Tsanev Robert, Tiigimägi Piret, Michelson Piret, Metsis Madis, Østerlund Torben, Kogerman Priit
Department of Gene Technology, Tallinn University of Technology, Tallinn, Estonia.
FEBS Lett. 2009 Jan 5;583(1):224-8. doi: 10.1016/j.febslet.2008.12.010. Epub 2008 Dec 10.
Gli transcription factors are downstream targets of the Hedgehog signaling pathway. Two of the three Gli proteins harbor gene transcription repressor function in the N-terminal half. We have analyzed the sequences and identified a potential repressor domain in Gli2 and Gli3 and have tested this experimentally. Overexpression studies confirm that the N-terminal parts harbor gene repression activity and we mapped the minimal repressor to residues 106 till 236 in Gli3. Unlike other mechanisms that inhibit Gli induced gene transcription, the repressor domain identified here does not utilize Histone deacetylases (HDACs) to achieve repression, as confirmed by HDAC inhibition studies and pull-down assays. This distinguishes the identified domain from other regulatory parts with negative influence on transcription.
Gli转录因子是Hedgehog信号通路的下游靶点。三种Gli蛋白中的两种在N端的一半区域具有基因转录抑制功能。我们分析了序列,在Gli2和Gli3中鉴定出一个潜在的抑制结构域,并进行了实验验证。过表达研究证实N端部分具有基因抑制活性,我们将最小抑制区域定位到Gli3中的第106至236位残基。与其他抑制Gli诱导基因转录的机制不同,此处鉴定的抑制结构域不利用组蛋白去乙酰化酶(HDACs)来实现抑制,HDAC抑制研究和下拉试验证实了这一点。这使得鉴定出的结构域与其他对转录有负面影响的调节部分区分开来。