OPA1 is a GTPase that controls mitochondrial fusion, cristae integrity, and mtDNA maintenance. In humans, eight isoforms are expressed as combinations of long and short forms, but it is unclear whether OPA1 functions are associated with specific isoforms and/or domains. To address this, we expressed each of the eight isoforms or different constructs of isoform 1 in Opa1(-/-) MEFs. We observed that any isoform could restore cristae structure, mtDNA abundance, and energetic efficiency independently of mitochondrial network morphology. Long forms supported mitochondrial fusion; short forms were better able to restore energetic efficiency. The complete rescue of mitochondrial network morphology required a balance of long and short forms of at least two isoforms, as shown by combinatorial isoform silencing and co-expression experiments. Thus, multiple OPA1 isoforms are required for mitochondrial dynamics, while any single isoform can support all other functions. These findings will be useful in designing gene therapies for patients with OPA1 haploinsufficiency.

Del Dotto, V., Mishra, P., Vidoni, S., Fogazza, M., Maresca, A., Caporali, L., et al. (2017). OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions. CELL REPORTS, 19(12), 2557-2571 [10.1016/j.celrep.2017.05.073].

OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions

DEL DOTTO, VALENTINA;VIDONI, SARA;FOGAZZA, MARIO;MARESCA, ALESSANDRA;CAPORALI, LEONARDO;CAPPELLETTI, MARTINA;RUGOLO, MICHELA;CARELLI, VALERIO;ZANNA, CLAUDIA
2017

Abstract

OPA1 is a GTPase that controls mitochondrial fusion, cristae integrity, and mtDNA maintenance. In humans, eight isoforms are expressed as combinations of long and short forms, but it is unclear whether OPA1 functions are associated with specific isoforms and/or domains. To address this, we expressed each of the eight isoforms or different constructs of isoform 1 in Opa1(-/-) MEFs. We observed that any isoform could restore cristae structure, mtDNA abundance, and energetic efficiency independently of mitochondrial network morphology. Long forms supported mitochondrial fusion; short forms were better able to restore energetic efficiency. The complete rescue of mitochondrial network morphology required a balance of long and short forms of at least two isoforms, as shown by combinatorial isoform silencing and co-expression experiments. Thus, multiple OPA1 isoforms are required for mitochondrial dynamics, while any single isoform can support all other functions. These findings will be useful in designing gene therapies for patients with OPA1 haploinsufficiency.
2017
Del Dotto, V., Mishra, P., Vidoni, S., Fogazza, M., Maresca, A., Caporali, L., et al. (2017). OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions. CELL REPORTS, 19(12), 2557-2571 [10.1016/j.celrep.2017.05.073].
Del Dotto, Valentina; Mishra, Prashant; Vidoni, Sara; Fogazza, Mario; Maresca, Alessandra; Caporali, Leonardo; Mccaffery, J Michael; Cappelletti, Mart...espandi
File in questo prodotto:
File Dimensione Formato  
1-s2.0-S2211124717307465-main.pdf

accesso aperto

Tipo: Versione (PDF) editoriale
Licenza: Licenza per Accesso Aperto. Creative Commons Attribuzione - Non commerciale - Non opere derivate (CCBYNCND)
Dimensione 4.34 MB
Formato Adobe PDF
4.34 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/602179
Citazioni
  • ???jsp.display-item.citation.pmc??? 75
  • Scopus 162
  • ???jsp.display-item.citation.isi??? 162
social impact