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Effects of α-synuclein overexpression in transgenic Caenorhabditis elegans strains.
- Source :
-
CNS & neurological disorders drug targets [CNS Neurol Disord Drug Targets] 2012 Dec; Vol. 11 (8), pp. 965-75. - Publication Year :
- 2012
-
Abstract
- The neural protein α-synuclein aggregates both in vivo and in vitro to form insoluble fibrils that are involved in Parkinson's disease pathogenesis. We have generated α-synuclein/fluorescent-protein fusion constructs overexpressed in muscle cells of the nematode, Caenorhabdtis elegans. Green Fluorescent Protein (GFP) variants, Cerulean (C) or Venus (V), were fused to the C-terminus of human α-synuclein (S); the resultant fusion genes were designated SV and SC, plus a CV fusion as well as S, C and V singly. The aggregation behavior of the purified fusion proteins (expressed in E. coli) will be described elsewhere. These constructs were fused to a C. elegans unc-54 myosin promoter, and integrated transgenic lines generated by microinjection, λ-irradiation, and outcrossing of fluorescent progeny. All transgenic lines expressing α- synuclein showed significant reductions (p <0.05) in lifespan, motility and pharyngeal pumping, as compared to wildtype worms or lines expressing CFP and/or YFP only. We showed that CFP and YFP labels colocalised in granular inclusions throughout the body wall in transgenic lines expressing both SC and SV fusions (SC+SV), whereas SV+C worms displayed YFP-labelled inclusions on a diffuse CFP background. These findings implied that the α-synuclein moieties of these fusion proteins still aggregated together in vivo, whereas CFP or YFP moieties alone did not. This in turn suggested that Foerster Resonanace Energy Transfer (FRET) between CFP and YFP labels in α-synuclein aggregates could allow the extent of aggregation to be quantified. Accordingly, we also showed that net FRET signals increased 2- fold between L4 and adult SC+SV worms.
- Subjects :
- Animals
Fluorescence Resonance Energy Transfer
Gene Expression Regulation
Green Fluorescent Proteins genetics
Humans
Longevity genetics
Luminescent Proteins genetics
Movement
Survival Analysis
alpha-Synuclein physiology
Animals, Genetically Modified genetics
Animals, Genetically Modified metabolism
Caenorhabditis elegans genetics
Caenorhabditis elegans metabolism
alpha-Synuclein biosynthesis
alpha-Synuclein genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1996-3181
- Volume :
- 11
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- CNS & neurological disorders drug targets
- Publication Type :
- Academic Journal
- Accession number :
- 23244416
- Full Text :
- https://doi.org/10.2174/1871527311211080005