Localization of the bacteriophage P1 cin recombinase promoter / by David L. Onks.

Author/creator Onks, David L. author.
Other author Kennedy, Kathleen E., 1946- degree supervisor.
Other author East Carolina University. Department of Biology.
Format Theses and dissertations
Production1990.
Description[iv], 62 leaves : illustrations ; 28 cm
Supplemental ContentAccess via ScholarShip
Subjects

Summary Site-specific inversion is a mechanism allowing an organism to express alternate phenotypes. Inversion frequency of a DNA segment may be under the control of the recombinase promoter. Promoter mapping studies, including endonuclease mapping and primer extension, localize the promoter of the bacteriophage P1 cin recombinase to a region less than 80 base pairs from the start codon. The endonuclease mapping gels were scanned using a densitometer to quantitate inversion relative to the parent plasmid. It was shown that additional promoters outside the invertible segment affect the frequency of inversion. One orientation of the invertible segment is favored as opposed to the other. Site-specific inversion systems could ultimately be used as promoter-probe vectors. These vectors would identify weak promoters cloned upstream from the recombinase gene.
General noteSubmitted to the faculty of the Department of Biology.
General noteAdvisor: Kathleen E. Kennedy
Dissertation noteM.S. East Carolina University 1990
Bibliography noteIncludes bibliographical references (leaves 60-62).
Genre/formdissertations.
Genre/formAcademic theses.
Genre/formAcademic theses.
Genre/formThèses et écrits académiques.

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