Genomic organization and chromosomal location of the mouse vasoactive intestinal polypeptide 1(VPAC1) receptor

被引:22
作者
Hashimoto, H
Nishino, A
Shintani, N
Hagihara, N
Copeland, NG
Jenkins, NA
Yamamoto, K
Matsuda, T
Ishihara, T
Nagata, S
Baba, A
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Mol Neuropharmacol Lab, Suita, Osaka 5650871, Japan
[2] NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program, Mammalian Genet Lab, Frederick, MD 21702 USA
[3] Natl Inst Genet, Struct Biol Ctr, Shizuoka 4118540, Japan
[4] Osaka Univ, Sch Med, Dept Genet, Suita, Osaka 5650871, Japan
关键词
D O I
10.1006/geno.1999.5805
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The gene encoding the mouse vasoactive intestinal polypeptide type 1 (VPAC(1)) receptor was cloned, and its structural organization was determined. The gene (Vipr1) is more than 16 kb in length and is divided into 13 exons. The 5'-flanking region is highly GC-rich and lacks an apparent TATA box, but contains a CCAAT box, three potential Spl-binding sites, and two potential AP-a-binding sites. Promoter analysis of the 5'-flanking region of Vipr1 using a luciferase gene reporter system revealed that the isolated 5'-flanking region has functional promoter activity. The mouse Vipr1 gene is encoded by a single gene, which was mapped to the distal region of mouse chromosome 9. This region is syntenic with human chromosome 3p, where the human VPAC(1) receptor gene has been mapped. (C) 1999 Academic Press.
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收藏
页码:90 / 93
页数:4
相关论文
共 23 条
[1]   STRUCTURE OF THE GENE ENCODING THE MOUSE PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE RECEPTOR [J].
AINO, H ;
HASHIMOTO, H ;
OGAWA, N ;
NISHINO, A ;
YAMAMOTO, K ;
NOGI, H ;
NAGATA, S ;
BABA, A .
GENE, 1995, 164 (02) :301-304
[2]  
ARIMURA A, 1992, REGUL PEPTIDES, V37, P287
[3]  
BREATHNACH R, 1981, ANNU REV BIOCHEM, V50, P349, DOI 10.1146/annurev.bi.50.070181.002025
[4]   DEVELOPMENT AND APPLICATIONS OF A MOLECULAR GENETIC-LINKAGE MAP OF THE MOUSE GENOME [J].
COPELAND, NG ;
JENKINS, NA .
TRENDS IN GENETICS, 1991, 7 (04) :113-118
[5]   VIP - MOLECULAR-BIOLOGY AND NEUROBIOLOGICAL FUNCTION [J].
GOZES, I ;
BRENNEMAN, DE .
MOLECULAR NEUROBIOLOGY, 1989, 3 (04) :201-236
[6]   Genetic structure and chromosomal mapping of MyD88 [J].
Hardiman, G ;
Jenkins, NA ;
Copeland, NG ;
Gilbert, DJ ;
Garcia, DK ;
Naylor, SL ;
Kastelein, RA ;
Bazan, JF .
GENOMICS, 1997, 45 (02) :332-339
[7]  
Harmar AJ, 1998, PHARMACOL REV, V50, P265
[8]   MULTIPLE RECEPTORS FOR PACAP AND VIP [J].
HARMAR, T ;
LUTZ, E .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1994, 15 (04) :97-99
[9]   MOLECULAR-CLONING AND TISSUE DISTRIBUTION OF A RECEPTOR FOR PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE [J].
HASHIMOTO, H ;
ISHIHARA, T ;
SHIGEMOTO, R ;
MORI, K ;
NAGATA, S .
NEURON, 1993, 11 (02) :333-342
[10]   STRUCTURE OF THE HUMAN PITUITARY ADENYLATE-CYCLASE ACTIVATING POLYPEPTIDE (PACAP) GENE [J].
HOSOYA, M ;
KIMURA, C ;
OGI, K ;
OHKUBO, S ;
MIYAMOTO, Y ;
KUGOH, H ;
SHIMIZU, M ;
ONDA, H ;
OSHIMURA, M ;
ARIMURA, A ;
FUJINO, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1129 (02) :199-206