Yamagami Sayaka, Xu Shan Hua, Tsutsumi Makiko, Hori Hiroshi, Suzuki Norio
Division of Biological Sciences, Graduate School of Science, Hokkaido University, Sapporo, Japan.
Zoolog Sci. 2003 May;20(5):591-606. doi: 10.2108/zsj.20.591.
A novel membrane guanylyl cyclase (membrane GC), OlGC8, was identified in the medaka fish Oryzias latipes by the isolation of full-length cDNA (4958 bp) and genomic DNA (14.3 kbp) clones. Phylogenetic analysis indicated that OlGC8 does not belong in any known vertebrate membrane GC subfamily. OlGC8 consists of an extracellular domain (214 residues), a transmembrane segment (19 residues), and an intracellular protein kinase-like domain (284 residues) and a cyclase catalytic domain (228 residues), although the extracellular domain is about half the length (around 450 residues) of other known vertebrate membrane GCs. OlGC8 transiently expressed in COS-7 cells exhibited only basal guanylyl cyclase activity. None of the known ligands (rat ANP, BNP, CNP, and C-ANF) and various medaka fish tissue extracts, which activated OlGC1, OlGC2, and OlGC7 differentially, stimulated basal activity, suggesting that OlGC8 is an orphan receptor. The OlGC8 gene consists of 24 exons and exists as a single copy on the medaka fish genome. Northern blot hybridization showed that a 5 kb-OlGC8 mRNA was expressed in the kidney and the testis at a high level and a 3.3 kb-OlGC8 mRNA was expressed only in the brain. The RNase protection, RNA Ligase-Mediated Rapid Amplification of cDNA Ends (RLM-RACE), and reverse transcription-polymerase chain reaction (RT-PCR) analyses demonstrated that the 3.3 kb-OlGC8 mRNA detected in the brain is transcribed from the second transcription initiation site, and contains an intron at the position prior to the catalytic domain, the translation product of which appears to be a protein lacking the cyclase catalytic domain.
通过分离全长cDNA(4958 bp)和基因组DNA(14.3 kbp)克隆,在青鳉鱼(Oryzias latipes)中鉴定出一种新型膜鸟苷酸环化酶(膜GC),即OlGC8。系统发育分析表明,OlGC8不属于任何已知的脊椎动物膜GC亚家族。OlGC8由一个细胞外结构域(214个残基)、一个跨膜片段(19个残基)、一个细胞内蛋白激酶样结构域(284个残基)和一个环化酶催化结构域(228个残基)组成,尽管其细胞外结构域长度约为其他已知脊椎动物膜GC的一半(约450个残基)。在COS-7细胞中瞬时表达的OlGC8仅表现出基础鸟苷酸环化酶活性。已知的配体(大鼠心房钠尿肽、脑钠肽、C型钠尿肽和C-ANF)以及能不同程度激活OlGC1、OlGC2和OlGC7的各种青鳉鱼组织提取物,均未刺激基础活性,这表明OlGC8是一种孤儿受体。OlGC8基因由24个外显子组成,在青鳉鱼基因组中以单拷贝形式存在。Northern印迹杂交显示,5 kb的OlGC8 mRNA在肾脏和睾丸中高水平表达,而3.3 kb的OlGC8 mRNA仅在脑中表达。核糖核酸酶保护分析、RNA连接酶介导的cDNA末端快速扩增(RLM-RACE)和逆转录-聚合酶链反应(RT-PCR)分析表明,在脑中检测到的3.3 kb OlGC8 mRNA是从第二个转录起始位点转录而来的,并且在催化结构域之前的位置含有一个内含子,其翻译产物似乎是一种缺乏环化酶催化结构域的蛋白质。