SCUBA

POLD4 — DNA polymerase delta 4, accessory subunit

POLD4 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.

POLD4's module in each cell type

Cell typeModuleShares the module with
Gamma-delta T cellsComplex I Assembly
Mitochondrial & OxPhos
AKR7A2, AP2S1, BLOC1S1, DCTN2, HSD17B10, LAMTOR2, MGMT, MRPL34 +13 more
Innate lymphoid cellsSeptin Cytoskeleton
Cytoskeleton & motility
ATP6V0C, C17orf49, CIAO2A, COX16, DARS1, DDOST, GET3, H2AC6 +18 moreView in SCUBA
MacrophagesAntimicrobial Oxidative Defense
Antibacterial
ADAMDEC1, ALDOA, APOL3, CALHM6, CLEC10A, COX16, CPVL, DEFA5 +30 moreView in SCUBA
Mucosal-associated invariant T cellER & Mitochondrial Assembly
Protein processing & ER
ANAPC11, ARRDC1, ATP5MC1, COA3, CSTB, DECR1, GSTK1, HINT2 +9 more
Natural Killer cellsSeptin Cytoskeletal Assembly
Cytoskeleton & motility
ALDOA, EEF1G, MIF, NME2, PLAAT3, SEPTIN1, SEPTIN2, SEPTIN6View in SCUBA

About the gene

Synonymsp12, POLDS
Chromosome11: 67350772-67356972
Predicted locationIntracellular
Essential geneNo
Protein classMetabolic proteins, Predicted intracellular proteins
Biological processDNA damage, DNA excision, DNA repair, DNA replication

Function

As a component of the tetrameric DNA polymerase delta complex (Pol-delta4), plays a role in high fidelity genome replication and repair. Within this complex, increases the rate of DNA synthesis and decreases fidelity by regulating POLD1 polymerase and proofreading 3' to 5' exonuclease activity. Pol-delta4 participates in Okazaki fragment processing, through both the short flap pathway, as well as a nick translation system. Under conditions of DNA replication stress, required for the repair of broken replication forks through break-induced replication (BIR), a mechanism that may induce segmental genomic duplications of up to 200 kb. Involved in Pol-delta4 translesion synthesis (TLS) of templates carrying O6-methylguanine or abasic sites. Its degradation in response to DNA damage is required for the inhibition of fork progression and cell survival.

Human Protein Atlas · Open Targets · UniProt

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