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首页> 外文期刊>Journal of Cell Science >MEI4-a central player in the regulation of meiotic DNA double-strand break formation in the mouse
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MEI4-a central player in the regulation of meiotic DNA double-strand break formation in the mouse

机译:MEI4-a在小鼠减数分裂DNA双链断裂形成中的调控作用

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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.
机译:在减数分裂前期开始时程序化DNA双链断裂(DSB)的形成标志着减数分裂重组的开始。 SPO11催化减数分裂DSB的形成,其修复发生在减数分裂的染色体轴上。进化保守的MEI4蛋白是减数分裂DSB形成所必需的,并且位于染色体轴上。在这里,我们显示,减数分裂染色体轴成分之一HORMAD1是MEI4定位所必需的。重要的是,轴相关的MEI4水平与DSB形成之间的定量相关性表明,轴相关的MEI4可能是DSB形成的限制因素。我们还表明,MEI1,REC8和RAD21L对于正确的MEI4定位很重要。这些关于减数分裂前期MEI4动力学的发现表明,DSB形成需要MEI4与染色体轴的关联,并且DSB修复后这种关联的丧失可能有助于关闭减数分裂DSB的形成。

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