Cited by 656RNA Research and SplicingRNA regulation and diseaseRNA and protein synthesis mechanisms

Regulation of cytoplasmic mRNA decay

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Schoenberg, Daniel R., Maquat, Lynne E.·2012·Nature Reviews Genetics

Abstract

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.”

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  1. [94]von Roretz C Di Marco S Mazroui R Gallouzi IE Turnover of AU-rich-containing mRNAs during stress: a matter of survival Wiley Interdisc Rev: RNA 2 336 347 2011 21957021

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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
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
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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