Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
EMBO J. 2009 Dec 16;28(24):3893-902. doi: 10.1038/emboj.2009.306.
In shade-intolerant plants such as Arabidopsis, a reduction in the red/far-red (R/FR) ratio, indicative of competition from other plants, triggers a suite of responses known as the shade avoidance syndrome (SAS). The phytochrome photoreceptors measure the R/FR ratio and control the SAS. The phytochrome-interacting factors 4 and 5 (PIF4 and PIF5) are stabilized in the shade and are required for a full SAS, whereas the related bHLH factor HFR1 (long hypocotyl in FR light) is transcriptionally induced by shade and inhibits this response. Here we show that HFR1 interacts with PIF4 and PIF5 and limits their capacity to induce the expression of shade marker genes and to promote elongation growth. HFR1 directly inhibits these PIFs by forming non-DNA-binding heterodimers with PIF4 and PIF5. Our data indicate that PIF4 and PIF5 promote SAS by directly binding to G-boxes present in the promoter of shade marker genes, but their action is limited later in the shade when HFR1 accumulates and forms non-DNA-binding heterodimers. This negative feedback loop is important to limit the response of plants to shade.
在不能忍受阴凉的植物(如拟南芥)中,表明与其他植物竞争的红光/远红光(R/FR)比值降低,会引发一系列被称为避阴综合征(SAS)的反应。光敏色素受体测量 R/FR 比值并控制 SAS。光敏色素相互作用因子 4 和 5(PIF4 和 PIF5)在阴凉处稳定,是完整 SAS 的必需条件,而相关的 bHLH 因子 HFR1(长下胚轴在 FR 光下)则被阴凉诱导转录,并抑制这种反应。在这里,我们表明 HFR1 与 PIF4 和 PIF5 相互作用,并限制它们诱导阴凉标记基因表达和促进伸长生长的能力。HFR1 通过与 PIF4 和 PIF5 形成非 DNA 结合的异二聚体直接抑制这些 PIF。我们的数据表明,PIF4 和 PIF5 通过直接结合存在于阴凉标记基因启动子中的 G 框来促进 SAS,但当 HFR1 积累并形成非 DNA 结合的异二聚体时,它们的作用在阴凉后期会受到限制。这种负反馈环对于限制植物对阴凉的反应非常重要。