CA2295210A1 - Prolactin secretion modulator - Google Patents

Abstract

The present invention relates to a ligand polypeptide prolactin secretion modulating activity, and has a function of modulating placental function. The ligand polypeptide can be used as a prolactin secretion-stimulating agent for the prevention and treatment of certain diseases associated with prolactin secretion, such as hypoovarianism, gonecyst cacogenesis, menopausal syndrome, and euthyroid hypometabolism. In addition, the ligand polypeptide of the invention can be used with advantage as an aphrodisiac. The ligand polypeptide of the invention can be used with advantage as a prolactin secretion inhibitory agent in the prevention and treatment of certain diseases associated with prolactin secretion, such as pituitary adenomatosis, brain tumor, emmeniopathy, autoimmune disease, prolactinoma, infertility, impotence, amenorrhea, galactorrhea, acromegaly, Chiari-Frommel syndrome, Argonz-del Castilo syndrome, Forbes-Albright syndrome, lymphoma, Sheehan syndrome or dyszoospermia. In addition, the ligand polypeptide of the present invention is used as an agent for treating or preventing chriocarcinomia, hydatid mole, irruption mole, abortion, unthrifty fetus, abnormal saccharometabolism, abnormal lipidmetabolism or oxytocia.

Description

W O 981589b2 PCT/JP98/02765 DESCRIPTION
PROLACTIN SECRETION MODULATOR
V
[Technical Field]
The present invention relates to an agent for ' modulating prolactin secretion and/or placental function, comprising a ligand polypeptide for a G
protein-coupled receptor protein.
[Background Art]
Many hormones and neurotransmitters mediate biological functions through specific receptors present on the cell membrane. Many of these receptors engage themselves in the intracellular transduction of signals through activation of the coupled guanine nucleotide-binding protein (hereinafter sometimes referred to briefly as G protein) and have the common structure comprising 7 transmembrane domains. Therefore, these receptors are collectively referred to as G protein-coupled receptor or 7-transmembrane receptor.
One of the pathways to modulate biological functions mediated by such hormones or neurotransmitters through G protein-coupled receptors is the hypothalamo-pituitary system. Thus, the secretion of pituitary hormone from the hypophysis is controlled by hypothalamic hormones (pitultatropic releasing factor) and the functions of the target cells or organs are regulated through the pituitary hormones released into the circulation. This pathway carries out functional modulations of importance to the living body, such as homeostasis and regulation of the reproduction, development, metabolism and growth of individuals. The secretion of pituitary hormones is controlled by a positive or negative feedback mechanism involving hypothalamic hormone and the peripheral hormone secreted from the target endocrine gland. The A:

various receptor proteins present in the hypophysis are playing a central role in the regulation of the hypothalamus-pituitary system.
Meanwhile, it is known that these hormones and factors as well as their receptors are not localized in the hypothalamus-pituitary system but are broadly distributed in the brain. Therefore, it is suspected that, in the central nervous system, this substance called hypothalamus hormone is functioning as a neurotransmitter or a neuromodulator. Moreover, the substance is distributed in peripheral tissues as well and thought to be playing important roles in the respective tissue.
The pancreas is playing a crucial role in the carbohydrate metabolism by secreting glucagon and insulin as well as digestive juice. While insulin is secreted from the pancreatic (3 cells, its secretion is mainly stimulated by glucose. However, it is known that a cells have a variety of receptors and the secretion of insulin is controlled by a number of factors in addition to glucose as well as peptide hormones, e.g. galanine, somatostatin, gastric inhibitory polypeptide, glucagon, amyrin, etc.; sugars, e.g. mannose etc.; amino acids, and neurotransmitters, among others.
The means only heretofore available for identifying ligands for said G protein-coupled receptor proteins is estimation from the homology in primary structure of G
protein-coupled receptor proteins.
Recently, investigation for novel opioid peptides by introducing a cDNA coding for a recept ~r protein tc:
which a ligand is unknown, i.e. an orphan G protein-coupled receptor protein, into animal cells has been reported (Reinsheid, R. K. et al., Science, 270, 792-794, 1995, Menular, J.-C., et al., Nature 377, 532-535, 1995). However, in view of similarities to known G

A:

protein-coupled receptor proteins and tissue distributions, it could be easily anticipated in these cases that the ligand would be belonging to the family of opioid peptides. The history of research and development in the realm of substances acting on the living body through the opioid receptor dates back to many years ago and various antagonists and agonists had been developed. Therefore, among the compounds artificially synthesized, an agonist of the receptor was picked out and, using it as a probe, expression of the receptor in the receptor cDNA-transfected cells was verified. Then, a search was made for an activator of the intracellular signal transduction which was similar to the agonist, the activator so found was purified, and the structure of the ligand was determined.

However, when the homology of an orphan receptor to known G protein-coupled receptor proteins is low, it was very difficult to predict its ligand.

As Examples of the orphan G protein-coupled receptor, a human receptor protein (Genomics, vo1.29, 335 (1995)) which is encoded by phGR3 (sometimes called GPR10) gene and a rat receptor protein, UHR-1 (Biochem.

Biophy. Res. Commun., vol/209, 606 (1995)), is known.

Ligands for orphan G protein-coupled receptors expressed in the hypophysis, central nervous system, and pancreatic a cells are considered to be useful for developing medicines, but their structures and functions have not been elucidated as yet.

[Disclosure of Invension]
Employing a cell in which a cDNA coding for orphan G protein-coupled receptor protein, phGR3 has been expressed by a suitable means and using measurement of a specific cell stimulation activity exemplified by a signal transduction activity as an indicator, the inventors of the present invention succeeded in A:

screening a polypeptide derived from bovine, human, rat and determined their amino acid sequences and nucleotide sequences.
Furthermore, the inventors found that the ligand polypeptide has prolactin secretion and/or placental function(s).
The present invention, therefore, relates to (1) an agent for modulating prolactin secretion which comprises a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein, (2) an agent as described in (1) above, wherein the ligand polypeptide is a polypeptide comprising an amino acid sequence represented by SEQ ID NO: 73 or a substantial equivalent thereto, or its amide or ester, or a salt thereof , {3) an agent as described in (2) above, wherein the polypeptide comprising an amino acid sequence represented by SEQ ID NO: 73 is a polypeptide comprising an amino acid sequence represented by SEQ ID
NO: 5, 8, 47, 50, 61 or 64, (4) an agent as described in (1) above, which is for promoting prolactin secretion, (5) an agent as described in {1) above, which is for inhibiting prolactin secretion, (6) an agent as described in (4) above, which is for treating or preventing hypoovarianism, gonecyst cacogenesis, menopausal symdrome, or euthyroid hypometabolism, (7) An agent as described in (5) above, which is for treating or preventing pituitary adenomat_~ s, brain tumor, emmeniopathy, autoimmune disease, pr :.ctinoma, infertility, impotence, amenorrhea, ga~actorrhea, -acromegaly, Chiari-Frommel symdrome, Argonz-del Castilo symdrome, Forbes-Albright symdrome, lymphoma, Sheehan _ syndrome or dyszoospermia, (8) An agent for modulating placental function, which r.
comprises a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein, (9) An agent as described in (8) above, which is for treating or preventing choriocarcinomia, hydatid mole, _ 5 irruption mole, abortion, unthrifty fetus, abnormal saccharometabolism, abnormal lipidmetabolism or oxytocia, (10) An agent as described in (4) above, which is for promoting lactation of domestic mammal, (11) An agent as described in (4) above, which is for an aphrodisiac, (12) An agent for diagnosing function of prolactin secretion, which comprises a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein, ( 13 ) Use of a ligand polypeptide , or a salt thereof , for a G protein-coupled receptor protein for maufacture of a medicament for modulating prolactin secretion, (14) A method for modulating prolactin secretion in a mammal, which comprises administering to said mammal a ligand polypeptide, or a salt thereof, for a G
protein-coupled receptor protein, ( 15 ) Use of a ligand polypeptide , or a salt thereof , for a G protein-coupled receptor protein for maufacture of a medicament for modulating placental function, and (16) A method for modulating placental function in a mammal, which comprises administering to said mammal a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein, and so on.
~ [Brief Description of the Drawings) Fig. 1 shows the nucleotide sequence of the human pituitary-derived G protein-coupled receptor protein cDNA fragment harbored in cDNA clone p19P2 isolated by PCR using human pituitary-derived cDNA and the amino h:

acid encoded by the nucleotide sequence. The primer used for sequencing was -21M13. The underscored region corresponds to the synthetic primer.
Fig. 2 shows the nucleotide sequence of the human pituitary-derived G protein-coupled receptor protein cDNA fragment harbored in cDNA clone p19P2 isolated by PCR using human pituitary-derived cDNA and the amino acid sequence encoded thereby. The primer used for sequencing was M13RV-N (Takara). The underscored region corresponds to the synthetic primer.
Fig. 3 shows a partial hydrophobic plot of the protein encoded by the human pituitary-derived G
protein-coupled receptor protein cDNA fragment harbored in p19P2 constructed according to the amino acid sequence shown in Fig. 1.
Fig. 4 shows a partial hydrophobic plot of the protein encoded by the human pituitary-derived G
protein-coupled receptor protein cDNA fragment harbored in p19P2 constructed according to the amino acid sequence shown in Fig. 2.
Fig. 5 is a diagram comparing the partial amino acid sequence of the protein encoded by the human pituitary-derived G protein-coupled receptor protein cDNA fragment harbored in p19P2 as shown in Figs. 1 and 2 with the known G protein-coupled receptor protein SI2863. The shadowed region represents the region of agreement.. The 1 to 9 amino acid sequence of p19P2 corresponds to the 1 to 99 amino acid sequence of Fig.
1 and the 156 to 230 amino acid sequence corresponds to the 1 to 68 amino acid sequence of Fig. 2.
Fig. 6 shows the .scleotide sequence of the MIN6-derived G protein-r:~oupled receptor protein cDNA
fragment based on the nucleotide sequences of the MIN6-derived G protein-coupled receptor protein cDNA _ fragments harbored in the cDNA clones pG3-2 and pGl-10 isolated by PCR using MIN6-derived cDNA and the amino acid sequence encoded by the nucleotide sequence. The underscored region corresponds to the synthetic primer.
Fig. 7 is a diagram comparing the partial amino acid sequence encoded by pG3-2/pGl-10 of the MIN6 derived G protein-coupled receptor protein shown in Fig.
6 with the partial amino acid sequence of the protein encoded by p19P2 shown in Figs. I and 2. The shadowed region corresponds to the region of agreement. The 1 to 99 amino acid sequence of the protein encoded by p19P2 corresponds to the 1 to 99 amino acid sequence of Fig. 1 and the 156 to 223 amino acid sequence corresponds to the 1 to 68 amino acid sequence of Fig .
2. The 1 to 223 amino acid sequence of the protein encoded by pG3-2/pGl-10 corresponds to the 1 to 223 amino acid sequence of Fig. 6.
Fig. 8 is a partial hydrophobic plot of the MIN6-derived G protein-coupled receptor protein constructed according to the partial amino acid sequence shown in Fig. 6. Fig. 9 shows the entire nucleotide sequence of the human pituitary-derived G protein-coupled receptor protein cDNA harbored in the cDNA clone phGR3 isolated from a human pituitary-derived cDNA library by the plaque hybridization method using the DNA fragment inserted in p19P2 as a probe and the amino acid sequence encorded by the nucleotide sequence.
Fig. 10 shows the result of Northern blotting of human pituitary mRNA hybridized with radioisotope-labeled human pituitary cDNA clone phGR3.
Fig. 11 shows a hydrophobic plot of the protein encoded by the human pituitary-derived G protein coupled receptor protein cDNA harbored in the phGR3 as ~ constructed according to the amino acid sequence shown in Fig. 9.
_ Fig. 12 shows the nucleotide sequence of the MIN6 derived G protein-coupled receptor protein cDNA
fragment harbored in the cDNA clone p5S38 isolated by h.
PCR using MIN6-derived cDNA and the amino acid sequence encoded by the nucleotide sequence. The underscored region corresponds to the synthetic primer.
Fig. 13 shows a diagram comparing the partial amino acid sequence of MIN6-derived G protein-coupled receptor protein encoded by p5S38 shown in Fig. 12 with the partial amino acid sequence of G protein-coupled receptor protein encoded by the cDNA fragment harbored in p19P2 as shown in Figs. 1 and 2 and the partial amino acid sequence of G protein-coupled receptor protein encoded by the nucleotide sequence generated from the nucleotide sequences of cDNA fragments contained in pG3-2 and pGl-10 shown in Fig. 6. The shadowed region represents the sequence region of agreement. The 1 to 144 amino acid sequence of the protein encoded by p5S38 corresponds to the 1 to 144 amino acid sequence of Fig. 12, the 1 to 99 amino acid sequence of the protein encoded by p19P2 corresponds to the 1 to 99 amino acid sequence of Fig. 1 and the 156 to 223 amino acid sequence corresponds to 1 to 68 amino acid sequence of Fig. 2. The 1 to 223 amino acid sequence of the protein encoded by pG3-2/pGl-10 corresponds to the 1 to 223 amino acid sequence of Fig.
6.
Fig. 14 shows a partial hydrophobic plot of the protein encoded by the MIN6-derived G protein-coupled receptor protein cDNA harbored in p5S38 as constructed according to the partial amino acid sequence shown in Fig. 12.
Fig. 15 shows the results of the following analysis.
Thus , RT-PCR was carried out to confirm the expression of mRNA in CHO cells transfected by pAKKO-19P2 . Lanes -1-7 represent the results obtained by performing PCRs using serial dilutions of pAKKO-19P2 for comparison, i.e. the 10~.c1/ml stock solution (lane 1), 1/2 dilution (lane 2), 1/4 dilution (lane 3), 1/64 dilution (Lane 4), A.

1/256 dilution (lane 5), 1/1024 dilution (lane 6), and 1/4096 dilution (lane 7) of the plasmid as templates, and analyzing the reaction mixtures by 1.2% agarose gel electrophoresis. Lanes 8 through 11 are the results obtained by performing PCRs using a 1/10 dilution (lane 8), a 1/100 dilution (lane 9), and a 1/1000 dilution (lane 10) of the cDNA prepared from the CHO-19P2 cell line as templates and subjecting the respective reaction mixtures to electrophoresis. Lane 11 was obtained by performing PCR using a.template obtained by carrying out cDNA synthesis without reverse transcriptase and subjecting the PCR reaction product to electrophoresis. Lanes 12 and 13 were obtained by performing PCR using cDNAs prepared from mock CHO cells with and without addition of reverse transcriptase, respectively, as templates and subjecting the respective reaction products to electrophoresis. M
represents the DNA size marker. The lanes at both ends were obtained by electrophoresing 1 a 1 of ~ /Sty I
digest (Nippon Gene) and the second lane from right was obtained with 1 a 1 of ~ x 174/Hinc II digest (Nippon Gene). The arrowmark indicates the position of the band amplified by PCR of about 400 bp.
Fig. 16 shows the activity of the crude ligand peptide fraction extracted from rat whole brain to promote release of arachidonic acid metabolites from CHO-19P2 cells. The arachidonic acid metabolite releasing activity was expressed as % of the amount of [3H] arachidonic acid metabolites released in the presence of the crude ligand polypeptide fraction with the amount of [3H] arachidonic acid metabolites . released in the presence of 0.05% BAS-HABB being taken as 100%. The activity to promote release of arachidonic acid metabolites from the CHO-19P2 cell line Was detected in a 30% CH,CN fraction.
Fig. 17 shows the activity of the crude ligand polypeptide fraction extracted from bovine hypothalamus to promote release of arachidonic acid metabolites from CHO-19P2 cells. The arachidonic acid metabolite release-promoting activity was expressed as % of the 5 amount of ['H] arachidonic acid metabolites released in the presence of the crude ligand polypeptide fraction with the amount of [3H] arachidonic acid metabolites released in the presence of 0.05% BAS-HABB being taken as 100%. The activity to promote release of 10 arachidonic acid metabolites from the CHO-19P2 cell line was detected in a 30% CH3CN fraction just as in the crude ligand polypeptide fraction from rat whole brain.
Fig. 18 shows the activity of the fraction purified with the reversed-phase column C18 218TP5415 to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells. The active fraction from RESOURCE S was fractionated on C18 218TP5415.
Thus , chromatography was carried out at a flow rate of 1 ml/min. on a concentration gradient of 20%-30% CH3CN
/0.1% TFA/HZO, the eluate was collected in 1 ml fractions, and each fraction was lyophilized. Then, the activity of each fraction to specifically promote release of arachidonic acid metabolites from the CHO-19P2 cell line was determined. As a result, the activity was fractionated into 3 fractions (designated, in the order of elution, as P-1, P-2, and P-3).
Fig. 19 shows the activity of the fraction purified with the reversed-phase column diphenyl 219TP5415 to specifically promote aracr.~ :W nic acid metabolite rel~:~.~e from CHO-19P2 cells. he P-3 active fraction from C18 218TP5415 was f~s;.tionated on diphenyl 219TP5415. The chromatography was carried out at a flow rate of 1 ml/min. on a concentration gradient of .
22%-25% CH3CN /0.1% TFA/ HZO, the eluate was collected in 1 ml fractions, and each fraction was lyophilized.

Then, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells in each fraction was determined. As a result, the activity converged in a single peak.
Fig. 20 shows the activity of the fraction purified by reversed-phase column ,u RPC C2/C18 SC 2.1/10 to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells. The peak active fraction from diphenyl 219TP5415 was fractionated on a RPC C2/C18 SC 2.1/10. The chromatography was carried out at a flow rate of 100 a 1/min. on a concentration gradient of 22%-23.5% CH,CN /0.1% TFA/ H20, the eluate was collected in 100 ~c 1 fractions, and each fraction was lyophilized. Then, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells in each fraction was determined. As a result, the activity was found as two peaks of apparently a single substance (peptide).
Fig. 21 shows the activity of the P-2 fraction purified by reversed-phase column pRPC C2/C18 SC 2.1/10 to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells. The chromatography was carried out at a flow rate of 100 pl/min. on a concentration gradient of 21.5%-23.0% CH3CN /0.1%
TFA/distilled H20, the eluate was collected in 100 ,u 1 fractions, and each fraction was lyophilized. Then, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells in each fraction was determined. As a result, the activity was found as a peak of apparently a single substance.
Fig. 22 shows the nucleotide sequence of bovine hypothalamus ligand polypeptide cDNA fragment as . derived from the nucleotide sequence of the bovine hypothalamus-derived ligand polypeptide cDNA fragment which specifically promotes release of arachidonic acid WO 98/58962 PC'f/JP98/02765 h, metabolites from CHO-19P2 cells as harbored in a cDNA
clone isolated by PCR using bovine hypothalamus-derived cDNA and the amino acid sequence encoded by said nucleotide sequence. The region indicated by the arrowmark corresponds to the synthetic primer.
Fig. 23 shows the nucleotide sequence of the bovine hypothalamus-derived ligand polypeptide cDNA fragment generated according to the nucleotide sequence of the bovine hypothalamus-derived ligand polypeptide cDNA
fragment which specifically promotes release of arachidonic acid metabolites from CHO-19P2 cells as harbored in a cDNA clone isolated by PCR using bovine hypothalamus-derived cDNA and the amino acid sequence encoded by said nucleotide sequence. The region indicated by the arrowmark corresponds to the synthetic primer.
Fig. 24 shows the amino acid sequences (a) and (b) of the bovine hypothalamus-derived ligand polypeptides which specifically promote release of arachidonic acid metabolites from CHO-19P2 cells and the cDNA sequence coding for the full coding region of the ligand poly-peptides defined by SEQ ID N0:1 and SEQ ID N0:44.
Fig. 25 shows the concentration-dependent activity of synthetic ligand polypeptide (19P2-L31) to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells. The synthetic peptide was dissolved in degassed distilled HZO at a final concentration of 10-'M and diluted with 0.05% BSA-HBSS
to concentrations of IO-1zM-10-'M. The arachidonic acid metabolite releasing activity was expressed in the measure:' radioactivity of [3H] arachidonic acid metabo~.tes released in :he supernatant when the dilution was added to the cells. As a result, the activity of 19P2-31 to specifically promote release of .
arachidonic acid metabolites from CHO-19P2 cells was found in a concentration-dependent manner.

Fig. 26 shows the concentration-dependent activity of synthetic ligand polypeptide (19P2-L31(O)) to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells. The synthetic ligand peptide was dissolved in degassed distilled HZO at a final concentration of 10''M and diluted with 0.05% BSA-HBSS to concentrations of 10-1zM-10'6M. The arachidonic acid metabolite releasing activity was expressed in the measured radioactivity of [3H] arachidonic acid metabolites released in the supernatant when the dilution was added to the cells. As a result, the activity of 19P2-L31{O) to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was found in a dose-dependent manner.
Fig. 27 shows the activity of synthetic ligand polypeptide 19P2-L20 to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells. The synthetic peptide was dissolved in degassed distilled HZO at a final concentration of 10''M and diluted with 0.05% BSA-HBSS to concentrations of 10'i~M-10'6M. The arachidonic acid metabolite releasing activity was expressed in the measured radioactivity of ['H]
arachidonic acid metabolites released in the supernatant when the dilution was added to the cells.
As a result, the activity of 19P2-L20 to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was found in a dose-dependent manner.
Fig. 28 shows the 1.2% agarose gel electrophoregram of the DNA fragments of the phages cloned from a bovine genomic library as digested with restriction enzymes BamHI{B) and SalI(S). As the DNA size marker (M), StyI
~ digests of ~ phage DNA were used. In lane B, two bands derived from the vector were detected in positions _ between the first (19,329 bp) and second {7.743 bp) marker bands, as well as 3 bands derived from the inserted fragment between the third (6,223 bp) and 5th (3,472 bp) bands. In lane S, two bands derived from the vector were similarly detected but due to the overlap of the band of the inserted fragment, the upper band is thicker than the band in lane B.
Fig. 29 shows the nucleotide sequence around the coding region as decoded from bovine genomic DNA. The 1st to 3rd bases (ATG) correspond to the translation start codon and the 767th to 769th bases (TAA) correspond to the translation end codon.
Fig. 30 shows a comparison between the nucleotide sequence {genome) around the coding region as deduced from bovine genomic DNA and the nucleotide sequence (cDNA) of bovine cDNA cloned by PCR. The sequence region of agreement is indicated by shading. As to the 101st to 572nd region, there is no corresponding region in the nucleotide sequence of cDNA, indicating that it is an intron.
Fig. 31 shows the translation of the amino acid sequence encoded after elimination of the intron from the nucleotide sequence around the coding region as decoded from bovine genomic DNA.
Fig. 32 shows the full-length amino acid sequence and the cDNA sequence coding for the full coding region of rat ligand polypeptide.
Fig. 33 shows amino acid sequence of bovine ligand polypeptide and the nucleotide sequences of DNAs coding for bovine polypeptide and rat polypeptide. The arrowmark indicates the region corresponding to the synthetic primer.
Fig. 34 shows the full-length amino acid sequence and the seauence of cDNA coding for the full coding region of human ligand polypeptide.
Fig. 35 shows a comparison of the amino acid sequences in the translation region of bovine ligand .
polypeptide, rat ligand polypeptide, and human ligand polypeptide.

A:
Fig. 36 shows the results of a receptor binding experiment with an iodine-labeled ligand polypeptide in living cells.
Fig. 37 shows the arachidonic acid metabolite 5 releasing activity of the ligand polypeptide in CHO
19P2-9 and CHO-UHR1.
Fig. 38 shows the results of RT-PCR assays of UHR-1 expressed in rat tissues. Each value is the mean S:E.M. of 3 experiments.
10 Fig. 39 shows the results of RT-PCR assays of the ligand polypeptide expressed in rat tissues. Each value is the mean t S.E.M. of 3 experiments.
Fig. 40 shows the influence of the ligand polypeptide on the glucose-induced plasma insulin 15 concentration determined by radioimmunoassay.
Fig. 41 shows the measured motor activity of mice treated with 10 nmol of the ligand polypeptide. (a):
spontaneous motor activity, (b): rearing Fig. 42 shows the measured motor activity of mice treated with 1 nmol of the ligand polypeptide. (a):
spontaneous motor activity, (b): rearing Fig. 43 shows the measured motor activity of mice treated with 0.1 nmol of the ligand polypeptide. (a):
spontaneous motor activity, (b): rearing Fig. 44 shows the measured motor activity of mice treated with 0.01 nmol of the ligand polypeptide. (a):
spontaneous motor activity, (b): rearing Fig. 45 shows the change in the body temperature of mice upon administration of the ligand polypeptide into the cerebral ventricle 15 hours following subcutaneous administration of 3 mg/kg reserpine. The single asterisk * stands for p<0.05 and the double asterisk ** for p<0.01.
Fig. 46 shows a schematic diagram showing a microinjection cannula inserted into the area postrema {AP) at an angle of 20 degrees.

A.

Fig. 47 shows a typical example of pulse wave and mean blood pressure following injection of the ligand polypeptide into AP [Conscious rat, 10 nmol at a flow rate of 1 ~.tl/min].
Fig. 48 shows the plasma GH level following administration of the ligand polypeptide 50 nmol into the third ventricle of rats under pentobarbital anesthesia.
Fig. 49 shows the plasma GH level following administration of the ligand polypeptide into the third ventricle.
To unrestrained conscious rats, the ligand polypeptide or PBS was administered into the third ventricle following intraatrial injection of GHRH 5 a g/kg. The point of time at which the polypeptide was administered was reckoned as 0 min. *: p<0.05; **:
p<0.01.
Fig. 50 shows the relationship of ligand polypeptide antiserum with absorbance.
Fig. 51 shows the results of determination of arachidonic acid metabolite releasing activity of the anti-ligand polypeptide polyclonal antibody.
Fig. 52 shows the nucleotide sequence of the full coding region of rat UHR-1 constructed on the expression vector pAKKO-UHR-1 and the amino acid sequence encoded thereby.
Fig. 53 shows the nucleotide sequence of the inserted fragment of plasmid pmGB3. ~ indicates the sequence corresponding to the primer.
Fig. 54 shows the predicted cDNA and translated protein based on the nucleotide seque~:~e of plasmic pmGB3. --~ indicates the sequence corre~.ponding to the .
primer. The sequence flanked by .~ .~ is the sequence predicted to be an intron.
Fig. 55 shows the change in prolactin release from rat pituitary RC-4B/C cells upon addition of h:

ligand polypeptide I9P2-L31.
Fig. 56 shows the change in prolactin secretion from primary cultured rat pituitary cells upon addition f of ligand polypeptide 19P2-L31.
Fig. 57 shows the time course of expression of UHR-1 gene in the rat placenta described in Example 48.
Fig. 58 shows the time course of plasma prolactin concentration after administration of 19P2-L31 in unrestrained male rats. *=p<0.05. Each value is the mean ~ S.E.M. of 3-4 experiments.
Fig. 59 shows the time course of plasma prolactin concentration after administration of 19P2-L31 in unrestrained female rats. *=p<0.05. Each value is the mean t S.E.M. of 3-4 experiments.
Fig. 60 shows the time course of plasma prolactin concentration was determined among the sexual cycle.
[Best Mode for Carrying Out the Invention]
In the specification and drawings of the present application, the abbreviations used for bases (nucleotides), amino acids and so forth are those recommended by the IUPAC-IUB Commission on Biochemical Nomenclature or those conventionally used in the art.
Examples thereof are given below. Amino acids for which optical isomerism is possible are, unless otherwise specified, in the L form.
DNA : Deoxyribonucleic acid cDNA : Complementary deoxyribonucleic acid A . Adenine T . Thymine G . Guanine C . Cytosine RNA . Ribonucleic acid mRNA : Messenger ribonucleic acid dATP . Deoxyadenoslne triphosphate dTTP . Deoxythymidine triphosphate A:

dGTP . Deoxyguanosine triphosphate dCTP . Deoxycytidine triphosphate ATP . Adenosine triphosphate EDTA : Ethylenediamine tetraacetic acid SDS . Sodium dodecyl sulfate EIA . Enzyme Immunoassay G, Gly: Glycine (or Glycyl) A, Ala: Alanine (or Alanyl) V, Val: Valine (or Valyl) L, Leu: Leucine (or Leucyl) I, Ile: Isoleucine (or Isoleucyl) S, Ser: Serine (or Seryl) T, Thr: Threonine (or Threonyl}

C, Cys: Cysteine (or Cysteinyl) M, Met: Methionine (or Methionyl) E, Glu: Glutamic acid (or Glutamyl}

D, Asp: Aspartic acid (or Aspartyl) K, Lys: Lysine (or Lysyl) R, Arg: Arginine (or Arginyl) H, His: Histidine (or Histidyl) F, Phe: Phenylalamine (or Phenylalanyl) Y, Tyr: Tyrossine (or Tyrosyl) W, Trp: Tryptophan (or Tryptophanyl) P, Pro: Proline (or Prolyl}

N, Asn: Asparagine (or Asparaginyl) Q, Gln: Glutamine (or Glutaminyl) pGlu:
Pyroglutamic acid (or Pyroglutamyl}

Me:
Methyl Et:
Ethyl Bu :
Butyl Ph:
Phenyl TC:
Thiazolidinyl-4(R)-carboxamide In this specification, substitutions, protective groups and reagents commonly used are indicated by the following abbreviations:

BHA
.
benzhydrylamine pMBHA . p-methylbenzhydrylamine Tos . p-toluenesulfonyl CHO . formyl HONB . N-hydroxy-5-norbornene-2,3-dicarboxyimide OcHex . cyclohexyl ester Bzl . benzyl C1Z-Bzl . dichloro-benzyl Bom , benzyloxymethyl Br-Z . 2-bromobenzyioxycarbonyl Boc . t-butoxycarbonyl DCM . dichloromethane HOBt . 1-hydroxybenztriazole DCC . N,N'-dicyclohexylcarbodiimide TFA . trifluoro acetate DIEA . diisopropylethylamine Fmoc . N-9-fluorenylmethoxycarbonyl DNP . dinitrophenyl Bum . t-butoxymethyl Trt . trityl As used herein the term "substantial equivalent(s)"
means that the activity of the protein, e.g., nature of the binding activity of the ligand and the receptor and physical characteristics are substantially the same.
Substitutions, deletions or insertions of amino acids often do not produce radical changes in the physical and chemical characteristics of a polypeptide, in which case polypeptides containing the substitution, deletion, or insertion would be considered to be substantially equivalent to polypeptides lacking the substitution, deletion, or insertion.
Substantially equivalent substitutes for an amino acid within the sequence may be selected from other members of the class to which the amino acid belongs.
(1) The non-polar (hydrophobic) amino acids include alanine, leucine, isoleucine, valine, proline, phenylalanine, tryptophan and methionine. (2) The polar neutral amino acids include glycine, serine, threonine, cysteine, tyrosine, asparagine, and glutamine. (3) The positively charged (basic) amino acids include arginine, lysine and histidine. (4) The 5 negatively charged (acidic) amino acids include aspartic acid and glutamic acid.
The amino acids being comprised the ligand polypeptide of the present invention may form D-form or L-form, but usually form L-form.
10 The ligand polypeptide according to the present invention is a polypeptide which is capable of binding to G protein-coupled receptor protein and comprising an amino acid sequence represented by SEQ ID N0:73 or its substantial equivalent thereto, or its amide or ester, 15 or a salt thereof(hereinafter sometimes referred to briefly as the ligand polypeptide or the polypeptide).
In SEQ ID N0:73, Xaa at 10th position is Ala or Thr; Xaa at 11th position is Gly or Ser; and Xaa at 2lth position is H, Gly, or GlyArg.

20 Preferable example of the amino acid sequence represented by SEQ ID N0:73 is the amino acid sequence represented by SEQ ID N0:5, 8, 47, 50, 61 or 64. Among them, the amino acid sequence represented by SEQ ID
N0:61 or 64 is more preferable. Further, the amino acid sequence represented by SEQ ID 64 is more preferable.
The above ligand polypeptide of the present invention includes any polypeptides derived from any tissues, e.g. pituitary gland, pancreas, brain, kidney, liver, gonad, thyroid gland, gall bladder, bone marrow, adrenal gland, skin, muscle, lung, digestive canal, blood vessel, heart, etc.; or cells o= rnan and other warm-blooded animals, e.g. guinea pig, rat, mouse, swine, sheep, bovine, monkey, etc. and comprising an amino acid sequence represented by SEQ ID N0:73, preferably the amino acid sequence represented by SEQ
ID N0:5, 8, 47, 50, 61 or 64, or its substantial equivalent thereto. For example, in addition to the protein comprising the amino acid sequence of SEQ ID
N0:73, preferably the amino acid sequence represented by SEQ ID N0:5, 8, 47, 50, 61 or 64, the ligand polypeptide of the present invention includes the protein comprising an amino acid sequence having a homology of about 50-99.9%, preferably 70-99.9%, more preferably 80-99.9% and especially preferably 90-99.9%
to the amino acid sequence of SEQ ID N0:73, preferably the amino acid sequence represented by SEQ ID N0:5, 8, 47, 50, 61 or 64, and having qualitatively substantially equivalent activity to the protein comprising the amino acid sequence of SEQ ID N0:73, preferably the amino acid sequence represented by SEQ
ID N0:5, 8, 47, 50, 61 or 64. The term "substantially equivalent" means the nature of the receptor-binding activity, signal transduction activity and the like is equivalent. Thus, it is allowable that even differences among grades such as the strength of receptor binding activity and the molecular weight of the polypeptide are present.
To be more specific, the ligand polypeptide of the present invention includes the polypeptide derived from the rat whole brain, bovine hypothalamus, or human whole brain and comprising the amino acid sequence of SEQ ID N0:73. In addition, the ligand polypeptide of the present invention includes the polypeptides which comprises substantially equivalent polypeptides such as (I) polypeptides wherein 1 to 15, preferably 1 to 10, and more preferably 1 to 5 amino acid residues are deleted from the amino acid sequence of SEQ ID N0:73, ( 2 ) polypeptides wherein 1 to 80 , preferably 1 to 50.
more preferably 1 to 10 amino acid residues are added to the amino acid sequence of SEQ ID N0:73, (3) polypeptides wherein 1 to 15, preferably 1 to 10, more preferably 1 to 5 amino acid residues are substituted with one or more other amino acid residues of the amino acid sequence of SEQ ID N0:73, or (4) polypeptide wherein the amino acid, especially its side chain, of the polypeptide of the above (1) to (3) is modified, or its amide thereof, or its ester thereof, or a salt thereof.
Among them, preferred is the polypeptide comprising the amino acid sequence of SEQ ID N0:73 and the polypeptide comprising the amino acid sequence which a - 10 peptide of SEQ ID N0:74 is added to the N-terminus of the polypeptide comprising the amino acid sequence of SEQ ID N0:73.
The ligand polypeptide of the present invention can be changed or mutated by substitution, deletion, addition or modification as mentioned above (1) to (4), to a polypeptide which is stable against heat or proteases, or a polypeptide whose physiological function is activated.
The ligand polypeptide or an amide thereof , or an ester thereof, or a salt thereof includes the changed or mutated polypeptide mentioned above.
The peptides described in this specification, the left ends are the N-terminus (amino terminus) and the right end is the C-terminus (carboxyl terminus) -. 25 according to the convention of the peptide indication.
Furthermore , the polypeptide or partial peptide of the present invention includes those wherein the N-terminal side of Gln is cleaved in vivo to form pyroglutamyl peptide.
While the C-terminus of the polypeptide of the present invention, for ~~~ample the polypeptide comprising the amino acid sequence of SEQ Ir: N0:73, is usually carboxyl (-COOH) or carboxylate (-COO-), it may be amide (-CONHZ) or ester (-COOR) form. The ester residue R includes a C1_6 alkyl group such as methyl, ethyl, n-propyl, isopropyl, n-butyl, etc., a C,_8 .:

cycloalkyl group such as cyclopentyl, cyclohexyl, etc., a C6_12 aryl group such as phenyl , a - naphthyl , etc . , and a C,_1~ aralkyl group such as a phenyl-Cl_Z alkyl group, e.g. benzyl, phenethyl, benzhydryl, etc. or an c~ - naphthyl-Cl_Z alkyl , a . g . cx - naphthylmethyl etc . In addition, the ester may be a pivaloyloxymethyl ester which is broadly used for oral administration.
When the polypeptide of the present invention, for example the polypeptide comprises the amino acid sequence of SEQ ID N0:73, has a carboxyl or carboxylate group in any position other than the C-terminus, the corresponding amide or ester are also included in the concept of the polypeptide of the present invention.
The ester mentioned just above includes the esters mentioned for the C-terminus.
The preferred ligand polypeptide of the present invention is a peptide which the C-terminus is amidated.
Especially preferred is a polypeptide comprising the amino acid sequence of SEQ ID N0:5, 8, 47, 50, 61 or 64 which the C-terminus is amidated.
The salt of polypeptide of the present invention includes salts with physiologically acceptable bases, e.g. alkali metals or acids such as organic or inorganic acids, and is preferably a physiologically acceptable acid addition salt. Examples of such salts are salts thereof with inorganic acids, e.g.
hydrochloric acid, phosphoric acid, hydrobromic acid or sulfuric acid, etc, and salts thereof with organic acids, e.g. acetic acid, formic acid, propionic acid, fumaric acid, malefic acid, succinic acid, tartaric acid, citric acid, malic acid, oxalic acid, benzoic acid, . methanesulfonic acid or benzenesulfonic acid, etc.
The ligand polypeptide or amide or ester, or a salt thereof of the present invention may be 3S (1) manufactured from the tissues or cells of warm-blooded animals inclusive of human by purifying A:

techniques or (2) manufactured by the peptide synthesis as described hereinafter .
(3) Moreover, it can be manufactured by culturing a transformant carrying a DNA coding for the polypeptide as described hereinafter.
( 1 ) In the production from the tissues or cells of human or other warm-blooded animals, the ligand polypeptide can be purified and isolated by a process which comprises homogenizing the tissue or cells of human or other warm-blooded animal, extracting the homogenate with an acid, for instance, and subjecting the extract to a combination of chromatographic procedures such as reversed-phase chromatography, ion-exchange chromatography, affinity chromatography, etc.
(2) As mentioned above, the ligand polypeptide in the present invention can be produced by the per se known procedures for peptide synthesis. The methods for peptide synthesis may be any of a solid-phase synthesis and a liquid-phase synthesis. Thus, the objective peptide can be produced by condensing a partial peptide or amino acid capable of constituting the protein with the residual part thereof and, when the product has a protective group, the protective group is detached whereupon a desired peptide can be manufactured. The known methods for condensation and deprotection includes the procedures described in the following literature (1)-(5).
(1) M. Bodanszky and M. A. Ondetti, Peptide Synthesis, Interscience Publishers, New York, 1966 (2) Schroeder and L~:.ebke, The Peptide, Academic Press, New York, 1965 (3) Nobuo Izumiya et al., Fundamentals and Experiments in Peptide Synthesis, Maruzen, 1975 (4) Haruaki Yajima and Shumpei Sakakibara, Biochemical Experiment Series 1, Protein Chemistry IV, 205, 1977 (5) Haruaki Yajima (ed.), Development of Drugs-_ Continued, 14, Peptide Synthesis, Hirokawa Shoten After the reaction, the protein can be purified and 5 isolated by a combination of conventional purification techniques such as solvent extraction, column chromatography, liquid chromatography, and recrystallization. Where the protein isolated as above is a free compound, it can be converted to a suitable 10 salt by the known method. Conversely where the isolated product is a salt, it can be converted to the free peptide by the known method.
The amide of polypeptide can be obtained by using a resin for peptide synthesis which is suited for 15 amidation. The resin includes chloromethyl resin, hydroxymethyl resin, benzhydrylamine resin, aminomethyl resin, 4-benzyloxybenzyl alcohol resin, 4-methylbenz-hydrylamine resin, PAM resin, 4-hydroxymethylmethylphenylacetamidomethyl resin, 20 polyacrylamide resin, 4-(2',4'-dimethoxyphenyl-hydroxymethyl)phenoxy resin, 4-(2',4'-dimethoxyphenyl-Fmoc aminoethyl)phenoxy resin, and so on. Using such a resin, amino acids whose cx- amino groups and functional groups of side-chain have been suitably protected are 25 condensed on the resin according to the sequence of the objective peptide by various condensation techniques which are known per se. At the end of the series of reactions, the peptide or the protected peptide is removed from the resin and the protective groups are removed to obtain the objective polypeptide.
For the condensation of the above-mentioned protected amino acids, a variety of activating reagents for peptide synthesis can be used but a carbodiimide compound is particularly suitable. The carbodiimide includes DCC, N,N'-diisopropylcarbodiimide, and N-ethyl-N'-(3-dimethylaminoprolyl)carbodiimide. For 35 (4) Haruaki Yajima and Shum w:

activation with such a reagent, a racemization inhibitor additive, e.g. HOBt and the protected amino acid are directly added to the resin or the protected amino acid pre-activated as symmetric acid anhydride, HOBt ester, or HOOBt ester is added to the resin. The solvent for the activation of protected amino acids or condensation with the resin can be properly selected from among those solvents which are known to be useful for peptide condensation reactions. For example, N,N-dimethylformamide, N-methylpyrrolidone, chloroform, trifluoroethanol, dimethyl sulfoxide, DMF, pyridine, dioxane, methylene chloride, tetrahydrofuran, acetonitrile, ethyl acetate, or suitable mixtures of them can be mentioned. The reaction temperature can be selected from the range hitherto-known to be useful for peptide bond formation and is usually selected from the range of about -20'~ - 50~ . The activated amino acid derivative is generally used in a proportion of 1.5-4 fold excess. If the condensation is found to be insufficient by a test utilizing the ninhydrin reaction, the condensation reaction can be repeated to achieve a sufficient condensation without removing the protective group. If repeated condensation still fails to provide a sufficient degree of condensation, the unreacted amino group can be acetylated with acetic anhydride or acetylimidazole.
The protecting group of amino group for the starting material amino acid includes Z, Boc, tertiary-amyloxycarbonyl, isobornyloxycarbonyl, 4-methoxybenzyloxycarbonyl, C1-Z, Br-Z, adamantyloxycarbonyl, trifluoroacetyl, pt.:.. =lyl, f,~rmyl, 2-nitropheny'aulfenyl, diphenylphosphinotz~ ~1, or Fmoc.
The carboxy-_,::rotecting group that can be used includes but is not limited to the above-mentioned C1_6 alkyl, C3_ 8 cycloalkyl and C,_1, aralkyl as well as 2-adamantyl, 4-nitrobenzyl, 4-methoxybenzyl, 4-chlorobenzyl, phenacyl, A:

'~ benzyloxycarbonylhydrazido, tertiary butoxycarbonylhydrazido, and tritylhydrazido.
The hydroxy group of serine and threonine can be protected by esterification or etherification. The group suited for said esterification includes carbon derived groups such as lower alkanoyl groups, e.g.
acetyl etc., aroyl groups, e.g. benzoyl etc., benzyloxycarbonyl, and ethoxycarbonyl. The group suited for said etherification includes benzyl, tetrahydropyranyl, and tertiary-butyl.
The protective group for the phenolic hydroxyl group of tyrosine includes Bzl, C12-Bzl, 2-nitrobenzyl, Br-Z, and tertiary-butyl.
The protecting group of imidazole for histidine includes Tos, 4-methoxy-2,3,6-trimethylbenzenesulfonyl, DNP, benzyloxymethyl, Bum, Boc, Trt, and Fmoc.
The activated carboxyl group of the starting amino acid includes the corresponding acid anhydride, azide, and active esters, e.g. esters with alcohols such as pentachlorophenol, 2,4,5-trichlorophenol, 2,4-dinitrophenol, cyanomethyl alcohol, p-nitrophenol, HONB, N-hydroxysuccinimide, N-hydroxyphthali.mide, HOBt, etc.
The activated amino group of the starting amino acid includes the corresponding phosphoramide.
The method for elimination of protective groups includes catalytic reduction using hydrogen gas in the presence of a catalyst such as palladium black or palladium-on-carbon, acid treatment with anhydrous hydrogen fluoride, methanesulfonic acid, trifluoromethanesulfonic acid, trifluoroacetic acid, or a mixture of such acids, base treatment with diisopropylethylamine, triethylamine, piperidine, piperazine, reduction with sodium metal in liquid ammonia. The elimination reaction by the above-mentioned acid treatment is generally carried out at a temperature of -20 °C - 40 °C and can be conducted h:

advantageously with addition of a canon acceptor such as anisole, phenol, thioanisole, m-cresol, p-cresol, dimethyl sulfide, 1,4-butanedithiol, 1,2-ethanedithiol.
The 2,4-dinitrophenyl group used for protecting the S imidazole group of histidine can be eliminated by treatment with thiophenol, while the formyl group used for protecting the indole group of tryptophan can be eliminated by alkali treatment with dilute sodium hydroxide solution or dilute aqueous ammonia as well as the above-mentioned acid treatment in the presence of 1,2-ethanedithiol, 1,4-butanedithiol.
The method for protecting functional groups which should not take part in the reaction of the starting material, the protective groups that can be used, the method of removing the protective groups, and the method of activating the functional groups that are to take part in the reaction can all be selected from among the known groups and methods.
An another method for obtaining the amide form of the polypeptide comprises amidating the ~x - carboxyl group of the C-terminal amino acid at first, then extending the peptide chain to the N-side until the desired chain length, and then selectively deprotecting theca- amino group of the C-terminal peptide and thecx carboxy group of the amino acid or peptide that is to form the remainder of the objective polypeptide and condensing the two fragments whose - amino group and side-chain functional groups have been protected with suitable protective groups mentioned above in a mixed solvent such ~.:~ that mentioned hereinbefore. The parameters o:~ :~is condensation reaction can be the same as desc;.~~bed hereinbefore. From the protected peptide obtained by condensation, all the protective groups are removed by the above-described method to thereby provide the desired crude peptide. This crude peptide can be purified by known purification A:

procedures and the main fraction be lyophilized to provide the objective amidated polypeptide.
To obtain an ester of the polypeptide, the a -carboxyl group of the C-terminal amino acid is S condensed with a desired alcohol to give an amino acid ester and then, the procedure described above for production of the amide is followed.
The ligand polypeptide of the present invention, its amide or ester, or a salt thereof can be any peptide that has the same activities, e.g. pituitary function modulating activity, central nervous system function modulating activity, pancreatic function modulating activity, prolactin secretion modulating activity or placental function modulating activity, as the polypeptide which has an amino acid sequence of SEQ
ID N0:73 or its substantial equivalent thereto. As such peptides , there can be mentioned peptides wherein 1 to 15 amino acids residues are deleted from the above-mentioned amino acid sequence of SEQ ID N0:73.
To be specific, the peptide having an amino acid sequence corresponding to the 2nd to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 3rd to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 4th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 5th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 6th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 7th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 8th to 21st positions of the amino . acid sequence of SEQ ID N0:73, the peptide corresponding to the 9th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide A:
corresponding to the 10th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 11th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide 5 corresponding to the 12th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 13th to 21st positions of the amino acid sequence of SEQ ID N0:73, the peptide corresponding to the 14th to 21st positions of the 10 amino acid sequence of SEQ ID N0:73, and the peptide corresponding to the 15th to 21st positions of the amino acid sequence of SEQ ID N0:73, can be mentioned as preferred examples. Moreover, the peptide having the amino acid sequence of SEQ ID N0:74 is also 15 preferred.
Examples of the ligand polypeptide for the polypeptide comprises the amino acid sequence of SEQ ID
N0:5, 8, 47, 50 or 61 each of which is an preferable example of the polypeptide comprising the amino acid 20 sequence of SEQ ID NO: 73 , are the same as the cases of the polypeptide comprising the amino acid sequence of SEQ ID N0:73, mentioned above.
The DNA coding for the ligand .polypeptide or a partial peptide thereof of the present invention may be 25 any DNA comprising the nucleotide sequence encoding a polypeptide having an amino acid sequence of SEQ ID
N0:73 or its substantial equivalent thereto.
Furthermore, the DNA may be any of genomic DNA, genomic DNA library, tissue- or cell-derived cDNA, tissue- or 30 cell-derived cDNA library, and synthetic DNA. The vector for such as library may be any of bacteriophage, plasmide, cosmide, and phagimide. Moreover, it can be directly amplified by the RT-PCR(reverse transcription PCR) method by using an RNA fraction may be prepared from a tissue or cells .
To be more specific, as the DNA coding for a h.

polypeptide derived from rat whole brain or bovine hypothalamus and comprising the amino acid sequence of _ SEQ ID NO:1 or SEQ ID N0:44, the DNA comprising the nucleotide sequence of SEQ ID N0:2 can be exemplified.
In SEQ ID N0:2, R at 129th position represents G or A, and Y at 179th and 240th positions represents C or T.
When Y at 179th position is C, the amino acid sequence of SEQ ID NO:l is encoded, and when Y at 179th position is T, the amino acid sequence of SEQ ID N0:44 is encoded.
As the DNA coding for a bovine-derived polypeptide comprising the amino acid sequence of SEQ ID N0:3, 4, 5, 6, 7, 8, 9 or 10, a DNA comprising the nucleotide sequence of SEQ ID NO:11, 12, 13, 14, 15, 16, 17 or 18 can be exemplified. Here, R at 63th position of SEQ ID
N0:11, 13 , 14 or 15 and R at 29th position of SEQ ID
N0:12, 16, 17, or 18 represent G or A.
As the DNA coding for a rat-derived polypeptide of SEQ ID N0:45, 47, 48, 49, 50, 51, or 52, a DNA
comprising the nucleotide sequence of SEQ ID N0:46, 53, 54, 55, 56, 57, or 58 can be exemplified.
Furthermore, as the DNA coding for a human-derived peptide of SEQ ID N0:59, 61, 62, 63, 64, 65, or 66, a DNA comprising the nucleotide sequence of SEQ ID N0:60, 67, 68, 69, 70, 71, or 72 can be exemplified.
Among DNAs coding for the bovine-derived polypeptide comprising the amino acid sequence of SEQ
ID NO:1 or SEQ ID N0:44, the rat-derived polypeptide comprising the amino acid sequence of SEQ ID NO:45, or the human-derived polypeptide comprising the amino acid sequence of SEQ ID N0:59, DNA fragments comprising partial nucleotide sequences of 6 to 90, preferably 6 to 60, more preferably 9 to 30, and especially . preferably 12 to 30 can be advantageously used as DNA
probes as well.
The DNA coding for the ligand polypeptide or a partial peptide thereof of the present invention can be produced by the following genetic engineering procedures.
( 3 ) The DNA fully encoding the polypeptide of the present invention can be cloned either by PCR
amplification using synthetic DNA primers having a partial nucleotide sequence of the polypeptide or partial peptide or by hybridization using the DNA
inserted in a suitable vector and labeled with a DNA
fragment comprising a part or full region of a human-derived polypeptide or a synthetic DNA. The hybridization can be carried out typically by the procedure described in Molecular Cloning (2nd ed., J.
Sambrook et al., Cold Spring Harbor Lab. Press, 1989).
When a commercial library is used, the instructions given in the accompanying manual can be followed.
The cloned DNA coding for the polypeptide or partial peptide can be used directly or after digestion with a restriction enzyme or addition of a linker depending on purposes. This DNA has ATG as the translation initiation codon at the 5' end and may have TAA, TGA, or TAG as the termination codon at the 3' end.
The translation initiation and termination codons can be added by means of suitable DNA adapters.
An expression vector for the polypeptide or partial peptide can be produced by, for example (a) cutting out a target DNA fragment from the DNA for the polypeptide or partial peptide of the present invention and (b) ligating the target DNA fragment with the downstream side of a promoter in a suitable expression vector.
The vector may include plasmids derived from Escherichia coli, e.g., pBR322, pBR325, pUCl2, puCl3, etc.; plasmids derived from Bacillus subtilis, e.g., pUB110, pTP5, pC194, etc.; plasmids derived from yeasts e.g., pSHl9, pSHl5, etc.; bacteriophages such as ~1 -phage, and animal virus such as retrovirus, vaccinia A:

' virus and baculovirus.
According to the present invention, any promoter can be used as long as it is compatible with the host cell which is used for expressing a gene. When the host for the transformation is E. coli, the promoters are preferably trp promoters, lac promoters, recA
promoters, ~ PL promoters, lpp promoters, etc. When the host for the transformation is Bacillus, the promoters are preferably SPOT promoters, SP02 promoters, penP
promoters, etc. When the host is a yeast, the promoters are preferably PH05 promoters, PGK promoters, GAP promoters, ADH promoters, etc. When the host is an animal cell, the promoters include SV40-derived promoters, retrovirus promoters, metallothionein promoters, heat shock promoters, cytomegalovirus (CMV) promoters, SR a promoters, etc. An enhancer can be effectively utilized for expression.
As required, furthermore, a host-compatible signal sequence is added to the N-terminal side of the polypeptide or partial peptide thereof . When the host is E. cola, the utilizable signal sequences may include alkaline phosphatase signal sequences, OmpA signal sequences, etc. When the host is Bacillus, they may include cx -amylase signal sequences, subtilisin signal sequences, etc. When the host is a yeast, they may include mating factor cx signal sequences, invertase signal sequences, etc. When the host is an animal cell, they may include insulin signal sequences, cx interferon signal sequences, antibody molecule signal sequences, etc.
A transformant or transfectant is produced by using the vector thus constructed, which carries the polypeptide or partial peptide-encoding DNA of the . present invention. The host may be, for example, Escherichia microorganisms, Bacillus microorganisms, yeasts, insect cells, animal cells, etc. Examples of h:

the Escherichia include Escherichia cola K12.DH1 [Proc.
Natl. Acad. Sci. USA, Vol. 60, 160 (1968)], JM103 [Nucleic Acids Research, Vol. 9, 309 (1981)], JA221 [Journal of Molecular Biology, Vol. 120, 517 (1978)], HB101 [Journal of molecular Biology, Vol, 41, 459 (1969)], C600 [Genetics, Vol. 39, 440 (1954)], etc.
Examples of the Bacillus microorganism are, for example Bacillus subtilis MI114 [Gene, Vol. 24, 255 (1983)], 207-21 [Journal of Biochemistry, Vol. 95, 76 (1984)], etc. The yeast may be, for example, Saccharomyces cerevisiae AH22, AH22R-, NA87-11A, DKD-5D, 20B-12, etc.
The insect may include a silkworm (Bombyx mori larva), [Maeda et al, Nature, Vol. 315, 592 (1985)] etc. The host animal cell may be, for example, monkey-derived cell line, COS-7, Vero, Chinese hamster ovary cell line (CHO cell), DHFR gene-deficient Chinese hamster cell line (dhfr- CHO cell), mouse L cell, mouse myeloma cell, human FL, etc.
Depending on the host cell used, transformation is done using standard techniques appropriate to such cells. Transformation of Escherichia microorganisms can be carried out in accordance with methods as disclosed in, for example, Proc. Natl. Acad. Sci. USA, Vol. 69, 2110 (1972), Gene, Vol. 17, 107 (1982), etc.
Transformation of Bacillus microorganisms can be carried out in accordance with methods as disclosed in, for example, Molecular & General Genetics, Vol. 168, 111 (1979), etc. Transformation of the yeast can be carried out in accordance with methods as disclosed in, for example, Proc. Natl. Acad. Sci. USA, Vol. 75, 1929 (1978), etc. The insect ce?ls can be transformed in - accordance with methods as disclosed in, for example, Bio/Technology, 6, 47-55, 1988. The animal cells can be transformed by methods as disclosed in, for example, .
Virology, Vol. 52, 456, 1973, etc. The transformants or transfectants harboring the expression vector A:
carrying a polypeptide or partial peptide thereof encoding DNA are produced according to the aforementioned techniques.
Cultivation of the transformant (transfectant) in 5 which the host is Escherichia or Bacillus microorganism can be carried out suitably in a liquid culture medium.
The culture medium may contains carbon sources, nitrogen sources, minerals, etc. necessary for growing the transformant. The carbon source may include 10 glucose, dextrin, soluble starch, sucrose, etc. The nitrogen source may include organic or inorganic substances such as ammonium salts, nitrates, corn steep liquor, peptone, casein, meat extracts, bean-cakes, potato extracts, etc. Examples of the minerals may 15 include calcium chloride, sodium dihydrogen phosphate, magnesium chloride, etc. It is further allowable to add yeasts, vitamines, growth-promoting factors, etc.
It is desired that the culture medium is pH from about 5 to about 8.
20 The culture medium for Escherichia microorganism is preferably an M9 medium containing, for example, glucose and casamino acids (Miller, 3ournal of Experiments in Molecular Genetics), 431-433, Cold Spring Harbor Laboratory, New York, 1972. Depending on 25 necessity, the medium may be supplemented with drugs such as 3 l3 -indolyl acrylic acid in order to improve efficiency of the promoter. In the case of an Escherichia host, the cultivation is carried out usually at about 15 to 43~ for about 3 to 24 hours. As 30 required, aeration and stirring may be applied. In the case of Bacillus host, the cultivation is carried out ~ usually at about 30 to 40'~ for about 6 to 24 hours. As required, aeration and stirring may be also applied.
In the case of the transformant in which the host is a 35 yeast, the culture medium used may include, for example, a Burkholder minimum medium [Bostian, K.L. et al., Proc.

S.

Natl. Acad. Sci. USA, Vol. 77, 4505 (1980)], an SD
medium containing 0.5% casamino acids [Bitter, G.A. et al., Proc. Natl. Acad. Sci. USA, Vol. 81, 5330 (1984)], etc. It is preferable that the pH of the culture medium is adjusted to be from about 5 to about 8. The cultivation is carried out usually at about 20 to 35 ~
for about 24 to 72 hours. As required, aeration and stirring may be applied. In the case of the transformant in which the host is an insect, the culture medium used may include those obtained by suitably adding additives such as passivated (or immobilized) 10% bovine serum and the like to the Grace's insect medium (Grace, T.C.C., Nature, 195, 788 (1962)). It is preferable that the pH of the culture medium is adjusted to be about 6.2 to 6.4. The cultivation is usually carried out at about 27'C for about 3 to 5 days. As desired, aeration and stirring may be applied. in the case of the transformant in which the host is an animal cell, the culture medium used may include MEM medium [Science, Vol. 122, 501 (1952)], DMEM medium [Virology, Vol. 8, 396 (1959)], RPMI 1640 medium [Journal of the American Medical Association, Vol. 199, 519 (1967)], 199 medium [Proceedings of the Society of the Biological Medicine, Vol. 73, 1 (1950)], etc. which are containing, for example, about 5 to 20% of fetal calf serum. It is preferable that the pH is from about 6 to about 8. The cultivation is usually carried out at about 30 to 40~
for about 15 to 60 hours. As required, medium exchange, aeration and stirring may be applied.
Separation and purification of the polypex- # de from the above-mentioned cultures can be carW,ed out according to methods described herein below.
To extract polypeptide from the cultured microorganisms or cells, the microorganisms or cells are collected by known methods after the cultivation, A:

' suspended in a suitable buffer solution, disrupted by ultrasonic waves, lysozyme and/or freezing and thawing, etc. and, then, a crude extract of the polypeptide or partial peptide is obtained by centrifugation or filtration. Other conventional extracting or isolating methods can be applied. The buffer solution may contain a protein-denaturing agent such as urea or guanidine hydrochloride or a surfactant such as Triton X-100 (registered trademark, hereinafter often referred lU t0 aS °TMn).
In the case where the polypeptide is secreted into culture medium, supernatant liquid is separated from the microorganisms or cells after the cultivation is finished and the resulting supernatant liquid is collected by widely known methods. The culture supernatant liquid and extract containing the polypeptide or partial peptide can be purified by a suitable combination of widely known methods for separation, isolation and purification. The widely known methods of separation, isolation and purification may include methods which utilizes solubility, such as salting out or sedimentation with solvents methods which utilizes primarily a difference in the molecular size or weight, such as dialysis, ultrafiltration, gel filtration and SDS-polyacrylamide gel electrophoresis, methods utilizing a difference in the electric charge, such as ion-exchange chromatography, methods utilizing specific affinity such as affinity chromatography, methods utilizing a difference in the hydrophobic property, such as reverse-phase high-performance liquid chromatography, and methods utilizing a difference in the isoelectric point such as isoelectric electrophoresis, or chromatofocusing, etc.
In cases where the polypeptide thus obtained is in a free form, the free protein can be converted into a salt thereof by known methods or method analogous thereto. In case where the polypeptide thus obtained is in a salt form vice versa, the protein salt can be converted into a free form or into any other salt thereof by known methods or method analogous thereto.
The polypeptide produced by the transformant can be arbitrarily modified or a polypeptide can be partly removed therefrom, by the action of a suitable protein-modifying enzyme before or after the purification. The protein-modifying enzyme may include trypsin, chymotrypsin, arginyl endopeptidase, protein kinase, glycosidase, etc. The activity of the polypeptide thus formed can be measured by experimenting the coupling (or binding) with receptor or by enzyme immunoassays (enzyme linked immunoassays) using specific antibodies.
The ligand polypeptide of the present invention has prolactin secretion modulating activity, i.e.
prolactin secretion promoting and/or inhibiting activities. Thus, as will be understood from the Examples presented hereinafter, the ligand polypeptide of the present invention has prolactin secretion promoting activity and, therefore, finds application as a drug for preventing and/or treating various diseases associated with prolactin hyposecretion. On the other hand, the ligand polypeptide of the invention has a high affinity for the receptor proteins and, therefore, when used in an increased dose, causes desensitization for prolactin secretion, thus exhibiting prolactin secretion inhibiting activity. In this sense, it can be used as a drug for preventing and/or treating various diseases associated with prolactin hypersecretion.
Therefore, the ligand polypeptide of the invention can be used with advantage as a prolactin secretion-stimulating agent for the prevention and treatment of certain diseases associated with prolactin secretion, such as hypoovarianism, gonecyst cacogenesis, ' menopausal symdrome, euthyroid hypometabolism. In addition, the ligand polypeptide of the invention can be used with advantage as a aphrodisiac.
On the other hand, the ligand polypeptide of the invention can be used with advantage as a prolactin secretion inhibitory agent in the prevention and treatment of certain diseases associated with prolactin secretion, such as pituitary adenomatosis, brain tumor, emmeniopathy, autoimmune disease, prolactinoma, infertility, impotence, amenorrhea, galactorrhea, acromegaly, Chiari-Frommel symdrome, Argonz-del Castilo symdrome, Forbes-Albright symdrome, lymphoma, Sheehan syndrome or dyszoospermia.
In addition, the ligand poltpeptide of the present invention is used as a contraceptives based on its prolactin secretion inhibitory activity.
In addition, the ligand polypeptide of the invention can be used as a test reagent for study of the prolactin secretory function or a veterinary drug for use as a lactogogue in mammalian farm animals such as bovine, goat, and swine, and is even expected to find application in the elaboration of useful substances in such farm mammals and harvesting of the substances secreted into their milk.
In addition, the ligand polypeptide of the present invention has a function of modulating placental function, and can be used as an agent for treating or preventing chriocarcinomia, hydatid mole, irruption mole, abortion, unthrifty fetus, abnormal saccharometabolism, abnormal lipic3metabolism or oxytocia.
When the llgand polypeptide of the present invention is used as a pharmaceutical composition as described above, it can be used by conventional methods.
For example, it can be used orally in the form of tablets which may be sugar coated as necessary, A:
capsules, elixirs, microcapsules etc., or non-orally in the form of injectable preparations such as aseptic solutions and suspensions in water or other pharmaceutically acceptable liquids. These preparations 5 can be produced by mixing the polypeptide with physiologically acceptable carriers, flavoring agents, excipients, vehicles, antiseptics, stabilizers, binders etc. in unit dosage forms required for generally accepted manners of pharmaceutical making. Active 10 ingredient contents in these preparations are set so that an appropriate dose within the specified range is obtained.
Additives which can be mixed in tablets, capsules etc. include binders such as gelatin, corn starch, 15 tragacanth and gum arabic, excipients such as crystalline cellulose, swelling agents such as corn starch, gelatin and alginic acid, lubricants such as magnesium stearate, sweetening agents such as sucrose, lactose and saccharin, and flavoring agents such as 20 peppermint, akamono oil and cherry. When the unit dosage form is the capsule, the above-mentioned materials may further incorporate liquid carriers such as oils and fats. Sterile compositions for injection can be formulated by ordinary methods of pharmaceutical 25 making such as by dissolving or suspending active ingredients, naturally occuring vegetable oils such as sesame oil and coconut oil, etc. in vehicles such as water for injection.
Aqueous liquids for injection include physiological 30 saline and isotonic solutions containing glucose and other auxiliary agents, P.g., D-surbitol, D-m:~nnitol and sodium chloride, any may be used in comb~.nation with appropriate dissolution aids such as alcohols, e.g., ethanol, polyalcohols, e.g., propylene glycol and 35 polyethylene glycol, nonionic surfactants, e.g., polysorbate 80 (TM) and HCO-50 etc. Oily liquids h.

' include sesame oil and soybean oil, and may be used in combination with dissolution aids such as benzyl benzoate and benzyl alcohol. Furthermore the above-mentioned materials may also be formulated with buffers, e.g., phosphate buffer and sodium acetate buffer;
soothing agents, e.g., benzalkonium chloride, procaine hydrochloride; stabilizers, e.g., human serum albumin, polyethylene glycol; preservatives, e.g., benzyl alcohol, phenol; antioxidants etc. Normally, an appropriate ampule is f filled in with the thus prepared injectable liquid. Because the thus-obtained preparation is safe and of low toxicity, it can be administered to humans or warm-blooded mammals, e.g., mouse, rats, guinea pig, rabbits, chicken, sheep, pigs, bovines, cats, dogs, monkeys, baboons, chimpanzees, for instance.
The dose of said polypeptide is normally about 0.1-100 mg, preferably 1.0-50 mg, and more preferably 1.0-mg per day for a patient of euthyroid hypometabolism 20 (weighing 60 kg) in oral administration, depending on symptoms etc. In non-oral administration, it is advantageous to administer the polypeptide in the form of injectable preparation at a daily dose of about 0.01-30 mg, preferably about 0.1-20 mg, and more preferably about 0.1-10 mg per administration by an intravenous infection for a patient of euthyroid hypometabolism (weighing 60 kg), depending on subject of administration, target organ, symptoms, method of administration etc. For other animal species, J
corresponding does as converted per 60 kg weight can be administered.
- The G protein-coupled receptor protein _~r the above ligand polypeptide of the present invention may be any of G protein-coupled receptor proteins derived from various tissues, e.g. hypophysis, pancreas, brain, kidney, liver, gonad, thyroid gland, gall bladder, bone h.

marrow, adrenal gland, skin, muscle, lung, alimentary canal, blood vessel, heart, etc. of human and other warm-blooded animals, e.g. guinea pig, rat, mouse, swine, sheep, bovine, monkey, etc.; and comprising an amino acid sequence of SEQ ID N0:19, 20, 21, 22 or 23, or a substantial equivalent thereto. Thus, the G
protein-coupled receptor protein includes, in addition to proteins comprising the SEQ ID N0:19, 20, 21, 22 or 23, those proteins comprising amino acid sequences of about 90-99.9 homology to the amino acid sequence of SEQ ID N0:19, 20, 21, 22 or 23 and having qualitatively substantially equivalent activity to proteins comprising the amino acid sequence of SEQ ID N0:19, 20, 21, 22, or 23. The activities which these proteins possess may include ligand binding activity and signal transduction activity. The term "substantially equivalent" means that the nature of the ligand binding activity and the like is equivalent. Therefore, it is allowable that even differences among grades such as the strength of ligand binding activity and the molecular weight of receptor protein are present.
To be further specific, the G protein-coupled receptor proteins include human pituitary-derived G
protein-coupled receptor proteins which comprises the amino acid sequence of SEQ ID N0:19 or/and SEQ ID N0:20, mouse pancreas-derived G protein-coupled receptor proteins which comprises the amino acid sequence of SEQ
ID N0:22, and mouse pancreas-derived G protein-coupled receptor proteins which comprises the amino acid sequence of SEQ ID N0:23. As the human pituitary-derived G protein-coupled receptor proteins which com~:rises the amino acid sequence of SEQ ID N0:19 and/or SEQ ID N0:20 include the human pituitary-derived G protein-coupled receptor protein which comprises the amino acid sequence of SEQ ID N0:21. The G protein-coupled receptor proteins further include proteins wherein 1 to 30 amino acid residues, preferably 1 to 10 amino acid residues are deleted from the amino acid sequence of SEQ ID N0:19, 20, 21, 22 or 23, proteins wherein 1 to 30 amino acid residues, preferably l to 10 amino acid residues are added to the amino acid sequence of SEQ ID N0:19, 20, 21, 22, or 23, the proteins wherein 1 to 30 amino acid residues, preferably 1 to 10 amino acid residues in the amino acid sequence of SEQ ID N0:19, 20, 21, 22, or 23 are substituted with one or more other amino acid residues.
Here, the protein which comprises an amino acid sequence of SEQ ID N0:21 or a substantial equivalent thereto contains the full-length of the amino acid sequence for human pituitary-derived G protein-coupled receptor protein. The protein which comprises an amino acid sequence of SEQ ID N0:19 or/and SEQ ID N0:20 or a substantial equivalent thereto may be a partial peptide of the protein which comprises an amino acid sequence of SEQ ID N0:21 or a substantial equivalent thereto.
The protein which comprises an amino acid sequence of SEQ ID N0:22 or SEQ ID N0:23 or a substantial equivalent thereto is a G protein-coupled receptor protein which is derived from mouse pancreas but since its amino acid sequence is quite similar to the amino acid sequence of SEQ ID N0:19 or/and SEQ ID N0:20 (cf.
Example 8, Fig. 13 in particular), the protein which comprises an amino acid sequence of SEQ ID N0:22 or 23 or a substantial equivalent thereto is also subsumed in the category of said partial peptide of the protein which comprises an amino acid sequence of SEQ ID N0:21 or a substantial equivalent thereto.
Thus, the above-mentioned protein comprising an amino acid sequence of SEQ ID N0:21 or a substantial . equivalent thereto or a partial peptide of the protein or a salt thereof, which will be described below, includes the protein comprising an amino acid sequence of SEQ ID N0:19, 20, 22, or 23 or a substantial equivalent thereto, or a salt thereof.
Furthermore, the G protein-coupled receptor protein includes the protein in which the N-terminal Met has been protected with a protective group, e.g. C1_6 aryl such as formyl or acetyl, the protein in which the N-terminal side of Gln has been cleaved in vivo to form pyroglutamic acid, the protein in which the side chain of any relevant constituent amino acid has been protected with a suitable protective group, e.g. C1_6 acyl such as formyl or acetyl, and the complex protein such as glycoproteins available upon attachment of sugar chains.
The salt of G protein-coupled receptor protein includes the same kinds of salts as mentioned for the ligand polypeptide.
The G protein-coupled receptor protein or a salt thereof or a partial peptide thereof can be produced from the tissues or cells of human or other warm-blooded animals by the per se known purification technology or, as described above, by culturing a transformant carrying a DNA coding for the G protein-coupled receptor protein. It can also be produced in accordance with the procedures for peptide synthesis which are described above. The procedures for peptide synthesis is described in W096/05302 in detail.
A partial peptide of G protein-coupled receptor protein may include, for example, a fragment containing an extracellular portion of the G protein-coupled receptor protein, i.e. the site which is exposed outside the cell membranes. Examples of the partial peptide are fragments containing a region w: ch is an extracellular area (hydrophilic region) as analyzed in a hydrophobic plotting analysis of the G protein-coupled receptor protein, such as shown in Fig. 3, Fig.
4, Fig. 8, Fig. 11, or Fig. 14. Furthermore, a S:
fragment which partly contains a hydrophobic region may also be used. While peptides which separately contains each domain may be used too, peptides which contains multiple domains at the same time will be used as well.
5 The salt of a partial peptide of G protein-coupled receptor protein may be the same one as mentioned for the salt of ligand polypeptide.
The DNA coding for the G protein-coupled receptor protein may be any DNA comprising a nucleotide sequence 10 encoding the G protein-coupled receptor protein which comprises an amino acid sequence of SEQ ID N0:19, 20, 21, 22, or 23 or a substantial equivalent thereto. It may also be any one of genomic DNA, genomic DNA library, tissue- or cell-derived cDNA, tissue- or cell-derived 15 cDNA library, and synthetic DNA. The vector for such a library may include bacteriophage, plasmid, cosmid, and phargimide. Furthermore, using an RNA fraction prepared from a tissue or cells, a direct amplification can be carried out by the RT-PCR method.
20 To be specific, the DNA encoding the human pituitary-derived G protein-coupled receptor protein which comprises the amino acid sequence of SEQ ID N0:19 include a DNA which comprises the nucleotide sequence of SEQ ID N0:24. The DNA encoding the human pituitary-25 derived G protein-coupled receptor protein which comprises the amino acid sequence of SEQ ID N0:20 include a DNA which comprises the nucleotide sequence of SEQ ID N0:25. The DNA encoding the human pituitary-derived G protein-coupled receptor protein which 30 comprises the amino acid sequence of SEQ ID N0:21 include a DNA which comprises the nucleotide sequence - of SEQ ID N0:26. The DNA encoding the mouse pancreas derived G protein-coupled receptor protein which comprises the amino acid sequence of SEQ ID N0:22 35 include a DNA which comprises the nucleotide sequence of SEQ ID N0:27. The DNA encoding the mouse pancreas-h.

derived G protein-coupled receptor protein which comprises the amino acid sequence of SEQ ID N0:23 include a DNA comprising the nucleotide sequence of SEQ
ID N0:28.
A method for cloning the DNA completely coding for the G protein-coupled receptor protein, vector, promoter, host cell, a method for transformation, a method for culturing the transformant or a method for separation and purification of the G protein-coupled receptor protein may include the same one as mentioned for the ligand polypeptide.
To be specific, the plasmid phGR3 obtained in Example 5, described hereinafter, is digested with the restriction enzyme SalI and the translation frame for IS the full-length cDNA encoding hGR3 is isolated. This frame is subjected to ligation to, for example, the expression vector pAKKO-111 for animal cell use which has been treated with BAP (bacterial alkaline phosphatase) after SalI digestion for inhibition of autocyclization. After completion of the ligation reaction, a portion of the reaction mixture is used for transfection of, for example, Escherichia coli DH5.
Among the transformants obtained, a transformant in which the cDNA coding for hGR3 has been inserted in the forward direction with respect to a promoter, such as SR c~, which has been inserted into the expression vector beforehand is selected by mapping after cleavage with restriction enzymes or by nucleotide sequencing and the plasmid DNA is prepared on a production scale.
The thus-constructed DNA of the expression vector is b.ntroduced into CHO dhfr- cells using a kit for introducing a gene into animal cells~-by the calcium _ phosphate method, the liposome method or the like to provide a high G protein-coupled receptor protein (hGR3) expression CHO cell line.
The resulting CHO cells are cultured in a nucleic ' acid-free screening medium in a COZ incubator at 37 ~
using 5% COZ for 1-4 days so as to give the G protein-coupled receptor protein (hGR3).
The G protein-coupled receptor protein is purified S from the above CHO cells using an affinity column prepared by conjugating an antibody to the G protein coupled receptor protein or a partial peptide thereof to a support or an affinity column prepared by conjugating a ligand for the G protein-coupled receptor protein.
The activity of the G protein-coupled receptor protein thus formed can be measured by experimenting the binding with a ligand or by enzyme immunoassays using specific antibodies.
Hereinafter, a method for determing a ligand to the G protein-coupled receptor protein is described in detail.
The G protein-coupled receptor protein, the partial peptide thereof or a salt thereof is useful as a reagent for investigating or determining a ligand to said G protein-coupled receptor protein.
According to the present invention, methods for determining a ligand to the G protein-coupled receptor protein which comprises contacting the G protein-coupled receptor protein or the partial peptide thereof with the compound to be tested, and measuring the binding amount, the cell stimulating activity, etc. of the test compound to the G protein-coupled receptor protein or the partial peptide thereof are provided.
The compound to be tested may include not only known ligands such as _ angiotensins, bombesins, canavinoids, cholecystokinins, glutamine, serotonin, melatonins, neuropeptides Y, opioids, purine, vasopressins, oxytocins, VIP (vasoactive intestinal and related peptides), somatostatins, dopamine, motilins, amylins, bradykinins, CGRP (calcitonin gene related h:

peptides), leukotrienes, pancreastatins, prostaglandins, thromboxanes, adenosine, adrenaline, cx - and a -chemokines such as IL-8, GRO a , GRO ~3 , GRO r , NAP-2, ENA-78, PF4, IP10, GCP-2, MCP-I, HC14, MCP-3, I-309, MIP1 (x , MIP-1 f3 , RANTES, etc.; endothelins, enterogastrins, histamine, neurotensins, TRH, pancreatic polypeptides, galanin, modified derivatives thereof, analogues thereof, family members thereof and the like but also tissue extracts, cell culture supernatants, etc. of human or warm-blooded aminals such as mice, rats, swines, cattle, sheep and monkeys, etc. For example, said tissue extract, said cell culture supernatant, etc. is added to the G protein-coupled receptor protein for measurement of the cell stimulating activity, etc. and fractionated by relying on the measurements whereupon a single ligand can be finally determined and obtained.
In one specific embodiment of the present invention, said method for determining the ligand includes a method for determining whether a sample (including a compound or a salt thereof) is capable of stimulating a target cell which comprises binding said compound with the G protein-coupled receptor protein either in the presence of the G protein-coupled receptor protein, the partial peptide thereof or a salt thereof, or in a receptor binding assay system in which the expression system for the recombinant receptor protein is constructed and used; and measuring the receptor-mediated cell stimulating activity, etc. Examples of said cell stimulating activities that can be measured include promoting or inhibiting biological responses, e.g. liberation of arachidonic acid, liberation of acetylcholine, liberation of endocellular Ca2', production of endocellular cAMP, production of endocellular cGMP, production of inositol phosphate, changes in the cell membrane potential, phosphorylation WO 98/58962 PCT/JP98/02~65 ' of endocellular protein, activation of c-fos, decrease in pH, etc, and preferably liberation of arachidonic acid. Examples of said compound or a salt thereof capable of stimulating the cell via binding with the G
protein-coupled receptor protein include peptides, proteins, nonpeptidic compounds, synthetic compounds, fermented products, etc.
In more specific embodiments of the present invention, said methods for screening and identifying a ligand includes:
1) a method of screening for a ligand to a G protein-coupled receptor protein, which comprises contacting a labeled test compound with a G protein-coupled receptor protein or a salt thereof or its partial peptide or a salt thereof, and measuring the amount of the labeled test compound binding with said protein or salt thereof or with said partial peptide or salt thereof;
2) a method of screening for a ligand to a G protein coupled receptor protein, which comprises contacting a labeled test compound with cells containing the G
protein-coupled receptor protein or the membrane fraction of said cell, and measuring the amount of the labeled test compound binding with said cells or said membrane fraction;
3) a method of screening for a ligand to a G protein-coupled receptor protein, which comprises contacting a labeled test compound with the G protein-coupled receptor protein expressed on cell membranes by culturing transformants carrying the G protein-coupled receptor protein-encoding DNA and measuring the amount of the labeled test compound binding with said G
protein-coupled receptor protein;
4) a method of screening for a ligan to a G protein coupled receptor protein, which comprises contacting a test compound with cells containing the G protein coupled receptor protein, and measuring the cell h.
stimulating activity, e.g. promoting or inhibiting activity on biological responses such as liberation of arachidonic acid, liberation of acetylcholine, liberation of endocellular Ca2', production of endocullular cAMP, production of endocellular cGMP, production of inositol phosphate, changes in the cell membrane potential, phosphorylation of endocellular protein, activation of c-fos, lowering in pH, etc. via the G protein-coupled receptor protein; and 5) a method of screening for a ligand to the G
protein-coupled receptor protein, which comprises contacting a test compound with the G protein-coupled receptor protein expressed on the cell membrane by culturing transformants carrying the G protein-coupled receptor protein-encoding DNA, and measuring at least one cell stimulating activity, e.g., an activity for promoting or inhibiting physiological responses such as liberation of arachidonic acid, liberation of acetylcholine, liberation of endocellular Ca2+, production of endocellular cAMP, production of endocellular cGMP, production of inositol phosphate, changes in the cell membrane potential, phosphorylation of endocellular protein, activation of c-fos, lowering in pH etc. via the G protein-coupled receptor protein.
Described below are specific illustrations of the method for screening and identifying ligands.
First, the G protein-coupled receptor protein used for the method for determining the ligand may include any material so far as it contains a G protein-coupled receptor protein, a partial peptide thereof or a salt thereof a ~ txou~~~, it is preferable to exp°ess large amounts o. '.:he G protein-coupled receptor proteins in animal cells.
In the manufacture of the G protein-coupled receptor protein, the above-mentioned method can be used and carried out by expressing said protein h:

encoding DNA in mammalian cells or in insect cells.
With respect to the DNA fragment coding for a particular region such as an extracellular epitope, the extracellular domains, etc., complementary DNA may be used although the method of expression is not limited thereto. For example, gene fragments or synthetic DNA
may be used as well.
In order to introduce the G protein-coupled receptor protein-encoding DNA fragment into host animal cells and to express it efficiently, it is preferred that said DNA fragment is incorporated into the downstream side of polyhedron promoters derived from nuclear polyhedrosis virus belonging to baculovirus, promoters derived from SV40, promoters derived from retrovirus, metallothionein promoters, human heat shock promoters, cytomegalovirus promoters, SR c~ promoters, etc. Examinations of the quantity and the quality of the expressed receptor can be carried out by methods per se known to those of skill in the art or methods similar thereto based upon the present disclosure. For example, they may be conducted by methods described in publications such as Nambi, P. et al: The Journal of Biochemical Society, vo1.267, pages 19555-19559 (1992).
Accordingly, with respect to the determination of the ligand, the material containing a G protein-coupled receptor protein or partial peptide thereof may include products containing G protein-coupled receptor proteins which are purified by methods per se known to those of skill in the art or methods similar thereto, peptide fragments of said G protein-coupled receptor protein, cells containing said G___ protein-coupled receptor protein, membrane fractions of the cell containing said protein, etc.
When the G protein-coupled receptor protein containing cell is used in the determining method of the ligand, said cell may be immobilized with binding agents including glutaraldehyde, formalin, etc. The immobilization may be carried out by methods per se known to those of skill in the art or methods similar thereto.
The G protein-coupled receptor protein-containing cells are host cells which express the G protein-coupled receptor protein. Examples of said host cells are microorganisms such as Escherichia coli, Bacillus subtilis, yeasts, insect cells, animal cells, etc.
The cell membrane fraction is a cell membrane-rich fraction which is prepared by methods per se known to those of skill in the art or methods similar thereto after disruption of cells. Examples of cell disruption may include a method for squeezing cells using a Potter-Elvehjem homogenizer, a disruption by a blaring blender or a Polytron manufactured by Kinematica, a disruption by ultrasonic waves, a disruption via blowing out cells from small nozzles together with applying a pressure using a French press or the like, etc. In the fractionation of the cell membrane, a fractionation method by means of centrifugal force such as a fractional centrifugal separation and a density gradient centrifugal separation is mainly used. For example, disrupted cellular liquid is centrifuged at a low speed (500 rpm to 3,000 rom) for a short period (usually, from about one to ten minutes), the supernatant liquid is further centrifuged at a high speed (15,000 rpm to 30,000 rpm) usually for 30 minutes to two hours and the resulting precipitate is used as a membrane fraction. Said membrane fraction contains a lot of the expresses. : protein-coupled receptor protein and a lot of membrar:a components such as phospholipids and membrane proteins derived from the cells.
The amount of the G protein-coupled receptor .
protein in the membrane fraction cell containing said G
protein-coupled receptor protein is preferably 10' to A.

' 108 molecules per cell or, more preferably, 105 to 10' molecules per cell. Incidentally, the greater the expressed amount, the higher the ligand binding activity (specific activity) per membrane fraction whereby the construction of a highly sensitive i screening system becomes possible and, moreover, it permits measurement of a large amount of samples within the same lot.
In conducting the above-mentioned methods 1) to 3) wherein ligands capable of binding with the G protein coupled receptor protein are determined, a suitable G
protein-coupled receptor fraction and a labeled test compound are necessary. The G protein-coupled receptor fraction is preferably a naturally occurring (natural type) G protein-coupled receptor, a recombinant G
protein-coupled receptor having the activity equivalent to that of the natural type . Here , the term "activity equivalent to" means the equivalent ligand binding activity, etc. as discussed above.
Suitable examples of the labeled test compound include above-mentioned compound to be tested which are labeled with [ 3H ] , [ lasl ] , [ "C ] , [ 35S ] , etc .
Specifically, the determination of ligands capable of binding with G protein-coupled receptor proteins is carried out as follows:
First, cells or cell membrane fractions containing the G protein-coupled receptor protein are suspended in a buffer suitable for the assay to prepare the receptor sample for conducting the method of determining the ligand binding with the G protein-coupled receptor protein. The buffer may include any buffer such as Tris-HCl buffer or phosphate buffer with pH 4-10, preferably, pH 6-8, etc., as long as it does not inhibit the binding of the ligand with the receptor.
In addition, surface-active agents such as CHAPS, Tween 80T''' (Kao-Atlas, Japan), digitonin, deoxycholate, etc.

and various proteins such as bovine serum albumin(BSA), gelatin, milk derivatives, etc. may be added to the buffer with an object of descreasing the non-specific binding. Further, a protease inhibitor such as PMSF, leupeptin, E-64 (manufactured by Peptide Laboratory), pepstatin, etc. may be added with an object of inhibiting the decomposition of the receptor and the ligand by protease. A test compound labeled with a predetermined (or certain) amount (5,000 cpm to 500,000 cpm ) of [ 3H ] , [ 125I ] , [ 1'C ] , [ 35S ] , etc . coexists in 0 . O 1 ml to 10 ml of said receptor solution. In order to know the non-specific binding amount (NSB) , a reaction tube to which a great excessive amount of the unlabeled test compound is added is prepared as well. The reaction is carried out at 0-50'~ , preferably at 4-37~
for 20 minutes to 24 hours, preferably 30 minutes to three hours. After the reaction, it is filtered through a glass fiber filter or the like, washed with a suitable amount of the same buffer and the radioactivity remaining in the glass fiber filter is measured by means of a liquid scintillation counter or a gamma-counter. The test compound in which the count (B - NSB) obtained by subtracting the non-specific binding amount (NSB) from the total binding amount (B) is more than 0 cpm is identified as a ligand to the G
protein-coupled receptor protein.
In conducting the above-mentioned methods 4) to 5) wherein ligands capable of binding with the G protein-coupled receptor protein are determined, the cell stimulating activity, e.g. the liberation of arachidonic acid, the liberation of acetylcholine, endocellular Ca2~ liberation, endocellular CAMP
production, the production of inositol phosphate, changes in the cell membrane potential, the phosphorylation of endocellular protein, the activation of c-fos, lowering of pH, the activation of G protein, cell promulgation, etc.; mediated by the G protein-coupled receptor protein may be measured by known methods or by the use of commercially available measuring kits. To be more specific, G protein-coupled 5 receptor protein-containing cells are at first cultured in a multi-well plate or the like.
In conducting the determination of ligand, it is substituted with a fresh medium or a suitable buffer which does not show toxicity to the cells in advance of 10 the experiment, and incubated under appropriate conditions and for sufficient time after adding a test compound, etc. thereto. Then, the cells are extracted or the supernatant liquid is recovered and the resulting product is determined by each of the methods.
15 When it is difficult to identify the production of the substance, e.g. arachidonic acid, etc. which is to be an index for the cell stimulating activity due to the decomposing enzyme contained in the cell, an assay may be carried out by adding an inhibitor against said 20 decomposing enzyme. With respect to an activity such as an inhibitory action against CAMP production, it may be detected as an inhibitory action against the production of the cells whose fundamental production is increased by forskolin or the like.
25 The kit used for the method of determining the ligand binding with the G protein-coupled receptor protein includes a G protein-coupled receptor protein or a partial peptide thereof, cells containing the G
protein-coupled receptor protein, a membrane fraction 30 from the cells containing the G protein-coupled receptor protein, etc.
Examples of the kit for determining the ligand are as follows:
1. Reagent for Determing the Ligand.
35 1 ) Buffer for Measurement and Buffer for Washing.
The buffering product wherein 0.05 of bovine serum albumin (manufactured by Sigma) is added to Hanks' Balanced Salt Solution (manufactured by Gibco).
This product may be sterilized by filtration through a membrane filter with a 0.45u m pore size, and stored at 4'C or may be formulated upon use.
2) G protein-coupled receptor Protein Sample.
CHO cells in which G protein-coupled receptor proteins are expressed are subcultured at the rate of 5 x 105 cells/well in a 12-well plate and cultured at 37~ in a humidified 5~ COZ/95~ air atmosphere for two days to prepare the sample.
3) Labeled Test Compound.
The compound which is labeled with commercially available [ 3H ] , [ 1~5I ] , [ "C ] , ~ 35S ] , etc . or labeled with a suitable method.
The product in a state of an aqueous solution is stored at 4~ or at -20'~ and, upon use, diluted to 1/.tM
with a buffer for the measurement. In the case of a test compound which is barely soluble in water, it may be dissolved in an organic solvent such as dimethylformamide, DMSO, methanol and the like.
4) Unlabeled Test Compound.
The same compound as the labeled one is prepared in a concentration of 100 to 1,000-fold concentrated state.
2. Method of Measurement 1) G protein-coupled receptor protein-expressing CHO
cells cultured in a 12-well tissue culture plate are washed twice with 1 ml of buffer for the measurement and then 490 ~t 1 of buffer for the measurement is added to each well.
2 ) Five a ~ of the 1 abe~'~ .~d test compound is ac=: -?ed and the mixture is made to react at room tempera: ~e for one hour. For measuring the nonspecific binding amount, 5I~ 1 of the unlabeled test compound is added.
3) The reaction solution is removed from each well, which is washed with 1 ml of a buffer for the h:

measurement three times. The labeled test compound which is binding with the cells is dissolved in 0.2N
w ~ NaOH-l~ SDS and mixed with 4 ml of a liquid w scintillator A manufactured by WAKO Pure Chemical, Japan.
4) Radioactivity is measured using a liquid scintillation counter such as one manufactured by Beckmann.
Each SEQ ID NO set forth in the SEQUENCE LISTING of the specification refers to the following sequence:
[SEQ ID NO:1] is an entire amino acid sequence of the bovine pituitary-derived ligand polypeptide encoded by the cDNA included in pBOV3.
[ SEQ ID NO: 2 ] is an entire nucleotide sequence of the bovine pituitary-derived ligand polypeptide cDNA.
[SEQ ID N0:3] is an amino acid sequence of the bovine pituitary-derived ligand polypeptide which was obtained by purification and analysis of N-terminal sequence for P-3 fraction. The amino acid sequence corresponds to 23rd to 51st positions of the amino acid sequence of SEQ ID NO:1. [ SEQ ID NO: 4 ] is an amino acid sequence of the bovine pituitary-derived ligand polypeptide which was obtained by purification and analysis of N-terminal sequence for P-2 fraction. The amino acid sequence corresponds to 34th to 52nd positions of the amino acid sequencce of SEQ ID NO: 1.
[SEQ ID N0:5] is an amino acid sequence of the bovine pituitary-derived ligand polypeptide. The amino acid sequence corresponds to 23rd to 53rd positions of the amino acid sequence of SEQ ID NO:1.
[ SEQ ID .NO: 6 ] is an amino acid sequence of the bovine pituitary-derived ligand polypeptide. The amino acid sequence corresponds to 23rd to 54th positions of the _ amino acid sequence of SEQ ID NO: 1.
[ SEQ ID NO: 7 ] is an amino acid sequence of the bovine pituitary-derived ligand polypeptide. The amino acid h.
SO
sequence corresponds to 23rd to 55th positions of the amino acid sequence of SEQ ID NO:1.

[ SEQ ID NO: 8 ] is an amino acid sequence the bovine of pitui tary-derived ligand polypeptide. The amino acid seque nce corresponds to 34th to 53rd positions of the amino acid sequence of SEQ ID NO:1.

[ SEQ ID NO : 9 ] is an amino acid sequence the bovine of pitui tary-derived ligand polypeptide. The amino acid seque nce corresponds to 34th to 54th positions of the amino acid sequence of SEQ ID NO:1.

[SEQ ID NO:10] is an amino acid sequence the bovine of pituitary-derived amino acid ligand polypeptide.
The sequence corresponds to 34th to 55th positions of the amino acid sequence of SEQ
ID
NO:1.

[SEQ ID NO:11] is a nucleotide sequence DNA coding of for the bovine pituitary-derived ligand polypeptide (SEQ ID N0:3).

[SEQ ID NO: I2] is a nucleotide sequence DNA coding of for the bovine pituitary-derived ligand polypeptide (SEQ ID NO:4).

[SEQ ID N0:13] is a nucleotide sequence DNA coding of for the bovine pituitary-derived ligand polypeptide (SEQ ID N0:5).

[SEQ ID N0:14] is a nucleotide sequence DNA coding of for the bovine pituitary-derived ligand polypeptide (SEQ ID N0:6).

[SEQ ID N0:15] is a nucleotide sequence DNA coding of for the bovine pituitary-derived ligand polypeptide (SEQ ID N0:7).

[SEQ ID N0:16] is a nucleotide sequence DNA coding of for the bovine pituitar=~-derived ligar~:3polypeptide (SEQ ID N0:8).

[ SEQ ID N0:17 ] is a nucleotide sequence DNA coding of for the bovine pituitary derived ligand polypeptide (SEQ ID N0:9).

[SEQ ID N0:18] is a nucleotide sequence DNA coding of for the bovine pituitary-derived ligand polypeptide (SEQ ID NO:10).
w [SEQ ID N0:19] is a partial amino acid sequence of the human pituitary-derived G protein-coupled receptor S protein encoded by the human pituitary-derived G
protein-coupled receptor protein cDNA fragment included in p19P2.
[SEQ ID N0:20] is a partial amino acid sequence of the human pituitary-derived G protein-coupled receptor protein encoded by the human pituitary-derived G
protein-coupled receptor protein cDNA fragment include in p19P2.
[SEQ ID N0:21] is an entire amino acid sequence of the human pituitary-derived G protein-coupled receptor protein encoded by the human pituitary-derived G
protein-coupled receptor protein cDNA include in phGR3.
[SEQ ID N0:22] is a partial amino acid sequence of the mouse pancreatic (3 -cell line, MIN6-derived G protein-coupled receptor protein encoded by the mouse pancreatic a-cell line, MIN6-derived G protein-coupled receptor protein cDNA fragment having a nucleotide sequence (SEQ ID N0:27), derived based upon the nucleotide sequences of the mouse pancreatic ~3 -cell line, MIN6-derived G protein-coupled receptor protein cDNA fragments each included in pG3-2 and pGl-10.
[SEQ ID N0:23] is a partial amino acid sequence of the mouse pancreatic (3 -cell line, MIN6-derived G protein-coupled receptor protein encoded by p5S38.
_ [SEQ ID N0:24] is a nucleotide sequence of the human pituitary-derived G protein-coupled receptor protein cDNA fragment include in p19P2.
- [SEQ ID N0:25] is a nucleotide sequence of the human pituitary-derived G protein-coupled receptor protein _ cDNA fragment include in p19P2.
[SEQ ID N0:26] is an entire nucleotide sequence of the human pituitary-derived G protein-coupled receptor protein cDNA include in phGR3.
[SEQ ID N0:27] is a nucleotide sequence of the mouse pancreatic a -cell line, MIN6-derived G protein-coupled receptor protein cDNA, derived based upon the 5 nucleotide sequences of the mouse pancreatic (3 -cell line, MIN6-derived G protein-coupled receptor protein cDNA fragments each included in pG3-2 and pGl-10.
[SEQ ID NO: 28] is a nucleotide sequence of the mouse pancreatic/3 -cell line, MIN6-derived G protein-coupled 10 receptor protein cDNA include in p5S38.
[SEQ ID N0:29] is a synthetic DNA primer for screening of cDNA coding for the G protein-coupled receptor protein.
[SEQ ID N0:30] is a synthetic DNA primer for screening 15 of cDNA coding for the G protein-coupled receptor protein.
[SEQ ID N0:31] is a synthetic DNA primer for screening of cDNA coding for the G protein-coupled receptor protein.
20 [SEQ ID N0:32] is a synthetic DNA primer for screening of cDNA coding for the G protein-coupled receptor protein:
[SEQ ID N0:33] is a synthetic DNA primer for screening of cDNA coding for the G protein-coupled receptor 25 protein.
[SEQ ID N0:34] is a synthetic DNA primer for screening of cDNA coding for the G protein-coupled receptor protein.
[SEQ ID NO:35] is a synthetic DNA primer for screening 30 of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer i.s repranted by P5-1.
[ SEQ ID NO: 36 ] is a synthetic I: "~A primp.. a for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by P3-1.
35 [SEQ ID N0:37] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand ,:

polypeptide, wherein the primer is represented by P3-2.
[SEQ ID N0:38] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by PE.
[SEQ ID N0:39] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by PDN.
[SEQ ID N0:40] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by FB.
[SEQ ID N0:41] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by FC.
[SEQ ID N0:42] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by BOVF.
[SEQ ID N0:43] is a synthetic DNA primer for screening of cDNA coding for the bovine pituitary-derived ligand polypeptide, wherein the primer is represented by BOVR.
[SEQ ID N0:44] is an entire amino acid sequence of the bovine genome-derived ligand polypeptide.
[SEQ ID NO: 45] is an entire amino acid sequence of the rat type ligand polypeptide encoded by the cDNA
included in pRAV3.
[ SEQ ID NO: 46 ] is an entire nucleotide sequence of the rat type ligand polypeptide cDNA.
[SEQ ID N0:47] is an amino acid sequence of the rat type ligand polypeptide. The amino acid sequence corresponds to 22nd to 52nd positions of the amino acid sequence of SEQ ID N0:45.
[SEQ ID N0:48] is an amino acid sequence of the rat type ligand polypeptide. The amino acid sequence corresponds to 22nd to 53rd positions of the amino acid sequence of SEQ ID N0:45.
[SEQ ID N0:49] is an amino acid sequence of the rat type ligand polypeptide. The amino acid sequence corresponds to 22nd to 54th positions of the amino acid sequence of SEQ ID N0:45.
[SEQ ID N0:50] is an amino acid sequence of the rat type ligand polypeptide. The amino acid sequence corresponds to 33rd to 52nd positions of the amino acid sequence of SEQ ID N0:45.
[SEQ ID N0:51] is an amino acid sequence of the rat type ligand polypeptide. The amino acid sequence corresponds to 33rd to 53rd positions of the amino acid sequence of SEQ ID N0:45.
[SEQ ID N0:52] is an amino acid sequence of the rat type ligand polypeptide. The amino acid sequence corresponds to 33rd to 54th positions of the amino acid sequence of SEQ ID N0.45.
[SEQ ID N0:53] is a nucleotide sequence encoding for the rat type ligand polypeptide of SEQ ID N0:47.
[SEQ ID N0:54] is a nucleotide sequence encoding for the rat type ligand polypeptide of SEQ ID N0:48.
[SEQ ID N0:55] is a nucleotide sequence encoding for the rat type ligand polypeptide of SEQ ID N0:49.
[SEQ ID N0:56] is a nucleotide sequence encoding for the rat type ligand polypeptide of SEQ ID N0:50.
[SEQ ID N0:57] is a nucleotide sequence encoding for the rat type ligand polypeptide of SEQ ID N0:51.
[SEQ ID N0:58] is a nucleotide sequence encoding for the rat type ligand polypeptide of SEQ ID N0:52.
[ SEQ ID NO: 59 ] is an entire amino acid sequence of the human type ligand polypeptide encoded by the cDNA
includedin pHOB7.
[ SEQ ID NO: 60 ] is an entire nucleotide sequence of the human type ligand polypept3:e cDNA.
[SEQ ID N0:61] is an amino acid sequence of the human =
type ligand polypeptide. The amino acid sequence corresponds to 23rd to 53rd positions of the amino acid .
sequence of SEQ ID N0.59.
[SEQ ID N0:62] is an amino acid sequence of the human type ligand polypeptide. The amino acid sequence corresponds to 23rd to 54th positions of the amino acid sequence of SEQ ID N0.59.

[SEQ ID N0:63] is an amino acid sequence of the human S type ligand polypeptide. The amino acid sequence corresponds to 23rd to 55th positions of the amino acid sequence of SEQ ID N0.59.

[SEQ ID N0:64] is an amino acid sequence of the human type ligand polypeptide. The amino acid sequence corresponds to 34th to 53rd positions of the amino acid sequence of SEQ ID N0.59.

[SEQ ID N0:65] is an amino acid sequence of the human type ligand polypeptide. The amino acid sequence corresponds to 34th to 54th positions of the amino acid sequence of SEQ ID N0.59.

[SEQ ID N0:66] is an amino acid sequence of the human type ligand polypeptide. The amino acid sequence corresponds to 34th to 55th positions of the amino acid sequence of SEQ ID N0.59.

[SEQ ID N0:67] is a nucleotide sequence encoding for the human type ligand polypeptide of SEQ ID N0:61.

[SEQ ID N0:68] is a nucleotide sequence encoding for the human type ligand polypeptide of SEQ ID N0:62.

[SEQ ID N0:69] is a nucleotide sequence encoding for the human type ligand polypeptide of SEQ ID N0:63.

[SEQ ID N0:70] is a nucleotide sequence encoding for the human type ligand polypeptide of SEQ ID N0:64.

[SEQ ID N0:71] is a nucleotide sequence encoding for the human type ligand polypeptide of SEQ ID N0:65.

[SEQ ID N0:72] is a nucleotide sequence encoding for the human type ligand polypeptide of SEQ ID N0:66.

= [SEQ ID N0:73] is a partial amino acid sequence of the ligand polypeptide, wherein Xaa of the 10th position is Ala or Thr, Xaa of the 11th position is Gly or Ser and Xaa of the 21st position is H, Gly or GlyArg.

[SEQ ID N0:74] is a partial amino acid sequence of the h.

ligand polypeptide, wherein Xaa of the 3rd position is -Ala or Thr, Xaa of the 5th position is Gln or Arg and Xaa of the 10th position is Ile or Thr.

[ SEQ ID NO: 75 ] synthetic DNA primer for screening is a of cDNA coding for the rat type ligand polypeptide, wherein the primer is represented by RA.

[SEQ ID N0:76] is synthetic DNA primer for screening a of cDNA coding for the rat type ligand polypeptide, wherein the primer is represented by RC.

[SEQ ID N0:77] is synthetic DNA primer for screening a of cDNA coding for the rat type ligand polypeptide, wherein the primer is represented by rF.

[SEQ ID N0:78] is synthetic DNA primer for screening a of cDNA coding for the rat type ligand polypeptide, wherein the primer is represented by rR.

[SEQ ID N0:79] is synthetic DNA primer for screening a of cDNA coding for the human type ligand polypeptide, wherein the primer is represented by R1.

[SEQ ID N0:80] is synthetic DNA primer for screening a of cDNA coding for the human type ligand polypeptide, wherein the primer s represented by R3.
i [SEQ ID N0:81] is synthetic DNA primer for screening a of cDNA coding for the human type ligand polypeptide, wherein the primer s represented by R4.
i [SEQ ID N0:82] is synthetic DNA primer for screening a of cDNA coding for the human type ligand polypeptide, wherein the primer is represented by HA.

[SEQ ID N0:83] is synthetic DNA primer for screening a of cDNA coding for the human type ligand polypeptide, wherein the primer is represented by HB.

[ SEQ ID NO: 84 ] synthefi~ c DNA primer for screening is a of cDNA coding for "he human type ligand polypeptide, _ Wherein the primer is represented by HE.

[SEQ ID N0:85] is synthetic DNA primer for screening a of cDNA coding for the human type ligand polypeptide, wherein the primer is represented by HF.

h:
LS
[SEQ ID N0:86] is a synthetic DNA primer for screening of cDNA coding for the human type ligand polypeptide, wherein the primer is represented by 5H.
[SEQ ID N0:87] is a synthetic DNA primer for screening of cDNA coding for the human type ligand polypeptide, wherein the primer is represented by 3HN.
[SEQ ID N0:88] is a synthetic DNA primer for screening of cDNA coding for the rat type G protein-coupled receptor protein (UHR-1), wherein the primer is represented by rRECF.
[SEQ ID N0:89] is a synthetic DNA primer for screening of cDNA coding for the rat type G protein-coupled receptor protein (UHR-1), wherein the primer is represented by rRECR.
[SEQ ID N0:90] is a synthetic DNA which is used for amplification of G3PDH, UHR-1 and ligand, wherein the primer represented by rl9F.
[SEQ ID N0:91] is a synthetic DNA which is used for amplification of G3PDH, UHR-1 and ligand, wherein the primer represented by rl9R.
[SEQ ID N0:92] is a N-terminal peptide of the ligand polypeptide, which is used for antigen. (Peptide-I) [SEQ ID N0:93] is a C-terminal peptide of the ligand polypeptide, which is used for antigen. (Peptide-II) (SEQ ID N0:94] is a peptide of the central portion in ligand polypeptide, which is used for antigen.
(Peptide-III) [SEQ ID N0:95] is a synthetic DNA primer for screening of cDNA coding for rat type G protein-coupled receptor protein (UHR-1).
[SEQ ID N0:96] is a synthetic DNA primer for screening of cDNA coding for rat type G protein-coupled-receptor protein (UHR-1).
[SEQ ID N0:97] is a synthetic DNA primer used in Example 48.
[SEQ ID N0:98] is a synthetic DNA primer used in a:

Example 48.
[SEQ ID N0:99] is a synthetic DNA prove used in Example 48.
The transformant Escherichia coli, designated INV a F' /p19P2 , which is obtained in the Example 2 mentioned herein below, is on deposit under the terms of the Budapest Treaty from August 9 , 1994 , with the National Institute of Bioscience and Human-Technology (NIBH), Agency of Industrial Science and Technology, Ministry of International Trade and Industry, Japan and has been assigned the Accession Number FERM BP-4776. It is also on deposit from August 22, 1994 with the Institute for Fermentation, Osaka, Japan (IFO) and has been assigned the Accession Number IFO 15739.
The transformant Escherichia coli, designated INV a F '/pG3-2, which is obtained in the Example 4 mentioned herein below, is on deposit under the terms of the Budapest Treaty from August 9, 1994, with NIBH and has been assigned the Accession Number FERM BP- 4775. It is also on deposit from August 22, 1994 with IFO and has been assigned the Accession Number IFO 15740.
The transformant Escherichia coli, designated JM109/phGR3, which is obtained in the Example 5 mentioned herein below, is on deposit under the terms of the Budapest Treaty from September 27, 1994, with NIBH and has been assigned the Accession Number FERM
BP-4807. It is also on deposit from September 22, 1994 with IFO and has been assigned the Accession Number IFO
15748 .
The transformant Esc: Hrichia -oli, designated JM109/p5S38, which is obtained i~ the example 8 _ mentioned herein below, is on deposit under the terms of the Budapest Treaty from October 27, 1994, with NIBH
and has been assigned the Accession Number FERM BP
4856. It is also on deposit from October 25, 1994 with ' IFO and has been assigned the Accession Number IFO
15754.
The transformant Escherichia cola, designated .
JM109/pBOV3, which is obtained in the Example 20 mentioned herein below, is on deposit under the terms of the Budapest Treaty from February 13, 1996, with NIBH and has been assigned the Accession Number FERM
BP-5391. It is also on deposit from January 25, 1996 with IFO and has been assigned the Accession Number IFO
15910.
The transformant Escherichia coli, designated JM109/pRAV3, which is obtained in the Example 29 mentioned herein below, is on deposit under the terms of the Budapest Treaty from September 12, 1996, with NIBH and has been assigned the Accession Number FERM
BP-5665. It is also on deposit from September 3, 1996 with IFO and has been assigned the Accession Number IFO
16012.
The transformant Escherichia cola, designated JM109/pHOV7, which is obtained in the Example 32 mentioned herein below, is on deposit under the terms of the Budapest Treaty from September 12, 1996, with NIBH and has been assigned the Accession Number FERM
BP-5666. It is also on deposit from September 5, 1996 with IFO and has been assigned the Accession Number IFO
16013.
[Industrial Application]
The ligand polypeptide of the present invention has prolactin secretion modulating activity, i.e. prolactin secretion promoting and/or inhibiting activities. Thus, as will be understood from the Examples presented hereinafter, the ligand polypeptide of the present invention has prolactin secretion promoting activity and, therefore, finds application as a drug for preventing and/or treating various diseases associated with prolactin hyposecretion. On the other hand, the -ligand polypeptide of the invention has a high affinity for the receptor proteins and, therefore, when used in an increased dose, causes desensitization for prolactin secretion, thus exhibiting prolactin secretion inhibiting activity. In this sense, it can be used as a drug for preventing and/or treating various diseases associated with prolactin hypersecretion.
Therefore, the ligand polypeptide of the invention can be used with advantage as a prolactin secretion-stimulating agent for the prevention and treatment of certain diseases associated with prolactin secretion, such as hypoovarianism, gonecyst cacogenesis, menopausal symdrome, euthyroid hypometabolism. In addition, the ligand polypeptide of the invention can be used with advantage as a aphrodisiac.
On the other hand, the ligand polypeptide of the invention can be used with advantage as a prolactin secretion inhibitory agent in the prevention and treatment of certain diseases associated with prolactin secretion, such as pituitary adenomatosis, brain tumor, emmeniopathy, autoimmune disease, prolactinoma, infertility, impotence, amenorrhea, galactorrhea, acromegaly, Chiari-Frommel symdrome, Argonz-del Castilo symdrome, Forbes-Albright symdrome, lymphoma, Sheehan syndrome or dyszoospermia.
In addition, the ligand poltpeptide of the present invention is used as a contraceptives based on its prolactin secretion inhibitory activity.
In addition, the ligand polypeptide of the invention can be used as a test reagent for study of the prolactin secretory function or a veterinary drug for use as a lactogogue in mammalian farm animals such as bovine, goat, and swine, and is even expected to find application in the elaboration of useful substances in such farm mammals and harvesting of the substances secreted into their milk.
In addition, the ligand polypeptide of the present invention has a function of modulating placental function, and can be used as an agent for treating or preventing chriocarcinomia, hydatid mole, irruption mole, abortion, unthrifty fetus, abnormal saccharometabolism, abnormal lipidmetabolism or oxytocia.
[Examples]
Described below are working examples of the present invention which are provided only for illustrative purposes, and not to limit the scope of the present invention. [Reference Example 1]
Preparation of Synthetic DNA Primer for Amplifying DNA Coding for G protein-coupled receptor Protein A comparitons of deoxyribonucleotide sequences coding for the known amino acid sequences corresponding to or near the first membrane-spanning domain each of human-derived TRH receptor protein (HTRHR), human-derived RANTES receptor protein (L10918, HUMRANTES), human Burkitt's lymphoma-derived unknown ligand receptor protein (X68149, HSBLR1A), human-derived somatostatin receptor protein (L14856, HUMSOMAT), rat-derived a - opioid receptor protein (U02083, RNU02083), rat-derivedr~-opioid receptor protein (U00442, U00442), human-derived neuromedin B receptor protein (M73482, HUr~IMBR), human-derived muscarinic acetylcholine . receptor protein (X15266, HSHM4), rat-derived 3D adrenaline cxlB receptor protein (L08609, RATAADRE01), human-derived somatostatin 3 receptor protein (M96738, HUMSSTR3X), human-derived CSa receptor protein (HUMCSAAR), human-derived unknown ligand receptor protein (HUMRDC1A), human-derived unknown ligand receptor protein (M84605, HUMOPIODRE) and rat-derived adrenaline a 2 B receptor protein (M91466, RATA2BAR) was made . As a result , highly homologous regions or parts -were found.
Further, a comparison of deoxynucleotide sequences coding for the known amino acid sequences corresponding 5 to or near the sixth membrane-spanning domain each of mouse-derived unknown ligand receptor protein (M80481, MUSGIR), human-derived bombesin receptor protein (L08893, HUMBOMB3S), human-derived adenosine A2 receptor protein (S46950, S46950), mouse-derived 10 unknown ligand receptor protein (D21061, MUSGPCR), mouse-derived TRH receptor protein (S43387, S43387), rat-derived neuromedin K receptor protein (J05189, RATNEURA), rat-derived adenosine A1 receptor protein (M69045, RATAlARA), human-derived neurokinin A receptor 15 protein (M57414, HUMNEKAR), rat-derived adenosine A3 receptor protein (M94152, DATADENREC), human-derived somatostatin 1 receptor protein (M81829, HUMSRIlA), human-derived neurokinin 3 receptor protein (S86390, S8637154), rat-derived unknown ligand receptor protein 20 (X61496, RNCGPCR), human-derived somatostatin 4 receptor protein (L07061, HUMSSTR4Z) and rat-derived GnRH receptor protein (M3I670, RATGNRHA) was made. As a result, highly homologous regions or parts were found.
The aforementioned abbreviations in the parentheses 25 are identifiers (reference numbers) which are indicated when GenBank/EMBL Data Bank is retrieved by using DNASIS Gene/Protein Sequencing Data Base (CD019, Hitachi Software Engineering, Japan) and are usually called "Accession Numbers" or "Entry Names". HTRHR is, 30 however, the sequence as disclosed in Japanese Patent Publication No. 304797/1993 (EPA 638645).
Specifically, it was planned to incorporate mixed bases relying upon the base regions that were in agreement with cDNAs coding for a large number of 35 receptor proteins in order to enhance base agreement of sequences with as many receptor cDNAs as possible even w ~ in other regions. Based upon these sequences, the degenerate synthetic DNA having a nucleotide sequence ~ represented by SEQ ID N0:29 or SEQ ID N0:30 which is complementary to the homologous nucleotide sequence were produced. [Synthetic DNAs] 5'-CGTGG (G or C) C (A
or C) T (G or C) (G or C) TGGGCAAC (A, G, C or T) (C or T) CCTG-3' (SEQ ID N0:29) 5'-GT (A, G, C or T) G (A or T) (A or G) (A or G) GGCA (A, G, C or T) CCAGCAGA (G or T) GGCAAA-3' (SEQ ID N0:30) The parentheses indicate the incorporation of a plurality of bases, leading to multiple oligonucleotides in the primer preparation. In other words, nucleotide resides in parentheses of the aforementioned DNAs were incorporated in the presence of a mixture of plural bases at the time of synthesis.
[Example 1]
Amplification of Receptor cDNA by PCR Using Human Pituitary Gland-Derived cDNA
By using human pituitary gland-derived cDNA
(QuickClone, CLONTECH Laboratories, Inc.) as a template, PCR amplification using the DNA primers synthesized in Reference Example 1 was carried out. The composition of the reaction solution consisted of the synthetic DNA
primers (SEQ: 5' primer sequence and 3' primer sequence) each in an amount of 1 ~t M, lng of the template cDNA, 0.25 mM dNTPs, 1 ~t 1 of Taq DNA
polymerise and a buffer attached to the enzyme kit, and the total amount of the reaction solution was made to be 100 !~ 1. The cycle for amplification including 95 'C
f or 1 min . , 5 5 °C f or 1 min . and 7 2 ~ f or 1 min . was repeated 30 times by using a Thermal Cycler (Perkin-Elmer Co.). Prior to adding Taq DNA polymerise, the remaining reaction solution was mixed and was heated at 95'C for 5 minutes and at 65'~ for 5 minutes. The amplified products were confirmed relying upon 1.2%
agarose gel electrophoresis and ethidium bromide a:

staining.
[Example 2]
Subcloning of PCR Product into Plasmid Vector and Selection of Novel Receptor Candidate Clone via Decoding Nucleotide Sequence of Inserted cDNA Region The PCR products were separated by using a 0.8~
low-melting temperature agarose gel, the band parts were excised from the gel with a razor blade, and were heat-melted, extracted with phenol and precipitated in ethanol to recover DNAs. According to the protocol attached to a TA Cloning Kit (Invitrogen Co.), the recovered DNAs were subcloned into the plasmid vector, pCRT'''II (TM represents registered trademark). The recombinant vectors were introduced into E. coli INV(x F' competent cells (Invitrogen Co.) to produce transformants. Then, transformant clones having a cDNA-inserted fragment were selected in an LB agar culture medium containing ampicillin and X-gal. Only transformant clones exhibiting white color were picked with a sterilized toothpick to obtain transformant Escherichia coli INV(xF'/p19P2.
The individual clones were cultured overnight in an LB culture medium containing ampicillin and treated with an automatic plasmid extracting machine (Kurabo Co., Japan) to prepare plasmid DNAs. An aliquot of the DNA thus prepared was cut by EcoRI to confirm the size of the cDNA fragment that was inserted. An aliquot of the remaining DNA was further processed with RNase, extracted with phenol/chloroform, and precipitated in ethanol so as to be condensed. Sequencing was carried out by ing a DyeDeoxy terminator cycle sequencing kit (ABI C;. t, the DNAs were decoded by using a fluorescent automatic sequencer, and the data of the nucleotide sequences obtained were read by using DNASIS (Hitachi System Engineering Co., Japan). The underlined portions represent regions corresponding to the " synthetic primers.
Homology retrieval was carried out based upon the determined nucleotide sequences [SEQ ID N0:24 and 25 (Here, the determined nucleotide sequence is the nucleotide sequence which the underlined portion is deleted from the sequence of Figure 1 or Figure 2 respectively)].
As a result, it was learned that a novel G protein coupled receptor protein was encoded by the cDNA
fragment insert in the plasmid, p19P2, possessed by the transformant Escherichia coli INV cx F'/p19P2. To further confirm this fact, by using DNASIS (Hitachi System Engineering Co., Japan) the nucleotide sequences were converted into amino acid sequences [SEQ ID N0:19 and 20], and homology retrieval was carried out in view of hydrophobicity plotting [Figures 3 and 4] and at the amino acid sequence level to find homology relative to neuropeptide Y receptor proteins [Figure 5].
[Example 3]
Preparation of Poly(A)'RNA Fraction from Mouse Pancreatic/3-Cell Strain, MIN6 and Synthesis of cDNA
A total RNA was prepared from the mouse pancreatic a -cell strain, MIN6 (Jun-ichi Miyazaki et al., Endocrinology, Vol. 127, No. 1, p.126-132) according to the guanidine thiocyanate method (Kaplan B.B. et al., Biochem. J., 183, 181-184 (1979) and, then, poly(A)'RNA
fractions were prepared with a mRNA purifying kit (Pharmacia Co.). Next, to 5 a g of the poly(A)'RNA
fraction was added a random DNA hexamer (BRL Co.) as a primer, and the resulting mixture was subjected to reaction with mouse Moloney Leukemia virus (1~V) reverse transcriptase (BRL Co. ) in the buffer attached to the MMLV reverse transcriptase kit to synthesize complementary DNAs. The reaction product was extracted with phenol/chloroform (1:1), precipitated in ethanol, and was then dissolved in 30 Lc 1 of TE buffer ( 10 mM

Tris-HCl at pH8.0, 1 mM EDTA at pH8.0).
[Example 4]
Amplification of Receptor cDNA by PCR Using MIN6-Derived cDNA and Sequencing By suing, as a template, 5 a 1 of cDNA prepared from the mouse pancreatic a -cell strain, MIN6 in the above Example 3, PCR amplification using the DNA
primers synthesized in Reference Example 1 was carried out under the same condition as in Example 1. The resulting PCR product was subcloned into the plasmid vector, pCRTMII, in the same manner as in Example 2 to obtain a plasmid, pG3-2. The plasmid pG3-2 was transfected into E . coli INV cx F' to obtain transformed Escherichia coli INVcxF'/pG3-2.
By using , as a template , 5 L.c 1 of the cDNA
parepared from the mouse pancreatic~3-cell strain, MIN6, PCR amplification using DNA primers as disclosed in Libert F. et al., "Science, 244:569-572, 1989", i.e., a degenerate synthetic primer represented by the following sequence: 5'-CTGTG (C or T) G (C or T) (G or C) AT (C or T) GCIIT (G or T) GA (C or T) (A or C) G (G
or C) TAC-3' (SEQ ID N0:31) wherein I is inosine; and a degenerate synthetic primer represented by the following sequence: 5'-A (G or T) G
(A or T) AG (A or T) AGGGCAGCCAGCAGAI (G or C) (A or G) (C or T) GAA-3' (SEQ
ID N0:32) wherein I is inosine, was carried out under the same conditions as in Example 1. The resulting PCR
product was subcloned into the plasmid vector, pCRT'''II , in the same manner as described in Example 2 to obtain a plasmid, pGl-10. -The reaction for determining the nucleotide sequence (sequencing) was carried out with a DyeDeoxy terminator cycle sequencing kit (ABI Co. ) , the DNA was decoded with the fluorescent automatic sequencer (ABI

h Co. ) , and the data of the nucleotide sequence obtained were analyzed with DNASIS (Hitachi System Engineering Co., Japan).
Figure 6 shows a mouse pancreatic a -cell strain 5 MIN6-derived G protein-coupled receptor protein encoding DNA (SEQ ID N0:27) and an amino acid sequence (SEQ ID N0:22) encoded by the isolated DNA based upon the nucleotide sequences of plasmids pG3-2 and pGl-10 which are possessed by the transformant Escherichia 10 cola INVCYF'/pG3-2. The underlined portions represent regions corresponding to the synthetic primers.
Homology retrieval was carried out based upon the determined necleotide sequence [Figure 6]. As a result, it was learned that a novel G protein-coupled receptor 15 protein was encoded by the cDNA fragment obtained. To further confirm this fact, by using DNASIS (Hitachi System Engineering Co., Japan) the nucleotide sequence was converted into an amino acid sequence [Figure 6], hydrophobicity plotting was carried out to confirm the 20 presence of six hydrophobic regions [Figure 8]. Upon comparing the amino acid sequence with that of p19P2 obtained in Example 2, furthermore, a high degree of homology was found as shown in [Figure 7]. As a result, it is strongly suggested that the G protein-coupled 25 receptor proteins encoded by pG3-2 and pGl-10 recognize the same ligand as the G protein-coupled receptor protein encoded by p19P2 while the animal species from which the receptor proteins encoded by pG3-2 and pGl-10 are derived is different from that from which the 30 receptor protein encoded by p19P2 is.
[Example 5]
_ Cloning of cDNA Comprising Whole Coding Regions for Receptor Protein from Human Pituitary Gland-Derived cDNA Library 35 The DNA library constructed by Clontech Co. wherein gtll phage vector is used (CLONTECH Laboratories, Inc.; CLH L1139b) was employed as a human pituitary -gland-derived cDNA library. The human pituitary gland cDNA library (2 x 106 pfu (plaque forming units)) was mixed with E. coli Y1090- treated with magnesium sulfate, and incubated at 37~ for 15 minutes followed by addition of 0.5% agarose (Pharmacia Co.) LB. The E.
coli was plated onto a 1.5% agar (Wako-Junyaku Co.) LB
plate (containing 50 a g /ml of ampicillin). A
nitrocellulose filter was placed on the plate on which plaques were formed and the plaque was transferred onto the filter. The filter was denatured with an alkali and then heated at 80~C for 3 hours to fix DNAs.
The filter was incubated overnight at 42~C together with the probe mentioned herein below in a buffer containing 50% formamide, 5 x SSPE (20 x SSPE (pH 7.4) a.s 3 M NaCl , 0 . 2 M NaHZPO, . H20 , 2 5 mM EDTA ) , 5 X
Denhardt's solution (Nippon Gene, Japan), 0.1% SDS and 100 !~ g /ml of salmon sperm DNA for hybridization.
The probe used was obtained by cutting the DNA
fragment inserted in the plasmid, p19P2, obtained in Example 2, with EcoRI, followed by recovery and labelling by incorporation of [3zP]dCTP (Dupont Co.) with a random prime DNA labelling kit (Amasham Co.).
It was washed with 2 x SSC (20 x SSC is 3 M NaCl, 0.3 M sodium citrate), 0.1% SDS at 55~ for 1 hour and, then, subjected to an autoradiography at -80 ~C to detect hybridized plaques.
In this screening, hybridization signals were recognized in three independent plaques. Each DNA was prepared from the three clones. The DNAs digested with EcoRI were subjecteQ to an garose elecwvophoresis and were analyzed by the southern blotting csing the same probe as the one used in the screening. Hybridizing bands were identified at about 0 . 7kb , 0 . 8kb and 2 . Okb , respectively. Among them, the DNA fragment corresponding to the band at about 2.Okb ( ~ hGR3) was h.

selected. The ~l hGR3-derived EcoRI fragment with a hybridizable size was subcloned to the EcoRI site of the plasmid, pUCl8 , and E . coli JM109 was transformed with the plasmid to obtain transformant E. cola JM109/phGR3. A restriction enzyme map of the plasmid, phGR3, was prepared relying upon a restriction enzyme map deduced from the nucleotide sequence as shown in Example 2. As a result, it was learned that it carried a full-length receptor protein-encoding DNA which was predicted from the receptor protein-encoding DNA as shown in Example 2.
[Example 6]
Sequencing of Human Pituitary Gland-Derived Receptor Protein cDNA
Among the EcoRI fragments inserted in the plasmid, phGR3, obtained in the above Example 5, the from EcoRI
to NheI nucleotide sequence with about 1330bp that is considered to be a receptor protein-coding region was sequenced. Concretely speaking, by utilizing restriction enzyme sites that exist in the EcoRI
fragments, unnecessary parts were removed or necessary fragments were subcloned in order to prepare template plasmids for analyzing the nucleotide sequence.
The reaction for determining the nucleotide sequence (sequencing) was carried out with a DyeDeoxy terminator cycle sequencing kit (ABI Co.), the DNA was decoded with the fluorescent automatic sequencer (ABI
Co.), and the data of the nucleotide sequence obtained were analyzed with DNASIS (Hitachi System Engineering Co., Japan).
Figure 9 shows a nucleotide sequence of from immediate after the EcoRI site up to the NheI site encoded by phGR3. The nucleotide sequence of the human pituitary gland-derived receptor protein-encoding DNA
corresponds to the nucleotide sequence (SEQ ID N0:26) of from 118th to 1227th nucleotides [Figure 9]. An amino acid sequence of the receptor protein that is encoded by the nucleotide sequence is shown in SEQ ID
N0:21.
[Example 7]
Northern Hybridization with Human Pituitary Gland-Derived Receptor Protein-Encoding phGR3 Northern blotting was carried out in order to detect the expression of phGR3-encoded human pituitary gland-derived receptor proteins obtained in Example 5 in the pituitary gland at a mRNA level. Human pituitary gland mRNA (2.5 a g , Clontech Co.) was used as a template mRNA and the same as the probe used in Example 5 was used as a probe. Nylon membrane (Pall Biodyne, U.S.A.) was used as a filter for northern blotting and migration of the mRNA and adsorption (sucking) thereof with the blotting filter was carried out according to the method as disclosed in Molecular Cloning, Cold Spring Harbor Laboratory Press, 1989.
The hybridization was effected by incubating the above-mentioned filter and probe in a buffer containing 50% formamide, 5 x SSPE, 5 X Denhardt's solution, 0.1%
SDS and 100 I~ g /ml of salmon sperm DNA overnight at 4 2 ~ . The f filter was washed with 0 .1 x SSC , 0 .1 % SDS
at 50 °C and, after drying with air, was exposed to an X-ray film ( XAR5 , Kodak ) for three days at -80 ~ . The results were as shown in Figure 10 from which it is considered that the receptor gene encoded by phGR3 is expressed in the human pituitary gland.
[Example 8]
Amplificatifln of Receptor cDNA by PCR Using MIN6-Deriv~:~d cDNA and Sequencing By using, as a template, 5 I-~. 1 of cDNA prepared from the mouse pancreatic (3 -cell strain, MIN6 in Example 3, PCR amplification using the DNA primers synthesized in Example 4 as disclosed in Libert F. et al., "Science, 244:569-572, 1989", i.e., a synthetic S.

- primer represented by the following sequence: 5'-CTGTG
(C or T) G (C or T) (G or C) AT (C or T) GCIIT {G or T) r GA {C or T) (A or C) G (G or C) TAC-3' (SEQ ID N0:31) wherein I is inosine; and a synthetic primer represented by the following sequence: 5'-A {G or T) G
(A or T) AG (A or T) AGGGCAGCCAGCAGAI (G or C) (A or G) (C or T) GAA-3' (SEQ ID N0:32) wherein I is inosine, was carried out under the same conditions as in Example 1. The resulting PCR product was subcloned to the plasmid vector, pCRTMII, in the same manner as in Example 2 to obtain a plasmid, p5S38. The plasmid p5S38 was transfected into E. cola JM109 to obtain transformant Escherichia coli JM109/p5S38.
The reaction for determining the nucleotide sequence (sequencing) was carried out with a DyeDeoxy terminator cycle sequencing kit ( ABI Co . ) , the DNA was decoded with the fluorescent automatic sequencer (ABI
Co . ) , and the data of the nucleotide sequence obtained were read with DNASIS (Hitachi System Engineering Co., Japan ) .
Figure 12 showns a mouse pancreatic (3 -cell strain MIN6-derived G protein-coupled receptor protein-encoding DNA (SEQ ID N0:28) and an amino acid sequence ( SEW ID NO: 23 ) encoded by the isolated DNA based upon the nucleotide sequence of plasmid, p5S38. The underlined portions represent regions corresponding to the synthetic primers.
Homology retrieval was carried out based upon the y determined nucleotide sequence [Figure 12]. As a result, it was learned that a novel G protein-coupled receptor protein was encoded by the cDNA fragment obtained. To further confirm this fact, by using DNASIS (Hitachi System Engineering Co., Japan), the nucleotide sequence was converted into an amino acid sequence [Figure 12], and hydrophobicity plotting was carried out to confirm the presence of tour hydrophobic regions [Figure 14]. Upon comparing the amino acid -sequence with those encoded by p19P2 obtained in Example 2 and encoded by pG3-2 obtained in Example 4, -_ furthermore, a high degree of homology was found as 5 shown in Figure 13. As a result, it a.s strongly suggested that the mouse pancreatic a -cell strain, MIN6-derived G protein-coupled receptor protein encoded by p5S38 recognizes the same ligand as the human pituitary gland-derived G protein-coupled receptor 10 protein encoded by p19P2 does while the animal species from which the receptor protein encoded by p5S38 is derived is different from that from which the receptor protein encoded by p19P2 is. It is also strongly suggested that the mouse pancreatic a -cell strain, 15 MIN6-derived G protein-coupled receptor protein encoded by p5S38 recognized the same ligand as the mouse pancreatic (3 -cell strain, MIN6-derived G protein coupled receptor proteins encoded by pG3-2 and pGl-10 do and they are analogous receptor proteins one another 20 (so-called "subtype").
[Example 9]
Preparation of CHO cells which express phGR3 The plasmid phGR3 (Example 5) containing a cDNA
encoding the full-length amino acid sequence of human 25 pituitary receptor protein was digested with the restriction enzyme Nco I and electrophoresed on agarose gel and a fragment of about lkb was recovered. Both ends of the recovered fragment were blunted with a DNA
blunting kit (Takara Shuzo Co., Japan) and, with the 30 SalI linker added, treated with SalI and inserted into the Sall site of pUC119 to yrovide p asmid S10 . Then S10 was treated with Sall and SacII to prw ,~ :are fragment of about 700 by (containing the N-terminal coding region). Then, a fragment of about 700 by 35 (containing the C-terminal coding region including initiation and termination codons) was cut out from h.

- phGR3 with Sac II and Nhe I. These two fragments were added to the animal cell expression vector plasmid pAKKO-111H (the vector plasmid identical to the pAKK01.11 H described in Biochim. Biophys. Acta, Hinuma, S., et al., 1219 251-259, 1994) and a ligation reaction was carried out to construct a full-length receptor protein expression plasmid pAKKO-19P2.
E. coli transfected with pAKKO-19P2 was cultured and the pAKKO-19P2 plasmid DNA was mass-produced using QUIAGEN Maxi . A 20 ~t g portion of the plasmid DNA was dissolved in 1 ml of sterile PBS, and in a gene transfer vial (Wako Pure Chemical Ind.), the solution was vortexed well for liposome formation. This liposome, 125 a 1, was added to CHOdhfr' cells subcultured at 1 x 106 per lOcm-dia. dish 24 hr before and placed 1n fresh medium immediately before addition and overnight culture was carried out. After a further one-day culture in fresh medium, the medium was changed to a screening medium and the incubation was further carried out for a day. For efficient screening of transformants, subculture was carried out at a low cell density and only the cells growing in the screening medium were selected to establish a full-length receptor protein expression CHO cell line CHO-19P2.
[Example IO]
Confirmation of the amount of expression of the full-length receptor protein in the CHO-19P2 cell line at the transcription level Using FastTrack Kit (Invitrogen), CHO cells transfscted with pAKKO-19P2 according to the kit manual and mock CHO cells were used to prepare poly(A)'RNA.
Using 0.02 ~t g of this poly(A)'RNA, a cDNA was synthesized by means of RNA PCR Kit {Takara Shuzo, Co., Japan). The kind of primer used was a random 9mer and the total volume of the reaction mixture was 40/.cl. As a negative control of cDNA synthesis, a reverse S.

transcriptase-free reaction mixture was also provided. -First, the reaction mixture was incubated at 30 ~ for minutes to conduct an amplification reaction to some extent. Then, it was incubated at 42~ for 30 minutes 5 to let the reverse transcription reaction proceed. The enzyme was inactivated by heating at 99~ for 5 minutes and the reaction system was cooled at 5~ for 5 minutes.
After completion of the reverse transcription reaction, a portion of the reaction mixture was 10 recovered and after dilution with distilled water, extraction was carried out with phenol/chloroform and further with diethyl ether. The extract was subjected to precipitation from ethanol and the precipitate was dissolved in a predetermined amount of distilled water for use as a cDNA sample. This cDNA solution and the plasmid DNA (pAKKO-19P2) were serially diluted and using primers specific to full-length receptor protein, PCR was carried out. The sequences of the primers prepared according to the base sequence of the coding region of the full-length receptor protein were CTGACTTATTTTCTGGGCTGCCGC (SEQ ID N0:33) for 5' end and AACACCGACACATAGACGGTGACC (SEQ ID N0:34) for 3' end.
The PCR reaction was carried out in a total volume of 100 ~t 1 using 1 Ic M each of the primers , 0 . 5 a 1 of Taq DNA polymerase ( Takara Shuzo Co . , Japan ) , the reaction buffer and dNTPs accompanying the enzyme, and 10 ~.t 1 of template DNA (cDNA or plasmid solution). First the reaction mixture was heat-treated at 94~C for 2 minutes for sufficient denaturation of the template DNA and subjected to 25 cycles of 95~ x 30 seconds, 65~ x 30 seconds, and 72~ x 60 seconds. After completion of the reaction, 10 ~.1 of the reaction mixture was subjected to agarose gel electrophoresis and the detection and quantitative comparison of amplification products were carried out. As a result, a PCR product of the size (400 bp) predictable from the sequence of the cDNA

A.

- coding for the full-length receptor protein was detected [Fig. 15]. In the lane of the PCR reaction r mixture using the product of the reverse transcriptase free transcription system as the template, no specific band was detected, thus extruding the possibility of its being a PCR product derived from the genomic DNA of CHO cells . Moreover, no specific band appeared in the lane of mock cells, either. Therefore, it was clear that the product was not derived from the mRNA
initially expressed in CHO cells [Fig. 15].
[Example 11]
Detection of the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells in a rat whole brain extract A crude peptide fraction was prepared from rat whole brain by the following procedure. The rat whole brain enucleated immediately after sacrifice was frozen in liquefied nitrogen and stored at -80~ . The frozen rat whole brain, 20 g (the equivalent of 10 rats) was finely divided and boiled in 80 ml of distilled water for 10 minutes. After the boiled tissue was quenched on ice, 4.7 ml of acetic acid was added at a final concentration of 1.0 M and the mixture was homogenized using a Polytron (20,000 rpm, 6 min. ) . The homogenate was stirred overnight and then centrifuged (10,000 rpm, 20 min.) to separate the supernatant. The sediment was homogenized in 40 ml of 1.0 M acetic acid and centrifuged again to recover the supernatant. The supernatants were pooled, diluted in 3 volumes of acetone, allowed to stand on ice for 30 minutes, and centrifuged (10,000 rpm, 20 min.) to recover the supernatant. The recovered supernatant was evaporated to remove acetone. To the resulting acetone-free concentrate was added 2 volumes of 0.05%
trifluoroacetic acid(TFA)/H20 and the mixture was applied to a reversed-phase C18 column (Prep C18 125, ,.

Millipore). After application of the supernatant, the column was washed with 0.05% TFA/HzO, and gradient elution was carried out with 10%, 20%, 30%, 40%, 50%, and 60% CH3CN/0.05%TFA/HZO. The fractions were respectively divided into 10 equal parts and lyophilized. The dried sample derived from one animal equivalent of rat whole brain was dissolved in 2011 of dimethyl sulfoxide (DMSO) and suspended in 1 ml of Hank's balanced saline solution (HBSS) supplemented with 0.05% bovine serum albumin (BSA) to provide a crude peptide fraction.
The full-length receptor protein-expressed CHO
... cells and mock CHO cells were seeded in a 24-well plate, 0.5 x 105 cells/well, and cultured for 24 hours. Then, i5 ['H ] arachidonic acid was added at a final concentration of 0.25 a Ci/well. Sixteen (16) hours after addition of [3H] arachidonic acid, the cells were rinsed with 0.05% BSA-HBSS and the above-mentioned crude peptide fraction was added, 400 Lt 1/well. The .- 20 mixture was incubated at 37~ for 30 minutes and a 3001 1 portion of the reaction mixture (4001 1) was added to 4 ml of a scintillator and the amount of ['H]
arachidonic acid metabolite released into the reaction mixture was determined with a scintillation counter.
25 As a result, an arachidonic acid metabolite-releasing activity specific to the full-length receptor protein expressed CHO cells ( CHO-19P2 ) was detected in the 30%
CH3CN fraction of the eluate [Fig. 16].
[Example 12]
30 Detection of the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells in a bovine hypothalamus extract A crude peptide fraction was prepared from 360 g (the equivalent of 1 animals) of bovine brain tissue 35 including hypothalamus in the same manner as in Example 11. A dried peptide sample per 0.05 animal was WO 98/58962 PCT/.1P98/02765 h.
dissolved in 40 a 1 of DMSO and suspended in 2 ml of 0.05% BSA-HBSS and the detection of arachidonic acid metabolite-releasing activity was attempted in the same manner as in Example 11. As a result , the activity to specifically promote release of arachidonic acid metabolites from the CHO-19P2 cell line was detected in the fraction eluted with 30% CH,CN from a C18 column to which the crude bovine hypothalamus peptide fraction had been applied [Fig. 17].
[Example 13]
Preparation of the activity (peptide) to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells by purification from bovine hypothalamus A typical process for harvesting the activity to specifically promote release of arachidonic acid metabolites from the CHO-19P2 cell line by purification from bovine hypothalamus is now described. A frozen bovine brain tissue specimen including hypothalamus, 4.0 kg (the equivalent of 80 animals) was ground and boiled in 8.0 L of distilled water for 20 minutes.
After quenching on ice, 540 ml of acetic acid was added at a final concentration of 1.0 M and the mixture was homogenized using a Polytron (10,000 rpm, 12 min.).
The homogenate was stirred overnight and then centrifuged (9,500 rpm, 20 min) to recover a supernatant. The sediment was suspended in 4.0 L of 1.0 M acetic acid and homogenized with the Polytron and centrifuged again to recover a further supernatant.
The supernatants were pooled and TFA was added at a final concentration of 0.05%. The mixture was applied to reversed-phase C18 (Prep C18 125, 160 ml;
Millipore) packed in a glass column. After addition, the column was washed with 320 mi of 0.05% TFA/H20 and 3-gradient elution was carried out with 10%, 30%, and 50% CH3CN/0.05% TFA/HZO. To the 30% CH3CN/0.05% TFA/H20 S:

fraction was added 2 volumes of 20 mM CH,COONH4/H20 and -the mixture was applied to the cation exchange column HiPrep CM-Sepharose FF (Pharmacia). After the column -was washed with 20 mM CH3COONH4/10% CH3CN/H20, 4-gradient elution was carried out with 100 mM, 200 mM, 500 mM, and 1000 mM CH,COONH4/10% CH3CN/H20. In the 200 mM CH3COONH4 fraction, activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 was detected. Therefore, this fraction was diluted with 3 volumes of acetone, centrifuged for deproteination, and concentrated in an evaporator. To the concentrated fraction was added TFA (final concentration 0.1%) and the mixture was adjusted to pH4 with acetic acid and applied to 3 ml of the reversed-phase column RESOURCE RPC (Pharmacia). Elution was carried out on a concentration gradient of 15%-30%
CH3CN. As a result, activity to specifically promote the release of arachidonic acid metabolites from the CHO-19P2 cell line was detected in the 19%-21% CH,CN
fraction. The active fraction eluted from RESOURCE RPC
was lyophilized, dissolved with DMSO, suspended in 50 mM MES pH 5.0/10% CH3CN, and added to 1 ml of the cation exchange column RESOURCE S. Elution was carried out on a concentration gradient of 0 M-0.7 M NaCl. As a result, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was detected in the 0.32 M-0.46 M NaCl fraction. The active eluate from RESOURCE S was lyophilized, dissolved with DMSO, suspended in 0.1% TFA/HzO, and added to reversed-phase column C18 218TP5415 (Vydac), and elution was carried out on a co wntration gradient of 20%-30% CH3CN. As a result the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was detected in the three fractions 22.5%, 23%, and 23.5% CH3CN (these active fractions are designated as P-1, P-2, and P-3) h:

[Fig. 18]. Of the three active fractions, the 23.5%

CH3CN fraction (P-3) was lyophilized, dissolved with .
DMSO, suspended in 0.1% TFA/H20, and added to the reversed-phase column diphenyl 219TP5415 (Vydac), and elution was carried out on a gradient of 22%-25% CH3CN.

As a result, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was converged by recovered in one elution peak obtained with 23% CH,CN [Fig. 19]. The peak activity fraction from the reverse-phased column diphenyl 219TP5415 was lyophilized, dissolved with DMSO, suspended in 0.1% TFA/H20, and added to the reversed-phase column a RPC C2/C18 SC 2.1/10 (Pharmacia), and elution was carried out on a gradient of 22%-23.5%

CH,CN. As a result, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was detected in the two peaks eluted with 23.0% and 23.2% CH3CN [Fig. 20].

[Example 14]

Determination of the amino acid sequence of the peptide having the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells as purified from bovine hypothalamus The amino acid sequence of the peptide (P-3) having activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells as purified in Example 13 was determined. The fraction of peak . activity from the reversed-phase a RPC C2/C18 SC 2.1/10 was lyophilized and dissolved in 20,u 1 of 70% CH,CN
and analyzed for amino acid sequence with the peptide sequencer (ABI.491). As a result, the sequence defined by SEQ ID N0:3 was obtained. However, the 7th and 19th amino acids were not determined by only the analysis of amino acid sequence.

[Example 15]

S.
Preparation of the active substance (peptide) which specifically promotes release of arachidonic acid metabolites from CHO-19P2 cells as purified from bovine hypothalamus Of the three active fractions obtained with Vydac C18 218TP5415 in Example 13, the active fraction (P-2) eluted with 23.0 CH3CN was further purified. This active fraction was lyophilized, dissolved with DMSO, suspended in 0.1~ TFA/distilled H20, and added to reversed-phase column diphenyl 219TP5415 (Vydac), and elution was carried out on a gradient of 21.0-24.0$
CH,CN. As a result, activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was detected in a peak eluted with 21.9 CH,CN.
This fraction was lyophilized, dissolved with DMSO, suspended in 0.1~ TFA/distilled H20, and added to reversed-phase a RPC C2/C18 SC 2.1/10 (Pharmacia), and elution was carried out on a CH3CN gradient of 21.5~-23.0%. As a result, the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells converged in one peak eluted with 22.0 CH3CN [ Fig . 21 ] .
[Example 16]
Determination of the amino acid sequence of the peptide (P-2) purified from bovine hypothalamus which specifically promotes release of arachidonic acid metabolites from CHO-19P2 cells The amino acid sequence of the peptide (P-2) having the activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells as purified in Example 15 was determined. The peak activity fraction from the reversed-phase column /.tRPC
C2/C18 SC 2.1/10 was lyophilized, dissolved in 20 a 1 of 70~ CH3CN, and analyzed for amino acid sequence with the peptide sequences (ABI, 492) (SEQ ID N0:4).
[Example 17]

S.

Preparation of a poly(A)+RNA fraction from bovine hypothalamus and synthesis of a cDNA
Using Isogen (Nippon Gene), total RNA was prepared from one animal equivalent of bovine hypothalamus.
Then, using Fast Track (Invitrogen), a poly(A)'RNA
fraction was prepared. From 1 ,u g of this poly(A)'RNA
fraction, cDNA was synthesized using 3' RACE system (GIBCO BRL) and Marathon cDNA amplification kit (Clontech) according to the manuals and dissolved in 20 IO and 10 a 1, respectively .
[Example 18]
Acquisition of cDNA coding for the amino acid sequence established in Example 14 To obtain a cDNA coding for a polypeptide comprising the amino acid sequence established in Example 14, the acquisition of a base sequence coding for SEQ ID NO:1 was attempted in the first place. Thus, primers P5-1 (SEQ ID N0:35), P3-1 (SEQ ID N0:36), and P3-2 (SEQ ID N0:37) were synthesized. (In the Sequence Table, I represents inosine). Using 0.5/~ 1 of the cDNA
prepared by 3' RACE in Example 17 as a template and EXTaq ( Takara Shuzo Co . , Japan ) as DNA polymerase , 2 . 5 a 1 of accompanying buffer, 200,u M of accompanying dNTP, and primers P5-1 and P3-1 Were added each at a final concentration of 200 nM, with water added to make 25u 1, and after one minute at 94 ~ , the cycle of 98 9C x 10 seconds, 50 ~ x 30 seconds, 68°~ x 10 seconds was repeated 30 times. This reaction mixture was diluted 50-fold with tricine-EDTA buffer and using 2.5 a 1 of the dilution as a template and the primer combination of P5-1 and P3-2, the reaction was carried out in otherwise the same manner as described above. As the thermal cycler, Gene Amp 9600 (Perkin Elmer) was used.
The amplification product was subjected to 4% agarose electrophoresis and ethidium bromide staining and a band of about 70 by was cut out and subjected to r:
thermal fusion, phenol extraction, and ethanol -precipitation. The recovered DNA was subcloned into plasmid vector PCRTMII according to the manual of TA
Cloning kit (Invitrogen). The vector was then 5 introduced into E. coli JM109 and the resultant transformant was cultured in ampicillin-containing LB
medium. The plasmid obtained with an automatic plasmid extractor (Kurabo) was reacted according to the manual of Dye Terminator Cycle Sequencing Kit (ABI) and 10 decoded with a fluorescent automatic DNA sequencer (ABI). As a result, the sequence shown in Fig. 22 was obtained and confirmed to be part of the base sequence coding for SEQ ID NO:1.
[Example 19]
15 Acquisition of a bioactive polypeptide cDNA by RACE using the sequence established in Example 18 First, for amplification (5' RACE) of the sequence at 5' end, the two primers PE (SEQ ID N0:38) and PDN
(SEQ ID N0:39) were synthesized by utilizing the 20 sequence shown in Fig. 22. The cDNA prepared using Marathon cDNA amplification kit in Example i7 was diluted 100-fold with tricine-EDTA buffer. Then, in the same manner as Example 2, a reaction mixture was prepared using 2.5u 1 of the dilution and a combination 25 of the adapter primer AP1 accompanying the kit and the primer PE and after one minute at 94 ~ , the cycle of 98~C x 10 seconds and 68~ x 5 minutes was repeated 30 times. This reaction system was further diluted 50-fold with tricine-EDTA buffer and using 2.5 l~ 1 of the 30 dilution as a template and the changed primer combination of AP1 and PDN, the reaction w~::~ conducted at 94'C for one minute, followed by 4 cycles of 94qC x 1 minute, 98~C x 10 seconds, 72~ x 5 minutes, 4 cycles of 98 °C x 10 seconds , 70 ~ x 5 minutes , and 26 cycles of 35 98~ x 10 seconds, 68~ x 5 minutes. The amplification product was electrophoresed on 1.2~ agarose gel and 4.

stained with ethidium bromide and a band of about 150 by was cut out and centrifugally filtered through a centrifugal filter tube (Millipore), extracted with phenol, and precipitated from ethanol. The recovered DNA was subcloned into plasmid vector PCR1''"'II according to the manual of TA Cloning Kit (Invitrogen). The vector was then introduced into E. coli JM109 and the resulting transformant was cultured and the sequence of the inserted cDNA fragment was analyzed as in Example 18. As a result, the sequence shown in Fig. 23 was obtained. Based on this sequence, primers FB (SEQ ID
NO: 40 ) and FG ( SEQ ID NO: 41 ) were synthesized and the 3' sequence was cloned (3' RACE). Using the same template as that for 5' RACE in the same quantity and the combination of the accompanying adapter primer AP1 with the primer FC , PCR was carried out at 94 °~ for 1 minute, followed by 5 cycles of 98~ x 10 seconds, 72qC
x 5 minutes , 5 cycles of 98 ~C x 10 seconds , 70 ~ x 5 minutes, and 25 cycles of 98 ~ x 10 seconds, 68°C x 5 minutes . Then, using 2 . 5 a 1 of a 50- fold dilution of this reaction mixture in tricine-EDTA buffer as the template and the combination of the accompanying primer AP2 with the primer FB, the reaction was further conducted at 94~C for one minute, followed by 4 cycles of 98~ x 10 seconds, 72~ x 5 minutes, 4 cycles of 98~
x 10 seconds, 70'C x 5 minutes, and 27 cycles of 98'~ x 10 seconds, 68~ x 5 minutes. The amplification product was electrophoresed on 1.2~ agarose gel and stained - with ethidium bromide and a band of about 400 by was cut out and the DNA was recovered as in 5' -RACE. This DNA fragment was subcloned into plasmid vector pCRTMII
and introduced into E. coli JM109 and the sequence of the inserted cDNA fragment in the resulting transformant was analyzed. From the results of 5' RACE
and 3' RACE, the DNA sequence [Fig. 24] coding for the complete coding region of the bioactive polypeptide WO 98/58962 PCTlJP98/02765 .:

defined by SEQ ID NO:1 was established. Thus, in Fig. -24 (a) and (b), the base134 is G, the base184 is T or C, and the base245 was T or C. -The cDNA shown in Fig. 24 was the cDNA encoding a polypeptide consisting of 98 amino acids. The fact that the amino acids in 1 - 22-positions comprise a cluster of hydrophobic amino acids taken together with the fact that the N-terminal region of the active peptide begins with Ser in 23-position as shown in Example 14 suggested that the amino acids 1-22 represent a secretion signal sequence. On the other hand, the Gly-Arg-Arg-Arg sequence in 54-57 positions of the polypeptide was found to be a typical amino acid sequence motif which exists in the event of cleavage of a bioactive peptide. As it is the case with this cleavage motif, it is known that because of the presence of Gly, the C-terminus of the product peptide is frequently amidated.
The P-3 N-terminal sequence data of Example 14 and P-2 N-terminal sequence data in Example 16 coupled with this GlyArgArgArg sequence suggest that at least same of the bioactive peptides cut out from the polypeptide encoded by this cDNA are defined by SEQ ID N0:3, SEQ ID
N0:4, SEQ ID N0:5, SEQ ID N0:6, SEQ ID N0:7, SEQ ID
N0:8, SEQ ID N0:9 or SEQ ID NO:10.
[Example 20]
Acquisition of a DNA fragment comprising the full coding region of bovine-derived bioactive polypeptide cDNA by PCR
Using the cDNA prepared with Marathon cDNA
amplification kit in Example 17 as a template, a DNA
fragment including the entire coding region of .
bioactive polypeptide cDNA was constructed. First, based on the sequence of cDNA elucidated in Example 19, two primers having base sequences defined by SEQ ID
N0:42 and SEQ ID N0:43, respectively, were synthesized.

S.

BOVF
5'-GTGTCGACGAATGAAGGCGGTGGGGGCCTGGC-3' (SEQ ID N0:42) BOVR (24 mer) 5'-AGGCTCCCGCTGTTATTCCTGGAC-3' (SEQ ID N0:43) BOVF contains the initiation codon of bioactive polypeptide cDNA and is a sense sequence corresponding to -2 - +22 (A of the initiation codon ATG being reckoned as +1) with restriction enzyme SalI site added. On the other hand, BOVR is an antisense sequence corresponding to +285 - +309 which includes the termination codon of bioactive polypeptide cDNA.
The PCR was conduced as follows. The cDNA
prepared using Marathon cDNA amplification kit in Example 17 was diluted 100-fold in tricine-EDTA buffer and using 2.5 a 1 of the dilution, a reaction mixture was prepared as in Example 2 and subjected to 94°~ x 1 minute, 3 cycles of 98'C x 10 seconds , 72'~ x 5 minutes, 3 cycles of 98'~ x 10 seconds, 70~ x 5 minutes, and 27 cycles of 98~ x 10 seconds, 68'C x 5 minutes. The amplification product was subjected to 2%
agarose electrophoresis and ethidium bromide staining and a band of about 320 by was cut out. The DNA was recovered and subcloned in plasmid vector pCRTMII as in Example 3. The vector was introduced into Escherichia cola JM109 to provide the transformant E. coli JM109/pBOV3. The sequence of the cDNA fragment inserted in the transformant was then analyzed. As a result, this DNA fragment was confirmed to be a fragment covering the entire coding region of the bioactive polypeptide cDNA.
[Example 21]
Synthesis of Ser-Arg-Ala-His-Gln-His-Ser-Met-Glu-Ile-Arg-Thr-Pro-Asp-Ile-Asn-Pro-Ala-Trp-Tyr-Ala-Gly-Arg-Gly-Ile-Arg-Pro-Val-Gly-Arg-Phe-NHZ (19P2-L31 ) 1) Synthesis of Ser(Bzl)-Arg(Tos)-Ala-His(Bom)-Gln-A.

His(Bom)-Ser(Bzl)-Met-Glu(OcHex)-Ile-Arg(Tos)-Thr(Bzl)-Pro-Asp(OcHex)-Ile-Asn-Pro-Ala-Trp(CHO)-Tyr(Br-Z}-Ala-Gly-Arg(Tos}-Gly-Ile-Arg(Tos)-Pro-Val-Gly-Arg(Tos}-Phe- y pMBHA-resin The reactor of a peptide synthesizer (Applied Biosystems 430A) was charged with 0.71 g (0.5 mmole) of commercial p-methyl-BHA resin (Applied Biosystems, currently Perkin Elmer). After wetting with DCM, the initial amino acid Boc-Phe was activated by the HOBt/DCC method and introduced into the p-methyl-BHA
resin. The resin was treated with 50% TFA/DCM to remove Boc and make the amino group free and neutralized with DIEA. To this amino group was condensed the next amino acid Boc-Arg (Tos} by the HOBt/DCC method. After the absence of unreacted amino function was verified by ninhydrin test, a sequential condensation of Boc-Gly, Boc-Val, Boc-Pro, Boc-Arg(Tos), Boc-Ile, Boc-Gly, Boc-Arg(Tos), Boc-Gly, Boc-Ala, Boc-Tyr(Br-Z) was carried out. The Boc-Ala, Boc-Tyr (Br-Z), the condensation of which was found insufficient by ninhydrin test, was recondensed to complete the reaction. The resin was dried and a half of the resin was withdrawn. To the remainder, Boc-Trp(CHO}, Boc-Ala, Boc-Pro, Boc-Asn, Boc-Ile, Boc-Asp(OcHex), Boc-Pro, Boc-Thr(Bzl), Boc-Arg(Tos), Boc-Ile, Boc-Glu(OcHex), Boc-Met, Boc-Ser(Bzl), Boc-His(Bom), Boc-Gln, Boc-His(Bom), Boc-Ala, Boc-Arg(Tos), Boc-Ser(Bzl) were serially condensed and recondensed until sufficient condensation was confirmed by ninhydrin test. After introduction of the full sequence of amino acids of 19P2-L31, t-~ 1 resi.:A ~~aas treated with 50% TFA/DCM to remove Boc :coups on the resin and, then, dried to provide 1.28 g of _the peptide resin.
2) Synthesis of Ser-Arg-Ala-His-Gln-His-Ser-Met-Glu-Ile-Arg-Thr-Pro-Asp-Ile-Asn-Pro-Ala-Trp-Tyr-Ala-Gly-Arg-Gly-Ile-Arg-Pro-Val-Gly-Arg-Phe-NHZ(I9P2-L31) In a Teflon hydrogen fluoride reactor, the resin obtained in 1) was reacted with 3.8 g of p-cresol, 1 ml of 1,4-butanedithiol, and 10 ml of hydrogen fluoride at 5 0°C for 60 minutes. The hydrogen fluoride and 1,4 butanedithiol (1 ml) were distilled off under reduced pressure and the residue was diluted with 100 ml of diethyl ether, stirred, filtered through a glass filter, and the fraction on the filter was dried. This 10 fraction was suspended in 50 ml of 50% acetic acid/H20 and stirred to extract the peptide. After separation of the resin, the extract was concentrated under reduced pressure to about 5 ml and chromatographed on Sephadex G-25 (2 x 90 cm). Development was carried out 15 with 50% acetic acid/ H20 and the 114 ml - 181 ml fraction was pooled and lyophilized to recover 290 mg of white powders containing 19P2-L31. The powders were applied to a reversed-phase column of LiChroprep RP-18 (Merck) and repeatedly purified by gradient elution 20 using 0.1% TFA/ H20 and 0.1% TFA-containing 30%
acetonitrile/ HZO. The fraction eluted at about 25%
acetonitrile was pooled and lyophilized to provide 71 mg of white powders.
Mass spectrum (M+H)' 3574.645 25 HPLC elution time 18.2 min.
Column conditions Column: Wakosil 5Ci8 (4.6 x 100 mm) Eluent: A (0.1% TFA/ HBO) B (0.1% TFA-containing 50 %
30 acetonitrile/ H20) Linear gradient elution from A to B (25 min.) Flow rate: 1.0 ml/min.
[Example 22]
Synthesis of Ser-Arg-Ala-His-Gln-His-Ser-Met(O)-Glu 35 Ile-Arg-Thr-Pro-Asp-Ile-Asn-Pro-Ala-Trp-Tyr-Ala-Gly Arg-Gly-Ile-Arg-Pro-Val-Gly-Arg-Phe-NH2(19P2-L31(O)) In 20 ml of 5% acetic acid/ H20 was dissolved 6 mg of synthetic I9P2-L31 and the Met only was selectively oxidized with 40 a 1 of 30% H20. After completion of -y the reaction, the reaction mixture was immediately applied to a reversed-phase column of LiChroprep RP-18 (Merck) for purification to provide 5.8 mg of the objective peptide.
Mass spectrum (M+H)+ 3590.531 HPLC elution time 17.9 min.
Column conditions Column: Wakosil 5C18 (4.6 x 100 mm) Eluent: A (0.1% TFA/ HZO) B (0.1% TFA-containing 50% acetonitrile/
HZO ) Linear gradient elution from A to B (25 min.) Flow rate: 1.0 ml/min.
(Example 23]
Synthesis of Thr-Pro-Asp-Ile-Asn-Pro-Ala-Trp-Tyr-Ala Gly-Arg-Gly-Ile-Arg-Pro-Val-Gly-Arg-Phe-NHZ(19P2-L20) To the resin subjected to condensations up to Boc Tyr(Br-Z) in Example 21-1) was further condensed Boc-Trp(CHO), Boc-Ala, Boc-Pro, Boc-Asn, Boc-Ile, Boc-Asp(OcHex), Boc-Pro, Boc-Thr(Bzl) serially in the same manner to provide 1.14 g of Boc-Thr(Bzl)-Pro-Asp(OcHex)-Ile-Asn-Pro-Ala-Trp(CHO)-Tyr(Br-Z)-Ala-Gly-Arg(Tos)-Gly-Ile-Arg(Tos)-Pro-Val-Gly-Arg(Tos)-Phe-pMBHA-resin. This resin was treated with hydrogen fluoride and columnwise purified in the same manner as Example 21-2) to provide 60 mg of white powders.
Mass vectrum (M+H)' 2242.149 HPLC ~:~ution time 10.4 min.
Column conditions -Column: Wakosil 5C18 (4.6 x 100 mm) Eluent: A (0.1% TFA-containing 15% acetonitrile/
H20 ) B (0.1% TFA-containing 45% aceto h.

' nitrile/ HZO) Linear gradient elution from A to 8 (15 min.) Flow rate: 1.0 ml/min.
[Example 24]
Determination of arachidonic acid metabolites-releasing activity of synthetic peptide (19P2-L31) The activity of the peptide (19P2-L31) synthesized in Example 21 to specifically release arachidonic acid metabolites from CHO-19P2 cells was assayed in the same manner as Example 11. The synthetic peptide was dissolved in degassed distilled HZO at a concentration of 10''M
and diluted with 0.05% BSA-HBSS and the activity to promote release of arachidonic acid metabolites from CHO-19P2 cells at each concentration was assayed using the amount of [3H]arachidonic acid metabolites as the indicator. As a result, concentration-dependent arachidonic acid metabolite-releasing activity was detected over the range of 10-12M - 10''M [ Fig . 25 ] .
When the arachidonic acid metabolite-releasing activity of peptide 19P2-L31(O), i.e. the methionine-oxidation product of 19P2-L31 synthesized in Example 22, was compared with that of 19P2-L31, it was found that the activity of 19P2-L31(O) was equivalent to the activity of 19P2-L31 as can be seen from Fig. 26.
[Example 25]
Determination of arachidonic acid metabolites-releasing activity of synthetic peptide (19P2-L20) The activity of the synthetic equivalent (19P2-L20) of natural peptide P-2 as synthesized in Example 23 to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells was determined as in Example 11. Thus, the synthetic peptide was dissolved in degassed distilled H20 at a final concentration of 10''M and this solution was serially diluted with 0.05%
BAS-HBSS.

S.

The activity to specifically promote release of arachidonic acid metabolites from CHO-19P2 cells at each concentration was assayed using the amount of a [3H]arachidonic acid metabolites as the indicator.
As a result, concentration-dependent arachidonic acid metabolite-releasing activity was detected over the range of 10-1z - 10-6M in nearly the same degree as 19P2-L31 [Fig. 27].
[Example 26]
Analysis of the coding region base sequence of bovine genomic DNA
pBOV3 was digested with restirction enzyme EcoRI
and after fractionation by agarose gel electrophoresis, the DNA corressponding to the cDNA fragment was recovered to prepare a probe. This DNA was labeled with 32P using a multiprime DNA labeling kit (Amersham). About 2.0x106 phages of Bovine Genomic Library (Clontech BL1015j) constructed using cloning vector EMBL3 SP6/T7 and Escherichia coli K802 as the host were seeded in an LB agar plate and cultured overnight for plaque formation. The plaques were transferred to a nitrocellulose filter and after alkaline modification and neutralization, heat-treated (80~, 2 hours) to inactivate the DNA. This filter was incubated with the labeled probe in 50% formamide-Hybri buffer (50% formamide, 5 x Denhardt solution, 4 x SSPE, 0.1 mg/ml heat-denatured salmon sperm DNA, 0.1% SDS) at 42~ overnight for hybridization. After this hybridization, the filter was washed with 2 x SSC, 0.1%
SDS at room temperature for 1.5 hours, and further washed in the same buffer at 55cC for 30 minutes.
Detection of the clone hybridizing with the probe was carried out on Kodak X-ray film (X-OMATTMAR) after 4 days of exposure using a sensitization screen at -8090.
After development of the film, the film was collated with plate positions and the phages which had ,.

hybridized were recovered. Then, plating and hybridization were repeated in the same manner for ' cloning of the pharges.
The cloned phages were prepared on a large scale by the plate lysate method and the phage DNA was extracted. Then, cleavage at the restriction enzyme SalI and BamHI cleavage sites at both ends of the cloning site of the vector and detection of the inserted fragment derived from bovine genomic DNA was carried out by 1.2% agarose gel electrophoresis [Fig.
28]. As a result, in the case of BamHI digestion, 3 fragments were detected in addition to the bands derived from the phages. In the case of SalI
digestion, one band overlapping the phage band was detected. The SalI-digested fragment being considered to harbor the full length and in order to subclone this fragment into a plasmid vector, it was ligated to BAP
(E. coli-derived alkaline phosphatase)-treated plasmid vector pUCl8 (Pharmacia) and introduced into E. cola JM109. From this microorganism, a genome-derived SalI
fragment-inserted plasmid DNA was prepared on a production scale and the base sequence in the neighborhood of its coding region was analyzed using Perkin Elmer Applied Biosystems 370A fluorecent sequencer and the same manufacturer's kit. As a result, the sequence shown in Fig. 29 was obtained.
Comparison with the coding region of cDNA reveals that because of its being derived from genomic DNA, the coding region is divided in two by a 472 by intron [Fig. 30]. Fig. 31 and SEQ ID N0:44 present the amino acid sequence predicted from this bovine genome coding region (excluding the intron region).
[Example 27]
Preparation of rat medulla oblongata poly(A)'RNA
fraction and synthesis of cDNA
Using Isogen (Nippon Gene), total RNA was prepared WO 98/589b2 PCT/JP98/02~65 a.

from the dorsal region of rat medulla oblongata and using FastTrack (Invitrogen), poly(A)'RNA fraction was prepared . To 5 ,u g of this poly ( A ) +RNA was added the primer random DNA hexamer (BRL) and using Moloney mouse leukemia reverse transcriptase (BRL) and the accompanying buffer, complementary DNA was synthesized.
The reaction product was precipitated from ethanol and dissolved in 12 a 1 of DW. In addition, from l ,u g of this poly(A)'RNA, a cDNA was synthesized using Marathon cDNA amplification kit (Clontech) according to the manual and dissolved in 1011 of DW.
[Example 28]
Acquisition of rat bioactive polypeptide cDNA by RACE
To obtain the full coding region of rat bioactive polypeptide cDNA, an experiment was performed in the same manner as the acquisition of bovine cDNA. First, PCR was carried out using the same primers P5-1 (SEQ ID
N0:35) and P3-1 (SEQ ID N0:36) as used in Example 18 as primers and the complementary DNA synthesized in Example 27 using the primer random DNA hexamer (BRL) and Moloney mouse leukemia reverse transcriptase (BRL) as a template. The reaction system was composed of 1. 25 !~ 1 of the template cDNA, 200 ~t M of dNTP , 1 ~t M each of the primers, ExTaq (Takara Shuzo Co., Japan) as DNA
polymerase, and 2.51 1 of the accompanying buffer, with a sufficient amount of water to make a total of 251 1.
The reaction was carried out at 94~ for 1 minute, followed by 40 cycles of 98~ x 10 seconds , 50'rC x 30 seconds, and 72°C x 5 seconds, and the reaction mixture was then allowed to stand at 72 ' for 20 seconds. The thermal cycler used was GeneAmp2400 (Perkin Elmer).
The amplification product was subjected to 4% agarose electrophoresis and ethidium bromide staining and the band of about 80 by was cut out. Then, in the manner described in Example 19, the DNA was recovered, H.

subcloned into plasmid vector pCRTMII, and introduced into E. coli JM109, and the inserted cDNA fragment was - sequenced. As a result, a partial sequence of rat bioactive polypeptide could be obtained. Based on this sequence, two primers, namely RA (SEQ ID N0:75) for 3' RACE and RC (SEQ ID N0:76) for 5' RACE were synthesized and 5' and 3' RACEs were carried out.
RA:5'-CARCAYTCCATGGAGACAAGAACCCC-3' (where R means A or G; Y means T or G) (SEQ ID N0:75) RC:5'-TACCAGGCAGGATTGATACAGGGG-3' (SEQ ID N0:76) As a template, the template synthesized using Marathon cDNA amplification kit (Clontech) in Example 27 was diluted 40-fold with the accompanying tricine-EDTA buffer and 2.5 a l of the dilution was used. As primers, RA and the adapter primer AP1 accompanying the kit were used for 3' RACE, and RC and AP1 for 5' RACE.
The reaction mixture was prepared in the same manner as above. The reaction conditions were 94°~ x 1 minute , 5 cycles of 98'c x 10 seconds , 72'~ x 45 seconds, 3 cycles of 98°~ x 10 seconds, 7090 x 45 seconds, and 40 cycles of 98~C x 10 seconds, 68~ x 45 seconds. As a result, a band of about 400 by was obtained from 3' RACE and bands of about 400 by and 250 by from 5' RACE. These bands were recovered in the same manner as above and using them as templates and the primers used in the reaction, sequencing was carried out with Dye Terminator Cycle Sequencing Kit (ABI). As a result, the sequence up to poly A could be obtained from the region considered to be the 5' noncoding region. .
[ Example 29 ] : _ .---Acquisition of the full-length cDNA of rat _ bioactive polypeptide by PCR
Based on the sequence obtained in Example 28, two primers, viz. rF for the region including the h:

initiation codon (SEQ ID N0:77) and rR for the 3' side from the termination codon (SEQ ID N0:78), were synthesized to amplify the fragment including the full-length cDNA.
rF:5'-GGCATCATCCAGGAAGACGGAGCAT-3' (SEQ ID N0:77) rR:S'-AGCAGAGGAGAGGGAGGGTAGAGGA-3' (SEQ ID N0:78) Using the cDNA prepared using Moloney mouse leukemia reverse transcriptase in Example 27 as a template and ExTaq (Takara Shuzo Co., Japan), PCR was carried out by repeating 40 cycles of 95~C x 30 seconds, 68cC x 60 seconds. The amplification product was subjected to agarose electrophoresis and ethidium bromide staining and a band of about 350 by was cut out. The DNA was recovered, subcloned into plasmid vector pCRTMII, and introduced into E. coli JM109 as in Example 19. The plasmid was extracted from the transformant and the base sequence was determined. As a result, E. coli JM 109/pRAV3 having the full-length cDNA of rat bioactive polypeptide was obtained [Fig.
3 2 ] .
[Example 30]
Synthesis of cDNA from the human total brain ply(A)'RNA fraction From 1 a g of human total brain poly(A)'RNA
fraction (Clontech), cDNA was synthesized with Marathon cDNA amplification kit (Clontech) according to the manual and dissolved in 10~t1. In addition, the random DNA hexamer (BRL) was added as primer to 5l~ g of the same poly(A)'RNA fraction and using Moloney mouse leukemia reverse transcriptase (BRL) and the accompanying buffer, complementary DNA was syntr:=-.:,ized.
The reaction product was precipitated from ethanol and dissolved in 30~.t1 of TE.
[Example 31]
Acquisition of human bioactive polypeptide cDNA by RACE

h:

From the amino acid sequence of rat bioactive polypeptide established in Example 28 [Fig. 33], the well-preserved regions of rat and bovine polypeptides were selected and the following 3 primers Rl (SEQ ID
N0:79), R3 (SEQ ID N0:80), and R4 (SEQ ID N0:81) were synthesized. Then, amplification of the region flanked by them was attempted by PCR using human cDNA as a template. Referring to Fig. 33, bovine. as represents the amino acid sequence of bovine polypeptide, bovine.
seq represents the base sequence of the DNA coding for bovine polypeptide, and rat. seq represents the base sequence of the DNA coding for rat polypeptide.
R1:5'-ACGTGGCTTCTGTGCTTGCTGC-3' (SEQ ID N0:79) R3:5'-GCCTGATCCCGCGGCCCGTGTACCA-3' (SEQ ID N0:80) R4:5'-TTGCCCTTCTCCTG.CCGAAGCGGCCC-3' (SEQ ID N0:81) The cDNA prepared using Marathon cDNA
amplification kit (Clontech) in Example 30 was diluted 30-fold with tricine-EDTA buffer and 0.25,u l of the dilution was used as a template. The reaction mixture was composed of 200 ~t M of dNTP , 0 . 2 !~ M each of the primers R1 and R4, a 50:50 mixture of Taq Start Antibody (Clontech) and DNA polymerase ExTaq (Takara Shuzo Co., Japan), 2.5~t1 of the accompanying buffer, and a sufficient amount of water to make a total of 25 ,u 1. The reaction conditions were 94'~ x 1 minute, followed by 42 cycles of 98'~ x 10 seconds, 68~ x 40 seconds, and 1 minute of standing at 72'~C. Then, using ll~ 1 of a 100-fold dilution of the above reaction mixture in tricine-EDTA buffer as a template, the same reaction mixture as above except that the primer combination was changed to R1 and R3 was prepared and PCR was carried out in the sequence of 94 ~ x 1 minute and 25 cycles of 98~ x 10 seconds, 68'~ x 40 seconds.
The amplification product was subjected to 4% agarose electrophoresis and ethidium bromide staining. As a result, a band of about 130 by was obtained as h:

expected. This band was recovered in the same manner as in Example 28 and using the recovered fragment as a template, sequencing was carried out with Dye .
Terminator Cycle Sequencing Kit (ABI). As a result, a partial sequence of human bioactive polypeptide could be obtained. Therefore, based on this sequence, primers HA (SEQ ID N0:82) and HB (SEQ ID N0:83) were synthesized for 3' RACE and primers HE (SEQ ID N0:84) and HF (SEQ ID N0:85) for 5' RACE and 5' and 3' RACES
were carried out.
HA:5'-GGCGGGGGCTGCAAGTCGTACCCATCG-3' (SEQ ID N0:82) HB:5'-CGGCACTCCATGGAGATCCGCACCCCT-3' (SEQ ID N0:83) HE:5'-CAGGCAGGATTGATGTCAGGGGTGCGG-3' (SEQ ID N0:84) HF:5'-CATGGAGTGCCGATGGGTACGACTTGC-3' (SEQ ID N0:85) As the template, 2.5/.tl of a 20-fold dilution of the cDNA prepared in Example 30 in tricine-EDTA buffer was used. For the initial PCR, reaction mixtures were prepared in the same manner as above except that HA and adapter primer AP1 were used for 3' RACE and HE and APl for 5' RACE. The reaction sequence was 94~C x 1 minute, 5 cycles of 98~ x 10 seconds, 72~ for 35 seconds, 5 cycles of 98~ x 10 seconds, 70~ x 35 seconds, and 40 cycles of 98~ x 10 seconds, 68~C x 35 seconds. Then, using l,u 1 of a 100-fold dilution of this reaction mixture in tricine-EDTA buffer as a template, a second PCR was carried out in the same cycles as the first PCR. However, the reaction mixture was prepared using primers HB and AP1 for 3' RACE or HF
and AP2 for 5' RACE and Klen Taq (Clontech) as DNA
polymerase and the accompanying buffer. As a result, a band of about 250 by was obtained from 3' RACE and a band of about 150 by from 5'-RACE. These bands.were sequenced by the same procedure as above and using them in combination with the partial sequence obtained previously, the sequence from the region presumed to be 5'-noncoding region to polyA of human bioactive A:

polypeptide was obtained.
[Example 32]
Acquisition of human bioactive polypeptide full-length cDNA by PCR
Based on the sequence obtained in Example 31, two primers 5H (SEQ ID N0:86) and 3HN (SEQ ID N0:87) were synthesized for amplification of a fragment including full-length cDNA.
5H:5'-GGCCTCCTCGGAGGAGCCAAGGGATGA-3' (SEQ ID N0:86) 3HN:5'-GGGAAAGGAGCCCGAAGGAGAGGAGAG-3' (SEQ ID N0:87) Using 2.5 a 1 of the cDNA prepared using Moloney mouse leukemia reverse transcriptase (BRL) in Example 30 as a template and the reaction mixture prepared using Klen Taq DNA polymerase (Clontech), the PCR
reaction was conducted in the sequence of 94~ x 1 minute and 40 cycles of 98'~ x 10 seconds, 68°~ x 30 seconds. The fragment of about 360 by obtained was recovered and subcloned (pCR~"' 2.1 was used as the vector) in otherwise the same manner as Example 29.
The plasmid was recovered and its base sequence was determined. As a result, E. coli JM109/pHOV7 harboring the human bioactive polypeptide full-length cDNA was obtained [Fig. 34]. In regard to the amino acid sequence of the translation region, a comparison was made between this human bioactive polypeptide and the bovine polypeptide shown in Example 20 or the rat polypeptide in Example 29 [Fig. 35].
[Example 33]
(1) Preparation of UHR-1 expression CHO cells Recently, the orphan receptor UHR-1 has been cloned from the rat suprachiasmatic nucleus by Susan K.
Welch and coworkers (Biochemical and Biophysical Research Communications , Vol . 209 , No . 2 , pp . 606-613 , 1995).
Based on this report, the inventors of the present invention compared the amino acid sequence of h.
lOb the protein encoded by the UHR-1 gene with the amino -acid sequence of the protein encoded by hGR3.
As a result, the two sequences had 91.6 identity over 359 amino acids, suggesting that UHR-1 is a phGR3 homolog. In order to confirm that the protein encoded by UHR-1 functions as a receptor for 19P2-L31, the inventors of the present invention carried out a cloning of UHR-1 cDNA and subcloned it into CHO cells to construct a stable expression cell line as described below.
By the extraction using FastTrackT''' Kit (Invitrogen), poly(A)'RNA was prepared from the anterior lobe of the rat hypophysis. Then, using 0.2 /~
g of the poly(A)'RNA as a template, a cDNA was synthesized on a total reaction scale of 40 J~ 1 using TaKaRa RNA PCR Kit (Takara Shuzo). The reaction product was extracted with phenol-chloroform (1:1), precipitated with ethanol, and dissolved in 10 a 1 of distilled water. Based on the known nucleotide sequence of rat UHR-1 cDNA {GenBank, Accession Number S77867), the following two synthetic DNA primers were prepared.
(1) 5'-GTTCACAG{GTCGAC)ATGACCTCAC-3' (SalI recognition sequence in parentheses) (SEQ ID
NO:95) (2) 5'-CTCAGA(GCTAGC)AGAGTGTCATCAG-3' (NheI recognition sequence in parentheses) {SEQ ID
N0:96) Using the above pair of primers (1) and (2) and the cDNA synthesized by the procedure described above as the template, a PCR was carried out. F. this reaction, 5 a 1 of a 5-fold dilution of the cDNA
solution, 1 a 1 of a 1:1 mixture of Ex Taq (Takara Shuzo) and Taq Start Antibody (Clontech), 5 I~1 of 10 x .
reaction buffer attached to Ex Taq, 4 /.c 1 of dNTP, and 1 a 1 each of the primers of 50 /.t. M concentration were r:

used and the whole amount was made up to 50 a 1 with distilled water.
,; The PCR was performed according to the schedule of denaturing at 95 ~ x 2 min. and 27 cycles each consisting of 95'C x 30 sec. , 65qC x 30 sec. and 72'x, 1 min., followed by final extension at 72 ~ x 7 min.
After completion of cycling, a portion of the reaction mixture was electrophoresed on an agarose gel. After ethidium bromide staining, a 1.1 kbp (approx.) band was excised, centrifugally filtered using a centrifugal filtration tube (Millipore), extracted with phenol, and precipitated from ethanol to recover the DNA. The recovered DNA was subcloned into the plasmid vector pCR1'''II according to the manual of TA Cloning Kit (Invitrogen) (pCRII-UHR-1) and introduced into Escherichia coli JM109. The resultant transformant was cultured in ampicillin-containing LB medium and the plasmid was extracted with an automatic plasmid extractor (Kurabo).
This plasmid was subjected to sequencing reaction using ABI PRISM Dye Teriminator Cycle Sequencing Kit, FS (Perkin-Elmer) according to the manual and the nucleotide sequence was read out using a fluorescent automatated DNA sequences (ABI).
The above sequencing revealed that the cDNA
fragment obtained by PCR was a 1116bp fragment [Fig.
52]. Fig. 52 shows the nucleotide sequence of the full coding region of the rat UHR-1 constructed on the expression vector pAKKO-UHR-1 and the amino acid sequence encoded thereby. In Fig. 52, the underscored sequences (1) and (2) correspond to portions= of the respective primer sequences. The bases different from those of the known nucleotide sequence (C in 664-position, G in 865-position, G in 897-position) are double-scored. The known nucleotide sequence presented here is a reproduction of GenBank Accession No. 577867.

,.

One of those base substitutions involves an amino acid substitution of z89Leu ( CTC ) -' Z89Val ( GTC } . The construction of the UHR-1 expression vector was carried -out as follows .
The pCRII-UHR-1 was cleaved with the restriction enzymes NheI (Takara Shuzo) and SalI (Takara Shuzo).
The sample available on cleavage was electrophoresed on an agarose gel and stained with ethidium bromide, and the gel portion corresponding to the band was cut out.
This gel fragment was put in a centrifuge tube with a filter (Millipore), frozen in a freezer, and thawed at room temperature. The tube was then centrifuged at 8000 rpm for 1 minute, whereupon a solution containing the DNA fragment was eluted out in the bottom of the filter. This solution was extracted with phenol, phenol-chloroform (1:I), and diethyl ether in the routine manner to remove impurities and the DNA was precipitated from ethanol to recover a cDNA fragment.
The pAKKO-111H was cleaved with the restriction enzymes NheI (Takara Shuzo) and SalI (Takara Shuzo) and the vector was isolated and extracted from an agarose gel in the same manner as above. Using Ligation System (Takara Shuzo), the cDNA fragment obtained above was reacted with the restriction enzyme digest of pAKKO
111H at 16 ~C for 30 minutes . Using a portion of this ligation product, Escherichia coli JM109 was transformed to construct a transformant, Escherichia coli JM109/pAKKO-UHR-1. This transformant was cultured overnight in 2 ml of ampicillin ( 50 ~t g/ml ) -containing LB medium and using an automatic plasmid extractor (Kurabo), the plasmid _:vA (pAKKO-UHR-1) was obtained.
The nucleotide sequence of the cDNA fragment-PAKKO-111H
ligation site was analyzed with a fluorescent sequences to confirm completion of the construction of the expression vector pAKKO-UHR-1.
(2) Introduction of the UHR-1 expression vector into h.

' CHO dhfr- cells In a 10 cm-diameter tissue culture dish, 1x106 CHO dhfr- cells were seeded and cultured for 24 hours .
From 20 a g of the UHR-1 expression vector pAKKO-UHR-1 obtained in (1), a DNA-liposome complex was prepared using a liposome-mediated gene transfer kit (Gene Transfer, Nippon Gene). The medium was replaced with fresh one and the DNA-liposome complex was added and incubated overnight. The medium was replaced with fresh one again and further incubated for 1 day. After the medium was replaced with a transformant screening medium, the complex was incubated for 2 days. The cells were harvested from the dish by trypsin-EDTA
treatment and recultured at a low cell density for an enhanced yield of the transformant. By the above procedure, a CHO-UHR-1 cell line capable of stable, high expression of UHR-1 could be cloned.
[Example 34]
~zsl labeling of 19P2-L31 and a receptor-binding experiment using the labeled 19P2-L31 The radiolabeling of 19P2-L31 was carried out using [lzsl]-Bolton-Hunter Reagent (NEN/DuPont; NEX-120).
First, 200 a 1 of [lzsl]_golton-Hunter Reagent (2200 Ci/mmol) was transferred to a 500 a 1 Eppendorf's tube and dried thoroughly with nitrogen gas. It was redissolved in 2 Ltl of acetonitrile and, then, 4 a 1 of 50 mM phosphate buffer ( pH 8 . 0 ) and 4 a 1 of 3x10-' M
synthetic 19P2-L31 were added. After mixing, the reaction was carried out at room temperature for 40 minutes. The reaction was then stopped with 5 a 1 of 1.0 M glycine buffer and the whole reaction mixture was applied onto a reversed phased column (Tosoh; TSK gel ODS-80TMCTP ) to separate [ ~ZSI ] -labeled 19P2-L31 ( [ lzsl ] -19P2-L31). The fraction containing [izsl]-19P2-L31 was diluted with 2 volumes of 50 mM Tris-HCl (pH 7 . 5 ) -0 .1%
BSA-0.05% CHAPS, distributed in small aliquots, and stored at -20~ .
The receptor binding experiment was performed using CHO-19P2-9, CHO-UHR-1, and mock CHO as receptor -expression CHO cells. CHO-19P2-9 cells were obtained by picking up a CHO-19P2 cell clone showing particularly high activity to stimulate the release of arachidonic acid metabolites by 19P2L-L31 from a limiting dilution culture in a 96-well microtiter plate.
The mock CHO cells were control cells obtained by transformation with the expression vector pAKKO alone.
Those cells, grown in tissue culture flasks, were respectively scraped off with 5 mM EDTA/PBS and resuspended in 0.05 BSA/0.05~ CHAPS-containing HBSS at a density of 0.5x10' cells/ml. To 100 ~t 1 of this cell suspension was added ~ 125I ] _ 19P2-L31 at a final concentration of 200 pM. In addition, as an NSB (non-specific binding) experiment, 19P2-L31 was added to portions of the cell suspensions at a concentration of 200 nM. The reaction was performed at room temperature for 2.5 hours. After the reaction, B/F separation was carried out with a glass filter GF/F (Wattman) and the radioactivity trapped by the filter was counted with a gamma-counter as a receptor binding amount.
The results of receptor binding experiments using (lzsl]_19P2-L31 in living cells are shown in Fig. 36.
To 100 a 1 of a cell suspension, 0.5x10' cells/ml, was added ~ lzsl ] _ 19P2-L31 at a final concentration of 200 pM, and after a 2.5-hour reaction at room temperature, the amount of [lzsl]_19P2-L31 bound to the receptor and the non-specific binding amount were determined with a ga3 za counter. The e:~ ~riments were performed in triplicate and the mean values and standard deviations were calculated.
In the CHO cells in which hGR3 and UHR-1 were expressed, specific binding of [ IzSI ] -19P2-L31 was observed. Those results indicate that the protein h:

' encoded by hGR3 or UHR-1 functions as a specific receptor of 19P2-L31.
~ [Example 35]
Specific stimulation of arachidonic acid metabolite release from CHO-19P2-9 and CHO-UHR1 by 19P2-L31 The action of 19P2-L31 to stimulate arachidonic acid metabolite release from CHO-19P2-9, CHO-UHRl, and mock CHO was assayed by the same procedure as described in Example 11.
Fig. 37 shows the results of assays of arachidonic acid metabolite releasing activity of 19P2-L31 in CHO-19P2-9 and CHO-UHR1. The experiments were performed in duplicate and the mean results are shown.
In CHO cells with expression of UHR1, too, a comparable degree of arachidonic acid metabolite releasing activity of 19P2-L31 was found as in CHO
19P2-9. Those results indicate that the protein encoded by UHR-1 functions as a specific receptor of 19P2-L31 as does hGR3.
[Example 36]
Assay of the expression of rat tissue ligand polypeptide and rat G protein-coupled receptor (UHR-1) by RT-PCR
(1) Preparation of poly(A)+RNA from rat tissues Using an 8 -week-old rat ( d' ) , poly ( A }'RNAs from various tissues were prepared in amounts ranging from about 5 to about 30 ~t g by the isolation of total RNA
with Isogen (Nippon Gene) and subsequent purification with an oligo(dT)cellulose column (Pharmacia).
To completely remove the genome DNA from the poly(A)'RNA fraction, one unit of DNaseI (Glbco BRL, amplification grade) was used to decompose the DNA at room temperature. After addition of 25 mM EDTA, the reaction mixture was incubated at 65 ~ for 10 minutes to inactivate the DNaseI. The mixture was diluted to ng/1~1 with water, and from a 160 ng portion thereof, WO 98!58962 PCT/JP98/02765 h:

a cDNA was synthesized using 10 U AMV reverse transcriptase XL (Takara), 2.5 a M random 9mer (Takara, final concentration 2. 5 I~ M) , 10 mM Tris-HC1 (pH 8. 3 ) , and 0.4 mM each dNTP. The synthetic reaction protocol was 30~ x 10 minutes followed by 42°rC x 30 min, 99~ x 5 min, and 5 ~ x 5 min. The reaction product was precipitated from ethanol and dissolved in Tricine-EDTA
buffer to give a total of 40 Lt 1 ( 4 ng poly(A)'RNA/ a 1) .
(2) Construction of a positive control plasmid vector Rat glyceraldehyde-3-phosphate dehydrogenase (G3PDH, GenBank Accession No. M17701) was amplified by PCR using the cDNA synthesized from the rat pituitary GH3 poly(A)'RNA prepared using FastTrack Kit (Invitrogen) in the same manner as in (1) above as a template and Clontech's G3PDH amplification primer set.
The UHR-1 was obtained by PCR using the cDNA of GH3, as a template, and the following primers, followed by subcloning into the pCRT''' 2.1 Vector of TA Cloning Kit (Invitrogen).
rRECF: 5'-CCTGCTGGCCATTCTCCTGTCTTAC-3' (SEQ ID N0:88) rRECR: 5'-GGGTCCAGGTCCCGCAGAAGGTTGA-3' (SEQ ID N0:89) Those were introduced into Escherichia coli JM109 to provide transformants. As the ligand peptide, JM109/pRAV3, already deposited, was used. After each of those transformants was cultured in ampicillin-containing LB medium, the plasmid was purified with Qiagen Plasmid Midi Kit (Qiagen) and, after the concentration was determined from optical density, used as a positive control plasmid vector.
(3) RT-PCR
The cDNA solution and the positive control plasmid vector prepared in (1) and (2) above were used as templates, with or without dilution to a suitable concentration with water. For the amplification of G3PDH, UHR-1, and ligand peptide, Clontech's G3PDH
Amplification Primer Set, rRECF/rRECR set, and the ' following primer set were used, respectively, at a final concentration of 200 nM.
rl9F: 5'-GAAGACGGAGCATGGCCCTGAAGAC-3' (SEQ ID N0:90) rl9R: 5'-GGCAGCTGAGTTGGCCAAGTCCAGT-3' (SEQ ID N0:91) The reaction mixture consisted of 4 a 1 of the diluted template, 200 nM each primers, dNTP (final concen-tration 100 a M each), and KlenTaq (Clontech) as DNA
polymerase and used after adjustment to 25 ~cl with the buffer attached to KlenTaq and water. The amplification reaction conditions were as follows.
G3PDH: 94~ x 1 min. followed by 26 cycles of 98~C x 10 sec, 65°~ x 20 sec., and 7290 x 40 sec.; UHR-1 and ligand peptide: 94~ x 1 min, followed by 34 cycles of 98 'rC x 10 sec. , 68 9C x 25 sec. The amplification product was electrophoresed on an ethidium bromide-stained 1.2% or 4% agarose gel. The electrophoretogram was photographed by a CCD camera (Fotodyne, Foto/Ecrips) and the concentration of the band was digitalized and quantitated using an analytical software (Advanced American Biotechnology). The data for G3PDH was expressed in pg per 4 ng poly(A)iRNA and the data for UHR-1 and ligand peptide were expressed in pg per 4 ng poly(A)'RNA and, additionally, in the value found by dividing the pg value by pg for G3PDH [Figs.
ZS 38 and 39].
As a result, UHR-1 and the ligand peptide were confirmed to be expressed in all tissues. The level of expression of UHR-1 was high in the hypophysis and a broad distribution was found in the brain, too, but the levels of expression in the peripheral tissues were not so high with the exception of the adrenal gland. On . the other hand, the level of expression of the ligand peptide was high in the medula oblongata and hypothalamus, among brain tissues, and low in the hypophysis. In the peripheral tissues, the ligand peptide was expressed at comparatively high levels in h.

the lung, thymus, pancreas, kidney, adrenal, and testis.
Those results suggest that UHR-1 and its ligand peptide are playing important roles in various tissues for the modulation of their functions.
(Example 37]
The influence of 19P2-L31 on glucose-induced increase in plasma insulin concentration Wistar rats (8-10 weeks old, d') anesthetized with pentobarbital (65 mg/kg, i.p.) were transitorily dosed with glucose ( 86 mg/rat ) alone or glucose in the same dose plus 19P2-L31 (675 pmol, 2.25 nmol, 6.75 nmol, or 67.5 nmol, per rat) via the common jugular vein, while the blood was serially drawn from the contralateral common jugular vein and the plasma insulin concentration was determined by radioimmunoassay. For this determination, Amersham's insulin assay kit was used.
19P2-L31 in a dose of 675 pmol, 2.25 nmol, or 6.75 nmol, suppressed the first-phase burst of plasma insulin concentration occurring 2 minutes following glucose loading and the second-phase moderate rise in plasma insulin concentration beginning around 6 minutes following administration. Administered in a dose of 67.5 nmol, 19P2-L31 completely inhibited both the first-phase and second-phase increases in insulin concentration [Fig. 40].
[Example 38]
The influence of the ligand polypeptide on the behaviors of mice The inventors investigated the influence of 19P2-L31 and 19P2-L20 administered into a lateral ventricle of mice on their behaviors. Thus, mature male ICR mice (body weights at operation: ca 35 g) were anesthetized with pentobarbital 50 mg/kg i.p. and immobilized in a rat brain stereotaxic apparatus. The skull was exposed and a hole was drilled with a dental drill for insertion of a guide cannula into one lateral ventricle.
Thus, a stainless steel guide cannula (24G, 5 mm long) for intraventricular medication was inserted with its tip set at AP: +0.6 mm (from bregma), L: 1 mm (left), and H: -1 mm (from data). The guide cannula was then rigidly secured to the skull with an adhesive. After operation, the mice were reared for at least 3 days for recuperation and then submitted to an experiment for behavioral analysis.
The spontaneous motor activity of mice was measured using a jiggle (spontaneous movement) cage made of clear acrylic resin, 24 x 37 x 30 cm, in a soundproof chamber. The mouse was individually housed in the above cage, and under a 12-hr light-and-dark cycle {ON: 6 to 18 o'clock) and with free access to water and food, the amount of spontaneous motor activity and the amount of rearing were respectively measured. The amount of spontaneous motor activity was measured with Supermex (Muromachi Machinery). The peptide or phosphate buffered saline (PBS) was administered at 2:30 ~ 30 min., p.m. For administration, a stainless steel microinjection cannula (30 G, 6 mm long) was passed through the guide cannula. The microinjection cannula was connected to a microsyringe pump via a Teflon tube and either PBS or a PBS solution of the peptide was infused at a flow rate of 2 a 1/min for 2 minutes. The microinjection cannula was left inserted for at least 2 minutes after completion of infusion and, then, removed and the amount of spontaneous motor activity was measured.
The results were-expressed in mean ~ S.E.M. and the significance of the relative effect of the-peptide and PBS treatments on motor activity was analyzed by Student's t-test. The difference at the 5% level of significance (p<5%) on a two-tailed basis was regarded as being statistically significant. It is clear from h.

Fig. 41 that when 10 nmol of 19P2-L31 was administered, the spontaneous motor activity of mice was increased significantly during the period from 70 to 105 minutes A
after administration. The rearing behavior also showed a significant change in the like fashion. When, 1 nmol of 19P2-L31 was administered, no change was found in spontaneous activity and the amount of rearing was decreased significantly only at 105 minutes following administration [Fig. 42]. With 0.1 nmol of 19P2-31, the amount of spontaneous motor activity was increased significantly at 25, 40, and 70 minutes following administration. The amount of rearing also showed a similar trend but did not change significantly [Fig.
43]. With 0.01 nmol of 19P2-L31, spontaneous motor activity was increased significantly at 20 and 40 minutes following administration. The amount of rearing also showed a similar tendency toward increase but the change was not significant [Fig. 44].
[Example 39]
The influence of the ligand peptide on reserpine-induced hypothermia in mice Mature male ICR mice ( body weights at operation ca 35 g) were anesthetized with pentobarbital 50 mg/kg i.p. and immobilized in a rat brain stereotaxic apparatus. The skull was exposed and a hole was drilled with a dental drill for indwelling a guide cannula in one lateral ventricle. A stainless steel guide cannula for intraventricular medication (24 G, 5 mm long ) was inserted with its tip set at AP : +0 . 6 mm (from bregma), L: 1 ~ (left), H: -1 mm (from dura).
The guide cannul~ :~a~ ~i~.dly :eacured to t%'a skull with an adhesive. After of ation, the mice we~~e reared for at least 3 days for recuperation and the body temperature was then measured. Then, reserpine (Apopron Inj. 1 mg, Daiichi Pharmaceutical), 3 mg/kg, was injected subcutaneously, and 15 hours later the mice were transferred to individual cages for body temperature measurement. A stainless steel microinjection cannula (30 G, 6 mm long) was passed into the guide cannula. The microinjection cannula was connected to a microinjection syringe pump via a Teflon tube and PBS or a PBS solution of the peptide was infused at a flow rate of 2 a 1/min. for 2 minutes . The microinjection cannula was left installed for at least 2 minutes following completion of infusion and, then, removed and the rectal temperature was measured.
The results were expressed in mean t S.E.M. and the significance of the relative effect of the peptide and PBS treatments on body temperature was analyzed by Student's t-test. The difference at the 5% level of significance on a two-tailed basis was regarded as being statistically significant. It is clear from Fig.
45 that when 10 nmol of 19P2-L31 was administered, the body temperature depressed by reserpine was elevated significantly as compared with the PBS control group.
This elevation of body temperature peaked at 45 minutes following administration of 19P2-L31. On the other hand, no difference was found between the 19P2-L20 1 nmol group and the control group.
[Example 40]
The influence of the ligand polypeptide on rat blood pressure The inventors of the present invention studied the influence of 19P2-L31 injected into the area postrema (AP) of medula oblongata on rat blood pressure.
Mature male Wistar rats (body weights at operation: ca 300 g) were anesthetized with pentobarbital 50 mg/kg i.p. and immobilized in a rat brain stereotaxic apparatus. The incisal bar was set 3.3 mm below the interoral line . The skull was exposed and a hole was drilled with a dental drill for indwelling a guide cannula. In addition, anchor screws were embedded in 2 h:

positions around the hole. A stainless steel guide cannula, AG-12 (inside dia. 0.4 mm, out. dia. 0.5 mm, Acorn), was inserted with its tip situated in the -superior domain of the area postrema. For this purpose, the guide cannula was inserted from the anterior direction at an angle of 20 degrees with the vertical direction (Fig. 46; the figure shows a microinjection cannula which is longer than the guide cannula by 1.0 mm). The stereotaxic coordinates of AP: -0.6 mm (from interoral line), L: 0.0 mm, H: +1.5 mm (from interoral line ) were used with reference to the atlas of Paxinos and Watson (1986). The guide cannula was secured to the skull with an instant adhesive, a dental cement, and said anchor screws. In the guide cannula, a stainless steel dummy cannula, AD-12 (out. dia. 0.35 mm, Acorn), was inserted and secured in position with a cap nut (Acorn). Thereafter, the rats were reared in individual cages.
The animals were reared for about a week following cannulation for recuperation and a surgery was performed for measurement of conscious blood pressure. Thus, the rat was anesthetized with pentobarbital 50 mg/kg i.p. and immobilized in supine position on a dissection pad, and the left femoral artery was exposed. A polyethylene tube, SP35 (in. dia.
0.5 mm, out. dia. 0.9 mm, Natsume Seisakusho) , was cut to about 60 cm in length and the cut tube was filled with 200 U/ml heparin-containing saline and inserted into the femoral artery over a distance of about 2.5 cm and secured in position. The other end of the tube was passed beneath the dorsal skin and exposed from the cervical (dorsal) region.
After one night following operation, the poly ethylene tube was connected to a pressure transducer (Spectramed) and the blood pressure was measured.
After the blood pressure reading had become steady, the h.

cap nut and dummy cannula were removed from the rat skull and, instead, a stainless steel microinjection cannula, AMI13 (in. dia. 0.17 mm, out. dia. 0.35 mm, Acom), connected to a Teflon tube (50 cm long, 0.1 mm in. dia., 0.4 mm out. dia., Acom), was inserted. The ' length of the microinjection cannula was adjusted beforehand so that its tip would be exposed from the guide cannula over a distance of 1 mm [Fig. 46] . The other end of the Teflon tube was connected to a microsyringe pump and 2 I~ 1 of either PBS or a PBS
solution of 19P2-L31 was injected into the area postrema at a flow rate of 1.0 a 1/min.
After blood pressure measurement, the micro injection cannula used for injection of 19P-L31 was removed and, instead, a microinjection cannula for infusion of a dye ( Evans blue ) was installed . The dye was similarly infused at a flow rate of 1. 0 ,u 1/min for 2 minutes and after a waiting time of about 3 minutes the microinjection cannula was removed. The rat was decapitated and the brain was quickly enucleated and frozen. Using a cryostat, frozen sections were prepared and the infusion position of the dye was confirmed.
The above experiment revealed that the infusion of 10 nmol of 19P2-L31 into the area postrema caused a rise in blood pressure. A typical example of pulse wave and mean blood pressure is shown in Fig. 47.
[Example 41]
The influence of the ligand polypeptide on the plasma pituitary hormone level The inventors of the present invention studied the influence of 19P2-L31 injected into the third ventricle on the plasma pituitary hormone levels.
Mature male Wistar rats (body weights at operation: ca 290~350 g) were anesthetized with pentobarbital 50 mg/kg i.p. and each animal was immobilized in a rat brain stereotaxic apparatus. The incisal bar was set 3.3 mm below the interoral line. The skull was exposed and using a dental bar a hole was drilled for indwelling a guide cannula. In addition, an anchor screw was embedded in one position around the hole. A
stainless steel guide cannula, AG-12 (in. dia. 0.4 mm, out. dia. 0.5 mm, Acorn), was inserted with its tip positioned in the superior domain of the third ventricle. The stereotaxic coordinates of AP: +7.2 mm ( from interoral line ) , I, : 0 . 0 mm, H : +2 . 0 mm ( from interoral line) were used with reference to the atlas of Paxinos and Watson (1986). The guide cannula was rigidly secured to the skull with an instant adhesive, a dental cement, and said anchor screw. In the guide cannula, a stainless steel dummy cannula, AD-12 (out.
dia. 0.35 mm, Acorn) was passed and secured in position with a cap nut (Acorn). After operation, the rats were reared in individual cages for at least 3 days for recuperation and then submitted to the experiment.
The rat operated on as above was anesthetized with pentobarbital 50 mg/kg i.p. and immobilized in supine position on a dissection pad. After the bilateral jugular veins were exposed, 400 /.c 1 of blood was collected into a 1 ml tuberculin syringe with a 24 G needle ( both from Terumo ) . To prevent clotting, the syringe was filled with 20 a 1 of 200 U/ml heparin-containing saline ahead of time. The cap nut and dummy cannula were removed from the rat skull and, instead, a stainless steel microinjection cannula, AMI13 (in. dia.
0.17 mm, out. dia. 0.35 mm, Acorn), connected to a Teflon tube (50 cm long. 0.1 mm in. dia 0.4 mrn out.
dia. .Acorn) was inserted. The le:-~th rthe microinjection cannula was adjusted beforehand so that its tip would be exposed from the guide cannula over a distance of 1 mm. The other end of the Teflon tube was connected to a microsyringe pump and 10 I-~.1 of PBS or a PBS solution of 19P2-L31 was injected into the third ventricle at a flow rate of 2.5 I~ 1/min. After a - waiting time of 1 minute following completion of injection, the microinjection cannula was removed and the dummy cannula was reinstalled and secured with the cap nut. Immediately before intraventricular administration and 10, 20, 30, 40, and 60 minutes after the start of intraventricular administration, 400 ~t 1 of blood was collected from the jugular vein. Each blood sample was centrifuged (5,000 rpm, 10 min.) using a high-speed refrigerated microcentrifuge (MR-150, Tomy precision Industry) and the supernatant (plasma) was recovered. The pituitary hormones [prolactin, luteinizing hormone (LH), adrenocorticotropic hormone (ACTH), and thyrotropin (TSH), and growth hormone (GH)]
in the plasma were respectively assayed by radioimmunoassays.
The results were expressed in mean ~ S.E.M. For the significance testing of the difference between the 19P2-L3I/PBS group and the PBS group, Student's t-test was used. As a test for statistical significance, the 5~ level was used. It can be seen from Fig. 48 that the plasmal level of growth hormone in the 19P2-L31 group was significantly decreased at 20 minutes after injection of 50 nmol into the third ventricle. The trend toward decrease was also observed at 10, 30, and 40 minutes as well but the changes were not significant.
At 60 minutes after injection, there was no difference from the control group. The plasma prolactin, LH, ACTH, and TSH levels were not altered significantly [Example 42]
Effects of ligand polypeptide on plasma growth hormone (GH) level in freely moving rats Mature male Wistar rats were anesthetized with pentobarbital 50 mg/kg i.p. and, as in Example 41, a stainless-steel guide cannula AG-12 {0.4 mm in. dia., 0.5 mm out. dia., EICOM) was implanted in position with its tip situated in the upper part of the third ventricle. After the operation the rats were housed in individual cages and kept for at least 3 days for recuperation and, then, a cannula (30 cm long, 0.5 mm in . dia . , 0 . 9 mm out . dia . , Natsume Seisakusho ) filled in with heparin (200 U/ml)-containing saline was inserted into the right atrium from the right jugular vein under pentobarbital anesthesia. The rats were maintained overnight for complete arousal from anesthesia and then transferred to transparent acrylic cages (30 cm x 30 cm . x 35 cm). ~A 1 ml tuberculin syringe with a 24-G needle (both by Termo) was connected to the cannula inserted in the atrium and 3001.11 of blood was drawn. To prevent clotting, the syringe was filled in with 20 E.t 1 of saline containing 200 U/ml of heparin beforehand. A
stainless-steel microinjection cannula (0.17 mm in.
dia., 0.35 mm out. dia.; EICOM) connected to Teflon tube (50 cm long, 0.1 mm in. dia., 0.4 mm out. dia., EICOM) was inserted into the guide cannula positioned in the third ventricle. The length of the microinjection cannula was adjusted beforehand so that its tip would be extend I mm from the guide cannula.
One end of the Teflon tube was connected to a microsyringe pump and either PBS or 19P2-L31 dissolved in PBS was injected, in a total volume of 10I~.il, into the third ventricle at a flow rate of 2.5L~.1/min. Ten minutes after initiation of administration into the third ventricle, 5/~g/kg GHRH-saline was adm.~~.stered via the cannula inserted ir. , the atriL~. Iv 3iatel~-before initiation of intraventricular admini:, ~~ration and 10, 20, 30, 40, and 60 minutes after administration of GHRH, 300,u 1 portions of blood were drawn from the jugular vein. Each blood sample was centrifuged (5,000 rpm, 10 min.) and the supernatant (plasma) was h:

recovered. The concentrations of GH in the plasma were determined by radioimmunoassay.
r The results were expressed as a mean 'f S.E.M. To test for significant difference between the group treated with 19P2-L31 dissolved in PBS and the control group treated with PBS alone, Student's t-test was used. According to the two tailed test, p<0.05 was assumed to be the minimal level of significance. As shown in Fig. 49, administration of 5 ~ g/kg of GHRH
elevated the plasma GH level. However, when 50 nmol of 19P2-L31 was administered into the third ventricle, the GHRH-induced elevation of plasma GH was significantly inhibited.
[Example 43]
Preparation of rabbit anti-bovine 19P2-L31 antibodies Synthetic peptides containing partial 19P2-L31 sequence [peptide-I: SRAHQHSMEIRTPDC (SEQ ID N0:92), peptide-II: CAWYAGRGIRPVGRFNH2 (SEQ ID N0:93), and peptide-III: CEIRTPDINPAWYAG (SEQ ID N0:94) were conjugated with KLH according to the standard method.
Each peptide conjugate (600~cg as a peptide) dissolved in saline was mixed with Freund's complete adjuvant, and the resultant emulsion was subcutaneously injected into three rabbits (NZW, male, 2.5 kg) respectively.
Hyperimmunization was carried out three times in total at the same dose of the conjugate as the first injection with Freund's incomplete adjuvant every three weeks. Antibody titers were determined as follows.
Two weeks after the last immunization, blood samples were obtained from the vein of the immunized rabbits respectively. After being incubated at 37°C for 1 hour, the blood samples were kept at 4°C over night.
Sera were then prepared by means of centrifugation. An aliquot (100,u l) of each serum sample diluted properly was introduced into 96-well polystyrene microplates A.

which were pre-coated with goat anti-rabbit IgG (Fc) antibodies, and then the microplates were incubated at 4°C for 16 hours. After removing the sera, horse r radish peroxidase (HRP)-conjugated peptide-I, II, and III were added to the wells respectively, and then the microplates were incubated at room temperature for 4 hours. After removing the peptides, coloring reaction was done by adding a substrate. The reaction was stopped by adding 100E.c.1 of a stopping solution, and then the absorbance at 450 nm in each well was measured. As shown in Fig. 50, serum samples obtained from the rabbits after the immunization showed binding activities to HRP-conjugated peptides respectively.
However, none of binding activities was detected in sera prepared before the immunization. These results indicated that the rabbits received the immunization produced antibodies against peptide-I, II, and III, respectively. To prepare purified IgG antibody fractions, sera obtained from the immunized rabbits was percipitated with anmonium sulfate. The resultant precipitates were dissolved in borate buffer, and then dialyzed with the same buffer. The IgG fractions thus obtained were then subjected onto affinity columns conjugated with peptide-I or 19P2-L31 respectively.
After washing the columns with borate buffer and following with acetate buffer (100 mM, pH 4.5), antibodies bound to the column were eluted with glycine buffer (200 mM, pH 2.0). After being neutralized with 1M Tris, the eluents were used as purified antibodies respectively.
[ E~:atnple 44 ]
Inhibitory activity of antibodies against the release of arachidonic acid metabolites induced by i9P2-L31 The purified antibodies prepared as described in Example 43 were tested their inhibitory activity ,:

against the release of arachidonic acid metabolites induced by 19P2-L31. The antibodies diluted as indicated in Fig. 51 were mixed with 19P2-L31 ( 5 x 10~
loM) at room temperature for 1 hour, and then the release of arachidonic acid metabolites was examined as ' described in Example 11. As shown in Fig. 51, the highest inhibitory activity was observed in anti-peptide-II antibodies.
[Example 45]
Based on the DNA sequence coding the murine-derived ligand polypeptide (Figure 32) obtained in Example 29, two primers, were synthesized.
rFBG:5'-AGATTGGCATCATCCAGGAAGACGGAGCAT-3'(SEQ ID N0:95) rRSA:5'-GTCGACTCAGCAGCACTGTCTTCTCGAGCTG-3' (SEQ ID N0:96) Using the cDNA prepared using 0.5 ng of m01.2212.....121urine genomic DNA (Mouse BALB/c genomic DNA as a template and PCR was carried out.
50 ~t 1 of reaction mixture comprises 200nM each of synthetic DNA primer, 0.5 nM of template DNA, 0.25mM of dNTPs, 0.5 a 1 of E X Taq polymerase, and buffers attached with enzyme. An amplification reaction was carried out in 30 cycles of 95~ x 30 sec and 67~C x 60 sec. The amplification product was identified by 1.2%
agarose gel electrophoresis with ethidium bromide staining and a 1 kb (approx.) band was recovered and subcloned using TA Cloning Kit (Invitrogen). This ligation mixture was used to transform E_. c i JM109 and clones harboring the inserted fragment were selected on ampicillin- and X-gal-containing LB agar.
A white clone was isolated to provide a transformant, EscherichEia coli JM109/pmGB3. This clone was cultured overnight in an ampicillin-containing LB medium and, using an automatic plasmid extractor, a plasmid DNA was h:

prepared. A portion of the DNA thus prepared was subjected to a sequencing reaction using ABI Dye Terminator Cycle Sequencing Kit (ABI) and analyzed with -a fluorescent automated sequencer. The oligonucleotide sequence data thus obtained was analyzed with DNASIS
(Hitachi System Engineering) (Fig. 53). The underscored sequences correspond to the primer sequences.
The nucleotide sequence determined in this manner was compared with the sequence of SEQ ID N0:2, 46, or 60. As a result, the DNA fragment inserted in the plasmid pmGB3 horbored by Escherichia coli JM109/pmGB3 was found to code for a novel mouse ligard polypeptide jFig. 54].
[Example 46]
The influence of 19P2-L31 on prolactin secretion from pituitary cell line RC-4B/C
The rat pituitary cell line RC-4B/C (Hurbain Kosmath et al., In Vitro Cell. Dev. Biol., ~, 431-440 (1990)) was seeded on a 12-well plate {Sumitomo Bakelite) at a density of 1x105 cells/well and cultured for 2 days. The medium composition was as suggested in the above literature (DMEM (Nissui): cx -MEM (Gibco) -1:1, 10~ fetal calf serum, 1.5 g/1 glucose (Wako), 0.2 mg/ml BSA (Sigma), 0.5~ nonessential amino acids solution (Flow Laboratories), 15 mM HEPES (Wako) pH 7.3, 2.5 ng/ml EGF (Genzyme), 50 ng/ml gentamicin (Gibco)) and the cultivation was carried out under 10~ COz at 34~ .
The cultured cells were washed with 3 portions of incubation buffer (DMEM: ~x--MEM = 1:1, 0.5 g/1 glucose, 0.1% BSA, 0.5$ nonessential=amino acids solution, 15 mM
HEPES pH 7 . 3 ) and after addition of the same buffer, a preincubation was carried out under 10~ COZ at 34~ for 15 minutes. The cells were re-washed with two portions of the same buffer. Then, a preparation of bovine S.

19P2-L31 peptide (SEQ ID N0:5) in incubation buffer was added at the varying concentration shown in Fig. 55 and an incubation was performed under 10% COz at 34~ for 30 minutes. To remove the floating cells, the culture was centrifuged with a high-speed microcentrifuge and the supernatant was stored at -30~.
The amount of prolactin in the culture supernatant sample obtained by the above procedure was determined with Rat Prolactin [lzsl] Assay System (Amersham).
It can be seen from Fig. 55 that addition of 19P2-L31 caused a concentration-dependent increase in prolactin secretion from RC-4B/C cells. The mark ** in the diagram indicates a significance with not less than 99% confidence versus the experiment without addition of 19P2-L31 as analyzed by Student's t-test.
(Example 47]
The influence of 19P2-L31 on prolactin secretion from primary cultured rat pituitary cells The primary cultured rat pituitary cells were prepared according to the method of Shiota et al. (Acta Endocrinologica, 1~(,~, 71-78 (1984).
A female Fischer 344/N rat (SLC) at about 11 lactation days was decapitated to death and the anterior lobe of hypophysis was isolated. The isolated pituitary specimen was washed with buffer A [137 mM
NaCl (Wako), 5 mM KC1 (Wako), 0.7 mM NazHPO, (Wako), 50 /t g/ml gentamicin (Gibco)] and treated with enzyme solution I [0.4% collagenase A (Boehringer-Mannheim), 10 a g/ml DNase (Sigma), 0.4% BSA (Sigma), 0.2% glucose ( Wako ) ] in buf f er A at 3 7 °C f or 1 hour . After the pituitary preparation was dispersed into cells by pipetting, the dispersion was centrifuged to remove the supernatant and the pellet was suspended in enzyme solution II (0.25% pancreatin (Sigma) in buffer A and incubated at 37 ~ for 8 minutes. The reaction was a.

stopped by adding fetal calf serum and the reaction mixture was centrifuged to remove the supernatant. The resulting cells were suspended in DMEM-I (DMEM:
Dulbecco's minimum essential medium, 10% fetal calf serum, 20 mM HEPES pH 7.3, 50 U/ml penicillin, 50 ~t g/ml streptomycin), passed through a cell strainer (Falcon) to remove cell conglomerates and fibrous contaminants, and washed with 2 portions of DMEM-I.
The cells thus obtained were diluted in DMEM-I , seeded at a cell density of 1.5x105/well, and cultured under 5% COZ at 37~C for 4 days .
On day 3 of culture the medium was replaced with fresh one and on day 4 a sample of culture supernatant was prepared. Thus, cells were washed with 3 portions of DMEM-II (DMEM, 0.2% BSA, 20 mM HEPES pH 7.3) , DMEM-II was added, and the mixture was preincubated under 5%
COZ at 37~ for 1 hour. After washing with 2 portions of DMEM-II, a solution of 19P2-L31 peptide (amide form of SEQ ID N0:5) in DMEM-II was added at the varying concentration shown in Fig. 56 and the reaction was carried out under 5% COZ at 37 ~ for 1 hour. The supernatant was recovered, centrifuged to remove floating cells, and stored at -30 ~ for use as a supernatant sample.
The concentration of prolactin in the culture supernatant was determined with Rat Prolactin [125/]
Assay System (Amersham).
It can be seen from Fig. 56 that addition of 19P2-L31 caused a concentration-dependent increase in prolactin secretion from the primary cultured pituitary cells. The mark ** in the diagram ir: :states that a analyzed by Student's t-test the particular value is statistically significant at p<0.01 compared with the corresponding value found without addition of 19P2-L31.
The mark * indicates that as analyzed by Student's t-test the particular value is significant at p<0.05 compared with the corresponding value found without addition of 19P2-L31.
~ [Example 48]
The time course of expression of UHR-1 gene in the rat placenta From female rats at 12 weeks of age, placental samples were isolated on days 11, 14, 17, and 20 of gestation. Those tissues were quickly frozen in liquid nitrogen and stored at -80°C. For the preparation of mRNA, each frozen tissue was homogenized with Isogen solution (Nippon Gene) and then total RNA was prepared in accordance with its manual. From 1 mg of each total RNA, mRNA was prepared using a mRNA Purification Kit (Pharmacia).
After 1 a g of the mRNA was treated with DNase I
(Amprification Grade, Gibco BRL), 160 ng was taken and synthesized a cDNA using a RNA PCR Kit (Takara Shuzo) with random 9mer primers at 42~ for 30 minutes. Each of the cDNAs thus prepared was dissolved in 40 ~.1 of TE buffer. Assay of the amount of expression of UHR-1 gene was carried out using ABI PRISM 7700 Sequence Detector (Perkin-Elmer). For the reaction, rUlF (5'-AACCCCTTCATCTATGCGTGG-3').and rUlR (5'-ATATTCTGGCCATGAGGCAC-3' (SEQ ID N0:98)) were used as primers and rUlP (5'-TTCCGAGAGGAGCTACGCAAGATGCTTC-3'(SEQ ID N0:99)) as the fluorescence-labeled probe.
The reaction mixture was prepared using the proprietary reagent kit TaqMan PCR Core Reagent Kit (Perkin-Elmer) in accordance with the manual. In this procedures, 4 ~t 1 of a 40-fold dilution of the sample cDNA in TE buffer was added to the reaction mixture.
A DNA fragment for which the number of moles of UHR-1 gene was determined by measuring the absorbance at 260 nm was diluted, and then used as templates for PCR to obtain a calibration curve for quantification. PCR was performed under the conditions of 50'~ x 2 min. and 4.

95~C x 10 min, followed by 40 cycles of 95~ x 10 sec.
and 55~ x 1.5 min. The results indicated that the amount of expression of UHR-1 gene in the rat placenta increased remarkably with an increasing gestation period.
[Example 49]
The influence of 19P2-L31 on plasma prolactin concentration in rats (1) Activity of I9P2-L31 on male rats The inventors studied the influence of 19P2-L31 administered i.v. on plasma prolactin concentration on male rats. Mature male Fischer rats (body weights: ca 150-180 g) were anesthetized with urethane I.5 mg/kg i.p. and each sides of the right jugular vein were exposed by operation, 20 minutes after anesthesia. 15 minutes after the operation, a solution of 19P2-L31 (50 or 500 nmol/kg) in 1~ bovine serum albumin (BSA)-saline or, in the control group, 1~ BSA-saline was administered by using a 1 ml tuberculin syringe.
Immediately before initiation of intravenous administration and 2, 5, 10, and 20 minutes after administration, 200 /-t 1 of blood was serially drawn from the jugular vein. To prevent clotting, the syringe was filled in with 10 ,cc 1 of 150 U/ml heparin-saline ahead of time. Each blood sample was centrifuged (10,000 rpm, 15 min.) using a high-speed refrigerated microcentrifuge (MR-150, Tomy Precision Machinery) and the supernatant (plasma) was recovered.
The amount of prolactin contained in the plasma was determined with a radi ~.anmunoassay kit (Amersham). The time course of pia~ prolactin <.r~ncentrati::~ w~ ~v expressed in mean ~ ._ .E.M. and the significa~:;:e o~
difference between the 19P2-L31/1~ BSA-saline group and the 1~ BSA-saline group was tested by Dunnett's method.
The 5~ level of significance ( ps 0 . 05 ) was used. It is clear from Fig. 58 that administration of 19P2-L31 in a 1.

' dose of 500 nmol/kg caused a significant increase in plasma prolactin concentration, compared with the control group, at 2 minutes following administration.
(2) Activity of 19P2-L31 on female rats Subsequently, the inventors studied the influence of 19P2-L31 administered i.v. on plasma concentration on female rats . Sexual cycles of mature female Fischer rats (body weight . ca 140 to 160g) were determined by ostium vaginae test, and the influence of 19P2-L31 administered i.v. on plasma prolactin concentration was studied by the same method as described on Example 49-(1) mentioned above. The time course of plasma prolactin concentration was expressed in mean ~ S.E.M.
and the significance of difference between the 19P2-L31/1% BSA-saline group and the 1% BSA-saline group was tested by Dunnett's method. The 5% level of significance (ps 0.05 ) was used. It is clear from Fig.
59 that administration of 19P2-L31 in a dose of 50 nmol/kg caused a significant increase in plasma prolactin concentration, compared with the control group, at 5 minutes following administration. It is also clear from Fig. 59 that administration of 19P2-L31 on female rats in a dose of about 1/10 showed the equevalent or superior activities compared with the case of the administration on male rats. In addition, As shown in Fig. 60, when the time course of plasma prolactin concentration was determined among the sexual cycle, a significant increase in plasma prolactin concentration was observed in estrus. This indicates that the effect of 19P2-L3I is different depending on the sexual cycles of the female rats.
[Preparation Example-1]
Fifty milligrams~~of the compound as obtained in Example 21 is dissolved in 50 ml of distilled water for injection (Japanese pharmacopoeial), and distilled water for injection (Japanese pharmacopoeial) is added thereto to make 100 ml. The resulting solution is filtered under a germ-free condition, and each vial for injection is filled in with 1 ml of the filtrate, freeze-dried and sealed therein also under a germ-free condition.
[Preparation Example 2]
One hundred milligrams of the compound as obtained in Example 21 is dissolved in 50 ml of distilled water for injection (Japanese pharmacopoeial), and distilled water for injection (Japanese pharmacopoeial) is added thereto to make 100 ml. The resulting solution is filtered under a germ-free condition, and each vial for injection is filled in with 1 ml of the filtrate, freeze-dried and sealed therein also under a germ-free condition.
[Sequence Listing]
(1) GENERAL INFORMATION:
(i) APPLICANT:
{A) NAME: Takeda Chemical Industries, Ltd.
(B) STREET: 1-1, Doshomachi 4-chome, Chuo-ku (C) CITY: Osaka (D) STATE: Osaka (E) COUNTRY: Japan (F) POSTAL CODE (ZIP): 541 (ii) TITLE OF INVENTION: Polypeptides, Their Production and Use (iii) NUMBER OF SEQUENCES: 94 (iv) COMPUTER READABLE FORM:
{A) MEDIUM TYPE:
(B) COMPUTER:
{C) OPERATING SYSTEM:
(D) SOFTWARE:
(v) CURRENT APPLICATION DATA:
APPLICATION NUMBER:

WO 98/589b2 PCT/JP98/02765 h.

(2) INFORMATION FOR SEQ ID NO:1:
( i ) SEQiJINCE C~~ARACTE'~RISTICS
- (A) LENGTIi: 98 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) 1~LECULE TYPE: Peptide ( xi ) SFQiJEnTCE DESCRIPTION : SEQ ID NO :1:
Met Lys Ala Val Gly Ala Trp Leu Leu Cys Leu Leu Leu Leu Gly Leu Ala Leu Gln Gly Ala Ala Ses Arg Ala His Gln His Ser Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Gly Arg Gly Ile Arg 15 Pro Val Gly Arg Phe Gly Arg Arg Arg Ala Ala Pro Gly Asp Gly Pm Arg Pro Gly Pro Arg Arg Val Pro Ala Cys Phe Ax~g Leu Glu Gly Gly Ala Glu Pro Ses Arg Ala Leu Pro Gly Arg Leu Thr Ala Gln Leu Val Gln Glu (2) INFORMATION
FOR SEQ ID N0:2:

(i) SEQUENCE CHARACTERISTICS:

(A) I~1GTH: 294 (B) TYPE: Nucleic acid (C) STRANDENESS: Double (D) TOPOLOGY: Linear (ii) N~LECULE TYPE: cDNA

(xi) FEATURE

( C ) IDENTIFICATION ME'T130D
: S

(x) SEQUENCE DESCROPTION; SEQ ID
N0:2:

ATGAAG~'~GG TGGGGGCCI~G GG'PCCrCI~GC CI,GCZGCTGC TGGGCCIGGC CC1GCAGGGG 60 GCDGCCAGCA GAGCCGAlCCA GCAGTCCATG GAGATCCGCA CCCOCGA~'AT CAACCCTGCC 120 TGGTFrCGC3tG GCOGrGGGAT CCGGCCCG'.LG GGCCGCITOG GCOGGCGAAG AGCTGCCCYG 180 .5.

GGGGAOGGAC CCHGGCCI'GG CCCCOGGCGP GrGCCGGCCT GCZTCCGCCT CiGAAGGOGGY 240 GCt'G~AGCCC~ CC:CGAGCCCT CCCGGGGCGG CTGACGGCCC F~GCrGGTCCA GGAA 294 (2) I1~'ORMATION FOR SEQ ID N0:3:
(i) SEQUErICE CHARACTERISTICS:
(A) LENC~'T~i: 29 (B) TYPE: Amino acid ( C ) 'I"OPOLOGY : Linear ( ii ) NIfJLECULE TYPE : Peptide (xi) SEQLIfl~ICE DESCRIPTION: SEQ ID N0:3:
Ser Arg Ala His Gln His Ser Met Glu Ile Arg Thr Pro Asp Ile Asn 1 5 . 10 15 pro Ala Ttp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly (2) INFORMATION FOR SEQ ID N0:4:
(i) SEQUE~1CE CHARACTERISTICS:
(A) LENGTH: 19 w 20 ( B ) TYPE : Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide ( xi. ) SFQL1ENCE DESCRIPTION : SEQ ID N0 : 4 Thr Pro Asp Ile Asn Pro Ala Ttp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg (2) INFORMATION FOR SEQ ID N0:5:
( i ) SEQLJF~1CE C~~ARACTERI STICS
(A) LENGTH: 31 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUErICE DESCRIPTION: SEQ ID N0:5:

Ses Arg Ala His Gln His Ses Met Glu Ile Arg Thr Pro Asp Ile Asn ~ 1 5 10 15 Pm Ala Trp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe (2) INFORMATION FOR SEQ ID N0:6:
( i ) SEA C~iARACTERISTICS :
(A) LENC~"rH: 32 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (fi) MOLECULE TYPE: Peptide (xi) SEQZIErTCE DESCRIPTION: SEQ ID N0:6:
Ser Arg Ala His Gln His Ser Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Ttp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly 20 {2) INFORMATION FOR SEQ ID N0:7:
( i ) SFQiJENCE CE1ARAG't'ERISTICS
(A) I~TG'I~i: 33 (B) TYPE: Amino acid (C) TOPOLOGY: Linear {ii) MOLECULE TYPE: Peptide (xi) SEQUENCE DESCRTPTION: SEQ ID N0:7:
Ser Arg Ala His Gln His Sex Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly Arg _ (2) INFORMATION FOR SEQ ID N0:8:
(i) SEQZJaICE CHARACTERISTICS:

S.

(A) LENGTH: 20 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUEnTCE DESCRIPTION: SEQ ID N0:8:
Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe (2) INFORMATION FOR SEQ ID N0:9:
(i) SEQUENCE CHARACTERISTICS:
(A) LE~1GTH: 21 ( B ) TYPE : Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUFTTCE DESCRIPTION: SEQ ID NO:9:
Thr Pro Asp Ile Asn Pro Ala Ttp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly 25 (2) INFORMATION FOR SEQ ID N0:10:
(i) SEQUINCE CHARACTERISTICS:
(A) Lfl~TGTH: 22 (B) TYPE: Amino acid (C) TOPOLOGY: Linear {ii) MOLECULE TYPE: Peptide ( xi ) SF~IEnICE DESCRIPTIC'' SEQ .T_ D NO :10 Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly Arg (2) INFORMATION FOR SEQ ID NO:11:
( i ) SEQiJENCE C~~ARACTERISTICS
(A) LENGTH: 87 (B) TYPE: Nucleic acid ' (C) STRANDEDNESS: Double (D) TOPOLOGY; Linear (ii) MOLECULE TYPE: cDNA
( xi ) SEQZJE'NCE DESCRIPTION : SEQ ID NO :11:

GCRGCCOGl~G GGATCGGGCC CGTGG~C 87 (2) INFORMATION FOR SEQ ID N0:12:
( i ) SEQUEnTCE CIiARACTERISTICS
(A) LENGTH: 57 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(xi) SFQUEnTCE DESCRIPTION: SEQ ID N0:12:
ACCCCCGACA '1'CAACCCrGC CTGGTACGCR GGCCGIGGGA TCOGGCCCGT GGGCOGC 57 (2} INFORMATION FOR SEQ ID N0:13:
( i ) SEQiJE~iCE CHARACTERISTICS
(A) LEIVG"rH: 93 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:13:
. A~CAGAiGCCC ACCAGC'.ACTC CATC'GAGATC CGCAiCCCCCG ACATCAACCC ZGCCT('~GTAC 60 G(RGC('.OGTG GGATCGGGOC CG1~GGG~'.C~C TTC 93 4.

(2) INFORMATION FOR SEQ ID N0:14:
( i ) SF~JEnICE CHARACTERISTICS
(A) LENGTH: 96 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUErICE DESCRIPTION: SEQ ID N0:14:

GCRGCCOG'PG GGATCOGGCC CCGC TI'CGGC 96 (2) INFORMATION FOR SEQ ID N0:15:
( i ) SEQUE~1CE C~3ARACTERISTICS
(A) LENGTH: 99 (B) TYPE: . Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:15:
AGrCAGAGCCC ACCAGCACIC CATGGAGATC CGCACCCCCG ACATCAACCC TGCCTGGTAC 60 G(~tGGCCGIG GGATCCCGCC CGTGGGCCCC TTCC~CCGG 99 (2) INFORMATION FOR SEQ ID N0:16:
(i) SEQUEnTCE CHARACTERISTICS:
(A) LF~IG'l~i: 60 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNpr ( xi ) SFQZJ~1CE DESCRIPTION : SEQ ID N0:16 ACCCCaGACA TCAACCCTGC CTGGTACGCR GGCOGI'GGGA TCCGGCC(7GT GCGCCGCTrC 60 (2) INFORMATION FOR SEQ ID N0:17:

A:

( i ) SF~tIErTCE CHARACTERISTICS
(A) LENGTH: 63 - (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear ( ii ) MOLECULE TYPE : c~lA
(xi) SE~IE~CE DESCRIPTION: SEQ ID N0:17:
ACCCC(7GACA TCAACC'.CrGC G'tG~'rACGCR GG('.CG'hGGGA TCCGGCOCGT GGGCCJGC'tTC 60 (2) INFORMATION FOR SEQ ID N0:18:
( i ) SF~QIJ~1CE CHARACTERISTICS
(A) LENGTH: 66 (B) TYPE: Nucleic acid (C) STRANDEDI~SS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
( xi ) SDQIJEnICE DESCRIPTION : SEQ ID N0:18 ACCCCCGACA TC'.AAGCCTGC ChC~IGTAQGCR GGCCGTGGGA TC~GCCCGT GGGCOGCTt'C 60 (2) INFORMATION FOR SEQ ID N0:19:
( i ) SEQIJEnICE C3iARACTERISTICS
(A) LENGi'~i: 91 (B) TYPE: Amino acid (C) TDPOI~OGY: Linear (ii) MOLECULE TYPE: Peptide ( xi ) SFQLJErTCE DESCRIPTION : SEQ ID N0:19 Leu Val Leu Val Ile Ala Arg Val Arg Arg I~eu His Asn Val Thr Asn Phe Leu Ile Gly Asn Leu Ala Leu Ser Asp Val Leu Meet Gds Thr Ala Cys Val Pro Leu Thr Leu Ala Tyr Ala Phe Glu Pm Arg Gly Tip Val Phe Gly Gly Gly Leu Gds His Leu Val Phe Phe Leu Gln Pro Val Thr Val Tyr Val Ser Val Phe Thr Leu Thr Thr Ile Ala Val Asp Arg Tyr Va1 Val Leu Val His Pro Leu Arg Arg Arg Ile (2) INFbRMATION FOR SEQ ID N0:20:
(i) SFQUErICE CHARACTERISTICS:
(A) LErlG'rH: 59 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUErICE DESCRIPTION: SEQ ID N0:20:
Gly Leu Leu Leu Val Thr Tyr Leu Leu Pro Leu Leu Val Ile Leu Leu Sex Tyr Val Arg Val Ser Val Lys Leu Arg Asn Arg Val Val Pro Gly G'ys Val Thr Gln Ser Gln Ala Asp Trp Asp Arg Ala Arg Arg Arg Arg Thr Phe Cys Leu Leu Val Val Val Val Val Val (2) INFORMATION FOR SEQ ID N0:21:
( i ) SEQt3ErICE CHARACTERISTICS
{A) Iii: 370 ( B ) TYPE : Amino acid (C) TOPOLOGY: Linear ( ii ) MOLECULE TYPE : Peptic (xi) SDESCRIPTION: ~:.Q ID N0:21:
Met Ala Ser Ser Thr Thr Arg Gly Pro Arg Val Ser Asp Leu Phe Ser Gly Leu Pro Pro Ala Val Thr Thr Pro Ala Asn Gln Ser Ala Glu Ala ' 20 25 30 Ser Ala Gly Asn Gly Ser Val Ala Gly Ala Asp Ala Pro Ala Val Thr Pro Phe Gln Ser Leu Gln Leu Val His Gln Leu Lys Gly Leu Ile Val a Leu Leu Tyr Ser Val Val Val Val Val Gly Leu Val Gly Asn Gds Leu Leu Val Leu Val Ile Ala Arg Val Arg Arg Leu His Asn Val Thr Asn Phe Leu Ile Gly Asn Leu Ala Leu Ser Asp Val Leu Met Gds Thr Ala Gds Val Pro Leu Thr Leu Ala Tyr Ala Phe Glu Pro Arg Gly Z'sp Val Phe Gly Gly Gly Leu Cys His Leu Val Phe Phe Leu Gln Pro Val Thr Val Tyr Val Ser Val Phe Thr Leu Thr Zhr Ile Ala Val Asp Arg Tyr Val Val Leu Val Isis Pro Leu Arg Arg Arg Ile Ser Leu Arg Leu Ser Ala Tyr Ala Val Leu Ala Ile Trp Ala Leu Sex Ala Val Leu Ala Leu Pro Ala Ala Val His Thr Tyr His Val Glu Leu Lys Pro His Asp Val Arg Leu Gds Glu Glu Phe Trp Gly Ser Gln Glu Arg Gln Arg Gln Leu Tyr Ala Trp Gly Leu Leu Leu Val Thr Tyr Leu Leu Pro Leu Leu Val Ile Leu Leu Ser err Val Arg Val Ser Val Lys Leu Arg Asn Arg Val Val Pro Gly Cys Val Thr Gln Ser Gln Ala Asp Trp AsP Arg Ala Arg Arg Arg Arg Thr Phe Cys Leu Leu Val Val Val Val Val Val Phe Ala Val Cys Trp Leu Pro Leu His Val Phe Asn Leu Leu Arg Asp Leu Asp Pro His Ala Ile Asp Pro Zyr Ala Phe Gly Leu Val Gln Leu Leu Gds His Trp Leu Ala Met Ses Ser Ala Cys Tyr Asn Pro Phe Ile Tyr Ala Trp Leu His Asp Ser Phe Arg Glu Glu Leu Arg Lys Leu Leu Val Ala Trp Pro Arg Lys Ile Ala Pro His Gly Gln Asn Met Thr Val Ser Val Val Ile ( 2 ) II~RN1ATION FOR SEQ ID NO: 22 (i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 206 ( B ) TYPE : Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUENCE DESCRIPTION: SEQ ID N0:22:
Leu Val Leu Val Ile Ala Arg Val Arg Arg Leu err Asn Val Thr Asn Phe Leu Ile Gly Asn Leu Ala Leu Ser Asp Val Leu Met Cys Thr Ala Cps Val Pro Leu Thr Leu Ala Tyr Ala Phe Glu Pro Arg Gly Trp Val Phe Gly Gly Gly Leu Gds His Leu Val Phe Phe Leu Gln Ala Val Thr Val Tyr Val Ser Val Phe Thr Leu Thr Thr Ile Ala Val Asp Arg Tyr Val Val Leu Val His Pro Leu Arg Arg Arg Ile Ser Leu Arg Leu Ser Ala Tyr Ala Val Leu Ala ~Le Trp Val Leu Ser Ala Val Leu Ala Leu Pro Ala Ala Val His Thr Tyr His Val Glu Leu Lys Pro His Asp Val Arg Leu G'ys Glu Glu Phe Trp Gly Ser Gln Glu Arg Gln Arg Gln Leu S.

' Tyr Ala Trp Gly Leu Leu Leu Val Thr Tyr Leu Leu Pro Leu Leu Val Ile Leu Leu Ser Tyr Ala Arg Val Ser Val Lys Leu Arg Asn Arg Val Val Pro Gly Axg Val Thr Gln Ser Gln Ala Asp Trp Asp Axg Ala Arg Arg Ark Arg Thr Phe Gds Leu Leu Val Val Val Val Val Val (2) INFORMATION FOR SEQ ID NO:23:
( i ) SEQtJEnICE CHARACTERISTICS
(A) LENGTH: 126 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) I~LECULE TYPE: Peptide (xi) SEQLTErICE DESCRIPTION: SEQ ID N0:23:
Val Val Leu Val His Pro Leu Arg Arg Arg Ile Ser Leu Arg Leu Ser Ala Tyr Ala Val Leu Gly Ile Trp Ala Leu Ser Ala Val Leu Ala Leu Pro Ala Ala Val His Thr Tyr His Val Glu Leu Lys Pro His Asp Val Ser Leu Gds Glu Glu Phe Trp Gly Ser Gln Glu Arg Gln Arg Gln Ile Tyr Ala Trp Gly Leu Leu Leu Gly Thr Tyr Leu Leu Pro Leu Leu Ala Ile Leu Leu Ser Tyr Val Arg Val Ser Val Lys Leu Arg Asn Arg Val Val Pro Gly Ser Val Thr Gln Ser Gln Ala Asp Txp Asp Arg Ala Arg Arg Arg Arg Thr Phe Cys Leu Leu Val Val Val Val Val Val (2) INFORMATION FOR SEQ ID N0:24:
( i ) SEQUn~ICE CHARACI~RI STICS

r.

(A) LE~1GTH: 273 -(B) TYPE: Nucleic acid (C) STRANDEDNESS: Double -(D) TOPOLOGY: Linear ( ii ) MDT-F.('f n-R TYPE : cDNA
(ix) FEATURE
(C) IDENTIFICATION METHOD: S
(xi) SEQUEnICE DESCRIPTION: SEQ ID N0:24:
CIGGTGCrGG TGAZ'OGOGCG GGTGCGCCGG C1'GCACAACG TGAOGAAClT CCTCATOC~'GC 60 AACC~GGCGT TGTCOGACGT GCTCATGTGC ACCGCCTGCG '1'GCGGCi'CAC GCTCGCGTAT 120 GCCTI'CGAGC CACGCGGCrG GG'i'GTI'CGGC GG~CGGCCTGT GCCACCIGGT CTI'C'ITCCTG 180 CAGCCGGTCA CCGI~.TATGT GTCGGTGITC ACGCTCACCA CCATCGCAGP GGACOGGTAC 240 (2) INFORMATION
FOR SEQ
ID N0:25:

(i) SCE CHARACTERISTICS:

(A) LENGTH: 177 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA

(ix) FEATURE

(C) IDENTIFICATION METHOD: S

(xi) SFQUF~ICE DESCRIPTION: SEQ ID
N0:25:

GGCCTGCTGC TGGTCP~CCTA CCTCCrCCCT CTGCI'GGTCA TCCTCCTGTC TI''ACGTCOGG 60 GzCrTCAG3GA AGC~CCGCAA CCGCGTGGTG CCGGGCTGCG TGACCCAGAG CCAGGCCGAC 120 TGGGACCGOG CTCGGCGCCG GCGCACCITC TGG~TGCTGG TGGTGG'iCGT GGTGGTG 177 p INFORMATION FOR SEQ ID N0:26:
(i) SFQtJENCE CHARACTERISTICS:
(A) LF~~1GTH: 1110 (B) TYPE: Nucleic acid ( C ) STRANDEDI~IESS : Double (D) TOPOLOGY: Linear h:

{ ii ) 1~I~ECUI~E TYPE : cDNA
(3x) FEATURE
(C) IDENTIFICATION NIET~: S
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:26:
ATGGCCTCAT OGAC(,'ACrCG GGGOCCCAGG GTITCrGAGT TAT1'1TCZGG GCi~GCCGCCG 60 COGG'1'CACAA C'lGCCGCCAA CCAG<AGOGCA GAGGCChC7GG C~('.AP~GG GTCGGZGGCT 120 GGOGGGGACG CZ~C(".AG(~GT CACGCCCTTC CAGi~t;CTGC AC'~('IGGTGCA TCAC'~C~GAAG 180 GGGCTGATCG TGCrGCrGTA CAGOG3nGTG GIGGl'OGZGG GGCLGG~GG CAAC1GOCZG 240 CTOGTGC'iGG TGATCGOGOG GG'PGOGC'.(7GG CTGCACAACG TGAIOGAAC1T CL'I'CAT.CGGC 300 AACClGGCCT TGTCOGHC<T GCrCFrTGrGC ACOGC;CTGCG TGCCGCTCAC GC1GGCCTAT 360 GCCTTOGAGC CAOC~GCTG GGZG'ITOGGC GGCGGCClGT GCCACCTGGT CTZC.Tl'CCTG 420 CAGCCGGTCA CCGTGTATGT GTCGGtGTTC AOGCTCA,iC',CA CCA',LbGCAG'.C GGACaGCTAC 480 G!'OGZGCTGG TGCACCOGCT GAGGCC'~OGC ATCrCGCTCC GCCTCAGCGC CTACGCZGTG 540 CTGGCCATCT GGGCGCTGTC CC'~OGGTGG'.LG GQGG'rGCCCG CCGCCGTGCA CACGTATCAC 600 GTGGAGCT(.'A AC~CCGCACGA Ct'iC TGOC~lAGGT~GT T~'~GGC'~ CCAGG~AGCGC 660 CAGOGCCHGC TCTACGCCIG C~GC~.C~TG C1G6TCACCT ACC',IGCTCGC TC1GCJ~TC 720 ATCCI~C~ C'ITACGICCG G~ AAGCrCOGCA ACOGCGTGGT GCCGGCCTGC 780 GrGACCCAIGA G~CCAGt'~F. CTC~GACCGC G('rCC~'~ GC'C'LT L'rGClZG~,'IG 840 GT~TCG TGGTGGZG'!T CGCCGTCTGC TC,~.'iGCCGC ZGC~'CIT CAACCiGCIG 900 CGGG~A(.''CI"OG ACGGCCACGC CATOGACCCr TA~OGC(:I~G GGGZGGTGCA GCTGCTCZGC 960 CAClGGCTCG CCATGA(~Tr'C GG(xTC'aC,TAC AACCCCTTCA TCTACC'~CCPG GC1GCA,CGAC1020 AGCiTCCGCG AGGAGC1GCG CAAACTGITG GTCGCT1GGC CCCGCAAGAT AGCC('.CCCAT1080 G(~CA~'~AATA TGA~70GT~'.AG OGIGGTCATC 1110 (2) INFORMATION
FOR SEQ ID N0:27:

i ) SEQtJEnICE CHARACTERISTICS

(A) I~'I~I: 618 (B) TYPE: Nucleic acid {C) STRANDEDNESS: Double (D) TOPOLOGY: Linear ( ii ) NDI~ECUI~E TYPE : cDNA

(ix) FEATURE

(C) IDENTIFICATION METHOD:
S

( xi ) SF,QLJEnICE DESCRIPTION : SEQ
ID N0: 27 h.

CI~GGTG(.TGG TGATCGCGOG CCCGG CTGrACAACG TGACGAATTT CCTCATOGGC 60 AACCTGGCCT TGTCOGACGT GCrCATGTGC ACCGCCTGCG TGCCGCTCAC GCTGGOCrAT 120 GCCTTOGAGC CACGCGGCZG GGTVTt'CGGC GGCGGCCTGT GCCA~CC.~T Ct'PCITCCTG 180 CAGGOGG.PCP. COGTCTATGT G'IbGGrGITC ACGCZCACCA CCATCGCAGT GGPrCCGCTAC 240 GZCGTGCTGG TGCACCCGCT GAGGCGGCGC ATCTCGCTGC GCCTCAGCGC GT19,CGCTGTG 300 CTGGC<'ATCT GGGTGCTGTC (7GOGGTGCTG GCGCrGCOCG CCGCOG1~C'zCA CAC(,TATCAC 360 GTGGAGCTCA AGCCGCACGA OGTGCGCCrC TGCGAGGAGT TCTGGGGCTC CCAC~GAGO('~C 420 CAGCGCCAGC TCTACGCCTG GGGGC1~GCPG CTGGTCACCT ACCTG(.'TCCC TCTGCrGG2'C 480 ATCCTCCTGT CZTACGCCCG GGT(~I'CAGTG AAGCTCCGCA ACCGCGTGGT GCCGGGCCGC 540 GrGA~CCCAGA GCCAGGCCGA CTGGGACGGC GC1~G(',GCC GGOGCACCTT Ct'GCTTGCTG 600 ~~ TG~G 618 (2) INFORMATION
FOR SEQ
ID N0:28:

( i ) SFQLJINCE CHARACTERISTICS

(A) LING'IIi: 378 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOIAGY: Tin~ga_r (ii) 1~LECULE TYPE: cDNA

(ix) FEATURE

(C) IDENTIFICATION N~THpD: S

(xi) SEQLTEnICE DESCRIPTION: SEQ
ID N0:28:

GTGGTrCrGG TGCACCCGCT ACGTCGGCGC AT1TCACrGA GGCIrAGOGC CTACGOGGTG 60 CTGGGCATCT GGGCTCTATC TGCAGiGCTG GC~CTGCCGG CCGCGGTGCA CACGTACCAT 120 GTGGAGCIrA AGOCCCACGA OGTGAGCCTC TGOGAGGAGT TCTGGGGC1'C GCAGGAGCGC 180 CAACGCCAGA TCTAQGCCTG GGGG(TGCiT CIGGGCACCT ATTTGCTCCC CCTGCiGGCC 240 GPGACCCAGA GTCAA~GCrGA CTGGGA~CCGA GCGOGTCGCC GCCGCACI~T CPGTCrGCTG 360 GTGGTGGTGC' TGGTAGTG 378 ( 2 ) INFOn,':.4TION FOR SF~ ~ NO: 29 ( i ) SEQiJ~ICE CHARACTERISTICS
(A) LENGTH: 25 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single h.

. (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:29:
' CV'IGGSQ~2TS STGCG~,'AACN YC~'I'G 25 (2) INFORMATION FOR SEQ ID N0:30:
(i) SEQUEnTCE CHARACTERISTICS:
(A) LENGTH: 27 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:30:
~'iNCWRRGCC ANCC.AGCAGA KGGCAAA 27 (2) INFORMATION FOR SEQ ID N0:31:
( i ) SEQ~JF~1CE CHARACTERISTICS
(A) LF,LVC~l~i. 27 {B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear {ii) MDLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SDQUEnTCE DESCRIPTION: SEQ ID N0:31:
CrGTGYGYSA TYGQ~iTfCGA YMGSTAC 27 ~ (2) INFORMATION FOR SEQ ID N0:32:
( i ) SEQUINCE Q~ARACTERISTICS
(A) LE(VGTH: 29 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single h.

{D) TOPOLOGY: Linear -(ii) N~LECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:32:
AK(~nTp,(~AGG GCAGCCAGCA GANSRYGAA 29 (2) INFORMATION FOR SEQ ID N0:33:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 24 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SFQUEnTCE DESCRIPTION: SEQ ID N0:33:
ChGACITATT TrCrGC~GGTG COGC 24 (2) INFORMATION FOR SEQ ID N0:34:
( i ) SEQIJINCE CHARACTERISTICS
(A) LE2'1GTH: 24 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
( xi. ) SEQZJErTCE DESCRIPTION : SEQ ID NO: 34 (2) INFORMATION FOR SEQ ID N0:35:
(i) SEQUEnTCE CHARACTERISTICS:
(A) LENGTH: 20 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single - (D) TOPOLOGY: Linear ( ii ) N~LEC:ULE TYPE : Other nucleic acid . Synthetic DNA
(xi) SEQUEnTC~E DESCRIPTION: SEQ ID N0:35:

(2) INFORMATION FOR SEQ ID N0:36:
( i ) SEQIJEniCE CfiARACTERISTICS
(A) LENGTH: 26 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:36:
CCIACGCGIC ImATCCCICK GCCIGC 26 (2) INFORMATION FOR SEQ ID N0:37:
( i ) SEQiJF~ICE CHARACTERISTICS
(A) I~fl~G~'I~i: 26 (B) TYPE: Nucleic acid (C) STRANDEDNES,S: Single (D) TOPOLOGY: Linear (ii) N~LECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUErICE DESCRIPTION: SEQ ID 1:37:
ACGGGCC:ImA TGCCICKGCC IG(~tTA 26 (2) INFORMATION FOR SEQ ID N0:38:
(i) SEA CHARACTERISTICS:
(A) I~ENGI~i: 20 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single s.

(D) TOPOLOGY: Linear -(ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUErICE DESCRIPTION: SEQ ID N0:38:
CCGGCGTACC AC,GCAGGGlT 20 (2) INFORMATION FOR SEQ ID N0:39:
(i) SEQUEnICE CHARACTERISTICS:
(A) LENGTH: 28 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single {D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:39:
AGGCA~GGZT GAT~TCGGGG GTCCGGAT 28 {2) INFORMATION FOR SEQ ID N0:40:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 27 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
{~.) SFQUEL~1CE DESCRIPTION: SEQ ID N0:40:

~i) INFORMATION FG. ~EQ In NO:41:
( i ) SEQUEnICE CHARACTERISTICS
(A) LENGTH: 27 (B) TYPE: Nucleic acid (C) SIRANDEDNESS: Single S.

(D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA

* (xi) SEQZ1ENGE DESCRIPTION: SEQ ID N0:41:

GTGGGGGCGT GGCTCCTCTG GCTGC'1!G 27 (2) INFORMATION FOR SEQ ID N0:42:

i ) SDQUEnICE CfiARACTERISTICS

(A) I~fl~iGTH: 32 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOhOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA

(xi) SEQZJEnICE DESCRIPTION: SEQ ID N0:42:

GTGTCGACGA ATGAAGGCGG TGGGGGCC'rG GC 32 (2) INFORMATION FOR SEQ ID N0:43:

( i ) SEQZJEnTCE C3iARACTERISTICS

(A) LENC~'TEI: 24 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA

(xi) SEQUENCE DESCRIPTION: SEQ ID N0:43:

AGGCI~GC TG'ITATTCGT GG~AC 24 (2) INFORMATION FOR SEQ ID N0:44:

( i ) SFQLIErICE CHARACTERISTICS

(A) LENGTH: 98 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SFQiJENCE DESCRIPTION: SEQ ID N0:44:
Met Lys Ala Val Gly Ala Trp Leu Leu Cys Leu Leu Leu Leu Gly Leu Ala Leu Gln Gly Ala Ala Ser Arg Ala His Gln His Sex Met Glu Ile Arg Thr Pro Asp Ile Asn Pm Ala Ttp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly Arg Arg Arg Ala Ala Leu Gly Asp Gly Pro Arg Pro Gly Pro Arg Arg Val Pro Ala Gds Phe Arg Leu Glu Gly Gly Ala Glu Pro Ser Arg Ala Leu Pro Gly Arg Leu Thr Ala Gln Leu Val Gln Glu (2} INFORMATION FOR SEQ ID N0:45:
(i) SEQUEnTCE CHARACTERISTICS:
(A) hflQGTH: 83 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SFQUErICE DESCRIPTION: SEQ ID N0:45:
Met Ala Leu Lys Thr Trp Leu Leu Gds Leu Leu Leu Leu Ser Leu Val Leu Pro Gly Ala Ser Ser Arg Ala His Gln His Ses Met Glu Thr Arg Thr Pro Asp Ile Asn Pro Ala Trp Tyr Thr Gly Arg Gly I1~ Arg Pro Val Gly Arg Phe Gly Arg Arg Arg Ala Thr Pro Arg Asp Va: ~Rlr Gly Leu Gly Gln Leu Ser Cps Leu Pro Leu Asp Gly Arg Thr Lys Phe Ses Gln Arg Gly h:

(2) INFORMATION FOR SEQ ID N0:46:
( i ) SEQi JE<~TCE CHARACTERISTICS

{A) I~GTH: 249 (B) TYPE: Nucleic acid ' ( C ) S'i'RANDEDNE.SS : Double (D) TOPOLOGY: Linear ( ii ) N~LEQ1L~E
TYPE : cDNA

(ix) FEATURE

(C) IDENTIFICATION METHOD: S

(xi.) SEQiIENCE DESCRIPTION: SEQ ID N0:46:
ATGGCCCI'C'~A AGAGGInGGT TC3'GI~GGTDG CrGC.ZGCTAA GLTt'GGTCCT CCCAGGGGCT 60 TCCAGCCGAG CCCACCAGCA CZCCATGGPrG ACAAGAACCC CTGATATCAA TCCTGCCTGG 120 TACA(7GGGCC G~GATCAG GCCl~'iGGGC CGCTZ'CGGCA GGAGAAGGGC AACCCCGAGG 180 GATGTCAClG GACT~CCA A('i'CAGCTGC CTCCCACZGG ATGC~ACGCAC CAAGZ'rCrCT 240 ~G~GA 249 (2) INFORMATION FOR SEQ ID N0:47:
( i ) SFQLJEfiCE CHARACTERISTICS
(A) LENG'I~i: 31 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide ( xi ) SEQiJErICE DESCRIPTION : SEQ ID N0 : 47 Ses Arg Ala His Gln His Ser Met Glu Thr Arg Thr Pro Asp Ile Asn Pro Ala Trp Tyr Thr Gly Arg Gly Ile Arg Pro Val Gly Arg Phe ' (2) INFORMATION FOR SEQ ID N0:48:
i ) SEQtJEnICE CfiARACTERISTICS
(A) LENC~'Tfi: 32 (B) TYPE: Amino acid (C) TOPOLOGY: Linear h.

(ii) MOLECULE TYPE: Peptide (~) SEQUINCE DESCRIPTION: SEQ ID N0:48:
Ser Arg Ala His Gln His Ser Met Glu Thr Arg Thr Pro Asp Ile Asn Pro Ala Txp Tyr Thr Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly (2) INFORMATION FOR SEQ ID N0:49:
( i ) SEQUF~~1CE CHARACTERISTICS
(A) LENGTH: 33 (B} TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUETiCE DESCRIPTION: SEQ ID NO:49:
Ser Arg Ala His Gln His Ser Met Glu Thr Arg Thr Pro Asp Ile Asn Pro Ala.Ttp Tyr Thr Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly (2) INFORMATION FOR SEQ ID N0:50:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUEnICE DESCRIPTION: SEQ ID N0:50:
Th: nro Asp Ile Asn Pro Ala Trp Tyr Thr Gly Arg Gly Ile Arg Pro Val Gly Arg Phe (2) INFORMATION FOR SEQ ID N0:51:

h:

( i ) SFC~iARACTERISTICS
(A) LENGTH: 21 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) N~LECULE TYPE: Peptide ( xi ) SEQiJEnICE DESCRIPTION : SEQ ID NO : 51:
Thr Pro Asp Ile Asn Pro Ala Tip Tyr Thr Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly (2) II~RMATION FOR SEQ ID N0:52:
(i) SFQUEnICE CHARACTERISTTCS:
15 (A) LF~NGTfi: 22 (B) TYPE: Amino acid (C) TOPOLOGY: Linear ( ii ) I~IOI~ECULE TYPE : Peptide (xi) SEQZJENCE DESCRIPTION: SEQ ID N0:52:
Thr Pro Asp Ile Asn Pro Ala Trp Tyr Thr Gly Arg Gly Ile Arg Pro Val Gly Arg Phe Gly Arg (2) INFORMATION
FOR SEQ ID N0:53:

( i ) SEQtJEnTCE CHARACTERISTICS

(A) LEnTGTfi: 93 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear ' (ii) MOLECULE TYPE: cDNA

(jx) FEATURE

(C) IDENTIFICATION METHOD:
S

(xi) SEQIJEnTCE DESCRIPTION: SEQ
ID N0:53:

A.

AGCCGAGCCC ACCAGCACTC CATGGA~GACA AGAACCCCZG ATATCAATCC TGOCTC~~AC 60 (2) INFORMATION
FOR SEQ
ID N0:54:

(i) SEQUENCE CHARACTERISTICS:

(A) LENG">'H: 96 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear IO (ii) MOLECULE TYPE: cDNA

(ix) FEATURE

(C) IDENTIFICATION METHOD: S

(xi) SFQUEnICE DESCRIPTION: SEQ ID
N0:54:

AGCCGAC~CCC ACCAGCACTC CAZGGAGACA AGAACCCCIG ATATCAATCC TCCCTL~TAC 60 ACCGGCCGCG GGATCAC,CCC TGrGGCCCGC Tt'OGGC 96 (2) INFORMATION
FOR SEQ
ID N0:55:

(i) SEQUENCE CHARACTERISTICS:

(A) LE~1GTH: 99 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA

(ix) FEATURE

(C) IDENTIFICATION METHOD: S

(xi) SEQUENCE DESCRIPTION: SEQ ID
NO:55:

AGCC;GAGCCC ACCAGCACTC CATGGP~ACA AGAACCCCTC ATATCAATCC TCCC'IG~GTAC 60 AOCGGCOGCG GGATCAGGCC TCTGGGC''"':,uC TTCGCCAGG 99 (2) INFORMATION FOR SEQ IL .40:56:
(i) SEQUE<3CE CHARACTERISTICS:
(A) LENGTH: 60 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double ' (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION METHOD: S
(xi) SEQUEnICE DESCRIPTION: SEQ ID NO:56:
ACCCCTGATA TCAATCCi'GC CIGGTACACG GGCCGCGGGA 'I'CAGGCCPGT GGGCCGCTTC 60 (2) INFORMATION FOR SDQ ID N0:57:
( i ) SF~QtJENCE (~~ARACTERISTICS
(A) I~GTH: 63 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOIAGY: Linear (ii) MOLECULE TYPE: cDNA
( i.x) FEATURE
(C) IDENTIFICATION METHOD: S
(xi) SFQUF.NCE DESCRIPTION: SEQ ID N0:57:
ACCCG'IGATA TGAFrTC~'I~GC CTGGTACACG GGCCGCGGGA TCAGGCCl~' GGGCCVCrI'C 60 (2) INFORMATION FOR SEQ ID N0:58:
( i ) SEQUEnTCE CIEiARACTERISTICS
(A) LF~TG'rH: 66 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION N~IOD: S
(xi) SEQUF~NCE DESCRIPTION: SEQ ID N0:58:
AGCCCI'GATA TGAATGCTGC CTGGTACACG GGCOGCGGGA TCAGGC'.CrGT GGGCCGCt'I'C 60 C~CAGG 66 h:

(2) INFORMATION FOR SEQ ID N0:59:
i ) SEQUEriCE CHp.RACTERISTICS
(A) LENGTH: 87 (B) TYPE: Amino acid (C) TOPOLOGY: Linear {ii) N~LECULE TYPE: Peptide (xi) SEQUENCE DESCRIPTION: SEQ ID N0:59:
Met Lys Val Leu Arg Ala Trp Leu Leu Cys Leu Leu Met Leu Gly Leu Ala Leu Arg Gly Ala Ala Ses Arg Thr His Arg Isis Ser Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Ser Arg Gly Ile Arg 15 Pro Val Gly Arg Phe Gly Arg Arg Arg Ala Thr Leu Gly Asp Val Pro Lys Pro Gly Leu Arg Pro Arg Leu Thr Cps Phe Pro Leu Glu Gly Gly Ala Met Ser Ser Gln Asp Gly (2) INFbRMATION FOR SEQ ID N0:60:
(i) SEQUENCE CHARACTERISTICS:
(A) I~NGTfi: 261 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION METHOD: S
( xi. ) SEQLJEnICE DESCRIPTION : SEQ ID N0 : 60 ATGAAGGTGC TGP~GGGCCIG GCTCCI'GTGC CTGCTGATGC TGGGCCTGGC CCI'GCGGGGA 60 GCTGCAAGIrC GTACCCATCG GCACI'CCATG GAGATCaGCA CCCCTGACAT CAATCCrGCC 120 TGGTACGCCA GrCGCC'~CGAT CAGGCCTGTG GGCCGGTI'CG GTCGGAGGAG GGCAACCCTG 180 GGGGACG1'CC CCAAGCCTGG CCTGCGACCC CGGCTGACCT GCTrCCCCCT GGAAGGCGGT 240 h:

GCrATGTCGT CCCAGGATGG C 261 ~ (2) INFORMATION FOR SEQ ID N0:61:
( i ) SEQLJINCE CHARACTERISTICS
S (A) LENGTf3: 31 (B} TYPE: Amino acid (C) TOPOLOGY: Linear (ii) N~LECULE TYPE: Peptide (xi) SEQLJBvICE DESCRIPTION: SEQ ID NO:61:
Ser Arg Thr His Arg His Ser Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Ttp Tyr Ala Ser Arg Gly Ile Arg Pro Val Gly Arg Phe (2) INFORMATION FOR SEQ ID NO:62:
(i) SEQUEriCE CHARACTERISTICS:
(A) I~fl~lG'I~i: 32 (B) TYPE: Amino acid (C) TOPOLOGY: Linear ( ii ) NI)LECULE TYPE : Peptide ( xi ) SEQL1F3QCE DESCRIPTION : SEQ ID NO: 62 Ser Arg Thr His Arg His Ser Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Ttp Tyr Ala Ser Arg Gly Ile Arg Pro Val Gly Arg Phe Gly (2} INFORMATION FOR SEQ ID N0:63:
( i ) SEQUENCE C~E1ARACTERISTICS
(A) LENGTH: 33 (B) TYPE: Amino acid (C) TOPOLOGY: Linear ( ii ) MOLECI,1I~E TYPE : Peptide (xi) SEQUaTCE DESCRIPTION: SEQ ID N0:63:

h.

Ser Arg Thr His Arg His Ser Met Glu Ile Arg Thr Pro Asp Ile Asn Pro Ala Tzp Tyr Ala Ser Arg Gly Ile Arg Pro Val Gly Arg Phe Gly Arg (2) INFORMATION FOR SEQ ID N0:64:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 20 {B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUENCE DESCRIPTION: SEQ ID N0:64:
Thr Pro Asp Ile Asn Pro Ala Tzp Tyr Ala Ser Arg Gly Ile Arg Pro Val Gly Arg Phe 20 {2) INFORMATION FOR SEQ ID N0:65:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 21 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUE1VCE DESCRIPTION: SEQ ID N0:65:
Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Ser Arg Gly Ile Arg Pro Val Gly Arg Phe Gly (2) INFORMATION FOR SEQ ID N0:66:
( i ) SEQLJFNCE C,IiARACTERISTICS
35 (A) LENGTH: 22 (B) TYPE: Amino acid ' {C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide w ~ {~) SEQUENCE DESCRIPTION: SEQ ID N0:66:
Thr Pro Asp Ile Asn Pro Ala Trp Tyr Ala Ser Arg Gly Ile Arg Pro Val Gly Arg Phe Gly Arg 10 (2) INFORMATION FOR SEQ ID N0:67:
{ i ) SEQiIErTCE CHARACTERISTICS
(A) LENGTH: 93 (B) TYPE: . Nucleic acid (C) STRANDEDNESS: Double 15 (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION METHOD: S
(xi) SFQiJErTCE DESCRIPTION: SEQ ID N0:67:
AGTOGTACCC ATCGGCAGTC CATGGAGATC CGCACCCCI"G ACATCAATCC TGCCi'GGTAC 60 ~CG GGATCAGC,cC ZG'.IGGGCCGC TTC 93 ' (2) INFORMATION FOR SEQ ID N0:68:
2s ( i ) sEQU~cE c~~ARACTERISTZCS
(A) : 96 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
{C) IDENTIFICATION METHOD: S
(xi) SE,QLIErICE DESCRIPTION: SEQ ID N0:68:
AGTCGTA(:CC ATCGGCACTC CATGGAGATC CGCACGCCI"G ACATCAATCC TGCCTGGTAC 60 C~CCAGZ~C('~OG GGA'I'CAGGCC TGTGGC'~COGC T1'OGGT 96 WO 98/58962 PCT/JP98/02~65 h.

(2) INFORMATION FOR SEQ ID N0:69:
(i) SEQUENCE Q~ARACTERISTICS:
(A) LENC~"I'li: 99 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION METHOD: S
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:69:
AGI'CGTACCC ATOGGCACTC CATGGP.GATC CGCACCCCTG ACATCAATCC TGCCTGGTAC 60 GCCAGTCGCG GGATCAGGCC TGrGGGCCGC TTCGGTCGG 99 (2) INFORMATION FOR SEQ ID N0:70:
(i) SEQUENCE CHARACTERISTICS:
(A) LENGTH: 60 ( B ) TYPE : Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION METfiOD: S
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:70:
ACCCCZGACA TCAATCCTGC CTCGTACGCC AGTOGaGGGA TCAGGCCTGT GGGCCGCTiC 60 {2) INFORMATION FOR SEQ ID N0:71:
(i) SEQUENCE CHARACTERISTICS:
(A) LF~"rH: 63 (B) TYPE: Nucleic acid C ) S'I'RANDEDNESS : Double (D) TOPOLOGY: Linear (ii) N~LECULE TYPE: cDNA
(ix) FEATURE

- (C) IDENTIFICATION METHOD: S
( xi ) SEQZIErTCE DESCRIPTION : SEQ ID N0 : 7I
ACCC(:TGACA TCAATCCTGC CTGGTACGCC AGl'CGOGGGA TCAGGCC1~CT GGGCCGCTrC 60 (2) INFORMATION FOR SEQ ID N0:72:
i ) SEQiJfl~iCE C~iARAG'1'ERISTICS
(A) LENC~'rH: 66 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Double (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: cDNA
(ix) FEATURE
(C) IDENTIFICATION METHOD: S
( xa. ) SEQiJEnTCE DESCRIPTION : SDQ ID N0: 72 ACCCC1~GACA TCAA'lCCrGC CTGGTACGCC AGTCGO~GGA 'I'CAGGCCTGT GC~GCCGCITC 60 (2) INFORMATION FOR SEQ ID N0:73:
( i ) SEQLTErICE CHARACTERISTICS
(A) I~1V"rH: 21 (B) TYPE: Amino acid ( C ) TOPOIpGY : Linear (ii) MOLECULE TYPE: Peptide (ix) FEATURE: Xaa of the 10th position is Ala or Thr.
Xaa of the 11th position is Gly or Ser.
Xaa of the 21st position is H, Gly or GlyArg.
(xi.) SEQUENCE DESCRIPTION: SEQ ID N0:73:
Thr Pro Asp Ile Asn Pro Ala Txp Tyr Xaa Xaa Arg Gly Ile Ax~g Pro Val Gly Arg Phe Xaa a:

(2) INFORMATION FOR SEQ ID N0:74:
( i ) SEQiJEnTCE C~iARACTERISTICS
(A) LINGI~i: 11 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (ix) FEATURE: Xaa of the 3rd position is Ala or Thr.
. Xaa of the 5th position is Gln or Arg.
Xaa of the 10th position is Ile or Thr.
{~) SEQUENCE DESCRIPTION: SEQ ID N0:74:
Ses Arg Xaa His Xaa H_is Ser Met Glu Xaa Arg (2) INFORMATION FOR SEQ ID N0:75:
{i) SEQUENCE CEiARACTERISTICS:
(A) hENGTH: 26 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQiJE~ICE DESCRIPTION: SEQ ID NO:75:
CARCAY'I'CCA ZGGAGACAAG AACCCC 26 {2) INFORMATION FOR SEQ ID N0:76:
(i) SEQUEnICE CHARACTERISTICS:
(A) LENGTH: 24 ( B ) TYPE : Nu ~- sic acid (C) STRANDEDNESS: S~.~gle .
(D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:76:

TACCA('~GCP~G GATTGATACA GGGG 24 (2) INFORMATION FOR SEQ ID NO:77;
{ i ) SEQUEnICE QiARACTERISTICS
' {A) LENGTH: 25 (B) TYPE: Nucleic acid ( C ) STRAI~1DEDNESS : Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
SCE DESCRIPTION: SEQ ID N0:77:
GGCATCATCC ACGAA~ACJGG AGCAT 25 (2) INFORMATION FOR SEQ ID N0:78:
i ) SFQLJ~ICE C~iARACTERISTICS
(A) I~fi: 25 {B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQtJEnICE DESCRIPTION: SEQ ID N0:78:

(2) INFORMATION FOR SEQ ID N0:79:
( i ) SF~LJE~TCE CHARACTERISTICS
(A) I~flVGTH: 22 (B) TYPE: Nucleic acid ', (C) STRANDEDNESS: Single ( D ) TOPOLOGSC : Linear {ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQtJEIJCE DESCRIPTION: SEQ ID N0:79:

h:

AOG'~GCi'I'C TGTG~(.T.LGCT GC 22 (2) INFORMATION FOR SEQ ID N0:80:
(i) SEQUENCE CHARACTERISTICS:
(A) I,ENG~'li: 25 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:80:
GCCTGATCCC GCGGCCOG'hG TACCA 25 {2) INFORMATION FOR SEQ ID N0:81:
( i ) SEQIJErICE CHARACTERISTICS
(A) LENGTH: 26 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:81:
TTGCCCTTCr CCTGCCGAAG CGGCCC 26 (2) INFORMATION FOR SEQ ID N0:82:
(i) SEQUENCE CHARACTERISTICS:
(A) LEL~1GTH: 27 (B ) TYPE: Nwc:leic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:82:

WO 98/58962 PCT/JP98/OZ'765 h:

(2) INFORMATION FOR SEQ ID NO:83:
( i ) SEQUEnICE C~~ARACTERISTICS
' (A) LENGTH: 27 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi.) SEQUENCE DESCRIPTION: SEQ ID N0:83:
CGGCAC'ICCA TGGAGATCCG CACCCCT 27 (2) INFORMATION FOR SEQ ID N0:84:
( i ) SFQtIErICE C:EiARAG'I'ERISTICS
(A) LENGTH: 27 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
( xi ) SFQIJEniCE DESCRIPTION : SEQ ID NO: 84 CAGGCAGGAT TGAZG'ICAC~G GGTGCGG 27 (2) INFORMATI~1 FOR SEQ ID N0:85:
(i) SEQUENCE CHARACTERISTICS:
(A) I~H: 27 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOhOGY: Linear ( ii ) N~LECUI~E TYPE : Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:85:

CATGGAGrGC CGATGGGTAC GACPJ.GC 27 (2) INFORMATION FOR SEQ ID N0:86:
(i) SEQUF~1CE CHARACTERISTICS:
(A) LI~lG'i~i: 27 (B) TYPE: Nucleic acid (C) STRP.NDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE 'TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUINCE DESCRIPTION: SEQ ID N0:86:
GGCCTCC'I'OG GAGGAC~CCAA GGGATGA 27 (2) INFORMATION FOR SEQ ID N0:87:
(i) SEQUEnICE CHARACTERISTICS:
(A) I~fl~IGTH: 27 {B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:87:
GGGAAAGGAG CCCGAAGGAG ACGA~GAG 27 (2) INFORMATION FOR SEQ ID N0:88:
(i) SEQUENCE CHARACTERISTICS:
(A) hflJGTfi: 25 (B) TYPE: Nucleic acid (C) S'TRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
{xi) SFQU~ICE DESCRIPTION: SEQ ID N0:88:

h.

CCTGC'rGGCC ATTCFCCTGr CTTAC 25 ( 2 ) I~'ORN1ATION FOR SEQ ID NO: 89 (i) SEQUW1CE CHARACTERISTICS:
(A) ?~"rH: 25 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQLJEnICE DESCRIPTION: SEQ ID N0:89:

(2) INFORMATION FOR SEQ ID N0:90:
( i ) SF~1CE Q~ARP~..'TERISTICS
(A) LENGTH: 25 (B) TYPE: Nucleic acid ( C ) S'!'RANDEDNESS : Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQ~JF~1CE DESCRIPTION: SEQ ID N0:90:

(2) INFORMATION FOR SEQ ID N0:91:
( i ) SEQ~JF~1CE CHARACTERISTICS

(A) I~'fi: 25 (B) TYPE: Nucleic acid ', (C) STRANDEDNES S: Single (D) TOPOLOGY: Linear (ii) NIaLECULE TYPE: Other nucleic acid Synthetic DNA

( xi ) SEQLJENC'.E DESCRI PTION : SEQ ID NO:
91:

GGCA,GCIGAG TIGGCCAAG'P CCAGT 25 (2) INFORMATION FOR SEQ ID N0:92:
$ (i) SFQUEnICE CHARACTERISTICS:
(A} LENGTH: 15 (B} TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SEQUENCE DESCRIPTION: SEQ ID N0:92:
Ser Arg Ala His Gln His Ser Met Glu Ile Arg Thr Pro Asp Cys (2) INFORMATION FOR SEQ ID N0:93:
(i) SEQUE~1CE CHARACTERISTICS:
(A) LENGTH: 15 (B) TYPE: Amino acid (C) TOPOLOGY: Linear (ii) MOLECULE TYPE: Peptide (xi) SFQUEnICE DESCRIPTION: SEQ ID N0:93:
Cys Ala Trp Tyr Ala Gly Arg Gly Ile Arg Pro Val Gly Arg Phe (2) INFORMATICiN FOR SEQ ID N0:94:
( i ) SFQUE2~1CE CHARACTERI STICS
(A} LENGTH: 15 (B) TYPE: Amino acid (C} TOPOLOGY: Linear (ii) MC°1.~CULE TYPE: Peptide (xi) 5,.xJENCE DESCRIPTION: SEQ ID N0:9=1:
Cys Glu Ile Arg ThT Pro Asp Ile Asn Pro Ala Trp Tyr Ala Gly A:

(2) INFORMATION FOR SEQ ID N0:95:
( i ) SEQLlErICE CHARACTERISTICS
{A) LENGTH: 30 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single ' ( D ) TOPOT~7GY : Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi.) SFQiJEnICE DESCRIPTION: SEQ ID N0:95:
AGATIGGCAT CAZCCAGGAA GACt'~GAGCAT 30 (2) INFbRMATION FOR SEQ ID N0:96:
( i ) SE;QUEnICE CHARACTERISTICS
(A} LENG'i~i: 31 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D} TOPOLOGY: Linear (i.i) 1H~LECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:96:
GCTGACTCGA CAGCACTG1'C TI'C.'I~C'~AiGLT G 31 (2) INFORMATION FOR SEQ ID N0:97:
(i) SDQUENCE CHARACTERISTICS:
(A) I~TH: 21 (B) TYPE: Nucleic acid (C) S'TRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) I~LECULE TYPE: Other nucleic acid ', Synthetic DNA
{xi) SEQtJE<~1CE DESCRIPTION: SEQ ID N0:97:

h:

(2) INFORMATION FOR SEQ ID N0:98:
(i) SEQUErTCE CHARACTERISTICS:
(A) LENGTH: 20 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUENCE DESCRIPTION: SEQ ID N0:98:

(2) INFORMATION FOR SEQ ID N0:99:
(i) SEQUE~1CE CHARACTERISTICS:
(A) I~1GTH: 28 (B) TYPE: Nucleic acid (C) STRANDEDNESS: Single (D) TOPOLOGY: Linear (ii) MOLECULE TYPE: Other nucleic acid Synthetic DNA
(xi) SEQUEnICE DESCRIPTION: SEQ ID N0:99:

Claims (16)

WHAT IS CLAIMED IS:

1. An agent for modulating prolactin secretion which comprises a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein.

2. An agent as claimed in claim 1, wherein the ligand polypeptide is a polypeptide comprising an amino acid sequence represented by SEQ ID NO: 73 or a substantial equivalent thereto, or its amide or ester, or a salt thereof.

3. An agent as claimed in claim 2, wherein the polypeptide comprising an amino acid sequence represented by SEQ ID NO: 73 is a polypeptide comprising an amino acid sequence represented by SEQ
ID NO: 5, 8, 47, 50, 61 or 64.

4. An agent as claimed in claim 1, which is for promoting prolactin secretion.

5. An agent as claimed in claim 1, which is for inhibiting prolactin secretion.

6. An agent as claimed in claim 4, which is for treating or preventing hypoovarianism, gonecyst cacogenesis, menopausal symdrome, euthyroid or hypometabolism.

7. An agent as claimed in claim 5, which is for treating or preventing pituitary adenomatosis, brain tumor, emmeniopathy, autoimmune disease, prolactinoma, infertility, impotence, amenorrhea, galactorrhea, acromegaly, Chiari-Frommel symdrome, Argonz-del Castilo symdrome, Forbes-Albright symdrome, lymphoma, Sheehan syndrome or dyszoospermia.

8. An agent for modulating placental function, which comprises a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein.

9. An agent as claimed in claim 8, which is for treating or preventing choriocarcinomia, hydatid mole, irruption mole, abortion, unthrifty fetus, abnormal saccharometabolism, abnormal lipidmetabolism or oxytocia.

10. An agent as claimed in claim 4, which is for promoting lactation of domestic mammal.

11. An agent as described in claim 4 , which is for an aphrodisiac.

12. An agent for diagnosing function of prolactin secretion, which comprises a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein.

13. Use of a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein for maufacture of a medicament for modulating prolactin secretion.

14. A method for modulating prolactin secretion in a mammal, which comprises administering to said mammal a ligand polypeptide, or a sat thereof, for a G
protein-coupled receptor protein.

15. Use of a ligand polypeptide, or a salt thereof, for a G protein-coupled receptor protein for maufacture of a medicament for modulating placental function.

16. A method for modulating placental function in a mammal, which comprises administering to said mammal a ligand polypeptide, or a salt thereof, for a G
protein-coupled receptor protein.