OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion

Cartes-Saavedra, Benjamin; Lagos, Daniel; Macuada, Josefa; Arancibia, Duxan; Burte, Florence; Sjoberg-Herrera, Marcela K.; Andres, Maria Estela; Horvath, Rita; Yu-Wai-Man, Patrick; Hajnoczky, Gyorgy; Eisnera, Veronica

Abstract

Inner mitochondrial membrane fusion and cristae shape depend on optic atrophy protein 1, OPA1. Mutations in OPA1 lead to autosomal dominant optic atrophy (ADOA), an important cause of inherited blindness. The Guanosin Triphosphatase (GTPase) and GTPase effector domains (GEDs) of OPA1 are essential for mitochon-drial fusion; yet, their specific roles remain elusive. Intriguingly, patients carrying OPA1 GTPase mutations have a higher risk of developing more severe multisystemic symptoms in addition to optic atrophy, suggesting pathogenic contributions for the GTPase and GED domains, respectively. We studied OPA1 GTPase and GED muta-tions to understand their domain-specific contribution to protein function by analyz-ing patient-derived cells and gain-of-function paradigms. Mitochondria from OPA1 GTPase (c.870+5G>A and c.889C>T) and GED (c.2713C>T and c.2818+5G>A) mutants display distinct aberrant cristae ultrastructure. While all OPA1 mutants inhibited mitochondrial fusion, some GTPase mutants resulted in elongated mito-chondria, suggesting fission inhibition. We show that the GED is dispensable for fusion and OPA1 oligomer formation but necessary for GTPase activity. Finally, splicing defect mutants displayed a posttranslational haploinsufficiency-like pheno-type but retained domain-specific dysfunctions. Thus, OPA1 domain-specific mutants result in distinct impairments in mitochondrial dynamics, providing insight into OPA1 function and its contribution to ADOA pathogenesis and severity.

Más información

Título según WOS: OPA1 disease-causing mutants have domain-specific effects on mitochondrial ultrastructure and fusion
Título de la Revista: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
Volumen: 120
Número: 12
Editorial: NATL ACAD SCIENCES
Fecha de publicación: 2023
DOI:

10.1073/pnas.2207471120

Notas: ISI