RESUMEN
Human Tim8a and Tim8b are members of an intermembrane space chaperone network, known as the small TIM family. Mutations in TIMM8A cause a neurodegenerative disease, Mohr-Tranebjærg syndrome (MTS), which is characterised by sensorineural hearing loss, dystonia and blindness. Nothing is known about the function of hTim8a in neuronal cells or how mutation of this protein leads to a neurodegenerative disease. We show that hTim8a is required for the assembly of Complex IV in neurons, which is mediated through a transient interaction with Complex IV assembly factors, in particular the copper chaperone COX17. Complex IV assembly defects resulting from loss of hTim8a leads to oxidative stress and changes to key apoptotic regulators, including cytochrome c, which primes cells for death. Alleviation of oxidative stress with Vitamin E treatment rescues cells from apoptotic vulnerability. We hypothesise that enhanced sensitivity of neuronal cells to apoptosis is the underlying mechanism of MTS.
Asunto(s)
Trastornos Sordoceguera/fisiopatología , Distonía/fisiopatología , Complejo IV de Transporte de Electrones/metabolismo , Discapacidad Intelectual/fisiopatología , Proteínas de Transporte de Membrana/metabolismo , Neuronas/metabolismo , Atrofia Óptica/fisiopatología , Multimerización de Proteína , Apoptosis , Proteínas Reguladoras de la Apoptosis/metabolismo , Línea Celular , Proteínas Transportadoras de Cobre/metabolismo , Humanos , Proteínas de Transporte de Membrana/deficiencia , Proteínas del Complejo de Importación de Proteínas Precursoras Mitocondriales , Estrés Oxidativo , Mapas de Interacción de ProteínasRESUMEN
Mitochondria are essential organelles which perform complex and varied functions within eukaryotic cells. Maintenance of mitochondrial health and functionality is thus a key cellular priority and relies on the organelle's extensive proteome. The mitochondrial proteome is largely encoded by nuclear genes, and mitochondrial proteins must be sorted to the correct mitochondrial sub-compartment post-translationally. This essential process is carried out by multimeric and dynamic translocation and sorting machineries, which can be found in all four mitochondrial compartments. Interestingly, advances in the diagnosis of genetic disease have revealed that mutations in various components of the human import machinery can cause mitochondrial disease, a heterogenous and often severe collection of disorders associated with energy generation defects and a multisystem presentation often affecting the cardiovascular and nervous systems. Here, we review our current understanding of mitochondrial protein import systems in human cells and the molecular basis of mitochondrial diseases caused by defects in these pathways.