USP7とは? わかりやすく解説

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USP7

出典: フリー百科事典『ウィキペディア(Wikipedia)』 (2021/04/30 15:43 UTC 版)

USP7(Ubiquitin-specific-processing protease)は、ヒトではUSP7遺伝子にコードされる酵素であり、HAUSP(herpesvirus-associated ubiquitin-specific protease)やubiquitin carboxyl-terminal hydrolase 7の名称でも知られる[5][6][7][8]


  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000187555 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000022710 - Ensembl, May 2017
  3. ^ Human PubMed Reference:
  4. ^ Mouse PubMed Reference:
  5. ^ “Human and mouse proteases: a comparative genomic approach”. Nature Reviews. Genetics 4 (7): 544–58. (Jul 2003). doi:10.1038/nrg1111. PMID 12838346. 
  6. ^ “Assignment1 of herpesvirus-associated ubiquitin-specific protease gene HAUSP to human chromosome band 16p13.3 by in situ hybridization”. Cytogenetics and Cell Genetics 83 (1–2): 100. (Mar 1999). doi:10.1159/000015142. PMID 9925944. 
  7. ^ Entrez Gene: USP7 ubiquitin specific peptidase 7 (herpes virus-associated)”. 2021年2月14日閲覧。
  8. ^ “A novel ubiquitin-specific protease is dynamically associated with the PML nuclear domain and binds to a herpesvirus regulatory protein”. The EMBO Journal 16 (7): 1519–30. (Apr 1997). doi:10.1093/emboj/16.7.1519. PMC: 1169756. PMID 9130697. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1169756/. 
  9. ^ “Protein interaction domains of the ubiquitin-specific protease, USP7/HAUSP”. The Journal of Biological Chemistry 278 (48): 47753–61. (Nov 2003). doi:10.1074/jbc.M307200200. PMID 14506283. 
  10. ^ Sherr, C. J.; Weber, J. D. (2000-02). “The ARF/p53 pathway”. Current Opinion in Genetics & Development 10 (1): 94–99. doi:10.1016/s0959-437x(99)00038-6. ISSN 0959-437X. PMID 10679383. https://pubmed.ncbi.nlm.nih.gov/10679383. 
  11. ^ Seavey, S. E.; Holubar, M.; Saucedo, L. J.; Perry, M. E. (1999-09). “The E7 oncoprotein of human papillomavirus type 16 stabilizes p53 through a mechanism independent of p19(ARF)”. Journal of Virology 73 (9): 7590–7598. doi:10.1128/JVI.73.9.7590-7598.1999. ISSN 0022-538X. PMC: PMC104286. PMID 10438849. https://pubmed.ncbi.nlm.nih.gov/10438849. 
  12. ^ Tolbert, Dawn; Lu, Xiangdong; Yin, Chaoying; Tantama, Mathew; Van Dyke, Terry (2002-01). “p19(ARF) is dispensable for oncogenic stress-induced p53-mediated apoptosis and tumor suppression in vivo”. Molecular and Cellular Biology 22 (1): 370–377. doi:10.1128/mcb.22.1.370-377.2002. ISSN 0270-7306. PMC: PMC134227. PMID 11739748. https://pubmed.ncbi.nlm.nih.gov/11739748. 
  13. ^ a b “Deubiquitination of p53 by HAUSP is an important pathway for p53 stabilization”. Nature 416 (6881): 648–53. (Apr 2002). doi:10.1038/nature737. PMID 11923872. 
  14. ^ a b “GMP synthetase stimulates histone H2B deubiquitylation by the epigenetic silencer USP7”. Molecular Cell 17 (5): 695–707. (Mar 2005). doi:10.1016/j.molcel.2005.02.013. PMID 15749019. 
  15. ^ “Biosynthetic enzyme GMP synthetase cooperates with ubiquitin-specific protease 7 in transcriptional regulation of ecdysteroid target genes”. Molecular and Cellular Biology 30 (3): 736–44. (Feb 2010). doi:10.1128/MCB.01121-09. PMC: 2812229. PMID 19995917. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2812229/. 
  16. ^ Meredith, M.; Orr, A.; Everett, R. (1994-05-01). “Herpes simplex virus type 1 immediate-early protein Vmw110 binds strongly and specifically to a 135-kDa cellular protein”. Virology 200 (2): 457–469. doi:10.1006/viro.1994.1209. ISSN 0042-6822. PMID 8178435. https://pubmed.ncbi.nlm.nih.gov/8178435. 
  17. ^ “HAUSP/USP7 as an Epstein-Barr virus target”. Biochemical Society Transactions 32 (Pt 5): 731–2. (Nov 2004). doi:10.1042/BST0320731. PMID 15494000. 
  18. ^ Speck, Samuel H., ed (Oct 2009). “EBNA1-mediated recruitment of a histone H2B deubiquitylating complex to the Epstein-Barr virus latent origin of DNA replication”. PLOS Pathogens 5 (10): e1000624. doi:10.1371/journal.ppat.1000624. PMC: 2757719. PMID 19834552. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2757719/. 
  19. ^ “USP7 Acts as a Molecular Rheostat to Promote WASH-Dependent Endosomal Protein Recycling and Is Mutated in a Human Neurodevelopmental Disorder”. Mol. Cell 59 (6): 956–69. (September 2015). doi:10.1016/j.molcel.2015.07.033. PMC: 4575888. PMID 26365382. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4575888/. 
  20. ^ USP7 Related Diseases”. National Organization for Rare Disorders (NORD). 2021年2月13日閲覧。
  21. ^ a b “Inhibition of USP7 activity selectively eliminates senescent cells in part via restoration of p53 activity”. Aging Cell 19 (3): e13117. (2020). doi:10.1111/acel.13117. PMC: 7059172. PMID 32064756. https://onlinelibrary.wiley.com/doi/full/10.1111/acel.13117. 
  22. ^ “USP7, a ubiquitin-specific protease, interacts with ataxin-1, the SCA1 gene product”. Molecular and Cellular Neurosciences 20 (2): 298–306. (Jun 2002). doi:10.1006/mcne.2002.1103. PMID 12093161. 
  23. ^ “USP7 counteracts SCFbetaTrCP- but not APCCdh1-mediated proteolysis of Claspin”. The Journal of Cell Biology 184 (1): 13–9. (Jan 2009). doi:10.1083/jcb.200807137. PMC: 2615094. PMID 19124652. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615094/. 
  24. ^ “Defining the human deubiquitinating enzyme interaction landscape”. Cell 138 (2): 389–403. (Jul 2009). doi:10.1016/j.cell.2009.04.042. PMC: 2716422. PMID 19615732. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716422/. 
  25. ^ “UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair”. Nature Genetics 44 (5): 598–602. (May 2012). doi:10.1038/ng.2230. PMID 22466611. 





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