Profiling of Accessible Chromatin Regions across Multiple Plant Species and Cell Types Reveals Common Gene Regulatory Principles and New Control Modules
Author(s) -
Kelsey A. Maher,
Marko Bajic,
Kaisa Kajala,
Mauricio Reynoso,
Germain Pauluzzi,
Donnelly A. West,
Kristina Zumstein,
Margaret Woodhouse,
Kerry L. Bubb,
Michael W. Dorrity,
Christine Queitsch,
Julia BaileySerres,
Neelima Sinha,
Siobhán M. Brady,
Roger B. Deal
Publication year - 2017
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.17.00581
Subject(s) - biology , medicago truncatula , chromatin , genetics , myb , arabidopsis , transcription factor , gene , promoter , genome , regulation of gene expression , regulatory sequence , computational biology , gene expression , symbiosis , bacteria , mutant
The transcriptional regulatory structure of plant genomes remains poorly defined relative to animals. It is unclear how many cis -regulatory elements exist, where these elements lie relative to promoters, and how these features are conserved across plant species. We employed the assay for transposase-accessible chromatin (ATAC-seq) in four plant species ( Arabidopsis thaliana , Medicago truncatula , Solanum lycopersicum , and Oryza sativa ) to delineate open chromatin regions and transcription factor (TF) binding sites across each genome. Despite 10-fold variation in intergenic space among species, the majority of open chromatin regions lie within 3 kb upstream of a transcription start site in all species. We find a common set of four TFs that appear to regulate conserved gene sets in the root tips of all four species, suggesting that TF-gene networks are generally conserved. Comparative ATAC-seq profiling of Arabidopsis root hair and non-hair cell types revealed extensive similarity as well as many cell-type-specific differences. Analyzing TF binding sites in differentially accessible regions identified a MYB-driven regulatory module unique to the hair cell, which appears to control both cell fate regulators and abiotic stress responses. Our analyses revealed common regulatory principles among species and shed light on the mechanisms producing cell-type-specific transcriptomes during development.
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