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首页> 外文期刊>BMC Bioinformatics >An improved method for identifying functionally linked proteins using phylogenetic profiles
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An improved method for identifying functionally linked proteins using phylogenetic profiles

机译:一种使用系统发育谱鉴定功能性连接蛋白的改进方法

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Background Phylogenetic profiles record the occurrence of homologs of genes across fully sequenced organisms. Proteins with similar profiles are typically components of protein complexes or metabolic pathways. Various existing methods measure similarity between two profiles and, hence, the likelihood that the two proteins co-evolve. Some methods ignore phylogenetic relationships between organisms while others account for such with metrics that explicitly model the likelihood of two proteins co-evolving on a tree. The latter methods more sensitively detect co-evolving proteins, but at a significant computational cost. Here we propose a novel heuristic to improve phylogenetic profile analysis that accounts for phylogenetic relationships between genomes in a computationally efficient fashion. We first order the genomes within profiles and then enumerate runs of consecutive matches and accurately compute the probability of observing these. We hypothesize that profiles with many runs are more likely to involve functionally related proteins than profiles in which all the matches are concentrated in one interval of the tree. Results We compared our approach to various previously published methods that both ignore and incorporate the underlying phylogeny between organisms. To evaluate performance, we compare the functional similarity of rank-ordered lists of protein pairs that share similar phylogenetic profiles by assessing significance of overlap in their Gene Ontology annotations. Accounting for runs in phylogenetic profile matches improves our ability to identify functionally related pairs of proteins. Furthermore, the networks that result from our approach tend to have smaller clusters of co-evolving proteins than networks computed using previous approaches and are thus more useful for inferring functional relationships. Finally, we report that our approach is orders of magnitude more computationally efficient than full tree-based methods. Conclusion We have developed an improved method for analyzing phylogenetic profiles. The method allows us to more accurately and efficiently infer functional relationships between proteins based on these profiles than other published approaches. As the number of fully sequenced genomes increases, it becomes more important to account for evolutionary relationships among organisms in comparative analyses. Our approach, therefore, serves as an important example of how these relationships may be accounted for in an efficient manner.
机译:背景系统发生谱记录了全序列生物中基因同源物的发生。具有相似特征的蛋白质通常是蛋白质复合物或代谢途径的组成部分。现有的各种方法可测量两个图谱之间的相似性,从而测量两个蛋白质共同进化的可能性。有些方法忽略了生物之间的系统发育关系,而另一些方法则用明确地模拟两种蛋白质在树上共同进化的可能性的度量标准来解释这种关系。后一种方法可以更灵敏地检测共同进化的蛋白质,但是计算成本很高。在这里,我们提出了一种新颖的启发式方法来改进系统发育谱分析,该分析以一种计算有效的方式解释了基因组之间的系统发育关系。我们首先在配置文件中对基因组进行排序,然后枚举连续匹配的序列,并准确计算观察到这些匹配的概率。我们假设,与所有匹配都集中在树的一个间隔中的谱相比,具有许多运行的谱更可能涉及功能相关的蛋白质。结果我们将我们的方法与各种先前发表的方法进行了比较,这些方法既忽略又合并了生物之间的潜在系统发育。为了评估性能,我们通过评估基因本体注释中重叠的重要性,比较了共享相似系统发育谱的蛋白质对的排序顺序列表的功能相似性。考虑系统发育谱匹配的运行,提高了我们鉴定功能相关的蛋白质对的能力。此外,与使用以前的方法计算得出的网络相比,由我们的方法得出的网络往往具有较小的共同进化蛋白簇,因此对于推断功能关系更有用。最后,我们报告说,与基于完整树的方法相比,我们的方法的计算效率更高。结论我们开发了一种改进的系统发育谱分析方法。与其他已发表的方法相比,该方法使我们能够基于这些配置文件更准确,更有效地推断蛋白质之间的功能关系。随着完全测序的基因组数量的增加,在比较分析中考虑生物之间的进化关系变得越来越重要。因此,我们的方法是如何有效解决这些关系的重要示例。

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