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利用一种新的计算方法揭示了插入缺失替换对 PVC 超门细菌进化的全基因组影响。

Genome-wide influence of indel Substitutions on evolution of bacteria of the PVC superphylum, revealed using a novel computational method.

机构信息

Department of Molecular Biology, University of Wyoming, USA.

出版信息

Genome Biol Evol. 2010;2:870-86. doi: 10.1093/gbe/evq071. Epub 2010 Nov 3.

Abstract

Whole-genome scans for positive Darwinian selection are widely used to detect evolution of genome novelty. Most approaches are based on evaluation of nonsynonymous to synonymous substitution rate ratio across evolutionary lineages. These methods are sensitive to saturation of synonymous sites and thus cannot be used to study evolution of distantly related organisms. In contrast, indels occur less frequently than amino acid replacements, accumulate more slowly, and can be employed to characterize evolution of diverged organisms. As indels are also subject to the forces of natural selection, they can generate functional changes through positive selection. Here, we present a new computational approach to detect selective constraints on indel substitutions at the whole-genome level for distantly related organisms. Our method is based on ancestral sequence reconstruction, takes into account the varying susceptibility of different types of secondary structure to indels, and according to simulation studies is conservative. We applied this newly developed framework to characterize the evolution of organisms of the Planctomycetes, Verrucomicrobia, Chlamydiae (PVC) bacterial superphylum. The superphylum contains organisms with unique cell biology, physiology, and diverse lifestyles. It includes bacteria with simple cell organization and more complex eukaryote-like compartmentalization. Lifestyles range from free-living organisms to obligate pathogens. In this study, we conduct a whole-genome level analysis of indel substitutions specific to evolutionary lineages of the PVC superphylum and found that indels evolved under positive selection on up to 12% of gene tree branches. We also analyzed possible functional consequences for several case studies of predicted indel events.

摘要

全基因组扫描正向达尔文选择被广泛用于检测基因组新颖性的进化。大多数方法基于评估进化谱系中非同义替换与同义替换的比率。这些方法对同义位点的饱和敏感,因此不能用于研究远缘生物的进化。相比之下,插入缺失发生的频率低于氨基酸替换,积累速度较慢,可用于描述分化生物的进化。由于插入缺失也受到自然选择的影响,它们可以通过正向选择产生功能变化。在这里,我们提出了一种新的计算方法,用于检测远缘生物全基因组水平插入缺失替换的选择约束。我们的方法基于祖先序列重建,考虑了不同类型二级结构对插入缺失的易感性差异,并根据模拟研究是保守的。我们将这个新开发的框架应用于表征浮霉菌门、疣微菌门和衣原体门(PVC)细菌超级门生物的进化。这个超级门包含具有独特细胞生物学、生理学和多样化生活方式的生物。它包括具有简单细胞组织和更复杂的真核样区室化的细菌。生活方式从自由生活的生物到专性病原体不等。在这项研究中,我们对 PVC 超级门进化谱系特有的插入缺失替换进行了全基因组水平分析,发现多达 12%的基因树分支上的插入缺失是在正向选择下进化的。我们还分析了几个预测插入缺失事件的可能功能后果。

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