Abstract |
Human PNPLA6 gene encodes Neuropathy Target Esterase protein (NTE). PNPLA6 gene mutations cause hereditary spastic paraplegia (SPG39 HSP), Gordon-Holmes syndrome, Boucher-Neuhäuser syndromes, Laurence-Moon syndrome, and Oliver-McFarlane syndrome. Mutations in the Drosophila NTE homolog swiss cheese (sws) cause early-onset, progressive behavioral defects and neurodegeneration characterized by vacuole formation. We investigated sws5 flies and show for the first time that this allele causes progressive vacuolar formation in the brain and progressive deterioration of negative geotaxis speed and endurance. We demonstrate that inducible, neuron-specific expression of full-length human wildtype NTE reduces vacuole formation and substantially rescues mobility. Indeed, neuron-specific expression of wildtype human NTE is capable of rescuing mobility defects after 10 days of adult life at 29°C, when significant degeneration has already occurred, and significantly extends longevity of mutants at 25°C. These results raise the exciting possibility that late induction of NTE function may reduce or ameliorate neurodegeneration in humans even after symptoms begin. In addition, these results highlight the utility of negative geotaxis endurance as a new assay for longitudinal tracking of degenerative phenotypes in Drosophila.
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Authors | Alyson Sujkowski, Shirley Rainier, John K Fink, Robert J Wessells |
Journal | PloS one
(PLoS One)
Vol. 10
Issue 12
Pg. e0145356
( 2015)
ISSN: 1932-6203 [Electronic] United States |
PMID | 26671664
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Drosophila Proteins
- Nerve Tissue Proteins
- SWS protein, Drosophila
- PNPLA6 protein, human
- Phospholipases
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Topics |
- Aging
- Animals
- Disease Progression
- Drosophila Proteins
(genetics)
- Drosophila melanogaster
(physiology)
- Humans
- Longevity
- Motor Activity
- Mutation
(genetics)
- Nerve Degeneration
(pathology)
- Nerve Tissue Proteins
(genetics)
- Phospholipases
(metabolism)
- Vacuoles
(metabolism)
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