SCUBA

BRD4 — Bromodomain containing 4

BRD4 belongs to a gene co-expression module in 5 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

BRD4's module in each cell type

Cell typeModuleShares the module with
Gamma-delta T cellsGPCR-AKT-MAPK Signaling
TCR Signaling
ADNP, AKT1, ALYREF, B3GALT6, BRI3, BTBD6, CENPB, CLPTM1L +29 more
Innate lymphoid cellsILC3 identity
Differentiation
BHLHE40, CASK, CITED2, GLUL, GNAS, HECA, IGFBP7, IQGAP1 +19 moreView in SCUBA
Lymphatic endothelialBasement Membrane ECM
migration & adhesion
COL4A1, COL4A2, GOLGA4, ITGAV, PITPNB, PXDN, RAI14, RB1CC1 +4 moreView in SCUBA
MacrophagesChromatin Regulatory Genes
Housekeeping
ACAP2, ARID4A, ATRX, BPTF, BRD10, EP300, ERBIN, ETNK1 +31 moreView in SCUBA
Mucosal-associated invariant T cellPI3K MAPK Signaling
TCR Signaling
AKT1, APH1A, CALM2, CMTM3, DAZAP1, GNAS, GRK2, MAP2K2 +11 more

About the gene

SynonymsCAP, HUNK1, HUNKI, MCAP
Chromosome19: 15235519-15332545
Predicted locationIntracellular
Essential geneYes
Protein classCancer-related genes, Disease related genes, Essential proteins, Predicted intracellular proteins
Molecular functionChromatin regulator
Biological processDNA damage, Host-virus interaction, Transcription, Transcription regulation

Function

Chromatin reader protein that recognizes and binds acetylated histones and plays a key role in transmission of epigenetic memory across cell divisions and transcription regulation. Remains associated with acetylated chromatin throughout the entire cell cycle and provides epigenetic memory for postmitotic G1 gene transcription by preserving acetylated chromatin status and maintaining high-order chromatin structure. During interphase, plays a key role in regulating the transcription of signal-inducible genes by associating with the P-TEFb complex and recruiting it to promoters. Also recruits P-TEFb complex to distal enhancers, so called anti-pause enhancers in collaboration with JMJD6. BRD4 and JMJD6 are required to form the transcriptionally active P-TEFb complex by displacing negative regulators such as HEXIM1 and 7SKsnRNA complex from P-TEFb, thereby transforming it into an active form that can then phosphorylate the C-terminal domain (CTD) of RNA polymerase II. Regulates differentiation of naive CD4(+) T-cells into T-helper Th17 by promoting recruitment of P-TEFb to promoters (By similarity). Promotes phosphorylation of 'Ser-2' of the C-terminal domain (CTD) of RNA polymerase II. According to a report, directly acts as an atypical protein kinase and mediates phosphorylation of 'Ser-2' of the C-terminal domain (CTD) of RNA polymerase II; these data however need additional evidences in vivo. In addition to acetylated histones, also recognizes and binds acetylated RELA, leading to further recruitment of the P-TEFb complex and subsequent activation of NF-kappa-B. Also acts as a regulator of p53/TP53-mediated transcription: following phosphorylation by CK2, recruited to p53/TP53 specific target promoters. Acts as a chromatin insulator in the DNA damage response pathway. Inhibits DNA damage response signaling by recruiting the condensin-2 complex to acetylated histones, leading to chromatin structure remodeling, insulating the region from DNA damage response by limiting spreading of histone H2AX/H2A.x phosphorylation

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.