| Literature DB >> 11284040 |
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.Entities:
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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