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RE-1 silencing transcription factor-4 (REST4) is neither a transcriptional repressor nor a de-repressor.

机译:RE-1沉默转录因子4(REST4)既不是转录阻遏物,也不是去阻遏物。

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摘要

The zinc finger protein RE-1 silencing transcription factor (REST) is a transcriptional repressor that represses neuronal genes in non-neuronal tissues. A neuronal splice form of REST, termed REST4, has been described in the rat. It encompasses the N-terminus of REST, including the N-terminal repressor domain and five of the eight zinc fingers of the DNA-binding domain. The biological function of REST4 is controversial. Transcriptional repression as well as transcriptional de-repression activity has been attributed to the REST4 protein of rat. Here, we have expressed a 'humanized' version of REST4 (hREST4) to facilitate a comparison of the biological functions of hREST4 and REST. The biological activity the human REST protein has been extensively studied in the past. Additionally, hREST4 has a high degree of homology with the REST4 protein of rat. An immunofluorescence analysis showed that hREST4 is expressed in the nucleus, indicating that the protein may have a potential impact on gene regulation. We analyzed the biological function of hREST4 in NS20Y neuroblastoma cells using human synapsin I promoter/reporter gene constructs. The human synapsin I gene is negatively regulated by REST. The results show that hREST4, in contrast to the full-length human REST protein, does not impair human synapsin I promoter activity. Moreover, co-transfection experiments with expression vectors encoding REST and hREST4 did not reveal any evidence that REST4 blocks the transcriptional repression activity of REST.
机译:锌指蛋白RE-1沉默转录因子(REST)是一种转录抑制子,可抑制非神经组织中的神经元基因。在大鼠中已经描述了称为REST4的神经元剪接形式的REST。它涵盖了REST的N端,包括N端阻遏域和DNA结合域的八个锌指中的五个。 REST4的生物学功能是有争议的。转录抑制以及转录抑制活性已经归因于大鼠的REST4蛋白。在这里,我们表达了REST4(hREST4)的“人性化”版本,以便于比较hREST4和REST的生物学功能。过去已经广泛研究了人类REST蛋白的生物学活性。另外,hREST4与大鼠的REST4蛋白具有高度同源性。免疫荧光分析表明,hREST4在细胞核中表达,表明该蛋白可能对基因调控具有潜在影响。我们使用人类突触素I启动子/报告基因基因结构分析了hREST4在NS20Y神经母细胞瘤细胞中的生物学功能。人突触素I基因受REST负调控。结果表明,与全长人REST蛋白相反,hREST4不会损害人突触素I启动子活性。此外,使用编码REST和hREST4的表达载体进行的共转染实验没有发现REST4阻断REST的转录抑制活性的任何证据。

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