Structure of the human VIPR2 gene for vasoactive intestinal peptide receptor type 2

被引:21
作者
Lutz, EM
Shen, S
Mackay, M
West, K
Harmar, AJ
机构
[1] Univ Edinburgh, Dept Neurosci, MRC, Brain Metab Unit, Edinburgh EH8 9JZ, Midlothian, Scotland
[2] Univ Edinburgh, Royal Edinburgh Hosp, MRC, Brain Metab Unit, Edinburgh EH10 5HF, Midlothian, Scotland
关键词
vasoactive intestinal peptide receptor type 2; vasoactive intestinal peptide; pituitary adenylate cyclase activating polypeptide; vasoactive intestinal peptide receptor type 2 gene; human;
D O I
10.1016/S0014-5793(99)01135-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The VPAC(2) (vasoactive intestinal peptide (VIP)(2)) receptor is a seven-transmembrane spanning G protein-coupled receptor which responds similarly to VIP and pituitary adenylate cyclase activating polypeptide (PACAP) in stimulating cAMP production. Recently, we reported the localisation of the human VPAC(2) receptor gene (VIPR2) to chromosome 7q36.3 (Mackay, M. et al. (1996) Genomics 37, 345-353). Here, we describe the characterisation of the VIPR2 gene structure and promoter region. The VIPR2 gene is encoded by 13 exons, the initiator codon of the 438 amino acid open reading frame is located in exon 1 and the termination signal and a poly-adenylation signal sequence are located in exon 13. The 5' untranslated region extends 187 bp upstream of the initiator codon and is extremely GC-rich (80%), The poly-adenylation signal is located 2416 bp downstream of the stop codon, Intron sizes range from 68 hp (intron 11) to 45 kb (intron 4) and the human gene spans 117 kb. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:197 / 203
页数:7
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