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Multiple Chromosomes in Bacteria: Low Level of Evolutionary Constraint Drives the Rapid Genetic Divergence of Chromosome II

机译:细菌中的多个染色体:低水平的进化约束驱动染色体II的快速遗传差异。

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Multiple chromosomes in bacteria are designated as a larger primary chromosome (CI) and smaller accessory chromosomes (CII and CIII). Although previous studies examined multiple chromosomes in several bacterial species, the evolutionary mechanisms for the origin of CIIs still remain unclear. In this study, the four following hypotheses were tested. 1) CIIs exhibit lower sequence conservation and sequence divergence compared to their corresponding CIs across species of Proteobacteria . 2) The differential sequence divergence of CI and CII depends on pathogenic and non-pathogenic lifestyles. 3) CIIs harbor a higher level of horizontal gene transfers (HGTs) than CIs. 4) Orthologs located on CIIs experience less purifying selection than their corresponding orthologs on CIs. Results reveal a higher level of sequence conservation of CIs than the sequence conservation of CIIs. There is no significant difference in HGT estimates between CIs and CIIs. A majority of orthologous genes of CIs and CIIs experience purifying selection; however, genes on CIIs were significantly less constrained than the corresponding ones on CIs. This finding is true for both pathogenic and non-pathogenic bacteria, but the selective constraints for non-pathogenic bacteria are relatively less constrained. It was concluded that the differential selective constraint is a potent driving force for the rapid evolution of CII. Therefore, gene expression analysis at the transcriptome and proteome levels may shed light on the gene regulation mechanisms that might affect the sequence divergence between CI and CII.
机译:细菌中的多个染色体被指定为较大的主染色体(CI)和较小的辅助染色体(CII和CIII)。尽管先前的研究检查了几种细菌物种中的多条染色体,但CII起源的进化机制仍不清楚。在这项研究中,检验了以下四个假设。 1)CII与所有Proteobacteria物种中的相应CI相比,具有较低的序列保守性和序列差异性。 2)CI和CII的差异序列差异取决于致病性和非致病性生活方式。 3)CII比CI具有更高水平的水平基因转移(HGT)。 4)位于CII上的直系同源物比其在CI上的相应直系同源物经历的纯化选择更少。结果显示,CI的序列保守性高于CII的序列保守性。 CI和CII之间的HGT估计值没有显着差异。大多数CI和CII的直系同源基因都经历纯化选择。然而,CIIs上的基因比CIs上的相应基因受到的约束要少得多。该发现对于病原性细菌和非病原性细菌都是正确的,但是对非病原性细菌的选择性限制相对较少。结论是,差异选择约束是CII快速发展的强大动力。因此,在转录组和蛋白质组水平上的基因表达分析可以阐明可能影响CI和CII之间序列差异的基因调控机制。

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