Redox Regulation of the Mitochondrial Quality Control Protease Oma1-Reference-Cited by-同舟云学术

Redox Regulation of the Mitochondrial Quality Control Protease Oma1

Published:2019-08-20 Issue:6 Volume:31 Page:429-443
ISSN:1523-0864
Container-title:Antioxidants & Redox Signaling
language:en
Short-container-title:Antioxidants & Redox Signaling

Author:

Bohovych Iryna¹,Dietz Jonathan V.¹,Swenson Samantha¹,Zahayko Nataliya¹,Khalimonchuk Oleh¹²³⁴

Affiliation:

1. Department of Biochemistry, University of Nebraska-Lincoln, Lincoln, Nebraska.

2. Nebraska Redox Biology Center, University of Nebraska-Lincoln, Lincoln, Nebraska.

3. Center for Integrated Biomolecular Communication, University of Nebraska-Lincoln, Lincoln, Nebraska.

4. Fred & Pamela Buffett Cancer Center, University of Nebraska Medical Center, Omaha, Nebraska.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry,Cell Biology,Clinical Biochemistry,Molecular Biology,Physiology,Biochemistry

Link

https://www.liebertpub.com/doi/pdf/10.1089/ars.2018.7642

Reference43 articles.

1. Ablation of the stress protease OMA1 protects against heart failure in mice

2. The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission

3. Stress-induced OMA1 activation and autocatalytic turnover regulate OPA1-dependent mitochondrial dynamics

4. Inaccurately Assembled CytochromecOxidase Can Lead to Oxidative Stress-Induced Growth Arrest

5. Redox-regulated dynamic interplay between Cox19 and the copper-binding protein Cox11 in the intermembrane space of mitochondria facilitates biogenesis of cytochrome c oxidase

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