Syne-1, a dystrophin- and klarsicht-related protein associated with synaptic nuclei at the neuromuscular junction

被引:217
作者
Apel, ED
Lewis, RM
Grady, RM
Sanes, JR
机构
[1] Washington Univ, Sch Med, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
关键词
D O I
10.1074/jbc.M004775200
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
We describe a novel protein, Syne-1, that is associated with nuclear envelopes in skeletal, cardiac, and smooth muscle cells. Syne-1 contains multiple spectrin repeats similar to those found in dystrophin and utrophin, as well as a domain homologous to the carboxyl-terminal of Klarsicht, a protein associated with nuclei and required for a subset of nuclear migrations in Drosophila. In adult skeletal muscle fibers, levels of Syne-1 are highest in the nuclei that lie beneath the postsynaptic membrane at: the neuromuscular junction. These nuclei are transcriptionally specialized, expressing genes for synaptic components at higher levels than extrasynaptic nuclei in the same cytoplasm. Syne-1 is the first protein found to be selectively associated with synaptic nuclei. Syne-1 becomes concentrated in synaptic nuclei postnatally. It remains synaptically enriched following denervation or degeneration/regeneration, and is also present at high levels in the central nuclei of dystrophic myotubes. The location and structure of Syne-1 suggest that it may participate in the migration of myonuclei in myotubes and/or their anchoring at the postsynaptic apparatus. Finally, we identify a homologous gene, syne-2, that is expressed in an overlapping but distinct pattern.
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收藏
页码:31986 / 31995
页数:10
相关论文
共 55 条
  • [1] Rapsyn is required for MuSK signaling and recruits synaptic components to a MuSK-containing scaffold
    Apel, ED
    Glass, DJ
    Moscoso, LM
    Yancopoulos, GD
    Sanes, JR
    [J]. NEURON, 1997, 18 (04) : 623 - 635
  • [2] Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
    Bonne, G
    Di Barletta, MR
    Varnous, S
    Bécane, HM
    Hammouda, EH
    Merlini, L
    Muntoni, F
    Greenberg, CR
    Gary, F
    Urtizberea, JA
    Duboc, D
    Fardeau, M
    Toniolo, D
    Schwartz, K
    [J]. NATURE GENETICS, 1999, 21 (03) : 285 - 288
  • [3] Brosamle C, 1996, J EXP BIOL, V199, P2359
  • [4] ACETYLCHOLINE-RECEPTOR CLUSTERS ARE ASSOCIATED WITH NUCLEI IN RAT MYOTUBES
    BRUNER, JM
    BURSZTAJN, S
    [J]. DEVELOPMENTAL BIOLOGY, 1986, 115 (01) : 35 - 43
  • [5] SYNAPSE-SPECIFIC GENE-EXPRESSION
    BURDEN, SJ
    [J]. TRENDS IN GENETICS, 1993, 9 (01) : 12 - 16
  • [6] Alternatively spliced isoforms of nerve- and muscle-derived agrin: Their roles at the neuromuscular junction
    Burgess, RW
    Nguyen, QT
    Son, YJ
    Lichtman, JW
    Sanes, JR
    [J]. NEURON, 1999, 23 (01) : 33 - 44
  • [7] HIGH-EFFICIENCY TRANSFORMATION OF MAMMALIAN-CELLS BY PLASMID DNA
    CHEN, C
    OKAYAMA, H
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (08) : 2745 - 2752
  • [8] REGULATION OF THE ACETYLCHOLINE-RECEPTOR EPSILON-SUBUNIT GENE BY RECOMBINANT ARIA - AN IN-VITRO MODEL FOR TRANSYNAPTIC GENE-REGULATION
    CHU, GC
    MOSCOSO, LM
    SLIWKOWSKI, MX
    MERLIE, JP
    [J]. NEURON, 1995, 14 (02) : 329 - 339
  • [9] STRUCTURE OF THE SUBSYNAPTIC SARCOPLASM IN THE INTERFOLDS OF THE FROG NEUROMUSCULAR-JUNCTION
    COUTEAUX, R
    [J]. JOURNAL OF NEUROCYTOLOGY, 1981, 10 (06): : 947 - 962
  • [10] COUTEAUX R, 1973, STRUCTURE FUNCTION M, V2, P483