从转座元件中提取蛋白质编码序列。

Genome dynamics Pub Date : 2007-01-01 DOI:10.1159/000107609
N J Bowen, I K Jordan
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引用次数: 27

摘要

转座因子(te)的活性对真核生物基因组的进化有着深远的影响。曾经被认为是纯粹自私的基因组实体,现在人们认识到te与其宿主基因组具有从寄生到互惠的连续关系。te对其所在基因组的功能和进化做出贡献的众多方式之一是通过宿主蛋白质编码序列(CDSs)的捐赠。在本章中,我们将描述几个由TEs衍生的真核宿主cds的著名例子。尽管存在一些这样的公认案例,但这一现象的总体范围和意义仍然是一个有争议的问题。基因组规模的计算分析对来自te的宿主cds的比例产生了截然不同的估计。我们解释了这些看似矛盾的发现是如何由用于检测te相关序列的不同方法引入的特定确定偏差的结果。鉴于这一问题,我们提出了一个全面和系统的框架来明确表征TEs对真核cds的贡献。
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Exaptation of protein coding sequences from transposable elements.

The activity of transposable elements (TEs) has had a profound impact on the evolution of eukaryotic genomes. Once thought to be purely selfish genomic entities, TEs are now recognized to occupy a continuum of relationships, ranging from parasitic to mutualistic, with their host genomes. One of the many ways that TEs contribute to the function and evolution of the genomes in which they reside is through the donation of host protein coding sequences (CDSs). In this chapter, we will describe several notable examples of eukaryotic host CDSs that are derived from TEs. Despite the existence of a number of such well-established cases, the overall extent and significance of this phenomenon remains a matter of controversy. Genome-scale computational analyses have yielded vastly different estimates for the fraction of host CDSs that are derived from TEs. We explain how these seemingly contradictory findings are the result of specific ascertainment biases introduced by the different methods used to detect TE-related sequences. In light of this problem, we propose a comprehensive and systematic framework for definitively characterizing the contribution of TEs to eukaryotic CDSs.

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The evolutionary dynamics of transposable elements in eukaryote genomes. SINEs as driving forces in genome evolution. Unstable microsatellite repeats facilitate rapid evolution of coding and regulatory sequences. Satellite DNA evolution. Satellite DNA-mediated effects on genome regulation.
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