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某属物种的高基因组重排率及致病性

High Rates of Genome Rearrangements and Pathogenicity of spp.

作者信息

Seferbekova Zaira, Zabelkin Alexey, Yakovleva Yulia, Afasizhev Robert, Dranenko Natalia O, Alexeev Nikita, Gelfand Mikhail S, Bochkareva Olga O

机构信息

Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Moscow, Russia.

Institute for Information Transmission Problems (The Kharkevich Institute, RAS), Moscow, Russia.

出版信息

Front Microbiol. 2021 Apr 12;12:628622. doi: 10.3389/fmicb.2021.628622. eCollection 2021.

Abstract

are pathogens originating within the lineage but frequently classified as a separate genus. genomes contain numerous insertion sequences (ISs) that lead to pseudogenisation of affected genes and an increase of non-homologous recombination. Here, we study 414 genomes of and strains to assess the contribution of genomic rearrangements to evolution. We found that experienced exceptionally high rates of intragenomic rearrangements and had a decreased rate of homologous recombination compared to pathogenic and non-pathogenic . The high rearrangement rate resulted in independent disruption of syntenic regions and parallel rearrangements in different lineages. Specifically, we identified two types of chromosomally encoded E3 ubiquitin-protein ligases acquired independently by all strains that also showed a high level of sequence conservation in the promoter and further in the 5'-intergenic region. In the only available enteroinvasive (EIEC) strain, which is a pathogenic with a phenotype intermediate between and non-pathogenic , we found a rate of genome rearrangements comparable to those in other and no functional copies of the two -specific E3 ubiquitin ligases. These data indicate that the accumulation of ISs influenced many aspects of genome evolution and played an important role in the evolution of intracellular pathogens. Our research demonstrates the power of comparative genomics-based on synteny block composition and an important role of non-coding regions in the evolution of genomic islands.

摘要

是起源于该谱系内但常被归类为一个单独属的病原体。其基因组包含大量插入序列(ISs),这些序列导致受影响基因的假基因化以及非同源重组的增加。在这里,我们研究了414个该病原体和相关菌株的基因组,以评估基因组重排对其进化的贡献。我们发现,与致病性和非致病性相关菌株相比,该病原体经历了异常高的基因组内重排率,且同源重组率降低。高重排率导致了同线性区域的独立破坏以及不同该病原体谱系中的平行重排。具体而言,我们鉴定出了两种所有该病原体菌株都独立获得的染色体编码的E3泛素蛋白连接酶,它们在启动子以及进一步的5'基因间区域也表现出高度的序列保守性。在唯一可用的肠侵袭性该病原体(EIEC)菌株中,它是一种致病性该病原体,其表型介于该病原体和非致病性之间,我们发现其基因组重排率与其他该病原体相当,且没有这两种该病原体特异性E3泛素连接酶的功能拷贝。这些数据表明,ISs的积累影响了基因组进化的许多方面,并在细胞内病原体的进化中发挥了重要作用。我们的研究证明了基于同线性块组成的比较基因组学的力量以及非编码区域在基因组岛进化中的重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2d2/8072062/c61d27e5f814/fmicb-12-628622-g001.jpg

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