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Updated: Jun 22, 2026

Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
Published on: March 7, 2018
From DNA sequence to transcriptional behaviour: a quantitative approach.
1Department of Computer Science and Applied Mathematics and Department of Molecular Cell Biology, Weizmann Institute of Science, Rehovot 76100, Israel. eran.segal@weizmann.ac.il
This study introduces a quantitative framework to understand gene regulation. It models how DNA sequences, transcription factors, and nucleosomes interact to control gene activity and transcriptional noise.
Area of Science:
- Molecular Biology
- Genomics
- Systems Biology
Background:
- Gene regulatory regions contain complex DNA sequences.
- Quantitative models describe molecular interactions with genomic sequences.
- Each regulatory sequence has a unique binding landscape for molecules.
Purpose of the Study:
- To present a unified quantitative framework for gene regulation.
- To explain experimental observations of factor and nucleosome binding.
- To model transcriptional dynamics, noise, and evolution.
Main Methods:
- Utilizing existing quantitative modeling methods.
- Developing a framework based on molecular binding affinities.
- Integrating sequence-specific binding and transcriptional output.
Main Results:
- The framework explains observed binding patterns of transcription factors and nucleosomes.
- It accurately models the dynamics of transcriptional activation.
- The model accounts for unique binding configurations and transcriptional outputs.
Conclusions:
- The unified framework advances understanding of transcriptional regulation.
- It provides a basis for modeling complex phenomena like transcriptional noise.
- This approach can be extended to study the evolution of gene regulation.
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