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Mammalian transposable elements and their impacts on genome evolution

机译:哺乳动物转座因子及其对基因组进化的影响

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摘要

Transposable elements (TEs) are genetic elements with the ability to mobilize and replicate themselves in a genome. Mammalian genomes are dominated by TEs, which can reach copy numbers in the hundreds of thousands. As a result, TEs have had significant impacts on mammalian evolution. Here we summarize the current understanding of TE content in mammal genomes and find that, with a few exceptions, most fall within a predictable range of observations. First, one third to one half of the genome is derived from TEs. Second, most mammalian genomes are dominated by LINE and SINE retrotransposons, more limited LTR retrotransposons, and minimal DNA transposon accumulation. Third, most mammal genome contains at least one family of actively accumulating retrotransposon. Finally, horizontal transfer of TEs among lineages is rare. TE exaptation events are being recognized with increasing frequency. Despite these beneficial aspects of TE content and activity, the majority of TE insertions are neutral or deleterious. To limit the deleterious effects of TE proliferation, the genome has evolved several defense mechanisms that act at the epigenetic, transcriptional, and post-transcriptional levels. The interaction between TEs and these defense mechanisms has led to an evolutionary arms race where TEs are suppressed, evolve to escape suppression, then are suppressed again as the defense mechanisms undergo compensatory change. The result is complex and constantly evolving interactions between TEs and host genomes.
机译:转座因子(TEs)是具有动员能力并在基因组中自我复制的遗传因子。哺乳动物的基因组主要由TEs所占据,TE可以达到数十万的拷贝数。结果,TE对哺乳动物的进化产生了重大影响。在这里,我们总结了当前对哺乳动物基因组中TE含量的理解,发现除少数例外,大多数都属于可预测的观察范围。首先,基因组的三分之一至一半来自TEs。其次,大多数哺乳动物基因组主要由LINE和SINE逆转座子,更有限的LTR逆转座子和最小的DNA转座子积累组成。第三,大多数哺乳动物基因组包含至少一个活跃积累的反转录转座子家族。最后,在血统之间TE的水平转移很少。越来越多的人认识到TE豁免事件。尽管TE含量和活性具有这些有益的方面,但是大多数TE插入是中性的或有害的。为了限制TE增殖的有害影响,基因组已经进化出了几种在表观遗传,转录和转录后水平上起作用的防御机制。 TE与这些防御机制之间的相互作用导致了一场演化军备竞赛,其中TE被抑制,演变为逃避抑制,然后随着防御机制发生补偿性变化而再次受到抑制。结果是TE与宿主基因组之间的相互作用复杂且不断发展。

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