Expression of mutant Ets protein at the neuromuscular synapse causes alterations in morphology and gene expression

被引:28
|
作者
d'Exaerde, AD
Cartaud, J
Ravel-Chapuis, A
Seroz, T
Pasteau, F
Angus, LM
Jasmin, BJ
Changeux, JP
Schaeffer, L
机构
[1] Inst Pasteur, CNRS, Mol Neurobiol Lab, URA 2182 Recepteurs & Cognit, F-75724 Paris 15, France
[2] Ecole Normale Super, CNR, UMR 5665, Equipe Differenciat Neuromusculaire, F-69364 Lyon 07, France
[3] Univ Paris 06, CNRS, UMR7592, Inst Jaques Monod, F-75251 Paris, France
[4] Univ Paris 07, CNRS, UMR7592, Inst Jaques Monod, F-75251 Paris, France
[5] Free Univ Brussels, Fac Med, Neurophysiol Lab, B-1070 Brussels, Belgium
[6] Univ Ottawa, Fac Med, Dept Cellular & Mol Med, Ottawa, ON K1H 8M5, Canada
[7] Univ Ottawa, Fac Med, Ctr Neuromuscular Dis, Ottawa, ON K1H 8M5, Canada
关键词
D O I
10.1093/embo-reports/kvf220
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
The localized transcription of several muscle genes at the motor endplate is controlled by the Ets transcription factor GABP. To evaluate directly its contribution to the formation of the neuromuscular junction, we generated transgenic mice expressing a general Ets dominant-negative mutant specifically in skeletal muscle. Quantitative RT-PCR analysis demonstrated that the expression of genes containing an Ets-binding site was severely affected in the mutant mice. Conversely, the expression of other synaptic genes, including MuSK and Rapsyn, was unchanged. in these animals, muscles expressing the mutant transcription factor developed normally, but examination of the post-synaptic morphology revealed marked alterations of both the primary gutters and secondary folds of the neuromuscular junction. Our results demonstrate that Ets transcription factors are crucial for the normal formation of the neuromuscular junction. They further show that Ets-independent mechanisms control the synaptic expression of a distinct set of synaptic genes.
引用
收藏
页码:1075 / 1081
页数:7
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