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Neuron restrictive silencer factor as a modulator of neuropeptide gene expression.

机译:神经元限制性沉默子因子作为神经肽基因表达的调节剂。

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We hypothesize that the transcription factor neuron restrictive silencer factor (NRSF) is an important determinant of the expression of the preprotachykinin (PPTA) gene (encoding substance P and Neurokinin A) and arginine vasopressin (AVP) both in neuronal and nonneuronal cells. NRSF, a zinc finger repressor protein, binds the NRSE motif found in many neuronal specific genes at a variety of promoter locations. However, it is found in a similar location at the major transcriptional start site, within both PPTA and AVP peptide promoters.We have correlated modulation of NRSF activity with expression of AVP and PPTA in a variety of cell types, indicating the general mechanism by which this protein may regulate expression. Specifically, they are as follows:(1) Expression of NRSF dramatically represses PPTA promoter activity in reporter gene constructs in primary cultures of DRG neurons.(2) The PPTA promoter activity is regulated differentially in osteoarthritic compared to normal chondrocytes. This regulation correlates with the region containing the NRSE site.(3) We have correlated a splice variant of NRSF with the establishment and progression of small cell lung carcinoma (SCLC) and demonstrated that NRSF variants can directly affect the activity of the AVP promoter in reporter gene constructs.If the deregulated expression of peptides in these diseases point to the mechanism determining the pathology, then perhaps targeting protocols that correct this deregulation may also reverse the specific disease phenotypes. Our data would indicate that modulation of NRSF activity would be a target for such intervention.
机译:我们假设转录因子神经元限制性沉默因子(NRSF)是神经元和非神经元细胞中前激肽激肽(PPTA)基因(编码物质P和神经激肽A)和精氨酸加压素(AVP)表达的重要决定因素。锌指阻遏蛋白NRSF与在许多启动子位置的许多神经元特异性基因中发现的NRSE基序结合。然而,它在PPTA和AVP肽启动子的主要转录起始位点的相似位置被发现。我们已经将NRSF活性的调节与AVP和PPTA在多种细胞类型中的表达相关联,表明了其基本机制这种蛋白质可能调节表达。具体来说,它们如下:(1)NRSF的表达显着抑制DRG神经元原代培养物中报告基因构建物中的PPTA启动子活性。(2)与正常软骨细胞相比,骨关节炎中PPTA启动子活性受到不同的调节。该调节与包含NRSE位点的区域相关。(3)我们已经将NRSF的剪接变体与小细胞肺癌(SCLC)的建立和进展相关联,并证明了NRSF变体可以直接影响AVP启动子的活性。如果这些疾病中肽的表达失调指向确定病理的机制,则可能纠正该失调的靶向方案也可能逆转特定疾病的表型。我们的数据表明,NRSF活性的调节将是此类干预的目标。

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