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EF-G 诱导核糖体沿着非编码 mRNA 滑动。

EF-G-induced ribosome sliding along the noncoding mRNA.

机构信息

Max Planck Institute for Biophysical Chemistry, Department of Physical Biochemistry, 37077 Göttingen, Germany.

出版信息

Sci Adv. 2019 Jun 5;5(6):eaaw9049. doi: 10.1126/sciadv.aaw9049. eCollection 2019 Jun.

Abstract

Translational bypassing is a recoding event during which ribosomes slide over a noncoding region of the messenger RNA (mRNA) to synthesize one protein from two discontinuous reading frames. Structures in the mRNA orchestrate forward movement of the ribosome, but what causes ribosomes to start sliding remains unclear. Here, we show that elongation factor G (EF-G) triggers ribosome take-off by a pseudotranslocation event using a small mRNA stem-loop as an A-site transfer RNA mimic and requires hydrolysis of about two molecules of guanosine 5'-triphosphate per nucleotide of the noncoding gap. Bypassing ribosomes adopt a hyper-rotated conformation, also observed with ribosomes stalled by the SecM sequence, suggesting common ribosome dynamics during translation stalling. Our results demonstrate a new function of EF-G in promoting ribosome sliding along the mRNA, in contrast to codon-wise ribosome movement during canonical translation, and suggest a mechanism by which ribosomes could traverse untranslated parts of mRNAs.

摘要

翻译转位是一种重编码事件,在此过程中核糖体在信使 RNA(mRNA)的非编码区滑动,以从两个不连续的阅读框合成一种蛋白质。mRNA 中的结构协调核糖体的向前运动,但导致核糖体开始滑动的原因尚不清楚。在这里,我们使用一个小的 mRNA 茎环作为 A 位转移 RNA 模拟物,显示延伸因子 G(EF-G)通过假转位事件触发核糖体起飞,并且需要每核苷酸非编码缺口的两个分子的鸟苷 5'-三磷酸水解。翻译延伸中核糖体被 SecM 序列阻断,转位核糖体采用超旋转构象,这表明核糖体动力学在翻译暂停时是共同的。我们的结果表明 EF-G 在促进核糖体沿 mRNA 滑动方面具有新的功能,与典型翻译中基于密码子的核糖体运动相反,并提出了核糖体可以穿过 mRNA 未翻译部分的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f52/6551183/0ce9fa6001f8/aaw9049-F1.jpg

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