Genomic DNA exons having exons encoding human pituitary adenylate cyclase activity peptide with 38 amino acids residues(PACAP38) and a promoter thereof

Abstract

Disclosed are (1) a genomic DNA of human PACAP38; (2) a DNA containing a DNA segment coding for human PACAP38; (3) a DNA of human PACAP 38 promotor; (4) a transformant carrying a vector which contains a DNA of (3) or further contains a DNA coding for a protein downstream from the promotor; and (5) a method for preparing a protein comprising cultivating the transformant described in the above (4), accumulating the protein in a culture product, and collecting the resulting protein such as mature PACAP 38. The DNA gives human PACAP 38 effectively and makes it possible to screen the chemical substance necessary for production of PACAP and is applied to experimental animals to understand their brain functions, which serves to elucidate human brain functions. Human PACAP38 can also be utilized as therapeutic agents about growth and maintenance of human brain nerves.

Description

FIELD OF THE INVENTION

The present invention relates to a genomic DNA of human pituitary adenylate cyclase activating polypeptide with 38 residues (PACAP38) which is a bioactive peptide derived from testes or brain hypothalami, a DNA containing a DNA sequence coding for the peptide, a promoter of human PACAP38, a vector containing the promoter, a vector containing a DNA coding for a structural gene of a peptide downstream from the promoter, a transformant bearing the vector, and a method for preparing a protein such as mature PACAP38 peptide using the transformant.

BACKGROUND OF THE INVENTION

Various hormones secreted by brain hypothalami and hypophyses are well known. Examples thereof include thyrotropin releasing hormone, luteinizing hormone releasing hormone, somatostatin, adrenocorticotropic hormone(ACTH), growth hormone(GH) and prolactin. The action of these hormones has been well studied. A novel peptide consisting of 38 amino acid residues which has the adenylate cyclase activity was discovered in a different hormone derived from sheep hypophyses. The structure thereof was determined and the peptide was named "PACAP38" (EPA 0 404 652).

The present inventors filed a patent application (Japanese Patent Application No. 1-155791/1990) on cDNA of sheep PACAP38. Further, cDNA of human PACAP38 was cloned from the cDNA library of testes and the amino acid sequence thereof was also determined (Japanese Patent Application No. 1-259924/1990).

The amino acid sequence corresponding to human PACAP38 is the same as that of sheep PACAP38, although there is substitution of some amino acids in the precursors thereof.

In general, when an amino acid sequence such as a bioactive peptide is determined and cDNA is cloned, its expression mechanism can be studied to determine the physical conditions under which transcription and translation of the gene take place. Understanding the expression mechanism aids in the development of drugs for inducing the expression of the gene. PACAP38, a peptide consisting of 38 amino acid residues which enhances adenylate cyclase activity, is one such peptide whose expression mechanism was unknown in the prior art.

Promoter regions, typically located upstream from genes, are activated by factors which result in the synthesis of mRNA coding for the protein.

Some factors which activate promoter regions have been reported. However, most of them are specific to the cells which specifically express the protein.

Human PACAP is a protein secreted by nerve cells and is specifically produced in the hypothalamas. Accordingly, a promoter of human PACAP can possibly produce substances specific to nerve cells.

SUMMARY OF THE INVENTION

The present inventors have undertaken the study of the mechanism of the expression of the human PACAP38 gene in order to develop methods for inducing the expression. Their study has led to the isolation of genomic DNA of PACAP38 from a human DNA library and the determination of its nucleotide sequence. This has made it possible to induce human PACAP38 through genetic engineering techniques, thus achieving the present invention.

Concurrently, the present inventors have further cloned the gene of human PACAP38, which has been compared with the structure of the previously cloned cDNA of human PACAP38 to determine the structure thereof and to elucidate the relationship between an intron and an exon. At the same time, a promoter region essential for the expression of the gene has been determined.

In accordance with the present invention, there are provided (1) a genomic DNA of human PACAP38; (2) a DNA containing a DNA sequence coding for human PACAP38; (3) a DNA of human PACAP38 promoter; (4) a transformant carrying a vector which contains a DNA of (3) or further contains a DNA coding for a protein downstream from the promoter; and (5) a method for preparing a protein comprising cultivating the transformant described in the above (4), accumulating the protein in a culture product, and collecting the resulting protein such as mature PACAP38.

The present invention further provides a method of producing substances specifically produced in nerve cells, such as human PACAP38. In the method, an expression vector is constructed containing a cDNA coding for a protein (e.g., PACAP38), specifically expressed in nerve cells, (e.g., astrocytes), is linked downstream from the promoter of the present invention. The expression vector is then introduced into the cultured cell, for example, astrocytes to produce the proteins specifically produced in nerve cells, such as PACAP. The promoter of the present invention can also be used for neuroscientific study regarding the production of substances in astrocytes, differentiation of the cells, morphological change of the cells and growth of the cells.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a simplified restriction enzyme map of a genomic DNA of human PACAP38; and

FIG. 2 [SEQ. ID. NO:1] shows a nucleotide sequence of the genomic DNA of human PACAP38 and an amino acid sequence (SEQ. ID. NO: 2) of a human PACAP38 precursor from which a mature peptide can be deduced.

FIG. 3 shows a construction of a plasmid into which a 5'-region of human PACAP38 genomic DNA was introduced.

FIG. 4 shows promoter activity of various DNA fragments from 2.5 to 1 kb located in a 5'-region of genomic DNA of human PACAP38.

FIG. 5 shows promoter activity of some shorter DNA fragments located in a 5'-region of genomic DNA of human PACAP38.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

In the present invention, a DNA having the nucleotide sequence coding for the precursor protein of human PACAP38 or mature PACAP38 and for a promoter of human PACAP38 can be prepared, for example, by the following process:

(i) Human cell DNA is extracted and treated with restriction enzyme such as EcoRI or SalI, and is introduced into a phage or a plasmid; (ii) The recombinant phage or plasmid thus obtained is introduced into an appropriate host cell to produce a transformant; (iii) After cultivation of the transformant thus obtained, the plasmid or the phage containing the desired DNA is isolated from the transformant by an appropriate method such as hybridization with a DNA probe coding for a portion of PACAP38; and (iv) The desired cloned DNA is cut out from the recombinant DNA.

Methods for cloning the PACAP38 DNA from the human DNA library include, for example, the plaque hybridization method [T. Maniatis et al., Molecular Cloning, Cold Spring Harbor Laboratory (1982)] using as a probe an oligonucleotide chemically synthesized reflecting phage vector .lambda.gt11 or EMBL and the amino acid sequence of PACAP38, or the cDNA of PACAP38.

The PACAP38 cDNA thus cloned is subcloned to a plasmid such as pBR322, pUC12, pUC13, pUC18, pUC19, pUC118, pUC119 or the like to obtain the human PACAP38 DNA, if necessary.

The nucleotide sequence of the DNA thus obtained is determined, for example, by the Maxam-Gilbert method [A. M. Maxam and W. Gilbert, Proc. Natl. Acad. Sci., U.S.A. 74, 560 (1977)] or the dideoxy method [J. Messing et al., Nucleic Acids Research 9, 309 (1981)], and the existence of the human PACAP38 DNA is confirmed in comparison with the known amino acid sequence.

As described above, the DNA (FIG. 2, SEQ ID NO:1) containing a DNA fragment coding for a portion of the precursor protein of human PACAP38 is obtained.

The restriction enzyme fragment map of the DNA coding for the precursor protein of human PACAP38 is shown in FIG. 1. The nucleotide sequence of the DNA determined by the dideoxy method and the amino acid sequence deduced from that nucleotide sequence are shown in FIG. 2.

A DNA coding for a precursor protein of human PACAP38 cloned as described above is compared with a cDNA of human PACAP38 previously cloned, and then the relationship of introns and exsons of the gene is determined and a promoter region essential for an expression of the gene is deduced. A DNA sequence essential as a promoter is determined from the portion which covers a promoter region of human PACAP38.

For example, a region containing a DNA sequence of SEQ ID NO:3 can be used as the promoter. The promoter can be obtained from pHPR10neo obtainable from the transformant, Escherichia coli MV1184/pHPR10 neo (FERM BP-4084) according to a method of Example 3. A DNA fragment having a DNA sequence of the promoter of the present invention can be synthesized using the phosphoamidide method using standard DNA synthesizing equipment(Applied Biosystems Co. Ltd.).

The plasmids into which the DNA is introduced include, for example, pBR322 [Gene 2, 95 (1977)], pBR325 [Gene 4, 121 (1978)], pUC12 [Gene 19, 259 (1982)] and pUC13 [Gene 19, 259 (1982)], each derived from Escherichia coli, and pUB110 derived from Bacillus subtilis [Biochemical and Biophysical Research Communication 112, 678 (1983)]. However, any other plasmid can be used as long as it is replicable and viable in the host. The phage vectors into which the DNA is introduced include, for example, .lambda.gt11 [R. Young and R. Davis, Proc. Natl. Acad. Sci., U.S.A. 80, 1194 (1983)] and EMBL3 [Prischauf et al., J. Mol. Biol. 170, 827 (1983)]. However, any other phage vector can be used as long as it is replicable and viable in the host.

Methods for introducing the DNA into the plasmid include, for example, the method described in T. Maniatis et al., Molecular Cloning, p.239, Cold Spring Laboratory, (1982). Methods for introducing the DNA into the phage vector include, for example, the method of T. V. Hyunh et al. [DNA Cloning, A Practical Approach 1, 49 (1985)].

The plasmid thus obtained is introduced into the appropriate host cells such as Escherichia and Bacillus.

Examples of Escherichia described above include Escherichia coli K12DH1 [Proc. Natl. Acad. Sci. U.S.A. 60, 160 (1968)], M103 [Nucleic Acids Research 9, 309 (1981)], JA221 [Journal of Molecular Biology 120, 517, (1978)], HB101 [Journal of Molecular Biology 41, 459 (1969)] and C600 [Genetics 39, 440 (1954)].

Examples of Bacillus described above include Bacillus subtilis MI114 [Gene 24, 255 (1983)] and 207-21 [Journal of Biochemistry 95, 87 (1984)].

Methods for transforming the host with the plasmid include, for example, the calcium chloride method and the calcium chloride/rubidium chloride method described in T. Maniatis et al., Molecular Cloning, p.249, Cold Spring Harbor Laboratory, (1982).

When the phage vector is used, for example, the phage vector can be transduced into proliferated E. coli, using the in vitro packaging method.

In the present invention, an expression vector containing a DNA having the nucleotide sequence coding for the precursor protein of human PACAP38, mature PACAP38 or other protein can be prepared, for example, by the following process:

(i) Human cell DNA is extracted and treated with restriction enzyme such as EcoRI or SalI, and is introduced into a phage or a plasmid; (ii) The recombinant phage or plasmid thus obtained is introduced into an appropriate host cell to produce a transformant; (iii) After cultivation of the transformant thus obtained, the plasmid or the phage containing the desired DNA is isolated from the transformant by an appropriate method such as hybridization with a DNA probe coding for a portion of PACAP38; (iv) The desired cloned DNA is cut out from the recombinant DNA; and (v) The cloned DNA or a portion thereof is ligated downstream from a promoter in a vector suitable for expression, whereby an expression vector can be obtained.

Expressible proteins other than PACAP38, include nerve cell-derived proteins such as Neuro Growth Factor(NGF), Brain Derived Neurotrophin-3(BDNT-3) and etc.

In obtaining a structural gene to be expressed, plasmids into which a DNA is incorporated, incorporation methods, hosts, transformation methods which are similar with the above-described ones can be used.

The region intended to be expressed is cut out from the cloned DNA and ligated downstream from the promoter in a vehicle (vector) suitable for expression, whereby the expression vector can be obtained.

The DNA has ATG as a translation initiating codon at the 5'-terminus thereof and may have TAA, TGA or TAG as a translation terminating codon at the 3'-terminus. Further, a consensus sequence reactive to cyclic AMP is observed upstream from ATG of the 5'-terminus. These translation initiating codons and translation terminating codon may be added by use of an appropriate synthetic DNA adaptor such as adaptor containing a translation initiating codon ATG or a translation terminating codon TAA, TAG or TGA.

The vectors include the above plasmids derived from E. coli such as pBR322, pBR325, pUC12 and pUC13, plasmids derived from Bacillus subtilis such as pUB110, pTP5 and pC194, plasmids derived from yeast such as pSH19 and pSH15, bacteriophages such as .lambda. phage, and animal viruses such as retroviruses and vaccinia viruses.

As a promoter, a promoter of the present invention containing a DNA sequence of SEQ ID NO:3 can be used. The promoter can be obtained from pHPR10neo obtainable from the transformant, Escherichia coli MV1184/pHPR10 neo (FERM BP-4084) according to a method of Example 3.

Further, pHPR9.5neo, pHPR8.8neo, pHPR8.1neo, pHPR4.9neo, pHPR4.1neo and pHPR2.6neo as shown in FIG. 5 can also be used.

When the host is an animal cell, a SV40-derived promoter, a retrovirus promoter, a metallothionein promoter, a heat shock promoter or the like can be used. The use of an enhancer such as an SV40-derived enhancer, a retrovirus-derived enhancer, is also effective for expression.

By using a vector containing the DNA coding for the precursor protein of human PACAP38, the mature peptide PACAP38 or other protein thus constructed, the transformant is prepared.

Hosts for transformants include Escherichia and Bacillus described above, and animal cells.

Examples of the animal cells include monkey cell COS-7, Vero, Chinese hamster cell (CHO), mouse L cell, human FL cell and human nerve cell 1MR-32.

The transformation of Escherichia described above is conducted, for example, according to the method described in Proc. Natl. Acad. Sci. U.S.A., 69, 2110 (1972), Gene, 17, 107 (1982) or the like.

The transformation of animal cells is carried out, for example, according to the method described in Virology, 52, 456 (1973).

Thus, the transformant transformed with the expression vector containing the DNA coding for the precursor protein of human PACAP38 or the mature peptide (PACAP38) is obtained.

When the animal cell transformants are cultivated, examples of the media which can be used include MEM medium containing about 5 to 20% fetal calf serum [Science, 122, 501 (1952)], DMEM medium [Virology, 8, 396 (1959)], RPMI1640 medium [The Journal of the American Medical Association, 199, 519 (1967)] and 199 medium [Proceeding of the Society for the Biological Medicine, 73, 1 (1950)]. The pH is preferably about 6 to about 8. The cultivation is usually carried out at about 30.degree. to 40.degree. C. for about 15 to about 60 hours, with aeration or agitation if necessary.

The gene product accumulated in a culture broth can be isolated and purified from the culture broth, for example, by the following method.

The collected cells are suspended in an appropriate buffer solution and disrupted by lysozyme such as zymolyace (Kirin Beer Co. Ltd) and/or mechanical disruption method using glass beads, and the desired substances are extracted. The buffer solution may contain a protein denaturant such as urea or guanidine hydrochloride, or a surface-active agent such as Triton X-100 for easier extraction.

The isolation and purification of the human PACAP38 precursor protein, mature peptide or other proteins contained in the culture supernatant or the exctracted solution thus obtained can be performed by an appropriate combination of isolating and purifying methods known in the art. The known isolating and purifying methods include methods utilizing solubility such as salt precipitation and solvent precipitation, methods mainly utilizing a difference in molecular weight such as dialysis, ultrafiltration, gel filtration and SDS-polyacrylamide gel electrophoresis, methods utilizing a difference in electric charge such as ion-exchange column chromatography, methods utilizing specific affinity such as affinity chromatography, methods utilizing a difference in hydrophobicity such as reverse phase high performance liquid chromatography and methods utilizing a difference in isoelectric point such as isoelectro-focussing electrophoresis.

Examples of the purification methods for proteins such as PACAP include a method described in Biochemical and Biophyrical Research Communications, 164,, No.1, p.567-574 (1989).

A system having a promoter of the present invention can express proteins specific to nerve cells or can be used to screen proteins specific to nerve cells.

Further, using an induction substance (chemical substance) for the PACAP gene, the amount of PACAP produced can be determined, for example, by the use of the sandwich EIA method. Furthermore, by using this assay system, it is possible to screen for chemical substances, e.g., drugs that are necessary for, or increase, production of PACAP. Substances showing promise during screening may be then given to experimental animals to understand their action, particularly on brain functions, more particularly on brain functions due to hormones. Moreover, the information thus obtained provides information which serves to elucidate human brain functions.

Such induction substances can also be screened in an assay using the promoter of the present invention operably linked in a vector to a gene encoding a marker protein such as chloramphenicol acetytransferase (CAT). Other suitable marker proteins include luciferase and alkaline phosphatase. Host cells, such as IMR-32 cells, are transformed with the vector using standard precedures. The resulting transformed cells are then exposed to a pre-determined induction substance, such as a drug or chemical, and the level of marker protein production is measured using methods standard for each marker. Substances capable of inducing or increasing marker protein expression can then be further evaluated.

The above methods may also be used to screen for substances that inhibit or decrease PACAP or marker protein expression.

The system employing a promoter of the present invention can express effectively PACAP38. Human PACAP38, including PACAP27, results in an increase in cAMP activity, and therefore can be utilized as therapeutic agents for growth and maintenance of human brain nerves.

There were hereinbefore described in detail the cloning of the DNA coding for human PACAP38, the preparation of the promoter activity expression vectors, the preparation of the transformants thereby, the production of a portion of human PACAP38 and the mature peptides by use of the transformants, and the utility thereof.

When the amino acids are capable of existing as optical isomers, it is understood that the L-forms are represented unless otherwise specified. When nucleotides, amino acids and so on are indicated by abbreviations in the specification and drawings, the abbreviations adopted by the IUPAC-IUB Commission on Biochemical Nomenclature or those commonly used in the art are employed. Accordingly, the following abbreviations are used.

DNA: Deoxyribonucleic acid cDNA: Complementary deoxyribonucleic acid A: Adenine T: Thymine G: Guanine C: Cytosine RNA: Ribonucleic acid mRNA: Messenger ribonucleic acid dATP: Deoxyadenosine triphosphate dTTP: Deoxythymidine triphosphate dGTP: Deoxyguanosine triphosphate dCTP: Deoxycytidine triphosphate ATP: Adenosine triphosphate EDTA: Ethylenediaminetetraacetic acid SDS: Sodium dodecyl sulfate BHA: Benzhydrylamine Cl-Z: 2-Chloro-benzyloxycarbonyl Br-Z: 2-Bromo-benzyloxycarbonyl Bzl: Benzyl OBzl: Benzyl ester HOBt: 1-Benzotriazole DCC: N,N'-Dichlorohexylcarbodiimide Gly or G: Glycine Ala or A: Alanine Val or V: Valine Leu or L: Leucine Ile or I: Isoleucine Ser or S: Serine Thr or T: Threonine Cys or C: Cysteine Met or M: Methionine Glu or E: Glutamic acid Asp or D: Aspartic acid Lys or K: Lysine Arg or R: Arginine His or H: Histidine Phe or F: Phenylalanine Tyr or Y: Tyrosine Trp or W: Tryptophan Pro or P: Proline Asn or N: Asparagine Gln or Q: Glutamine

With respect to the human PACAP38 precursor proteins or the mature peptide of the present invention, a portion of the amino acid sequence may be modified, through addition, elimination of amino acid(s) or substitution with other amino acid(s).

The present invention will be described in more detail with the following Reference Examples and Examples. It is understood of course that these Reference Examples and Examples are not intended to limit the scope of the invention.

Transformants E. coli MV1184/pHGP2312 and MV1184/pHGP2306 obtained in Example 2 described below were deposited with the Fermentation Research Institute, the Agency of Industrial Science and Technology, the Ministry of International Trade and Industry, Japan (FRI) under the accession number FERM BP-3054 on Aug. 10, 1990, and under the accession number FERM BP-3033 on Jul. 30, 1990, respectively. These microorganisms were also deposited with the Institute for Fermentation, Osaka, Japan (IFO) under the accession numbers IFO 15068 and IFO 15067, respectively, on Jul. 24, 1990.

Transformant E. coli MV1184/pGPR10neo in Example 3 described below was deposited with FRI under the accession number FERM BP-4084 on Nov. 26, 1992.

REFERENCE EXAMPLE 1

The amino acid sequence of sheep PACAP38 is believed to be identical to that of human PACAP38. When PACAP38 purified from sheep hypothalami (hereinafter, "Nat. 38p") and synthesized PACAP38 (hereinafter, "Syn.38p") were allowed to act on rat pituicytes in vitro, an increase in adenylate cyclase activity was identified by observing an increase of cAMP observed. The result is shown in Table 1. The minimum effective amount was 10.sup.-12 M, and it was shown that the activity increased with increasing concentration.

Further, similar activity was also observed for synthesized 27-NH.sub.2, the amino acids situated in the 132nd to 158th positions of FIG. 2 (hereinafter, "Syn.27p-NH.sub.2 "). In contrast, a similar increase in activity could not be observed for a synthesized porcine vasoactive intestinal polypeptide (hereinafter, Syn. pVIP).

TABLE 1______________________________________Adenylate Cyclase Stimulating Test in Rat Pituicyte Culture cAMP p mol/ml (M .+-. SEM)______________________________________Experiment 1Syn.pVIP 10.sup.-12 M 1.35 .+-. 0.05Syn.pVIP 10.sup.-11 M 1.40 .+-. 0.00Syn.pVIP 10.sup.-10 M 1.45 .+-. 0.15Syn.pVIP 10.sup.-9 M 1.75 .+-. 0.05Syn.pVIP 10.sup.-8 M 2.55 .+-. 0.25Syn.pVIP 10.sup.-7 M 3.30 .+-. 0.20Control (Blank) 1.55 .+-. 0.15Experiment 2Syn.27p-NH.sub.2 10.sup.-12 M 2.05 .+-. 0.15Syn.27p-NH.sub.2 10.sup.-11 M 2.55 .+-. 0.15Syn.27p-NH.sub.2 10.sup.-10 M 4.00 .+-. 0.20Syn.27p-NH.sub.2 10.sup.-9 M 7.90 .+-. 0.30Syn.27p-NH.sub.2 10.sup.-8 M 9.20 .+-. 0.00Syn.27p-NH.sub.2 10.sup.-7 M 9.20 .+-. 0.20Syn.38p 10.sup.-12 M 2.15 .+-. 0.05Syn.38p 10.sup.-11 M 3.05 .+-. 0.35Syn.38p 10.sup.-10 M 4.60 .+-. 0.20Syn.38P 10.sup.-9 M 6.20 .+-. 0.10Syn.38p 10.sup.-8 M 8.60 .+-. 0.20Syn.38p 10.sup.-7 M 8.70 .+-. 0.20Nat.38p 10.sup.-12 M 1.50 .+-. 0.10Nat.38p 10.sup.-11 M 1.75 .+-. 0.05Nat.38p 10.sup.-10 M 2.60 .+-. 0.10Nat.38P 10.sup.-9 M 4.60 .+-. 0.00Nat.38p 10.sup.-8 M 8.05 .+-. 0.35Control (Blank) 1.35 .+-. 0.05______________________________________

REFERENCE EXAMPLE 2

The materials used in Reference Example 1 were similarly allowed to act on rat pituicytes in vitro. As a result, the releasing activity of prolactin (PRL), ACTH and GH was confirmed therein.

EXAMPLE 1

Preparation of cDNA Probe Coding for Human PACAP38

The cDNA of cloned human PACAP38 was labelled by the random prime method using .sup.32 P-dCTP for use in screening of the human genomic DNA library.

EXAMPLE 2

Isolation of Human PACAP Genomic DNA and Determination of Nucleotide Sequence Thereof

E. coli LE392 was infected with a human leukocyte-derived DNA library (Clontech Laboratories, Inc., Catalog No. HL1006d) and plated to cause phage plaques to appear. A portion of plaque DNA was transferred to a nitrocellulose film according to the method of W. Benton and R. Davis [Science 196, 180-182 (1977)] and hybridized with the cDNA probe labeled with .sup.32 p in Example 1. Hybridization was carried out in the absence of formaldehyde at 60.degree. C. Clones positive to hybridization were isolated. Then, a cDNA portion of .lambda.HGP23, which was one of the clones described above, was cut out with SalI and recloned into the SalI site of plasmid pUC18 to prepare plasmids pHGP2312 and pHGP2306. By transforming E. coli MV1184 with these plasmids, transformants E. coli MV1184/pHGP2312 (FERM BP-3054) and E. coli MV1184/pHGP2306 (FERM BP-3033) were obtained. The cDNA portions included in these plasmids were 11.1 kbp and 6 kbp, respectively. The simplified restriction enzyme maps thereof are shown in FIG. 1. In the figure, black box () shows a mature human PACAP38 code region. The nucleotide sequence of this DNA portion was determined by the method of Sanger [Proc. Natl. Acad. Sci. U.S.A. 74, 5463-5467 (1977)]. This nucleotide sequence is shown in FIG. 2. The region from amino acid Nos. 132 to 169 is the mature peptide portion of human PACAP38.

Referring to FIG. 2, the 7540th to 7650th nucleotides form the first exon, which codes for amino acid residues M(1) to R(37) in the lower row. The amino acid numbers are designated in parentheses. The 9814th to 9945th nucleotides form the second exon, which codes for amino acid residues P(38) to R(81). The 10421st to 10519th nucleotides form the third exon, which codes for amino acid residues D(82) to G(114). The 11602nd to 11787th nucleotides form the fourth exon, which codes for amino acid residues G(115) to L(176).

Analysis of the genomic DNA revealed that the precursor of human PACAP38 consisted of 176 amino acid residues (SEQ ID NO:2).

EXAMPLE 3

Plasmid pHGP 2312 into which 5'-region of a genomic DNA of the cloned human PACAP had been incorporated was digested with EcoRI and Eco47III to obtain a DNA fragment of 2.5 kb (4646 to 7159 nucleotides). The DNA fragment was inserted into puc118 at the sites of EcoRI and SmaI.

A terminater of SV40 of 519 bp (to 0.52 Kbp) was incorporated at the sites of BamHI and SalI of the above described plasmid, and then a gene of chloramphenicol acetytransferase was incorporated into BamHI site of the plasmid.

A DNA fragment (pMCIneo.polyA, Stragene, USA) which has a promoter of thymidine kinase and a polyA signal.neomycin resistance gene was linked at SalI site of the above-described plasmid to construct a plasmid of FIG. 3.

FIG. 3 shows a plasmid into which a 2.5 kb of PACAP gene.

The plasmids which have each 2.2 kb, 1.5 kb and 1 kb of PACAP gene were named pHPR22neo, pHPR15neo. and pHPR10neo, respectively. Each 50 .mu.g of the purified plasmids was applied to IMR-32 cells, neuroblastoma, grown up in a petri dish of 9 cm diameter with calcium phosphate method(Graham, PL1973, Virology 52, 456-457), which were cultivated in Eagles' MEM (EMEM) medium with 10% serum containing 0.5mg/ml of G418. The survived cells were further cultivated. The CAT assay according to Gorman et al (Mol. Cell. Biol., 2, 1044) was used.

Each plasmid was applied to IMR-32 cells and CAT produced in the cells was assayed. The results are shown in FIG. 4. The black bands indicated by an arrow show CAT amount expressed. The stronger the black is, the more CAT is expressed, which means stronger promoter activity.

Plasmids into which DNA fragments of 2.5 kb to 1.0 kb of PACAP were incorporated respectively were found to produce CAT. Among them, the plasmid which has a 1 kb fragment had the highest activity and a promoter on the gene of human PACAP was shown to be located in a 17 kb nucleotide sequence of 6143rd to 7159th previously cloned.

A plasmid into which a further shortened PACAP gene was incorporated was constructed and the resulting plasmid was applied to IMR-32 cells to assay CAT produced. The plasmid pHPRneo6.6 (657 bp, 6503rd to 7159th nucleotides)(SEQ ID NO:3) had the highest activity as shown in FIG. 5.

The above results show that the promoter region is located in an EcoRI to Eco47III region of the PACAP gene (4644th to 7159th nucleotides). The promoter region deduced from the results can be used for an expression system utilizing nerve cells.

EXAMPLE 4

Synthesis of PACAP38 NH.sub.2

PACAP38 NH.sub.2 was synthesized by using 1.04 g (0.5 mmole) of a commercially available p-methyl BHA resin (Applied Biosystems Inc., California USA) and a peptide synthesizer (Model 430A, Applied Biosystems Inc.).

A starting amino acid, Boc-Lys(Cl-Z), was activated with HOBt/DCC and then condensed to the resin. Thereafter, the Boc group on the resin was treated with 50% trifluoroacetic acid/methylene chloride to deprotect the amino group. To this free amino group, the following protected amino acids activated with HOBt/DCC were reacted in turn according to the amino acid sequence of PACAP3:

Boc-Asn, Boc-Lys(Cl-Z), Boc-Val, Boc-Arg(Tos), Boc-Gln, Boc-Tyr(Br-Z), Boc-Gly, Boc-Leu, Boc-Ala, Boc-Met, Boc-Ser(Bzl), Boc-Asp(OBzl), Boc-Thr(Bzl), Boc-Phe, Boc-Ile and Boc-His(Tos) After the completion of each reaction, the residual amino groups were acetylated with acetic anhydride to obtain 2.42 g of a protected PACAP38 NH.sub.2 resin.

0.51 g of the resulting protected PACAP38 NH.sub.2 resin was treated with 5 ml of hydrogen fluoride in the presence of 0.6 g of p-cresol at 0.degree. C. for 60 minutes, followed by removal of excess hydrogen fluoride by distillation under reduced pressure. The treated resin was washed twice with 5 ml of ethyl ether, and then extracted with 6 ml of 50% aqueous acetic acid. The insoluble material was removed by filtration and washed with 5 ml of 50% aqueous acetic acid. The filtrate and the washings were combined, and the combined solution was concentrated under reduced pressure to 2 to 3 ml. The concentrated solution was applied to a Sephadex LH-20 column (2.times.90 cm) for elution with 50% acetic acid. The main fractions were collected, and then removed by distillation under reduced pressure. Then, the residue was dissolved in 100 ml of 0.1% aqueous trifluoroacetic acid. The resulting solution was subjected to a YMC-ODS AM120 S-50 resin column (2.6.times.7 cm) and eluted by a linear gradient of 0.1% aqueous trifluoroacetic acid and 50% acetonitrile containing 0.1% trifluoroacetic acid.

The main fractions were combined, followed by lyophilization. Thus, 60 mg of a white powder was obtained. This powder was dissolved in 20 ml of 0.05M aqueous ammonium acetate. The resulting solution was subjected to a CM-Cellulofine resin column (1.times.6 cm) and eluted by a linear gradient of ammonium acetate from 0.05M to 1M. The main fractions were combined. The combined solution was subjected to a YMC-ODS column (2.6.times.7 cm) again and eluted by a linear gradient of from 0% to 40% aqueous acetonitrile containing 0.1% trifluoroacetic acid. The fractions of 28% to 30% acetonitrile were collected, followed by lyophilization. 21.6 mg of a white powder was obtained. Anal. of amino acids:

Asp 2.90(3), Thr 0.84(1), Ser 2.10(3), Glu 2.21(2), Gly 2.00(2), Ala 3.29(3), Val 3.19(3), Met 1.01(1), Ile 0.87(1), Leu 2.19(2), Tyr 3.93(4), Phe 0.92(1),

Lys 7.18(7), His 0.96(1), Arg 4.19(4)

(M+H).sup.+ by mass spectrography (SIMS): 4530

HPLC elution time: 19.6 minutes

Column conditions

Column: YMC-ODS (AM-301, S-5 120A) Eluent: A (0.1% aqueous trifluoroacetic acid) B (acetonitrile containing 0.1% trifluoroacetic acid) A linear gradient elution from the eluent A to the eluent B for 50 minutes Flow rate: 1.0 ml/minute

EXAMPLE 5

Synthesis of PACAP27 NH.sub.2

PACAP27 NH.sub.2 was synthesized by using 1.04 g (0.5 mmole) of a commercially available p-methyl BHA resin (Applied Biosystems Inc.) and a peptide synthesizer (Model 430A, Applied Biosystems Inc.).

A starting amino acid, Boc-Leu, was activated with HOBt/DCC and then condensed to the resin. Thereafter, the Boc group on the resin was treated with 50% trifluoroacetic acid/methylene chloride to deprotect the amino group. To this free amino group, the following protected amino acids activated with HOBt/DCC were reacted in turn according to the amino acid sequence of PACAP38 (1-27):

Boc-Val, Boc-Ala, Boc-Leu, Boc-Tyr(Br-Z), Boc-Lys(Cl-Z), Boc-Met, Boc-Gln, Boc-Arg(Tos), Boc-Ser(Bzl), Boc-Asp(OBzl), Boc-Thr(Bzl), Boc-Phe, Boc-Ile and Boc-His(Tos) After the completion of each reaction, the residual amino groups were acetylated with acetic anhydride to obtain 2.31 g of a protected PACAP27 NH.sub.2 resin.

0.50 g of the resulting protected PACAP27 NH.sub.2 resin was treated with 5 ml of hydrogen fluoride in the presence of 0.6 g of p-cresol at 0.degree. C. for 60 minutes, followed by removal of excess hydrogen fluoride by distillation under reduced pressure. The treated resin was washed twice with 5 ml of ethyl ether, and then extracted with 6 ml of 50% aqueous acetic acid. The insoluble material was removed by filtration and washed with 5 ml of 50% aqueous acetic acid. The filtrate and the washings were combined, and the combined solution was concentrated under reduced pressure to 2 to 3 ml. The concentrated solution was applied on a Sephadex LH-20 column (2.times.90 cm) for elution with 50% acetic acid. The main fractions were collected, followed by removal by distillation under reduced pressure. 129 mg of a white powder was obtained. This powder was dissolved in 5 ml of 0.1% aqueous trifluoroacetic acid. The resulting solution was subjected to a TSK-GEL (ODS-120T) column (21.5.times.300 mm) and eluted with 27% acetonitrile containing 0.1% aqueous trifluoroacetic acid.

The main fractions were collected, followed by lyophilization. 17.2 mg of a white powder was obtained. Anal. for amino acids:

Asp 1.99(2), Thr 0.98(1), Ser 2.76(3), Glu 1.25(1), Gly 1.05(1), Ala 3.00(3), Val 1.56(2), Met 0.78(1), Ile 0.72(1), Leu 1.88(2), Tyr 2.22(3), Phe 0.75(1), Lys 2.73(3), His 1.51(1), Arg 1.94(2)

(M+H).sup.+ by mass spectrography (SIMS): 3145

HPLC elution time: 21.2 minutes

Column conditions

Column: YMC-ODS (AM-301, S-5 120A) Eluent: A (0.1% aqueous trifluoroacetic acid) B (acetonitrile containing 0.1% trifluoroacetic acid) A linear gradient elution from the eluent A to the eluent B for 50 minutes Flow rate: 1.0 ml/minute

EXAMPLE 6

Using male Wistar rats having a body weight of 350 g under nembutal anesthesia, the hypotensive activity was measured. The value shows the decrease from normal value. The results are shown in Table 2.

TABLE 2______________________________________Hypotensive activity of PACAP Dosage (n mole/kg)Compound 0.3 1.0 3.0______________________________________PACAP38 NH.sub.2 3.2 .+-. 1.9 17.4 .+-. 2.4 29.8 .+-. 3.6 (n = 6) (n = 6) (n = 6)PACAP27 NH.sub.2 14.5 .+-. 3.1 51.9 .+-. 9.6 4.1 (n = 5) (n = 5) (n = 1)______________________________________ Unit: mm Hg

The following references, which are referred to for their disclosures at various points in this application, are incorporated herein by reference.

European Patent Publication 0 404 652 A1 Japanese Patent Application 1-155791/1990 Japanese Patent Application 1-259924/1990 __________________________________________________________________________SEQUENCE LISTING(1) GENERAL INFORMATION:(iii) NUMBER OF SEQUENCES: 3(2) INFORMATION FOR SEQ ID NO:1:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 17041 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: double(D) TOPOLOGY: linear(ii) MOLECULE TYPE: DNA (genomic)(ix) FEATURE: (A) NAME/KEY: CDS(B) LOCATION: join(7540..7650, 9814..9945, 10421..10519,11602..11787)(xi) SEQUENCE DESCRIPTION: SEQ ID NO:1:GATCACGAGGTCACGAGATCGAGACCATCCTGGCCAACATGGTGAAACCCCATCTCTACT60AAAAATACAAAAAATAGCTGGGCATGGTGGCCCATGCCTGTAGTCC CAGCTACTCGGGAG120GCTGAGGCAGGAGAATTGCTTAAACCCGGGAAGCGGAGGTTGCAGTGAGCCAAGATCGCA180CCACTGCCTCCCAGCCTGGTGATGGAGTGAGACTCCATCTCAAAAAAAAAAAAAAAAAAT240TCCTAGAGAAAATAAATATG CCAGTATAACATATTATAGTCATTAAGACTGTCTGGAGTC300ATTGAGACTTGAATCTGAAGTTCAGCATTACAATGTAGCAGCTGTGTAACTTTGGATAAG360GTACCTGAGCTCTTTTAGTCCCGATTTCTTGTCTGTAAAATGGAGGTAATAACAGTGCCT4 20ACAAAGAAGTTTGTTGTGAGGGAAAGGAAATAAGTAGTCAAGCACTTAGCCCAGGAAGTG480TTCATTAAACAGTTGTTGCTGTTGCTGTTATTCACTGGTGAATAACAAAACCATACAGTC540CCTTTGGAAGGAAGGATTTAAAATAATTTAAACAAATAA TCACTAAAAATTTCAACCAGT600ACATTTATGACAAATGTAATAGTATTCCAAGCAGATGATAGTTTTTAAAAATTTATGCCT660GTGTATATTTGGGTAGAGACAAAGGATTATTTAAAAAGTATTTTCAGGTTGGGCACACTG720GCTCATCCTTGCA ACCCCTGCACTTTGGGAGGCTTGAGTCCAGGAGTTTGTGACCAGCCT780GGGCAACACAGGGAGACCTTGTCTCTGCAAAGTAATAATAATAACAATAATAATAAATAA840AATTAGCCAGGCATGGTGGTGGCATGTGCCTGTAGTCCCAGGTATTCAAGAGGTTGA GGC900AGGAGTCTCACTTAAGCCCAAGAGTTTGAGGTTGCTGTGAGCTATGAATGCACTACTGCA960CTCCAGCCTGGGTGACCGAGGAAGACTCAGTAAAAACAAAACAAAACAAACAAACAAACA1020AAAACTGCAAAGCCGTGATTACCATACAGTG CTAGTAATAATGATAATAAAAACAAAGGC1080TCCAAAATTATTACATGTAAACCTATATTCACAGGTAGATAATGCCAAGCCTGAGCCCAA1140AGGGAAGAGGGATGCTAGGGGCTCACAGAGGAAGACCTTCTTTTGATTTTACACACAAAA1200ACCTTG TTTTATTTTGCATATAGATTCCCCTTCCAACATTTTCTGAAGTGGTCTCAAAAG1260CTTATTTAGGATATTGGTTTTCCTGGATCCTGTCCAAGCTTTTCCTTCTGCATTTAAGCC1320TTATGTCAGCAGAGGATTTAGACTAAGTAGAGAGAAGACTTTCTTCTCCT TGGCTTTTTA1380GAGGAGGTGCTCTGGAATTTGGAAGATGCTACACAGTGAAGTCTGGGATATACATTTTTG1440GTACCCAGTAAACTCATGTTCAGAGAATAAGGCCTTAGTAGAGCCATATATGTGAGATAT1500TTGGAATCATCCAAACCTGTAGCA AAGGTTAGATCCTGGTTTTTGTTTCTCAGATGTCTG1560CTTTATATCTCAAAACAACAAGCAAAATTTCTTGGCTCTGTGAATATGCAATTCTGTTCT1620TAGATTAGAGAGAAGCTTTACTCATGTGGTTTGGAAGGCTTCCTTTCCTAGTTGTTTTCA1680GTGTGTGAGAAGCACTACATTTTGAAGGTCAGAGAAGTCATGACACATTATAGGTAAGCT1740CATCAGCTTCTTACTTCACAGTGAGTTCTGAAAGGCATGATGCATGCAGTCCAGTAAGTG1800ATGGTCATGATGTTCTGGTTCAGAACATTTGGGTTTCCCTAC AGGTGTAATCGGTATGAA1860GTGAGTCATTAGTCATTGCATTTTCTGGAAAAGTCGGTAGAGAAAAGTTTAAGTGAAATG1920TAATACAGTGTTATAATTCACTTTTGTCACTCACAGGAGAGGATGATGTTTTGCATCAGG1980CTTGTTTACTGAAAAAG CTTATTATAGCCTGGTTCTTATGCTAAGTACTGGCTAAAAAAG2040AATAGAATGTGCCAGGCACGGTGGCTCACGCCTGTAATCCCATTACTTTGAAAGGCTGAG2100GCAGGTGGATCACAAGGTCAGGAGTTCGAGACCAGCCTGGCGAACACGGTGAAACTCTGT 2160CTGTACTAAAAATACAAAAATTAGCAGGGTGTGGTGGTGGGTGCCTGTAGTCCCAGCTGC2220TTGGGAGGCTGAGACAGGAGAATCACTTGAACCTGGGAGGCGGAGGTGGCAGTGAGCCGA2280GATTGTGCCACTGCACTCCAGCCTGGGGGACAGAG CGAGACTTCATCTCAAAAAAAAAAA2340AAAAAAATGCACAACTTTTCCAATCTTGATTTAGATTATTTATACTAGGAATGTGTGAGG2400ATGCCTTGAACAAACATGTCCTTTTATATGGTTAAGAAAATCAAATGTTGTAGGATATAG2460AGATAGTGGT AGTAAAAGGTAATGGTGTAGAGATATGTACCTAAGGAAAGAGAATGTCAT2520GGAGAAACCCTGGGTACTATGGGTGACTGAGCCAAAAAGAAAGTAGTGGAAATCTTATCT2580AAGTGACCAGAAGCCGCACTTCACTGGGCTGCTTAAAGGCAAAAATACTTTTA GCTCACC2640ACTGATTTGCAATATGGGGATGGAGGGGAGCAGTGTTTAAAAGATGCTGAAGATTCCCAT2700GCAATATAGGGAAAGCCAATTTCCCAAGTGGTGATGGTCCAAAGGCAGGAACCTGGCACA2760GACACAACAGTACAAACACTATAGTATT TGCTAATGTTGTGAAGCCATCTGCAATTCAAA2820CTCCCAGTATATATACTAGACATATTCCTCCTGTTTGAATACAAAAACCCACTTCCTCAA2880AGGCTAGAGTTCTTTAAATTGAATGTTAATTCAAGGTTCAAGGATTAACCCTTCAACAAA2940GG CGGATGTGTTAGCCACCAGGAAAAACAATTCGGGGAAGGGTTAGTTTGACTTTTAGCT3000ATTATTTATCATTTCTTACCCAAACTTGTTTTCACATCTGAAGGACCAACAGGATAAAAG3060TTGATACATTAGGGACTTGAAGTTCAGAGTATTATTAAATCATTTC CAACAAATATATAT3120AAACAGCGTCTTCCGGGCAGGTCAGGGCTTAGCTCAAGTCACTTTCAGTTGCTGTGCCTC3180AGGGAGGATGCTGGTTAGACCTCCCACTGAAAGATTTCCATTGTTCTTCTAACTTTTCTA3240GCCAAACATGATTCCAGTTA ATGTAACAATCTCATAGCCTGGAAAGAAACTGCCAGCCTG3300GGAAATCTACTTTTCTGGCCTGGGAAGTATTCTGGTGAGCACTGAGGGAAGGGAGTAGGG3360GTGTTGGAAAGAAGACTTGAAATTCCTTTGTGTTATCTGTAAATAGAACGTTCTAACTCT34 20TTGGTCTCTTCTTCCTCCTCTCCCCCAACCCCCTCTTTCATCATTTTCAATTATATATAG3480GAGGTTGGAAAGTTTCTCTTGAGCTCTTAACCCCAGTCACCTAAATACCCTTTGTGAGGG3540AAACTGGGTAAGAACAATTAAAGTGGAAGGCTCTCCTAC CCTGGTCTTGCTCTTCCCCAA3600TTCTCCTCTAGCTCCTCCTCCCTTTATCTCTCTCTCTTCTCATAAAAGTGCTTTAGTTGA3660GGCTTCCTAGGATTCACCCTCCAGCTCCTATCTGCACTTGAAGCCAGGCTGGGGTCTGCA3720CTTGCAATTAGTA TGTCTGTTGGACTGGGCCACGGTATCCCACCTGGCCACTGCCGCATG3780CCTCCTCAGTGCATGCCGGGGCTCCTGGTCTCTCTAGCCTGGGGCTTTGGGCTGACAAGT3840CCCCTCTTCCTTGCAGCTCCCTCAAAGTCCCAGACACAAAGGCCTCCAGGATGCTCT GTT3900AATGCTTGACTGGAGCCTTCCAAGATTAGAATCAAAGGGGCATTTGGGGGTAGTTTTGGT3960CTTTGAGACTTCAGTCATCCCATATTCCCTCTACCCAATAGAAAGCAGAAGGGGCCTATA4020CTCTCATCTAGCAGCTTCTAGTTCCTCCTAT TTATTGGCCTTTTCCCTTGGCCCAGGGCC4080AAGGCCAGATTTTCATGAATAGGAAAGCTCTCCTGCAGAGAGATGTCAAACATGCCCAGC4140TAGACAATGGCCATGAGCAACAAAAGATCTGTGGGTGATCCTGTAGGAGTTTGATTCCCC4200CAGGCT GCTGTGGGCAGGGCTGTGTGGGTCTTTAGATTGTGTTGAGCAATTGGTGGGTCT4260AGGAAGCTTGATTTTCTGGAGTTCAGTGACCTTGAATCTCAAGTTCTCTGTTTAGTCTTT4320CACTCTCGTGAATGGGTTCAGGTCTGAAGGCCTGTAATTTTTGGGTGCTG AGCCCCGAGT4380TCTGAGCTGAGAGTATCTAAGCTGAGAAGAGCACGGGGTCACAGCCTTGGTAAGTCAGAG4440GCACAGTTCAGCCTCTGTTGGCCCTTGGAGCCAGCAGTTAGTTGTCCTCCCCAGATAGTT4500AATCGTGTTTGTGGTTTTCCCCCT TTAATGGGCCGTGAAGTCAGCAAACTCCCCACATGG4560TGGCTCCCTTTACTAAAGTTGAGTAGTGAATTGTACAAGGAGTCTTGGAAATTTTCAAAT4620ATTTCTCCAGATTGAACTCAACTCAGAATTCGTGTGGGAGGAAAGAGTAAGGATTTTAAT4680GGGGTTCACCTTTGACGTGAAGCAAGGCGGAAGACAGGAAAGCCACAGTGGGGAATAGCT4740TTGGGCGCTTTAGTAAGAAAGACATCTCTGCTTGATTATCTGGTAGTGTTCACCGCAGGC4800TCTTTGTGTGCGAGCTTGCTGCAGAGGCAGAGCTGAACACGG AAAACACGCATGTAAACA4860GTCCAACATAAATCAGTGAGCATATGTATCAGAGAAAAAGAGACATATTCCCATGTAGAT4920GTGGTTTGAAGCTTTATTGAAGGCAGACAATCTGAAGCACGGCCAGGAATAAACTAAGAG4980GAAGCAGACAGTTTTCG GTCATTCATGGCCAGGAATAAACAAAACTTAGTTTTTTTTTTA5040AGAAGGAGGAAGTATTAAATCTCAAATAAGAGCAGGAACAGCATTTAGAAGGAGAAATAT5100AATATCTTGGAAAAAGCAAGCAGAACTAATATAGCTTATTTAAATGTGAGATCCAAATCG 5160TAGTAACAGGAAACCCTCCCACTAAACTGGAATTTCCCCTAATTTTTGTGTAAGATCCAA5220ATAATTAAAATGCACTCTAATGGTTATTGATGGCTCTATTTTCTTTCTTTCTTTCTTCTT5280CTTCTTTTTTTTTTTTTTAAAGAAATAGACCTGAG TTCTCTTACTGGAGTAGAAATATAT5340GAACCTTCTTCAATTACCCAGGAAATTGGAAGCCTCTGGGTGGATATGGTCTTCCCTTAT5400TGCTTTCCTCTTCCCACATCATTTTCAGTTAAAAAAATTAACTGTTTCCAGCAGAGGGAT5460TCCTGTTAGA AACCTTCATCAGGTGAACTTGTACTGGGAACCCTCATGCTTTCCCAGTCT5520GTCTGTGTCTCCCAAACAGAGCTGAAGTTGTAAACAAAGTGGAAAAACATATTTCTCACC5580CCAAAATTCTTAAAATTTCACTTCTTGTGGAAAACACAATTTCACAACATCAA TTTTTAA5640AATCTGTAAGAGCCACAGAAGGTGTGAAAGTAGCCAAACAGCCGGTCTAGAAATCCAAAA5700GCCAGGACTAACGGGGGACAGAATGCTTTTTCCTCAAATCCAGGCAGGGATGGGGAGCAT5760TCTCAGCATTAGGGCATTTATGGACGCT ACAAGGGGAAAGGATGTATCTGAACGGTGGGG5820GTGATTTAGCGATGAATCGCCACGTTAATAGCACTACTGCCAAATCTTCAAATTTAGAGG5880CTCTGGTGAAAAATTAAACCGGTGGCAATTTTCAACGTTTGTAGCATCTGTTACCCTACA5940CT TCAGCACCCGGAGTCTGGACAGCTCCGCAGGCCGCGCTCCGGAGGCAGCATGAGCTCT6000CATCAATCTACTCATAGCCCTACTGTCAACGGCAGCCAGACTCAGGAGAGATTTACTGAA6060AATCCTCCAAGACTTCCCTTTAAAAACAAAACGACTTCCACATTTA ATGGTCTATCTGAA6120AGAACATACGCAAGAAATTAGGAGATCTAAATTAAATTTATTAATAGGAGAGCTTGATGA6180TGCTTAATTCCAGAGACCAGAGCTCCGATTGGTGAGGCTTGATGAAAAAGTAAAGAGAAA6240TCGTAATTGTATAGTTAAAA ACATAACTTTTGTCATCCTCAAAATTCTAAAAATTCTTTA6300CCTGTCCTTGGGAAATGGGTGAAATTGAAAACCATCAAAACAATTGGACTTCTTAAAAAT6360TGGATTGTATGAGTGAAAGGTGTTTATGAGAAGTCGATGACTCCGGATCTTATCATCCAA64 20GAGGACAGCACAGAATAGTTAATATGTTCCTTGAGGGACTAGGATGCTGACGTCTTTTTC6480TGATACCCGATCATTACGTGACTGAGAAAAAAAAAAAGGAAGTCATTTCATGAATAAAAA6540TCGGAGCGCAACAGTGCAACAAAATATTCTGTACTTAAA GGCAACAGGCAGGCAGATGTT6600GACAAAGAGGGCTCTCCAAAAACCATGTTCGGATAGATTTTTGCGAACTGCACAGATAAA6660TAGGAGCAGAAGGCCGGTCACCTCTGTAACCAGCGGTAGCAGCAGCAGAAGCCGCAGCTT6720CAGAGGCAGCCGG AGAGACCTCGGAGCAGAGAAGGCGCCGCCGACCCTCGCGGCTGCCTG6780GCCCGCGGCTCCTACAAAGGCGGGCTAGCCGCCCGCCCTCTCCCTTGCCTTCCTCCCCTT6840CTTTTCTGACTTTCCCTCTTTCCCTTAATCGCCTGCTTCTTCCTCCGGGTGGACTTA CGG6900CCACCTTGCTCCTCCGCGCTTCACCTCATCGCCCCCTCTTTCTTTCTTCTGCCTCTCTCT6960CTGCGCCCCCTTCTCTCCGTGTCACGCTCCCTCCTGGTTCTGCGCGTCTACAAACTTTTG7020AGCAGAACACGAGCCTCGGCAAACGAGTCCC GCAGCTCCTCCTGCTGCTCCCGCTGGTTC7080CTGCGGCTTCTGCTCAGACACCAACGCCAGACGGCGATGCCTCTCGGGTGGTGACTCCAG7140CGCAGGAACTTGAAGAAGCGCTTTGCCCGCCGTCCTACCTGGCAGCTCTCCTGGCAGCGG7200GAGGAG TTGAAGGGTAAGGGAGGGAAAATCTTACCAAAGCGACCGGCTCACTCGACTGCT7260GATTCTTTCGCTTGGCGTCGCGTCAGGGGAGTTAGCTTTCCTTCAGCCGGGTCTGGCTAG7320TTATTGGGCGCCGGGTAGATGCATATATATATATTTTTTTCTAACTATAG CAAGCAAGAA7380GTGGCAGGGCGCGCACCGGCTGTCGCCAAGTGCTGTTCAACTCAGGGAGCCGGGGCTTCG7440CTCCGTCCCTCCCCCGGCTTCCAGAGCTTTTTGGGGTTGGAGGGTGGGAGGCCAGGGGCG7500TTCTCACAGCTGTGTGTCCTCTTT CCCATCCTGCGCAGAATGACCATGTGTAGC7554MetThrMetCysSer15GGAGCGAGGCTGGCC CTGCTGGTCTATGGGATAATCATGCACAGCAGC7602GlyAlaArgLeuAlaLeuLeuValTyrGlyIleIleMetHisSerSer101520GTCTACAGCTCA CCTGCCGCCGCCGGACTCCGGTTCCCCGGGATCAGG7650ValTyrSerSerProAlaAlaAlaGlyLeuArgPheProGlyIleArg253035TAGGTGCTGGCTGC CTGGCCCAAGCAGGAGCTGGGGCTCCCCAGGCACAGACGCTTCCTC7710ACGGTCTCCTTCCTGCAGTCCTTTGGGTCCAGACTACTAGCATCGCCCTCTGCGCCCCCG7770GTGCGCCTCCGCCAGCCTCGGCTGGACAGCGGGTCCCCATTCTAGCCGAGGGTCTGGC AG7830GCTCCGCGACTGCTCGGACGCCTCCCCCAGCCCTAGGCAGCTCAGGGTCCCGGGTAGAGC7890CAGTGAGCTTCTGGCCGCTGGAGAACCCCCCCTCCCCCAACCCGGCCCACAGGATGGGGG7950CAGGGCACGGCCCCTAGCTTGGTTTCTTTTAC CTATTCTTGGGACGAGTTAGGAGAACTT8010CAGCTCTGGAGCCTGGCCGGGGGTTGAGCGTGAAGCTCCCTCGGACTTTGCTTTGTTACT8070GCTTGTTCTGGACTATCCGGGTGGGGTCTCTCTCTCTCCTCCACCCTTTCTTTTCATTTC8130ATTCCAA TTCTTTCCCCTGAAGAGCTTTCTTTCAAGTGATCCGTGTTCCAACTGCATTTT8190GAATCCCAGGCTGTCTTGGGGGGCGTGCGGTGGGGAGGGTGTTGGCCCGGTGTGATTGAG8250GAAAAGCGACTTAAGAGAGGGAAGAACAAGGACGAGACTGCGAAGGAGGG GGAAAAACAG8310GCGCAAAGGAGGAGGAAGGGAAAGCCAGCAGGCAGGCAGGACCGGGAGAGCAGCCCTGCC8370TGGCCCGGGATGGAGGAACCTTGGCTTTTTTCTTAACCCCGGGTTTCTAACCCGCAGGCG8430CGGCCCAGGTTCCCGGAGGCAGCCC CAGAGTCGCGGGCCGATGTGCCAGGCTGTGGATGA8490GCCCCGGGTAGGGGAGGGTTCGTACCAGCGGCGCCTGGGGCAGCGAGGAGCGCGCGTTCT8550GCCTGCGAAGCTGCCTTCTCCGAGCCCCGCCCAGGAACATTAGCTCTGGGGGGCCGCTGA8610 TCATTGATTTGGACGGAGAGATGGGTTCTGGGTTCTGTATTAGGATTCCAGCATCTGGGC8670TCGAGGCAGGGCAATATCCAGAAAGACCCCAGGGTTCGGGGTACCCGGGCCAGGGCTGAG8730GCGCATCGCCGAGCAAAGGCTGGGTGCGAGGCGTGCGGAATGA TGCGCTTGCCTTGCCCG8790GGCCTCTCCAAGGATGGAGAAAAGGCGAGTGAAGTAGCGAAGTACGACTCCAACCCCGCC8850CAGAGAGTGCTACTAGCGCTGGCTGCACGCCAAGTCTCTCCAGGGGTCCAAAGCGAGAGG8910GATTTGTTTTAACCCATC TCTACCCGTCCTGTGTCAAGAACGGAGGCTGTAGAGGGCGAC8970TGCGAAGTCGCCAGGCACTCGCTGGATCTCGGTCCCCCTCCTCGTGCTCTGGGGTTGAGA9030TGGGGCACCGCCATCGATAACAGATCAGCGCGAACTATTCGTTTAGTGGCCTTAAAACAC 9090CCTGGTTTCACCCTCAGCTATTTTCAAGTTCCCGTGTGCCTGGCACTTTCTCCGTGCGAG9150AAGCACCGGAGGGTGCGGACGCGCCACAGTCTGAGCCGCCGCCGAACTGGCTAAGTTTAG9210GGGCATTTATTATTCATGTTCCTGCCAGATCCTCGC CTGCCCAAAATAGAAACCGAGGTT9270CTCCGTGACCTACATCTGCTCGGGGAAGGGCTCCCCTGGGCTCGGAGGCTGGGGTGGGGG9330TGGCTGAGGAGTTGGCCCCCGCACGCCCCACGCATCCTCTCCTTTGCTTTCTGGGCCTCC9390CCATTCGGGT CTTCGCGTGGGTCAGCGCCCGGTCTCCCAGGGCCTTTCTCGTCCCCGCCC9450GTTGCTGCTTTGGGGAGGCTCGGGAGCCAGGCGGGGAGGGGGGCGGTCCTTTTCCGTAGA9510CAGGTGTGCGCGATCGGCGGAGACGCCTCGGTTTCCCAGCGCTTGTTGAGGCCG TGGCCC9570GCAGGACGACCCTTTACCCGCGAAGGGGGGGTGGGCGGGACCGCCCGGCGGGGTAGGAGT9630GGTTGGGTGTCGTTGCCTCCTCCTTACCTCTGCTCCCACCCCCAGTCCTGGGAGAAGAGA9690CAATTCTCAGCGGAGGACTTTTATCACCT GTGAAAATCCGCGCGAGCCCCTTACTTTGGA9750TCCTCGCCGAGCTGGGGAGGAACTTGCACTGACCACACCTTCTGTCCCCGGCCACCCCGC9810AGGCCAGAGGAAGAGGCGTACGGCGAGGACGGAAACCCGCTGCCAGAC9858 ProGluGluGluAlaTyrGlyGluAspGlyAsnProLeuProAsp404550TTCGGTGGCTCGGAGCCGCCGGGCGCAGGGAGCCCCGCCTCCGCGCCG9906Phe GlyGlySerGluProProGlyAlaGlySerProAlaSerAlaPro556065CGCGCCGCCGCCGCCTGGTACCGCCCGGCCGGGAGAAGGTGAGATTCGC9955ArgAla AlaAlaAlaTrpTyrArgProAlaGlyArgArg707580GCGGCCTCGCGCACACCCGCGGCTGGGAGCTCGGGACTGCGGTGACGGGAGGGGCAGTGT10015GGTGACCCACCCAGGATTTTTTTTT TTTTTCCCGTGAAAGTCCTCAAGCCTGTCCTCTCC10075CTGGCCCGATCCTATTGCAGCGACAGAAAATCAGCAGCGGGCGGGTCTGTGTGGACCTGA10135GGGCCGCGTGGGGACCGAGGGGGGCTGTGGCCCAAAGAGTGGCAGTGAGTGGCGTCAAGG10195 AACCCACACTCCGCATCTGCCACTCCTAGAGCCGGGACTAGCTCCCGATCCTAGCAGTTG10255CTCTCGAGATCATCCCGGGAGTTATTGGCGAGTTCTGGGCCTCTGGAGGTTTCCCTGTCA10315GCCTCCCCGGCCGCCGAGGGGGCGCGCGCCCAACAAGGGGGTC TCTAGCGGCCACCTGGG10375GACAGAAACAGTGACCCTGGGCGCGCACTTTGCCTCCCCGTTAGAGATGTCGCC10429AspValAlaCACGGGATCCTTAACGAGGCCTAC CGCAAAGTGCTGGACCAGCTGTCC10477HisGlyIleLeuAsnGluAlaTyrArgLysValLeuAspGlnLeuSer859095100GCCGGGAAGCACCTGCAG TCGCTCGTGGCCCGGGGCGTGGGG10519AlaGlyLysHisLeuGlnSerLeuValAlaArgGlyValGly105110TAAGAGTTTGTGGAAGGATTAACCTGCGCGCGCCGGGGTGGGT GCCTGTGCGGGGCGCGC10579GGGGCGGGCGGCGGTGGGTGCCCGTGGGGGCCAGGGTGAGTCTGCGCCCCTGGGTCTGGG10639GTGGGCATCCGCCACGGGTCGCAGTTGGAGATTTTGAAGTGGCACTTTAAATTTGCCCAG10699AGAGCTCTGGAAGAGGCA AAAAGGGAACGCGAGCCAGGGAGTTTGATCCGTTTTGAATGA10759AAAGAAAGAGAAACCAAACCAAACCTCTCAGTCATCCAAAACCTTCAGGCTTCCAGGGAG10819GTTTTGCTATAATTTTCTCTAAGCATGACTGTTTCTGGGGGAGGGGAAAGGGGTGGTTGT 10879ATTTACTGAAAATTCAAATCGAAATAATAAATGGCCAAATGTGGACACTTATGGACCCAA10939ACAGTTTTGCTCACGCCAGAGAAACTGAGAGCACAGGGCTTGCGTGAAGCCTATCTCGGC10999AGAAGGCAACATTCTAATAAAGCCCGTGGGAAAACA GATTACATTTTCGCCATGAATAAG11059TCATGCAGTGAAAAATATTGCCTACAGCCTGTCGACTTATATTATTATCACGTTTTTCAA11119CTCGGCGTGAGGAGGGAGAGGAGTGTTCATATTTGACTAGGAATTGCAGGATCGATGCAA11179ACTCCAGGGC AGCAGCCAGACTGGCATATGTAGGGCTCTCCGGTTACTTTCTCTGTATGT11239CGCGGGTGAGAGGAACAGCGAGGACAATTTAGCGCAAACACACGAAGGGTCGGATCTCAA11299GGGGGCAGCGCTGGGAGAAAGGTTAGGCTTGAAGCGCGCGTCGCCTGCCCGGAT CTTATC11359CCGGGCCCCCTCCGCAGGGTTTGGTGCCAGGAGATCCTGCGTGGGGAGGGGGGCATCGAG11419GGGCTGCCGTCTCGGCCCTCCCCACGGCTGCTTCCAGGCAGAGGCGGGCGACGCGGTGGG11479CAGTGCGAGCCCCGGGCCCTCCCCGAAGG CTCCCGCGTGGGGTGGGGCCCGCCTGCTCCC11539CGCGGCGATTGAACCTGTGTCTCCCGCCCCGCCACCCTCTTCCCGACCCCTTTGCTTGCA11599GTGGGAGCCTCGGCGGCGGCGCGGGGGACGACGCGGAGCCGCTCTCC11646G lySerLeuGlyGlyGlyAlaGlyAspAspAlaGluProLeuSer115120125AAGCGCCACTCGGACGGGATCTTCACGGACAGCTACAGCCGCTACCGG11694LysArgHisSe rAspGlyIlePheThrAspSerTyrSerArgTyrArg130135140145AAACAAATGGCTGTCAAGAAATACTTGGCGGCCGTCCTAGGGAAGAGG11742LysGl nMetAlaValLysLysTyrLeuAlaAlaValLeuGlyLysArg150155160TATAAACAAAGGGTTAAAAACAAAGGACGCCGAATAGCTTATTTG11787Ty rLysGlnArgValLysAsnLysGlyArgArgIleAlaTyrLeu165170175TAGCGATGGGTTACCAGCTACCCTGTGTATACAGCCCTGACGCAATGAAAAGTCGTTTTC11847CAAAC TGACTCAACAGTCATCGCTCGTGTGTTCTATCCAAACATGTATTTATGTAATGAA11907GTAAAGCCATTAAATGAATATTTTGATAATAATATTGTTTTTCTTTCTACAAAGCACTAG11967AGAATGCACAGATATACTTTGTGGACCAATTATTGATATATATTATAAA TATATATAAAG12027AATATATATATATATATATATATAAAGTATAGAGAGAAGTTCATACAAAGCGTGCACAAG12087GATTGAAAATTCGCCCGAGCTGTTTATGTTTTTATAAAAATAAATAGAAAAGTAGACAAT12147CATTGTTTTGAATATTACTCCTA TTTTTGTAAACTGGAATTAAAAGGATAGTATTTTTAT12207CCATGACAGGCCTGAAGATATTACTACTTACCATTTGCTACTGTACATAAACAATGATGC12267CCTGCTCCAGGGAGATTTTGAGGTAAAGATATGGAGAATTGCTGAAGGGCATTCTTTCCC12327AGTGAGTCTCTGGGGCAGGCTGCTTCAATCCCAGCCTAACTCAACTGGGCTCTGTCCCCC12387TGGTTGGGTGGCAATTCCAATATTTCTGCTTTCTTTGATTCTCCTTTTATGTGTAGTTGT12447CTCTCTTCAGACTCTCAGCCCAGAAGAAAATTCTCCTGATA AAACAACAGCTCGATCCAA12507ATTGTGCTTCTCCCCAGAATTCACGCCTCTCCCTAGGAGAAGAGTTGAGGAACTGTACAG12567AAAAGGGCGGCTTCGTTAGACCGCTCTCTTTTCTGTACTTCCTGAGTGGCCAGGGAATCT12627AATATCCCCAAATTAG GGCAATTGGAACAAAGTGAAGGACATAGAGGTATATTGGAAGAG12687GCAGAGCCTGAGGTGGTAGGAGGACGACCCTGGAAATGGACTGGTTTGAGATTGCCCCAG12747GTCTGGGAAGCTGAGGGCAAATCCAGTCCCAGTGGTCCTGACTTTGGGCGCTGGGTATTG 12807GAAATGGATGCAAAGTACAATGTGTTTTTCTCCAGTGCTGTCCATGCTTCTCATCTTGTG12867AAATGGCCAGGATCCTCTCCTTTGAAACCTGCTCTGTAGGAGCTACCCTTTTCCTTTGTG12927GTTTTATGGAGACCTCTCCTTCCTACCCTCCTGC ACTGTTTAAGTACTGTTTACCATTTT12987TCATTCACTTCTCTTAAACTTGTGAATGCTTCTCACTTTTTTTTTTGTTTGATGCAGGCA13047CTTATTGTAAATTTTAGAAACCCCTCTGTAGCCACTAGTAAGTAATTATGCACTAAATAT13107GAACCCTTT GTTTCTTGTTTATTGAGTTTGTAGGTAAAATGTATTTTTCTACATTATTGC13167TTATTGCTTAGTAAAATTTATTTCATAAAACCAACCTTTGTCATATTAGAATGTGTAGTG13227TTCACATGTTGCTCAGTTTTGCTAACTGATAAATCATTTAATCCTCTTCTTC ATATGTAT13287GAGTACTATCTTATATCTGTGGTCAAGAGTGAGGTAAGCAAGCTCCAACAGACCCTGAGA13347ACCTACGCTTGTATCCTTTCTTTGGCTAAAGAAAGCATGTCTGTTTCCTGTCAATTCTTT13407GAACATACAGAGTAATCTTTATAAACA AAAGAACCTTCACCCAGCAATCAGATCGAGCAG13467CAACAGACAAACCAGCCAGCCAATCTCCCAAATTTCAGGCACAAGTTTATTTTTTTTTTT13527TTTATGTTTTGAAAAAAGAAGATGAAGAAGAAGAAAAAAAAAAGAACAAGGAAAGATTAA13587A CGTTAGCTTGTAAAGTTTAAAGGACCTTTCCTTTTCCTTTACGGATTTGATCAGTATGA13647AGTCATAAATCAAAGAAAACAGAATTGGATTTGCATTCCCAGGCGGGATGGATGCTGCCA13707GGAGATCACATTGCAAATAGTGAAAACAGAGGCATTCGGTCTATG CCTGAGTCCTGTGTA13767TAGGATCAATCTTCCTTTAATTCCGCAGTCTCCTCAGGCAATGTGACACGGGATGCAGTT13827TGCAGCTTTAGTGCCTTTCTTCGCCTTTTAAATTGCCACGAATCACAGATGGCTATTTAG13887TGGCCCTACAATGCTGCAAC ACATCAGCTTGCATTTTAGTCTTAATTATTTGTTTCTTGG13947ATAATGGGCAGAGTTTTCTGTATTTGTATCGACTGTTAGTGGTGAAATAGGGCTCTAGTT14007AACCTTTTATTTATGAAGTCTAATTTAGTGTTCCCGTGGCTAGTTGCAAGCATTTTACAG14 067TGATCACCCAGTTTAATCTTTTGTATACTTTTTAGAAATGCCAAGAGCCTTACTAAACTG14127AAGCAGATTTATGATATAGTGATAATTTAGGTAGATGTTAGTCTTGAAGCTCTTATTTTG14187TGTGCAACTGATTATAAAAACACCTTAACCAAGTATTA TTACACACATGATATCTATAAC14247TAGGACTTTGATAACTGTTATATAAAGTGTGTAAAATTTGTATGAATAAATTTTTGTAAA14307CAATGCAACTTGGTCTAATGTTTGGGAAAAAAGACATTCAGGAAATAATTACTTTAAAAT14367CTCTTAAAGTAT TATATTTCTTTAGCAACCATAAGATTTTTTTACGTCTGGAATATATAT14427CTATCTAAGCACCCTTGTATTTTCATGAACTGCACTTTAATAATTGATGGGCAACTGGAT14487TCTGCTAAAAATTTAAAGTAGCTACTCAGATGGAGATGCCTAAGAAGGTTTTAAGC TCAT14547AAACAGGCATGATGTTGCAACATTATAAGACACACAATTTAGATTAATTTCCATCCCCTA14607GTGTGTATATACTTTGCTCAATATTCAGAAAGTTACTAGGTAGTAGTGGGAGACAATGCT14667GGAGCATTAGTTACACATCTAAAATAGCAA TCTAACATTGTTCTTTTATTTTTTATTTTA14727GTGGCCAGGTCTCACTATGTTGCCCAGGCTGGTCTTGCTCAAGCGATCCTCCCACCTCAG14787CCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCACACCCAGCCTAAAATAGGGATCT14847AACAT TGTTCTTATACAAGTAACTCTGCAGACTAAACTTGTCTTGATAAAATTTTGTATA14907AAATGATCTAAATAATCAGTTTTTGGAGGTTTTAAAATGTATTTAGAGACATACAAACTA14967CTGTCTCTGATTAAAATGCTTTAGGTAGAAGGAACGTGAACATGAGTAA GTAAAGAGTTA15027ATTAGATGCCTTTAAAAGAAAATGTACTTTGAAGTCCAGGAAGAAACACAAGAAGTCATT15087TGTGGATTGTATGCTTTCTTAGTTCATATTTACAAACTTTAGGGCAAAGCTTTCATACGA15147AATTCCTTCAAATTCCGTAGTGG TGTGTGTTTTGGCACCTTTGACTATTTCTGGCTTAGA15207AAATGTATAGAAAGTCACACAATAATTGACATACCATTTAATTTAAAATGCCAGGGTTTC15267ATCCTAAAAATTAATGGTCTCAATTAGTAAATCAATAAATATGTTACGATAGAATTAAAG15327GATGAGTGAGGATTCTAAAATTATCTTCAGAATTTAGCTCAGTATTTAAGGCCTAGAATC15387AAATAGGGAGGAGCCCACAGTCTAGAAATCCCGTTTGTAGTCAATGAAAAAATGAATCCA15447GTACAGTTCATATTTGCATTTGATTTTATTGGATAAGGAAT TTTTCTTCTCCATCTTTAA15507CTGCCCCTCTTTGTCCTTGAAGACATAGTGTGGTAGATGAAAAAATGAAGAAGACTTTAT15567TCGGTTGGGGCTAGGCTAATGACTTGTCAAGAACATAAAGATAAACCCCAGACTTGGCTG15627ACTTCAAGTGAATTTC ATGTATTTAGCAACTTGCCATATTATCTTCGGTGATAACTCAAA15687TTACATCTTTTTAAAGGCAGACTTGATACATATGGGTATTCAAGAAGCTGTAATAGGTGC15747CTTAATGCTGTTAGGGCGGAGAACACACTTATTCAATACAATGCACACTTATTGAACACA 15807TGAAATGGGCCACCGCACTGGTCGAGAGAGCTTGACTAACACCTGGGAGCTCAGGTAGTA15867TTTTTTTCAGAATGTTTTTCTGAAATGTGATCATCTTTGGGGCGGGGGGAGCTTAAAAAT15927GCAAAATTGTAGGGCTCTGCCAGATCCAGTGAAT CTGCATTTTAAATAAAAACCCTAGAT15987TACTGTGCACTAAAATTTGAGACTGCCTAGATTTAGAATTGGTGACATATGTAGGCATAC16047ATATGTGCTGGTCTGAATGTTTTTTTCATATGAAATAAGCAAAAGGTCATGTTACCTGCA16107TACAGTAAT AAATACATAACTGTGCCATATTCTTCCAAGATATCTGGTCATTAAGCTCTT16167TGACAATTTCAGTATTTCCTTTAGGTCACTAAAACTACTAGTTAGCATTATTTTACTTGT16227ACAGTCTGGTTGGACCTCTCCTACAGGAGCTTGTGGAAGGAGAGTGATCCTC TAAGTTGG16287GTCCAAAATATTCAATCACAGGACTAAGAGATTATGGCTATAATGAGGAGAACTTGTGCA16347GCTAGCTAGCCATAATTCTGGGGATCCAGAAGTCAACTTCCAGTTGCATTATATCCCAAT16407TTGGTTTGAATGTATTTACTGCTCCCC AACTGTTTACATGATGGTTTCTCTTGGATGGCT16467CACTATGACCTTCAACCCAACCCTACTGTTCACATGATCACAAGATTGGAAGCCAAGATC16527AAGTCATCCCTCTTCTCTTTTGTTGCCACTCTTTTTTGTAGAAGGGAGATGCCAGCTGCC16587C CTGCTGCTGCAGATTGCATCACTGCTGGATTCTTACATTGGTTTGTAGTTGGTCATCCT16647GGTCACTTCCCCTGCAACCACATAGTTTTAGCTCCATCTTAGTATCATGTCCCTCTGATC16707AGATGTTCCAGAGTAGCTTCCATTGTCAAAGGGTTAAAGGGTTTA AGGTAATCAGTAGTC16767AATTTTACCTCTCTGTTCTTCAACACGATCCTTCCTCTTTTTTTTGTTTTGAGAAAGGGT16827CTTACTCTGTTGCCCAGGCTGGAGTGCAGTGGCACGATCTCGGCTCACTGCAACCTCTGC16887CTCCCGGGTTTAAGCGATTC TCCTGTCTCAACCTCCCGAGTAGCTGGGATTACAGGTGCA16947TGCCAACGCGCCCGGCTAATTTTTGTATTTTTAGTAGAGACGGGGTTTCACTGTGTTGGC17007CAGGCTGGTCTTGGACTCTTGTCCCCAAATGATC17 041(2) INFORMATION FOR SEQ ID NO:2:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 176 amino acids(B) TYPE: amino acid(D) TOPOLOGY: linear(ii) MOLECULE TYPE: protein(xi) SEQUENCE DESCRIPTION: SEQ ID NO:2:MetThrMetCysSerGlyAlaArgLeuAlaLeuLeuValTyrGlyIle1 51015IleMetHisSerSerValTyrSerSerProAlaAlaAlaGlyLeuArg202530PheProGlyIleArgPro GluGluGluAlaTyrGlyGluAspGlyAsn354045ProLeuProAspPheGlyGlySerGluProProGlyAlaGlySerPro5055 60AlaSerAlaProArgAlaAlaAlaAlaTrpTyrArgProAlaGlyArg65707580ArgAspValAlaHisGlyIleLeuAsnGluAlaTyrArg LysValLeu859095AspGlnLeuSerAlaGlyLysHisLeuGlnSerLeuValAlaArgGly100105110ValGlyGlySerLeuGlyGlyGlyAlaGlyAspAspAlaGluProLeu115120125SerLysArgHisSerAspGlyIlePheThrAspSerTyrSerArgTyr130 135140ArgLysGlnMetAlaValLysLysTyrLeuAlaAlaValLeuGlyLys145150155160ArgTyrLysGlnArgValLys AsnLysGlyArgArgIleAlaTyrLeu165170175(2) INFORMATION FOR SEQ ID NO:3:(i) SEQUENCE CHARACTERISTICS:(A) LENGTH: 657 base pairs(B) TYPE: nucleic acid(C) STRANDEDNESS: double(D) TOPOLOGY: linear(ii) MOLECULE TYPE: DNA (genomic)(xi) SEQUENCE DESCRIPTION: SEQ ID NO:3:TGAGAAAAAAAAAAAGGAAGTCATTTCATGAATAAAAATCGGAGCGCAACAGTGCAACAA60AATATTCTGTACTTAAAGGCAACAGGCAGGCAGATGTTGACAAAGAGGGCTCTCCAAAAA120CCATGTTCGG ATAGATTTTTGCGAACTGCACAGATAAATAGGAGCAGAAGGCCGGTCACC180TCTGTAACCAGCGGTAGCAGCAGCAGAAGCCGCAGCTTCAGAGGCAGCCGGAGAGACCTC240GGAGCAGAGAAGGCGCCGCCGACCCTCGCGGCTGCCTGGCCCGCGGCTCCTACA AAGGCG300GGCTAGCCGCCCGCCCTCTCCCTTGCCTTCCTCCCCTTCTTTTCTGACTTTCCCTCTTTC360CCTTAATCGCCTGCTTCTTCCTCCGGGTGGACTTACGGCCACCTTGCTCCTCCGCGCTTC420ACCTCATCGCCCCCTCTTTCTTTCTTCTG CCTCTCTCTCTGCGCCCCCTTCTCTCCGTGT480CACGCTCCCTCCTGGTTCTGCGCGTCTACAAACTTTTGAGCAGAACACGAGCCTCGGCAA540ACGAGTCCCGCAGCTCCTCCTGCTGCTCCCGCTGGTTCCTGCGGCTTCTGCTCAGACACC600AAC GCCAGACGGCGATGCCTCTCGGGTGGTGACTCCAGCGCAGGAACTTGAAGAAGC657

Claims

1. An isolated DNA having the nucleotide sequence of SEQ ID NO: 3.

2. A vector in which a structural gene coding for a protein is operably linked downstream from the DNA of claim 1.

3. A vector according to claim 2 in which the protein is human pituitary adenylate cyclase activating polypeptide with 38 residues.

4. A transformant containing a vector according to claim 2 or 3.

5. A transformant according to claim 4, wherein the transformant is a prokaryotic host cell.

6. A transformant according to claim 4 wherein the transformant is an eukaryotic host cell.

7. A method for preparing a protein comprising:

1) cultivating a nerve cell containing a vector according to claim 2, or 3 under appropriate conditions for expression of the protein,

2) accumulating the protein in a culture broth; and

3) collecting the resulting accumulated protein.

8. A method according to claim 7, wherein the protein is human pituitary adenylate cyclase activating polypeptide with 38 amino acid residues.

9. The DNA of claim 1, wherein said DNA when operably linked to a gene directs expression of said gene in nerve cells.