Ribosome-based quality control of mRNA and nascent peptides.

Ribosome-based quality control of mRNA and nascent peptides.
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DOI:
10.1002/wrna.1366
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发表时间:
2017-01
影响因子:
7.3
通讯作者:
Zaher, Hani S.
Zaher, Hani S.
中科院分区:
生物学2区
文献类型:
--
作者:
Simms, Carrie L.;Thomas, Erica N.;Zaher, Hani S.

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Quality control processes are widespread and play essential roles in detecting defective molecules and removing them in order to maintain organismal fitness. Aberrant mRNA molecules, unless properly managed, pose a significant hurdle to cellular proteostasis. Often mRNAs harbor premature stop codons, possess structures that present a block to the translational machinery, or lack stop codons entirely. In eukaryotes, the three cytoplasmic mRNA-surveillance processes, nonsense-mediated decay (NMD), no-go decay (NGD) and non-stop decay (NSD), evolved to cope with these aberrant mRNAs, respectively. Non-stop mRNAs and mRNAs that inhibit translation elongation are especially problematic as they sequester valuable ribosomes from the translating ribosome pool. As a result, in addition to RNA degradation, NSD and NGD are intimately coupled to ribosome rescue in all domains of life. Furthermore, protein products produced from all three classes of defective mRNAs are more likely to malfunction. It is not surprising then that these truncated nascent protein products are subject to degradation. Over the past few years, many studies have begun to document a central role for the ribosome in initiating the RNA and protein quality control processes. The ribosome appears to be responsible for recognizing the target mRNAs, as well as for recruiting the factors required to carry out the processes of ribosome rescue and nascent protein decay.
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