cell. Biol., 3:1803-1814); and sperm- mediated gene transfer (Lavitrano et al, 1989, Cell 57:717-723); etc. For a review of such techniques, see Gordon, 1989, "Transgenic Animals", Intl. Rev. Cytol. 115:171-229, which is incorporated by reference herein in its entirety.

The present invention relates to knock-out animals engineered by homologous recombination to be deficient in the production of the IGPcR27. The present invention is directed to a knock-out animal having a phenotype characterized by the substantial absence of !GPcR27, otherwise naturally occurring in the animal. In addition, the invention encompasses the DNA constructs and embryonic stem cells used to develop the knock-out animals and assays which utilize either the animals or tissues derived from the animals. Preferably, these cells, tissues and cell lines are characterized by the substantial absence of IGPcR27 that would otherwise be naturally occurring in their normal counterparts.

Gene targeting is a procedure in which foreign DNA sequences are introduced into a specific locus within the genome of a host cell. In another embodiment of the invention, endogenous IGPcR27 gene expression can be reduced by inactivating or knocking out the IGPcR27 gene or its promoter using targeted homologous recombination, (e.g., see Smithies et al., 1985, Nature 317:230-234; Thomas & Capecchi, 1987, Cell 51:503-512; Thompson et al, 1989, Cell 5:313-321; each of which is incorporated by reference herein in its entirety). For example, a mutant, non-functional IGPcR27 (or a completely unrelated DNA sequence) flanked by DNA homologous to the endogenous IGPcR27 gene (either the coding regions or regulatory regions of the IGPcR27 gene) can be used, with or without a selectable marker and/or a negative selectable marker, to transfect cells that express IGPcR27 in vivo. Insertion of the DNA construct, via targeted homologous recombination into the genome, results in abolishing IGPcR27 gene function.

One preferred technique for targeted mutagenesis in this invention is based on homologous recombination. The general methodologies of targeting mutations into the genome of cells, and the process of generating mouse lines from genetically altered embryonic stem (ES) cells with specific genetic lesions are well known

(Bradley, 1991, Cur. Opin. Biotech. 2: 823-829). See also U.S. patents 5,557,032 by Mak et al, and U.S. Patent No. 5,487,992 by Capecchi et al, included by reference herein. Preferred in this invention is a synthetic recombination vector which contains the genetic information of the targeted chromosomal locus recombines with the genomic DNA after introduction into a cell. A strategy of "positive/negative selection" can be used to enrich the cell population for cells in which targeting vectors have integrated into the host cell genome, and recombination has occurred at the desired gene locus (Mansour, et al, 1988, Nature 336:348). The vector usually contains a positive selection cassette which is flanked by the genetic information of the target locus to enrich for cells where the vector successfully recombines with the chromosomal DNA against the pool of non-recombinant cells. The likelihood of obtaining an homologous recombination event increases with the size of the chromosomal vector DNA and is further dependent on the isogenicity between the genomic DNA of the vector and the target cell (See Reile TE et al, 1992, P.N.A.S. USA 89:5128-5132; Deng et al, 1991, Mol. Cell. Biol., 12, 3365-

3371). Also preferred in this invention are large stretches of genomic DNA flanking the IGPcR27 gene ortholog in the target animal species. The cloning of large chromosomal fragments of the target gene, the sub-cloning of this DNA into a bacterial plasmid vector, the mapping of the gene structure, the integration of the positive selection cassette into the vector and finally, the flanking of one or both homologous vector arms by a negative selection marker are well described in the literature. Also preferred are replacement-type targeting vectors using yeast host cells are described by Storck et al, 1996, Nuc. Acids Res. 24:4594-4596. The use of other vectors such as bacteriophage λ and vectors for phage-plasmid recombination have been described by Tsuzuki et al, 1998, Nuc. Acids Res 26:988-993; transposon-generated gene targeting constructs have also been described by Westphal et al, 1997, Curr. Biol., 7:530-533 and are within the scope of the invention.

The most highly preferred method in this invention is described by Wattler S &

Nehls M, German patent application DE 100 16 523.0, "Klonierungssystem zur Konstruktion von homologen Rekombiationsvektoren", filed April 03, 2000, included by reference in whole herein,, and described in part in Example 9. This method reduces the time required for the construction of such vectors from 3-6 months to about 14 days. The vector includes a linear lambda vector (lambda-KO-

Sfi) that comprises a stuffer fragment; an E. coli origin of replication; an antibiotic resistance gene for bacterial selection, two negative selection markers suitable for use in mammalian cells; LoxP sequences for cre-recombinase mediated conversion of linear Lambda phages into high copy plasmids. In a final targeting vector, the stuffer fragment is replaced by nucleotide sequences representing a left arm of homology, an ES cell selection cassette, and a right arm of homology. The transformation of mouse 129 ES cells with the final vector construct is done according to standard procedures. The targeting vector is linearized and then introduced by electroporation into ES cells. Cell clones are positively selected with G418 and negatively selected with GANC (ganciclovir, 0.2 μM). Targeted ES-cell clones with single integration sites are identified, confirmed by hybridization, and expanded in culture for injection.

The invention also encompasses embryonic stem (ES) cells derived from a developing mouse embryo at the blastocyst stage, that are modified by homologous recombination to contain a mutant IGPcR27 gene allele. The modified ES cells are reintroduced into a blastocyst by microinjection, where they contribute to the formation of all tissues of the resultant chimeric animal, including the germ line (Capecchi, 1989, Trends Genet., 5:70; Bradley, et al, 1984, Nature, 309:255). Modified ES cells may also be stored before reimplantation into blastocysts. The chimeric blastocysts are implanted into the uterus of a pseudopregnant animal, prepared by mating females with vasectomized males of the same species. Typically chimeras have genes coding for a coat color or another phenotypic marker that is different from the corresponding marker encoded by the stem cell genes.

Also within the scope of the invention are chimeric male non-human animals and their heterozygous offspring carrying the IGPcR27 gene mutation which are bred to obtain animals which are homozygous for the mutation, preferred animals being mice. A phenotype selection strategy may be employed, or chromosomal DNA may be obtained from the tissue of offspring, screened using Southern blots and/or PCR amplification for the presence of a modified nucleotide sequence at the IGPcR27 gene locus, liked described in the above section of identifying positivlly targeted ES cells. Other means for identifying and characterizing transgenic knock-out animals are also available. For example, Northern blots can be used to probe mRNA obtained from tissues of offspring animals for the presence or absence of transcripts coding for either the IGPcR27, the marker gene, or both. In addition, Western blots might be used to assess IGPcR27 expression by probing with antibody specific for the receptor.

These animals are characterized by including, but not limited to, a loss in the ability to bind ligands specific for IGPcR27 and/or by a loss in expression from the

IGPcR27 gene locus. Preferably, the animals produce no functional forms of IGPcR27 at all. Once homozygous transgenic animals have been identified, they may preferably be interbred to provide a continual supply of animals that can be used in identifying pathologies dependent upon the absence of a functional lGPcR27 and in evaluating drugs in the assays described above. Also highly preferred in this invention, are these animals as providing a source of cells, tissues and cell lines that differ from the corresponding cells, tissues and cell lines from normal animals by the absence of fully functional forms of IGPcR27.

The methodology needed to make such animals can be adapted to any non-human animal, preferably rodents such as hamsters, rats or mice, and most preferably, mice. In another embodiment, clones of the non-human transgenic animals can be produced according to methods described in Wilmut et al, 1997, Nature, 385:810- 813.

EXAMPLES

Example 1. Identification of a full-length human cDNA coding for a novel GPcR, IGPcR27.

A coding sequence of 1353 bp was identified as follows from the EMBL alert HTGH (High Throughput Genome) database (see Fig.l, SEQ ID NO:l). A search was performed using the nucleotide sequences of known GPcRs. A sequence with a statistically significant score was returned and searched for open reading frames. Subsequently a putative coding region was assigned and used in primer design. The tracked human genomic IGPcR27 sequence contains the full-length cDNA sequence, identified as a single exon coding GPcR. IGPcR27 encodes a protein of 451 amino acids (see Fig.2; SEQ ID NO:2).

A BLASTP search (Basic Local Alignment Search Tool for Proteins, National Institutes of Health, Bethesda MD, U.S.A.) revealed that the protein most closely related to human IGPcR27 is a Medaka fish (Oryzais latipes) GPcR, named p47MNR, and 428 amino acids in size, has 41% amino acid sequence identity and 60%) sequence homology (with conserved substitutions) to p47MNR, which is a 7TM receptor related to human catecholamine, histamine, and serotonin receptors. The gene was isolated from a fish genomic DNA library using consensus sequences from the sixth transmembrane domain of human adrenergic receptor proteins (Yasuoka et al, 1995, Biochim. Biophys. Acta, 1235:467-469).

Example 2. Tissue-specific expression of human IGPcR27, analysis by RT-

PCR.

A panel of cDNAs derived from total RNA from 29 human tissues (Clontech Laboratories, Inc., Palo Alto CA, USA; Invitrogen Corp., Carlsbad CA, USA) was tested in a reverse transcription-polymerase chain reaction (RT-PCR) assay. The sequence of the primers used to amplify a 390 bp product (SEQ ID No:5), which spans a region including transmembrane domains 2 to 4, is as follows: 5' - GTCTTCGTCTTCCACCTCTG (coding sequence position 229-246; SEQ ID NO:3) 5' - CTGGCAGTAGGCACTGTGG (coding sequence position 600-618; SEQ ID NO:4)

The conditions for the PCR were: denaturation at 94°C for 45 seconds, annealing at 56°C for 1 minute, and extension at 72°C for 30 seconds, for a total of 35 cycles, in a Thermocycler (MJ Research, Watertown MA, USA; type PTC-225). The PCR products were analyzed on an 1.8% agarose gel and stained with ethidium bromide to visualize DNA by ultraviolet imaging. The tissues analyzed were: skin, whole brain, fetal brain, cerebellum, thymus, esophagus, trachea, lung, breast, mammary gland, heart, liver, fetal liver, kidney, spleen, adrenal gland, pancreas, stomach, small intestine, skeletal muscle, adipose tissue, uterus, placenta, bladder, prostate, testis, colon, rectum and cervix. Positive (human genomic DNA) and negative (water) controls were included.

Positive signals for PCR products of 390 bps in size were observed in cDNA prepared from human whole brain and cerebellum (strong signals) as well as in adipose tissue, breast, pancreas, spleen, mammary gland, testis, trachea, rectum, liver, stomach, small intestine, skeletal muscle, trachea, and cervix (weak signals).

The correct identity of the sequence amplified was confirmed by sequencing of the PCR products.

Example 3. Tissue-specific expression of human IGPcR27, analysis by

Northern hybridization.

Northern hybridization of polyA+ RNAs from several human tissues was carried out using a IGPcR27 specific DNA-probe. The probe was generated by radiolabelling the purified and sequenced PCR product generated using primers as described in Example 2. The probe spans sequences coding for transmembrane regions 2 to 4 and is 390 bp in length. Commercially available Multiple Tissue Northern Blots (BioChain Institute, Hayward CA, USA) each containing 3 micrograms of poly A + RNA per lane, were hybridized, following the manufacturer's instructions. These blots are optimized to give best resolution in the 1.0-4.0 kb range, and marker RNAs of 9.5, 7.5, 4.4, 2.4, 1.35 and 0.24 kb are run for reference. Membranes were pre- hybridized for 30 minutes and hybridized overnight at 68°C in ExpressHyb hybridization solution (Clontech Laboratories, Palo Alto CA, USA) as per the manufacturer's instructions. The cDNA probe used was labeled with [α³²P] dCTP using a random primer labeling kit (Megaprime DNA labeling system; Amersham Pharmacia Biotech, Piscataway NJ, USA) and had a specific activity of 1 x 10⁹ dpm/μg. The blots were washed several times in 2X SSC, 0.05% SDS for 30-40 min at room temperature, and were then washed in O.IX SSC, 0.1%) SDS for 40 min at 50°C (see Sambrook et al, 1989, "Molecular Cloning, A Laboratory Manual", Cold Spring Harbor Press, New York, USA). The blots were covered with standard domestic plastic wrap and exposed to X-ray film at -70°C with two intensifying screens for 36 hours.

The tissues represented in the BioChain Institute Multiple Tissue Northern Blots are as follows:

Blot #I Blot #11 Blot #V Blot#VIII

Heart Stomach Uterus Brain

Brain Jejunum Cervix Kidney

Liver Ileum Ovary Spleen

Pancreas Colon Testis Intestine

Skeletal Muscle Lung Prostate Uterus

Lung Lung Cervix

Placenta

Lung

The results of this experiment indicate that IGPcR27 is exclusively in human brain, with a predominant transcript of approximately 4.2 kb and a faint band representing an RNA species of about 3 kb in size (see Fig. 3).

Example 4. Characterization of human IGPcR27 protein.

Hydrophobicity analysis of the predicted amino acid sequence showed seven hydrophobic regions corresponding to the seven transmembrane regions, a conserved structural feature of G protein-coupled receptors. Human IGPcR27 is a protein of 451 amino acid residues (Fig. 2; SEQ ID NO:2). The encoded protein was compared to amino acid sequences present in public databases EMBL and Genbank.

IGPcR27 has 41%) amino acid sequence identity and 60%) similarity to a Medaka fish GPCR sequence, protein ID BAA07741.1, a protein of 428 amino acids in size. This 7TM receptor is related distantly to human catecholamine, histamine, and serotonin receptors.

Fig. 4a shows the amino acid sequence of IGPcR27 ('query') compared to the amino acid sequence of Medaka fish p47MNR ('sbjct'), as abstracted from the SWISSPROT database and analyzed using a BLASTP alignment program. The predicted transmembrane domains of IGPcR27 are flanked by amino acids 44-66 (TM1), 78-98 (TM2), 116-137 (TM3), 160-177 (TM4), 210-230 (TM5), 291-309 (TM6), 324-346 (TM7), as underlined.

Fig. 5a shows a hydropathy plot for the predicted amino acid sequence of the human IGPcR27 protein compared to the sequences predicted for Medaka fish p47MNR. The analysis was performed using the method of Kyte and DooLittle (1982, J. Mol. Biol., 157:105-32), with the DAMBE program (Data Analysis in Molecular Biology and Evolution), University of Hong Kong, version 3.7.49.

Example 5. Identification of mouse ortholog of IGPcR27 by "touch-up" PCR. A cDNA stretch of the mouse ortholog of human IGPcR27 was identified by polymerase chain reaction (PCR) amplification of 129 mouse genomic ES cell DNA with human IGPcR27 primers SEQ ID NO:6 and SEQ ID NO:7, under the following conditions ("touch-up" PCR): - denaturation at 94°C for 45 seconds, annealing at 42°C for 1 minute, and extension at 72°C for 45 seconds, for a total of two cycles; followed by denaturation at 94°C for 45 seconds, annealing at 48°C for 1 minute, and extension at 72°C for 45 seconds, for a total of 2 cycles; followed by denaturation at 94°C for 45 seconds, annealing at 54°C for 1 minute, and extension at 72°C for 45 seconds; for a total of 35 cycles in a Thermocycler (MJ Research; type PTC-225). The PCR products were analyzed on an 1.8% agarose gel and stained with ethidium bromide to visualize DNA by ultraviolet imaging. The sequence of the human primers used to amplify a mouse 261 bp product (SEQ ID NO:8) is as follows:

5' - GACCACGCCCTCTTTGGG (SEQ ID NO:6 ) 5' - GGGGACACTGGGAGCTCC (SEQ ID NO: 7)

An isolated mouse PCR product of the 261 bp in size was sequenced (SEQ ID NO: 8), the mouse sequence used for mouse primer design. Clones from a mouse strain 129 genomic library, containing the full-length cDNA (Figure 7; SEQ ID NO:9) and flanking genomic sequences are isolated by hybridization, using a mouse

IGPcR27 specific DNA probe. Genomic clones are utilized in the construction of targeting vectors.

Example 6. Tissue-specific expression of mouse IGPcR27, analysis by RT-

PCR.

A mouse tissue cDNA panel, including 34 different types of cDNA from freshly prepared tissue RNAs, was tested in a RT-PCR assay. The sequences of the primers used in amplification of a 280 bp product (SEQ ID NO 13) were as follows:

5' - CTCTACTATGGTTACCAGCTC (SEQ IDNOT1) 5'-CTGTTTGCTAAGCTCGCCCCGG (SEQ IDNO:12)

The conditions for the PCR were: denaturation at 94°C for 45 seconds, annealing at 56°C for 1 minute, and extension at 72°C for 30 seconds, for a total of 35 cycles in a

Thermocycler (MJ Research; type PTC-225). The PCR products were analyzed on a 1.8% agarose gel and stained with ethidium bromide to visualize DNA by ultraviolet imaging.

The tissues analyzed were: lung, kidney, heart, skeletal muscle, total brain, cerebrum, cerebrum left hemisphere, cerebrum right hemisphere, cerebellum, medulla oblongata, olfactory lobe, thymus, adipose tissue, thyroid/ trachea, gall bladder, tongue, esophagus, bladder, eye, salivary gland, stomach, rectum, large intestine, trachea, adrenal gland, spleen, testis, epididymis, prostate, liver, trachea, embryonic stem cell, ovary, uterus. A negative control (water) was included.

PCR products of 280 bp in size were observed in cDNA prepared from total brain, cerebrum, cerebrum right hemisphere, cerebrum left hemisphere, cerebellum, medulla oblongata, olfactory lobe and testis. The correct identity of the 280 bp products amplified was confirmed by sequencing.

Example 7. Tissue-specific expression of human IGPcR27, analysis by Northern hybridization.

A mouse Multi Tissue Northern Blot containing 15 μg of total RNA from each of total brain, cerebrum, cerebellum, medulla oblongata, testis and skeletal muscle was hybridized with a 280 bp mouse IGPcR27 probe, as explained in Example 6.

The result of this experiment indicates that mouse IGPcR27 is expressed exclusively in neural tissues, represented by two transcripts of approximately 4.5kb and 4kb in size (see Fig. 8).

Example 8. Characterization of mouse IGPcR27 protein.

The mouse IGPcR27 protein is of 449 amino acid residues in length (Figure 8; SEQ ID NO: 10).

Fig. 4b shows the amino acid sequence of IGPcR27 ('query') compared to the amino acid sequence of the mouse ortholog of IGPcR27 ('sbjct'), analyzed using the BLASTP alignment program. The amino acid identity is 95,4% in an 452 amino acid residues overlap. The predicted transmembrane domains (TM) of human lGPcR27 are flanked by amino acids 44-66 (TM1), 78-98 (TM2), 116-137 (TM3),

160-177 (TM4), 210-230 (TM5), 291-309 (TM6), 324-346 (TM7); and the predicted transmembrane domains (TM) of the mouse ortholog of IGPcR27 are flanked by amino acids 44-66 (TM1), 80-102 (TM2), 114-136 (TM3), 154-176 (TM4), 207-229 (TM5), 286-308 (TM6), 324-346 (TM7), as underlined in Fig. 4b.

Fig. 5b shows a hydropathy plot for the predicted sequence of the human IGPcR27 protein compared to that of mouse IGPcR27. The analysis was performed using the method of Kyte and DooLittle (1982, J. Mol. Biol., 157:105-32), with the DAMBE program (Data Analysis in Molecular Biology and Evolution), University of Hong Kong, version 4.0.41.

Example 9. Generation of ES cells with a modified IGPcR27 allele, produced by homologous recombination.

The most preferred method in this invention is described in Wattler S & Nehls M, German patent application DE 100 16 523.0, "Klonierungssystem zur Konstruktion von homologen Rekombiationsvektoren", filed April 03, 2000. This method reduces the time required for the construction of such a vector from 3-6 months to about 14 days. The vector includes a linear lambda vector (lambda-KO-Sfi) that comprises a stuffer fragment; an E. coli origin of replication; an antibiotic resistance gene for bacteria selection, two negative selection markers suitable for use in mammalian cells; LoxP sequences for cre-recombinase mediated conversion of linear lambda phages into high copy plasmids. In a final targeting vector, the stuffer fragment is replaced by nucleotide sequences representing a left arm of homology, an ES cell selection cassette, and a right arm of homology.

To abolish the gene function of mouse IGPcR27 (mIGPcR27) a deletion of approximately 880 bp of the coding region starting approximately 10 bp downstream of the ATG was performed (see Fig. 9). The left arm of homology (hereafter referred to as A/C) is PCR amplified with the primers C and A. The primers contain Sfi I restriction sites A and C in their 5 '-ends, respectively. Sfi recognizes and cuts the nucleotide sequence 5-GGCCNNNNNGGCC-3'. By changing the nucleotides designated N, unique and non-compatible Sfi restriction sites are generated. The 3'- end of primer A is homologous to 25 bp of mouse IGPcR27, ending with the 10 bp downstream of the ATG. The 3'-end (25 bp) of primer C is homologous to a position approximately 2500 bp upstream of the ATG. The right arm of homology (hereafter referred to as B/D) is PCR amplified with primers B and D: B is located approximately 880 bp downstream of the ATG, and D approximately 2000 bp downstream of the stop codon. Both primers contain S i-restriction sites B or D in their 5 '-ends, respectively. To avoid the introduction of point mutations the Expand high fidelity PCR-System, (Boehringer Mannheim / Roche Diagnostics, Basel CH) is used. A ligation of A/C with B/D and a selection cassette leads to an approximately

800 bp deletion of the mIGPcR27 coding region, thereby creating a null allelle. Both PCR-products A/C and B/D are purified using Qiaquick PCR Purification Kit according to the manufacturer (Quiagen, Venlo, NL). The PCR-products are cleaved 3 hours at 50°C with 60 U Sfi and subsequently purified (Qiaquick PCR Purification kit). The final volume is 30 μl/product. The ES-cell selection cassette (IRES-β- lactamase-MCSneo) contains S r-sites A and B 5'- and 3'-, respectively (Wattler S, et al., 1999, Biotechniques, 26:1150-1159). A typical ligation is 50 ng lambda-KO-Sfi- arm (S/z-cleaved), 10 ng selection cassette, 1 ng A/C, 1 ng B/D, 1 x ligation buffer and 1U T4 ligase (Boehringer Mannheim / Roche Diagnostics, Basel CH). The ligation is carried out for 2 hours at room temperature. Two μl of the ligation are used for in vitro packaging ('Gigapack plus' from Stratagene, La Jolla CA, USA) for 1.5 hours at room temperature according to the manufacturer's instructions. Aliquots of 10 μl and 50 μl are used to infect C600 bacteria (Stratagene, La Jolla CA, USA) and infection is performed overnight. Single plaques in SM-buffer (Ausubel FM et al, 1994, "Current Protocols in Molecular Biology", John Wiley & Sons, New

York) are taken to infect BNN 132 bacteria (30 min at 30°C) for plasmid conversion and infection. Bacteria are cultured over 16 hours at 30°C in TB media (Ausubel FM et al, 1994, "Current Protocols in Molecular Biology", John Wiley & Sons, New York), containing 100 μg/ l ampicillin (Amersham Pharmacia Biotech, Piscataway NJ, USA; cat. no. US 11259-25). Plasmids are harvested using the Qiagen plasmid kit (Qiagen cat. no. 12143) according to the manufacturer's instructions. To verify plasmid integrity, Sfi and EcoRI -digests are performed.

The transformation of mouse 129 ES cells with the final targeting vector is performed according to standard procedures. Electroporated 129 mouse ES cells are double-selected with G418 (400 μg/ml) for 7 days and GANC (ganciclovir, 0.2 μM) for 3 days, starting on day 3 after electroporation, for positive and negative selection, respectively, thereby enriching for transformants having the neomycin resistance gene integrated into an endogenous IGPcR27 allele. Single cell clones are propagated, frozen down and expanded for DNA isolation. To identify positively targeted clones, ES cell DNA is isolated from selected clones, incubated with an appropriate restriction enzyme, and the digestion products separated on an agarose gel. Southern blots are hybridized with a 5' external probe and positive targeted candidates are verified by hybridization with a 3' external probe. A single integration is confirmed by hybridization with a probe derived from the neomycin gene, Positive ES cells are isolated and expanded in culture.

Example 10. Mice Deficient in the Expression of the IGPcR27 Gene.

Male chimeric mice are generated by micro-injection of ES cells carrying a recombined allele into 129/SvEv mouse blastocysts, using standard methodology.

The chimeric blastocyst is implanted into the uterus of a pseudopregnant mouse, prepared by mating females with vasectomized males of the same species. The chimeras are bred to wild type animals. Tail DNA is isolated from the offspring of these chimeric mice and analyzed by incubation with appropriate restriction enzymes followed by Southern analysis, using the same strategy as outlined above to determine germline transmission. The blots demonstrate the transmission into the mouse genome of the mutation altering the IGPcR27 allele in transfoxmant ES cells. The chimeric male mouse and its heterozygous progeny (+/-) are bred to produce mice homozygous for the mutation (-/-).

Northern blots are used to probe mRNA obtained from tissues of offspring for the presence or absence of transcripts encoding either the IGPcR27, the marker gene, or both. In addition, Western blots are used to assess IGPcR27 expression by probing with antibody specific for the receptor.

Those skilled in the art will be able to recognize, or be able to ascertain, using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the invention.

Claims

1. An isolated nucleic acid molecule, wherein said nucleic acid molecule comprises at least one of: (a) the nucleotide sequence of SEQ ID NO: 1 ;

(b) the nucleotide sequence of SEQ ID NO:9;

(c) a nucleotide sequence which encodes a polypeptide comprising the amino acid sequence of SEQ ID NO:2, or any unique fragment thereof wherein the amino acid sequence of the fragment is greater than ten amino acids in length.

(d) a nucleotide sequence which encodes a polypeptide comprising the amino acid sequence of SEQ ID NO: 10, or any unique fragment thereof wherein the amino acid sequence of the fragment is greater than ten amino acids in length.

2. An isolated nucleic acid molecule comprising an allelic variant of a nucleotide sequence which encodes a polypeptide comprising the amino acid sequence selected from the group of:

(a) the amino acid sequence of SEQ ID NO:2; and (b) the amino acid sequence of SEQ ID NOT 0; wherein said allelic variant contains at least 80%) nucleic acid homology and hybridizes to the complement of SEQ ID NO:l under highly stringent conditions equivalent to hybridization in 42°C in a hybridization solution comprising 50%) formamide, 1%> SDS, 1M NaCl, 10%> Dextran sulfate, and washing twice for 30 minutes in a wash solution comprising 0. lxSSC and 1%> SDS.

3. The isolated nucleic acid molecule of claims 1 or 2, comprising a nucleotide sequence which encodes at least one of the group of polypeptides, peptides and fusion proteins, comprising an amino acid sequence at least 70%) similar to an amino acid sequence selected from the group of:

(a) the amino acid sequence of SEQ ID NO:2; and (b) the amino acid sequence of SEQ ID NO: 10.

4. The isolated nucleic acid molecule of claims 1 to 3 operatively linked with a nucleotide regulatory sequence capable of controlling expression of the nucleic acid molecule in a host cell or non-human animal.

5. A vector comprising the isolated nucleic acid molecule of any of claims 1 to 4.

6. A host cell genetically engineered to contain at least one of: (a) the nucleic acid molecule of any of claims 1 to 4; or

(b) the vector of claim 5.

7. The host cell of claim 6 wherein said host cell is a eucaryotic cell, being at least one of: (a) a yeast cell;

(b) an insect cell; or

(c) a mammalian cell.

8. The human IGPcR27 protein of SEQ ID NO:2, or any unique fragment thereof wherein the amino acid sequence of the fragment is greater than ten amino acids in length, including but not limited to polypeptides, peptides, isolated domains and fusion proteins.

9. The mouse IGPcR27 protein of SEQ ID NO: 10, or any unique fragment thereof wherein the amino acid sequence of the fragment is greater than ten amino acids in length, including but not limited to polypeptides, peptides, isolated domains and fusion proteins.

10. Antibodies specifically targeting the IGPcR27 proteins of any of claims 8 or 9, and/or polypeptides, peptides, isolated domains and the IGPcR27 component of fusion proteins of said IGPcR27 proteins.

11. Agonists and antagonists of IGPcR27 protein that compete selectively with native natural IGPcR27 ligand and which modulate IGPcR27 gene expression or gene product activity, including: (a) 'small molecules' of molecular mass less than 6 kDa; (b) molecules of intermediate size, having molecular mass between 5 kDa to 15 kDa; and (c) large molecules of molecular mass greater than 12 kDa; the latter including mutant natural IGPcR27 ligand proteins that compete with native natural IGPcR27 ligand and which modulate IGPcR27 gene expression or gene product activity.

12. Anti-sense and ribozyme molecules that can be used to inhibit IGPcR27 gene expression or expression constructs used to enhance IGPcR27 gene expression.

13. Methods of identifying compounds of any of claims I I or 12, which modulate the activity of IGPcR27 or IGPcR27 gene expression.

14. Embryonic stem cells containing a disrupted endogenous IGPcR27 gene.

15. Non-human knock-out animals that do not express IGPcR27, wherein the endogenous animal ortholog of the IGPcR27 gene is functionally disrupted.

16. The non-human knock-out animals of claim 15, wherein the endogenous animal ortholog of the IGPcR27 gene is functionally disrupted by an homologous recombination method.

17. Mutated non-human animals that express a non-functional or partially functional form of IGPcR27.

18. A non-human transgenic animal model expressing the human IGPcR27 cDNA sequence as shown in SEQ ID NOT or the nucleic acid molecule of any of claims 1 to 4.

19. The non-human animal model according to any one of claims 17 to 18, whereby the human IGPcR27 is encoded by a nucleic acid sequence which is homozygous in said animal model.

20. Progeny of non-human animals of any of claims 15 to 19, including both heterozygous and homozygous offspring.

21. Non-human animals of any of claims 15 to 20, wherein the animal is from a genus selected from the group consisting of Mus (e.g., mice), Rattus (e.g., rats), Oryctologus (e.g., rabbits) and Mesocricetus (e.g., hamsters).

22. Use of the non-human animal according to any one of claims 15 to 21, for the dissection of the molecular mechanisms of the IGPcR27 pathway, for the identification and cloning of genes able to modify, reduce or inhibit the phenotype associated with IGPcR27 activity or deficiency.

23. Use of the animal model according to any of claims 15 to 21 for the identification of gene and protein diagnostic markers for diseases.

24. Use of the animal model according to any of claims 15 to 21 for the identification and testing of compounds useful in the prevention, amelioration or treatment of diseases associated with IGPcR27 activity or deficiency.

25. The use of any of claims 23 or 24 wherein the disease is selected from the group of diseases associated with signal processing in the central nervous system (CNS).

26. The use of claim 25 wherein the disease is selected from the group of diseases selected from the group of movement dysfunctions, disorders or diseases: tics, tremor, Tourette's syndrome, Parkinson's disease, Huntington's disease, dyskinesias, dystonia, pain and spasms.

27. A method of identifying compounds suitable for modulating the activity of the protein according to claim 8, for treatment of diseases characterized by aberrant expression or activity of IGPcR27.

28. A method of prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27, by the administration of compounds that bind specifically to the IGPcR27 gene or protein and/or which modulate IGPcR27 expression or IGPcR27 activity; the compounds that that bind specifically to the IGPcR27 gene or protein and/or which modulate IGPcR27 expression or IGPcR27 activity for the prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27; and the use of compounds that that bind specifically to the IGPcR27 gene or protein and/or which modulate IGPcR27 expression or IGPcR27 activity for prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27.

29. A gene therapy method of prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27, by the administration of vectors and/or host cells containing nucleotide sequences according to any of claims 1 to 7, that modulate IGPcR27 expression or IGPcR27 activity; the vectors and/or host cells containing nucleotide sequences according to any of claims 1 to 7 which modulate IGPcR27 expression or IGPcR27 activity for the prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27; and the use of vectors and/or host cells containing nucleotide sequences according to any of claims 1 to 7 which modulate IGPcR27 expression or IGPcR27 activity for prevention, amelioration or treatment of diseases characterized by aberrant expression or activity of IGPcR27.

30. The method of any of claims 27 to 29 wherein the disease is selected from the group of diseases associated with signal processing in the central nervous system

(CNS).

1. The method of claim 30 wherein the disease is selected from the group of diseases selected from the group of movement dysfunctions, disorders or diseases: tics, tremor, Tourette's syndrome, Parkinson's disease, Huntington's disease, dyskinesias, dystonia, pain and spasms.