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Series GSE218019 Query DataSets for GSE218019
Status Public on Jun 27, 2023
Title Localization of the pioneer factor GAF to subnuclear foci is driven by DNA binding and required to silence satellite repeat expression [ChIP-Seq]
Organism Drosophila melanogaster
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary The eukaryotic genome is organized to enable the precise regulation of gene expression required for development. This organization is established during early development when the embryo transitions from a fertilized germ cell to the totipotent zygote. To understand the factors and processes that drive genomic organization, we focused on the pioneer factor GAGA factor (GAF) that is required for early embryonic development in Drosophila. GAF transcriptionally activates the zygotic genome and is localized to subnuclear foci. We show that this non-uniform distribution is driven by binding to the highly abundant GA-satellite repeats. At GA-repeats, GAF is necessary to form heterochromatin and silence transcription. Thus, GAF is required to establish both active and silent regions. We propose that the foci formation enables GAF to have opposing transcriptional roles within a single nucleus. Our data support a model in which modulation of the subnuclear concentration of transcription factors acts to organize the nucleus into functionally distinct domains that are essential for the robust regulation of gene expression.
 
Overall design ChIP-seq was performed using the anti-GFP antibody (Abcam #abcam290) on 2-3 hr AEL embryos from mothers expressing endogenously tagged sfGFP-GAF (sfGFP-GAF/+) or endogenously tagged sfGFP-GAF with the polyQ region of the short isoform deleted (sfGFP-GAFS-delta-PQ/sfGFP-GAFS-delta-PQ). DBD-sfGFP ChIP-seq was performed using the anti-GFP antibody on 2-2.5 hr AEL embryos laid by mothers expressing a truncated version of GAF from a transgene that contained only the DNA-binding domain (310-391aa) tagged with sfGFP. Anti-H3K9me3 ChIP-seq was performed using the anti-H3K9me3 antibody (Active motif #39161) on 2-2.5 hr AEL sfGFP-GAF homozygous controls and GAFdeGradFP embryos that have GAF knocked down. All experiments were done in duplicate, and sequencing was performed on immunoprecipitated samples as well as input controls.
 
Contributor(s) Gaskill MM, Soluri IV, Branks AE, Boka AP, Stadler MR, Vietor K, Huang HS, Gibson TJ, Mir M, Blythe SA, Harrison MM
Citation(s) 37478844
Submission date Nov 15, 2022
Last update date Sep 26, 2023
Contact name Melissa M Harrison
E-mail(s) [email protected]
Organization name University of Wisconsin Madison
Department Biomolecular Chemistry
Lab 1135 Biochemical Sciences Bldg
Street address 420 Henry Mall
City Madison
State/province WI
ZIP/Postal code 53706
Country USA
 
Platforms (3)
GPL19132 Illumina NextSeq 500 (Drosophila melanogaster)
GPL21306 Illumina HiSeq 4000 (Drosophila melanogaster)
GPL25244 Illumina NovaSeq 6000 (Drosophila melanogaster)
Samples (20)
GSM6732877 DBD-sfGFP, GFP Input, 1
GSM6732878 DBD-sfGFP, GFP Input, 2
GSM6732879 DBD-sfGFP, GFP IP, 1
This SubSeries is part of SuperSeries:
GSE218020 Localization of the Drosophila pioneer factor GAF to subnuclear foci is driven by DNA binding and required to silence satellite repeat expression
Relations
BioProject PRJNA901932

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

Supplementary file Size Download File type/resource
GSE218019_2-3H_PQ-mut_IP.bw 59.6 Mb (ftp)(http) BW
GSE218019_2-3H_PQ-mut_IP.narrowPeak.gz 78.4 Kb (ftp)(http) NARROWPEAK
GSE218019_2-3H_PQ-mut_input.bw 60.5 Mb (ftp)(http) BW
GSE218019_2-3H_control_IP.bw 59.2 Mb (ftp)(http) BW
GSE218019_2-3H_control_IP.narrowPeak.gz 111.2 Kb (ftp)(http) NARROWPEAK
GSE218019_2-3H_control_input.bw 59.3 Mb (ftp)(http) BW
GSE218019_H3K9me3_log2ratioIPvInput_control.bw 4.2 Mb (ftp)(http) BW
GSE218019_H3K9me3_log2ratioIPvInput_degrad.bw 4.2 Mb (ftp)(http) BW
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Processed data are available on Series record

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