Seki T, Ihara I, Sugimura A, Shimonishi M, Nishizawa T, Asami O, Hagiya M, Nakamura T, Shimizu S
Pharmaceutical Research Center, Toyobo Co. Ltd., Otsu, Japan.
Biochem Biophys Res Commun. 1990 Oct 15;172(1):321-7. doi: 10.1016/s0006-291x(05)80212-8.
Human leukocyte cDNA library was screened to isolate cDNA clones coding for hepatocyte growth factor using cDNA from human liver as a probe. Nucleotide and deduced amino acid sequences were analyzed for two of four clones obtained. One of them contained an open reading frame coding for a polypeptide chain of 728 amino acid residues like that of cDNA clone derived from human liver. In another clone a spontaneous deletion of 15 base pairs was found within the coding sequence. When expressed transiently using COS-1 cells both clones produced protein with similar biological activity against rat hepatocyte in vitro.
用人肝cDNA作为探针,筛选人白细胞cDNA文库以分离编码肝细胞生长因子的cDNA克隆。对获得的四个克隆中的两个进行了核苷酸和推导氨基酸序列分析。其中一个含有一个开放阅读框,编码一条728个氨基酸残基的多肽链,与人肝来源的cDNA克隆的多肽链相似。在另一个克隆中,在编码序列内发现了15个碱基对的自发缺失。当使用COS-1细胞瞬时表达时,两个克隆在体外对大鼠肝细胞均产生具有相似生物学活性的蛋白质。