Tales of Detailed Poly(A) Tails
Open accessAbstract
Poly(A) tails are non-templated additions of adenosines at the 3' ends of most eukaryotic mRNAs. In the nucleus, these RNAs are co-transcriptionally cleaved at a poly(A) site and then polyadenylated before being exported to the cytoplasm. In the cytoplasm, poly(A) tails play pivotal roles in the translation and stability of the mRNA. One challenge in studying poly(A) tails is that they are difficult to sequence and accurately measure. However, recent advances in sequencing technology, computational algorithms, and other assays have enabled a more detailed look at poly(A) tail length genome-wide throughout many developmental stages and organisms. With the help of these advances, our understanding of poly(A) tail length has evolved over the past 5 years with the recognition that highly expressed genes can have short poly(A) tails and the elucidation of the seemingly contradictory roles for poly(A)-binding protein (PABP) in facilitating both protection and deadenylation.
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Translational efficiency of mRNA improves with increasing poly(A) size up to a length of 300 A.
“who showed that the translational efficiency of mRNA was improved in conjunction with increasing poly(A) size until a length of 300 A”
From Combining an optimized mRNA template with a double purification process allows strong expression of in vitro transcribed mRNA (2021) · cites this paper as [24]
Poly(A) tail plays an important function in the stability and regulation of translation efficiency of mRNA.
“Poly(A) tail plays an important function in the stability and regulation of translation efficiency of the mRNA.24”
From Combining an optimized mRNA template with a double purification process allows strong expression of in vitro transcribed mRNA (2021) · cites this paper as [24]
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Hanson, G., & Coller, J. (2018) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2017.91 · Cited by 825 · see citing works
Multifunctional deadenylase complexes diversify mRNA control
Goldstrohm, A. C., & Wickens, M. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2370 · Cited by 377 · see citing works
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Linares-Fernández, S., Moreno, J., Lambert, E., Mercier-Gouy, P., Vachez, L., Verrier, B., & Exposito, J.-Y. (2021) · Molecular Therapy - Nucleic Acids · doi:10.1016/j.omtn.2021.10.007 · Cited by 62 · see citing works
- Authors
- Nicholson, A. L., & Pasquinelli, A. E.
- Affiliations
- University of California San Diego (US)
- Corresponding author
- Pasquinelli, Amy E.
- Venue
- Trends in Cell Biology
- Publisher
- Elsevier BV
- Published
- 2019-03
- Volume
- 29
- Issue
- 3
- Pages
- 191-200
- ISSN
- 0962-8924 (ISSN-L)
- PMC
- PMC7083203
- OpenAlex
- W2903167102
- Cited by
- 209
- References
- 3
- Citations by year
- 2026: 21 · 2025: 22 · 2024: 31 · 2023: 31 · 2022: 37 · 2021: 33 · 2020: 27 · 2019: 7
- FWCI
- 1.66
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Trends in Cell Biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- National Institute of General Medicine (T32 GM007240)
- National Science Foundation Graduate Research Fellowship (DGE-1650112)
- National Institutes of Health (R35 GM127012)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Keywords
- poly(A) tail, mRNA 3' end, poly(A) site, polyadenylation, mRNA stability, translation (biology), poly(A)-binding protein, deadenylation, poly(A) tail length, gene expression, mRNA export
- MeSH terms
- Algorithms, Animals, Cell Nucleus, Cytoplasm, Humans, Poly A, RNA, Messenger, Sequence Analysis, RNA, Computational Biology
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