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Frequency-based time-series gene expression recomposition using PRIISM

BACKGROUND: Circadian rhythm pathways influence the expression patterns of as much as 31% of the Arabidopsis genome through complicated interaction pathways, and have been found to be significantly disrupted by biotic and abiotic stress treatments, complicating treatment-response gene discovery meth...

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Autores principales: Rosa, Bruce A, Jiao, Yuhua, Oh, Sookyung, Montgomery, Beronda L, Qin, Wensheng, Chen, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464900/
https://www.ncbi.nlm.nih.gov/pubmed/22703599
http://dx.doi.org/10.1186/1752-0509-6-69
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author Rosa, Bruce A
Jiao, Yuhua
Oh, Sookyung
Montgomery, Beronda L
Qin, Wensheng
Chen, Jin
author_facet Rosa, Bruce A
Jiao, Yuhua
Oh, Sookyung
Montgomery, Beronda L
Qin, Wensheng
Chen, Jin
author_sort Rosa, Bruce A
collection PubMed
description BACKGROUND: Circadian rhythm pathways influence the expression patterns of as much as 31% of the Arabidopsis genome through complicated interaction pathways, and have been found to be significantly disrupted by biotic and abiotic stress treatments, complicating treatment-response gene discovery methods due to clock pattern mismatches in the fold change-based statistics. The PRIISM (Pattern Recomposition for the Isolation of Independent Signals in Microarray data) algorithm outlined in this paper is designed to separate pattern changes induced by different forces, including treatment-response pathways and circadian clock rhythm disruptions. RESULTS: Using the Fourier transform, high-resolution time-series microarray data is projected to the frequency domain. By identifying the clock frequency range from the core circadian clock genes, we separate the frequency spectrum to different sections containing treatment-frequency (representing up- or down-regulation by an adaptive treatment response), clock-frequency (representing the circadian clock-disruption response) and noise-frequency components. Then, we project the components’ spectra back to the expression domain to reconstruct isolated, independent gene expression patterns representing the effects of the different influences. By applying PRIISM on a high-resolution time-series Arabidopsis microarray dataset under a cold treatment, we systematically evaluated our method using maximum fold change and principal component analyses. The results of this study showed that the ranked treatment-frequency fold change results produce fewer false positives than the original methodology, and the 26-hour timepoint in our dataset was the best statistic for distinguishing the most known cold-response genes. In addition, six novel cold-response genes were discovered. PRIISM also provides gene expression data which represents only circadian clock influences, and may be useful for circadian clock studies. CONCLUSION: PRIISM is a novel approach for overcoming the problem of circadian disruptions from stress treatments on plants. PRIISM can be integrated with any existing analysis approach on gene expression data to separate circadian-influenced changes in gene expression, and it can be extended to apply to any organism with regular oscillations in gene expression patterns across a large portion of the genome.
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spelling pubmed-34649002012-10-10 Frequency-based time-series gene expression recomposition using PRIISM Rosa, Bruce A Jiao, Yuhua Oh, Sookyung Montgomery, Beronda L Qin, Wensheng Chen, Jin BMC Syst Biol Research Article BACKGROUND: Circadian rhythm pathways influence the expression patterns of as much as 31% of the Arabidopsis genome through complicated interaction pathways, and have been found to be significantly disrupted by biotic and abiotic stress treatments, complicating treatment-response gene discovery methods due to clock pattern mismatches in the fold change-based statistics. The PRIISM (Pattern Recomposition for the Isolation of Independent Signals in Microarray data) algorithm outlined in this paper is designed to separate pattern changes induced by different forces, including treatment-response pathways and circadian clock rhythm disruptions. RESULTS: Using the Fourier transform, high-resolution time-series microarray data is projected to the frequency domain. By identifying the clock frequency range from the core circadian clock genes, we separate the frequency spectrum to different sections containing treatment-frequency (representing up- or down-regulation by an adaptive treatment response), clock-frequency (representing the circadian clock-disruption response) and noise-frequency components. Then, we project the components’ spectra back to the expression domain to reconstruct isolated, independent gene expression patterns representing the effects of the different influences. By applying PRIISM on a high-resolution time-series Arabidopsis microarray dataset under a cold treatment, we systematically evaluated our method using maximum fold change and principal component analyses. The results of this study showed that the ranked treatment-frequency fold change results produce fewer false positives than the original methodology, and the 26-hour timepoint in our dataset was the best statistic for distinguishing the most known cold-response genes. In addition, six novel cold-response genes were discovered. PRIISM also provides gene expression data which represents only circadian clock influences, and may be useful for circadian clock studies. CONCLUSION: PRIISM is a novel approach for overcoming the problem of circadian disruptions from stress treatments on plants. PRIISM can be integrated with any existing analysis approach on gene expression data to separate circadian-influenced changes in gene expression, and it can be extended to apply to any organism with regular oscillations in gene expression patterns across a large portion of the genome. BioMed Central 2012-06-15 /pmc/articles/PMC3464900/ /pubmed/22703599 http://dx.doi.org/10.1186/1752-0509-6-69 Text en Copyright ©2012 Rosa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Rosa, Bruce A
Jiao, Yuhua
Oh, Sookyung
Montgomery, Beronda L
Qin, Wensheng
Chen, Jin
Frequency-based time-series gene expression recomposition using PRIISM
title Frequency-based time-series gene expression recomposition using PRIISM
title_full Frequency-based time-series gene expression recomposition using PRIISM
title_fullStr Frequency-based time-series gene expression recomposition using PRIISM
title_full_unstemmed Frequency-based time-series gene expression recomposition using PRIISM
title_short Frequency-based time-series gene expression recomposition using PRIISM
title_sort frequency-based time-series gene expression recomposition using priism
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464900/
https://www.ncbi.nlm.nih.gov/pubmed/22703599
http://dx.doi.org/10.1186/1752-0509-6-69
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