Literature DB >> 7490101

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

L Xia1, K A St Denis, B Bapat.   

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.

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Year:  1995        PMID: 7490101     DOI: 10.1006/geno.1995.1195

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  7 in total

1.  Alternative genetic pathways in colorectal carcinogenesis.

Authors:  S Olschwang; R Hamelin; P Laurent-Puig; B Thuille; Y De Rycke; Y J Li; F Muzeau; J Girodet; R J Salmon; G Thomas
Journal:  Proc Natl Acad Sci U S A       Date:  1997-10-28       Impact factor: 11.205

2.  Constitutional high expression of an APC mRNA isoform in a subset of attenuated familial adenomatous polyposis patients.

Authors:  Tiziana Venesio; Antonella Balsamo; Christian Sfiligoi; Luca Fuso; Sara Molatore; Guglielmina Nadia Ranzani; Mauro Risio
Journal:  J Mol Med (Berl)       Date:  2006-12-02       Impact factor: 4.599

Review 3.  Alternative splicing and disease.

Authors:  Jamal Tazi; Nadia Bakkour; Stefan Stamm
Journal:  Biochim Biophys Acta       Date:  2008-10-17

4.  Molecular analysis of the APC gene in 205 families: extended genotype-phenotype correlations in FAP and evidence for the role of APC amino acid changes in colorectal cancer predisposition.

Authors:  Y L Wallis; D G Morton; C M McKeown; F Macdonald
Journal:  J Med Genet       Date:  1999-01       Impact factor: 6.318

5.  Novel mutations of the APC gene and genetic consequences of splicing mutations in the Czech FAP families.

Authors:  Lucie Schwarzová; Jitka Štekrová; Martina Florianová; Aleš Novotný; Michaela Schneiderová; Petr Lněnička; Věra Kebrdlová; Jaroslav Kotlas; Kamila Veselá; Milada Kohoutová
Journal:  Fam Cancer       Date:  2013-03       Impact factor: 2.375

6.  A novel indel in exon 9 of APC upregulates a 'skip exon 9' isoform and causes very severe familial adenomatous polyposis.

Authors:  Peh Yean Cheah; Yu Hui Wong; Poh Koon Koh; Carol Loi; Min Hoe Chew; Choong Leong Tang
Journal:  Eur J Hum Genet       Date:  2013-10-30       Impact factor: 4.246

7.  APC Splicing Mutations Leading to In-Frame Exon 12 or Exon 13 Skipping Are Rare Events in FAP Pathogenesis and Define the Clinical Outcome.

Authors:  Vittoria Disciglio; Giovanna Forte; Candida Fasano; Paola Sanese; Martina Lepore Signorile; Katia De Marco; Valentina Grossi; Filomena Cariola; Cristiano Simone
Journal:  Genes (Basel)       Date:  2021-02-28       Impact factor: 4.096

  7 in total

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