P bodies and the control of mRNA translation and degradation
Open accessAbstract
Recent results indicate that many untranslating mRNAs in somatic eukaryotic cells assemble into related mRNPs that accumulate in specific cytoplasmic foci referred to as P bodies. Transcripts associated with P body components can either be degraded or return to translation. Moreover, P bodies are also biochemically and functionally related to some maternal and neuronal mRNA granules. This suggests an emerging model of cytoplasmic mRNA function in which the rates of translation and degradation of mRNAs are influenced by a dynamic equilibrium between polysomes and the mRNPs seen in P bodies. Moreover, some mRNA-specific regulatory factors, including miRNAs and RISC, appear to repress translation and promote decay by recruiting P body components to individual mRNAs.
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P-bodies are cytoplasmic foci depleted of ribosomes and enriched with enzymatic mRNA degradation machinery such as mRNA decapping proteins, the CCR4-NOT complex, XRN1, and GW182 family proteins.
“They are cytoplasmic foci depleted of ribosomes (79) and enriched with enzymatic mRNA degradation machinery, such as mRNA decapping proteins, the CCR4-NOT complex, XRN1, and GW182 family proteins (78).”
From Overview of MicroRNA Biogenesis, Mechanisms of Actions, and Circulation (2018) · cites this paper as [79]
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- Authors
- Parker, R., & Sheth, U.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Parker, Roy
- ORCID
- Parker, Roy
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2007-03
- Volume
- 25
- Issue
- 5
- Pages
- 635-646
- ISSN
- 1097-2765 (ISSN-L)
- OpenAlex
- W2003911773
- Cited by
- 1,335
- References
- 94
- Citations by year
- 2026: 33 · 2025: 49 · 2024: 38 · 2023: 30 · 2022: 44 · 2021: 44 · 2020: 54 · 2019: 57 · 2018: 44 · 2017: 47 · 2016: 66 · 2015: 62 · 2014: 78 · 2013: 86 · 2012: 119
- FWCI
- 9.76
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 2366 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R37GM045443)
- 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 Interference and Gene Delivery
- Keywords
- P-bodies, mRNA translation, mRNA degradation, mRNA granules, polysomes, microRNA, RNA-induced silencing complex, protein synthesis inhibition
- MeSH terms
- Animals, Humans, Models, Biological, Neurons, Protein Biosynthesis, RNA Stability, Cytoplasmic Structures, RNA, Messenger, Stored
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