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Updated: Jun 22, 2026

Enhanced Yeast One-hybrid Screens To Identify Transcription Factor Binding To Human DNA Sequences
Published on: February 11, 2019
Dynamic and complex transcription factor binding during an inducible response in yeast.
Li Ni1, Can Bruce, Christopher Hart
1Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, Connecticut 06520, USA.
Transcription factors exhibit diverse binding patterns to regulate yeast salt response. This study defines temporal binding classes and reveals a dynamic, hierarchical gene regulatory circuit coordinating cellular responses.
Area of Science:
- Molecular Biology
- Systems Biology
- Genetics
Background:
- Gene regulation is crucial for complex biological processes.
- Transcription factor binding dynamics are poorly understood.
- Understanding temporal binding patterns is key to deciphering regulatory circuits.
Purpose of the Study:
- To analyze the temporal order of transcription factor binding in yeast during salt response.
- To define distinct temporal binding patterns of transcription factors.
- To integrate binding and gene expression data to reveal regulatory circuit dynamics.
Main Methods:
- Global analysis of transcription factor binding to target genes.
- Identification of temporal binding classes (constant, rapid, slow, transient induction).
- Co-association analysis of multiple transcription factors.
- Correlation of binding patterns with gene expression data.
Main Results:
- Identified four distinct temporal binding patterns for Yap4 and Sko1.
- Demonstrated that individual transcription factors can display multiple binding patterns.
- Found significant co-association among seven transcription factors involved in osmotic regulation.
- Correlated transcription factor binding patterns with specific gene expression profiles.
Conclusions:
- Eukaryotic gene regulation utilizes diverse temporal binding patterns.
- A complex, dynamic, and hierarchical regulatory circuit coordinates yeast salt response.
- Specific combinations of transcription factors target distinct genes at discrete times.
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