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dc.contributor.advisorKunkel, Gary R.
dc.creatorShah, Uma
dc.date.accessioned2022-04-04T13:49:02Z
dc.date.available2022-04-04T13:49:02Z
dc.date.issued1991
dc.identifier.urihttps://hdl.handle.net/1969.1/CAPSTONE-JonesK_1979
dc.descriptionProgram year: 1990/1991en
dc.descriptionDigitized from print original stored in HDRen
dc.description.abstractThe 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.extent34 pagesen
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.subjectS. cerevisiaeen
dc.subjectRNA polymerase III transcribed genesen
dc.subjectU6 promoteren
dc.subjectligation-mediated PCRen
dc.subjectprotein-DNA interactionsen
dc.subjectgenomic footprintingen
dc.titlePCR-aided Amplification: A Tool for the Study of In Vivo Protein-DNA Interactions in the Yeast U6 Promoteren
dc.typeThesisen
thesis.degree.departmentBiochemistry and Biophysicsen
thesis.degree.grantorUniversity Undergraduate Fellowen
thesis.degree.levelUndergraduateen
dc.type.materialtexten


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