Apoptotic-induced cleavage shifts HuR from being a promoter of survival to an activator of caspase-mediated apoptosis

作者：von Roretz C; Lian X Jin; Macri A M; Punjani N; Clair E; Drouin O; Dormoy Raclet V; Ma J F; Gallouzi I E^*

来源：Cell Death and Differentiation, 2013, 20(1): 154-168.

DOI：10.1038/cdd.2012.111

• caspases
• HuR
• apoptosis
• mRNA stability

Little is known about the cellular mechanisms modulating the shift in balance from a state of survival to cell death by caspase-mediated apoptosis in response to a lethal stress. Here we show that the RNA-binding protein HuR has an important function in mediating this switch. During caspase-mediated apoptosis, HuR is cleaved to generate two cleavage products (CPs). Our data demonstrate that the cleavage of HuR switches its function from being a prosurvival factor under normal conditions to becoming a promoter of apoptosis in response to a lethal stress. In the absence of an apoptotic stimuli, HuR associates with and promotes the expression of caspase-9 and prothymosin alpha (ProT) mRNAs, and pro- and antiapoptotic factors, respectively, both of which have been characterized as important players in determining cell fate. During the early steps of caspase-mediated apoptosis, however, the level of caspase-9 protein increases, while ProT remains unchanged. Under these conditions, the two HuR-CPs selectively bind to and stabilize caspase-9 mRNA, but do not bind to ProT. Hence, taken together, our data show that by maintaining a threshold of expression of proapoptotic factors such as caspase-9 in response to a lethal stress, the HuR-CPs help a cell to switch from resisting death to undergoing apoptosis. Cell Death and Differentiation (2013) 20, 154-168; doi:10.1038/cdd.2012.111; published online 7 September 2012

• 出版日期2013-1
• 单位McGill