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OASIS:用于细菌和古菌插入序列全球调查的自动化程序。

OASIS: an automated program for global investigation of bacterial and archaeal insertion sequences.

机构信息

Department of Organismic and Evolutionary Biology and Faculty of Arts and Sciences Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA.

出版信息

Nucleic Acids Res. 2012 Dec;40(22):e174. doi: 10.1093/nar/gks778. Epub 2012 Aug 16.

Abstract

Insertion sequences (ISs) are simple transposable elements present in most bacterial and archaeal genomes and play an important role in genomic evolution. The recent expansion of sequenced genomes offers the opportunity to study ISs comprehensively, but this requires efficient and accurate tools for IS annotation. We have developed an open-source program called OASIS, or Optimized Annotation System for Insertion Sequences, which automatically annotates ISs within sequenced genomes. OASIS annotations of 1737 bacterial and archaeal genomes offered an unprecedented opportunity to examine IS evolution. At a broad scale, we found that most IS families are quite widespread; however, they are not present randomly across taxa. This may indicate differential loss, barriers to exchange and/or insufficient time to equilibrate across clades. The number of ISs increases with genome length, but there is both tremendous variation and no increase in IS density for genomes >2 Mb. At the finer scale of recently diverged genomes, the proportion of shared IS content falls sharply, suggesting loss and/or emergence of barriers to successful cross-infection occurs rapidly. Surprisingly, even after controlling for 16S rRNA sequence divergence, the same ISs were more likely to be shared between genomes labeled as the same species rather than as different species.

摘要

插入序列(ISs)是存在于大多数细菌和古菌基因组中的简单转座元件,在基因组进化中发挥着重要作用。最近测序基因组的扩展提供了全面研究 ISs 的机会,但这需要高效、准确的 IS 注释工具。我们开发了一个名为 OASIS 的开源程序,即插入序列的优化注释系统,它可以自动注释测序基因组中的 IS。对 1737 个细菌和古菌基因组的 OASIS 注释提供了一个前所未有的机会来研究 IS 进化。在广泛的范围内,我们发现大多数 IS 家族非常普遍;然而,它们并不是随机分布在各个分类单元中的。这可能表明存在差异丢失、交换障碍和/或在进化枝之间没有足够的时间来达到平衡。IS 的数量随基因组长度的增加而增加,但对于 >2 Mb 的基因组,IS 密度既有巨大的变化,也没有增加。在最近分化的基因组的更精细尺度上,共享 IS 内容的比例急剧下降,表明成功的交叉感染的障碍的丢失和/或出现迅速发生。令人惊讶的是,即使在控制 16S rRNA 序列分歧后,相同的 IS 也更有可能在被标记为相同物种的基因组之间共享,而不是在不同物种之间共享。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/833b/3526298/b31667352c4d/gks778f1.jpg

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