ATAC-Seq Data for Genome-Wide Profiling of Transcription Factor Binding Sites in the Rice False Smut Fungus Ustilaginoidea virens.
Xiaoyang ChenHao LiuXiaolin ChenJunbin HuangTom HsiangLu ZhengPublished in: Molecular plant-microbe interactions : MPMI (2021)
Identification of transcription factor binding sites is one of the most important steps in understanding the function of transcription factors and regulatory networks in organisms. The assay for transposase accessible chromatin sequencing (ATAC-seq) is a simple protocol for detection of open chromatin that could be a powerful tool to advance studies of protein-DNA interactions. Although ATAC-seq has been used in systematic identification of cis-regulatory regions in animal and plant genomes, this method has been rarely applied in fungi. Here, we describe a valuable ATAC-seq resource in the genome of an economically important phytopathogen, the rice false smut fungus Ustilaginoidea virens. The ATAC-seq data of U. virens mycelia collected from potato sucrose broth (PSB) and PSB supplied with rice spikelet extract were both generated. This is the first genome-wide profiling of open chromatin and transcription factor binding sites in U. virens.[Formula: see text] Copyright © 2021 The Author(s). This is an open access article distributed under the CC BY-NC-ND 4.0 International license.
Keyphrases
- genome wide
- transcription factor
- dna methylation
- single cell
- dna binding
- copy number
- rna seq
- electronic health record
- genome wide identification
- randomized controlled trial
- gene expression
- high throughput
- smoking cessation
- single molecule
- bioinformatics analysis
- human milk
- circulating tumor
- dna damage
- multidrug resistant
- protein protein
- deep learning