期刊
BIOCHEMISTRY
卷 55, 期 23, 页码 3285-3302出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.6b00306
关键词
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资金
- Department of Defense Prostate Cancer Research Program [W81XWH-08-1-0045]
- American Cancer Society [RSG-09-166-01-CCG]
- State of North Dakota Experimental Program to Stimulate Competitive Research (ND-EPSCoR) [FAR0022246]
Apoptosis inducing factor (AIF) plays a well-defined role in controlling cell death but is also a critical factor for maintaining mitochondrial energy homeostasis; how these dueling activities are balanced has remained largely elusive. To identify new AIF binding partners that may define the continuum of AIF cellular regulation, a biochemical screen was performed that identified the mitochondrial phosphoglycerate mutase 5 (PGAM5) as an AIF associated factor. AIF binds both the short and long isoforitis of PGAM5. and can reduce the ability of PGAM5 to control antioxidant responses. Transient overexpression of either PGAM5 isoform triggers caspase activation and cell death, and while AIF could reduce this caspase activation neither AIF expression nor caspase activity is required for PGAM5-mediated death. PGAM5 toxicity Morphologically and biochemically resembles mitophagic cell death and is inhibited by the AIF binding protein X-linked inhibitor of apoptosis (XIAP) in a manner that depends on the ubiquitin ligase activity of XIAP. The phosphatase activity of PGAM5 was not required for cell death, and comparison of phosphatase activity between short and long PGAM5 isoforms suggested that only the long isoform is catalytically competent. This property correlated with an increased ability Of PGAM5(L) to form dimers and/or higher order oligomers in intact cells compared to PGAM5s. Overall this study identifies an AIF/PGAM5/XIAP axis that can regulate PGAM5 activities related to the antioxidant response and mitophagy.
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