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.
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Authors | Peter J Tatnell, Matthew Cook, John Kay |
Journal | Biochimica et biophysica acta
(Biochim Biophys Acta)
Vol. 1625
Issue 2
Pg. 203-6
(Jan 27 2003)
ISSN: 0006-3002 [Print] Netherlands |
PMID | 12531480
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Enzyme Precursors
- RNA, Messenger
- Cathepsins
- procathepsin E
- Cathepsin E
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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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