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. 2024 Aug 16;17(1):228.
doi: 10.1186/s13104-024-06879-5.

Phenotypic assessment of Cox10 variants and their implications for Leigh Syndrome

Thomas-Shadi Voges  1   2 , Eun Bi Lim  1   3 , Abigail MacKenzie  1 , Kyle Mudler  1 , Rebecca DeSouza  1 , Nmesoma E Onyejekwe  1 , Stephen D Johnston  4
Affiliations

Phenotypic assessment of Cox10 variants and their implications for Leigh Syndrome

Thomas-Shadi Voges et al. BMC Res Notes. .

Abstract

Objectives: Cox10 is an enzyme required for the activity of cytochrome c oxidase. Humans who lack at least one functional copy of Cox10 have a form of Leigh Syndrome, a genetic disease that is usually fatal in infancy. As more human genomes are sequenced, new alleles are being discovered; whether or not these alleles encode functional proteins remains unclear. Thus, we set out to measure the phenotypes of many human Cox10 variants by expressing them in yeast cells.

Results: We successfully expressed the reference sequence and 25 variants of human Cox10 in yeast. We quantitated the ability of these variants to support growth on nonfermentable media and directly measured cytochrome c oxidase activity. 11 of these Cox10 variants supported approximately half or more the cytochrome c oxidase activity compared to the reference sequence. All of the strains containing those 11 variants also grew robustly using a nonfermentable carbon source. Cells expressing the other variants showed low cytochrome c oxidase activity and failed to grow on nonfermentable media.

Keywords: Saccharomyces cerevisiae; Cox10; Cytochrome c oxidase; Leigh syndrome.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
Activity of human COX10 variants. (A) Ten-fold serial dilutions of yeast cells carrying the indicated COX10 variant or an empty vector were plated on rich media with either glucose or glycerol as the carbon source. (B) The same strains were lysed and COX activity was measured. The resulting specific activities were normalized to the sample containing the human COX10 reference sequence. Error bars show one standard deviation
See this image and copyright information in PMC

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