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An order estimation based approach to identify response genes for microarray time course data
Zhiheng K Lu1, O Brian Allen, Anthony F Desmond
1Metastract Inc.
Abstract:
Gene expression profiles from microarray time course experiments provide a unique opportunity to examine genome-wide signal processing and gene responses. A fundamental issue in microarray experiments is that the treatment condition can only be controlled at the cell level rather than at the gene level. The treatment condition does not affect all genes equally. Some genes depend on other genes to detect external changes. The dependency between genes is not fully deterministic and may vary with treatment condition. Thus the expression of each gene is potentially affected by two confounding effects: the treatment effect and the gene context effect arising from the regulatory interactions among genes. This gene context effect is hard to isolate. Neither can it be simply ignored. Instead, this gene context information which may be different under different treatment conditions is of primary biological interest. We introduce an approach which deals with the confounding effects and takes into account the uncontrollable gene context effect. Our method is based on the estimation of the number of hidden states, which, in our development, corresponds to the order of a hidden Markov model (HMM). For each gene, its observed expression is modeled by a gamma distribution determined by the corresponding hidden state at each time point. Those genes showing evidence for more than one hidden state can be categorized as the signalling genes, or in a wider sense, as the response genes which are coordinated by a cell system in reaction to a specific external condition. These response genes can be used in the comparison of different treatment conditions, to investigate the gene context effect under different treatments. Microarray time course data are also analyzed to demonstrate our method.
Insights
This study introduces a novel method to analyze gene expression data from microarray time course experiments. It accounts for both treatment and gene context effects, identifying response genes crucial for understanding cellular systems and treatment impacts.
Area of Science:
- Genomics
- Systems Biology
- Bioinformatics
Background:
- Microarray time course experiments offer insights into genome-wide gene responses.
- Gene expression is influenced by both external treatments and complex gene regulatory interactions (gene context effect).
- Isolating the gene context effect, which can vary with treatment, is challenging but biologically significant.
Purpose of the Study:
- To develop an approach that addresses confounding effects in gene expression analysis.
- To incorporate uncontrollable gene context information into the analysis of microarray time course data.
- To identify and categorize response genes that are coordinated by cellular systems.
Main Methods:
- Utilizing a hidden Markov model (HMM) to estimate the number of hidden states.
- Modeling individual gene expression using a gamma distribution dependent on hidden states at each time point.
- Categorizing genes with multiple hidden states as signaling or response genes.
Main Results:
- The proposed method effectively handles confounding treatment and gene context effects.
- Genes exhibiting multiple hidden states are identified as response genes.
- The approach allows for the investigation of gene context effects across different treatment conditions.
Conclusions:
- The developed method provides a robust framework for analyzing complex gene expression patterns.
- Identified response genes are valuable for comparing treatment conditions and understanding cellular responses.
- This approach enhances the biological interpretation of microarray time course data.
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