Sreedharan S P, Huang J X, Cheung M C, Goetzl E J
Department of Medicine, University of California Medical Center, San Francisco 94143-0711, USA.
Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2939-43. doi: 10.1073/pnas.92.7.2939.
Vasoactive intestinal peptide (VIP) and other members of the pituitary adenylyl cyclase-activating peptide (PACAP) and secretin neuroendocrine peptide family are recognized with specificity by related G protein-coupled receptors. We report here the cloning, characterization, and chromosomal location of the gene encoding the human type I VIP receptor (HVR1), also termed the type II PACAP receptor. The gene spans approximately 22 kb and is composed of 13 exons ranging from 42 to 1400 bp and 12 introns ranging from 0.3 to 6.1 kb. Primer extension analysis with poly(A)+ RNA from human HT29 colonic adenocarcinoma cells indicated that the transcription initiation site is located at position -110 upstream of the first nucleotide (+1) of the translation start codon, and 75 nt downstream of a consensus CCAAT-box motif. The G+C-rich 5' flanking region contains potential binding sites for several nuclear factors, including Sp1, AP2, ATF, interferon regulatory factor 1, NF-IL6, acute-phase response factor, and NF-kappa B. The HVR1 gene is expressed selectively in human tissues with a relative prevalence of lung > prostate > peripheral blood leukocytes, liver, brain, small intestine > colon, heart, spleen > placenta, kidney, thymus, testis. Fluorescence in situ hybridization localized the HVR1 gene to the short arm of human chromosome 3 (3p22), in a region associated with small-cell lung cancer.
血管活性肠肽(VIP)以及垂体腺苷酸环化酶激活肽(PACAP)和促胰液素神经内分泌肽家族的其他成员,可被相关的G蛋白偶联受体特异性识别。我们在此报告人类I型VIP受体(HVR1,也称为II型PACAP受体)编码基因的克隆、特征分析及染色体定位。该基因跨度约22kb,由13个外显子(长度从42到1400bp)和12个内含子(长度从0.3到6.1kb)组成。用人HT29结肠腺癌细胞的聚腺苷酸加尾RNA进行引物延伸分析表明,转录起始位点位于翻译起始密码子第一个核苷酸(+1)上游110位,在共有CCAAT框基序下游75nt处。富含G+C的5'侧翼区域包含几个核因子的潜在结合位点,包括Sp1、AP2、ATF、干扰素调节因子1、NF-IL6、急性期反应因子和NF-κB。HVR1基因在人类组织中选择性表达,相对表达量为肺>前列腺>外周血白细胞、肝脏、脑、小肠>结肠、心脏、脾脏>胎盘、肾脏、胸腺、睾丸。荧光原位杂交将HVR1基因定位到人类3号染色体短臂(3p22),该区域与小细胞肺癌相关。