A tale of two termini:
Abstract
A quarter of century following the prediction that mRNAs are translated in a circular form, recent biochemical and genetic evidence has accumulated to support the idea that communication between the termini of an mRNA is necessary to promote translation initiation. The poly(A)-binding protein (PABP) interacts with the cap-associated eukaryotic initiation factor (eIF) 4G (in yeast and plants) and eIF4B (in plants), a functional consequence of which is to increase the affinity of PABP for poly(A) and to increase the affinity of the cap-binding complex, eIF4F (of which eIF4G is a subunit) for the 5' cap structure. In mammals, PABP interacts with a novel PABP-interacting protein that also binds eIF4A. The interaction between PABP and those initiation factors associated with the 5' terminus of an mRNA may also explain the role of PABP during mRNA turnover, as it protects the 5' cap from attack by Dcp1p, the decapping enzyme. Several of those mRNAs that have evolved functional equivalents to a cap or a poly(A) tail nevertheless require a functional interaction between terminal regulatory elements similar to that observed between the 5' cap and poly(A) tail, suggesting that efficient translation is predicated on communication between largely-separated regulatory elements within an mRNA.
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The poly(A) tail regulates the fate of mRNA by synergy with the 5' cap, the internal ribosomal entry site, and various RNA stability determinants.
“The poly(A) tail regulates the fate of mRNA by synergy with the 5Ј cap, with the internal ribosomal entry site, and with various RNA stability determinants.31,[38][39][40][41]”
From Modification of antigen-encoding RNA increases stability, translational efficacy, and T-cell stimulatory capacity of dendritic cells (2006) · cites this paper as [31]
mRNA stability and translation are controlled by a complex network of RNA/protein interactions and depend on the primary and secondary structures of mRNAs, their rates of translation, and the initiation of one of the various degradation mechanisms.
“mRNA stability and translation are controlled by a complex network of RNA/protein interactions and depend on the primary and secondary structures of mRNAs, their rates of translation, and the initiation of one of the various degradation mechanisms.[28][29][30][31]”
From Modification of antigen-encoding RNA increases stability, translational efficacy, and T-cell stimulatory capacity of dendritic cells (2006) · cites this paper as [31]
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Kahvejian, A., Svitkin, Y. V., Sukarieh, R., M'Boutchou, M.-N., & Sonenberg, N. (2005) · Genes & Development · doi:10.1101/gad.1262905 · Cited by 491 · see citing works
Rate-Limiting Steps in Yeast Protein Translation
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Evading innate immunity in nonviral mRNA delivery: don't shoot the messenger.
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Youn, H., & Chung, J.-K. (2015) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.2015.1057563 · Cited by 114 · see citing works
- Authors
- Gallie, D. R.
- Affiliations
- University of California, Riverside (US)
- Corresponding author
- Gallie, Daniel R
- ORCID
- Gallie, Daniel R
- Venue
- Gene
- Publisher
- Elsevier BV
- Published
- 1998-08
- Volume
- 216
- Issue
- 1
- Pages
- 1-11
- ISSN
- 0378-1119 (ISSN-L)
- OpenAlex
- W100014517
- Cited by
- 280
- References
- 0
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 2 · 2023: 2 · 2022: 3 · 2020: 10 · 2019: 7 · 2018: 3 · 2017: 5 · 2016: 9 · 2015: 8 · 2014: 4 · 2013: 8 · 2012: 7
- FWCI
- 1.71
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Gene (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Keywords
- poly(A)-binding protein, mRNA translation initiation, 5' cap, poly(A) tail, eIF4G, eIF4B, eIF4A, mRNA turnover
- MeSH terms
- Animals, Nucleic Acid Conformation, Peptide Initiation Factors, Protein Binding, RNA Caps, RNA, Messenger, Protein Biosynthesis, RNA-Binding Proteins, Poly(A)-Binding Proteins
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