Sapru M K, Florance S K, Kirk C, Goldman D
Mental Health Research Institute and Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109, USA.
Proc Natl Acad Sci U S A. 1998 Feb 3;95(3):1289-94. doi: 10.1073/pnas.95.3.1289.
At the neuromuscular synapse, innervation induces endplate-specific expression of adult-type nicotinic acetylcholine receptors by selective expression of their subunit-encoding genes (alpha2betaepsilondelta) in endplate-associated myonuclei. These genes are specifically regulated by protein-tyrosine phosphatase (PTPase) activity. In addition, neuregulin/acetylcholine-receptor-inducing activity, a nerve-derived factor that stimulates nicotinic acetylcholine receptor synthesis, induces adult-type specific epsilon subunit gene expression via activation of a Ras/mitogen-activated protein kinase pathway. However, the DNA regulatory elements and the binding proteins that mediate PTPase and neuregulin-dependent gene expression remain unknown. Herein we report that PTPase, neuregulin, and Ras-dependent regulation of the epsilon subunit gene map to a 15-bp promoter sequence. Interestingly, this same 15-bp sequence appears to be necessary for low epsilon subunit gene expression in extrajunctional regions of the muscle fiber. Site-directed mutagenesis of a putative Ets binding site located within this 15-bp sequence, reduced PTPase, neuregulin, and Ras-dependent regulation. Overexpression of the rat muscle Ets-2 transcription factor resulted in a sequence-specific induction of epsilon subunit promoter activity. Further, a dominant negative mutant of Ets-2 abolished neuregulin-dependent induction of epsilon subunit gene expression. Thus, these results indicate a crucial role for the 15-bp element in determining synapse-specific and neuregulin-mediated motor neuron control of epsilon subunit gene expression and suggest the participation of Ets transcription factor(s) in this control.
在神经肌肉突触处,神经支配通过在终板相关肌细胞核中选择性表达其亚基编码基因(α2βεδ)来诱导成年型烟碱型乙酰胆碱受体在终板特异性表达。这些基因受蛋白酪氨酸磷酸酶(PTPase)活性的特异性调控。此外,神经调节蛋白/乙酰胆碱受体诱导活性是一种神经源性因子,可刺激烟碱型乙酰胆碱受体的合成,它通过激活Ras/丝裂原活化蛋白激酶途径诱导成年型特异性ε亚基基因表达。然而,介导PTPase和神经调节蛋白依赖性基因表达的DNA调控元件和结合蛋白仍不清楚。在此我们报告,PTPase、神经调节蛋白和Ras对ε亚基基因的依赖性调控定位于一个15bp的启动子序列。有趣的是,这个相同的15bp序列似乎是肌纤维结外区域低水平ε亚基基因表达所必需的。对位于这个15bp序列内的一个假定的Ets结合位点进行定点诱变,降低了PTPase、神经调节蛋白和Ras依赖性调控。大鼠肌肉Ets-2转录因子的过表达导致ε亚基启动子活性的序列特异性诱导。此外,Ets-2的显性负性突变体消除了神经调节蛋白依赖性的ε亚基基因表达诱导。因此,这些结果表明15bp元件在决定突触特异性和神经调节蛋白介导的运动神经元对ε亚基基因表达的控制中起关键作用,并提示Ets转录因子参与了这种控制。