Literature DB >> 8242607

APC gene messenger RNA: novel isoforms that lack exon 7.

M Oshima1, H Sugiyama, K Kitagawa, M Taketo.   

Abstract

The APC gene at human chromosome 5q21 is responsible for familial adenomatous polyposis coli. Furthermore, sporadic cancers of not only colon but also other digestive organs often contain mutations in the APC gene. A dominant mouse mutation Min that was generated by chemical mutagenesis and causes polyposis in the digestive tract is in the mouse homologue of the human APC gene. The APC mRNA is generated from 15 exons. Two mRNA isoforms were reported which are produced by alternative splicing in the 9th exon. Here, we report novel mRNA isoforms that lack the 7th exon in both mouse and human cells.

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Year:  1993        PMID: 8242607

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  6 in total

1.  Allele-specific expression of APC in adenomatous polyposis families.

Authors:  Ester Castellsagué; Sara González; Elisabet Guinó; Kristen N Stevens; Ester Borràs; Victoria M Raymond; Conxi Lázaro; Ignacio Blanco; Stephen B Gruber; Gabriel Capellá
Journal:  Gastroenterology       Date:  2010-04-29       Impact factor: 22.682

2.  A novel coding exon of the human adenomatous polyposis coli gene.

Authors:  Z Suleková; W G Ballhausen
Journal:  Hum Genet       Date:  1995-10       Impact factor: 4.132

3.  cDNA cloning of the rat APC gene and assignment to chromosome 18.

Authors:  M Toyota; T Ushijima; H Kakiuchi; M Watanabe; K Imai; A Yachi; T Sugimura; M Nagao
Journal:  Mamm Genome       Date:  1995-10       Impact factor: 2.957

4.  Loss of Apc heterozygosity and abnormal tissue building in nascent intestinal polyps in mice carrying a truncated Apc gene.

Authors:  M Oshima; H Oshima; K Kitagawa; M Kobayashi; C Itakura; M Taketo
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

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.  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

  6 in total

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