Kageyama T, Ichinose M, Tsukada-Kato S, Omata M, Narita Y, Moriyama A, Yonezawa S
Center for Human Evolutionary Modeling Research, Primate Research Institute, Kyoto University, Inuyama, 484-8506, Japan.
Biochem Biophys Res Commun. 2000 Jan 27;267(3):806-12. doi: 10.1006/bbrc.1999.2047.
To clarify the nature of rat neonate/infant-specific pepsinogens, we carried out their purification and molecular cloning. Prochymosin was found to be the major neonatal pepsinogen. The general proteolytic activity of its active form, chymosin, was, however, lower than those of pepsins A and C which are predominant in adult animals. Molecular cloning of rat prochymosin cDNA was achieved along with cDNA for another neonate-specific pepsinogen, pepsinogen F, although determination of pepsinogen F in neonatal gastric mucosa was unsuccessful, presumably due to its lack of proteolytic activity or different proteolytic specificity. Northern blot analysis confirmed that genes for prochymosin and pepsinogen F are expressed only at neonatal/infant stages and the switching of gene expression to that of pepsinogen C occurred at late infant stages. A phylogenetic tree based on nucleotide sequences showed clearly that pepsinogens fall into four major groups, namely prochymosin and pepsinogen F of the neonate/infant and pepsinogens A and C of adult animals. Although, to date, prochymosin and pepsinogen F were believed to be expressed in only a limited number of mammals, the present results suggest that they might be expressed at the neonatal/infant stage in a variety of mammals.
为了阐明大鼠新生儿/婴儿特异性胃蛋白酶原的性质,我们对其进行了纯化和分子克隆。发现凝乳酶原是主要的新生儿胃蛋白酶原。然而,其活性形式凝乳酶的一般蛋白水解活性低于成年动物中占主导地位的胃蛋白酶A和C。我们成功实现了大鼠凝乳酶原cDNA的分子克隆,同时还克隆了另一种新生儿特异性胃蛋白酶原——胃蛋白酶原F的cDNA,尽管在新生儿胃黏膜中未能成功测定胃蛋白酶原F,推测是由于其缺乏蛋白水解活性或具有不同的蛋白水解特异性。Northern印迹分析证实,凝乳酶原和胃蛋白酶原F的基因仅在新生儿/婴儿阶段表达,而在婴儿后期基因表达转换为胃蛋白酶原C。基于核苷酸序列的系统发育树清楚地表明,胃蛋白酶原可分为四大类,即新生儿/婴儿的凝乳酶原和胃蛋白酶原F以及成年动物的胃蛋白酶原A和C。尽管迄今为止,人们认为凝乳酶原和胃蛋白酶原F仅在少数哺乳动物中表达,但目前的结果表明它们可能在多种哺乳动物的新生儿/婴儿阶段表达。