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Abstract

In eukaryotes, poly(A) tails are present on almost every mRNA. Early experiments led to the hypothesis that poly(A) tails and the cytoplasmic polyadenylate-binding protein (PABPC) promote translation and prevent mRNA degradation, but the details remained unclear. More recent data suggest that the role of poly(A) tails is much more complex: poly(A)-binding protein can stimulate poly(A) tail removal (deadenylation) and the poly(A) tails of stable, highly translated mRNAs at steady state are much shorter than expected. Furthermore, the rate of translation elongation affects deadenylation. Consequently, the interplay between poly(A) tails, PABPC, translation and mRNA decay has a major role in gene regulation. In this Review, we discuss recent work that is revolutionizing our understanding of the roles of poly(A) tails in the cytoplasm. Specifically, we discuss the roles of poly(A) tails in translation and control of mRNA stability and how poly(A) tails are removed by exonucleases (deadenylases), including CCR4–NOT and PAN2–PAN3. We also discuss how deadenylation rate is determined, the integration of deadenylation with other cellular processes and the function of PABPC. We conclude with an outlook for the future of research in this field.

Recent studies have revolutionized our understanding of the interplay between mRNA poly(A) tails and the processes of translation and mRNA decay in the cytoplasm. Poly(A) tails interact with dedicated RNA-binding proteins and deadenylases, which together determine the impact of poly(A) tails on gene expression.

Details

Title
Roles of mRNA poly(A) tails in regulation of eukaryotic gene expression
Author
Passmore, Lori A 1   VIAFID ORCID Logo  ; Coller, Jeff 2   VIAFID ORCID Logo 

 MRC Laboratory of Molecular Biology, Cambridge, UK (GRID:grid.42475.30) (ISNI:0000 0004 0605 769X) 
 Johns Hopkins University, Department of Molecular Biology and Genetics and Department of Biology, Baltimore, USA (GRID:grid.21107.35) (ISNI:0000 0001 2171 9311) 
Pages
93-106
Publication year
2022
Publication date
Feb 2022
Publisher
Nature Publishing Group
ISSN
14710072
e-ISSN
14710080
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2623201316
Copyright
© Springer Nature Limited 2021.