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dc.identifier.urihttp://hdl.handle.net/1951/60292
dc.identifier.urihttp://hdl.handle.net/11401/71549
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 expression of the sloppy-paired 1 (slp1) gene in the gastrula stage Drosophila embryo is controlled by the interplay of four transcription factors Runt, Even-skipped (Eve), Fushi-tarazu (Ftz), and Odd-paired (Opa) with two distinct cis-regulatory enhancer elements, the distal early stripe element (DESE) and the proximal early stripe element (PESE). The stripe pattern of slp1 is the result of non-additive interactions between these two enhancers and is context-dependent. Using chromatin immunoprecipitation (ChIP) to examine a number of reporter constructs, I found DESE mediates Runt dependent activation by facilitating pre-initiation complex formation on the slp1 promoter. This DESE-dependent activation is influenced by the extent of promoter- proximal DNA upstream of the transcription start site and involves a mechanism that induces nucleosome depletion around the promoter. This effect is specifically important for DESE activation but not PESE activation. ChIP experiments comparing wild-type versus repressed states of DESE-lacZ and PESE-lacZ reporter genes indicate that Eve represses PESE-lacZ expression by blocking the elongation step of the transcription cycle. This repression involves the regulated association of the elongation factor P-TEFb and phosphorylation of Ser2 in the C-terminal domain of RNA polymerase II. Runt and Ftz repress both DESE and PESE. Interestingly, Runt and Ftz repress DESE-lacZ by the same mechanism as Eve dependent repression of PESE, that is by inhibition of transcription elongation. However, Runt and Ftz repress PESE-lacZ by blocking transcription initiation. Analysis of the conserved domains of Runt revealed that C-terminal domain of Runt (region VIII) is involved in the repression of both DESE and PESE, and that this region is not required for activation of DESE.
dcterms.available2013-05-24T16:38:22Z
dcterms.available2015-04-24T14:47:52Z
dcterms.contributorThomsen, Gerald Hen_US
dcterms.contributorGergen, J Peteren_US
dcterms.contributorSternglanz, Rolfen_US
dcterms.contributorHaltiwanger, Robert Sen_US
dcterms.contributorKernan, Mauriceen_US
dcterms.creatorHang, Saiyu
dcterms.dateAccepted2013-05-24T16:38:22Z
dcterms.dateAccepted2015-04-24T14:47:52Z
dcterms.dateSubmitted2013-05-24T16:38:22Z
dcterms.dateSubmitted2015-04-24T14:47:52Z
dcterms.descriptionDepartment of Biochemistry and Structural Biologyen_US
dcterms.extent97 pg.en_US
dcterms.formatMonograph
dcterms.formatApplication/PDFen_US
dcterms.identifierhttp://hdl.handle.net/1951/60292
dcterms.identifierhttp://hdl.handle.net/11401/71549
dcterms.issued2012-08-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2013-05-24T16:38:22Z (GMT). No. of bitstreams: 1 StonyBrookUniversityETDPageEmbargo_20130517082608_116839.pdf: 41286 bytes, checksum: 425a156df10bbe213bfdf4d175026e82 (MD5) Previous issue date: 1en
dcterms.provenanceMade available in DSpace on 2015-04-24T14:47:52Z (GMT). No. of bitstreams: 3 StonyBrookUniversityETDPageEmbargo_20130517082608_116839.pdf.jpg: 1934 bytes, checksum: c116f0e1e7be19420106a88253e31f2e (MD5) StonyBrookUniversityETDPageEmbargo_20130517082608_116839.pdf.txt: 336 bytes, checksum: 84c0f8f99f2b4ae66b3cc3ade09ad2e9 (MD5) StonyBrookUniversityETDPageEmbargo_20130517082608_116839.pdf: 41286 bytes, checksum: 425a156df10bbe213bfdf4d175026e82 (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectdevelopment, Drosophila, enhancer, sloppy-paired 1, transcription, transcription factor
dcterms.subjectDevelopmental biology--Molecular biology--Genetics
dcterms.titleCis-regulatory contributions to the regulation of sloppy-paired 1 transcription initiation and elongation
dcterms.typeDissertation


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