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PMID: 26306039 Published · ppublish English

Death-associated Protein 3 Regulates Mitochondrial-encoded Protein Synthesis and Mitochondrial Dynamics.

The Journal of biological chemistry ·Vol. 290 ·No. 41 ·2016-01-15

Xiao Lin, Xian Hongxu, Lee Kit Yee, Xiao Bin, Wang Hongyan, Yu Fengwei, Shen Han-Ming, Liou Yih-Cherng

Abstract

Mitochondrial morphologies change over time and are tightly regulated by dynamic machinery proteins such as dynamin-related protein 1 (Drp1), mitofusion 1/2, and optic atrophy 1 (OPA1). However, the detailed mechanisms of how these molecules cooperate to mediate fission and fusion remain elusive. DAP3 is a mitochondrial ribosomal protein that involves in apoptosis, but its biological function has not been well characterized. Here, we demonstrate that DAP3 specifically localizes in the mitochondrial matrix. Knockdown of DAP3 in mitochondria leads to defects in mitochondrial-encoded protein synthesis and abnormal mitochondrial dynamics. Moreover, depletion of DAP3 dramatically decreases the phosphorylation of Drp1 at Ser-637 on mitochondria, enhancing the retention time of Drp1 puncta on mitochondria during the fission process. Furthermore, autophagy is inhibited in the DAP3-depleted cells, which sensitizes cells to different types of death stimuli. Together, our results suggest that DAP3 plays important roles in mitochondrial function and dynamics, providing new insights into the mechanism of a mitochondrial ribosomal protein function in cell death.

Keywords
Drp1 DAP3 autophagy cell death cell signaling metabolism mitochondria
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
Published
2016-01-15
Indexed
2015-10-10
Updated
2016-10-19
Language
English
Country/Region
United States
NLM ID
2985121R
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