Literature DB >> 3969306

Maturation of sucrase-isomaltase complex in human fetal small and large intestine during gestation.

N Triadou, A Zweibaum.   

Abstract

Sucrase-isomaltase complex is expressed in human small intestine throughout gestation and in the large intestine between 12 and 30 wk. The molecular form of the enzyme was studied in the brush-border membrane fractions by the immunoblotting method. Before 30 wk of gestation, the enzyme is present only as the high molecular weight prosucrase-isomaltase, while from 30 wk until birth the two subunits are also present. The fetal enzyme, as its proform and as its two subunits, has a faster mobility in sodium-dodecylsulfate polyacrylamide gel electrophoresis, than the adult enzyme (removal of sialic acid residues from fetal enzymes emphasizes this difference). The colonic and the small intestinal fetal enzymes are identical.

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Year:  1985        PMID: 3969306     DOI: 10.1203/00006450-198501000-00035

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  5 in total

Review 1.  Ontogeny, growth and development of the small intestine: Understanding pediatric gastroenterology.

Authors:  Laurie A Drozdowski; Tom Clandinin; Alan B R Thomson
Journal:  World J Gastroenterol       Date:  2010-02-21       Impact factor: 5.742

2.  Clonal analysis of sucrase-isomaltase expression in the human colon adenocarcinoma Caco-2 cells.

Authors:  J F Beaulieu; A Quaroni
Journal:  Biochem J       Date:  1991-12-15       Impact factor: 3.857

3.  Intrinsic factor receptor during fetal development of the human intestine.

Authors:  H Schohn; J L Guéant; B Leheup; M Saunier; G Grignon; J P Nicolas
Journal:  Biochem J       Date:  1992-08-15       Impact factor: 3.857

Review 4.  Intestinal mucosal atrophy and adaptation.

Authors:  Darcy Shaw; Kartik Gohil; Marc D Basson
Journal:  World J Gastroenterol       Date:  2012-11-28       Impact factor: 5.742

5.  The posttranslational processing of sucrase-isomaltase in HT-29 cells is a function of their state of enterocytic differentiation.

Authors:  G Trugnan; M Rousset; I Chantret; A Barbat; A Zweibaum
Journal:  J Cell Biol       Date:  1987-05       Impact factor: 10.539

  5 in total

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