Chirgwin J M, Schaefer I M, Rotwein P S, Piccini N, Gross K W, Naylor S L
Somat Cell Mol Genet. 1984 Jul;10(4):415-21. doi: 10.1007/BF01535637.
DNA sequences encoding kidney renin were localized to region p21----qter of human chromosome 1 by Southern blot analysis of mouse-human somatic cell hybrids with a cloned human renin DNA probe. The renin gene may be a member of a chromosome 1 linkage group which is conserved in mouse and man. Available evidence suggests this gene is present in one copy per haploid genome. Thus those renin-like molecules detected immunologically in tissues other than the kidney (such as brain, placenta, uterus, pituitary, vasculature, and adrenal) may be derived from this single gene. Since renin messenger RNA in human kidney is about 1550 nucleotides long, reported molecular weights in excess of 45,000 for circulating renin represent posttranslational or postsecretory modifications of the polypeptide.
通过用克隆的人肾素DNA探针分析小鼠 - 人杂种体细胞的Southern印迹,将编码肾素的DNA序列定位到人类第1号染色体的p21----qter区域。肾素基因可能是在小鼠和人类中保守的1号染色体连锁群的成员。现有证据表明该基因在每个单倍体基因组中以单拷贝存在。因此,在肾脏以外的组织(如脑、胎盘、子宫、垂体、血管和肾上腺)中通过免疫检测到的那些肾素样分子可能来自这个单一基因。由于人肾中的肾素信使RNA约为1550个核苷酸长,报道的循环肾素分子量超过45,000代表该多肽的翻译后或分泌后修饰。