An arginine/lysine-rich motif is crucial for VCP/p97-mediated modulation of ataxin-3 fibrillogenesis

被引:131
作者
Boeddrich, A
Gaumer, S
Haacke, A
Tzvetkov, N
Albrecht, M
Evert, BO
Müller, EC
Lurz, R
Breuer, P
Schugardt, N
Plassmann, S
Xu, KX
Warrick, JM
Suopanki, J
Wüllner, U
Frank, R
Hartl, UF
Bonini, NM
Wanker, EE
机构
[1] Max Delbruck Ctr Mol Med, MDC, Dept Neuroprote, D-13092 Berlin, Germany
[2] Univ Penn, Howard Hughes Med Inst, Dept Biol, Philadelphia, PA 19104 USA
[3] Max Planck Inst Biochem, D-82152 Martinsried, Germany
[4] Max Planck Inst Informat, Saarbrucken, Germany
[5] Univ Bonn, Dept Neurol, D-5300 Bonn, Germany
[6] Max Planck Inst Mol Genet, Berlin, Germany
[7] GBF, Dept Chem Biol, Braunschweig, Germany
关键词
ataxin-3; VCP; polyglutamine aggregation;
D O I
10.1038/sj.emboj.7601043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Arginine/lysine-rich motifs typically function as targeting signals for the translocation of proteins to the nucleus. Here, we demonstrate that such a motif consisting of four basic amino acids in the polyglutamine protein ataxin-3 (Atx-3) serves as a recognition site for the interaction with the molecular chaperone VCP. Through this interaction, VCP modulates the fibrillogenesis of pathogenic forms of Atx-3 in a concentration-dependent manner, with low concentrations of VCP stimulating fibrillogenesis and excess concentrations suppressing it. No such effect was observed with a mutant Atx-3 variant, which does not contain a functional VCP interaction motif. Strikingly, a stretch of four basic amino acids in the ubiquitin chain assembly factor E4B was also discovered to be critical for VCP binding, indicating that arginine/lysine-rich motifs might be generally utilized by VCP for the targeting of proteins. In vivo studies with Drosophila models confirmed that VCP selectively modulates aggregation and neurotoxicity induced by pathogenic Atx-3. Together, these results define the VCP-Atx-3 association as a potential target for therapeutic intervention and suggest that it might influence the progression of spinocerebellar ataxia type 3.
引用
收藏
页码:1547 / 1558
页数:12
相关论文
共 43 条
[11]   Spinocerebellar ataxia 3 and Machado-Joseph disease: Clinical, molecular, and neuropathological features [J].
Durr, A ;
Stevanin, G ;
Cancel, G ;
Duyckaerts, C ;
Abbas, N ;
Didierjean, O ;
Chneiweiss, H ;
Benomar, A ;
LyonCaen, O ;
Julien, J ;
Serdaru, M ;
Penet, C ;
Agid, Y ;
Brice, A .
ANNALS OF NEUROLOGY, 1996, 39 (04) :490-499
[12]  
Frank R, 1996, Methods Mol Biol, V66, P149
[13]   SPOT-SYNTHESIS - AN EASY TECHNIQUE FOR THE POSITIONALLY ADDRESSABLE, PARALLEL CHEMICAL SYNTHESIS ON A MEMBRANE SUPPORT [J].
FRANK, R .
TETRAHEDRON, 1992, 48 (42) :9217-9232
[14]   A mutant ataxin-3 putative-cleavage fragment in brains of Machado-Joseph disease patients and transgenic mice is cytotoxic above a critical concentration [J].
Goti, D ;
Katzen, SM ;
Mez, J ;
Kurtis, N ;
Kiluk, J ;
Ben-Haïem, L ;
Jenkins, NA ;
Copeland, NG ;
Kakizuka, A ;
Sharp, AH ;
Ross, CA ;
Mouton, PR ;
Colomer, V .
JOURNAL OF NEUROSCIENCE, 2004, 24 (45) :10266-10279
[15]   Identification of ter94, Drosophila VCP, as a modulator of polyglutamine-induced neurodegeneration [J].
Higashiyama, H ;
Hirose, F ;
Yamaguchi, M ;
Inoue, YH ;
Fujikake, N ;
Matsukage, A ;
Kakizuka, A .
CELL DEATH AND DIFFERENTIATION, 2002, 9 (03) :264-273
[16]   VCP/p97 in abnormal protein aggregates, cytoplasmic vacuoles, and cell death, phenotypes relevant to neurodegeneration [J].
Hirabayashi, M ;
Inoue, K ;
Tanaka, K ;
Nakadate, K ;
Ohsawa, Y ;
Kamei, Y ;
Popiel, AH ;
Sinohara, A ;
Iwamatsu, A ;
Kimura, Y ;
Uchiyama, Y ;
Hori, S ;
Kakizuka, A .
CELL DEATH AND DIFFERENTIATION, 2001, 8 (10) :977-984
[17]   Polyglutamine-expanded human huntingtin transgenes induce degeneration of Drosophila photoreceptor neurons [J].
Jackson, GR ;
Salecker, I ;
Dong, XZ ;
Yao, X ;
Arnheim, N ;
Faber, PW ;
MacDonald, ME ;
Zipursky, SL .
NEURON, 1998, 21 (03) :633-642
[18]   Characterization of the mouse gene for the U-box-type ubiquitin lipase UFD2a [J].
Kaneko, C ;
Hatakeyama, S ;
Matsumoto, M ;
Yada, M ;
Nakayama, K ;
Nakayama, KI .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 300 (02) :297-304
[19]   p47 is a cofactor for p97-mediated membrane fusion [J].
Kondo, H ;
Rabouille, C ;
Newman, R ;
Levine, TP ;
Pappin, D ;
Freemont, P ;
Warren, G .
NATURE, 1997, 388 (6637) :75-78
[20]   Can flies help humans treat neurodegenerative diseases? [J].
Marsh, JL ;
Thompson, LM .
BIOESSAYS, 2004, 26 (05) :485-496