Fission 1 (FIS1) is a small tail-anchored protein embedded in the outer mitochondrial membrane that serves as an adaptor for the [DRP1](/proteins/drp1-protein) GTPase during mitochondrial fission. FIS1 recruits and anchors DRP1 to the mitochondrial surface, initiating the fission process that divides mitochondria. Dysregulated FIS1 expression contributes to excessive mitochondrial fragmentation in Alzheimer's disease, Parkinson's disease, and Huntington's disease.[@james2003][@stojanovski2004]
Structure and Domains
FIS1 has a compact architecture optimized for fission machinery recruitment:
N-terminal arm: Flexible region that regulates DRP1 interaction
Two TPR-like helical domains: Form a concave surface for protein-protein interactions
C-terminal transmembrane domain: Anchors FIS1 in the outer mitochondrial membrane
Cytoplasmic exposure: Bulk of protein faces cytosol for DRP1 recruitment
The TPR domains create a platform that docks DRP1 and associated factors.[@dohm2004]
Normal Function
Mitochondrial Fission Initiation
FIS1 mediates fission through several steps:[@yu2005]
DRP1 recruitment: Cytosolic DRP1 binds to FIS1's TPR domains
Oligomerization: DRP1 forms spiral oligomers around mitochondria
GTP hydrolysis: Drives constriction and division
Membrane scission: Mitochondrion divides into two fragments
Peroxisomal Fission
FIS1 also regulates peroxisome division:[@koch2004]
Similar DRP1 recruitment mechanism
Important for peroxisome proliferation
Impacts fatty acid β-oxidation
Links to oxidative stress response
Mitophagy Priming
FIS1-mediated fission prepares damaged mitochondria for clearance:[@gomes2013]
Segregates damaged mitochondrial regions
Produces smaller fragments for autophagic engulfment
Works upstream of PINK1/Parkin pathway
FIS1 overexpression can induce mitophagy
Role in Neurodegeneration
Alzheimer's Disease
FIS1 is upregulated in AD with pathological consequences:[@wang2016]
Elevated FIS1 in AD brains and [neurons](/entities/neurons) exposed to [Aβ](/proteins/amyloid-beta)
Excessive mitochondrial fragmentation
Impaired energy production
Synaptic dysfunction correlates with fission activation