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RNA-Seq 分析揭示了嗜热古菌 Methanopyrus kandleri 中 tRNA 加工事件的顺序以及 C/D 盒和 CRISPR RNA 的成熟过程。

RNA-Seq analyses reveal the order of tRNA processing events and the maturation of C/D box and CRISPR RNAs in the hyperthermophile Methanopyrus kandleri.

机构信息

Max-Planck-Institute for Terrestrial Microbiology, Max Planck Research Group: Prokaryotic Small RNA Biology, Karl-von-Frisch Strasse 10, 35037 Marburg, Germany.

出版信息

Nucleic Acids Res. 2013 Jul;41(12):6250-8. doi: 10.1093/nar/gkt317. Epub 2013 Apr 25.

Abstract

The methanogenic archaeon Methanopyrus kandleri grows near the upper temperature limit for life. Genome analyses revealed strategies to adapt to these harsh conditions and elucidated a unique transfer RNA (tRNA) C-to-U editing mechanism at base 8 for 30 different tRNA species. Here, RNA-Seq deep sequencing methodology was combined with computational analyses to characterize the small RNome of this hyperthermophilic organism and to obtain insights into the RNA metabolism at extreme temperatures. A large number of 132 small RNAs were identified that guide RNA modifications, which are expected to stabilize structured RNA molecules. The C/D box guide RNAs were shown to exist as circular RNA molecules. In addition, clustered regularly interspaced short palindromic repeats RNA processing and potential regulatory RNAs were identified. Finally, the identification of tRNA precursors before and after the unique C8-to-U8 editing activity enabled the determination of the order of tRNA processing events with termini truncation preceding intron removal. This order of tRNA maturation follows the compartmentalized tRNA processing order found in Eukaryotes and suggests its conservation during evolution.

摘要

产甲烷古菌 Methanopyrus kandleri 生长在接近生命上限温度的环境中。基因组分析揭示了适应这些恶劣条件的策略,并阐明了在 30 种不同 tRNA 物种的碱基 8 处存在独特的转移 RNA(tRNA)C 到 U 编辑机制。在这里,RNA-Seq 深度测序方法与计算分析相结合,用于描述这种高温嗜热生物的小 RNA 组,并深入了解极端温度下的 RNA 代谢。鉴定出大量的 132 种小 RNA,它们可以指导 RNA 修饰,从而稳定结构 RNA 分子。C/D 框引导 RNA 被证明以环状 RNA 分子的形式存在。此外,还鉴定了簇状规则间隔短回文重复 RNA 加工和潜在的调节 RNA。最后,在独特的 C8 到 U8 编辑活性前后鉴定出 tRNA 前体,从而确定了具有末端截断的 tRNA 加工事件的顺序,在前导序列切除之前。这种 tRNA 成熟的顺序遵循真核生物中发现的分隔 tRNA 加工顺序,并表明其在进化过程中的保守性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3efc/3695527/32dbb2ca8575/gkt317f1p.jpg

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