AI Article Synopsis

  • Meiotic recombination begins with DNA double-strand breaks (DSBs), crucial for genetic diversity and fertility, facilitated by the TOPOVIL complex in mice.
  • The study reveals that REC114 forms homodimers and interacts with MEI4 and IHO1 to create complex structures, with IHO1 forming tetramers.
  • Findings suggest REC114 may play a regulatory role, allowing it to interact with various partners in a ternary complex with IHO1 and MEI4, emphasizing the importance of these interactions in meiotic processes.

Article Abstract

Meiotic recombination is initiated by the formation of DNA double-strand breaks (DSBs), essential for fertility and genetic diversity. In the mouse, DSBs are formed by the catalytic TOPOVIL complex consisting of SPO11 and TOPOVIBL. To preserve genome integrity, the activity of the TOPOVIL complex is finely controlled by several meiotic factors including REC114, MEI4, and IHO1, but the underlying mechanism is poorly understood. Here, we report that mouse REC114 forms homodimers, that it associates with MEI4 as a 2:1 heterotrimer that further dimerizes, and that IHO1 forms coiled-coil-based tetramers. Using AlphaFold2 modeling combined with biochemical characterization, we uncovered the molecular details of these assemblies. Finally, we show that IHO1 directly interacts with the PH domain of REC114 by recognizing the same surface as TOPOVIBL and another meiotic factor ANKRD31. These results provide strong evidence for the existence of a ternary IHO1-REC114-MEI4 complex and suggest that REC114 could act as a potential regulatory platform mediating mutually exclusive interactions with several partners.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425845PMC
http://dx.doi.org/10.15252/embj.2023113866DOI Listing

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