SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorder.

Published online

Journal Article

Inherited optic neuropathies include complex phenotypes, mostly driven by mitochondrial dysfunction. We report an optic atrophy spectrum disorder, including retinal macular dystrophy and kidney insufficiency leading to transplantation, associated with mitochondrial DNA (mtDNA) depletion without accumulation of multiple deletions. By whole-exome sequencing, we identified mutations affecting the mitochondrial single strand binding protein (SSBP1) in four families with dominant and one with recessive inheritance. We show that SSBP1 mutations in patient-derived fibroblasts variably affect its amount and alter multimer formation, but not the binding to ssDNA. SSBP1 mutations impaired mtDNA, nucleoids and 7S-DNA amounts as well as mtDNA replication, impacting replisome machinery. The variable mtDNA depletion in cells reflected in severity of mitochondrial dysfunction, including respiratory efficiency, OXPHOS subunits and complexes amount and assembly. mtDNA depletion and cytochrome c oxidase-negative cells were found ex-vivo in biopsies of affected tissues, like kidney and skeletal muscle. Reduced efficiency of mtDNA replication was also reproduced in vitro, confirming the pathogenic mechanism. Furthermore, ssbp1 suppression in zebrafish induced signs of nephropathy and reduced optic nerve size, the latter phenotype complemented by wild-type mRNA but not by SSBP1 mutant transcripts. This previously unrecognized disease of mtDNA maintenance implicates SSBP1 mutations as cause of human pathology.

Full Text

Duke Authors

Cited Authors

  • Del Dotto, V; Ullah, F; Di Meo, I; Magini, P; Gusic, M; Maresca, A; Caporali, L; Palombo, F; Tagliavini, F; Baugh, EH; Macao, B; Szilagyi, Z; Péron, C; Gustafson, MA; Khan, K; La Morgia, C; Barboni, P; Carbonelli, M; Valentino, ML; Liguori, R; Shashi, V; Sullivan, JA; Nagaraj, S; El-Dairi, M; Iannaccone, A; Cutcutache, I; Bertini, E; Carrozzo, R; Emma, F; Diomedi-Camassei, F; Zanna, C; Armstrong, M; Page, MJ; Boesch, S; Wortmann, SB; Kopajtich, R; Stong, N; Sperl, W; Davis, E; Copeland, WC; Seri, M; Falkenberg, M; Prokisch, H; Katsanis, N; Tiranti, V; Pippucci, T; Carelli, V

Published Date

  • September 24, 2019

Published In

PubMed ID

  • 31550240

Pubmed Central ID

  • 31550240

Electronic International Standard Serial Number (EISSN)

  • 1558-8238

Digital Object Identifier (DOI)

  • 10.1172/JCI128514

Language

  • eng

Conference Location

  • United States