[1] DaRosa PA, Wang Z, Jiang X, et al. Allosteric activation of the RNF146 ubiquitin ligase by a poly(ADP-ribosyl)ation signal[J]. Nature, 2014, doi:10.1038/nature13826.[Epud ahead of print].
[2] Matsumura Y, Sakai J, Skach WR. Endoplasmic reticulum protein quality control is determined by cooperative interactions between Hsp/c70 protein and the CHIP E3 ligase[J]. J Biol Chem, 2013, 288(43):31069-31079.
[3] Ballinger CA, Connell P, Wu Y, et al. Identification of CHIP, a novel tetratricopeptide repeat-containing protein that interacts with heat shock proteins and negatively regulates chaperone functions[J]. Mol Cell Biol, 1999, 19(6):4535-4545.
[4] Rosser MF, Washburn E, Muchowski PJ, et al.Chaperone functions of the E3 ubiquitin ligase CHIP[J]. J Biol Chem,2007, 282(31):22267-22277.
[5] Zhu X, Zhang J, Sun H, et al. Ubiquitination of Inositol-requiring Enzyme 1 (IRE1) by the E3 Ligase CHIP Mediates the IRE1/TRAF2/JNK Pathway [J]. J Biol Chem, 2014, 289(44):30567-30577.
[6] Hirayama S, Yamazaki Y, Kitamura A, et al. MKKS is a centrosome-shuttling protein degraded by disease-causing mutations via CHIP-mediated ubiquitination[J]. Mol Biol Cell, 2008, 19(3):899-911.
[7] Tsvetkov P, Adamovich Y, Elliott E, et al. E3 ligase STUB1/CHIP regulates NAD(P)H: quinoneoxidoreductase 1 (NQO1) accumulation in aged brain, a process impaired in certain Alzheimer disease patients [J]. J Biol Chem, 2011, 286(11):8839-8845.
[8] Synofzik M, Schule R, Schulze M, et al. Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts[J]. Orphanet J Rare Dis, 2014, 9:57.
[9] Xie P, Fan Y, Zhang H, et al. CHIP represses myocardin-induced smooth muscle cell differentiation via ubiquitin-mediated proteasomal degradation[J]. Mol Cell Biol, 2009, 29(9):2398-2408.
[10] Li X, Huang M, Zheng H, et al. CHIP promotes Runx2 degradation and negatively regulates osteoblast differentiation[J]. J Cell Biol, 2008, 181(6):959-972.
[11] Li S, Shu B, Zhang Y, et al. Carboxyl terminus of Hsp70-interacting protein regulation of osteoclast formation in mice through promotion of tumor necrosis factor receptor-associated factor 6 protein degradation[J]. Arthritis Rheumatol, 2014, 66(7):1854-1863.
[12] Loffek S, Woll S, Hohfeld J, et al. The ubiquitin ligase CHIP/STUB1 targets mutant keratins for degradation[J]. Hum Mutat, 2010, 31(4):466-476.
[13] Sun C, Li HL, Shi ML, et al. Diverse roles of C-terminal Hsp70-interacting protein (CHIP) in tumorigenesis[J]. J Cancer Res Clin Oncol, 2014, 140(2):189-197.
[14] McDonough H, Charles PC, Hilliard EG, et al. Stress-dependent Daxx-CHIP interaction suppresses the p53 apoptotic program[J]. J Biol Chem, 2009, 284(31):20649-20659.
[15] Choi YN, Lee SK, Seo TW, et al. C-Terminus of Hsc70-interacting protein regulates profilin1 and breast cancer cell migration[J]. Biochem Biophys Res Commun, 2014, 446(4):1060-1066.
[16] Tsuchiya M, Nakajima Y, Hirata N, et al. Ubiquitin ligase CHIP suppresses cancer stem cell properties in a population of breast cancer cells[J]. Biochem Biophys Res Commun, 2014,452(4):928-932.
[17] Jan CI, Yu CC, Hung MC, et al. Tid1, CHIP and ErbB2 interactions and their prognostic implications for breast cancer patients[J]. J Pathol, 2011, 225(3):424-437.
[18] Wang Y, Ren F, Wang Y, et al. CHIP/Stub1 functions as a tumor suppressor and represses NF-kappaB-mediated signaling in colorectal cancer[J]. Carcinogenesis, 2014, 35(5):983-991. |