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An alternatively spliced variant of cathepsin E in human gastric adenocarcinoma cells.

Abstract
Splice variant and authentic mRNAs for procathepsin E were measured at a ratio of 5:1 and 1:2 in Kato 3 and AGS cells, two human gastric adenocarcinoma cell lines. As a result of the precise splicing of the 3'-end of exon 6 to the 5'-end of exon 8, the variant lacked the 142 bp of exon 7 which encodes the second of the Asp residues that operate the catalytic mechanism of aspartic proteinases.
AuthorsPeter J Tatnell, Matthew Cook, John Kay
JournalBiochimica et biophysica acta (Biochim Biophys Acta) Vol. 1625 Issue 2 Pg. 203-6 (Jan 27 2003) ISSN: 0006-3002 [Print] Netherlands
PMID12531480 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Enzyme Precursors
  • RNA, Messenger
  • Cathepsins
  • procathepsin E
  • Cathepsin E
Topics
  • Adenocarcinoma (metabolism)
  • Alternative Splicing
  • Cathepsin E (genetics, metabolism)
  • Cathepsins (genetics, metabolism)
  • Enzyme Precursors (genetics, metabolism)
  • Exons
  • Genetic Variation
  • Humans
  • Introns
  • Polymerase Chain Reaction
  • RNA, Messenger (analysis, isolation & purification)
  • Stomach Neoplasms (metabolism)
  • Tumor Cells, Cultured

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