TY - JOUR
T1 - Large-scale analysis of Arabidopsis transcription reveals a basal co-regulation network.
AU - Atias, Osnat
AU - Chor, Benny
AU - Chamovitz, Daniel A.
N1 - Funding Information:
We thank Drs. Kris Gunsalus and Shiri Freilich for critical reading of the manuscript. We thank Dr. Saharon Rosset for helpful discussions. OA was supported in part by fellowships from the Edmund J. Safra Bioinformatics Program at Tel Aviv University, and from the Beville Family through Australian Friends of Tel Aviv University. DAC was supported by Israel Science Foundation grant 783/05.
PY - 2009
Y1 - 2009
N2 - Analyses of gene expression data from microarray experiments has become a central tool for identifying co-regulated, functional gene modules. A crucial aspect of such analysis is the integration of data from different experiments and different laboratories. How to weigh the contribution of different experiments is an important point influencing the final outcomes. We have developed a novel method for this integration, and applied it to genome-wide data from multiple Arabidopsis microarray experiments performed under a variety of experimental conditions. The goal of this study is to identify functional globally co-regulated gene modules in the Arabidopsis genome. Following the analysis of 21,000 Arabidopsis genes in 43 datasets and about 2 x 10(8) gene pairs, we identified a globally co-expressed gene network. We found clusters of globally co-expressed Arabidopsis genes that are enriched for known Gene Ontology annotations. Two types of modules were identified in the regulatory network that differed in their sensitivity to the node-scoring parameter; we further showed these two pertain to general and specialized modules. Some of these modules were further investigated using the Genevestigator compendium of microarray experiments. Analyses of smaller subsets of data lead to the identification of condition-specific modules. Our method for identification of gene clusters allows the integration of diverse microarray experiments from many sources. The analysis reveals that part of the Arabidopsis transcriptome is globally co-expressed, and can be further divided into known as well as novel functional gene modules. Our methodology is general enough to apply to any set of microarray experiments, using any scoring function.
AB - Analyses of gene expression data from microarray experiments has become a central tool for identifying co-regulated, functional gene modules. A crucial aspect of such analysis is the integration of data from different experiments and different laboratories. How to weigh the contribution of different experiments is an important point influencing the final outcomes. We have developed a novel method for this integration, and applied it to genome-wide data from multiple Arabidopsis microarray experiments performed under a variety of experimental conditions. The goal of this study is to identify functional globally co-regulated gene modules in the Arabidopsis genome. Following the analysis of 21,000 Arabidopsis genes in 43 datasets and about 2 x 10(8) gene pairs, we identified a globally co-expressed gene network. We found clusters of globally co-expressed Arabidopsis genes that are enriched for known Gene Ontology annotations. Two types of modules were identified in the regulatory network that differed in their sensitivity to the node-scoring parameter; we further showed these two pertain to general and specialized modules. Some of these modules were further investigated using the Genevestigator compendium of microarray experiments. Analyses of smaller subsets of data lead to the identification of condition-specific modules. Our method for identification of gene clusters allows the integration of diverse microarray experiments from many sources. The analysis reveals that part of the Arabidopsis transcriptome is globally co-expressed, and can be further divided into known as well as novel functional gene modules. Our methodology is general enough to apply to any set of microarray experiments, using any scoring function.
UR - http://www.scopus.com/inward/record.url?scp=77956679288&partnerID=8YFLogxK
U2 - 10.1186/1752-0509-3-86
DO - 10.1186/1752-0509-3-86
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
AN - SCOPUS:77956679288
SN - 1752-0509
VL - 3
SP - 86
JO - BMC Systems Biology
JF - BMC Systems Biology
ER -