Developmentally regulated GTP-binding protein 2 depletion leads to mitochondrial dysfunction through downregulation of dynamin-related protein 1
- Authors
- Vo, Mai-Tram; Ko, Myoung Seok; Lee, Unn Hwa; Yoon, Eun Hye; Lee, Byung Ju; Cho, Wha Ja; Ha, Chang Man; Kim, Kyungjin; Park, Jeong Woo
- Issue Date
- May-2017
- Publisher
- ACADEMIC PRESS INC ELSEVIER SCIENCE
- Keywords
- DRG2; Mitochondrial dysfunction; Drpl; Mitochondrial swelling
- Citation
- BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.486, no.4, pp.1014 - 1020
- Journal Title
- BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Volume
- 486
- Number
- 4
- Start Page
- 1014
- End Page
- 1020
- URI
- http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/826
- DOI
- 10.1016/j.bbrc.2017.03.154
- ISSN
- 0006-291X
- Abstract
- Mitochondrial dynamics, including constant fusion and fission, play critical roles in maintaining mitochondrial morphology and function. Here, we report that developmentally regulated GTP-binding protein 2 (DRG2) regulates mitochondrial morphology by modulating the expression of the mitochondrial fission gene dynamin-related protein 1 (Drp1). shRNA-mediated silencing of DRG2 induced mitochondrial swelling, whereas expression of an shRNA-resistant version of DRG2 decreased mitochondrial swelling in DRG2-depleted cells. Analysis of the expression levels of genes involved in mitochondrial fusion and fission revealed that DRG2 depletion significantly decreased the level of Drpl. Overexpression of Drpl rescued the defect in mitochondrial morphology induced by DRG2 depletion. DRG2 depletion reduced the mitochondrial membrane potential, oxygen consumption rate (OCR), and amount of mitochondrial DNA (mtDNA), whereas it increased reactive oxygen species (ROS) production and apoptosis. Taken together, our data demonstrate that DRG2 acts as a regulator of mitochondrial fission by controlling the expression of Drp1. (C) 2017 Elsevier Inc. All rights reserved.
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