Phenotypic assessment of Cox10 variants and their implications for Leigh Syndrome.

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

SUBMITTER: Voges TS 

PROVIDER: S-EPMC11328382 | biostudies-literature | 2024 Aug

REPOSITORIES: biostudies-literature