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dc.identifier.urihttp://hdl.handle.net/11401/76892
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.typeThesis
dcterms.abstractThe Kin28 subunit of the general transcription factor complex, TFIIH, is a kinase that phosphorylates the heptapeptide repeats at serine position 5 (Ser5) on the C-terminal domain of RNA polymerase II (Pol II). Optimal Ser5 phosphorylation is important during transcription for Pol II to transition from the initiation step to the elongation step in a process called promoter escape. During transcription initiation, the nucleosome directly downstream of the promoter, called +1, must be disassembled before Pol II can engage the transcription start site. Previous work showed that the transcription machinery plays a direct role in the disassembly of the +1 nucleosome, but the exact mechanism is currently unknown. We hypothesize that the disassembly of the +1 nucleosome occurs during promoter escape. To test this idea, I attempted to conditionally deplete Kin28, in the yeast, Saccharomyces cerevisiae, to block promoter escape. I then applied a modified genomic approach to map nascent Pol II-associated RNA molecules before and after Kin28 depletion. The Kin28 depletion failed to block promoter escape, possibly due to incomplete removal of Kin28 from the nucleus. Instead, I found that the Kin28 depleted strain accumulated Pol II-associated read-through transcripts beyond the transcription termination site suggesting that Kin28 plays a role in the processing of the nascent RNA of protein-coding genes.
dcterms.available2017-09-20T16:51:23Z
dcterms.contributorLuk, Eden_US
dcterms.contributorHollingsworth, Nancy Men_US
dcterms.creatorLabuz, Daniel Roy
dcterms.dateAccepted2017-09-20T16:51:23Z
dcterms.dateSubmitted2017-09-20T16:51:23Z
dcterms.descriptionDepartment of Biochemistry and Cell Biologyen_US
dcterms.extent49 pg.en_US
dcterms.formatApplication/PDFen_US
dcterms.formatMonograph
dcterms.identifierhttp://hdl.handle.net/11401/76892
dcterms.issued2016-12-01
dcterms.languageen_US
dcterms.provenanceMade available in DSpace on 2017-09-20T16:51:23Z (GMT). No. of bitstreams: 1 Labuz_grad.sunysb_0771M_13119.pdf: 3574928 bytes, checksum: 84a7cd55029d3655d59b938d7d5602c2 (MD5) Previous issue date: 1en
dcterms.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.
dcterms.subjectBiochemistry -- Molecular biology
dcterms.titleThe role of the Kin28 protein kinase in chromatin remodeling and transcription termination
dcterms.typeThesis


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