Analysis of MT-ATP8 gene variants reported in patients by modeling in silico and in yeast model organism.

Autor: Panja C; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland., Niedzwiecka K; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland., Baranowska E; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland., Poznanski J; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland., Kucharczyk R; Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warsaw, Poland. roza@ibb.waw.pl.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2023 Jun 20; Vol. 13 (1), pp. 9972. Date of Electronic Publication: 2023 Jun 20.
DOI: 10.1038/s41598-023-36637-9
Abstrakt: Defects in ATP synthase functioning due to the substitutions in its two mitochondrially encoded subunits a and 8 lead to untreatable mitochondrial diseases. Defining the character of variants in genes encoding these subunits is challenging due to their low frequency, heteroplasmy of mitochondrial DNA in patients' cells and polymorphisms of mitochondrial genome. We successfully used yeast S. cerevisiae as a model to study the effects of variants in MT-ATP6 gene and our research led to understand how eight amino acid residues substitutions impact the proton translocation through the channel formed by subunit a and c-ring of ATP synthase at the molecular level. Here we applied this approach to study the effects of the m.8403T>C variant in MT-ATP8 gene. The biochemical data from yeast mitochondria indicate that equivalent mutation is not detrimental for the yeast enzyme functioning. The structural analysis of substitutions in subunit 8 introduced by m.8403T>C and five other variants in MT-ATP8 provides indications about the role of subunit 8 in the membrane domain of ATP synthase and potential structural consequences of substitutions in this subunit.
(© 2023. The Author(s).)
Databáze: MEDLINE
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