The Effects of T-DNA Integration Sites on Transgene Expression in Arabidopsis

dc.contributor.advisorMark Conkling, Committee Memberen_US
dc.contributor.advisorWilliam F. Thompson, Committee Co-Chairen_US
dc.contributor.advisorSteven Spiker, Committee Chairen_US
dc.contributor.advisorArthur Weissinger, Committee Memberen_US
dc.contributor.authorFrancis, Kirk Ericen_US
dc.date.accessioned2010-04-02T18:26:56Z
dc.date.available2010-04-02T18:26:56Z
dc.date.issued2004-06-28en_US
dc.degree.disciplineGeneticsen_US
dc.degree.leveldissertationen_US
dc.degree.namePhDen_US
dc.description.abstractSeveral recent investigations of T-DNA integration sites in Arabidopsis thaliana have reported "cold spots" of integration, especially near centromeric regions. These observations have contributed to the ongoing debate over whether T-DNA integration is random, or if integration preferentially occurs in transcriptionally active regions. When transgenic plants are identified by selecting or screening for transgene activity, transformants with integrations into genomic regions that suppress transcription, such as heterochromatin, may not be identified. This phenomenon, which we call selection bias, may explain the perceived non-random distribution of T-DNA integration in previous studies. In order to investigate this possibility, I have characterized the sites of T-DNA integration in the genomes of transgenic plants identified by pooled PCR, a procedure that does not required expression of the transgene and is therefore free of selection bias. Over 100 transgenic Arabidopsis plants were identified by PCR and compared to kanamycin-selected transformants from the same T1 seed pool. A higher perceived transformation efficiency and a higher frequency of transgene silencing were observed in the PCR-identified lines. Together, the data suggest approximately 30% of transformation events may result in non-expressing transgenes that would preclude identification by selection. Genomic integration sites in PCR-identified lines were compared to those in existing T-DNA integration databases. In PCR-identified lines with silenced transgenes, the integration sites mapped to regions significantly underrepresented by T-DNA integrations in studies where transformants were identified by selection. The data presented here suggest that selection bias can account for at least some of the observed non-random integration of T-DNA into the Arabidopsis genome.en_US
dc.identifier.otheretd-03262004-105111en_US
dc.identifier.urihttp://www.lib.ncsu.edu/resolver/1840.16/3119
dc.rightsI hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. I hereby grant to NC State University or its agents the non-exclusive license to archive and make accessible, under the conditions specified below, my thesis, dissertation, or project report in whole or in part in all forms of media, now or hereafter known. I retain all other ownership rights to the copyright of the thesis, dissertation or project report. I also retain the right to use in future works (such as articles or books) all or part of this thesis, dissertation, or project report.en_US
dc.subjectAgrobacterium tumefaciensen_US
dc.subjectmatrix attachment regions (MARs)en_US
dc.subjectchromatinen_US
dc.subjectinsertional mutagenesisen_US
dc.subjectpost-transcriptional gene silencing (PTGS)en_US
dc.subjecttranscriptional gene silencing (TGS)en_US
dc.titleThe Effects of T-DNA Integration Sites on Transgene Expression in Arabidopsisen_US

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