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   	<dc:title>Coevolution of transcription factors and their binding sites in sequence space</dc:title>
   	<dc:title>ISTA Thesis</dc:title>
   	<dc:creator>Prizak, Roshan</dc:creator>
   	<dc:subject>ddc:576</dc:subject>
   	<dc:description>Transcription factors, by binding to specific sequences on the DNA, control the precise spatio-temporal expression of genes inside a cell. However, this specificity is limited, leading to frequent incorrect binding of transcription factors that might have deleterious consequences on the cell. By constructing a biophysical model of TF-DNA binding in the context of gene regulation, I will first explore how regulatory constraints can strongly shape the distribution of a population in sequence space. Then, by directly linking this to a picture of multiple types of transcription factors performing their functions simultaneously inside the cell, I will explore the extent of regulatory crosstalk -- incorrect binding interactions between transcription factors and binding sites that lead to erroneous regulatory states -- and understand the constraints this places on the design of regulatory systems. I will then develop a generic theoretical framework to investigate the coevolution of multiple transcription factors and multiple binding sites, in the context of a gene regulatory network that performs a certain function. As a particular tractable version of this problem, I will consider the evolution of two transcription factors when they transmit upstream signals to downstream target genes. Specifically, I will describe the evolutionary steady states and the evolutionary pathways involved, along with their timescales, of a system that initially undergoes a transcription factor duplication event. To connect this important theoretical model to the prominent biological event of transcription factor duplication giving rise to paralogous families, I will then describe a bioinformatics analysis of C2H2 Zn-finger transcription factors, a major family in humans, and focus on the patterns of evolution that paralogs have undergone in their various protein domains in the recent past. </dc:description>
   	<dc:publisher>Institute of Science and Technology Austria</dc:publisher>
   	<dc:date>2019</dc:date>
   	<dc:type>info:eu-repo/semantics/doctoralThesis</dc:type>
   	<dc:type>doc-type:DoctoralThesis</dc:type>
   	<dc:type>DoctoralThesis</dc:type>
   	<dc:type>http://purl.org/coar/resource_type/c_db06</dc:type>
   	<dc:identifier>https://research-explorer.ista.ac.at/record/6071</dc:identifier>
   	<dc:identifier>https://research-explorer.ista.ac.at/download/6071/6072</dc:identifier>
   	<dc:source>Prizak R. Coevolution of transcription factors and their binding sites in sequence space. 2019. doi:&lt;a href=&quot;https://doi.org/10.15479/at:ista:th6071&quot;&gt;10.15479/at:ista:th6071&lt;/a&gt;</dc:source>
   	<dc:language>eng</dc:language>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.15479/at:ista:th6071</dc:relation>
   	<dc:relation>info:eu-repo/semantics/altIdentifier/issn/2663-337X</dc:relation>
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