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dc.identifier.urihttp://hdl.handle.net/1951/55432
dc.identifier.urihttp://hdl.handle.net/11401/70993
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.abstractThe spatial and temporal control of gene expression is key to generation of specific cellular fates during development. Studies of the transcriptional repressor REST/NRSF (RE1 Silencing Transcription factor/Neural Restrictive Silencing Factor) have provided important insight into the role that epigenetic modifications play in differential gene expression. Functional studies place REST within multiple developmental pathways and transcriptional networks. However, findings between different groups are often incongruent, and little progress has been made on understanding the embryonic lethality of the Rest knockout mice. What emerges from the controversies surrounding REST function is that the cellular context of REST is paramount. Here, zebrafish embryos are used to study REST function within the broader context of a developing organism. The approach was to assay changes in gene expression following Rest knockdown in various backgrounds. This method revealed a novel interaction between zebrafish Rest and the Hedgehog (Hh) signaling pathway. It was observed that Rest knockdown enhances or represses Hh signaling in a context-dependent manner. In wild-type embryos and embryos with elevated Hh signaling, Rest knockdown augments transcription of Hh target genes. Conversely, in contexts where Hh signaling is diminished, Rest knockdown has the opposite effect and Hh target gene expression is further attenuated. Epistatic analysis revealed that Rest interacts with the Hh pathway at a step downstream of Smo. Furthermore, the findings demonstrate that the bifunctional transcription factor Gli2a is key to Rest modulation of the Hh response. The role of Rest as a regulator of Hh signaling has broad implications for many developmental contexts where REST and Hh signaling act.
dcterms.available2012-05-15T18:03:39Z
dcterms.available2015-04-24T14:45:28Z
dcterms.contributorJoel Levineen_US
dcterms.contributorSirotkin, Howard I.en_US
dcterms.contributorGary Matthewsen_US
dcterms.contributorVitaly Citovosky.en_US
dcterms.creatorGates, Keith Pendleton
dcterms.dateAccepted2012-05-15T18:03:39Z
dcterms.dateAccepted2015-04-24T14:45:28Z
dcterms.dateSubmitted2012-05-15T18:03:39Z
dcterms.dateSubmitted2015-04-24T14:45:28Z
dcterms.descriptionDepartment of Neuroscienceen_US
dcterms.formatApplication/PDFen_US
dcterms.formatMonograph
dcterms.identifierhttp://hdl.handle.net/1951/55432
dcterms.identifierGates_grad.sunysb_0771E_10004.pdfen_US
dcterms.identifierhttp://hdl.handle.net/11401/70993
dcterms.issued2010-05-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2012-05-15T18:03:39Z (GMT). No. of bitstreams: 1 Gates_grad.sunysb_0771E_10004.pdf: 16979599 bytes, checksum: 1358cfbf012d201d59648caec7d9bf4e (MD5) Previous issue date: 1en
dcterms.provenanceMade available in DSpace on 2015-04-24T14:45:28Z (GMT). No. of bitstreams: 3 Gates_grad.sunysb_0771E_10004.pdf.jpg: 1894 bytes, checksum: a6009c46e6ec8251b348085684cba80d (MD5) Gates_grad.sunysb_0771E_10004.pdf.txt: 225206 bytes, checksum: 288d93b34a832d1c881d21fdb615ea09 (MD5) Gates_grad.sunysb_0771E_10004.pdf: 16979599 bytes, checksum: 1358cfbf012d201d59648caec7d9bf4e (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectBiology, Neuroscience -- Developmental Biology -- Biology, Genetics
dcterms.subjectGli, neural tube, REST/NRSF, Sonic Hedgehog, Transcription factor, zebrafish
dcterms.titleA Role for the Transcriptional Repressor REST in Patterning the Zebrafish Neural Tube
dcterms.typeDissertation


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