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分析由 DiGReF 程序生成的多样性产生逆转录元件的综合数据集。

Analysis of a comprehensive dataset of diversity generating retroelements generated by the program DiGReF.

机构信息

Department of Molecular Genetics, University of Kaiserslautern, Kaiserslautern, Germany.

出版信息

BMC Genomics. 2012 Aug 28;13:430. doi: 10.1186/1471-2164-13-430.

Abstract

BACKGROUND

Diversity Generating Retroelements (DGRs) are genetic cassettes that can introduce tremendous diversity into a short, defined region of the genome. They achieve hypermutation through replacement of the variable region with a strongly mutated cDNA copy generated by the element-encoded reverse transcriptase. In contrast to "selfish" retroelements such as group II introns and retrotransposons, DGRs impart an advantage to their host by increasing its adaptive potential. DGRs were discovered in a bacteriophage, but since then additional examples have been identified in some bacterial genomes.

RESULTS

Here we present the program DiGReF that allowed us to comprehensively screen available databases for DGRs. We identified 155 DGRs which are found in all major classes of bacteria, though exhibiting sporadic distribution across species. Phylogenetic analysis and sequence comparison showed that DGRs move between genomes by associating with various mobile elements such as phages, transposons and plasmids. The DGR cassettes exhibit high flexibility in the arrangement of their components and easily acquire additional paralogous target genes. Surprisingly, the genomic data alone provide new insights into the molecular mechanism of DGRs. Most notably, our data suggest that the template RNA is transcribed separately from the rest of the element.

CONCLUSIONS

DiGReF is a valuable tool to detect DGRs in genome data. Its output allows comprehensive analysis of various aspects of DGR biology, thus deepening our understanding of the role DGRs play in prokaryotic genome plasticity, from the global down to the molecular level.

摘要

背景

多样性产生 retroelements(DGRs)是遗传盒,可以在基因组的一个短定义区域中引入巨大的多样性。它们通过用元素编码的逆转录酶生成的强烈突变的 cDNA 副本替换可变区来实现超突变。与诸如组 II 内含子和 retrotransposons 等“自私” retroelements 相反,DGRs 通过增加其适应潜力赋予宿主优势。DGRs 在噬菌体中被发现,但此后在一些细菌基因组中又发现了其他例子。

结果

在这里,我们介绍了程序 DiGReF,该程序使我们能够全面筛选可用数据库以查找 DGRs。我们鉴定了 155 个 DGRs,它们存在于所有主要的细菌类别中,但在物种间分布稀疏。系统发育分析和序列比较表明,DGRs 通过与噬菌体、转座子和质粒等各种移动元件相关联在基因组之间移动。DGR 盒在其组件的排列上具有高度的灵活性,并且容易获得额外的旁系靶基因。令人惊讶的是,仅基因组数据就为 DGRs 的分子机制提供了新的见解。最值得注意的是,我们的数据表明,模板 RNA 是与元件的其余部分分开转录的。

结论

DiGReF 是在基因组数据中检测 DGRs 的有价值的工具。它的输出允许对 DGR 生物学的各个方面进行全面分析,从而加深我们对 DGR 在原核基因组可塑性中的作用的理解,从全局到分子水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c472/3521204/978cd27f96fa/1471-2164-13-430-1.jpg

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