RIKEN Plant Science Center, Plant Productivity Systems Research Group, Tsurumi, Yokohama 230-0045, Japan.
Plant Cell. 2010 Mar;22(3):594-605. doi: 10.1105/tpc.109.072892. Epub 2010 Mar 16.
An interlocking transcriptional-translational feedback loop of clock-associated genes is thought to be the central oscillator of the circadian clock in plants. TIMING OF CAB EXPRESSION1 (also called PSEUDO-RESPONSE REGULATOR1 [PRR1]) and two MYB transcription factors, CIRCADIAN CLOCK ASSOCIATED1 (CCA1) and LATE ELONGATED HYPOCOTYL (LHY), play pivotal roles in the loop. Genetic studies have suggested that PRR9, PRR7, and PRR5 also act within or close to the loop; however, their molecular functions remain unknown. Here, we demonstrate that PRR9, PRR7, and PRR5 act as transcriptional repressors of CCA1 and LHY. PRR9, PRR7, and PRR5 each suppress CCA1 and LHY promoter activities and confer transcriptional repressor activity to a heterologous DNA binding protein in a transient reporter assay. Using a glucocorticoid-induced PRR5-GR (glucorticoid receptor) construct, we found that PRR5 directly downregulates CCA1 and LHY expression. Furthermore, PRR9, PRR7, and PRR5 associate with the CCA1 and LHY promoters in vivo, coincident with the timing of decreased CCA1 and LHY expression. These results suggest that the repressor activities of PRR9, PRR7, and PRR5 on the CCA1 and LHY promoter regions constitute the molecular mechanism that accounts for the role of these proteins in the feedback loop of the circadian clock.
植物生物钟的中央振荡器被认为是由时钟相关基因的连锁转录-翻译反馈环构成的。TIMING OF CAB EXPRESSION1(也称为 PSEUDO-RESPONSE REGULATOR1 [PRR1])和两个 MYB 转录因子 CIRCADIAN CLOCK ASSOCIATED1(CCA1)和 LATE ELONGATED HYPOCOTYL(LHY)在这个反馈环中起着关键作用。遗传研究表明,PRR9、PRR7 和 PRR5 也在环内或附近发挥作用;然而,它们的分子功能仍然未知。在这里,我们证明 PRR9、PRR7 和 PRR5 作为 CCA1 和 LHY 的转录抑制剂发挥作用。PRR9、PRR7 和 PRR5 均抑制 CCA1 和 LHY 启动子活性,并在瞬时报告基因测定中赋予异源 DNA 结合蛋白转录抑制活性。使用糖皮质激素诱导的 PRR5-GR(糖皮质激素受体)构建体,我们发现 PRR5 直接下调 CCA1 和 LHY 的表达。此外,PRR9、PRR7 和 PRR5 在体内与 CCA1 和 LHY 启动子结合,与 CCA1 和 LHY 表达减少的时间一致。这些结果表明,PRR9、PRR7 和 PRR5 对 CCA1 和 LHY 启动子区域的抑制活性构成了这些蛋白在生物钟反馈环中作用的分子机制。