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卷尺蛋白的进化:单位、重复和丢失。

The evolution of the tape measure protein: units, duplications and losses.

机构信息

Information and Computer Sciences, University of Hawaii, Honolulu, Hawaii, USA.

出版信息

BMC Bioinformatics. 2011 Oct 5;12 Suppl 9(Suppl 9):S10. doi: 10.1186/1471-2105-12-S9-S10.

Abstract

BACKGROUND

A large family of viruses that infect bacteria, called phages, is characterized by long tails used to inject DNA into their victims' cells. The tape measure protein got its name because the length of the corresponding gene is proportional to the length of the phage's tail: a fact shown by actually copying or splicing out parts of DNA in exemplar species. A natural question is whether there exist units for these tape measures, and if different tape measures have different units and lengths. Such units would allow us to retrace the evolution of tape measure proteins using their duplication/loss history. The vast number of sequenced phages genomes allows us to attack this problem with a comparative genomics approach.

RESULTS

Here we describe a subset of phages whose tape measure proteins contain variable numbers of an 11 amino acids sequence repeat, aligned with sequence similarity, structural properties, and simple arithmetics. This subset provides a unique opportunity for the combinatorial study of phage evolution, without the added uncertainties of multiple alignments, which are trivial in this case, or of protein functions, that are well established. We give a heuristic that reconstructs the duplication history of these sequences, using divergent strains to discriminate between mutations that occurred before and after speciation, or lineage divergence. The heuristic is based on an efficient algorithm that gives an exhaustive enumeration of all possible parsimonious reconstructions of the duplication/speciation history of a single nucleotide. Finally, we present a method that allows, when possible, to discriminate between duplication and loss events.

CONCLUSIONS

Establishing the evolutionary history of viruses is difficult, in part due to extensive recombinations and gene transfers, and high mutation rates that often erase detectable similarity between homologous genes. In this paper, we introduce new tools to address this problem.

摘要

背景

一类能够感染细菌的病毒家族,被称为噬菌体,其特征是用于将 DNA 注入其宿主细胞的长尾巴。 量尺蛋白之所以得名,是因为相应基因的长度与噬菌体尾巴的长度成正比:这一事实通过实际复制或拼接范例物种的 DNA 部分来证明。 一个自然的问题是是否存在这些量尺的单位,以及不同的量尺是否具有不同的单位和长度。 这些单位将使我们能够使用其重复/丢失历史来追溯量尺蛋白的进化。 大量已测序的噬菌体基因组使我们能够使用比较基因组学方法来解决这个问题。

结果

在这里,我们描述了一类噬菌体,其量尺蛋白包含可变性数量的 11 个氨基酸序列重复,通过序列相似性、结构特性和简单的算术进行对齐。 这个子集为噬菌体进化的组合研究提供了一个独特的机会,而无需进行多次比对的不确定性,在这种情况下,多次比对是微不足道的,或者蛋白质功能是确定的。 我们提出了一种启发式方法,使用分歧菌株来区分在物种形成或谱系分化之前和之后发生的突变,从而重建这些序列的复制历史。 该启发式方法基于一种有效的算法,该算法可以对单个核苷酸的复制/物种形成历史的所有可能简约重建进行详尽枚举。 最后,我们提出了一种方法,当可能时,可以区分复制和丢失事件。

结论

建立病毒的进化历史具有挑战性,部分原因是广泛的重组和基因转移,以及高突变率经常消除同源基因之间可检测的相似性。 在本文中,我们引入了新的工具来解决这个问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b3a/3271669/f679756f5eb0/1471-2105-12-S9-S10-1.jpg

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