Puhl Henry L, Ikeda Stephen R
Laboratory of Molecular Physiology, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, Maryland 20892-9411, USA.
J Neurochem. 2008 Aug;106(3):1209-24. doi: 10.1111/j.1471-4159.2008.05466.x. Epub 2008 May 7.
Voltage-gated sodium channels (VGSC) are critical membrane components that participate in the electrical activity of excitable cells. The type one VGSC family includes the tetrodotoxin insensitive sodium channel, Na(V)1.8, encoded by the Scn10a gene. Na(V)1.8 expression is restricted to small and medium diameter nociceptive sensory neurons of the dorsal root ganglia and cranial sensory ganglia. To understand the stringent transcriptional regulation of the Scn10a gene, the sensory neuron specific promoter was functionally identified. While identifying the mRNA 5'-end, alternative splicing within the 5'-UTR was observed to create heterogeneity in the RNA transcript. Four kilobases of upstream genomic DNA was cloned and the presence of tissue specific promoter activity was tested by microinjection and adenoviral infection of fluorescent protein reporter constructs into primary mouse and rat neurons, and cell lines. The region contained many putative transcription factor-binding sites and strong homology with the predicted rat ortholog. Homology to the predicted human ortholog was limited to the proximal end and several conserved cis elements were noted. Two regulatory modules were identified by microinjection of reporter constructs into dorsal root ganglia and superior cervical ganglia neurons: a neuron specific proximal promoter region between -1.6 and -0.2 kb of the transcription start site cluster, and a distal sensory neuron switch region beyond -1.6 kb that restricted fluorescent protein expression to a subset of primary sensory neurons.
电压门控钠通道(VGSC)是参与可兴奋细胞电活动的关键膜成分。1型VGSC家族包括由Scn10a基因编码的河豚毒素不敏感钠通道Na(V)1.8。Na(V)1.8的表达局限于背根神经节和颅感觉神经节中小直径的伤害性感觉神经元。为了解Scn10a基因严格的转录调控,对感觉神经元特异性启动子进行了功能鉴定。在确定mRNA 5'端时,观察到5'-UTR内的可变剪接在RNA转录本中产生了异质性。克隆了4千碱基的上游基因组DNA,并通过将荧光蛋白报告构建体显微注射和腺病毒感染原代小鼠和大鼠神经元以及细胞系来测试组织特异性启动子活性的存在。该区域包含许多假定的转录因子结合位点,与预测的大鼠直系同源物具有高度同源性。与预测的人类直系同源物的同源性仅限于近端,并且注意到了几个保守的顺式元件。通过将报告构建体显微注射到背根神经节和颈上神经节神经元中,鉴定出两个调控模块:转录起始位点簇-1.6至-0.2 kb之间的神经元特异性近端启动子区域,以及-1.6 kb以外的远端感觉神经元开关区域,该区域将荧光蛋白表达限制在初级感觉神经元的一个子集中。