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dc.contributor.authorTran, Helene
dc.contributor.authorAlmeida, Sandra
dc.contributor.authorMoore, Jill
dc.contributor.authorGendron, Tania F.
dc.contributor.authorChalasani, UmaDevi
dc.contributor.authorLu, Yubing
dc.contributor.authorDu, Xing
dc.contributor.authorNickerson, Jeffrey A.
dc.contributor.authorPetrucelli, Leonard
dc.contributor.authorWeng, Zhiping
dc.contributor.authorGao, Fen-Biao
dc.date2022-08-11T08:07:59.000
dc.date.accessioned2022-08-23T15:38:25Z
dc.date.available2022-08-23T15:38:25Z
dc.date.issued2015-09-23
dc.date.submitted2016-01-07
dc.identifier.citationNeuron. 2015 Sep 23;87(6):1207-14. doi: 10.1016/j.neuron.2015.09.015. <a href="http://dx.doi.org/10.1016/j.neuron.2015.09.015">Link to article on publisher's site</a>
dc.identifier.issn0896-6273 (Linking)
dc.identifier.doi10.1016/j.neuron.2015.09.015
dc.identifier.pmid26402604
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25931
dc.description.abstractDipeptide repeat (DPR) proteins are toxic in various models of FTD/ALS with GGGGCC (G4C2) repeat expansion. However, it is unclear whether nuclear G4C2 RNA foci also induce neurotoxicity. Here, we describe a Drosophila model expressing 160 G4C2 repeats (160R) flanked by human intronic and exonic sequences. Spliced intronic 160R formed nuclear G4C2 sense RNA foci in glia and neurons about ten times more abundantly than in human neurons; however, they had little effect on global RNA processing and neuronal survival. In contrast, highly toxic 36R in the context of poly(A)(+) mRNA were exported to the cytoplasm, where DPR proteins were produced at >100-fold higher level than in 160R flies. Moreover, the modest toxicity of intronic 160R expressed at higher temperature correlated with increased DPR production, but not RNA foci. Thus, nuclear RNA foci are neutral intermediates or possibly neuroprotective through preventing G4C2 RNA export and subsequent DPR production.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26402604&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/j.neuron.2015.09.015
dc.subjectAmyotrophic Lateral Sclerosis
dc.subjectAnimals
dc.subjectAnimals, Genetically Modified
dc.subjectDipeptides
dc.subject*Disease Models, Animal
dc.subjectDrosophila
dc.subjectDrosophila Proteins
dc.subjectFrontotemporal Dementia
dc.subjectHumans
dc.subjectProteins
dc.subjectRNA, Nuclear
dc.subjectALS
dc.subjectC9ORF72
dc.subjectDPR
dc.subjectDrosophila
dc.subjectFTD
dc.subjectRNA foci
dc.subjectRan translation
dc.subjectrepeats
dc.subjectBioinformatics
dc.subjectCell Biology
dc.subjectComputational Biology
dc.subjectComputational Neuroscience
dc.subjectMolecular and Cellular Neuroscience
dc.subjectNervous System Diseases
dc.subjectNeurology
dc.titleDifferential Toxicity of Nuclear RNA Foci versus Dipeptide Repeat Proteins in a Drosophila Model of C9ORF72 FTD/ALS
dc.typeJournal Article
dc.source.journaltitleNeuron
dc.source.volume87
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/bioinformatics_pubs/72
dc.identifier.contextkey7992040
html.description.abstract<p>Dipeptide repeat (DPR) proteins are toxic in various models of FTD/ALS with GGGGCC (G4C2) repeat expansion. However, it is unclear whether nuclear G4C2 RNA foci also induce neurotoxicity. Here, we describe a Drosophila model expressing 160 G4C2 repeats (160R) flanked by human intronic and exonic sequences. Spliced intronic 160R formed nuclear G4C2 sense RNA foci in glia and neurons about ten times more abundantly than in human neurons; however, they had little effect on global RNA processing and neuronal survival. In contrast, highly toxic 36R in the context of poly(A)(+) mRNA were exported to the cytoplasm, where DPR proteins were produced at >100-fold higher level than in 160R flies. Moreover, the modest toxicity of intronic 160R expressed at higher temperature correlated with increased DPR production, but not RNA foci. Thus, nuclear RNA foci are neutral intermediates or possibly neuroprotective through preventing G4C2 RNA export and subsequent DPR production.</p>
dc.identifier.submissionpathbioinformatics_pubs/72
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.contributor.departmentDepartment of Cell and Developmental Biology
dc.contributor.departmentDepartment of Neurology
dc.source.pages1207-14


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