======= 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 |}}