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含 TISU 元件的 mRNAs 的独特翻译起始。

Unique translation initiation of mRNAs-containing TISU element.

机构信息

Department of Biological Chemistry, The Weizmann Institute of Science, Rehovot, Israel.

出版信息

Nucleic Acids Res. 2011 Sep 1;39(17):7598-609. doi: 10.1093/nar/gkr484. Epub 2011 Jun 25.

Abstract

Translation Initiator of Short 5' UTR (TISU) is a unique regulatory element of both transcription and translation initiation. It is present in a sizable number of genes with basic cellular functions and a very short untranslated region (5' UTR). Here, we investigated translation initiation from short 5' UTR mRNAs with AUG in various contexts. Reducing 5' UTR length to the minimal functional size increases leaky scanning from weak and strong initiators but hardly affects translation initiation and ribosomal binding directed by TISU. Ribosome interaction with TISU mRNA is cap dependent and involves AUG downstream nucleotides that compensate for the absent 5' UTR contacts. Interestingly, eIF1 inhibits cap-proximal AUG selection within weak or strong contexts but not within TISU. Furthermore, TISU-directed translation is unaffected by inhibition of the RNA helicase eIF4A. Thus, TISU directs efficient cap-dependent translation initiation without scanning, a mechanism that would be advantageous when intracellular levels of eIF1 and eIF4A fluctuate.

摘要

短 5'UTR(TISU)的翻译起始子是转录和翻译起始的独特调节元件。它存在于许多具有基本细胞功能和非常短的非翻译区(5'UTR)的基因中。在这里,我们研究了具有不同上下文 AUG 的短 5'UTR mRNA 的翻译起始。将 5'UTR 长度减少到最小功能大小会增加从弱和强起始子的渗漏扫描,但几乎不会影响 TISU 指导的翻译起始和核糖体结合。核糖体与 TISU mRNA 的相互作用依赖于帽,并涉及 AUG 下游核苷酸,这些核苷酸补偿了不存在的 5'UTR 接触。有趣的是,eIF1 在弱或强情况下抑制帽近端 AUG 选择,但在 TISU 中不抑制。此外,TISU 指导的翻译不受 RNA 解旋酶 eIF4A 抑制的影响。因此,TISU 指导无扫描的高效帽依赖性翻译起始,当细胞内 eIF1 和 eIF4A 水平波动时,这种机制将是有利的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/417e/3177215/27811869cbd8/gkr484f1.jpg

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