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The TRC8 Ubiquitin Ligase Is Sterol Regulated and Interacts with Lipid and Protein Biosynthetic Pathways
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Abstract
TRC8/RNF139 encodes an endoplasmic reticulum–resident E3 ubiquitin ligase that inhibits growth in a RING- and ubiquitylation-dependent manner. TRC8 also contains a predicted sterol-sensing domain. Here, we report that TRC8 protein levels are sterol responsive and that it binds and stimulates ubiquitylation of the endoplasmic reticulum anchor protein INSIG. Induction of TRC8 destabilized the precursor forms of the transcription factors SREBP-1 and SREBP-2. Loss of SREBP precursors was proteasome dependent, required a functional RING domain, occurred without generating processed nuclear forms, and suppressed SREBP target genes. TRC8 knockdown had opposite effects in sterol-deprived cells. In Drosophila, growth inhibition by DTrc8 was genetically suppressed by loss of specific Mprlp, Padlp N-terminal domain–containing proteins found in the COP9 signalosome and eIF3. DTrc8 genetically and physically interacted with two eIF3 subunits: eIF3f and eIF3h. Coimmunoprecipitation experiments confirmed these interactions in mammalian cells, and TRC8 overexpression suppressed polysome profiles. Moreover, high–molecular weight ubiquitylated proteins were observed in eIF3 immunoprecipitations from TRC8-overexpressing cells. Thus, TRC8 function may provide a regulatory link between the lipid and protein biosynthetic pathways. Mol Cancer Res; 8(1); 93–106
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Effects of GP78 and TRC8 are consistent with previous reports that they target INSIGs and HMG-CoA reductase for degradation.
“These effects of GP78 and TRC8 are consistent with previous reports that they target INSIGs and HMG-CoA reductase for degradation.”
From Inhibition of cholesterol biosynthesis through RNF145-dependent ubiquitination of SCAP (2017) · cites this paper as Lee et al., 2010
Analysis of domain structure suggests RNF145 may harbor a sterol-sensing domain, like TRC8.
“analysis of domain structure of RNF145 suggests the protein, like TRC8, may harbor a sterol-sensing domain (Lee et al., 2010).”
From Inhibition of cholesterol biosynthesis through RNF145-dependent ubiquitination of SCAP (2017) · cites this paper as Lee et al., 2010
TRC8 reduces stability of SREBP and inhibits SREBP processing in cultured cells.
“TRC8 was reported to reduce the stability of SREBP, and to inhibit SREBP processing in cultured cells (Irisawa et al., 2009; Lee et al., 2010).”
From Inhibition of cholesterol biosynthesis through RNF145-dependent ubiquitination of SCAP (2017) · cites this paper as Lee et al., 2010
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SREBPs: activators of the complete program of cholesterol and fatty acid synthesis in the liver
Horton, J. D., Goldstein, J. L., & Brown, M. S. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0215593 · Cited by 4,092
The Multiple Leiomyoma Consortium (2002) · Nature Genetics · doi:10.1038/ng849 · Cited by 1,635
Isaacs, J. S., Jung, Y. J., Mole, D. R., Lee, S., Torres-Cabala, C., Chung, Y.-L., Merino, M., Trepel, J., Zbar, B., Toro, J., et al. (2005) · Cancer Cell · doi:10.1016/j.ccr.2005.06.017 · Cited by 958
Vanharanta, S., Buchta, M., McWhinney, S. R., Virta, S. K., Peçzkowska, M., Morrison, C. D., Lehtonen, R., Januszewicz, A., Järvinen, H., Juhola, M., et al. (2004) · The American Journal of Human Genetics · doi:10.1086/381054 · Cited by 389
Flagged first, then by citations
Research works printed but not linked: 50
- Jemal, 2006, Cancer statistics, 2006, CA Cancer J Clin, 56, 106, 10.3322/canjclin.56.2.106 · DOI
- Kaelin, 2005, The von Hippel-Lindau protein, HIF hydroxylation, and oxygen sensing, Biochem Biophys Res Commun, 338, 627, 10.1016/j.bbrc.2005.08.165 · DOI
- Hughes, 2007, HIF-2α downregulation in the absence of functional VHL is not sufficient for renal cell differentiation, Cancer Cell Int, 7, 13, 10.1186/1475-2867-7-13 · DOI
- Mandriota, 2002, HIF activation identifies early lesions in VHL kidneys: evidence for site-specific tumor suppressor function in the nephron, Cancer Cell, 1, 459, 10.1016/S1535-6108(02)00071-5 · DOI · Paper page
- Schmidt, 1997, Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas, Nature Genet, 16, 68, 10.1038/ng0597-68 · DOI
- Bjornsson, 1996, Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features, Am J Pathol, 149, 1201
- Inoki, 2003, TSC2 mediates cellular energy response to control cell growth and survival, Cell, 115, 577, 10.1016/S0092-8674(03)00929-2 · DOI · Paper page
- Baba, 2006, Folliculin encoded by the BHD gene interacts with a binding protein, FNIP1, and AMPK, and is involved in AMPK and mTOR signaling, Proc Natl Acad Sci U S A, 103, 15552, 10.1073/pnas.0603781103 · DOI
- Siridechadilok, 2005, Structural roles for human translation factor eIF3 in initiation of protein synthesis, Science, 310, 1513, 10.1126/science.1118977 · DOI
- Cohen, 1979, Hereditary renal-cell carcinoma associated with a chromosomal translocation, N Engl J Med, 301, 592, 10.1056/NEJM197909133011107 · DOI
- Li, 1993, Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinoma, Ann Intern Med, 118, 106, 10.7326/0003-4819-118-2-199301150-00005 · DOI
- Gemmill, 1998, The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8, Proc Natl Acad Sci U S A, 95, 9572, 10.1073/pnas.95.16.9572 · DOI
- Poland, 2007, A constitutional balanced t(3;8)(p14;q24.1) translocation results in disruption of the TRC8 gene and predisposition to clear cell renal cell carcinoma, Genes Chromosomes Cancer, 46, 805, 10.1002/gcc.20466 · DOI
- Gemmill, 2002, The TRC8 hereditary kidney cancer gene suppresses growth and functions with VHL in a common pathway, Oncogene, 21, 3507, 10.1038/sj.onc.1205437 · DOI
- Lorick, 1999, RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination, Proc Natl Acad Sci U S A, 96, 11364, 10.1073/pnas.96.20.11364 · DOI
- Brauweiler, 2007, RING-dependent tumor suppression and G2/M arrest induced by the TRC8 hereditary kidney cancer gene, Oncogene, 26, 2263, 10.1038/sj.onc.1210017 · DOI
- Stagg, 2009, The TRC8 E3 ligase ubiquitinates MHC class I molecules before dislocation from the ER, J Cell Biol, 186, 685, 10.1083/jcb.200906110 · DOI
- Gemmill, 2005, Growth suppression induced by the TRC8 hereditary kidney cancer gene is dependent upon JAB1/CSN5, Oncogene, 24, 3503, 10.1038/sj.onc.1208509 · DOI
- Cope, 2002, Role of predicted metalloprotease motif of Jab1/Csn5 in cleavage of Nedd8 from Cul1, Science, 298, 608, 10.1126/science.1075901 · DOI
- Maytal-Kivity, 2002, MPN+, a putative catalytic motif found in a subset of MPN domain proteins from eukaryotes and prokaryotes, is critical for Rpn11 function, BMC Biochem, 3, 28, 10.1186/1471-2091-3-28 · DOI
- Gebhard, 1987, Abnormal cholesterol metabolism in renal clear cell carcinoma, J Lipid Res, 28, 1177, 10.1016/S0022-2275(20)38606-5 · DOI
- Clayman, 1986, Renal cell carcinoma in the Wistar-Lewis rat: a model for studying the mechanisms of cholesterol acquisition by a tumor in vivo, Cancer Res, 46, 2958
- Tosi, 2005, Cholesteryl esters in malignancy, Clin Chim Acta, 359, 27, 10.1016/j.cccn.2005.04.003 · DOI
- Goldstein, 2006, Protein sensors for membrane sterols, Cell, 124, 35, 10.1016/j.cell.2005.12.022 · DOI · Paper page
- Song, 2005, Gp78, a membrane-anchored ubiquitin ligase, associates with Insig-1 and couples sterol-regulated ubiquitination to degradation of HMG CoA reductase, Mol Cell, 19, 829, 10.1016/j.molcel.2005.08.009 · DOI · Paper page
- Sever, 2003, Accelerated degradation of HMG CoA reductase mediated by binding of insig-1 to its sterol-sensing domain, Mol Cell, 11, 25, 10.1016/S1097-2765(02)00822-5 · DOI
- Epand, 2006, Cholesterol and the interaction of proteins with membrane domains, Progress Lipid Res, 45, 279, 10.1016/j.plipres.2006.02.001 · DOI
- Horton, 2003, Combined analysis of oligonucleotide microarray data from transgenic and knockout mice identifies direct SREBP target genes, Proc Natl Acad Sci U S A, 100, 12027, 10.1073/pnas.1534923100 · DOI · Paper page
- Hughes, 2005, SREBP pathway responds to sterols and functions as an oxygen sensor in fission yeast, Cell, 120, 831, 10.1016/j.cell.2005.01.012 · DOI · Paper page
- Abdulrahman, 2006, Identification of novel VHL targets that are associated with the development of renal cell carcinoma, Oncogene, 26, 1661, 10.1038/sj.onc.1209932 · DOI
- Goldstein, 1983, Receptor-mediated endocytosis of low-density lipoprotein in cultured cells, Methods Enzymol, 98, 241, 10.1016/0076-6879(83)98152-1 · DOI
- Sakai, 1997, Identification of complexes between the COOH-terminal domains of sterol regulatory element-binding proteins (SREBPs) and SREBP cleavage-activating protein, J Biol Chem, 272, 20213, 10.1074/jbc.272.32.20213 · DOI · Paper page
- Feramisco, 2005, Intramembrane aspartic acid in SCAP protein governs cholesterol-induced conformational change, Proc Natl Acad Sci U S A, 102, 3242, 10.1073/pnas.0500206102 · DOI
- Roche, 2004, Hox expression in AML identifies a distinct subset of patients with intermediate cytogenetics, Leukemia, 18, 1059, 10.1038/sj.leu.2403366 · DOI
- Drabkin, 2002, Quantitative HOX expression in chromosomally defined subsets of acute myelogenous leukemia, Leukemia, 16, 186, 10.1038/sj.leu.2402354 · DOI
- Vandesompele, 2002, Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes, Genome Biol, 3, 1, 10.1186/gb-2002-3-7-research0034 · DOI · Paper page
- Johannes, 1998, Cap-independent polysomal association of natural mRNAs encoding c-myc, BiP, and eIF4G conferred by internal ribosome entry sites, RNA, 4, 1500, 10.1017/S1355838298981080 · DOI
- Yabe, 2002, Insig-2, a second endoplasmic reticulum protein that binds SCAP and blocks export of sterol regulatory element-binding proteins, Proc Natl Acad Sci U S A, 99, 12753, 10.1073/pnas.162488899 · DOI · Paper page
- Yang, 2002, Crucial step in cholesterol homeostasis: sterols promote binding of SCAP to INSIG-1, a membrane protein that facilitates retention of SREBPs in ER, Cell, 110, 489, 10.1016/S0092-8674(02)00872-3 · DOI · Paper page
- Chang, 2006, Cholesterol sensing, trafficking, and esterification, Ann Rev Cell Dev Biol, 22, 129, 10.1146/annurev.cellbio.22.010305.104656 · DOI
- Gong, 2006, Sterol-regulated ubiquitination and degradation of Insig-1 creates a convergent mechanism for feedback control of cholesterol synthesis and uptake, Cell Metabolism, 3, 15, 10.1016/j.cmet.2005.11.014 · DOI · Paper page
- Lee, 2006, Sterol-regulated degradation of Insig-1 mediated by the membrane-bound ubiquitin ligase gp78, J Biol Chem, 281, 39308, 10.1074/jbc.M608999200 · DOI
- Nohturfft, 1998, Sterols regulate processing of carbohydrate chains of wild-type SREBP cleavage-activating protein (SCAP), but not sterol-resistant mutants Y298C or D443N, Proc Natl Acad Sci U S A, 95, 12848, 10.1073/pnas.95.22.12848 · DOI
- Marygold, 2007, The ribosomal protein genes and Minute loci of Drosophila melanogaster, Genome Biol, 8, R216, 10.1186/gb-2007-8-10-r216 · DOI · Paper page
- Zhou, 2008, Special Feature: Mass spectrometry reveals modularity and a complete subunit interaction map of the eukaryotic translation factor eIF3, Proc Natl Acad Sci U S A, 105, 18139, 10.1073/pnas.0801313105 · DOI
- Beg, 1979, Characterization and regulation of reductase kinase, a protein kinase that modulates the enzymic activity of 3-hydroxy-3-methylglutaryl-coenzyme A reductase, Proc Natl Acad Sci U S A, 76, 4375, 10.1073/pnas.76.9.4375 · DOI
- Carling, 1989, Purification and characterization of the AMP-activated protein kinase. Copurification of acetyl-CoA carboxylase kinase and 3-hydroxy-3-methylglutaryl-CoA reductase kinase activities, Eur J Biochem, 186, 129, 10.1111/j.1432-1033.1989.tb15186.x · DOI
- Hardie, 2007, AMP-activated/SNF1 protein kinases: conserved guardians of cellular energy, Nat Rev Mol Cell Biol, 8, 774, 10.1038/nrm2249 · DOI
- Menendez, 2007, Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis, Nat Rev Cancer, 7, 763, 10.1038/nrc2222 · DOI · Paper page
- Meyer, 1982, Immunochemical characterization of mammalian protein synthesis initiation factors, Biochemistry, 21, 4206, 10.1021/bi00261a003 · DOI
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Inhibition of cholesterol biosynthesis through RNF145-dependent ubiquitination of SCAP
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Metadata
- Authors
- Lee, J. P., Brauweiler, A., Rudolph, M., Hooper, J. E., Drabkin, H. A., & Gemmill, R. M.
- Affiliations
- Authors' Affiliations: 1Division of Hematology/Oncology, Department of Medicine and Hollings Cancer Center, Medical University of South Carolina, Charleston, South Carolina and Departments of 2Medical Oncology, 3Physiology and Biophysics, and 4Cell and Developmental Biology, University of Colorado at Denver and Health Science Center, Aurora, Colorado
- Venue
- Molecular Cancer Research
- Published
- 2010-01-17
- Volume
- 8
- Issue
- 1
- Pages
- 93-106
- ISSN
- 1541-7786
- 1557-3125
- PMC
- PMC3086825
- Cited by
- 76
- References
- 4
- Language
- en
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