Syne proteins anchor muscle nuclei at the neuromuscular junction

被引:177
作者
Grady, RM
Starr, DA [1 ]
Ackerman, GL
Sanes, JR
Han, M
机构
[1] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[2] Univ Colorado, Howard Hughes Med Inst, Boulder, CO 80309 USA
[3] Washington Univ, Dept Anat & Neurobiol, St Louis, MO 63110 USA
[4] Washington Univ, Dept Pediat, St Louis, MO 63110 USA
[5] Univ Calif Davis, Sect Mol & Cellular Biol, Davis, CA 95616 USA
[6] Univ Calif Davis, Ctr Genet & Dev, Davis, CA 95616 USA
[7] Harvard Univ, Dept Mol & Cellular Biol, Cambridge, MA 02138 USA
关键词
acetylcholine receptors; nuclear envelope; nuclear aggregates; synaptic nuclei; Syne-1;
D O I
10.1073/pnas.0500711102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Vertebrate skeletal muscle fibers contain hundreds of nuclei, of which three to six are functionally specialized and stably anchored beneath the postsynaptic membrane at the neuromuscular junction (NMJ). The mechanisms that localize synaptic nuclei and the roles they play in neuromuscular development are unknown. Syne-1 is concentrated at the nuclear envelope of synaptic nuclei; its Caenorhabditis elegans orthologue ANC-1 functions to tether nuclei to the cytoskeleton. To test the involvement of Syne proteins in nuclear anchoring, we generated transgenic mice overexpressing the conserved C-terminal Klarsicht/ANC-1/Syne homology domain of Syne-1. The transgene acted in a dominant interfering fashion, displacing endogenous Syne-1 from the nuclear envelope. Muscle nuclei failed to aggregate at the NMJ in transgenic mice, demonstrating that localization and positioning of synaptic nuclei require Syne proteins. We then exploited this phenotype to show that synaptic nuclear aggregates are dispensable for maturation of the NMJ.
引用
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页码:4359 / 4364
页数:6
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