由HORMAD蛋白质结合的染色质调节了介质重组的启动
Carolyn R Milano1, Sarah N Ur2,3, Yajie Gu2
1Department of Biology, New York University, New York, NY, 10003, USA.
The EMBO journal
|February 9, 2024
概括
介质染色体轴蛋白Hop1通过其中央染色体结合区域 (CBR) 结合曲折的DNA,这对于组织染色体和调节化期间的DNA断裂至关重要. 破坏这种相互作用会损害染色体突触和生育能力.
科学领域:
- 分子生物学分子生物学
- 遗传学 遗传学 是一个
- 结构生物学 结构生物学
背景情况:
- 介质染色体轴对染色体组织,同源重组和生育至关重要.
- 在酵母中,HORMAD蛋白Hop1通过其中央染色体结合区域 (CBR) 促进了轴蛋白在富含核细胞位点的积累.
研究的目的:
- 阐明Hop1 CBR与核细胞DNA相互作用的结构机制.
- 研究破坏Hop1 CBR-核酶体相互作用对介质过程的功能后果.
主要方法:
- 低温电子显微镜 (cryo-EM) 用于确定与核体DNA结合的Hop1 CBR的结构.
- 针对Hop1 CBR突变的基因分析.
- 介质性HORMAD蛋白的遗传学分析.
主要成果:
- 克里奥-EM揭示了Hop1 CBR通过一个涉及其PHD和翼螺旋转螺旋域的组合接口来识别曲的核体DNA.
- 干扰Hop1 CBR-核细胞体接口减少了轴蛋白结合和轴岛上的介质DNA双链断裂 (DSB),导致突触缺陷.
- 与Pch2突变体的合成遗传相互作用表明,核细胞结合调节了Hop1的构造,以控制DSB的形成.
结论:
- 霍普1 CBR 直接结合曲的核细胞体DNA,建立了介质染色体轴组合的保存机制.
- 这种相互作用对于调节介质性DSB形成和确保适当的染色体突触和生育是至关重要的.
- CBR的古老起源表明,HORMAD蛋白在物种间的多变性中具有保留的作用.
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