The cardiac-enriched microprotein mitolamban regulates mitochondrial respiratory complex assembly and function in mice

Author:

Makarewich Catherine A.12,Munir Amir Z.3,Bezprozvannaya Svetlana3,Gibson Aaron M.2,Young Kim Soo4,Martin-Sandoval Misty S.5,Mathews Thomas P.56,Szweda Luke I.4ORCID,Bassel-Duby Rhonda3,Olson Eric N.3ORCID

Affiliation:

1. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229

2. The Heart Institute, Division of Molecular Cardiovascular Biology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229

3. Department of Molecular Biology, Hamon Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390

4. Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390

5. Children’s Research Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390

6. Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390

Abstract

Significance Microproteins are a growing class of versatile small proteins previously overlooked by standard gene annotation methods due to their small size. Here we characterize mitolamban as a cardiac-enriched inner mitochondrial membrane–localized microprotein, which interacts with complex III of the electron transport chain and contributes to complex III assembly and function. Mitolamban gene deletion in mice leads to a reduction in complex III activity and metabolic perturbations in the heart that are consistent with complex III deficiency, as well as altered complex III assembly into respiratory supercomplexes. These findings define a functional role for mitolamban in the heart and highlight the importance of microproteins in regulating mitochondrial function and cardiomyocyte biology.

Funder

HHS | National Institutes of Health

Welch Foundation

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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