======= POLQ ======= == Gene Information == * **Official Symbol**: POLQ * **Official Name**: DNA polymerase theta * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=10721|10721]] * **UniProt**: [[https://www.uniprot.org/uniprot/O75417|O75417]] * **Interactions**: [[https://thebiogrid.org/search.php?search=POLQ&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20POLQ|Open PubMed]] * **OMIM**: [[https://omim.org/entry/604419|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: DNA polymerase that promotes microhomology-mediated end- joining (MMEJ), an alternative non-homologous end-joining (NHEJ) machinery triggered in response to double-strand breaks in DNA (PubMed:25642963, PubMed:25643323). MMEJ is an error-prone repair pathway that produces deletions of sequences from the strand being repaired and promotes genomic rearrangements, such as telomere fusions, some of them leading to cellular transformation (PubMed:25642963, PubMed:25643323). POLQ acts as an inhibitor of homology-recombination repair (HR) pathway by limiting RAD51 accumulation at resected ends (PubMed:25642963). POLQ-mediated MMEJ may be required to promote the survival of cells with a compromised HR repair pathway, thereby preventing genomic havoc by resolving unrepaired lesions (By similarity). The polymerase acts by binding directly the 2 ends of resected double-strand breaks, allowing microhomologous sequences in the overhangs to form base pairs. It then extends each strand from the base-paired region using the opposing overhang as a template. Requires partially resected DNA containing 2 to 6 base pairs of microhomology to perform MMEJ (PubMed:25643323). The polymerase activity is highly promiscuous: unlike most polymerases, promotes extension of ssDNA and partial ssDNA (pssDNA) substrates (PubMed:18503084, PubMed:21050863, PubMed:22135286). Also exhibits low-fidelity DNA synthesis, translesion synthesis and lyase activity, and it is implicated in interstrand-cross-link repair, base excision repair and DNA end-joining (PubMed:14576298, PubMed:18503084, PubMed:19188258, PubMed:24648516). Involved in somatic hypermutation of immunoglobulin genes, a process that requires the activity of DNA polymerases to ultimately introduce mutations at both A/T and C/G base pairs (By similarity). {ECO:0000250|UniProtKB:Q8CGS6, ECO:0000269|PubMed:14576298, ECO:0000269|PubMed:18503084, ECO:0000269|PubMed:19188258, ECO:0000269|PubMed:21050863, ECO:0000269|PubMed:22135286, ECO:0000269|PubMed:24648516, ECO:0000269|PubMed:25642963, ECO:0000269|PubMed:25643323}. |Helicase C| |DNA pol A| |DEAD| |double-strand break repair via alternative nonhomologous end joining| |5-deoxyribose-5-phosphate lyase activity| |single-stranded DNA helicase activity| |somatic hypermutation of immunoglobulin genes| |negative regulation of double-strand break repair via homologous recombination| |somatic diversification of immune receptors via somatic mutation| |DNA-directed DNA polymerase activity| |negative regulation of double-strand break repair| |negative regulation of DNA repair| |somatic diversification of immunoglobulins| |base-excision repair| |negative regulation of DNA recombination| |regulation of double-strand break repair via homologous recombination| |somatic diversification of immune receptors| |damaged DNA binding| |double-strand break repair via nonhomologous end joining| |non-recombinational repair| |regulation of double-strand break repair| |negative regulation of response to DNA damage stimulus| |double-strand break repair via homologous recombination| |recombinational repair| |regulation of DNA recombination| |DNA biosynthetic process| |DNA duplex unwinding| |DNA geometric change| |DNA-dependent DNA replication| |negative regulation of DNA metabolic process| |chromosome| |regulation of DNA repair| |immunoglobulin production| |production of molecular mediator of immune response| |double-strand break repair| |DNA replication| |regulation of response to DNA damage stimulus| |DNA recombination| |DNA conformation change| |protein homooligomerization| |regulation of DNA metabolic process| |chromatin binding| |DNA repair| |protein complex oligomerization| |immune system development| |regulation of cellular response to stress| |DNA metabolic process| |cellular response to DNA damage stimulus| |chromosome organization| |nucleobase-containing compound biosynthetic process| |heterocycle biosynthetic process| |aromatic compound biosynthetic process| |organic cyclic compound biosynthetic process| |negative regulation of nucleobase-containing compound metabolic process| |regulation of response to stress| |ATP binding| |protein-containing complex assembly| |negative regulation of response to stimulus| |cellular nitrogen compound biosynthetic process| |cellular response to stress| |cellular macromolecule biosynthetic process| |macromolecule biosynthetic process| |protein-containing complex subunit organization| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp294|Nutlin-3A 1.6μM R06 exp294]]|-2.89| |[[:results:exp360|Genistein 15μM R07 exp360]]|-1.74| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 7/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|1/28| |blood|1/28| |bone|0/26| |breast|1/33| |central nervous system|0/56| |cervix|0/4| |colorectal|1/17| |esophagus|0/13| |fibroblast|0/1| |gastric|1/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|1/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 6059 * **Expression level (log2 read counts)**: 7.26 {{:chemogenomics:nalm6 dist.png?nolink |}}