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神经元限制性沉默因子在可卡因和苯丙胺调节转录物基因特异性表达中的调控作用

Regulatory role of neuron-restrictive silencing factor in the specific expression of cocaine- and amphetamine-regulated transcript gene.

作者信息

Li Yanhua, Liu Qingbin, Yang Yinxiang, Lv Yang, Chen Lin, Bai Cixian, Nan Xue, Wang Yunfang, Pei Xuetao

机构信息

Stem Cells and Regenerative Medicine Lab, Beijing Institute of Transfusion Medicine, Beijing, China.

出版信息

J Neurochem. 2008 Aug;106(3):1314-24. doi: 10.1111/j.1471-4159.2008.05487.x. Epub 2008 May 15.

Abstract

Cocaine- and amphetamine-regulated transcript (CART) peptide is an endogenous peptide which is widely expressed in the CNS and PNS as well as in endocrine cells. Despite the functional knowledge about CART, the mechanisms that regulate CART gene transcription are poorly characterized. Here, we showed that neuron-restrictive silencer factor (NRSF) functions as a negative regulator of CART gene expression in neuroendocrine cells. A putative neuron-restrictive silencer element (NRSE) conserved between the rodent and human CART promoter was identified and demonstrated to bind to NRSF in sequence-specific manner by the electrophoretic mobility shift and chromatin immunoprecipitation assays. Ectopic expression of NRSF in pheochromocytoma cells (PC12) and insulin-secreting cells (INS-1) induced a marked reduction in the level of CART mRNA and the activity of CART promoter or NRSE reporter. The CART promoter showed very low activity in endogenous NRSF-expressing HeLa cells. When expression of NRSF was down-regulated in HeLa cells using a RNA interfering technique, the transcriptional activity of the CART promoter or a NRSE reporter was significantly increased. Taken together, our data suggested that CART gene expression in neuroendocrine cells is strictly controlled by NRSF, via a mechanism dependent upon the CART NRSE.

摘要

可卡因和苯丙胺调节转录物(CART)肽是一种内源性肽,在中枢神经系统、外周神经系统以及内分泌细胞中广泛表达。尽管对CART的功能有所了解,但调节CART基因转录的机制仍知之甚少。在此,我们表明神经元限制性沉默因子(NRSF)在神经内分泌细胞中作为CART基因表达的负调节因子发挥作用。通过电泳迁移率变动分析和染色质免疫沉淀分析,在啮齿动物和人类CART启动子之间鉴定出一个假定的神经元限制性沉默元件(NRSE),并证明其以序列特异性方式与NRSF结合。在嗜铬细胞瘤细胞(PC12)和胰岛素分泌细胞(INS-1)中异位表达NRSF可导致CART mRNA水平以及CART启动子或NRSE报告基因的活性显著降低。CART启动子在内源性表达NRSF的HeLa细胞中活性极低。当使用RNA干扰技术下调HeLa细胞中NRSF的表达时,CART启动子或NRSE报告基因的转录活性显著增加。综上所述,我们的数据表明神经内分泌细胞中CART基因的表达受到NRSF的严格控制,其机制依赖于CART NRSE。

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