State Key Laboratory of Genetic Engineering, Institute of Plants Biology, School of Life Sciences, Fudan University, Shanghai, China.
State Key Laboratory of Genetic Engineering, Department of Biochemistry, Institute of Plants Biology, School of Life Sciences, Fudan University, Shanghai, China.
EMBO J. 2023 Apr 17;42(8):e111472. doi: 10.15252/embj.2022111472. Epub 2023 Mar 13.
For shade-intolerant plants, changes in light quality through competition from neighbors trigger shade avoidance syndrome (SAS): a series of morphological and physiological adaptations that are ultimately detrimental to plant health and crop yield. Phytochrome-interacting factor 7 (PIF7) is a major transcriptional regulator of SAS in Arabidopsis; however, how it regulates gene expression is not fully understood. Here, we show that PIF7 directly interacts with the histone chaperone anti-silencing factor 1 (ASF1). The ASF1-deprived asf1ab mutant showed defective shade-induced hypocotyl elongation. Histone regulator homolog A (HIRA), which mediates deposition of the H3.3 variant into chromatin, is also involved in SAS. RNA/ChIP-sequencing analyses identified the role of ASF1 in the direct regulation of a subset of PIF7 target genes. Furthermore, shade-elicited gene activation is accompanied by H3.3 enrichment, which is mediated by the PIF7-ASF1-HIRA regulatory module. Collectively, our data reveal that PIF7 recruits ASF1-HIRA to increase H3.3 incorporation into chromatin to promote gene transcription, thus enabling plants to effectively respond to environmental shade.
对于耐荫植物来说,来自邻居的光质变化会引发避荫综合征(SAS):一系列形态和生理适应,最终对植物健康和作物产量造成损害。光敏色素相互作用因子 7(PIF7)是拟南芥 SAS 的主要转录调控因子;然而,它如何调节基因表达还不完全清楚。在这里,我们表明 PIF7 直接与组蛋白伴侣抗沉默因子 1(ASF1)相互作用。ASF1 缺失的 asf1ab 突变体表现出缺陷的遮荫诱导下胚轴伸长。组蛋白调节因子同源物 A(HIRA)介导 H3.3 变体进入染色质的沉积,也参与了 SAS。RNA/ChIP-seq 分析确定了 ASF1 在 PIF7 靶基因子集的直接调控中的作用。此外,遮荫引发的基因激活伴随着 H3.3 的富集,这是由 PIF7-ASF1-HIRA 调控模块介导的。总的来说,我们的数据揭示了 PIF7 招募 ASF1-HIRA 增加 H3.3 掺入染色质以促进基因转录,从而使植物能够有效地响应环境遮荫。