4.6 Article

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

期刊

HUMAN GENETICS
卷 130, 期 5, 页码 685-699

出版社

SPRINGER
DOI: 10.1007/s00439-011-1003-z

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资金

  1. National Institutes of Health, National Cancer Institute, Center for Cancer Research
  2. Starr Foundation
  3. Breast Cancer Research Foundation
  4. Sabin Family Fund
  5. CRUK
  6. Ligue National Contre le Cancer
  7. Association for International Cancer Research [AICR-07-0454]
  8. Association Le cancer du sein, parlons-en
  9. NHMRC
  10. National Breast Cancer Foundation
  11. Cancer Australia [628333]
  12. Queensland Cancer Fund
  13. Cancer Councils of New South Wales, Victoria, Tasmania and South Australia
  14. Cancer Foundation of Western Australia
  15. Italian citizens
  16. Fondazione IRCCS Istituto Nazionale Tumori
  17. Komen Foundation
  18. National Cancer Institute, National Institutes of Health [RFA-CA-06-503]
  19. ISCIII [RD06/0020/0021]
  20. Dutch Cancer Society [NKI1998-1854, NKI2004-3088, NKI2007-3756]
  21. OSU Comprehensive Cancer Center
  22. Cancer Care Ontario
  23. US National Cancer Institute, National Institutes of Health [RFA CA-06-503]
  24. Cancer Research UK [C1287/A10118, C1287/A11990, C5047/A8385]
  25. NIHR
  26. Biomedical Research Centre, Manchester
  27. Biomedical Research Centre at The Institute of Cancer Research
  28. Royal Marsden NHS Foundation Trust
  29. NEYE foundation
  30. [NIHCA116167]
  31. Cancer Research UK [11174, 10118, 11022] Funding Source: researchfish
  32. National Institute for Health Research [NF-SI-0510-10096] Funding Source: researchfish

向作者/读者索取更多资源

Three founder mutations in BRCA1 and BRCA2 contribute to the risk of hereditary breast and ovarian cancer in Ashkenazi Jews (AJ). They are observed at increased frequency in the AJ compared to other BRCA mutations in Caucasian non-Jews (CNJ). Several authors have proposed that elevated allele frequencies in the surrounding genomic regions reflect adaptive or balancing selection. Such proposals predict long-range linkage disequilibrium (LD) resulting from a selective sweep, although genetic drift in a founder population may also act to create long-distance LD. To date, few studies have used the tools of statistical genomics to examine the likelihood of long-range LD at a deleterious locus in a population that faced a genetic bottleneck. We studied the genotypes of hundreds of women from a large international consortium of BRCA1 and BRCA2 mutation carriers and found that AJ women exhibited long-range haplotypes compared to CNJ women. More than 50% of the AJ chromosomes with the BRCA1 185delAG mutation share an identical 2.1 Mb haplotype and nearly 16% of AJ chromosomes carrying the BRCA2 6174delT mutation share a 1.4 Mb haplotype. Simulations based on the best inference of Ashkenazi population demography indicate that long-range haplotypes are expected in the context of a genome-wide survey. Our results are consistent with the hypothesis that a local bottleneck effect from population size constriction events could by chance have resulted in the large haplotype blocks observed at high frequency in the BRCA1 and BRCA2 regions of Ashkenazi Jews.

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