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首页> 外文期刊>PLoS Computational Biology >The Ortholog Conjecture Is Untestable by the Current Gene Ontology but Is Supported by RNA Sequencing Data
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The Ortholog Conjecture Is Untestable by the Current Gene Ontology but Is Supported by RNA Sequencing Data

机译:Ortholog猜想无法通过当前的基因本体论进行检验,但得到RNA测序数据的支持

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The ortholog conjecture posits that orthologous genes are functionally more similar than paralogous genes. This conjecture is a cornerstone of phylogenomics and is used daily by both computational and experimental biologists in predicting, interpreting, and understanding gene functions. A recent study, however, challenged the ortholog conjecture on the basis of experimentally derived Gene Ontology (GO) annotations and microarray gene expression data in human and mouse. It instead proposed that the functional similarity of homologous genes is primarily determined by the cellular context in which the genes act, explaining why a greater functional similarity of (within-species) paralogs than (between-species) orthologs was observed. Here we show that GO-based functional similarity between human and mouse orthologs, relative to that between paralogs, has been increasing in the last five years. Further, compared with paralogs, orthologs are less likely to be included in the same study, causing an underestimation in their functional similarity. A close examination of functional studies of homologs with identical protein sequences reveals experimental biases, annotation errors, and homology-based functional inferences that are labeled in GO as experimental. These problems and the temporary nature of the GO-based finding make the current GO inappropriate for testing the ortholog conjecture. RNA sequencing (RNA-Seq) is known to be superior to microarray for comparing the expressions of different genes or in different species. Our analysis of a large RNA-Seq dataset of multiple tissues from eight mammals and the chicken shows that the expression similarity between orthologs is significantly higher than that between within-species paralogs, supporting the ortholog conjecture and refuting the cellular context hypothesis for gene expression. We conclude that the ortholog conjecture remains largely valid to the extent that it has been tested, but further scrutiny using more and better functional data is needed.
机译:直系同源猜想假定直系同源基因在功能上比旁系同源基因更相似。该推测是系统发育组学的基石,计算生物学和实验生物学家每天都在预测,解释和理解基因功能中使用它。然而,最近的一项研究基于实验得出的人和小鼠中的基因本体论(GO)注释和微阵列基因表达数据,挑战了直系同源猜想。相反,它提议同源基因的功能相似性主要由基因起作用的细胞环境决定,这解释了为什么观察到(物种内)旁系同源物比(物种间)直系同源物具有更大的功能相似性。在这里,我们显示了在过去的五年中,人类和小鼠直系同源物之间相对于旁系同源物之间基于GO的功能相似性一直在增加。此外,与直系同源物相比,直系同源物不太可能包含在同一研究中,从而导致低估了它们的功能相似性。对具有相同蛋白质序列的同源物的功能研究进行的仔细检查发现,实验偏见,注释错误和基于同源性的功能推论在GO中被标记为实验性推论。这些问题以及基于GO的发现的暂时性使得当前的GO不适合测试直系同源猜想。已知RNA测序(RNA-Seq)在比较不同基因或不同物种的表达方面优于微阵列。我们对来自8个哺乳动物和鸡的多种组织的大型RNA-Seq数据集的分析表明,直系同源物之间的表达相似性显着高于种内旁系同源物之间的表达相似性,支持直系同源物推测并驳斥了基因表达的细胞背景假设。我们得出结论,直向同源猜想在经过测试的范围内仍在很大程度上有效,但是需要使用更多和更好的功能数据进行进一步的审查。

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