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The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the...
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Real-time Analysis of Transcription Factor Binding, Transcription, Translation, and Turnover to Display Global Events During Cellular Activation
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Inferring transcriptional logic from multiple dynamic experiments.

Giorgos Minas1,2, Dafyd J Jenkins2, David A Rand1,2

  • 1Mathematics Institute.

Bioinformatics (Oxford, England)
|July 2, 2017
PubMed
Summary
This summary is machine-generated.

This study introduces a new computational method to uncover gene regulatory logic using dynamic gene expression data. The approach effectively identifies transcription factor networks controlling gene expression across multiple experiments.

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Area of Science:

  • Systems Biology
  • Computational Biology
  • Genomics

Background:

  • Dynamic gene expression data under multiple conditions is crucial for understanding gene regulation.
  • Identifying transcriptional regulators and their logical interactions is a key goal in systems biology.

Purpose of the Study:

  • To develop a novel, interpretable computational method for inferring gene transcriptional regulation.
  • To identify the logical structure of gene regulation by transcription factors (TFs).

Main Methods:

  • A dynamic model linking target gene mRNA transcription rates to TF activation states.
  • Utilizing a trans-dimensional Markov Chain Monte Carlo (MCMC) algorithm for efficient sampling of regulatory logic.
  • Validating the method with simulations and applying it to Arabidopsis thaliana microarray time series data.

Main Results:

  • The proposed method successfully infers gene regulatory logic with biological interpretability.
  • The dynamic model captures TF interactions consistent across multiple experiments and time.
  • The MCMC algorithm efficiently ranks potential regulatory models by posterior probabilities.

Conclusions:

  • The novel method accurately detects complex regulatory interactions consistent across diverse experimental conditions.
  • This approach advances the understanding of gene regulatory networks using dynamic expression data.
  • The developed tool is available for use in further systems biology research.