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首页> 外文期刊>Genome Biology and Evolution >A Novel Approach to Investigate the Effect of Tree Reconstruction Artifacts in Single-Gene Analysis Clarifies Opsin Evolution in Nonbilaterian Metazoans
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A Novel Approach to Investigate the Effect of Tree Reconstruction Artifacts in Single-Gene Analysis Clarifies Opsin Evolution in Nonbilaterian Metazoans

机译:一种新的探讨树木重建伪影在单基因分析中的影响的方法阐明了非银行美唑烷的Opsin演变

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Our ability to correctly reconstruct a phylogenetic tree is strongly affected by both systematic errors and the amount of phylogenetic signal in the data. Current approaches to tackle tree reconstruction artifacts, such as the use of parameter-rich models, do not translate readily to single-gene alignments. This, coupled with the limited amount of phylogenetic information contained in single-gene alignments, makes gene trees particularly difficult to reconstruct. Opsin phylogeny illustrates this problem clearly. Opsins are G-protein coupled receptors utilized in photoreceptive processes across Metazoa and their protein sequences are roughly 300 amino acids long. A number of incongruent opsin phylogenies have been published and opsin evolution remains poorly understood. Here, we present a novel approach, the canary sequence approach, to investigate and potentially circumvent errors in single-gene phylogenies. First, we demonstrate our approach using two well-understood cases of long-branch attraction in single-gene data sets, and simulations. After that, we apply our approach to a large collection of well-characterized opsins to clarify the relationships of the three main opsin subfamilies.
机译:我们能够正确重建系统发育树的能力受系统误差和数据中的系统发育量的影响。目前解决树形重建工件的方法,例如使用富有参数的模型,请勿容易地转换为单基因对齐。这与单基因取向中包含的有限量的系统发育信息耦合,使基因树特别难以重建。 Opsin phylogeny清楚地说明了这个问题。 Opsins是用于跨甲基菌的光接收过程的G蛋白偶联受体,并且它们的蛋白质序列大约是300氨基酸长。已经公布了许多不一致的OPSIN,并且OPSIN进化仍然明白。在这里,我们提出了一种新的方法,金丝雀序列方法,在单基因发育中调查和潜在地避难的误差。首先,我们展示了我们使用单基因数据集中的两个良好的长分支吸引力的案例和模拟的方法。之后,我们将我们的方法应用于大量特征的Opsins,以澄清三个主要Opsin亚属的关系。

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