ATAD3C regulates ATAD3A assembly and function in the mitochondrial membrane

Gaudó, Paula ; de Tomás-Mateo, Elena ; Garrido-Pérez, Nuria (Universidad de Zaragoza) ; Santana, Alfredo ; Ruiz-Pesini, Eduardo (Universidad de Zaragoza) ; Montoya, Julio (Universidad de Zaragoza) ; Bayona-Bafaluy, Pilar (Universidad de Zaragoza)

Resumen: Mitochondrial ATAD3A is an ATPase Associated with diverse cellular Activities (AAA) domain containing enzyme, involved in the structural organization of the inner mitochondrial membrane and of increasing importance in childhood disease. In humans, two ATAD3A paralogs arose by gene duplication during evolution: ATAD3B and ATAD3C. Here we investigate the cellular activities of the ATAD3C paralog that has been considered a pseudogene. We detected unique ATAD3C peptides in HEK 293T cells, with expression similar to that in human tissues, and showed that it is an integral membrane protein that exposes its carboxy-terminus to the intermembrane space. Overexpression of ATAD3C, but not of ATAD3A, in fibroblasts caused a decrease in cell proliferation and oxygen consumption rate, and an increase of cellular ROS. This was due to the incorporation of ATAD3C monomers in ATAD3A complex in the mitochondrial membrane reducing its size. Consistent with a negative regulation of ATAD3A function in mitochondrial membrane organization, ATAD3C expression led to increased accumulation of respiratory chain dimeric CIII in the inner membrane, to the detriment to that assembled in respiratory supercomplexes. Our results demonstrate a negative dominant role of the ATAD3C paralog with implications for mitochondrial OXPHOS function and suggest that its expression regulates ATAD3A in the cell.

Idioma: Inglés

DOI: 10.1016/j.freeradbiomed.2023.12.006

Año: 2023

Publicado en: FREE RADICAL BIOLOGY AND MEDICINE 211 (2023), 114-126
ISSN: 0891-5849

Factor impacto JCR: 7.1 (2023)

Categ. JCR: ENDOCRINOLOGY & METABOLISM rank: 15 / 186 = 0.081 (2023) - Q1 - T1
Categ. JCR: BIOCHEMISTRY & MOLECULAR BIOLOGY rank: 35 / 313 = 0.112 (2023) - Q1 - T1

Factor impacto CITESCORE: 14.0 - Physiology (medical) (Q1) - Biochemistry (Q1)

Factor impacto SCIMAGO: 1.752 - Physiology (medical) (Q1) - Biochemistry (Q1)

Financiación: info:eu-repo/grantAgreement/ES/ISCIII-EDRF/PT17-0019

Tipo y forma: Artículo (Versión definitiva)

Área (Departamento): Área Bioquímica y Biolog.Mole. (Dpto. Bioq.Biolog.Mol. Celular)