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Series GSE68052 Query DataSets for GSE68052
Status Public on Jan 01, 2017
Title Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription [ChIP-Seq]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Cancer metabolism has been actively studied to gain insights into tumorigenic survival mechanisms and susceptibilities. In melanoma, we identify HEXIM1, a transcription elongation regulator, as a novel melanoma suppressor that participates in nucleotide stress regulation. HEXIM1 expression is low in melanoma. Its overexpression suppresses melanoma while its inactivation accelerates tumor onset in vivo. HEXIM1 responds to nucleotide stress. Knockdown of HEXIM1 rescues neural crest and melanoma nucleotide stress phenotypes in vivo. Mechanistically, under nucleotide stress, HEXIM1 is induced to form an inhibitory complex with P-TEFb, the kinase that initiates transcription elongation, to pause transcription at tumorigenic genes. The resulting alteration in gene expression also causes anti-tumorigenic transcripts to bind to and be stabilized by HEXIM1. HEXIM1 therefore plays an important role in inhibiting cancer cell-specific gene transcription while also facilitating anti-cancer gene expression. Our study reveals a novel role for HEXIM1 in coupling nucleotide metabolism with transcriptional regulation in melanoma.
 
Overall design ChIP-seq analysis of HEXIM1, CDK9 and RNA Pol II chromatin binding in human A375 melanoma cells treated with either DMSO or 25 μM A771726 for 48 hrs.
 
Contributor(s) Tan JL, Yang S, Fan ZP, Zhou Y, Young RA, Zon LI
Citation(s) 27058786
Submission date Apr 20, 2015
Last update date May 15, 2019
Contact name Leonard Zon
E-mail(s) zon@enders.tch.harvard.edu
Organization name Boston Children's Hospital
Department Oncology/Hematology
Street address 1 Blackfan Circle
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (8)
GSM1661784 Input ChIP on DMSO-treated cells-2
GSM1661785 Input ChIP on A771726-treated cells-2
GSM1661786 CDK9 ChIP on DMSO-treated cells.
This SubSeries is part of SuperSeries:
GSE68053 Nucleotide stress induction of HEXIM1 suppresses melanoma by modulating cancer cell-specific gene transcription
Relations
BioProject PRJNA281627
SRA SRP057456

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Supplementary file Size Download File type/resource
GSE68052_CDK9_A771.MACS2_in_Galaxy_treat_pileup.bedgraph.gz 129.0 Mb (ftp)(http) BEDGRAPH
GSE68052_CDK9_DMSO.MACS2_in_Galaxy_treat_pileup.bedgraph.gz 138.2 Mb (ftp)(http) BEDGRAPH
GSE68052_HEXIM1_A771.MACS2_in_Galaxy_treat_pileup.bedgraph.gz 141.1 Mb (ftp)(http) BEDGRAPH
GSE68052_HEXIM1_DMSO.MACS2_in_Galaxy_treat_pileup.bedgraph.gz 161.0 Mb (ftp)(http) BEDGRAPH
GSE68052_PolII_A771.MACS2_in_Galaxy_treat_pileup.bedgraph.gz 183.5 Mb (ftp)(http) BEDGRAPH
GSE68052_PolII_DMSO.MACS2_in_Galaxy_treat_pileup.bedgraph.gz 156.7 Mb (ftp)(http) BEDGRAPH
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Processed data are available on Series record

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