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Variation in the ratio of nucleotide substitution and indel rates across genomes in mammals and bacteria.

机译:哺乳动物和细菌中整个基因组的核苷酸取代率和插入缺失率的差异。

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摘要

Rates of nucleotide substitution and insertion/deletion (indel) are known to vary across the functional components of a genome. Little attention has been paid, however, to the quantitative relationship between the two. Here we investigate the ratio of nucleotide substitutions to indels (S/I) in different regions of 4 primates, 70 bacteria, and 8 other genomes. We find that the ratio differs at 5.4-times between coding and noncoding, 3.3-times between conserved and less conserved coding sequences, and 1.46-times between nonrepeat and repeat regions. The S/I ratio is also positively correlated with the level of divergence between the genomes compared. Our results suggest that the S/I ratio may reflect differences in the efficacy of selection against indels. Due to the sensitivity of indel density in different regions, this ratio varies over a much larger range. With the recent discovery suggesting that indels act as local enhancers of mutation in surrounding sequences, nucleotide substitution rates are expected to be accelerated in regions of low constraint, where indels tend to accumulate, but will otherwise be modulated in proportion to the level of a sequence's functional constraint. Indels, therefore, may play a nontrivial role in controlling differences in genetic variation and divergence across functional regions of a genome.
机译:已知核苷酸取代和插入/缺失(插入缺失)的速率在基因组的功能组件之间变化。然而,很少关注两者之间的定量关系。在这里,我们研究了4个灵长类,70个细菌和8个其他基因组的不同区域中核苷酸取代与indels(S / I)的比率。我们发现该比率在编码和非编码之间相差5.4倍,在保守和较不保守的编码序列之间相差3.3倍,在非重复和重复区域之间相差1.46倍。 S / I比也与所比较的基因组之间的差异水平正相关。我们的结果表明,信噪比可能反映了针对插入缺失的选择功效的差异。由于在不同区域中插入缺失密度的敏感性,该比率在更大的范围内变化。随着最近的发现表明插入缺失在周围序列中起局部突变的增强作用,预期核苷酸取代率将在低限制的区域中加速,在该区域中插入缺失往往会积累,但否则会与序列的水平成比例地被调节。功能约束。因此,插入缺失可以在控制基因组功能区域中遗传变异和发散的差异中起重要作用。

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