A chaperone-assisted mechanism of outer mitochondrial membrane TOM70 insertion protective against diet-induced obesity

Author:

Latorre-Muro Pedro1ORCID,Vitale Tevis1ORCID,Ravichandran Matthew2ORCID,Zhang Katherine2ORCID,Palozzi Jonathan M.1,Bennett Christopher F.1ORCID,Lamas-Paz Arantza2,Sohn Jee Hyung1ORCID,Jackson Thomas D.1ORCID,Jedrychowski Mark3,Gygi Steven P.3ORCID,Kajimura Shingo4ORCID,Schmoker Anna2ORCID,Jeon Hyesung5ORCID,Eck Michael J.5ORCID,Puigserver Pere1ORCID

Affiliation:

1. Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Cell Biology, Harvard Medical School

2. Department of Cancer Biology, Dana-Farber Cancer Institute

3. Department of Cell Biology, Harvard Medical School

4. Division of Endocrinology, Diabetes, and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School, Howard Hughes Medical Institute

5. Department of Cancer Biology, Dana-Farber Cancer Institute, Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School

Abstract

Abstract

Outer mitochondrial membrane (OMM) proteins communicate with the cytosol and other organelles including the endoplasmic reticulum (ER)1,2. This communication is important in thermogenic adipocytes to increase energy expenditure that controls body temperature and weight3,4. However, the regulatory mechanisms of OMM protein insertion are poorly understood. Herein, stress-induced cytosolic chaperone PPID (peptidyl-prolyl isomerase D/cyclophilin 40/Cyp40) drives OMM insertion of the mitochondrial import receptor TOM70 regulating body temperature and weight in obese mice, and respiratory/thermogenic function in brown adipocytes. PPID PPIase activity and C-terminal tetratricopeptide repeats (TPR), which show specificity towards TOM70 core and C-tail domains, facilitate OMM insertion. Our results provide an unprecedented role for ER-stress-activated chaperones in controlling energy metabolism through a selective OMM protein insertion mechanism with implications in adaptation to cold temperatures and high-calorie diets.

Publisher

Springer Science and Business Media LLC

Reference74 articles.

1. Navigating the landscape of mitochondrial-ER communication in health and disease;Ronayne CT;Front Mol Biosci,2024

2. Mechanisms of mitochondrial respiratory adaptation;Bennett CF;Nat Rev Mol Cell Biol,2022

3. A cold-stress-inducible PERK/OGT axis controls TOM70-assisted mitochondrial protein import and cristae formation;Latorre-Muro P;Cell Metab,2021

4. ER-to-mitochondria miscommunication and metabolic diseases;López-Crisosto C;Biochim Biophys Acta Mol Basis Dis,2015

5. The epidemic of obesity and diabetes: Trends and treatments;Barnes AS;Tex Heart Inst J,2011

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