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PMID: 16341810 已发表 · ppublish 英语

Lack of germ-line mutations at the specific BRCA1-IRIS coding sequence in 114 Spanish high-risk breast/ovarian families.

Familial cancer ·第 4 卷 ·第 4 期 ·2006-03-14

de la Hoya Miguel, Fernández Juan Manuel, Sánchez de Abajo Ana, Tosar Alicia, Díaz-Rubio Eduardo, Caldés Trinidad

摘要

A new BRCA1 locus product called BRCA1-IRIS has been identified recently. High-risk breast/ovarian families have not been screened for germ-line mutations at the specific BRCA1-IRIS coding sequence, as it was considered merely as part of BRCA1 intron 11. Here we report the first comprehensive screening of germ-line mutations in a cohort of 116 index cases from high-risk breast/ovarian families in which no germ-line mutation was identified in BRCA1 or BRCA2. We did not find germ-line mutations at the specific BRCA1-IRIS coding sequence in any sample. The only heterozygous patter identified by DGGE was caused by a C to A substitution in the non-coding 3' sequence, 123 bases downstream of the BRCA1-IRIS stop codon (IVS11+268C/A). The data indicates that it is probably a neutral change not associated with cancer risk. Our analysis suggests that the role of germ-line mutations at the specific BRCA1-IRIS sequence in breast cancer susceptibility, if any, is marginal and do not explain a significant fraction of high-risk breast/ovarian families, at least in the population analyzed.

文献信息
期刊
Familial cancer
期刊简称
Fam Cancer
发表日期
2006-03-14
收录日期
2005-12-12
更新日期
2009-11-19
语言
英语
国家/地区
Netherlands
NLM ID
100898211
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