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内含子 II 作为自我保护和细菌接合的冷传感器。

Group II intron as cold sensor for self-preservation and bacterial conjugation.

机构信息

Department of Biological Sciences and RNA Institute, University at Albany, Albany, NY 12222, USA.

College of Life Sciences, Hebei University, Baoding, Hebei 071002, China.

出版信息

Nucleic Acids Res. 2020 Jun 19;48(11):6198-6209. doi: 10.1093/nar/gkaa313.

DOI:10.1093/nar/gkaa313
PMID:32379323
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7293003/
Abstract

Group II introns are self-splicing ribozymes and mobile genetic elements. Splicing is required for both expression of the interrupted host gene and intron retromobility. For the pRS01 plasmid-encoded Lactococcus lactis group II intron, Ll.LtrB, splicing enables expression of the intron's host relaxase protein. Relaxase, in turn, initiates horizontal transfer of the conjugative pRS01 plasmid and stimulates retrotransposition of the intron. Little is known about how splicing of bacterial group II introns is influenced by environmental conditions. Here, we show that low temperatures can inhibit Ll.LtrB intron splicing. Whereas autocatalysis is abolished in the cold, splicing is partially restored by the intron-encoded protein (IEP). Structure profiling reveals cold-induced disruptions of key tertiary interactions, suggesting that a kinetic trap prevents the intron RNA from assuming its native state. Interestingly, while reduced levels of transcription and splicing lead to a paucity of excised intron in the cold, levels of relaxase mRNA are maintained, partially due to diminished intron-mediated mRNA targeting, allowing intron spread by conjugal transfer. Taken together, this study demonstrates not only the intrinsic cold sensitivity of group II intron splicing and the role of the IEP for cold-stress adaptation, but also maintenance of horizontal plasmid and intron transfer under cold-shock.

摘要

内含子 II 是自我剪接的核酶和移动遗传元件。对于表达中断的宿主基因和内含子反向移动,剪接都是必需的。对于 pRS01 质粒编码的乳球菌属 II 类内含子 Ll.LtrB,剪接使内含子的宿主松弛酶蛋白得以表达。松弛酶反过来又启动了可移动的 pRS01 质粒的水平转移,并刺激了内含子的反向转座。关于环境条件如何影响细菌内含子 II 的剪接知之甚少。在这里,我们表明低温会抑制 Ll.LtrB 内含子的剪接。虽然在寒冷条件下自动催化被废除,但内含子编码的蛋白 (IEP) 部分恢复了剪接。结构分析揭示了低温诱导的关键三级相互作用的破坏,这表明动力学陷阱阻止了内含子 RNA 呈现其自然状态。有趣的是,虽然转录和剪接水平降低导致低温下切除的内含子数量减少,但松弛酶 mRNA 的水平保持不变,部分原因是内含子介导的 mRNA 靶向减少,允许通过接合转移进行内含子传播。总之,这项研究不仅证明了内含子 II 剪接的固有低温敏感性和 IEP 对冷应激适应的作用,还证明了在冷休克下质粒和内含子的水平转移得以维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868b/7293003/d56452dbd7f2/gkaa313fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868b/7293003/d56452dbd7f2/gkaa313fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/868b/7293003/d56452dbd7f2/gkaa313fig2.jpg

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