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The alternative enzymes-bearing tunicates lack multiple widely distributed genes coding for peripheral OXPHOS subunits.
- Source :
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Biochimica et biophysica acta. Bioenergetics [Biochim Biophys Acta Bioenerg] 2024 Aug 01; Vol. 1865 (3), pp. 149046. Date of Electronic Publication: 2024 Apr 19. - Publication Year :
- 2024
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Abstract
- The respiratory chain alternative enzymes (AEs) NDX and AOX from the tunicate Ciona intestinalis (Ascidiacea) have been xenotopically expressed and characterized in human cells in culture and in the model organisms Drosophila melanogaster and mouse, with the purpose of developing bypass therapies to combat mitochondrial diseases in human patients with defective complexes I and III/IV, respectively. The fact that the genes coding for NDX and AOX have been lost from genomes of evolutionarily successful animal groups, such as vertebrates and insects, led us to investigate if the composition of the respiratory chain of Ciona and other tunicates differs significantly from that of humans and Drosophila, to accommodate the natural presence of AEs. We have failed to identify in tunicate genomes fifteen orthologous genes that code for subunits of the respiratory chain complexes; all of these putatively missing subunits are peripheral to complexes I, III and IV in mammals, and many are important for complex-complex interaction in supercomplexes (SCs), such as NDUFA11, UQCR11 and COX7A. Modeling of all respiratory chain subunit polypeptides of Ciona indicates significant structural divergence that is consistent with the lack of these fifteen clear orthologous subunits. We also provide evidence using Ciona AOX expressed in Drosophila that this AE cannot access the coenzyme Q pool reduced by complex I, but it is readily available to oxidize coenzyme Q molecules reduced by glycerophosphate oxidase, a mitochondrial inner membrane-bound dehydrogenase that is not involved in SCs. Altogether, our results suggest that Ciona AEs might have evolved in a mitochondrial inner membrane environment much different from that of mammals and insects, possibly without SCs; this correlates with the preferential functional interaction between these AEs and non-SC dehydrogenases in heterologous mammalian and insect systems. We discuss the implications of these findings for the applicability of Ciona AEs in human bypass therapies and for our understanding of the evolution of animal respiratory chain.<br />Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 Elsevier B.V. All rights reserved.)
- Subjects :
- Animals
Humans
Oxidoreductases genetics
Oxidoreductases metabolism
Protein Subunits metabolism
Protein Subunits genetics
Drosophila melanogaster genetics
Drosophila melanogaster enzymology
Urochordata genetics
Urochordata enzymology
Electron Transport
Electron Transport Complex I metabolism
Electron Transport Complex I genetics
Phylogeny
Plant Proteins
Oxidative Phosphorylation
Mitochondrial Proteins genetics
Mitochondrial Proteins metabolism
Ciona intestinalis genetics
Ciona intestinalis enzymology
Subjects
Details
- Language :
- English
- ISSN :
- 1879-2650
- Volume :
- 1865
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochimica et biophysica acta. Bioenergetics
- Publication Type :
- Academic Journal
- Accession number :
- 38642871
- Full Text :
- https://doi.org/10.1016/j.bbabio.2024.149046