Cox7a1 controls skeletal muscle physiology and heart regeneration through complex IV dimerization.

The oxidative phosphorylation (OXPHOS) system is intricately organized, with respiratory complexes forming super-assembled quaternary structures whose assembly mechanisms and physiological roles remain under investigation. Cox7a2l, also known as Scaf1, facilitates complex III and complex IV (CIII-CI...

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Detalhes bibliográficos
Autores: García-Poyatos, Carolina, Arora, Prateek, Calvo, Enrique, Marques, Ines J, Kirschke, Nick, Galardi-Castilla, Maria, Lembke, Carla, Meer, Marco, Fernández-Montes, Paula, Ernst, Alexander, Haberthür, David, Hlushchuk, Ruslan, Vázquez, Jesús, Vermathen, Peter, Enríquez, José Antonio, Mercader, Nadia
Formato: artículo
Fecha de publicación:2024
País:España
Recursos:Instituto de Salud Carlos III (ISCIII)
Repositorio:Repisalud
Idioma:inglés
OAI Identifier:oai:repisalud.isciii.es:20.500.12105/25850
Acesso em linha:https://hdl.handle.net/20.500.12105/25850
Access Level:acceso abierto
Palavra-chave:Ca(2+) signaling
cox7a1
cox7a2l
electron transport chain
heart regeneration
metabolic rewiring
mitochondria
muscle physiology
scaf1
supercomplex assembly
zebrafish
Descrição
Resumo:The oxidative phosphorylation (OXPHOS) system is intricately organized, with respiratory complexes forming super-assembled quaternary structures whose assembly mechanisms and physiological roles remain under investigation. Cox7a2l, also known as Scaf1, facilitates complex III and complex IV (CIII-CIV) super-assembly, enhancing energetic efficiency in various species. We examined the role of Cox7a1, another Cox7a family member, in supercomplex assembly and muscle physiology. Zebrafish lacking Cox7a1 exhibited reduced CIV formation, metabolic alterations, and non-pathological muscle performance decline. Additionally, cox7a1 hearts displayed a pro-regenerative metabolic profile, impacting cardiac regenerative response. The distinct phenotypic effects of cox7a1 and cox7a2l underscore the diverse metabolic and physiological consequences of impaired supercomplex formation, emphasizing the significance of Cox7a1 in muscle maturation within the OXPHOS system.