以APC/C为媒介,对缺乏正规降解子的核糖体外组织素复合体进行无处不在
Aleksandra Skrajna1,2,3, Tatyana Bodrug2,4, Raquel C Martinez-Chacin2,5
1Division of Chemical Biology and Medicinal Chemistry and Center for Integrated Chemical Biology and Drug Discovery, UNC Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, NC, USA.
Nature communications
|March 16, 2025
概括
酶促进复合体/循环体 (APC/C) 意外地在任何地方都存在于外核细胞组组基因组,而不是核细胞组基因组基因组. 这种机制通过向基因组的降解来调节基因表达和细胞循环的进展.
科学领域:
- 细胞生物学 细胞生物学
- 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.
- 分子生物学分子生物学
背景情况:
- 非降解性基因组无处不在对于基因调节和DNA修复至关重要.
- 在基因组过程中降解性基因素普遍存在的作用仍然在很大程度上是未知的.
- 亚纳酶促进复合体/循环体 (APC/C) 已涉及到多能细胞中基因表达的基因素普遍存在,但机制尚不清楚.
研究的目的:
- 阐明APC/C无处不在的基因组的分子机制.
- 为了研究APC/C介导的基因素普遍存在在细胞过程中的作用.
主要方法:
- 低温电子显微镜 (cryo-EM) 是一种电子显微镜.
- 生物物理测定试验
- 酶性检测试验 酶性检测试验
主要成果:
- 该APC/C通过亚单元APC3结合核细胞体,但不能无处不在核细胞体组织体.
- 在APC/C有效地 ubiquitylates 核细胞外H2A/H2B和H3/H4复合体.
- 在APC8和基因组尾巴中介于APC/C-依赖的核心基因组的多基化,没有正规的降解序列.
结论:
- 在APC/C核酶体中,核酶体结合促进了细胞外核酶体组织蛋白和其他染色质相关蛋白质的降解.
- 这一过程对于调节转录,细胞循环,以及防止细胞中过多的组织蛋白毒性至关重要.
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