A Novel Group of Dynamin-Related Proteins Shared by Eukaryotes and Giant Viruses Is Able to Remodel Mitochondria From Within the Matrix

0574455 - BC 2024 RIV US eng J - Článek v odborném periodiku
Sheikh, Shaghayegh - Panek, T. - Gahura, Ondřej - Týč, Jiří - Záhonová, Kristýna - Lukeš, Julius - Eliaš, M. - Hashimi, Hassan
A Novel Group of Dynamin-Related Proteins Shared by Eukaryotes and Giant Viruses Is Able to Remodel Mitochondria From Within the Matrix.
Molecular Biology and Evolution. Roč. 40, č. 6 (2023), č. článku msad134. ISSN 0737-4038. E-ISSN 1537-1719
Grant CEP: GA MŠMT(CZ) EF16_013/0001775; GA ČR(CZ) GJ20-04150Y; GA ČR(CZ) GX23-06479X; GA ČR(CZ) GA20-23513S; GA MŠMT(CZ) LM2018129
Institucionální podpora: RVO:60077344
Klíčová slova: dynamin superfamily * Mgm1 * mitochondria * Nucleocytoviricota * Opa1 * protists
Obor OECD: Cell biology
Impakt faktor: 10.7, rok: 2022
Způsob publikování: Omezený přístup
https://academic.oup.com/mbe/article/40/6/msad134/7190697?login=true

The diverse GTPases of the dynamin superfamily play various roles in the cell, as exemplified by the dynamin-related proteins (DRPs) Mgm1 and Opa1, which remodel the mitochondrial inner membrane in fungi and metazoans, respectively. Via an exhaustive search of genomic and metagenomic databases, we found previously unknown DRP types occurring in diverse eukaryotes and giant viruses (phylum Nucleocytoviricota). One novel DRP clade, termed MidX, combined hitherto uncharacterized proteins from giant viruses and six distantly related eukaryote taxa (Stramenopiles, Telonemia, Picozoa, Amoebozoa, Apusomonadida, and Choanoflagellata). MidX stood out because it was not only predicted to be mitochondria-targeted but also to assume a tertiary structure not observed in other DRPs before. To understand how MidX affects mitochondria, we exogenously expressed MidX from Hyperionvirus in the kinetoplastid Trypanosoma brucei, which lacks Mgm1 or Opa1 orthologs. MidX massively affected mitochondrial morphology from inside the matrix, where it closely associates with the inner membrane. This unprecedented mode of action contrasts to those of Mgm1 and Opa1, which mediate inner membrane remodeling in the intermembrane space. We speculate that MidX was acquired in Nucleocytoviricota evolution by horizontal gene transfer from eukaryotes and is used by giant viruses to remodel host mitochondria during infection. MidX's unique structure may be an adaptation for reshaping mitochondria from the inside. Finally, Mgm1 forms a sister group to MidX and not Opa1 in our phylogenetic analysis, throwing into question the long-presumed homology of these DRPs with similar roles in sister lineages.
Trvalý link: https://hdl.handle.net/11104/0345920