Title |
HuR and mRNA stability
|
---|---|
Published in |
Cellular and Molecular Life Sciences, February 2001
|
DOI | 10.1007/pl00000854 |
Pubmed ID | |
Authors |
C. M. Brennan, J. A. Steitz* |
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. |
X Demographics
Geographical breakdown
Country | Count | As % |
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Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Members of the public | 1 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
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United States | 7 | 2% |
Canada | 4 | 1% |
Austria | 3 | <1% |
United Kingdom | 2 | <1% |
Brazil | 1 | <1% |
India | 1 | <1% |
Italy | 1 | <1% |
Germany | 1 | <1% |
Russia | 1 | <1% |
Other | 1 | <1% |
Unknown | 335 | 94% |
Demographic breakdown
Readers by professional status | Count | As % |
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Student > Ph. D. Student | 94 | 26% |
Researcher | 60 | 17% |
Student > Master | 44 | 12% |
Student > Bachelor | 35 | 10% |
Student > Doctoral Student | 19 | 5% |
Other | 48 | 13% |
Unknown | 57 | 16% |
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Medicine and Dentistry | 24 | 7% |
Chemistry | 10 | 3% |
Immunology and Microbiology | 8 | 2% |
Other | 23 | 6% |
Unknown | 68 | 19% |