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细菌抗病毒防御途径编码了类似于真核生物的无处不在系统
Lydia R Chambers1, Qiaozhen Ye2, Jiaxi Cai3
1Department of Chemistry and Biochemistry, University of California San Diego, La Jolla CA, USA.
bioRxiv : the preprint server for biology
|October 9, 2023
概括
细菌拥有完整的无处不在途径,此前人们认为这种途径仅限于真核生物. 这一发现揭示了蛋白质结合系统的古代起源,影响了我们对细胞过程和进化的理解.
科学领域:
- 分子生物学分子生物学
- 生物化学 生物化学
- 进化生物学 进化生物学
背景情况:
- 乌比基因化是一种重要的翻译后修饰,它调节了真核生物中的蛋白质稳态,信号和免疫力.
- 虽然细菌具有相关的蛋白质,但已知 prokaryotes 中没有完整的无处不在途径.
研究的目的:
- 为了调查细菌是否可以进行类似于无处不在的蛋白质结合.
- 描述细菌无处不在系统的结构和功能.
主要方法:
- 使用X射线晶体学对细菌E1:E2:Ubl复合物的结构分析.
- 生物化学测试以证明Ubl对与点蛋白的结合.
- 研究了duebiquitinase (DUB) 在UBL处理中的作用.
主要成果:
- 在抗病毒免疫系统中确定了一条完整的细菌无处不在途径.
- 结构数据揭示了细菌和真核生物无处不在机制之间的惊人相似之处.
- 证明了细菌E1和E2酶结合Ubl以准氨酸残留物,并进行DUB预处理.
结论:
- 细菌拥有真正的无处不在系统,挑战了对这些通路的真核细胞中心观点.
- 这些发现表明,无处不在的途径可能起源于真核生物进化之前的细菌.
- 这一发现为研究细菌免疫和细胞调节的进化开辟了新的途径.
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