Preserved respiratory chain capacity and physiology in mice with profoundly reduced levels of mitochondrial respirasomes
Open accessPreprint — published as 10.1016/j.cmet.2023.07.015 · Paper page
Abstract
SUMMARY: The mammalian respiratory chain complexes I, III 2 and IV (CI, CIII 2 and CIV) are critical for cellular bioenergetics and form a stable assembly, the respirasome (CI- CIII 2 -CIV), that is biochemically and structurally well documented. The role of the respirasome in bioenergetics and regulation of metabolism is subject to intense debate and is difficult to study because the individual respiratory chain complexes coexist together with high levels of respirasomes. To critically investigate the in vivo role of the respirasome, we generated homozygous knock-in mice that have normal levels of respiratory chain complexes but profoundly decreased levels of respirasomes. Surprisingly, the mutant mice are healthy, with preserved respiratory chain capacity and normal exercise performance. Our findings show that high levels of respirasomes are dispensable for maintaining bioenergetics and physiology in the mouse, but raises questions about their alternate functions, such as relating to regulation of protein stability and prevention of age-associated protein aggregation.
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Highly accurate protein structure prediction with AlphaFold
Jumper, J., Evans, R., Pritzel, A., Green, T., Figurnov, M., Ronneberger, O., Tunyasuvunakool, K., Bates, R., Žídek, A., Potapenko, A., et al. (2021) · Nature · doi:10.1038/s41586-021-03819-2 · Cited by 43,764 · see citing works
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- Authors
- Milenkovic, D., Misic, J., Hevler, J. F., Molinié, T., Chung, I., Atanassov, I., Li, X., Filograna, R., Mesaros, A., Mourier, A., Heck, A. J. R., Hirst, J., & Larsson, N.-G.
- Affiliations
- Max Planck Institute for Biology of Ageing (DE)
- Karolinska Institutet (SE)
- Utrecht University (NL)
- Centre National de la Recherche Scientifique (FR)
- University of Cambridge (GB)
- Corresponding author
- Hirst, Judy
- Larsson, Nils-Göran
- ORCID
- Venue
- Cell Metabolism
- Publisher
- openRxiv
- Published
- 2023-06-22
- Volume
- 35
- Issue
- 10
- Pages
- 1799-1813.e7
- ISSN
- 1550-4131 (ISSN-L)
- OpenAlex
- W4386171179
- Cited by
- 68
- References
- 1
- Citations by year
- 2026: 14 · 2025: 25 · 2024: 23 · 2023: 6
- FWCI
- 6.01
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- cc-by
- Locations
- Cell Metabolism (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion, cc-by)
- Apollo (University of Cambridge) (submittedVersion, cc-by)
- Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
- Funders
- Swedish Cancer Foundation
- Nederlandse Organisatie voor Wetenschappelijk Onderzoek (SPI.2017.028, 184.034.019)
- Knut och Alice Wallenbergs Stiftelse (2019.0109, 2016.0050)
- Max-Planck-Gesellschaft
- Novo Nordisk
- Vetenskapsrådet (2015-00418)
- Novo Nordisk Fonden (NNF22OC0078444, NNF20OC0063616, NNF20OC006316)
- Medical Research Council (MC_UU_00015/2, MC_U105663141, MC_UU_00015/7)
- H2020 European Research Council (741366)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- respirasome, electron transport chain, cytochrome c oxidase, mitochondrial bioenergetics, knock-in mice, exercise performance, protein stability, protein aggregation
- MeSH terms
- Animals, Electron Transport Complex IV, Electron Transport, Energy Metabolism, Mammals, Mitochondria, Mitochondrial Membranes, Mice
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