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 α (ProTaα) and enhanced its translation and cytoplasmic abundance. More recently, HuR was shown to increase the stability of a target mRNA encoding the pro-survival deacetylase 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. ©2007 Landes Bioscience.
CITATION STYLE
Abdelmohsen, K., Lal, A., Hyeon, H. K., & Gorospe, M. (2007, June 1). Posttranscriptional orchestration of an anti-apoptotic program by HuR. Cell Cycle. Taylor and Francis Inc. https://doi.org/10.4161/cc.6.11.4299
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