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基因转移因子中DNA包装的演变

Evolution of DNA packaging in gene transfer agents.

作者信息

Esterman Emma S, Wolf Yuri I, Kogay Roman, Koonin Eugene V, Zhaxybayeva Olga

机构信息

Department of Biological Sciences, Dartmouth College, Hanover, NH 03755, USA.

National Center for Biotechnology Information, National Library of Medicine, Bethesda, MD 20894, USA.

出版信息

Virus Evol. 2021 Feb 19;7(1):veab015. doi: 10.1093/ve/veab015. eCollection 2021 Jan.

Abstract

Gene transfer agents (GTAs) are virus-like particles encoded and produced by many bacteria and archaea. Unlike viruses, GTAs package fragments of the host genome instead of the genes that encode the components of the GTA itself. As a result of this non-specific DNA packaging, GTAs can transfer genes within bacterial and archaeal communities. GTAs clearly evolved from viruses and are thought to have been maintained in prokaryotic genomes due to the advantages associated with their DNA transfer capacity. The most-studied GTA is produced by the alphaproteobacterium (RcGTA), which packages random portions of the host genome at a lower DNA density than usually observed in tailed bacterial viruses. How the DNA packaging properties of RcGTA evolved from those of the ancestral virus remains unknown. To address this question, we reconstructed the evolutionary history of the large subunit of the terminase (TerL), a highly conserved enzyme used by viruses and GTAs to package DNA. We found that RcGTA-like TerLs grouped within viruses that employ the headful packaging strategy. Because distinct mechanisms of viral DNA packaging correspond to differences in the TerL amino acid sequence, our finding suggests that RcGTA evolved from a headful packaging virus. Headful packaging is the least sequence-specific mode of DNA packaging, which would facilitate the switch from packaging of the viral genome to packaging random pieces of the host genome during GTA evolution.

摘要

基因转移因子(GTAs)是由许多细菌和古菌编码并产生的病毒样颗粒。与病毒不同,GTAs包装的是宿主基因组片段,而非编码GTA自身组分的基因。由于这种非特异性的DNA包装,GTAs能够在细菌和古菌群落内转移基因。GTAs显然是从病毒进化而来的,并且由于其DNA转移能力带来的优势,被认为在原核生物基因组中得以保留。研究最多的GTA是由α-变形菌(RcGTA)产生的,它以低于尾部细菌病毒通常观察到的DNA密度包装宿主基因组的随机部分。RcGTA的DNA包装特性如何从其祖先病毒演变而来仍然未知。为了解决这个问题,我们重建了末端酶大亚基(TerL)的进化历史,末端酶是病毒和GTAs用于包装DNA的一种高度保守的酶。我们发现,类似RcGTA的TerL聚集在采用满头部包装策略的病毒之中。由于病毒DNA包装的不同机制对应于TerL氨基酸序列的差异,我们的发现表明RcGTA是从一种满头部包装病毒进化而来的。满头部包装是DNA包装中序列特异性最低的模式,这将有助于在GTA进化过程中从包装病毒基因组转变为包装宿主基因组的随机片段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a1e/7947584/cb27442d9e07/veab015f1.jpg

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