Statistical mechanical modeling of eukaryotic gene regulation

Chen, Chieh-Chun

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https://hdl.handle.net/2142/42149 Copy

Description

Title

Statistical mechanical modeling of eukaryotic gene regulation

Author(s)

Chen, Chieh-Chun

Issue Date

2013-02-03T19:17:29Z

Director of Research (if dissertation) or Advisor (if thesis)

Zhong, Sheng

Doctoral Committee Chair(s)

Zhong, Sheng

Committee Member(s)

• Jakobsson, Eric
• Ma, Jian
• Zhao, Huimin

Department of Study

Bioengineering

Discipline

Bioengineering

Degree Granting Institution

University of Illinois at Urbana-Champaign

Degree Name

Ph.D.

Degree Level

Dissertation

Keyword(s)

• Statistical mechanics
• transcriptional regulation
• transcription factors
• epignomes
• gene expression

Abstract

Gene expression patterns are regulated by gene regulatory networks. Central to transcriptional regulation of gene expression is the regulation of the quantities of transcription factors (TFs) bound to genomic regulatory sequences. This thesis work is built on statistical mechanics to study the stochastic interactions of TFs and regulatory sequences. We present a predictive model to learn how TFs interact with cis-regulatory sequences and with each other. By analyzing large scale TF-DNA binding data, the model can discover cooperative interactions among TFs and predict the strength of TF-DNA binding. Less clear is how the genome and the epigenome jointly instruct TFs binding. We present an epigenome-sensitive model to systematically analyze the epigenomic functions in modulating transcription factor-DNA binding. We discovered preferences of TFs for specific combinations of epigenomic modifications, termed as epigenomic motifs. Epigenomic motifs explain why some TFs appear to have different DNA binding motifs derived from in vivo and in vitro experiments. The data suggest that the epigenome can modulate transcriptional noise and boost the cooperativity of weak TF binding sites. We also show that the epigenome might suppress the TF binding differences on SNP-containing binding sites in two people, in theory and in real data. To identify regulatory relationships between TFs and target genes is another major topic in gene regulation. We developed an analytical method to identify a statistical thermodynamic model that best describes the form of TF-TF interaction among a set of TFs for every target gene. Based on this method, we developed a computational framework to infer regulatory relationships from multiple time course gene expression datasets. RNA interference data and large scale TF-DNA binding data independently validated a statistically significant fraction of these regulatory relationships. Moreover, this framework has the flexibility to incorporate other independent datasets to increase prediction accuracy.

Graduation Semester

2012-12

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http://hdl.handle.net/2142/42149

Copyright and License Information

Copyright 2012 Chieh-Chun Chen

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