Xie Qiguang, Wang Peng, Liu Xian, Yuan Li, Wang Lingbao, Zhang Chenguang, Li Yue, Xing Hongya, Zhi Liya, Yue Zhiliang, Zhao Chunsheng, McClung C Robertson, Xu Xiaodong
Hebei Key Laboratory of Molecular and Cellular Biology, Key Laboratory of Molecular and Cellular Biology of the Ministry of Education, College of Life Sciences, Hebei Normal University, Hebei Collaboration Innovation Center for Cell Signaling, Shijiazhuang, Hebei 050024, China.
Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire 03755-3563.
Plant Cell. 2014 Jul;26(7):2843-57. doi: 10.1105/tpc.114.126573. Epub 2014 Jul 10.
Transcriptional feedback loops are central to the architecture of eukaryotic circadian clocks. Models of the Arabidopsis thaliana circadian clock have emphasized transcriptional repressors, but recently, Myb-like REVEILLE (RVE) transcription factors have been established as transcriptional activators of central clock components, including PSEUDO-RESPONSE REGULATOR5 (PRR5) and TIMING OF CAB EXPRESSION1 (TOC1). We show here that NIGHT LIGHT-INDUCIBLE AND CLOCK-REGULATED1 (LNK1) and LNK2, members of a small family of four LNK proteins, dynamically interact with morning-expressed oscillator components, including RVE4 and RVE8. Mutational disruption of LNK1 and LNK2 function prevents transcriptional activation of PRR5 by RVE8. The LNKs lack known DNA binding domains, yet LNK1 acts as a transcriptional activator in yeast and in planta. Chromatin immunoprecipitation shows that LNK1 is recruited to the PRR5 and TOC1 promoters in planta. We conclude that LNK1 is a transcriptional coactivator necessary for expression of the clock genes PRR5 and TOC1 through recruitment to their promoters via interaction with bona fide DNA binding proteins such as RVE4 and RVE8.
转录反馈环是真核生物钟结构的核心。拟南芥生物钟模型一直强调转录抑制因子,但最近,类Myb的唤醒(REVEILLE,RVE)转录因子已被确立为核心生物钟组分的转录激活因子,包括伪应答调节因子5(PSEUDO-RESPONSE REGULATOR5,PRR5)和CAB表达时间1(TIMING OF CAB EXPRESSION1,TOC1)。我们在此表明,夜灯诱导和生物钟调节1(NIGHT LIGHT-INDUCIBLE AND CLOCK-REGULATED1,LNK1)和LNK2是由4个LNK蛋白组成的小家族成员,它们与早晨表达的振荡器组分动态相互作用,包括RVE4和RVE8。LNK1和LNK2功能的突变破坏会阻止RVE8对PRR5的转录激活。LNKs缺乏已知的DNA结合结构域,但LNK1在酵母和植物中均作为转录激活因子发挥作用。染色质免疫沉淀表明,LNK1在植物中被招募到PRR5和TOC1启动子区域。我们得出结论,LNK1是一种转录共激活因子,通过与诸如RVE4和RVE8等真正的DNA结合蛋白相互作用,被招募到PRR5和TOC1启动子区域,从而对生物钟基因PRR5和TOC1的表达是必需的。