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Volumn 16, Issue 5, 2013, Pages 562-570

Identification of NUB1 as a suppressor of mutant Huntingtin toxicity via enhanced protein clearance

Author keywords

[No Author keywords available]

Indexed keywords

BETA INTERFERON; HUNTINGTIN;

EID: 84876917897     PISSN: 10976256     EISSN: 15461726     Source Type: Journal    
DOI: 10.1038/nn.3367     Document Type: Article
Times cited : (83)

References (51)
  • 1
    • 0027480960 scopus 로고
    • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
    • The Huntington's Disease Collaborative Research Group
    • The Huntington's Disease Collaborative Research Group. A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72, 971-983 (1993).
    • (1993) Cell , vol.72 , pp. 971-983
  • 2
    • 28644433087 scopus 로고    scopus 로고
    • Normal huntingtin function: An alternative approach to Huntington's disease
    • DOI 10.1038/nrn1806
    • Cattaneo, E., Zuccato, C. & Tartari, M. Normal huntingtin function: an alternative approach to Huntington's disease. Nat. Rev. Neurosci. 6, 919-930 (2005). (Pubitemid 41753086)
    • (2005) Nature Reviews Neuroscience , vol.6 , Issue.12 , pp. 919-930
    • Cattaneo, E.1    Zuccato, C.2    Tartari, M.3
  • 3
    • 84855499458 scopus 로고    scopus 로고
    • Huntington's disease: Molecular basis of neurodegeneration
    • Rubinsztein, D.C. & Carmichael, J. Huntington's disease: molecular basis of neurodegeneration. Expert Rev. Mol. Med. 5, 1-21 (2003).
    • (2003) Expert Rev. Mol. Med , vol.5 , pp. 1-21
    • Rubinsztein, D.C.1    Carmichael, J.2
  • 4
    • 33846225133 scopus 로고    scopus 로고
    • Huntington's disease
    • DOI 10.1016/S0140-6736(07)60111-1, PII S0140673607601111
    • Walker, F.O. Huntington's disease. Lancet 369, 218-228 (2007). (Pubitemid 46107685)
    • (2007) Lancet , vol.369 , Issue.9557 , pp. 218-228
    • Walker, F.O.1
  • 5
    • 77950584656 scopus 로고    scopus 로고
    • Proteolysis of mutant huntingtin produces an exon 1 fragment that accumulates as an aggregated protein in neuronal nuclei in Huntington disease
    • Landles, C. et al. Proteolysis of mutant huntingtin produces an exon 1 fragment that accumulates as an aggregated protein in neuronal nuclei in Huntington disease. J. Biol. Chem. 285, 8808-8823 (2010).
    • (2010) J. Biol. Chem , vol.285 , pp. 8808-8823
    • Landles, C.1
  • 6
    • 80051951102 scopus 로고    scopus 로고
    • FAT10 protein binds to polyglutamine proteins and modulates their solubility
    • Nagashima, Y., Kowa, H., Tsuji, S. & Iwata, A. FAT10 protein binds to polyglutamine proteins and modulates their solubility. J. Biol. Chem. 286, 29594-29600 (2011).
    • (2011) J. Biol. Chem , vol.286 , pp. 29594-29600
    • Nagashima, Y.1    Kowa, H.2    Tsuji, S.3    Iwata, A.4
  • 7
    • 66749167799 scopus 로고    scopus 로고
    • Rhes a striatal specific protein, mediates mutant-huntingtin cytotoxicity
    • Subramaniam, S., Sixt, K.M., Barrow, R. & Snyder, S.H. Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity. Science 324, 1327-1330 (2009).
    • (2009) Science , vol.324 , pp. 1327-1330
    • Subramaniam, S.1    Sixt, K.M.2    Barrow, R.3    Snyder, S.H.4
  • 8
    • 72149124383 scopus 로고    scopus 로고
    • IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome
    • Thompson, L.M. et al. IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome. J. Cell Biol. 187, 1083-1099 (2009).
    • (2009) J. Cell Biol , vol.187 , pp. 1083-1099
    • Thompson, L.M.1
  • 9
    • 0034737299 scopus 로고    scopus 로고
    • Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease
    • Yamamoto, A., Lucas, J.J. & Hen, R. Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease. Cell 101, 57-66 (2000).
    • (2000) Cell , vol.101 , pp. 57-66
    • Yamamoto, A.1    Lucas, J.J.2    Hen, R.3
  • 10
    • 36749033738 scopus 로고    scopus 로고
    • Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits
    • DiFiglia, M. et al. Therapeutic silencing of mutant huntingtin with siRNA attenuates striatal and cortical neuropathology and behavioral deficits. Proc. Natl. Acad. Sci. USA 104, 17204-17209 (2007).
    • (2007) Proc. Natl. Acad. Sci. USA , vol.104 , pp. 17204-17209
    • Difiglia, M.1
  • 12
    • 25144464388 scopus 로고    scopus 로고
    • Intrastriatal rAAV-mediated delivery of anti-huntingtin shRNAs induces partial reversal of disease progression in R6/1 Huntington's disease transgenic mice
    • DOI 10.1016/j.ymthe.2005.05.006, PII S1525001605002005
    • Rodriguez-Lebron, E., Denovan-Wright, E.M., Nash, K., Lewin, A.S. & Mandel, R.J. Intrastriatal rAAV-mediated delivery of anti-huntingtin shRNAs induces partial reversal of disease progression in R6/1 Huntington's disease transgenic mice. Mol. Ther. 12, 618-633 (2005). (Pubitemid 41350143)
    • (2005) Molecular Therapy , vol.12 , Issue.4 , pp. 618-633
    • Rodriguez-Lebron, E.1    Denovan-Wright, E.M.2    Nash, K.3    Lewin, A.S.4    Mandel, R.J.5
  • 13
    • 67349100160 scopus 로고    scopus 로고
    • Nonallele-specific silencing of mutant and wild-type huntingtin demonstrates therapeutic efficacy in Huntington's disease mice
    • Boudreau, R.L. et al. Nonallele-specific silencing of mutant and wild-type huntingtin demonstrates therapeutic efficacy in Huntington's disease mice. Mol. Ther. 17, 1053-1063 (2009).
    • (2009) Mol. Ther , vol.17 , pp. 1053-1063
    • Boudreau, R.L.1
  • 14
    • 65249131740 scopus 로고    scopus 로고
    • Sustained effects of nonallele-specific Huntingtin silencing
    • Drouet, V. et al. Sustained effects of nonallele-specific Huntingtin silencing. Ann. Neurol. 65, 276-285 (2009).
    • (2009) Ann. Neurol , vol.65 , pp. 276-285
    • Drouet, V.1
  • 15
    • 77749319356 scopus 로고    scopus 로고
    • Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein
    • Bauer, P.O. et al. Harnessing chaperone-mediated autophagy for the selective degradation of mutant huntingtin protein. Nat. Biotechnol. 28, 256-263 (2010).
    • (2010) Nat. Biotechnol , vol.28 , pp. 256-263
    • Bauer, P.O.1
  • 16
    • 57649227693 scopus 로고    scopus 로고
    • Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamine-expanded huntingtin and related proteinopathies
    • Sarkar, S., Ravikumar, B., Floto, R.A. & Rubinsztein, D.C. Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamine-expanded huntingtin and related proteinopathies. Cell Death Differ. 16, 46-56 (2009).
    • (2009) Cell Death Differ , vol.16 , pp. 46-56
    • Sarkar, S.1    Ravikumar, B.2    Floto, R.A.3    Rubinsztein, D.C.4
  • 17
    • 77950903972 scopus 로고    scopus 로고
    • The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy
    • Filimonenko, M. et al. The selective macroautophagic degradation of aggregated proteins requires the PI3P-binding protein Alfy. Mol. Cell 38, 265-279 (2010).
    • (2010) Mol. Cell , vol.38 , pp. 265-279
    • Filimonenko, M.1
  • 19
    • 34249715853 scopus 로고    scopus 로고
    • Huntingtin interacting proteins are genetic modifiers of neurodegeneration
    • Kaltenbach, L.S. et al. Huntingtin interacting proteins are genetic modifiers of neurodegeneration. PLoS Genet. 3, e82 (2007).
    • (2007) PLoS Genet , vol.3
    • Kaltenbach, L.S.1
  • 20
    • 84863833900 scopus 로고    scopus 로고
    • Network organization of the huntingtin proteomic interactome in mammalian brain
    • Shirasaki, D.I. et al. Network organization of the huntingtin proteomic interactome in mammalian brain. Neuron 75, 41-57 (2012).
    • (2012) Neuron , vol.75 , pp. 41-57
    • Shirasaki, D.I.1
  • 21
    • 70349675573 scopus 로고    scopus 로고
    • RNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation
    • Doumanis, J., Wada, K., Kino, Y., Moore, A.W. & Nukina, N. RNAi screening in Drosophila cells identifies new modifiers of mutant huntingtin aggregation. PLoS ONE 4, e7275 (2009).
    • (2009) PLoS ONE , vol.4
    • Doumanis, J.1    Wada, K.2    Kino, Y.3    Moore, A.W.4    Nukina, N.5
  • 22
    • 77955870526 scopus 로고    scopus 로고
    • A genomewide RNA interference screen for modifiers of aggregates formation by mutant Huntingtin in Drosophila
    • Zhang, S., Binari, R., Zhou, R. & Perrimon, N. A genomewide RNA interference screen for modifiers of aggregates formation by mutant Huntingtin in Drosophila. Genetics 184, 1165-1179 (2010).
    • (2010) Genetics , vol.184 , pp. 1165-1179
    • Zhang, S.1    Binari, R.2    Zhou, R.3    Perrimon, N.4
  • 23
    • 77955500335 scopus 로고    scopus 로고
    • Matrix metalloproteinases are modifiers of huntingtin proteolysis and toxicity in Huntington's disease
    • Miller, J.P. et al. Matrix metalloproteinases are modifiers of huntingtin proteolysis and toxicity in Huntington's disease. Neuron 67, 199-212 (2010).
    • (2010) Neuron , vol.67 , pp. 199-212
    • Miller, J.P.1
  • 24
    • 67650258745 scopus 로고    scopus 로고
    • Enhanced degradation of mutant huntingtin by rho kinase inhibition is mediated through activation of proteasome and macroautophagy
    • Bauer, P.O. & Nukina, N. Enhanced degradation of mutant huntingtin by rho kinase inhibition is mediated through activation of proteasome and macroautophagy. Autophagy 5, 747-748 (2009).
    • (2009) Autophagy , vol.5 , pp. 747-748
    • Bauer, P.O.1    Nukina, N.2
  • 25
    • 0027160708 scopus 로고
    • Targeted gene expression as a means of altering cell fates and generating dominant phenotypes
    • Brand, A.H. & Perrimon, N. Targeted gene expression as a means of altering cell fates and generating dominant phenotypes. Development 118, 401-415 (1993). (Pubitemid 23214028)
    • (1993) Development , vol.118 , Issue.2 , pp. 401-415
    • Brand, A.H.1    Perrimon, N.2
  • 27
    • 0035827621 scopus 로고    scopus 로고
    • NUB1 a NEDD8-interacting protein, is induced by interferon and down-regulates the NEDD8 expression
    • Kito, K., Yeh, E.T. & Kamitani, T. NUB1, a NEDD8-interacting protein, is induced by interferon and down-regulates the NEDD8 expression. J. Biol. Chem. 276, 20603-20609 (2001).
    • (2001) J. Biol. Chem , vol.276 , pp. 20603-20609
    • Kito, K.1    Yeh, E.T.2    Kamitani, T.3
  • 28
    • 84863178573 scopus 로고    scopus 로고
    • TR-FRET-based duplex immunoassay reveals an inverse correlation of soluble and aggregated mutant huntingtin in Huntington's disease
    • Baldo, B. et al. TR-FRET-based duplex immunoassay reveals an inverse correlation of soluble and aggregated mutant huntingtin in Huntington's disease. Chem. Biol. 19, 264-275 (2012).
    • (2012) Chem. Biol , vol.19 , pp. 264-275
    • Baldo, B.1
  • 29
    • 0033119123 scopus 로고    scopus 로고
    • Nuclear and neuropil aggregates in Huntington's disease: Relationship to neuropathology
    • Gutekunst, C.A. et al. Nuclear and neuropil aggregates in Huntington's disease: relationship to neuropathology. J. Neurosci. 19, 2522-2534 (1999).
    • (1999) J. Neurosci , vol.19 , pp. 2522-2534
    • Gutekunst, C.A.1
  • 30
    • 84877139837 scopus 로고    scopus 로고
    • A novel human embryonic stem cell-derived Huntington's disease neuronal model exhibits mutant huntingtin (mHTT) aggregates and soluble mHTT-dependent neurodegeneration
    • doi:10.1096/fj.12-219220 16 January 2013
    • Lu, B. & Palacino, J. A novel human embryonic stem cell-derived Huntington's disease neuronal model exhibits mutant huntingtin (mHTT) aggregates and soluble mHTT-dependent neurodegeneration. FASEB J . doi:10.1096/fj.12- 219220 (16 January 2013).
    • FASEB J
    • Lu, B.1    Palacino, J.2
  • 31
    • 84864628471 scopus 로고    scopus 로고
    • Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes
    • The HD iPSC Consortium
    • The HD iPSC Consortium. Induced pluripotent stem cells from patients with Huntington's disease show CAG-repeat-expansion-associated phenotypes. Cell Stem Cell 11, 264-278 (2012).
    • (2012) Cell Stem Cell , vol.11 , pp. 264-278
  • 32
    • 0035824559 scopus 로고    scopus 로고
    • Targeting of NEDD8 and its conjugates for proteasomal degradation by NUB1
    • Kamitani, T., Kito, K., Fukuda-Kamitani, T. & Yeh, E.T. Targeting of NEDD8 and its conjugates for proteasomal degradation by NUB1. J. Biol. Chem. 276, 46655-46660 (2001).
    • (2001) J. Biol. Chem , vol.276 , pp. 46655-46660
    • Kamitani, T.1    Kito, K.2    Fukuda-Kamitani, T.3    Yeh, E.T.4
  • 33
    • 0041856380 scopus 로고    scopus 로고
    • Regulation of the NEDD8 conjugation system by a splicing variant, NUB1L
    • DOI 10.1074/jbc.M212057200
    • Tanaka, T., Kawashima, H., Yeh, E.T. & Kamitani, T. Regulation of the NEDD8 conjugation system by a splicing variant, NUB1L. J. Biol. Chem. 278, 32905-32913 (2003). (Pubitemid 37055733)
    • (2003) Journal of Biological Chemistry , vol.278 , Issue.35 , pp. 32905-32913
    • Tanaka, T.1    Kawashima, H.2    Yeh, E.T.H.3    Kamitani, T.4
  • 34
    • 1942533448 scopus 로고    scopus 로고
    • NEDD8 ultimate buster-1l interacts with the ubiquitin-like protein fat10 and accelerates its degradation
    • DOI 10.1074/jbc.M310114200
    • Hipp, M.S., Raasi, S., Groettrup, M. & Schmidtke, G. NEDD8 ultimate buster-1L interacts with the ubiquitin-like protein FAT10 and accelerates its degradation. J. Biol. Chem. 279, 16503-16510 (2004). (Pubitemid 38509349)
    • (2004) Journal of Biological Chemistry , vol.279 , Issue.16 , pp. 16503-16510
    • Hipp, M.S.1    Raasi, S.2    Groettrup, M.3    Schmidtke, G.4
  • 35
    • 64749098830 scopus 로고    scopus 로고
    • An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer
    • Soucy, T.A. et al. An inhibitor of NEDD8-activating enzyme as a new approach to treat cancer. Nature 458, 732-736 (2009).
    • (2009) Nature , vol.458 , pp. 732-736
    • Soucy, T.A.1
  • 36
    • 34447135496 scopus 로고    scopus 로고
    • Substrate-mediated regulation of cullin neddylation
    • DOI 10.1074/jbc.M701153200
    • Chew, E.H. & Hagen, T. Substrate-mediated regulation of cullin neddylation. J. Biol. Chem. 282, 17032-17040 (2007). (Pubitemid 47093199)
    • (2007) Journal of Biological Chemistry , vol.282 , Issue.23 , pp. 17032-17040
    • Chew, E.-H.1    Hagen, T.2
  • 37
    • 0027521002 scopus 로고
    • Interferon beta-1b is effective in relapsing-remitting multiple sclerosis. II. MRI analysis results of a multicenter, randomized, double-blind, placebo- controlled trial
    • Paty, D.W., Li, D.K. & the UBC MS/MRI Study Group & the IFNB Multiple Sclerosis Study Group. Interferon beta-1b is effective in relapsing-remitting multiple sclerosis. II. MRI analysis results of a multicenter, randomized, double-blind, placebo-controlled trial. Neurology 43, 662-667 (1993). (Pubitemid 23121952)
    • (1993) Neurology , vol.43 , Issue.4 , pp. 662-667
    • Paty, D.W.1    Li, D.K.B.2
  • 38
    • 12644263394 scopus 로고    scopus 로고
    • Targeted inactivation of the mouse Huntington's disease gene homolog Hdh
    • MacDonald, M.E. et al. Targeted inactivation of the mouse Huntington's disease gene homolog Hdh. Cold Spring Harb. Symp. Quant. Biol. 61, 627-638 (1996).
    • (1996) Cold Spring Harb. Symp. Quant. Biol , vol.61 , pp. 627-638
    • MacDonald, M.E.1
  • 39
    • 0029082383 scopus 로고
    • Inactivation of the mouse Huntington's disease gene homolog Hdh
    • Duyao, M.P. et al. Inactivation of the mouse Huntington's disease gene homolog Hdh. Science 269, 407-410 (1995).
    • (1995) Science , vol.269 , pp. 407-410
    • Duyao, M.P.1
  • 40
    • 84860192454 scopus 로고    scopus 로고
    • Six-month partial suppression of Huntingtin is well tolerated in the adult rhesus striatum
    • Grondin, R. et al. Six-month partial suppression of Huntingtin is well tolerated in the adult rhesus striatum. Brain 135, 1197-1209 (2012).
    • (2012) Brain , vol.135 , pp. 1197-1209
    • Grondin, R.1
  • 42
    • 60849106643 scopus 로고    scopus 로고
    • Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction
    • Weiss, A., Roscic, A. & Paganetti, P. Inducible mutant huntingtin expression in HN10 cells reproduces Huntington's disease-like neuronal dysfunction. Mol. Neurodegener. 4, 11 (2009).
    • (2009) Mol. Neurodegener , vol.4 , pp. 11
    • Weiss, A.1    Roscic, A.2    Paganetti, P.3
  • 43
    • 69249232195 scopus 로고    scopus 로고
    • An efficient and reversible transposable system for gene delivery and lineage-specific differentiation in human embryonic stem cells
    • Lacoste, A., Berenshteyn, F. & Brivanlou, A.H. An efficient and reversible transposable system for gene delivery and lineage-specific differentiation in human embryonic stem cells. Cell Stem Cell 5, 332-342 (2009).
    • (2009) Cell Stem Cell , vol.5 , pp. 332-342
    • Lacoste, A.1    Berenshteyn, F.2    Brivanlou, A.H.3
  • 44
    • 62149125434 scopus 로고    scopus 로고
    • Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling
    • Chambers, S.M. et al. Highly efficient neural conversion of human ES and iPS cells by dual inhibition of SMAD signaling. Nat. Biotechnol. 27, 275-280 (2009).
    • (2009) Nat. Biotechnol , vol.27 , pp. 275-280
    • Chambers, S.M.1
  • 45
    • 0035502934 scopus 로고    scopus 로고
    • New anti-huntingtin monoclonal antibodies: Implications for huntingtin conformation and its binding proteins
    • DOI 10.1016/S0361-9230(01)00599-8, PII S0361923001005998
    • Ko, J., Ou, S. & Patterson, P.H. New anti-huntingtin monoclonal antibodies: implications for huntingtin conformation and its binding proteins. Brain Res. Bull. 56, 319-329 (2001). (Pubitemid 33062356)
    • (2001) Brain Research Bulletin , vol.56 , Issue.3-4 , pp. 319-329
    • Ko, J.1    Ou, S.2    Patterson, P.H.3
  • 46
    • 70349103737 scopus 로고    scopus 로고
    • Single-step detection of mutant huntingtin in animal and human tissues: A bioassay for Huntington's disease
    • Weiss, A. et al. Single-step detection of mutant huntingtin in animal and human tissues: a bioassay for Huntington's disease. Anal. Biochem. 395, 8-15 (2009).
    • (2009) Anal. Biochem , vol.395 , pp. 8-15
    • Weiss, A.1
  • 47
    • 84867148826 scopus 로고    scopus 로고
    • Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression
    • Weiss, A. et al. Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression. J. Clin. Invest. 122, 3731-3736 (2012).
    • (2012) J. Clin. Invest , vol.122 , pp. 3731-3736
    • Weiss, A.1
  • 49
    • 0041691176 scopus 로고    scopus 로고
    • Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats
    • DOI 10.1002/cne.10776
    • Menalled, L.B., Sison, J.D., Dragatsis, I., Zeitlin, S. & Chesselet, M.F. Time course of early motor and neuropathological anomalies in a knock-in mouse model of Huntington's disease with 140 CAG repeats. J. Comp. Neurol. 465, 11-26 (2003). (Pubitemid 37075677)
    • (2003) Journal of Comparative Neurology , vol.465 , Issue.1 , pp. 11-26
    • Menalled, L.B.1    Sison, J.D.2    Dragatsis, I.3    Zeitlin, S.4    Chesselet, M.-F.5
  • 50
    • 73949155373 scopus 로고    scopus 로고
    • Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease
    • Valencia, A. et al. Mutant huntingtin and glycogen synthase kinase 3-beta accumulate in neuronal lipid rafts of a presymptomatic knock-in mouse model of Huntington's disease. J. Neurosci. Res. 88, 179-190 (2010).
    • (2010) J. Neurosci. Res , vol.88 , pp. 179-190
    • Valencia, A.1
  • 51
    • 77955284657 scopus 로고    scopus 로고
    • The pseudokinase tribbles homolog 3 interacts with ATF4 to negatively regulate insulin exocytosis in human and mouse beta cells
    • Liew, C.W. et al. The pseudokinase tribbles homolog 3 interacts with ATF4 to negatively regulate insulin exocytosis in human and mouse beta cells. J. Clin. Invest. 120, 2876-2888 (2010).
    • (2010) J. Clin. Invest , vol.120 , pp. 2876-2888
    • Liew, C.W.1


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