Department of Horticulture, Zhejiang University, Hangzhou, Zhejiang 310058, People's Republic of China.
Zhejiang Provincial Key Laboratory of Integrative Biology of Horticultural Plants, Hangzhou, Zhejiang 310058, People's Republic of China.
Plant Physiol. 2020 Dec;184(4):1684-1701. doi: 10.1104/pp.20.01188. Epub 2020 Oct 22.
Light is indispensable for the anthocyanin accumulation of red pear (). Anthocyanin biosynthesis is catalyzed by a series of enzymes encoded by structural genes, which are regulated by a MYB-basic/helix-loop-helix-WD repeat (MYB-bHLH-WDR [MBW]) complex. The bHLH proteins of subgroup (SG) IIIf are believed to be involved in the regulation of anthocyanin accumulation. In this study, we revealed that pear PpbHLH64, which belongs to SGIIIb, positively regulates anthocyanin biosynthesis and is regulated by light at the transcriptional and posttranslational levels. Specifically, an exposure to light induced expression and anthocyanin accumulation in pear fruit and calli. Under light conditions, pear calli overexpressing exhibited enhanced red coloration, whereas the anthocyanin accumulation decreased in the -RNA interference calli. Additionally, the transient overexpression of in pear fruit peel increased anthocyanin accumulation, whereas the virus-induced gene silencing of had the opposite effect. Further analyses indicated that PpbHLH64 is a transcriptional activator that directly binds to the promoter of to upregulate expression. Moreover, PpbHLH64 interacted with PpMYB10, but not with PpMYB114, to form an MBW complex that significantly induces the accumulation of anthocyanins. Furthermore, PpbHLH64 was targeted by CONSTITUTIVE PHOTOMORPHOGENIC1 in darkness for subsequent degradation by the 26S proteasome. A genetic analysis indicated that PpbHLH64 functions downstream of B-BOX18, a component of the light signal transduction pathway. However, we were unable to detect the direct interaction between PpbHLH64 and PpBBX18. The characterization of PpbHLH64 in this study highlights the importance of SGIIIb bHLH proteins for light-induced anthocyanin accumulation.
光是红梨()中花色苷积累所必需的。花色苷生物合成由一系列结构基因编码的酶催化,这些酶受 MYB-碱性/螺旋-环-螺旋-WD 重复(MYB-bHLH-WDR [MBW])复合物调节。亚群(SG)IIIf 的 bHLH 蛋白被认为参与了花色苷积累的调节。在这项研究中,我们揭示了属于 SGIIIb 的梨 PpbHLH64 正向调控花色苷生物合成,并在转录和翻译后水平受光调控。具体来说,光照诱导了梨果实和愈伤组织中 的表达和花色苷积累。在光照条件下,过表达 的梨愈伤组织表现出增强的红色着色,而 -RNA 干扰愈伤组织中的花色苷积累减少。此外,在梨果皮中瞬时过表达 增加了花色苷的积累,而 的病毒诱导基因沉默则产生了相反的效果。进一步的分析表明,PpbHLH64 是一种转录激活因子,它直接结合到 的启动子上,上调其表达。此外,PpbHLH64 与 PpMYB10 相互作用,但不与 PpMYB114 相互作用,形成一个 MBW 复合物,显著诱导花色苷的积累。此外,PpbHLH64 在黑暗中被 CONSTITUTIVE PHOTOMORPHOGENIC1 靶向,随后被 26S 蛋白酶体降解。遗传分析表明,PpbHLH64 是光信号转导途径的组成部分 B-BOX18 的下游因子。然而,我们未能检测到 PpbHLH64 与 PpBBX18 之间的直接相互作用。本研究中 PpbHLH64 的特性强调了 SGIIIb bHLH 蛋白在光诱导花色苷积累中的重要性。