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DNA helicase HIM-6/BLM both promotes mutSγ-dependent crossovers and antagonizes mutSγ-independent interhomolog associations during Caenorhabditis elegans meiosis

  • Author(s): Schvarzstein, M
  • Pattabiraman, D
  • Libuda, DE
  • Ramadugu, A
  • Tam, A
  • Martinez-Perez, E
  • Roelens, B
  • Zawadzki, KA
  • Yokoo, R
  • Rosu, S
  • Severson, AF
  • Meyer, BJ
  • Nabeshima, K
  • Villeneuve, AM
  • et al.

Published Web Location

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174932/
No data is associated with this publication.
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Public License
Abstract

© 2014 by the Genetics Society of America. Meiotic recombination is initiated by the programmed induction of double-strand DNA breaks (DSBs), lesions that pose a potential threat to the genome. A subset of the DSBs induced during meiotic prophase become designated to be repaired by a pathway that specifically yields interhomolog crossovers (COs), which mature into chiasmata that temporarily connect the homologs to ensure their proper segregation at meiosis I. The remaining DSBs must be repaired by other mechanisms to restore genomic integrity prior to the meiotic divisions. Here we show that HIM-6, the Caenorhabditis elegans ortholog of the RecQ family DNA helicase BLM, functions in both of these processes. We show that him-6 mutants are competent to load the MutSg complex at multiple potential CO sites, to generate intermediates that fulfill the requirements of monitoring mechanisms that enable meiotic progression, and to accomplish and robustly regulate CO designation. However, recombination events at a subset of CO-designated sites fail to mature into COs and chiasmata, indicating a pro-CO role for HIM-6/BLM that manifests itself late in the CO pathway. Moreover, we find that in addition to promoting COs, HIM-6 plays a role in eliminating and/or preventing the formation of persistent MutSg-independent associations between homologous chromosomes. We propose that HIM-6/BLM enforces biased outcomes of recombination events to ensure that both (a) CO-designated recombination intermediates are reliably resolved as COs and (b) other recombination intermediates reliably mature into noncrossovers in a timely manner.

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