Kangawa K, Tawaragi Y, Oikawa S, Mizuno A, Sakuragawa Y, Nakazato H, Fukuda A, Minamino N, Matsuo H
Nature. 1984;312(5990):152-5. doi: 10.1038/312152a0.
Diuretic and smooth muscle-relaxing peptides, designated atrial natriuretic peptides (ANPs), have been identified in human and rat atrial tissues and implicated in the control of fluid volume and vascular function. Recently, cDNAs encoding the human and rat ANP precursors have been sequenced. We previously isolated from human tissue a natriuretic peptide of molecular weight (MW) 13,000 (gamma-hANP) comprising 126 amino acid residues, the largest natriuretic peptide so far identified, and showed that it is directly derived from the 151-residue human ANP precursor by the removal of a signal peptide. We now report the isolation and sequence analysis of a novel rat atrial natriuretic peptide (gamma-rANP) of MW 13,000, which derives from the rat ANP precursor. We also report the molecular cloning and nucleotide sequence analysis of the cDNA of the 152-residue rat ANP precursor, which is remarkably similar to the human 151-residue precursor (pre-hANP) except at the C-terminus. Differences in the rat and human precursor nucleotide sequences around the termination codons lead to a difference in processing pattern.
利尿和舒张平滑肌的肽,即心房利钠肽(ANP),已在人和大鼠的心房组织中被鉴定出来,并与体液量和血管功能的控制有关。最近,编码人和大鼠ANP前体的cDNA已被测序。我们之前从人体组织中分离出一种分子量为13,000的利钠肽(γ-hANP),它由126个氨基酸残基组成,是迄今为止鉴定出的最大的利钠肽,并表明它是通过去除信号肽直接从151个残基的人ANP前体衍生而来。我们现在报告一种分子量为13,000的新型大鼠心房利钠肽(γ-rANP)的分离和序列分析,它来源于大鼠ANP前体。我们还报告了152个残基的大鼠ANP前体cDNA的分子克隆和核苷酸序列分析,该前体除了在C端外,与人151个残基的前体(pre-hANP)非常相似。终止密码子周围大鼠和人前体核苷酸序列的差异导致加工模式的不同。