Evidence for a novel exon in the coding region of the adenomatous polyposis coli (APC) gene

Genomics. 1995 Aug 10;28(3):589-91. doi: 10.1006/geno.1995.1195.

Abstract

Germline mutations of the tumor suppressor gene APC cause familial adenomatous polyposis. Somatic APC alterations are involved in several sporadic neoplasms, including colorectal, duodenal, gastric, and esophageal carcinoma. The APC mRNA is encoded by 15 exons. Additional transcripts have been reported, due to alternative splicing of coding as well as noncoding regions. Two mRNA isoforms occur due to a deletion of exon 7 or a partial deletion of exon 9. We have identified a novel exon, flanked by APC exons 10 and 11, which is expressed as an alternatively transcribed product of the gene. Further, we have shown that the novel exon consists of a heptad repeat motif and is conserved across species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenomatous Polyposis Coli / genetics*
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • DNA Primers
  • DNA, Complementary / analysis
  • Exons*
  • Humans
  • Introns
  • Mice
  • Molecular Sequence Data
  • Mutation
  • RNA, Messenger

Substances

  • DNA Primers
  • DNA, Complementary
  • RNA, Messenger

Associated data

  • GENBANK/M88127