Interhomolog recombination and loss of heterozygosity in wild-type and Bloom syndrome helicase (BLM)-deficient mammalian cells Journal Article


Authors: La Rocque, J. R.; Stark, J. M.; Oh, J.; Bojilova, E.; Yusa, K.; Horie, K.; Takeda, J.; Jasin, M.
Article Title: Interhomolog recombination and loss of heterozygosity in wild-type and Bloom syndrome helicase (BLM)-deficient mammalian cells
Abstract: Genomic integrity often is compromised in tumor cells, as illustrated by genetic alterations leading to loss of heterozygosity (LOH). One mechanism of LOH is mitotic crossover recombination between homologous chromosomes, potentially initiated by a double-strand break (DSB). To examine LOH associated with DSB-induced interhomolog recombination, we analyzed recombination events using a reporter in mouse embryonic stem cells derived from F1 hybrid embryos. In this study, we were able to identify LOH events although they occur only rarely in wild-type cells (≤2.5%). The low frequency of LOH during interhomolog recombination suggests that crossing over is rare in wild-type cells. Candidate factors that may suppress crossovers include the RecQ helicase deficient in Bloom syndrome cells (BLM), which is part of a complex that dissolves recombination intermediates. We analyzed interhomolog recombination in BLM-deficient cells and found that, although interhomolog recombination is slightly decreased in the absence of BLM, LOH is increased by fivefold or more, implying significantly increased interhomolog crossing over. These events frequently are associated with a second homologous recombination event, which may be related to the mitotic bivalent structure and/or the cell-cycle stage at which the initiating DSB occurs.
Keywords: nonhuman; mitosis; animal cell; mouse; homologous recombination; cell cycle; embryo; embryonic stem cell; gene frequency; wild type; gene conversion; reporter gene; chromosome breakage; heterozygosity loss; enzyme structure; double-strand break repair; mammal cell; crossing over; bloom syndrome helicase; recq helicase
Journal Title: Proceedings of the National Academy of Sciences of the United States of America
Volume: 108
Issue: 29
ISSN: 0027-8424
Publisher: National Academy of Sciences  
Date Published: 2011-07-19
Start Page: 11971
End Page: 11976
Language: English
DOI: 10.1073/pnas.1104421108
PROVIDER: scopus
PMCID: PMC3141969
PUBMED: 21730139
DOI/URL:
Notes: --- - "Export Date: 3 October 2011" - "CODEN: PNASA" - "Source: Scopus"
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MSK Authors
  1. Jeremy M Stark
    8 Stark
  2. Maria Jasin
    249 Jasin
  3. Jeannine Larocque Kappas
    6 Kappas
  4. Jin Jung Oh
    3 Oh