Literature DB >> 10673373

Molecular cloning of neonate/infant-specific pepsinogens from rat stomach mucosa and their expressional change during development.

T Kageyama1, M Ichinose, S Tsukada-Kato, M Omata, Y Narita, A Moriyama, S Yonezawa.   

Abstract

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. Copyright 2000 Academic Press.

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Year:  2000        PMID: 10673373     DOI: 10.1006/bbrc.1999.2047

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  12 in total

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3.  Association between pepsinogen C gene polymorphism and genetic predisposition to gastric cancer.

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Journal:  World J Gastroenterol       Date:  2003-01       Impact factor: 5.742

4.  Mitogen-activated protein kinase activator with WD40 repeats (MAWD) and MAWD-binding protein induce cell differentiation in gastric cancer.

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5.  Identification of Novel Placentally Expressed Aspartic Proteinase in Humans.

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7.  Neonatal- maternal separation primes zymogenic cells in the rat gastric mucosa through glucocorticoid receptor activity.

Authors:  Daniela Ogias; Isadora C Rattes; Larissa Y M Hosoya; Juliana G Zulian; Chao Yun Irene Yan; Patrícia Gama
Journal:  Sci Rep       Date:  2018-06-29       Impact factor: 4.379

8.  A time-resolved multi-omic atlas of the developing mouse stomach.

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Journal:  Nat Commun       Date:  2018-11-21       Impact factor: 14.919

9.  The co-expression of functional gastric proteins in dynamic gastric diseases and its clinical significance.

Authors:  Qian Xu; Li-Ping Sun; Ben-Gang Wang; Jing-Wei Liu; Ping Li; Cai-Yun He; Yuan Yuan
Journal:  BMC Clin Pathol       Date:  2013-08-09

10.  Calcium-binding protein S100A14 induces differentiation and suppresses metastasis in gastric cancer.

Authors:  Min Zhu; Hongyi Wang; Jiantao Cui; Wenmei Li; Guo An; Yuanming Pan; Qingying Zhang; Rui Xing; Youyong Lu
Journal:  Cell Death Dis       Date:  2017-07-20       Impact factor: 8.469

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