Literature DB >> 11284040

A deletion/insertion mutation in the BRCA2 gene in a breast cancer family: a possible role of the Alu-polyA tail in the evolution of the deletion.

T Wang1, I Lerer, Z Gueta, M Sagi, L Kadouri, T Peretz, D Abeliovich.   

Abstract

Patients with breast and/or ovarian cancer were screened for gross rearrangements in the BRCA2 gene by Southern hybridization, with exon 10 and a fragment of exon 11 used as probes. One breast cancer patient with a positive family history had a 6.2-kb deletion including exons 12 and 13. The deletion breakpoint in intron 11 was in the 3' polyA tail of an Alu element, where a track of approximately 60 adenine nucleotide residues was inserted. Expansion of the Alu-polyA tail may have resulted from polymerase slippage during replication, representing a novel mechanism in which Alu elements mediate deletion/insertion mutations. Copyright 2001 Wiley-Liss, Inc.

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Year:  2001        PMID: 11284040     DOI: 10.1002/gcc.1110

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  12 in total

1.  Multiple fates of L1 retrotransposition intermediates in cultured human cells.

Authors:  Nicolas Gilbert; Sheila Lutz; Tammy A Morrish; John V Moran
Journal:  Mol Cell Biol       Date:  2005-09       Impact factor: 4.272

2.  Accuracy of MSI testing in predicting germline mutations of MSH2 and MLH1: a case study in Bayesian meta-analysis of diagnostic tests without a gold standard.

Authors:  Sining Chen; Patrice Watson; Giovanni Parmigiani
Journal:  Biostatistics       Date:  2005-04-14       Impact factor: 5.899

3.  The contribution of germline rearrangements to the spectrum of BRCA2 mutations.

Authors:  F Casilli; I Tournier; O M Sinilnikova; F Coulet; F Soubrier; C Houdayer; A Hardouin; P Berthet; H Sobol; V Bourdon; D Muller; J P Fricker; C Capoulade-Metay; A Chompret; C Nogues; S Mazoyer; P Chappuis; P Maillet; C Philippe; A Lortholary; P Gesta; S Bézieau; C Toulas; L Gladieff; C M Maugard; D M Provencher; C Dugast; C Delvincourt; T D Nguyen; L Faivre; V Bonadona; T Frébourg; R Lidereau; D Stoppa-Lyonnet; M Tosi
Journal:  J Med Genet       Date:  2006-09       Impact factor: 6.318

Review 4.  A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease.

Authors:  Jian-Min Chen; Peter D Stenson; David N Cooper; Claude Férec
Journal:  Hum Genet       Date:  2005-06-28       Impact factor: 4.132

5.  Analysis of BRCA1/BRCA2 genes' contribution to breast cancer susceptibility in high risk Jewish Ashkenazi women.

Authors:  Tal Distelman-Menachem; Tal Shapira; Yael Laitman; Bella Kaufman; Frida Barak; Sean Tavtigian; Eitan Friedman
Journal:  Fam Cancer       Date:  2008-09-17       Impact factor: 2.375

6.  Active Alu element "A-tails": size does matter.

Authors:  Astrid M Roy-Engel; Abdel-Halim Salem; Oluwatosin O Oyeniran; Lisa Deininger; Dale J Hedges; Gail E Kilroy; Mark A Batzer; Prescott L Deininger
Journal:  Genome Res       Date:  2002-09       Impact factor: 9.043

7.  Genomic rearrangements in BRCA1 and BRCA2: A literature review.

Authors:  Ingrid Petroni Ewald; Patricia Lisboa Izetti Ribeiro; Edenir Inêz Palmero; Silvia Liliana Cossio; Roberto Giugliani; Patricia Ashton-Prolla
Journal:  Genet Mol Biol       Date:  2009-09-01       Impact factor: 1.771

8.  LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease: mutation detection bias and multiple mechanisms of target gene disruption.

Authors:  Jian-Min Chen; Claude Férec; David N Cooper
Journal:  J Biomed Biotechnol       Date:  2006

9.  Prevalence of p.V37I variant of GJB2 in mild or moderate hearing loss in a pediatric population and the interpretation of its pathogenicity.

Authors:  So Young Kim; Gibeom Park; Kyu-Hee Han; Ahreum Kim; Ja-Won Koo; Sun O Chang; Seung Ha Oh; Woong-Yang Park; Byung Yoon Choi
Journal:  PLoS One       Date:  2013-04-25       Impact factor: 3.240

10.  Inherited and acquired alterations in development of breast cancer.

Authors:  Piera Rizzolo; Valentina Silvestri; Mario Falchetti; Laura Ottini
Journal:  Appl Clin Genet       Date:  2011-11-14
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