<<< Full experiment listing

PXD016586-1

PXD016586 is an original dataset announced via ProteomeXchange.

Dataset Summary
TitleHigh mobility group protein-mediated transcription requires DNA damage marker γ-H2AX
DescriptionThe eukaryotic genome is organized into chromatins, the physiological template for DNA-dependent processes including replication, recombination, repair, and transcription. Chromatin-mediated transcription regulation involves DNA methylation, chromatin remodeling, and histone modifications. However, chromatin also contains non-histone chromatin-associated proteins, of which the high-mobility group (HMG) proteins are the most abundant. Although it is known that HMG proteins induce structural changes of chromatin, the processes underlying transcription regulation by HMG proteins are poorly understood. Here we decipher the molecular mechanism of transcription regulation mediated by the HMG AT-hook 2 protein (HMGA2). We combined proteomic, ChIP-seq, and transcriptome data to show that HMGA2-induced transcription requires phosphorylation of the histone variant H2AX at S139 (H2AXS139ph; γ-H2AX) mediated by the protein kinase ataxia telangiectasia mutated (ATM). Furthermore, we demonstrate the biological relevance of this mechanism within the context of TGFβ1 signaling. The interplay between HMGA2, ATM, and H2AX is a novel mechanism of transcription initiation. Our results link H2AXS139ph to transcription, assigning a new function for this DNA damage marker. Controlled chromatin opening during transcription may involve intermediates with DNA breaks that may require mechanisms that ensure the integrity of the genome.
HostingRepositoryPRIDE
AnnounceDate2020-12-15
AnnouncementXMLSubmission_2020-12-15_00:06:37.xml
DigitalObjectIdentifier
ReviewLevelPeer-reviewed dataset
DatasetOriginOriginal dataset
RepositorySupportUnsupported dataset by repository
PrimarySubmitterGuillermo Barreto
SpeciesList scientific name: Mus musculus (Mouse); NCBI TaxID: 10090;
ModificationListmonohydroxylated residue; acetylated residue; iodoacetamide derivatized residue
InstrumentQ Exactive
Dataset History
RevisionDatetimeStatusChangeLog Entry
02019-12-04 03:54:31ID requested
12020-12-15 00:06:37announced
22021-04-06 02:15:34announced2021-04-06: Updated publication reference for PubMed record(s): 33594057.
32024-10-22 05:16:43announced2024-10-22: Updated project metadata.
Publication List
Dataset with its publication pending
Keyword List
curator keyword: Biological
submitter keyword: HMGA2, FACT, H2A.X, R-Loops, DNA demethylation, TGFB1
Contact List
Guillermo Barreto
contact affiliationLung Cancer Epigenetics Research Group Max Planck Institute for Heart and Lung Research
contact emailguillermo.barreto@mpi-bn.mpg.de
lab head
Guillermo Barreto
contact affiliationMax-Planck-Institute for Heart and Lung Research
contact emailguillermo.barreto@mpi-bn.mpg.de
dataset submitter
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2020/12/PXD016586
PRIDE project URI
Repository Record List
[ + ]