A Ferroptosis-mediated regulation of the biogenesis of the oxidative phosphorylation system

Murari, A.; Rhooms, S.-k.; Hossain, K.; Liu, T.; Li, H.; Goparaju, N. S.; Osei, C.; Owusu-Ansah, E.

doi:10.1101/2022.02.17.480976

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bioRxiv · 10.1101/2022.02.17.480976

A Ferroptosis-mediated regulation of the biogenesis of the oxidative phosphorylation system

Murari, A.·Rhooms, S.-k.·Hossain, K.·Liu, T.·Li, H.·Goparaju, N. S.·Osei, C.·Owusu-Ansah, E.

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Abstract

Several subunits in the matrix domain of mitochondrial complex I (CI) have been posited to be redox sensors for CI; but how elevated levels of reactive oxygen species (ROS) impinge on CI assembly is unknown. We report that when the mitochondrial NADPH-generating enzyme - Isocitrate Dehydrogenase 2 - is genetically disrupted, ROS levels are elevated and assembly of the oxidative phosphorylation system (OXPHOS) is impaired. Mechanistically, this begins with a ROS-mediated inhibition of biosynthesis of the matrix domain of CI, which progresses to a point where ferroptotic signals are induced, the mitochondrial unfolded protein response is activated and multiple OXPHOS complexes are impaired. Disruption of other enzymes that eliminate hydrogen peroxide, but not those that eliminate the superoxide radical, recapitulates the phenotype; implicating hydrogen peroxide as the signaling molecule involved. Thus, the redox status of the mitochondrion modulates the assembly of the matrix domain of CI and ultimately that of the entire OXPHOS.

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Murari, A., Rhooms, S.-k., Hossain, K., Liu, T., Li, H., Goparaju, N. S., Osei, C., Owusu-Ansah, E.. 2022-02-19. A Ferroptosis-mediated regulation of the biogenesis of the oxidative phosphorylation system. https://doi.org/10.1101/2022.02.17.480976

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