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GRSR: a tool for deriving genome rearrangement scenarios from multiple unichromosomal genome sequences

机译:GRSR:一种用于从多个单同位素基因组序列中衍生基因组重排感的工具

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摘要

Abstract Background Genome rearrangements describe changes in the genetic linkage relationship of large chromosomal regions, involving reversals, transpositions, block interchanges, deletions, insertions, fissions, fusions and translocations etc. Many algorithms for calculating rearrangement scenarios between two genomes have been proposed. Very often, the calculated rearrangement scenario is not unique for the same pair of permutations. Hence, how to decide which calculated rearrangement scenario is more biologically meaningful becomes an essential task. Up to now, several mechanisms for genome rearrangements have been studied. One important theory is that genome rearrangement may be mediated by repeats, especially for reversal events. Many reversal regions are found to be flanked by a pair of inverted repeats. As a result, whether there are repeats at the breakpoints of the calculated rearrangement events can shed a light on deciding whether the calculated rearrangement events is biologically meaningful. To our knowledge, there is no tool which can automatically identify rearrangement events and check whether there exist repeats at the breakpoints of each calculated rearrangement event. Results In this paper, we describe a new tool named GRSR which allows us to compare multiple unichromosomal genomes to identify “independent” (obvious) rearrangement events such as reversals, (inverted) block interchanges and (inverted) transpositions and automatically searches for repeats at the breakpoints of each rearrangement event. We apply our tool on the complete genomes of 28 Mycobacterium tuberculosis strains and 24 Shewanella strains respectively. In both Mycobacterium tuberculosis and Shewanella strains, our tool finds many reversal regions flanked by a pair of inverted repeats. In particular, the GRSR tool also finds an inverted transposition and an inverted block interchange in Shewanella, where the repeats at the ends of rearrangement regions remain unchanged after the rearrangement event. To our knowledge, this is the first time such a phenomenon for inverted transposition and inverted block interchange is reported in Shewanella. Conclusions From the calculated results, there are many examples supporting the theory that the existence of repeats at the breakpoints of a rearrangement event can make the sequences at the breakpoints remain unchanged before and after the rearrangement events, suggesting that the conservation of ends could possibly be a popular phenomenon in many types of genome rearrangement events.
机译:摘要背景基因组重排描述了大染色体区域的遗传联系关系的变化,涉及逆转,转置,块交换,缺失,插入,裂缝,融合和易位等。已经提出了用于计算两个基因组之间的重新排列情景的许多算法。通常,计算的重排方案对于同一对排列不是唯一的。因此,如何确定哪些计算的重排方案更生物学意义成为必不可少的任务。到目前为止,已经研究了几种基因组重排机制。一个重要的理论是可以通过重复介导的基因组重新排列,特别是对于逆转事件。发现许多逆转区域被一对倒置重复侧翼。结果,在计算的重排事件的断点中是否存在重复,可以在决定是否计算的重排事件是生物学上有意义的。据我们所知,没有工具可以自动识别重新安排事件并检查每个计算的重新安排事件的断点是否存在重复。结果在本文中,我们描述了一个名为GRSR的新工具,它允许我们比较多个单同位素基因组,以识别诸如逆转,(倒的)块交换和(倒置)换位等“独立”(明显)的重新排列事件,并自动搜索重复的重复每个重新排列事件的断点。我们将工具应用于28个分枝杆菌菌株和24个肺癌菌株的完整基因组。在结核分枝杆菌和沉肠菌株中,我们的工具发现了许多倒置的逆转区域,由一对倒置重复。特别地,GRSR工具还在雪松中找到倒置的转置和倒置块交换,其中重排区域的末端的重复在重新排列事件之后保持不变。为了我们的知识,这是第一次在雪松报告倒置转置和倒置块交汇处的这种现象。结论来自计算结果,有许多示例支持该理论,即重新排列事件的断点的重复存在的理论可以使断点的序列在重排事件之前和之后保持不变,这表明终止的守恒可能是一种在许多类型的基因组重新排列事件中的流行现象。

著录项

  • 作者

    Dan Wang; Lusheng Wang;

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  • 年度 2018
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  • 原文格式 PDF
  • 正文语种 eng
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