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来自蓝细菌的Ago核酸酶进行全基因组DNA采样

Genome-wide DNA sampling by Ago nuclease from the cyanobacterium .

作者信息

Olina Anna, Kuzmenko Anton, Ninova Maria, Aravin Alexei A, Kulbachinskiy Andrey, Esyunina Daria

机构信息

Institute of Molecular Genetics, Russian Academy of Sciences, Moscow, Russia.

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.

出版信息

RNA Biol. 2020 May;17(5):677-688. doi: 10.1080/15476286.2020.1724716. Epub 2020 Feb 16.

Abstract

Members of the conserved Argonaute (Ago) protein family provide defence against invading nucleic acids in eukaryotes in the process of RNA interference. Many prokaryotes also contain Ago proteins that are predicted to be active nucleases; however, their functional activities in host cells remain poorly understood. Here, we characterize the and properties of the SeAgo protein from the mesophilic cyanobacterium . We show that SeAgo is a DNA-guided nuclease preferentially acting on single-stranded DNA targets, with non-specific guide-independent activity observed for double-stranded substrates. The SeAgo gene is steadily expressed in ; however, its deletion or overexpression does not change the kinetics of cell growth. When purified from its host cells or from heterologous , SeAgo is loaded with small guide DNAs whose formation depends on the endonuclease activity of the argonaute protein. SeAgo co-purifies with SSB proteins suggesting that they may also be involved in DNA processing. The SeAgo-associated small DNAs are derived from diverse genomic locations, with certain enrichment for the proposed sites of chromosomal replication initiation and termination, but show no preference for an endogenous plasmid. Therefore, promiscuous genome sampling by SeAgo does not have great effects on cell physiology and plasmid maintenance.

摘要

保守的Argonaute(Ago)蛋白家族成员在RNA干扰过程中为真核生物抵御入侵核酸。许多原核生物也含有预测具有活性核酸酶的Ago蛋白;然而,它们在宿主细胞中的功能活性仍知之甚少。在这里,我们表征了嗜温蓝藻中SeAgo蛋白的特性。我们表明,SeAgo是一种DNA引导的核酸酶,优先作用于单链DNA靶标,对双链底物观察到非特异性的非引导依赖性活性。SeAgo基因在中稳定表达;然而,其缺失或过表达不会改变细胞生长动力学。当从其宿主细胞或异源中纯化时,SeAgo会装载小引导DNA,其形成取决于argonaute蛋白的内切核酸酶活性。SeAgo与SSB蛋白共纯化,表明它们也可能参与DNA加工。与SeAgo相关的小DNA来自不同的基因组位置,在拟议的染色体复制起始和终止位点有一定富集,但对内源质粒没有偏好。因此,SeAgo的混杂基因组采样对细胞生理学和质粒维持没有很大影响。

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