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OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions
Author(s) -
Valentina Del Dotto,
Prashant Mishra,
Sara Vidoni,
Mario Fogazza,
Alessandra Maresca,
Leonardo Caporali,
J. Michael McCaffery,
Martina Cappelletti,
Enrico Baruffini,
Guy Lenaers,
David C. Chan,
Michela Rugolo,
Valério Carelli,
Claudia Zanna
Publication year - 2017
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2017.05.073
Subject(s) - gene isoform , biology , microbiology and biotechnology , mitochondrion , mitochondrial fusion , haploinsufficiency , mitochondrial dna , phenotype , genetics , gene
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.

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