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PMID: 11289308 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

HuR and mRNA stability.

Cellular and molecular life sciences : CMLS ·Vol. 58 ·No. 2 ·2001-02-00 ·Pages 266-77

Brennan CM, Steitz JA

Abstract

An important mechanism of posttranscriptional gene regulation in mammalian cells is the rapid degradation of messenger RNAs (mRNAs) signaled by AU-rich elements (AREs) in their 3' untranslated regions. HuR, a ubiquitously expressed member of the Hu family of RNA-binding proteins related to Drosophila ELAV, selectively binds AREs and stabilizes ARE-containing mRNAs when overexpressed in cultured cells. This review discusses mRNA decay as a general form of gene regulation, decay signaled by AREs, and the role of HuR and its Hu-family relatives in antagonizing this mRNA degradation pathway. The influence of newly identified protein ligands to HuR on HuR function in both normal and stressed cells may explain how ARE-mediated mRNA decay is regulated in response to environmental change.

MeSH Terms
Amino Acid Sequence Animals Antigens, Surface Base Sequence Biological Transport, Active Carrier Proteins/metabolism Cell Differentiation Cytoplasm/metabolism ELAV Proteins ELAV-Like Protein 1 Humans Models, Biological Molecular Sequence Data RNA Stability RNA, Messenger/genetics,metabolism RNA-Binding Proteins/genetics,metabolism Sequence Homology, Amino Acid
Chemicals
Antigens, Surface Carrier Proteins ELAV Proteins ELAV-Like Protein 1 ELAVL1 protein, human RNA, Messenger RNA-Binding Proteins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Brennan C M
Department of Molecular Biophysics and Biochemistry, Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut 06536, USA.
Steitz J A
Article Info
Journal
Cellular and molecular life sciences : CMLS
Abbr.
Cell Mol Life Sci
ISSN
1420-682X
Published
2001-02-00
Pages
266-77
Language
English
Region
Switzerland
NLM ID
9705402
Subset
IM
Grants
NCI NIH HHS · CA16038 · United States
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