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The Genomic Distribution of L1 Elements: The Role of Insertion Bias and Natural Selection

机译:L1元素的基因组分布:插入偏差和自然选择的作用

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摘要

LINE-1 (L1) retrotransposons constitute the most successful family of retroelements in mammals and account for as much as 20% of mammalian DNA. L1 elements can be found in all genomic regions but they are far more abundant in AT-rich, gene-poor, and low-recombining regions of the genome. In addition, the sex chromosomes and some genes seem disproportionately enriched in L1 elements. Insertion bias and selective processes can both account for this biased distribution of L1 elements. L1 elements do not appear to insert randomly in the genome and this insertion bias can at least partially explain the genomic distribution of L1. The contrasted distribution of L1 and Alu elements suggests that postinsertional processes play a major role in shaping L1 distribution. The most likely mechanism is the loss of recently integrated L1 elements that are deleterious (negative selection) either because of disruption of gene function or their ability to mediate ectopic recombination. By comparison, the retention of L1 elements because of some positive effect is limited to a small fraction of the genome. Understanding the respective importance of insertion bias and selection will require a better knowledge of insertion mechanisms and the dynamics of L1 inserts in populations.
机译:LINE-1(L1)逆转座子是哺乳动物中最成功的逆转录家族,占哺乳动物DNA的20%。 L1元素可以在所有基因组区域找到,但在基因组中富含AT的,基因贫乏的和低重组的区域中,它们的含量要高得多。此外,性染色体和某些基因似乎不成比例地富含L1元素。插入偏差和选择性过程均可解决L1元素的这种偏差分布。 L1元素似乎不会随机插入基因组中,这种插入偏向至少可以部分解释L1的基因组分布。 L1和Alu元素的对比分布表明,插入后过程在塑造L1分布中起主要作用。最可能的机制是由于基因功能的破坏或其介导异位重组的能力而使最近整合的有害L1元件(负选择)丧失。相比之下,由于某些积极作用,L1元素的保留仅限于基因组的一小部分。了解插入偏差和选择的各自重要性将需要对插入机制和种群中L1插入的动力学有更好的了解。

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