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PMID: 22392217 Published · epublish English Journal Article Research Support, Non-U.S. Gov't Review

Regulation of cytoplasmic mRNA decay.

Nature reviews. Genetics ·Vol. 13 ·No. 4 ·2012-03-06 ·Pages 246-59

Schoenberg DR, Maquat LE

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.

MeSH Terms
Active Transport, Cell Nucleus Animals Cytoplasm/genetics,metabolism Histones/genetics,metabolism Mammals/genetics Organ Specificity Phosphorylation Protein Biosynthesis RNA Stability Receptors, Cytoplasmic and Nuclear/metabolism Signal Transduction
Chemicals
Histones Receptors, Cytoplasmic and Nuclear
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Schoenberg Daniel R
Department of Molecular and Cellular Biochemistry and Center for RNA Biology, The Ohio State University, Columbus, Ohio 43210, USA. [email protected]
Maquat Lynne E
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Article Info
Journal
Nature reviews. Genetics
Abbr.
Nat Rev Genet
ISSN
1471-0064
Published
2012-03-06
Epub
2012-00-06
Pages
246-59
Language
English
Region
England
NLM ID
100962779
PMCID
PMC3351101
Subset
IM
Grants
NIGMS NIH HHS · R01 GM038277 · United States
NIGMS NIH HHS · R01 GM074593 · United States
NIGMS NIH HHS · R01 GM079707 · United States
NIGMS NIH HHS · R01 GM059614 · United States
NIGMS NIH HHS · R01 GM084177 · United States
Corrections
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