dc.contributor.advisor | Kunkel, Gary R. | |
dc.creator | Shah, Uma | |
dc.date.accessioned | 2022-04-04T13:49:02Z | |
dc.date.available | 2022-04-04T13:49:02Z | |
dc.date.issued | 1991 | |
dc.identifier.uri | https://hdl.handle.net/1969.1/CAPSTONE-JonesK_1979 | |
dc.description | Program year: 1990/1991 | en |
dc.description | Digitized from print original stored in HDR | en |
dc.description.abstract | The classification of RNA polymerase III transcribed genes into genes with internal promoters (within the coding region) and those with external promoters is no longer a clear one. The S. cerevisiae U6 promoter is comprised of control elements outside the coding region (on the 5' and 3' sides) and a possible internal control element. In the following study I demonstrate the optimization of ligation-mediated PCR for the S. cerevisiae system as a technique that is instrumental in genomic footprinting for determination of protein-DNA interactions in the yeast U6 promoter. | en |
dc.format.extent | 34 pages | en |
dc.format.medium | electronic | en |
dc.format.mimetype | application/pdf | |
dc.subject | S. cerevisiae | en |
dc.subject | RNA polymerase III transcribed genes | en |
dc.subject | U6 promoter | en |
dc.subject | ligation-mediated PCR | en |
dc.subject | protein-DNA interactions | en |
dc.subject | genomic footprinting | en |
dc.title | PCR-aided Amplification: A Tool for the Study of In Vivo Protein-DNA Interactions in the Yeast U6 Promoter | en |
dc.type | Thesis | en |
thesis.degree.department | Biochemistry and Biophysics | en |
thesis.degree.grantor | University Undergraduate Fellow | en |
thesis.degree.level | Undergraduate | en |
dc.type.material | text | en |