Achaz G, Rocha E P C, Netter P, Coissac E
Structure et Dynamique des Génomes, Institut Jacques Monod, Tour 43-44, 1 degrees Etage, 4 Place Jussieu, F-75251 Paris Cedex 05, France.
Nucleic Acids Res. 2002 Jul 1;30(13):2987-94. doi: 10.1093/nar/gkf391.
We investigated 53 complete bacterial chromosomes for intrachromosomal repeats. In previous studies on eukaryote chromosomes, we proposed a model for the dynamics of repeats based on the continuous genesis of tandem repeats, followed by an active process of high deletion rate, counteracted by rearrangement events that may prevent the repeats from being deleted. The present study of long repeats in the genomes of Bacteria and Archaea suggests that our model of interspersed repeats dynamics may apply to them. Thus the duplication process might be a consequence of very ancient mechanisms shared by all three domains. Moreover, we show that there is a strong negative correlation between nucleotide composition bias and the repeat density of genomes. We hypothesise that in highly biased genomes, non-duplicated small repeats arise more frequently by random effects and are used as primers for duplication mechanisms, leading to a higher density of large repeats.
我们研究了53条完整的细菌染色体中的染色体内部重复序列。在之前对真核生物染色体的研究中,我们基于串联重复序列的持续产生提出了一个重复序列动态模型,随后是一个高缺失率的活跃过程,该过程会被可能阻止重复序列被删除的重排事件所抵消。目前对细菌和古菌基因组中长重复序列的研究表明,我们的散布重复序列动态模型可能适用于它们。因此,复制过程可能是所有三个域共有的非常古老机制的结果。此外,我们表明核苷酸组成偏差与基因组的重复密度之间存在很强的负相关。我们假设,在高度偏差的基因组中,未复制的小重复序列通过随机效应更频繁地出现,并被用作复制机制的引物,从而导致大重复序列的密度更高。