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Causes of Insertion Sequences Abundance in Prokaryotic Genomes

机译:原核基因组中插入序列丰富的原因

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Insertion sequences (ISs) are the smallest and most frequent transposable elements in prokaryotes where they play an important evolutionary role by promoting gene inactivation and genome plasticity. Their genomic abundance varies by several orders of magnitude for reasons largely unknown and widely speculated. The current availability of hundreds of genomes renders testable many of these hypotheses, notably that IS abundance correlates positively with the frequency of horizontal gene transfer (HGT), genome size, pathogenicity, nonobligatory ecological associations, and human association. We thus reannotated ISs in 262 prokaryotic genomes and tested these hypotheses showing that when using appropriate controls, there is no empirical basis for IS family specificity, pathogenicity, or human association to influence IS abundance or density. HGT seems necessary for the presence of ISs, but cannot alone explain the absence of ISs in more than 20% of the organisms, some of which showing high rates of HGT. Gene transfer is also not a significant determinant of the abundance of IS elements in genomes, suggesting that IS abundance is controlled at the level of transposition and ensuing natural selection and not at the level of infection. Prokaryotes engaging in obligatory associations have fewer ISs when controlled for genome size, but this may be caused by some being sexually isolated. Surprisingly, genome size is the only significant predictor of IS numbers and density. Alone, it explains over 40% of the variance of IS abundance. Because we find that genome size and IS abundance correlate negatively with minimal doubling times, we conclude that selection for rapid replication cannot account for the few ISs found in small genomes. Instead, we show evidence that IS numbers are controlled by the frequency of highly deleterious insertion targets. Indeed, IS abundance increases quickly with genome size, which is the exact inverse trend found for the density of genes under strong selection such as essential genes. Hence, for ISs, the bigger the genome the better.
机译:插入序列(ISs)是原核生物中最小,最常见的转座元件,它们通过促进基因失活和基因组可塑性发挥重要的进化作用。它们的基因组丰度变化了几个数量级,原因很多未知且被广泛推测。目前数百个基因组的可用性使上述假设中的许多成为可检验的,特别是IS丰度与水平基因转移(HGT)的频率,基因组大小,致病性,非强制性的生态联系和人类联系呈正相关。因此,我们对262个原核基因组中的IS进行了重新注释,并检验了这些假设,表明使用适当的对照时,没有IS家族特异性,致病性或人类关联影响IS丰度或密度的经验基础。 HGT似乎对于IS的存在是必要的,但是不能单独解释20%以上的生物体中IS的缺失,其中某些生物显示HGT的发生率很高。基因转移也不是基因组中IS元素丰度的重要决定因素,这表明IS丰度在转座和随后的自然选择水平上受到控制,而不在感染水平上受到控制。当受基因组大小控制时,参与强制性关联的原核生物的IS较少,但这可能是由于某些人被性隔离所致。令人惊讶的是,基因组大小是IS数量和密度的唯一重要预测指标。它单独解释了IS丰度差异的40%以上。因为我们发现基因组大小和IS丰度与最小倍增时间负相关,所以我们得出结论,快速复制的选择不能解释在小基因组中发现的少数IS。相反,我们显示出证据表明IS编号受高度有害插入目标的频率控制。确实,IS丰度随基因组大小的增加而迅速增加,这是在强选择下诸如必需基因之类的基因密度的确切逆趋势。因此,对于IS来说,基因组越大越好。

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  • 来源
    《Molecular Biology and Evolution 》 |2007年第4期| 969-981| 共13页
  • 作者单位

    Génétique des Génomes Bactériens CNRS URA2171 Institut Pasteur Paris France;

    Atelier de Bioinformatique Université Pierre et Marie Curie-Paris6 Paris France;

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