Identification of Transcription Factor Target Genes by Integrative Omics Data Analysis

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dc.contributor.ISNI0000 0001 1707 1372 (Zhang, MQ)
dc.contributor.advisorZhang, Michael Q.
dc.creatorLiu, Yuxuan
dc.date.accessioned2018-02-01T16:24:28Z
dc.date.available2017-12-01
dc.date.created2016-12
dc.date.issued2016-12
dc.date.submittedDecember 2016
dc.date.updated2018-02-01T16:24:28Z
dc.description.abstractTranscription factors (TFs) are proteins that control the rate of transcription. They are main regulators of gene transcription. Knowing their targets is very important for understanding developmental processes, cellular stress response and genetic causes of disease. Most of prokaryotic genome is coding and TF binding sites are usually close to genes. However, for the mammalian system, most of its genome is non-coding and TFs usually bind to gene distal regions and they regulate gene transcription via chromosome looping. In our study, we were trying to identify TF targets in both the simple prokaryotic system and the complex mammalian system by integrative omics data analysis. Considering the differences between prokaryotic and mammalian systems, we integrated different omics data in each system to identify TF targets. In prokaryotes, DNA is organized in operon which contains a cluster of genes under the control of a single promoter. There is stronger correlation between TF binding and gene expression in prokaryotes than in the mammalian system. And TF motif in prokaryotes is usually longer and more specific than that in eukaryotes. Therefore, in prokaryotes, we integrated TF genome-wide binding data, expression data and motif information to identify TF targets. We conducted our study using TF NsrR and tried to identify its genome-wide binding targets in Uropathogenic Escherchia coli (UPEC) CFT073 to understand UPEC’s response to nitric oxide. In the mammalian system, DNA is wrapped on histone to form nucleosome. Histone modification and chromatin accessibility are important for transcription factor binding. DNA can form looping interactions to regulate gene expression. Therefore for TF targets identification in the mammalian system, we integrated TF genome-wide binding data, epigenetic data and chromatin looping interaction data. We built a classifier to predict TP53-associated looping interactions and genome-wide long-distance targets of TP53.
dc.format.mimetypeapplication/pdf
dc.identifier.urihttp://hdl.handle.net/10735.1/5629
dc.language.isoen
dc.rightsCopyright ©2016 is held by the author. Digital access to this material is made possible by the Eugene McDermott Library. Further transmission, reproduction or presentation (such as public display or performance) of protected items is prohibited except with permission of the author.
dc.subjectTranscription factors
dc.subjectChromatin
dc.subjectp53 protein
dc.subjectBinding sites (Biochemistry)
dc.subjectGene expression
dc.subjectGenomics
dc.subjectBioinformatics
dc.titleIdentification of Transcription Factor Target Genes by Integrative Omics Data Analysis
dc.typeDissertation
dc.type.materialtext
thesis.degree.departmentBiology - Molecular and Cell Biology
thesis.degree.grantorThe University of Texas at Dallas
thesis.degree.levelDoctoral
thesis.degree.namePHD

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