Eastman C, Horvitz H R, Jin Y
Department of Biology, Sinsheimer Laboratories, University of California, Santa Cruz, California 95064, USA.
J Neurosci. 1999 Aug 1;19(15):6225-34. doi: 10.1523/JNEUROSCI.19-15-06225.1999.
An important aspect of the specification of neuronal fate is the choice of neurotransmitter. In Caenorhabditis elegans the neurotransmitter GABA is synthesized by the UNC-25 glutamic acid decarboxylase (GAD) and packaged into synaptic vesicles by the UNC-47 transporter. Both unc-25 and unc-47 are expressed in 26 GABAergic neurons of five different types. Previously, we have identified that the unc-30 homeobox gene controls the fate of 19 type D GABAergic neurons. We report here that the UNC-30 homeodomain protein transcriptionally regulates the expression of unc-25 and unc-47 in the 19 type D neurons. UNC-30 bound to the unc-25 and unc-47 promoters sequence-specifically. Mutations in the UNC-30 binding sites of the unc-25 and unc-47 promoters abolished the expression of reporter genes in the D neurons. The ectopic expression of UNC-30 induced the ectopic expression of reporter genes driven by the wild-type unc-25 and unc-47 promoters. Our data establish a mechanism for cell type-specific transcriptional coregulation of genes required for the synthesis and packaging of the neurotransmitter GABA.
神经元命运特化的一个重要方面是神经递质的选择。在秀丽隐杆线虫中,神经递质γ-氨基丁酸(GABA)由UNC-25谷氨酸脱羧酶(GAD)合成,并通过UNC-47转运体包装到突触小泡中。unc-25和unc-47在五种不同类型的26个GABA能神经元中均有表达。此前,我们已确定unc-30同源框基因控制着19个D型GABA能神经元的命运。我们在此报告,UNC-30同源结构域蛋白在转录水平上调节19个D型神经元中unc-25和unc-47的表达。UNC-30特异性地结合到unc-25和unc-47启动子上。unc-25和unc-47启动子中UNC-30结合位点的突变消除了报告基因在D型神经元中的表达。UNC-30的异位表达诱导了由野生型unc-25和unc-47启动子驱动的报告基因的异位表达。我们的数据建立了一种机制,用于对神经递质GABA合成和包装所需基因进行细胞类型特异性的转录共调节。