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Why Selection Might Be Stronger When Populations Are Small: Intron Size and Density Predict within and between-Species Usage of Exonic Splice Associated cis-Motifs

机译:为什么当种群较小时选择可能更强:内含子大小和密度预测外显子剪接相关顺式基序的物种内和物种间使用

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The nearly neutral theory predicts that small effective population size provides the conditions for weakened selection. This is postulated to explain why our genome is more "bloated" than that of, for example, yeast, ours having large introns and large intergene spacer. If a bloated genome is also an error prone genome might it, however, be the case that selection for error-mitigating properties is stronger in our genome? We examine this notion using splicing as an exemplar, not least because large introns can predispose to noisy splicing. We thus ask whether, owing to genomic decay, selection for splice error-control mechanisms is stronger, not weaker, in species with large introns and small populations. In humans much information defining splice sites is in cis-exonic motifs, most notably exonic splice enhancers (ESEs). These act as splice-error control elements. Here then we ask whether within and between-species intron size is a predictor of the commonality of exonic cis-splicing motifs. We show that, as predicted, the proportion of synonymous sites that are ESE-associated and under selection in humans is weakly positively correlated with the size of the flanking intron. In a phylogenetically controlled framework, we observe, also as expected, that mean intron size is both predicted by Ne.mu and is a good predictor of cis-motif usage across species, this usage coevolving with splice site definition. Unexpectedly, however, across taxa intron density is a better predictor of cis-motif usage than intron size. We propose that selection for splice-related motifs is driven by a need to avoid decoy splice sites that will be more common in genes with many and large introns. That intron number and density predict ESE usage within human genes is consistent with this, as is the finding of intragenic heterogeneity in ESE density. As intronic content and splice site usage across species is also well predicted by Ne.mu, the result also suggests an unusual circumstance in which selection (for cis-modifiers of splicing) might be stronger when population sizes are smaller, as here splicing is noisier, resulting in a greater need to control error-prone splicing.
机译:近乎中性的理论预测,较小的有效种群规模为弱化选择提供了条件。这可以解释为什么我们的基因组比酵母的基因组更“臃肿”,例如酵母的基因组具有大的内含子和大的基因间间隔区。然而,如果一个臃肿的基因组也是一个容易出错的基因组,那么在我们的基因组中,对减少错误的特性的选择是否更强?我们以剪接为例来研究这个概念,尤其是因为大内含子会导致嘈杂的剪接。因此,我们想知道,由于基因组衰变,在具有大内含子和小种群的物种中,剪接错误控制机制的选择是否更强,而不是更弱。在人类中,定义剪接位点的许多信息都存在于顺式外显子基序中,最显着的是外显子剪接增强子 (ESE)。它们充当拼接错误控制元件。在这里,我们问物种内和物种之间的内含子大小是否是外显子顺式剪接基序共性的预测因子。我们发现,正如预测的那样,在人类中与ESE相关且处于选择状态的同义位点的比例与侧翼内含子的大小呈弱正相关。在系统发育控制的框架中,我们观察到,正如预期的那样,平均内含子大小既可以通过 Ne.mu 预测,也可以很好地预测跨物种的顺式基序使用,这种使用与剪接位点定义共同发展。然而,出乎意料的是,在整个分类群中,内含子密度比内含子大小更能预测顺式基序的使用。我们提出,剪接相关基序的选择是由避免诱饵剪接位点的需要驱动的,这些位点在具有许多大内含子的基因中更为常见。内含子数量和密度预测人类基因中ESE的使用与此一致,ESE密度的基因内异质性的发现也是如此。由于 Ne.mu 也很好地预测了跨物种的内含子含量和剪接位点的使用,因此该结果还表明了一种不寻常的情况,即当种群规模较小时,选择(对于剪接的顺式修饰剂)可能更强,因为这里的剪接噪声更大,导致更需要控制容易出错的剪接。

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