Structure of murine enterokinase (enteropeptidase) and expression in small intestine during development.

Academic Article

Abstract

  • Enterokinase (enteropeptidase) is expressed only in proximal small intestine, where it initiates digestive enzyme activation by converting trypsinogen into trypsin. To investigate this restricted expression pattern, mouse enterokinase cDNA was cloned, and the distribution of enterokinase mRNA and enzymatic activity were determined in adult mice and during gestation. Analysis of enterokinase sequences showed that a mucinlike domain near the NH2 terminus is composed of repeated approximately 15-amino acid Ser/Thr-rich motifs. By Northern blotting and trypsinogen activation assays, enterokinase mRNA and enzymatic activity were undetectable in stomach, abundant in duodenum, and decreased distally until they were undetectable in midjejunum, ileum, and colon. By in situ mRNA hybridization, enterokinase mRNA was localized to the enterocytes throughout the villus. Expression was not observed in goblet cells, Paneth cells, or Brunner's glands. Enterokinase mRNA and enzymatic activity were not detected in the duodenum of fetal mice but were easily detected in the duodenum on postnatal days 2-6. Both enterokinase mRNA and enzymatic activity decreased to very low levels after day 7 but increased after weaning and reached a high level characteristic of adult life by day 60. Therefore, in mice, duodenal enterocytes are the major type of cells expressing enterokinase, which appears to be regulated at the level of mRNA abundance.
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    Published In

    Keywords

  • Amino Acid Sequence, Animals, DNA, Complementary, Duodenum, Enteropeptidase, Gene Expression Regulation, Developmental, Gene Expression Regulation, Enzymologic, In Situ Hybridization, Intestine, Small, Mice, Mice, Inbred C57BL, Molecular Sequence Data, Polymerase Chain Reaction, RNA, Messenger
  • Digital Object Identifier (doi)

    Author List

  • Yuan X; Zheng X; Lu D; Rubin DC; Pung CY; Sadler JE
  • Start Page

  • G342
  • End Page

  • G349
  • Volume

  • 274
  • Issue

  • 2