4.6 Article

Posttranscriptional orchestration of an anti-apoptotic program by HuR

Journal

CELL CYCLE
Volume 6, Issue 11, Pages 1288-1292

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/cc.6.11.4299

Keywords

mRNA-binding protein; mRNA turnover; translational control; ELAV; SIRT1; ProT alpha; Bcl-2; Mcl-1

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Funding

  1. Intramural NIH HHS Funding Source: Medline

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The RNA-binding protein HuR can stabilize and/ or regulate the translation of target mRNAs, thereby affecting the cellular responses to immune, proliferative, and damaging agents. Here, we discuss emerging evidence that HuR elicits a broad anti-apoptotic function through its influence on the expression of multiple target mRNAs. HuR was previously shown to bind to the mRNA encoding the apoptosome inhibitor prothymosin a (ProT alpha) and enhanced its translation and cytoplasmic abundance. More recently, HuR was shown to increase the stability of a target mRNA encoding the pro-survival deacety lase SIRT1. The discovery that HuR likewise binds to and promotes the expression of mRNAs encoding Bcl-2 and Mcl-1, two major anti-apoptotic effectors, strongly supports HuR's role as a key upstream coordinator of a constitutive pro-survival program.

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