======= USP10 ======= == Gene Information == * **Official Symbol**: USP10 * **Official Name**: ubiquitin specific peptidase 10 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=9100|9100]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q14694|Q14694]] * **Interactions**: [[https://thebiogrid.org/search.php?search=USP10&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20USP10|Open PubMed]] * **OMIM**: [[https://omim.org/entry/609818|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Hydrolase that can remove conjugated ubiquitin from target proteins such as p53/TP53, BECN1, SNX3 and CFTR. Acts as an essential regulator of p53/TP53 stability: in unstressed cells, specifically deubiquitinates p53/TP53 in the cytoplasm, leading to counteract MDM2 action and stabilize p53/TP53. Following DNA damage, translocates to the nucleus and deubiquitinates p53/TP53, leading to regulate the p53/TP53-dependent DNA damage response. Component of a regulatory loop that controls autophagy and p53/TP53 levels: mediates deubiquitination of BECN1, a key regulator of autophagy, leading to stabilize the PIK3C3/VPS34- containing complexes. In turn, PIK3C3/VPS34-containing complexes regulate USP10 stability, suggesting the existence of a regulatory system by which PIK3C3/VPS34-containing complexes regulate p53/TP53 protein levels via USP10 and USP13. Does not deubiquitinate MDM2. Deubiquitinates CFTR in early endosomes, enhancing its endocytic recycling. Involved in a TANK-dependent negative feedback response to attenuate NF-kappaB activation via deubiquitinating IKBKG or TRAF6 in response to interleukin-1-beta (IL1B) stimulation or upon DNA damage (PubMed:25861989). Deubiquitinates TBX21 leading to its stabilization (PubMed:24845384). {ECO:0000269|PubMed:11439350, ECO:0000269|PubMed:18632802, ECO:0000269|PubMed:19398555, ECO:0000269|PubMed:20096447, ECO:0000269|PubMed:21962518, ECO:0000269|PubMed:24845384, ECO:0000269|PubMed:25861989}. |UCH| |translesion synthesis| |negative regulation of I-kappaB kinase/NF-kappaB signaling| |DNA synthesis involved in DNA repair| |postreplication repair| |thiol-dependent ubiquitinyl hydrolase activity| |p53 binding| |DNA damage response, signal transduction by p53 class mediator| |cysteine-type endopeptidase activity| |signal transduction in response to DNA damage| |thiol-dependent ubiquitin-specific protease activity| |DNA biosynthetic process| |signal transduction by p53 class mediator| |ion channel binding| |cellular response to interleukin-1| |response to interleukin-1| |regulation of I-kappaB kinase/NF-kappaB signaling| |early endosome| |autophagy| |process utilizing autophagic mechanism| |protein deubiquitination| |protein modification by small protein removal| |regulation of autophagy| |negative regulation of intracellular signal transduction| |DNA repair| |ubiquitin-dependent protein catabolic process| |modification-dependent protein catabolic process| |modification-dependent macromolecule catabolic process| |proteolysis involved in cellular protein catabolic process| |protein-containing complex| |cellular protein catabolic process| |protein catabolic process| |DNA metabolic process| |cellular response to DNA damage stimulus| |regulation of cellular catabolic process| |cellular macromolecule catabolic process| |protein modification by small protein conjugation or removal| |regulation of catabolic process| |cellular response to cytokine stimulus| |macromolecule catabolic process| |organonitrogen compound catabolic process| |nucleobase-containing compound biosynthetic process| |response to cytokine| |heterocycle biosynthetic process| |aromatic compound biosynthetic process| |negative regulation of signal transduction| |proteolysis| |organic cyclic compound biosynthetic process| |negative regulation of cell communication| |negative regulation of signaling| |RNA binding| |negative regulation of response to stimulus| |cellular nitrogen compound biosynthetic process| |intracellular signal transduction| |cellular response to stress| |cellular macromolecule biosynthetic process| |macromolecule biosynthetic process| |organic substance catabolic process| |cellular catabolic process| |regulation of intracellular signal transduction| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp6|Bortezomib 0.005μM R00 exp6]]|-2.5| |[[:results:exp501|Methotrexate 0.01μM R08 exp501]]|-2.48| |[[:results:exp335|Aminopterin 0.005μM R07 exp335]]|-1.95| |[[:results:exp164|Q15 1 to 2μM on day4 R04 exp164]]|1.72| |[[:results:exp216|Erlotinib 10μM R05 exp216]]|1.78| |[[:results:exp198|Etoposide 0.1μM R05 exp198]]|1.79| |[[:results:exp434|Vemurafenib 6.6μM R08 exp434]]|1.93| |[[:results:exp189|Temozolomide 200μM R04 exp189]]|2.07| |[[:results:exp35|TRAIL 5ng/ml R00 exp35]]|2.15| |[[:results:exp211|AICAR 240μM R05 exp211]]|2.25| |[[:results:exp485|GSK626616 14μM R08 exp485]]|2.42| |[[:results:exp36|TRAIL 50ng/ml R00 exp36]]|2.69| 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|0/28| |blood|0/28| |bone|0/26| |breast|1/33| |central nervous system|1/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|1/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |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|2/29| |uterus|1/5| == Essentiality in NALM6 == * **Essentiality Rank**: 9723 * **Expression level (log2 read counts)**: 7.07 {{:chemogenomics:nalm6 dist.png?nolink |}}