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Series GSE186667 Query DataSets for GSE186667
Status Public on Apr 27, 2022
Title Smarcb1 is indispensable for the nervous system development and its loss results in a deregulation of esBAF binding [ChIP-seq]
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Using ChIP-seq technology, we aimed to provide insight into the consequences of the knockdown of Smarcb1, an essential esBAF subunit, for the binding of the esBAF complex (Smarca4), the PRC2 complex (Ezh2) as well as for histone marks H3K27me3, H3K27ac and H3K4me3. We show that Smarcb1 knockdown results in the change of BAF complex binding in both directions: decreased binding (potentially by loss of function) as well as increased binding (potentially by retargeting). Furthermore, we see that binding changes especially occur in regions important for basic cellular functions (adhesion, cell organization, metabolism) as well as regions crucial for development (especially nervous system development). In addition, we depicted binding changes in enhancer regions in which a decrease of BAF binding was much more prominent than in gene regions.
 
Overall design Genome-wide binding of Smarca4, Ezh2, H3K27me3, H3K27ac and H3K4me3 in Smarcb1 wildtype and Smarcb1 knockdown mESC
 
Contributor(s) Kerl K, Alfert A, Walter C
Citation(s) 35456033
Submission date Oct 27, 2021
Last update date Apr 29, 2022
Contact name Carolin Walter
E-mail(s) c_walt03@uni-muenster.de
Organization name Westfälische Wilhelms-Universität Münster
Department Medical Faculty of the WWU Münster
Lab Institute of Medical Informatics
Street address Domagkstraße 9
City Münster
ZIP/Postal code 48149
Country Germany
 
Platforms (1)
GPL19057 Illumina NextSeq 500 (Mus musculus)
Samples (14)
GSM5658765 ChIP-seq Input (Ezh2, H3K4me3, H3K27ac) (ctrl)
GSM5658766 ChIP-seq Input (Ezh2, H3K4me3, H3K27ac) (kd)
GSM5658767 ChIP-seq Input (Smarca4, H3K27me3) (ctrl)
This SubSeries is part of SuperSeries:
GSE186669 Smarcb1 is indispensable for the nervous system development and its loss results in a deregulation of esBAF binding.
Relations
BioProject PRJNA775008
SRA SRP343413

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE186667_RAW.tar 5.0 Mb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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