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功能分歧相关进化情景下的重组检测。

Recombination detection under evolutionary scenarios relevant to functional divergence.

机构信息

Department of Biology, Dalhousie University, Halifax, NS B3H 4J1, Canada.

出版信息

J Mol Evol. 2011 Dec;73(5-6):273-86. doi: 10.1007/s00239-011-9473-0. Epub 2012 Jan 1.

Abstract

Recombination can negatively impact methods designed to detect divergent gene function that rely on explicit knowledge of a gene tree. However, we know little about how recombination detection methods perform under evolutionary scenarios encountered in studies of functional molecular divergence. We use simulation to evaluate false positive rates for six recombination detection methods (GENECONV, MaxChi, Chimera, RDP, GARD-SBP, GARD-MBP) under evolutionary scenarios that might increase false positives. Broadly, these scenarios address: (i) asymmetric tree topology and sequence divergence, (ii) non-stationary codon bias and selection pressure, and (iii) positive selection. We also evaluate power to detect recombination under truly recombinant history. As with previous studies, we find that power increases with sequence divergence. However, we also find that accuracy to correctly infer the number of breakpoints is extremely low. When recombination is absent, increased sequence divergence leads to increased false positives. Furthermore, one method (GARD-SBP) is sensitive to tree shape, with higher false positive rates under an asymmetric tree topology. Somewhat surprisingly, all methods are robust to the simulated heterogeneity in codon bias, shifts in selection pressure and presence of positive selection. Based on these findings, we recommend that studies of functional divergence in systems where recombination is plausible can, and should, include a pre-test for recombination. Application of all methods to the core genome of Prochlorococcus reveals a substantial lack of concordance among results. Based on analysis of both real and simulated datasets we present some guidelines for the investigation of recombination in genes that may have experienced functional divergence.

摘要

重组可能会对依赖于基因树明确知识的旨在检测基因功能分歧的方法产生负面影响。然而,我们对重组检测方法在功能分子分歧研究中遇到的进化场景下的表现知之甚少。我们使用模拟来评估六种重组检测方法(GENECONV、MaxChi、Chimera、RDP、GARD-SBP、GARD-MBP)在可能增加假阳性的进化场景下的假阳性率。这些场景大致涵盖:(i)不对称树拓扑和序列分歧,(ii)非平稳密码子偏向和选择压力,以及(iii)正选择。我们还评估了在真正重组历史下检测重组的能力。与之前的研究一样,我们发现随着序列分歧的增加,能力也随之增加。然而,我们还发现,正确推断断点数量的准确性非常低。在不存在重组的情况下,增加序列分歧会导致假阳性增加。此外,一种方法(GARD-SBP)对树形状敏感,在不对称树拓扑下假阳性率更高。有些令人惊讶的是,所有方法都对模拟的密码子偏向异质性、选择压力的变化和正选择的存在具有鲁棒性。基于这些发现,我们建议在可能存在重组的系统中进行功能分歧研究时,可以而且应该包括对重组的预测试。所有方法应用于聚球藻核心基因组揭示了结果之间存在很大的不一致性。基于对真实和模拟数据集的分析,我们提出了一些用于调查可能经历过功能分歧的基因中重组的指南。

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