Connections Underlying Translation and mRNA Stability. Issue 18 (11th September 2016)

• Record Type: Journal Article
• Authors: Radhakrishnan, Aditya; Green, Rachel
• Is Part Of: Journal of molecular biology. Volume 428:Issue 18(2016:Sep. 15)
• Page Start: 3558
• Page End: 3564
• Publication Date: 2016-09-11
• Subjects: 3′-UTR 3′-untranslated region -- NMD nonsense-mediated decay -- ORF open reading frame; mRNA decay -- codon optimality -- mRNA surveillance -- microRNAs; Molecular biology -- Periodicals; Biology -- Periodicals; Biochemistry -- Periodicals; Bacteriology -- Periodicals; Molecular Biology -- Periodicals; Biochemistry -- Periodicals; Biologie moléculaire -- Périodiques; Biologie -- Périodiques; Biochimie -- Périodiques; Moleculaire biologie; Biochemistry; Biology; Molecular biology; Periodicals; 572.805
• DOI: 10.1016/j.jmb.2016.05.025
• Languages: English
• ISSNs: 0022-2836

Abstract

Abstract: Gene expression and regulation in organisms minimally depends on transcription by RNA polymerase and on the stability of the RNA product (for both coding and non-coding RNAs). For coding RNAs, gene expression is further influenced by the amount of translation by the ribosome and by the stability of the protein product. The stabilities of these two classes of RNA, non-coding and coding, vary considerably: tRNAs and rRNAs tend to be long lived while mRNAs tend to be more short lived. Even among mRNAs, however, there is a considerable range in stability (ranging from seconds to hours in bacteria and up to days in metazoans), suggesting a significant role for stability in the regulation of gene expression. Here, we review recent experiments from bacteria, yeast and metazoans indicating that the stability of most mRNAs is broadly impacted by the actions of ribosomes that translate them. Ribosomal recognition of defective mRNAs triggers "mRNA surveillance" pathways that target the mRNA for degradation [Shoemaker and Green (2012) ]. More generally, even the stability of perfectly functional mRNAs appears to be dictated by overall rates of translation by the ribosome [Herrick et al. (1990), Presnyak et al. (2015) ]. Given that mRNAs are synthesized for the purpose of being translated into proteins, it is reassuring that such intimate connections between mRNA and the ribosome can drive biological regulation. In closing, we consider the likelihood that these connections between protein synthesis and mRNA stability are widespread or whether other modes of regulation dominate the mRNA stability landscape in higher organisms. Graphical Abstract: Highlights: mRNAs, even within an organism, have vast differences in stabilities, ranging many orders of magnitude, but the mechanistic basis of this heterogeneity is poorly understood. Recent findings show aberrant translation by a ribosome on an mRNA greatly modulates the stability of the mRNA. Coupling of mRNA stability to translation helps inform and resolve outstanding mechanistic issues in the field of microRNA-mediated repression. Regulation of mRNA stability through translation appears to be a widely used mechanism in regulation of gene expression.