丰富的细菌核相关蛋白H-NS限制了质粒通过DNA的机械修饰转移。

IF 13.1 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Mingyue Fei,Mengdie Fang,Qi Zhou,Ziyan Chen,Mengxin Gong,Fabai Wu,Changfu Tian,Dongchang Sun
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引用次数: 0

摘要

原核生物和可移动遗传元件(MGEs)之间正在进行的军备竞赛产生了无数的宿主防御系统,这些系统可以检测和降解入侵的核酸。然而,目前尚不清楚改变核酸的机械性质是否会影响质粒/噬菌体的侵袭。在这里,我们证明了丰富的核相关蛋白(NAP) H-NS通过与转化双链DNA直接结合和寡聚化来限制质粒转移。H-NS的本构防御功能可由来自不同门的收敛进化的nap补充。H-NS蛋白在传入质粒内的DNA双链之间形成分子内桥梁。与其他防御系统在检测到MGEs之前存在低水平不同,主要nap存在高丰度,可能作为一种恒定的质粒监视剂。我们的研究表明,核酸的机械修饰可能是一种未被探索的原核免疫机制,它可以帮助平衡MGEs的优缺点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abundant bacterial nucleoid-associated protein H-NS limits plasmid transfer through mechanical modification of DNA.
The ongoing arms race between prokaryotes and mobile genetic elements (MGEs) gives rise to a myriad of host-defense systems that detect and degrade invading nucleic acids. However, it is yet unclear whether changing the mechanical properties of nucleic acids can impact plasmid/phage invasion. Here, we demonstrate that H-NS, an abundant nucleoid-associated protein (NAP), limits plasmid transfer by directly binding to and oligomerizing along with transforming double-stranded DNA. The constitutive defense function of H-NS can be complemented by convergently evolved NAPs from different phyla. H-NS proteins form intramolecular bridges between DNA duplexes within incoming plasmids. Different from other defense systems that exist at low levels prior to detecting MGEs, major NAPs exist in high abundance, which may moonlight as a constant plasmid surveillance agent. Our study implies that mechanical modification of nucleic acids may be an underexplored mechanism for prokaryotic immunity, which could help balance the advantages and disadvantages of MGEs.
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来源期刊
Nucleic Acids Research
Nucleic Acids Research 生物-生化与分子生物学
CiteScore
27.10
自引率
4.70%
发文量
1057
审稿时长
2 months
期刊介绍: Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.
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