Gene-specific transcriptional silencing directed by dephosphorylation of RNAP II

描述（由申请人提供）：真核细胞中的转录过程由RNA聚合酶II的c端结构域通过其翻译后修饰状态控制。然而，在CTD中识别相同磷酸化位点的酶可能导致不同的转录结果。解决CTD调控酶如何实现基因特异性调控的核心问题；我们研究了Scp的结构功能机制，Scp是一种人类CTD Ser5磷酸酶，作为神经元基因表达的共同抑制因子。通过比较基因特异性CTD磷酸酶Scp和一般转录CTD磷酸酶Ssu72，我们将检验两种不同但不相互排斥的假设，以解释不同的转录结果：分子靶向和基因特异性CTD编码。最后，我们将鉴定受Scp调控的神经元基因，并开发化学工具来研究神经发生过程中的基因级联表达。这项研究在理解ctd定向转录调控方面开辟了新的领域。本研究开发的化合物将成为了解神经干细胞分化生物学机制的有力工具。最后，在不同细胞类型中对Scp定向基因沉默的研究为确定Scp是否可以作为治疗神经退行性疾病（如阿尔茨海默病）的有效药物靶点铺平了道路。

DESCRIPTION (provided by applicant): The transcription process in eukaryotic cells is controlled by the C-terminal domain of RNA polymerase II through its post-translational modification states. However enzymes that recognize the same phosphorylation site in CTD can lead to different transcriptional outcomes. To address the central question that how gene-specific regulation was achieved by CTD regulatory enzymes; we investigate the structure function mechanism of Scp, a human CTD Ser5 phosphatase that functions as a co-repressor for neuronal gene expression. By comparing gene-specific CTD phosphatase Scp, to general-transcription CTD phosphatase Ssu72, we will test two different yet not mutually exclusive hypotheses to explain the differentiated transcription outcomes: molecular targeting and gene-specific CTD code. Finally, we will identify neuronal genes that are subject to Scp regulation and develop chemical tools to investigate the gene expression cascade during neurogenesis. The research breaks new ground in understanding CTD-directed transcription regulation. The chemical compounds developed in this study will become powerful tools to understand the biological mechanism of neuronal stem cell differentiation. Finally, the study of Scp-directed gene silencing in various cell types pave the way to establish if Scp can be a valid drug target for neurodegenerative diseases such as Alzheimer's.