Qiu Yongjian, Li Meina, Pasoreck Elise K, Long Lingyun, Shi Yiting, Galvão Rafaelo M, Chou Conrad L, Wang He, Sun Amanda Y, Zhang Yiyin C, Jiang Anna, Chen Meng
Department of Biology, Duke University, Durham, North Carolina 27708.
Department of Biology, Duke University, Durham, North Carolina 27708
Plant Cell. 2015 May;27(5):1409-27. doi: 10.1105/tpc.114.136093. Epub 2015 May 5.
Phytochromes (phys) are red and far-red photoreceptors that control plant development and growth by promoting the proteolysis of a family of antagonistically acting basic helix-loop-helix transcription factors, the PHYTOCHROME-INTERACTING FACTORs (PIFs). We have previously shown that the degradation of PIF1 and PIF3 requires HEMERA (HMR). However, the biochemical function of HMR and the mechanism by which it mediates PIF degradation remain unclear. Here, we provide genetic evidence that HMR acts upstream of PIFs in regulating hypocotyl growth. Surprisingly, genome-wide analysis of HMR- and PIF-dependent genes reveals that HMR is also required for the transactivation of a subset of PIF direct-target genes. We show that HMR interacts with all PIFs. The HMR-PIF interaction is mediated mainly by HMR's N-terminal half and PIFs' conserved active-phytochrome B binding motif. In addition, HMR possesses an acidic nine-amino-acid transcriptional activation domain (9aaTAD) and a loss-of-function mutation in this 9aaTAD impairs the expression of PIF target genes and the destruction of PIF1 and PIF3. Together, these in vivo results support a regulatory mechanism for PIFs in which HMR is a transcriptional coactivator binding directly to PIFs and the 9aaTAD of HMR couples the degradation of PIF1 and PIF3 with the transactivation of PIF target genes.
光敏色素(phys)是红色和远红光光感受器,通过促进一类起拮抗作用的碱性螺旋-环-螺旋转录因子——光敏色素相互作用因子(PIFs)的蛋白水解来控制植物的发育和生长。我们之前已经表明,PIF1和PIF3的降解需要HEMERA(HMR)。然而,HMR的生化功能及其介导PIF降解的机制仍不清楚。在这里,我们提供了遗传证据,表明HMR在调节下胚轴生长中作用于PIFs的上游。令人惊讶的是,对HMR和PIF依赖性基因的全基因组分析表明,HMR对于一部分PIF直接靶基因的反式激活也是必需的。我们表明HMR与所有PIFs相互作用。HMR-PIF相互作用主要由HMR的N端一半和PIFs保守的活性光敏色素B结合基序介导。此外,HMR拥有一个酸性的九氨基酸转录激活结构域(9aaTAD),该9aaTAD中的功能丧失突变会损害PIF靶基因的表达以及PIF1和PIF3的降解。总之,这些体内结果支持了一种PIFs的调控机制,其中HMR是一种直接与PIFs结合的转录共激活因子,并且HMR的9aaTAD将PIF1和PIF3的降解与PIF靶基因的反式激活联系起来。