Ataxin-3 is transported into the nucleus and associates with the nuclear matrix

被引:101
作者
Tait, D
Riccio, M
Sittler, A
Scherzinger, E
Santi, S
Ognibene, A
Maraldi, NM
Lehrach, H
Wanker, EE
机构
[1] Max Planck Inst Mol Genet, D-14195 Berlin, Dahlem, Germany
[2] Univ Bologna, Ist Istol, Bologna, Italy
[3] CNR, Ist Citomorfol Normale & Patol, I-40126 Bologna, Italy
[4] IOR, Lab Biol Cellulare & Microscopia Elettron, Bologna, Italy
关键词
D O I
10.1093/hmg/7.6.991
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
It has been reported that the ataxin-3 protein containing a polyglutamine sequence in the pathological range (61-84Q) is localized within the nucleus of neuronal cells, whereas ataxin-3 with a normal repeat length (12-37Q) is predominantly a cytoplasmic protein, In this study, the subcellular localization of the full-length ataxin-3 protein with a glutamine sequence in the normal range (Q(3)KQ(22)) was analysed in two mammalian cell lines. Using two affinity-purified polyclonal antibodies raised against the N- or C-terminal portion of ataxin-3, the protein was detected predominantly, but not exclusively, in the nucleus of COS-7 as well as neuroblastoma cells by immunofluorescence and confocal laser scanning microscopy (CLSM). The distribution of the protein in these cellular compartments was confirmed by biochemical subcellular fractionations, Furthermore, CLSM revealed that the ataxin-3 protein present in the nucleus of neuroblastoma cells is associated with the inner nuclear matrix. Our results taken together with the finding of a nuclear localization signal in ataxin-3 indicate that the ataxin-3 protein per se translocates to the nucleus and that an expanded glutamine repeat is not essential for this transport.
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页码:991 / 997
页数:7
相关论文
共 31 条
  • [1] Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation
    Davies, SW
    Turmaine, M
    Cozens, BA
    DiFiglia, M
    Sharp, AH
    Ross, CA
    Scherzinger, E
    Wanker, EE
    Mangiarini, L
    Bates, GP
    [J]. CELL, 1997, 90 (03) : 537 - 548
  • [2] Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain
    DiFiglia, M
    Sapp, E
    Chase, KO
    Davies, SW
    Bates, GP
    Vonsattel, JP
    Aronin, N
    [J]. SCIENCE, 1997, 277 (5334) : 1990 - 1993
  • [3] EPITHELIAL CYTOSKELETAL FRAMEWORK AND NUCLEAR MATRIX INTERMEDIATE FILAMENT SCAFFOLD - 3-DIMENSIONAL ORGANIZATION AND PROTEIN-COMPOSITION
    FEY, EG
    WAN, KM
    PENMAN, S
    [J]. JOURNAL OF CELL BIOLOGY, 1984, 98 (06) : 1973 - 1984
  • [4] HIGH-EFFICIENCY GENE-TRANSFER INTO MAMMALIAN-CELLS
    GORMAN, CM
    LANE, DP
    RIGBY, PWJ
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES, 1984, 307 (1132) : 343 - &
  • [5] A VERSATILE INVIVO AND INVITRO EUKARYOTIC EXPRESSION VECTOR FOR PROTEIN ENGINEERING
    GREEN, S
    ISSEMANN, I
    SHEER, E
    [J]. NUCLEIC ACIDS RESEARCH, 1988, 16 (01) : 369 - 369
  • [6] GU J, 1994, BIOTECHNIQUES, V17, P257
  • [7] HARDING AE, 1993, ADV NEUROL, V61, P1
  • [8] SPINOCEREBELLAR DEGENERATIONS IN JAPAN - A NATIONWIDE EPIDEMIOLOGIC AND CLINICAL-STUDY
    HIRAYAMA, K
    TAKAYANAGI, T
    NAKAMURA, R
    YANAGISAWA, N
    HATTORI, T
    KITA, K
    YANAGIMOTO, S
    FUJITA, M
    NAGAOKA, M
    SATOMURA, Y
    SOBUE, I
    IIZUKA, R
    TOYOKURA, Y
    SATOYOSHI, E
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 1994, 89 : 1 - 22
  • [9] Expanded polyglutamine in the Machado-Joseph disease protein induces cell death in vitro and in vivo
    Ikeda, H
    Yamaguchi, M
    Sugai, S
    Aze, Y
    Narumiya, S
    Kakizuka, A
    [J]. NATURE GENETICS, 1996, 13 (02) : 196 - 202
  • [10] CAG EXPANSIONS IN A NOVEL GENE FOR MACHADO-JOSEPH DISEASE AT CHROMOSOME 14Q32.1
    KAWAGUCHI, Y
    OKAMOTO, T
    TANIWAKI, M
    AIZAWA, M
    INOUE, M
    KATAYAMA, S
    KAWAKAMI, H
    NAKAMURA, S
    NISHIMURA, M
    AKIGUCHI, I
    KIMURA, J
    NARUMIYA, S
    KAKIZUKA, A
    [J]. NATURE GENETICS, 1994, 8 (03) : 221 - 228