Počet záznamů: 1  

Two mitochondrial DNA polymorphisms modulate cardiolipin binding and lead to synthetic lethality

  1. 1.
    0582771 - FGÚ 2025 RIV US eng J - Článek v odborném periodiku
    Chiang, A. C. Y. - Ježek, J. - Mu, P. - Di, Y. - Klucnika, A. - Jabůrek, Martin - Ježek, Petr - Ma, H.
    Two mitochondrial DNA polymorphisms modulate cardiolipin binding and lead to synthetic lethality.
    Nature Communications. Roč. 15, č. 1 (2024), č. článku 611. E-ISSN 2041-1723
    Grant CEP: GA ČR(CZ) GA22-17173S; GA ČR(CZ) GA21-01205S
    Institucionální podpora: RVO:67985823
    Klíčová slova: mitochondria * eukaryote * genetic interaction
    Obor OECD: Biochemistry and molecular biology
    Impakt faktor: 16.6, rok: 2022
    Způsob publikování: Open access
    https://doi.org/10.1038/s41467-024-44964-2

    Genetic screens have been used extensively to probe interactions between nuclear genes and their impact on phenotypes. Probing interactions between mitochondrial genes and their phenotypic outcome, however, has not been possible due to a lack of tools to map the responsible polymorphisms. Here, using a toolkit we previously established in Drosophila, we isolate over 300 recombinant mitochondrial genomes and map a naturally occurring polymorphism at the cytochrome c oxidase III residue 109 (CoIII109) that fully rescues the lethality and other defects associated with a point mutation in cytochrome c oxidase I (CoIT300I). Through lipidomics profiling, biochemical assays and phenotypic analyses, we show that the CoIII109 polymorphism modulates cardiolipin binding to prevent complex IV instability caused by the CoIT300I mutation. This study demonstrates the feasibility of genetic interaction screens in animal mitochondrial DNA. It unwraps the complex intra-genomic interplays underlying disorders linked to mitochondrial DNA and how they influence disease expression.
    Trvalý link: https://hdl.handle.net/11104/0351176

     
     
Počet záznamů: 1  

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