4.5 Article

MEI4-a central player in the regulation of meiotic DNA double-strand break formation in the mouse

Journal

JOURNAL OF CELL SCIENCE
Volume 128, Issue 9, Pages 1800-1811

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/jcs.165464

Keywords

Meiosis; Recombination; DNA double strand break; Synapsis

Categories

Funding

  1. Swedish Cancer Society
  2. Swedish Research Council
  3. Scientific Research on Innovative Areas
  4. MEXT, Japan
  5. Axa Research Fund
  6. ANR
  7. EDF
  8. Deutsche Forschungsgemeinschaft [SPP1384: TO 421/4-1, TO 421/4-2, TO 421/5-1]
  9. Fondation pour le Recherche Medicale
  10. Association pour la Recherche contre le Cancer
  11. Agence Nationale pour la Recherche [ANR-09-BLAN-0269-01]
  12. Centre National pour la Recherche Scientifique (CNRS)
  13. European Research Council Executive Agency under the European Community's Seventh Framework Programme [322788]
  14. Grants-in-Aid for Scientific Research [25000014, 26440003] Funding Source: KAKEN
  15. Agence Nationale de la Recherche (ANR) [ANR-09-BLAN-0269] Funding Source: Agence Nationale de la Recherche (ANR)

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The formation of programmed DNA double-strand breaks (DSBs) at the beginning of meiotic prophase marks the initiation of meiotic recombination. Meiotic DSB formation is catalyzed by SPO11 and their repair takes place on meiotic chromosome axes. The evolutionarily conserved MEI4 protein is required for meiotic DSB formation and is localized on chromosome axes. Here, we show that HORMAD1, one of the meiotic chromosome axis components, is required for MEI4 localization. Importantly, the quantitative correlation between the level of axis-associated MEI4 and DSB formation suggests that axis-associated MEI4 could be a limiting factor for DSB formation. We also show that MEI1, REC8 and RAD21L are important for proper MEI4 localization. These findings on MEI4 dynamics during meiotic prophase suggest that the association of MEI4 to chromosome axes is required for DSB formation, and that the loss of this association upon DSB repair could contribute to turning off meiotic DSB formation.

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