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具有催化活性的原核生物 Argonaute 蛋白利用磷脂酶 D 家族蛋白来增强对不同基因入侵者的免疫反应。

Catalytically active prokaryotic Argonautes employ phospholipase D family proteins to strengthen immunity against different genetic invaders.

作者信息

Cheng Feiyue, Wu Aici, Li Zhihua, Xu Jing, Cao Xifeng, Yu Haiying, Liu Zhenquan, Wang Rui, Han Wenyuan, Xiang Hua, Li Ming

机构信息

Department of Microbial Physiological & Metabolic Engineering, State Key Laboratory of Microbial Resources, Institute of Microbiology Chinese Academy of Sciences Beijing China.

College of Life Science University of Chinese Academy of Sciences Beijing China.

出版信息

mLife. 2024 Sep 4;3(3):403-416. doi: 10.1002/mlf2.12138. eCollection 2024 Sep.

Abstract

Prokaryotic Argonautes (pAgos) provide bacteria and archaea with immunity against plasmids and viruses. Catalytically active pAgos utilize short oligonucleotides as guides to directly cleave foreign nucleic acids, while inactive pAgos lacking catalytic residues employ auxiliary effectors, such as nonspecific nucleases, to trigger abortive infection upon detection of foreign nucleic acids. Here, we report a unique group of catalytically active pAgo proteins that frequently associate with a phospholipase D (PLD) family protein. We demonstrate that this particular system employs the catalytic center of the associated PLD protein rather than that of pAgo to restrict plasmid DNA, while interestingly, its immunity against a single-stranded DNA virus relies on the pAgo catalytic center and is enhanced by the PLD protein. We also find that this system selectively suppresses viral DNA propagation without inducing noticeable abortive infection outcomes. Moreover, the pAgo protein alone enhances gene editing, which is unexpectedly inhibited by the PLD protein. Our data highlight the ability of catalytically active pAgo proteins to employ auxiliary proteins to strengthen the targeted eradication of different genetic invaders and underline the trend of PLD nucleases to participate in host immunity.

摘要

原核生物的Argonaute蛋白(pAgos)为细菌和古细菌提供针对质粒和病毒的免疫能力。具有催化活性的pAgos利用短寡核苷酸作为向导,直接切割外源核酸,而缺乏催化残基的无活性pAgos则利用辅助效应物,如非特异性核酸酶,在检测到外源核酸时引发流产感染。在此,我们报道了一组独特的具有催化活性的pAgo蛋白,它们经常与磷脂酶D(PLD)家族蛋白结合。我们证明,这个特殊的系统利用相关PLD蛋白的催化中心而非pAgo的催化中心来限制质粒DNA,而有趣的是,其针对单链DNA病毒的免疫依赖于pAgo催化中心,并由PLD蛋白增强。我们还发现,这个系统选择性地抑制病毒DNA的传播,而不会引发明显的流产感染结果。此外,单独的pAgo蛋白可增强基因编辑,而这一作用出人意料地被PLD蛋白抑制。我们的数据突出了具有催化活性的pAgo蛋白利用辅助蛋白加强对不同遗传入侵者进行靶向清除的能力,并强调了PLD核酸酶参与宿主免疫的趋势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c263/11442185/5692a887bb03/MLF2-3-403-g002.jpg

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