4 research outputs found
Tex19.1 Promotes Spo11-Dependent Meiotic Recombination in Mouse Spermatocytes
Meiosis relies on the SPO11 endonuclease to generate the recombinogenic DNA double strand breaks (DSBs) required for homologous chromosome synapsis and segregation. The number of meiotic DSBs needs to be sufficient to allow chromosomes to search for and find their homologs, but not excessive to the point of causing genome instability. Here we report that the mammal-specific gene Tex19.1 promotes Spo11-dependent recombination in mouse spermatocytes. We show that the chromosome asynapsis previously reported in Tex19.1-/- spermatocytes is preceded by reduced numbers of recombination foci in leptotene and zygotene. Tex19.1 is required for normal levels of early Spo11-dependent recombination foci during leptotene, but not for upstream events such as MEI4 foci formation or accumulation of H3K4me3 at recombination hotspots. Furthermore, we show that mice carrying mutations in Ubr2, which encodes an E3 ubiquitin ligase that interacts with TEX19.1, phenocopy the Tex19.1-/- recombination defects. These data suggest that Tex19.1 and Ubr2 are required for mouse spermatocytes to accumulate sufficient Spo11-dependent recombination to ensure that the homology search is consistently successful, and reveal a hitherto unknown genetic pathway promoting meiotic recombination in mammals
De la physiopathologie à la stratégie thérapeutique d'une psychose neurodéveloppementale (la schizophrénie)
TOULOUSE3-BU Santé-Centrale (315552105) / SudocSudocFranceF
Succeeding Failure: A Comprehensive Approach to Strengthening Fragile States
Created as part of the 2010 Jackson School for International Studies SIS 495: Task Force. Scott Radnitz, Task Force Advisor; Ryan Crocker, Evaluator; Amanda Piro, Coordinator