Regulation of cytoplasmic mRNA decay
Open accessAbstract
Discoveries made over the past 20 years highlight the importance of mRNA decay as a means of modulating gene expression and thereby protein production. Up until recently, studies largely focused on identifying cis-acting sequences that serve as mRNA stability or instability elements, the proteins that bind these elements, how the process of translation influences mRNA decay and the ribonucleases that catalyse decay. Now, current studies have begun to elucidate how the decay process is regulated. This Review examines our current understanding of how mammalian cell mRNA decay is controlled by different signalling pathways and lays out a framework for future research.
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Because no exon-exon boundary in ADNP mRNA lies downstream of any of the mutations, nonsense-mediated RNA decay is unlikely.
“Since no exon-exon boundary in the ADNP mRNA is present downstream from any of the mutations, nonsense mediated RNA decay (NMD) is unlikely28-30.”
From A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP (2014) · cites this paper as [29]
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- Authors
- Schoenberg, D. R., & Maquat, L. E.
- Affiliations
- The Ohio State University (US)
- University of Rochester Medicine (US)
- Corresponding author
- Schoenberg, Daniel R.
- Maquat, Lynne E.
- Venue
- Nature Reviews Genetics
- Published
- 2012-03-06
- Volume
- 13
- Issue
- 4
- Pages
- 246-259
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- PMC
- PMC3351101
- OpenAlex
- W2003230246
- Cited by
- 656
- References
- 119
- Citations by year
- 2026: 20 · 2025: 30 · 2024: 31 · 2023: 29 · 2022: 30 · 2021: 42 · 2020: 51 · 2019: 40 · 2018: 66 · 2017: 49 · 2016: 45 · 2015: 61 · 2014: 58 · 2013: 77 · 2012: 26
- FWCI
- 6.47
- Type
- journal article
- Language
- en
- Update notices
- erratum (2012-05-09)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM074593, R01GM079707, R01GM084177, R01GM038277, R01GM059614)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA regulation and disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
- Keywords
- mRNA degradation, post-transcriptional regulation, mRNA stability, ribonuclease, translation (biology), signaling pathways, protein expression regulation, mammalian cells
- MeSH terms
- Animals, Cytoplasm, Histones, Mammals, Organ Specificity, Phosphorylation, Protein Biosynthesis, Signal Transduction, Receptors, Cytoplasmic and Nuclear, RNA Stability, Active Transport, Cell Nucleus
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