MICU1 confers protection from MCU-dependent manganese toxicity

The mitochondrial calcium uniporter is a highly selective ion channel composed of species- and tissue-specific subunits. However, the functional role of each component still remains unclear. Here, we establish a synthetic biology approach to dissect the interdependence between the pore-forming subun...

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Detalles Bibliográficos
Autores: Wettmarshausen, Jennifer, Goh, Valerie, Huang, Kai-Ting, Arduino, Daniela M., Tripathi, Utkarsh, Leimpek, Anja, Cheng, Yiming, Pittis, Alexandros, 1982-, Gabaldón Estevan, Juan Antonio, 1973-, Mokranjac, Dejana, Hajnóczky, György, Perocchi, Fabiana
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2018
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/42590
Acceso en línea:http://hdl.handle.net/10230/42590
http://dx.doi.org/10.1016/j.celrep.2018.10.037
Access Level:acceso abierto
Palabra clave:Mitochondria
Calcium
MCU
MICU1
Yeast
Manganese
Signaling
Descripción
Sumario:The mitochondrial calcium uniporter is a highly selective ion channel composed of species- and tissue-specific subunits. However, the functional role of each component still remains unclear. Here, we establish a synthetic biology approach to dissect the interdependence between the pore-forming subunit MCU and the calcium-sensing regulator MICU1. Correlated evolutionary patterns across 247 eukaryotes indicate that their co-occurrence may have conferred a positive fitness advantage. We find that, while the heterologous reconstitution of MCU and EMRE in vivo in yeast enhances manganese stress, this is prevented by co-expression of MICU1. Accordingly, MICU1 deletion sensitizes human cells to manganese-dependent cell death by disinhibiting MCU-mediated manganese uptake. As a result, manganese overload increases oxidative stress, which can be effectively prevented by NAC treatment. Our study identifies a critical contribution of MICU1 to the uniporter selectivity, with important implications for patients with MICU1 deficiency, as well as neurological disorders arising upon chronic manganese exposure.