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Mol Cell. 2015 Sep 17;59(6):941-55. doi: 10.1016/j.molcel.2015.08.001.

MAPL SUMOylation of Drp1 Stabilizes an ER/Mitochondrial Platform Required for Cell Death.

Author information

1
Montreal Neurological Institute, McGill University, 3801 University Ave, Montreal, QC H3A 2B4, Canada.
2
McIntyre Medical Sciences Building, Department of Biochemistry, McGill University, Montreal, QC H3G 1Y6, Canada.
3
Montreal Neurological Institute, McGill University, 3801 University Ave, Montreal, QC H3A 2B4, Canada. Electronic address: heidi.mcbride@mcgill.ca.

Abstract

There has been evidence that mitochondrial fragmentation is required for apoptosis, but the molecular links between the machinery regulating dynamics and cell death have been controversial. Indeed, activated BAX and BAK can form functional channels in liposomes, bringing into question the contribution of mitochondrial dynamics in apoptosis. We now demonstrate that the activation of apoptosis triggers MAPL/MUL1-dependent SUMOylation of the fission GTPase Drp1, a process requisite for cytochrome c release. SUMOylated Drp1 functionally stabilizes ER/mitochondrial contact sites that act as hotspots for mitochondrial constriction, calcium flux, cristae remodeling, and cytochrome c release. The loss of MAPL does not alter the activation and assembly of BAX/BAK oligomers, indicating that MAPL is activated downstream of BAX/BAK. This work demonstrates how interorganellar contacts are dynamically regulated through active SUMOylation during apoptosis, creating a stabilized platform that signals cytochrome c release.

KEYWORDS:

BAX/BAK; Drp1; MAPL; MUL1; SUMO; SenP5; apoptosis; mitochondria; mitochondria/ER contact sites

PMID:
26384664
DOI:
10.1016/j.molcel.2015.08.001
[Indexed for MEDLINE]
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