The SAC 1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals
Presynaptic terminals are metabolically active and accrue damage through continuous vesicle cycling. How synapses locally regulate protein homeostasis is poorly understood. We show that the presynaptic lipid phosphatase synaptojanin is required for macroautophagy, and this role is inhibited by the P...
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Veröffentlicht in: | The EMBO journal 2017-05, Vol.36 (10), p.1392-1411 |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Presynaptic terminals are metabolically active and accrue damage through continuous vesicle cycling. How synapses locally regulate protein homeostasis is poorly understood. We show that the presynaptic lipid phosphatase synaptojanin is required for macroautophagy, and this role is inhibited by the Parkinson's disease mutation R258Q. Synaptojanin drives synaptic endocytosis by dephosphorylating
PI
(4,5)P
2
, but this function appears normal in
Synaptojanin
RQ
knock‐in flies. Instead, R258Q affects the synaptojanin
SAC
1 domain that dephosphorylates
PI
(3)P and
PI
(3,5)P
2
, two lipids found in autophagosomal membranes. Using advanced imaging, we show that
Synaptojanin
RQ
mutants accumulate the
PI
(3)P/
PI
(3,5)P
2
‐binding protein Atg18a on nascent synaptic autophagosomes, blocking autophagosome maturation at fly synapses and in neurites of human patient induced pluripotent stem cell‐derived neurons. Additionally, we observe neurodegeneration, including dopaminergic neuron loss, in
Synaptojanin
RQ
flies. Thus, synaptojanin is essential for macroautophagy within presynaptic terminals, coupling protein turnover with synaptic vesicle cycling and linking presynaptic‐specific autophagy defects to Parkinson's disease.
image
Parkinson's disease‐related human synaptojanin 1 (
SYNJ
1) or
Drosophila
synaptojanin (Synj)
SAC
1 function drives autophagosome biogenesis within synapses by dephosphorylating
PI
(3)P/
PI
(3,5)P
2
, releasing
WIPI
2/Atg18a from immature autophagosomes, independent from Synj function in endocytosis.
Parkinson's disease related synaptojanin
RQ SAC
1 mutation does not affect synaptic vesicle endocytosis at fly excitatory glutamatergic neurons and photoreceptors.
Synaptojanin is required for autophagosome formation in presynaptic terminals, analogous to synaptic vesicle uncoating by synaptojanin.
The
PI
(3)P/
PI
(3,5)P
2
‐binding protein,
WIPI
2/Atg18a accumulates in Synj mutant flies and
SYNJ
1 R258Q patient‐derived human induced neurons.
Synaptojanin regulates Atg18a mobility at autophagosomal membranes.
Synaptojanin
RQ
knock‐in flies show neurodegeneration. |
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ISSN: | 0261-4189 1460-2075 |
DOI: | 10.15252/embj.201695773 |