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Updated: May 16, 2026

Genome-wide Analysis using ChIP to Identify Isoform-specific Gene Targets
Published on: July 7, 2010
Co-expression analysis identifies putative targets for CBP60g and SARD1 regulation
William Truman1, Jane Glazebrook
1Department of Plant Biology, Microbial and Plant Genomics Institute, University of Minnesota, 1500 Gortner Avenue, Saint Paul, MN 55108, USA. wtruman@umn.edu
Calmodulin binding protein CBP60g and SARD1 regulate plant defense by controlling salicylic acid (SA) biosynthesis. Co-expression analysis identified new genes in this signaling network, revealing insights into plant immunity.
Area of Science:
- Plant Molecular Biology
- Plant Immunity
- Gene Regulation
Background:
- Salicylic acid (SA) is crucial for plant defense signaling.
- Isochorismate synthase (SID2) is essential for SA biosynthesis in Arabidopsis.
- CBP60g and SARD1 bind the SID2 promoter, and their loss impairs SA production and increases susceptibility to pathogens.
Purpose of the Study:
- To identify novel components of the CBP60g and SARD1 signaling pathway.
- To understand the gene regulatory network controlling salicylic acid biosynthesis.
Main Methods:
- Gene expression profiling using custom microarrays.
- Co-expression analysis across ATH1 full genome microarray experiments.
- Clustering analysis to group co-expressed genes.
- Electrophoretic mobility shift assay (EMSA) to confirm DNA binding.
Main Results:
- Identified genes, including calmodulin-like genes, co-expressed with SID2 and regulated by CBP60g and SARD1.
- SID2 and co-expressed genes show promoter enrichment for GAAATT motifs.
- Genes regulated by CBP60g and SARD1 exhibit varied expression patterns in the double mutant.
Conclusions:
- Co-expression analysis successfully uncovered putative components of the CBP60g/SARD1 signaling network.
- Some identified genes are repressed by CBP60g and SARD1, highlighting their regulatory role.
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