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dc.identifier.urihttp://hdl.handle.net/11401/76588
dc.description.sponsorshipThis work is sponsored by the Stony Brook University Graduate School in compliance with the requirements for completion of degree.en_US
dc.formatMonograph
dc.format.mediumElectronic Resourceen_US
dc.language.isoen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dc.typeDissertation
dcterms.abstractThis thesis explores the consequences of mutated neurofibromin gene, NF1, on memory. NF1 disorder is an inheritable genetic disease in humans that is produced by mutation of the gene that encodes the large protein neurofibromin. Mutations in this gene produce fairly non-specific and widespread cognitive defects in human patients, in addition to a variety of other pathologies, such as benign tumors of the peripheral nervous system. It is unknown how NF1 disorder leads to cognitive deficits. Uncovering the mechanism is hampered by the fact that mutations in the NF1 gene have very unpredictable effects. Even identical (monozygotic) twins who have the same mutation sites can manifest wildly different symptoms. It is unclear why this is the case, but it certainly shows that mutated neurofibromin causes different pathologies in different tissues. Whilst NF1 is widely expressed throughout the body, it is not known if cognitive defects arise from its action in a particular region of the brain or throughout the whole brain. Here I explore this issue using the powerful genetic and behavioral techniques in the model organism, Drosophila melanogaster. I show that normal NF1 protein is required in octopamine neurons. Lacking of correct NF1 gene expression in these neurons leads to impaired long term memory, but not impaired learning. Manipulating the excitability of octopamine neurons after consolidation modulated appetitive LTM. NF1-dependent memory does not require the mushroom body, the insect learning and memory center. This the first time a specific neuron type has been identified as playing a role in the cognitive deficits in Drosophila NF1 research.
dcterms.available2017-09-20T16:50:42Z
dcterms.contributorKernan, Mauriceen_US
dcterms.contributorZhong, Yien_US
dcterms.contributorDubnau, Joshuaen_US
dcterms.contributorTurner, Glennen_US
dcterms.contributorGan, Wenbiao.en_US
dcterms.creatorXu, Chunsu
dcterms.dateAccepted2017-09-20T16:50:42Z
dcterms.dateSubmitted2017-09-20T16:50:42Z
dcterms.descriptionDepartment of Neuroscience.en_US
dcterms.extent91 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/11401/76588
dcterms.issued2015-08-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:50:42Z (GMT). No. of bitstreams: 1 Xu_grad.sunysb_0771E_12203.pdf: 2682124 bytes, checksum: dbd6afb2f9a2ff7997e658729927b79d (MD5) Previous issue date: 2014en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectNeurosciences
dcterms.subjectdrosophila behaivor, learning and memory, long term memory, neurofibromatosis type 1, octopamine
dcterms.titleThe role of NF1 in Drosophila appetitive long term memory
dcterms.typeDissertation


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