Cardoso J C R, Clark M S, Viera F A, Bridge P D, Gilles A, Power D M
Centre of Marine Sciences, Universidade do Algarve, Campus de Gambelas, 8000-810 Faro, Portugal.
J Mol Endocrinol. 2005 Jun;34(3):753-65. doi: 10.1677/jme.1.01730.
Twenty-one members of the secretin family (family 2) of G-protein-coupled receptors (GPCRs) were identified via directed cloning and data-mining of the Fugu Genome Consortium database, representing the most comprehensive description of secretin GPCRs in a teleost fish to date. Duplicated genes were identified for many of the family members, namely the receptors for pituitary adenylate cyclase-activating polypeptide (PACAP)/vasoactive intestinal peptide (VIP), calcitonin, calcitonin gene-related peptide (CGRP), growth hormone releasing hormone (GHRH), glucagon receptor/glucagon-like peptide (GLP) and parathyroid hormone-related peptide (PTHrP)/PTH. Mining of other teleost genomes (zebrafish and Tetraodon) revealed that the duplicated genes identified in the Takifugu genome were also present in these fish. Additional database searching of the Escherichia coli, yeast, Drosophila, Caenorhabditis elegans and Ciona genomes revealed that the family 2 of GPCRs were only present in the multicellular organisms. Orthologues of all the human secretin receptors were identified with the exception of secretin itself. Additional database searches in the Fugu Genome Consortium database also failed to reveal a secretin ligand and so it is hypothesised that both the receptor and the ligand evolved after the divergence of teleost/tetrapod lineages. Phylogenetic analysis at both the protein and the DNA level provided strong support for each of the individual receptor family groupings, but weak support between groups, making evolutionary inferences difficult. A more critical analysis of the PACAP/VIP receptor family confirmed previous hypotheses that the vasoactive intestinal peptide receptor (VPAC(1)R) gene is the ancestral form of the receptor.
通过对河豚基因组协会数据库进行定向克隆和数据挖掘,鉴定出了21个G蛋白偶联受体(GPCR)促胰液素家族(第2家族)的成员,这是迄今为止对硬骨鱼中促胰液素GPCR最全面的描述。许多家族成员都鉴定出了重复基因,即垂体腺苷酸环化酶激活多肽(PACAP)/血管活性肠肽(VIP)、降钙素、降钙素基因相关肽(CGRP)、生长激素释放激素(GHRH)、胰高血糖素受体/胰高血糖素样肽(GLP)以及甲状旁腺激素相关肽(PTHrP)/甲状旁腺激素(PTH)的受体。对其他硬骨鱼基因组(斑马鱼和红鳍东方鲀)的挖掘表明,在河豚基因组中鉴定出的重复基因在这些鱼中也存在。对大肠杆菌、酵母、果蝇、秀丽隐杆线虫和海鞘基因组进行的额外数据库搜索表明,GPCR第2家族仅存在于多细胞生物中。除了促胰液素本身外,鉴定出了所有人类促胰液素受体的直系同源物。在河豚基因组协会数据库中进行的额外数据库搜索也未能揭示促胰液素配体,因此推测受体和配体都是在硬骨鱼/四足动物谱系分化后进化而来的。蛋白质和DNA水平的系统发育分析为每个单独的受体家族分组提供了有力支持,但组间支持较弱,难以进行进化推断。对PACAP/VIP受体家族进行的更严格分析证实了先前的假设,即血管活性肠肽受体(VPAC(1)R)基因是该受体的祖先形式。