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Series GSE266972 Query DataSets for GSE266972
Status Public on May 13, 2024
Title Ubiquitylation of Pol II controls early stages of the transcription cycle [ChIP-seq]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Control of RNA Polymerase II (Pol II) through ubiquitylation is essential for the DNA-damage response. Here we reveal a distinct ubiquitylation pathway in human cells that targets excessive and defective Pol II molecules at the initial stages of the transcription cycle. This pathway, mediated by ARMC5CUL3 ubiquitin ligase, drives homeostatic Pol II turnover, and is further enhanced when early stages of transcription - initiation and pausing - are perturbed. Upon ARMC5 loss, Pol II accumulates in the free pool and in the promoter-proximal zone, but is not permitted into elongation. We identify Integrator subunit 8 (INTS8) as a gatekeeper preventing the release of excess Pol II molecules into gene bodies. Combined loss of ARMC5 and INTS8 has strong detrimental effects on cell growth, with ARMC5 loss exacerbating transcriptional defects seen in INTS8-depleted cells. These findings uncover that ARMC5CUL3 and INTS8 form a collaborative checkpoint, monitoring the quantity and quality of transcription complexes before they are licensed into elongation.
 
Overall design We aimed to study how ARMC5 loss affects Pol II occupancy on chromatin and how is a partial resistance to XBP inhibition by triptolide achieved in ARMC5 KO cells in HEK293 Trex flp In background. We treated WT and ARMC5 KO cells with triptolide at 300 nM for 2 h. We then performed double cross-linking, first we incubated the washed cells with disuccinimidyl glutarate (DSG) for 15 minutes, followed by washing and incubation with formaldehyde. Immunoprecipitation was performed against total Pol II (D8L4Y Antibody) and Serine 5 phosphorylated Pol II (3E8 Antibody).
 
Contributor(s) Zeller A, Shlamovitz I, Vidaković AT
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Submission date May 07, 2024
Last update date May 13, 2024
Contact name Ana Tufegdzic Vidakovic
E-mail(s) atv@mrc-lmb.cam.ac.uk
Organization name MRC-LMB
Street address Cambridge Biomedical Campus, Francis Crick Ave
City Cambridge
State/province Cambridge
ZIP/Postal code CB2 0QH
Country United Kingdom
 
Platforms (1)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (36)
GSM8257580 Input_ARMC5_KO_TPL_rep1
GSM8257581 Input_ARMC5_KO_TPL_rep2
GSM8257582 Input_ARMC5_KO_TPL_rep3
This SubSeries is part of SuperSeries:
GSE266979 Ubiquitylation of Pol II controls early stages of the transcription cycle.
Relations
BioProject PRJNA1108872

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Supplementary file Size Download File type/resource
GSE266972_RAW.tar 6.7 Gb (http)(custom) TAR (of BW)
SRA Run SelectorHelp
Raw data are available in SRA

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