Tawaragi Y, Fuchimura K, Tanaka S, Minamino N, Kangawa K, Matsuo H
Suntory Institute for Biomedical Research, Osaka, Japan.
Biochem Biophys Res Commun. 1991 Mar 15;175(2):645-51. doi: 10.1016/0006-291x(91)91614-i.
We have isolated the gene for human C-type natriuretic peptide (CNP) from a human genomic library using a cloned porcine CNP genomic DNA fragment as probe. Human CNP gene consists of at least two coding blocks and an intron, and encodes a 126-residue CNP precursor (human prepro-CNP). From a comparison of the amino acid sequences of porcine and rat prepro-CNPs, human prepro-CNP is found to be processed to generate 22-and 53-residue peptides (human CNP-22 and human CNP-53, respectively) as major endogenous CNPs in human. Interestingly, human CNP-53 has two amino acid substitutions as compared to the porcine and rat CNP-53s, whereas human CNP-22 is identical to the porcine and rat CNP-22s. Intravenous injection of human CNP-53 into anesthetized rats induces diuretic-natriuretic and hypotensive activities with same potencies as porcine CNP-53 does, although these activities were considerably lower (about 1/100) than those of human alpha-ANP.
我们以克隆的猪C型利钠肽(CNP)基因组DNA片段为探针,从人类基因组文库中分离出了人类C型利钠肽(CNP)基因。人类CNP基因至少由两个编码区和一个内含子组成,编码一个含126个氨基酸残基的CNP前体(人类前CNP原)。通过比较猪和大鼠前CNP原的氨基酸序列,发现人类前CNP原被加工生成22个和53个氨基酸残基的肽(分别为人类CNP - 22和人类CNP - 53),作为人类主要的内源性CNP。有趣的是,与猪和大鼠的CNP - 53相比,人类CNP - 53有两个氨基酸替换,而人类CNP - 22与猪和大鼠的CNP - 22相同。将人类CNP - 53静脉注射到麻醉大鼠体内,会诱导出与猪CNP - 53相同效力的利尿、利钠和降压活性,尽管这些活性比人类α - 心钠素(alpha - ANP)的活性低得多(约为1/100)。