Center for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, Campus UAB, Edifici CRAG, Bellaterra, 08193 Barcelona, Spain.
Lancaster Environment Center, Lancaster University, Lancaster LA1 4YQ, UK; The University of Edinburgh, CH Waddington Building, Max Born Crescent, Edinburgh EH9 3BF, UK.
Curr Biol. 2018 Jan 22;28(2):311-318.e5. doi: 10.1016/j.cub.2017.12.021. Epub 2018 Jan 11.
Plants coordinate their growth and development with the environment through integration of circadian clock and photosensory pathways. In Arabidopsis thaliana, rhythmic hypocotyl elongation in short days (SD) is enhanced at dawn by the basic-helix-loop-helix (bHLH) transcription factors PHYTOCHROME-INTERACTING FACTORS (PIFs) directly inducing expression of growth-related genes [1-6]. PIFs accumulate progressively during the night and are targeted for degradation by active phytochromes in the light, when growth is reduced. Although PIF proteins are also detected during the day hours [7-10], their growth-promoting activity is inhibited through unknown mechanisms. Recently, the core clock components and transcriptional repressors PSEUDO-RESPONSE REGULATORS PRR9/7/5 [11, 12], negative regulators of hypocotyl elongation [13, 14], were described to associate to G boxes [15], the DNA motifs recognized by the PIFs [16, 17], suggesting that PRR and PIF function might converge antagonistically to regulate growth. Here we report that PRR9/7/5 and PIFs physically interact and bind to the same promoter region of pre-dawn-phased, growth-related genes, and we identify the transcription factor CDF5 [18, 19] as target of this interplay. In SD, CDF5 expression is sequentially repressed from morning to dusk by PRRs and induced pre-dawn by PIFs. Consequently, CDF5 accumulates specifically at dawn, when it induces cell elongation. Our findings provide a framework for recent TIMING OF CAB EXPRESSION 1 (TOC1/PRR1) data [5, 20] and reveal that the long described circadian morning-to-midnight waves of the PRR transcriptional repressors (PRR9, PRR7, PRR5, and TOC1) [21] jointly gate PIF activity to dawn to prevent overgrowth through sequential regulation of common PIF-PRR target genes such as CDF5.
植物通过整合生物钟和光感受途径来协调其生长和发育与环境的关系。在拟南芥中,短日照下(SD)的下胚轴节律性伸长在黎明时通过基本螺旋-环-螺旋(bHLH)转录因子 PHYTOCHROME-INTERACTING FACTORS(PIFs)增强,这些因子直接诱导生长相关基因的表达[1-6]。PIF 在夜间逐渐积累,并在光照下被活性光敏色素靶向降解,此时生长受到抑制。尽管 PIF 蛋白也在白天被检测到[7-10],但其促进生长的活性通过未知机制受到抑制。最近,核心时钟组件和转录抑制因子 PSEUDO-RESPONSE REGULATORS PRR9/7/5[11,12],作为下胚轴伸长的负调节剂[13,14],被描述为与 G 盒[15](PIF 识别的 DNA 基序)相关联[16,17],表明 PRR 和 PIF 的功能可能通过拮抗作用汇聚来调节生长。在这里,我们报告 PRR9/7/5 和 PIFs 物理相互作用并结合到与预曙光相关的生长相关基因的相同启动子区域,并且我们鉴定出转录因子 CDF5[18,19]作为这种相互作用的靶标。在 SD 中,CDF5 的表达从早晨到黄昏被 PRRs 依次抑制,并被 PIFs 提前到黎明诱导。因此,CDF5 专门在黎明时积累,此时它诱导细胞伸长。我们的发现为最近的 TIMING OF CAB EXPRESSION 1(TOC1/PRR1)数据[5,20]提供了一个框架,并揭示了长描述的 PRR 转录抑制因子(PRR9、PRR7、PRR5 和 TOC1)的昼夜节律性晨至午夜波[21]共同门控 PIF 活性至黎明,以防止通过对 CDF5 等常见 PIF-PRR 靶基因的顺序调节而过度生长。