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Regulation of Notch signaling by the chromatin-modeling protein Hat-trick

机译:染色质模拟蛋白帽子戏剧的陷波信号调节

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摘要

Notch signaling plays a pleiotropic role in a variety of cellular processes, including cell fate determination, differentiation, proliferation and apoptosis. The increasingly complex regulatory mechanisms of Notch signaling account for the many functions of Notch during development. Using a yeast two-hybrid screen, we identified the Drosophila DNA-binding protein Hat-trick (Htk) to be an interacting partner of Notch-intracellular domain (Notch-ICD); their physical interaction was further validated by co-immunoprecipitation experiments. htk genetically interacts with Notch pathway components in trans-heterozygous combinations. Loss of htk function in htk mutant somatic clones resulted in the downregulation of Notch targets, whereas its overexpression caused ectopic expression of Notch targets, without affecting the level of the Notch protein. In the present study, immunocytochemical analyses demonstrate that Htk and overexpressed Notch-ICD colocalize in the same nuclear compartment. Here, we also show that Htk cooperates with Notch-ICD and Suppressor of Hairless to form an activation complex and binds to the regulatory sequences of Notch downstream targets such as Enhancer of Split complex genes, to direct their expression. Together, our results suggest a novel mode of regulation of Notch signaling by the chromatin-modeling protein Htk.
机译:Notch信号传导在各种细胞过程中发挥型抗性作用,包括细胞命运测定,分化,增殖和凋亡。开发期间缺口缺口功能越来越复杂的Notch信号传导账户的监管机制。使用酵母双杂交筛网,我们将果蝇DNA结合蛋白帽子特征(HTK)鉴定为Notch细胞内域(Notch-ICD)的相互作用伴侣;通过共免疫沉淀实验进一步验证了它们的物理相互作用。 HTK在反式杂合组合中与陷波途径组分进行遗传相互作用。 HTK突变体克隆中HTK功能的丧失导致了缺口靶的下调,而其过表达引起缺口靶的异位表达,而不会影响缺口蛋白的水平。在本研究中,免疫细胞化学分析表明,HTK和过度表达的NOTCH-ICD在同一核隔室中叠加。在这里,我们还表明,HTK与缺苗的Notch-ICD和抑制器配合,形成活化复合物,并结合凹口下游靶标的调节序列,例如分裂复合基因的增强子,以引导其表达。我们的结果表明了染色质模拟蛋白HTK的陷波信号传导的新型调节模式。

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