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Series GSE211953 Query DataSets for GSE211953
Status Public on Apr 19, 2024
Title The SAGA complex maintains the oncogenic gene expression program in MYCN-amplified neuroblastoma [ChIP-Seq]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Pediatric cancers are frequently driven by fusion or amplification events that result in aberrant transcription factor activity. As transcription factors themselves remain challenging to target, an emerging therapeutic approach for these cancers is to target epigenetic complexes that help maintain oncogenic transcriptional programs. It is therefore critical to identify the complete set of epigenetic modulators maintaining the oncogenic epigenetic landscape of pediatric cancers. Here, we used functional genomic screens to identify epigenetic complexes critical for viability in cell line models of MYCN-amplified neuroblastoma, a disease of dysregulated development driven by an aberrant oncogenic transcriptional program. We identified multiple genes within the transcriptional coactivator Spt-Ada-Gcn5-acetyltransferase (SAGA) complex as selective dependencies in MYCN-amplified neuroblastoma. Integrating ChIP-seq, ATAC-seq, and RNA-seq with targeted protein-degradation and gene editing tools, we characterized the DNA recruitment sites of the SAGA complex in neuroblastoma, and the consequences of SAGA complex lysine acetyltransferase (KAT) activity loss on histone acetylation and gene expression. We demonstrate that loss of SAGA KAT activity suppresses MYC and MYCN gene expression programs and impairs cell cycle progression. Further, we showed that the SAGA complex is pharmacologically targetable with a KAT2A/KAT2B proteolysis targeting chimera molecule that demonstrated significant activity in vitro and in vivo. Our findings expand our understanding of the histone modifying complexes that maintain the oncogenic transcriptional state in this disease and suggest therapeutic potential for inhibitors of SAGA KAT activity in MYCN-amplified neuroblastoma.
 
Overall design Investigate alterations in TADA2B binding after TADA2B loss (degradation dTAG v1 TADA2B vs. DMSO at 6 hours) in KELLY, NGP and NB1 neuroblastoma cells, one replicate per condition. Investigate alterations in MYCN, H3K27ac and H3K9ac binding after TADA2B loss (degradation dTAG v1 TADA2B vs. DMSO at 6 hours) in KELLY neuroblastoma cells, one replicate per condition. Investigate alterations in MYCN, H3K27ac and H3K9ac binding after KAT2A/KAT2B targeting (PROTAC GSK-699-1 vs. DMSO at 6 hours) in KELLY neuroblastoma cells, two replicates per condition.
 
Contributor(s) Stegmaier K, Alexe G
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Aug 24, 2022
Last update date Apr 19, 2024
Contact name Gabriela Alexe
E-mail(s) galexe@broadinstitute.org
Organization name Broad Institute
Department Computational Biology and Bioinformatics
Street address 415 Main St.
City Cambridge
State/province MA
ZIP/Postal code 02142
Country USA
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)
Samples (35)
GSM6506050 KELLY-TADA2Bdeg cells, DMSO, HA antibody, 6 hours
GSM6506051 KELLY-TADA2Bdeg cells, DMSO, Input, 6 hours
GSM6506052 KELLY-TADA2Bdeg cells, dTAGv1, HA antibody, 6 hours
This SubSeries is part of SuperSeries:
GSE211355 The SAGA complex maintains the oncogenic gene expression program in MYCN-amplified neuroblastoma
Relations
BioProject PRJNA873048

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
GSE211953_ChIPSeq_KELLY_DMSO.H3K27ac_06h.bw 289.9 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_DMSO.H3K9ac_06h.bw 121.5 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_DMSO.Input.TADA2B_06h.bw 266.4 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_DMSO.Input_06h.bw 381.7 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_DMSO.MYCN_06h.bw 312.1 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_DMSO.TADA2B_06h.bw 146.5 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_dTAGv1.H3K27ac_06h.bw 328.0 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_dTAGv1.H3K9ac_06h.bw 142.7 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_dTAGv1.Input.TADA2B_06h.bw 321.0 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_dTAGv1.Input_06h.bw 310.1 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_dTAGv1.MYCN_06h.bw 340.5 Mb (ftp)(http) BW
GSE211953_ChIPSeq_KELLY_dTAGv1.TADA2B_06h.bw 103.8 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NB1_DMSO.Input_06h.bw 455.5 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NB1_DMSO.TADA2B_06h.bw 285.6 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NB1_dTAGv1.Input_06h.bw 438.9 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NB1_dTAGv1.TADA2B_06h.bw 305.9 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NGP_DMSO.Input_06h.bw 417.8 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NGP_DMSO.TADA2B_06h.bw 233.7 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NGP_dTAGv1.Input_06h.bw 430.8 Mb (ftp)(http) BW
GSE211953_ChIPSeq_NGP_dTAGv1.TADA2B_06h.bw 362.7 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_DMSO_06h_H3K27ac.bw 165.4 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_DMSO_06h_H3K9ac.bw 133.6 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_DMSO_06h_Input.bw 258.0 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_DMSO_06h_MYCN.bw 72.3 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_GSK6991_06h_H3K27ac.bw 195.2 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_GSK6991_06h_H3K9ac.bw 152.7 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_GSK6991_06h_Input.bw 257.8 Mb (ftp)(http) BW
GSE211953_PROTAC_ChIPSeq_KELLY_GSK6991_06h_MYCN.bw 130.7 Mb (ftp)(http) BW
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