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修饰核糖体:核糖体蛋白基因的同工基因决定翻译调控。

Pimp My Ribosome: Ribosomal Protein Paralogs Specify Translational Control.

机构信息

Department of Molecular Genetics, Weizmann Institute of Science, Rehovot 7610001, Israel.

出版信息

Trends Genet. 2018 Nov;34(11):832-845. doi: 10.1016/j.tig.2018.08.004. Epub 2018 Sep 5.

Abstract

The ability of cells to grow and divide, differentiate and function, and even senesce is dependent on the fine-tuning of both gene and protein expression. Protein concentration in the cell is regulated not only at the transcriptional and post-translational levels, but also at the level of translation. Ribosomes, the molecular machines behind translation, were once considered to be an invariant driving force behind protein expression. However, studies over the past decade paint a rather different picture; namely, that ribosomes constitute an additional layer of regulatory control that might define which subsets of mRNAs are translated, to what extent, and to what purpose. Recent works summarized herein directly implicate ribosome heterogeneity and, in particular, ribosomal protein (RP) paralog specificity in regulating mRNA translation and control of the cellular translatome.

摘要

细胞的生长和分裂、分化和功能,甚至衰老的能力都依赖于基因和蛋白质表达的精细调控。细胞内的蛋白质浓度不仅受转录和翻译后水平的调节,还受翻译水平的调节。核糖体是翻译背后的分子机器,曾经被认为是蛋白质表达不变的驱动力。然而,过去十年的研究描绘了一幅截然不同的图景;即核糖体构成了额外的一层调节控制,可能决定哪些 mRNA 亚群被翻译、以何种程度和何种目的进行翻译。本文总结的最近的研究工作直接表明核糖体的异质性,特别是核糖体蛋白(RP)同工型的特异性,在调节 mRNA 翻译和控制细胞翻译组方面发挥了作用。

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