State Key Laboratory of Crop Stress Biology for Arid Areas/Shaanxi Key Laboratory of Apple, College of Horticulture, Northwest A&F University, Yangling, Shaanxi 712100, China.
College of Horticulture, Northwest A&F University, Yangling, Shaanxi 712100, China.
Plant Physiol. 2023 Nov 22;193(4):2711-2733. doi: 10.1093/plphys/kiad468.
Understanding the molecular regulation of plant response to drought is the basis of drought-resistance improvement through molecular strategies. Here, we characterized apple (Malus × domestica) histone deacetylase 6 (MdHDA6), which negatively regulates apple drought tolerance by catalyzing deacetylation on histones associated with drought-responsive genes. Transgenic apple plants over-expressing MdHDA6 were less drought-tolerant, while those with down-regulated MdHDA6 expression were more drought-resistant than nontransgenic apple plants. Transcriptomic and histone 3 acetylation (H3ac) Chromatin immunoprecipitation-seq analyses indicated that MdHDA6 could facilitate histone deacetylation on the drought-responsive genes, repressing gene expression. Moreover, MdHDA6 interacted with the abscisic acid (ABA) signaling transcriptional factor, ABSCISIC ACID-INSENSITIVE 5 (MdABI5), forming the MdHDA6-MdABI5 complex. Interestingly, MdHDA6 facilitated histone deacetylation on the drought-responsive genes regulated by MdABI5, resulting in gene repression. Furthermore, a dual-Luc experiment showed that MdHDA6 could repress the regulation of a drought-responsive gene, RESPONSIVE TO DESICCATION 29A (MdRD29A) activated by MdABI5. On the one hand, MdHDA6 can facilitate histone deacetylation and gene repression on the positive drought-responsive genes to negatively regulate drought tolerance in apple. On the other hand, MdHDA6 directly interacts with MdABI5 and represses the expression of genes downstream of MdABI5 via histone deacetylation around these genes to reduce drought tolerance. Our study uncovers a different drought response regulatory mechanism in apple based on the MdHDA6-MdABI5 complex function and provides the molecular basis for drought-resistance improvement in apple.
理解植物对干旱响应的分子调控是通过分子策略提高抗旱性的基础。在这里,我们对苹果(Malus × domestica)组蛋白去乙酰化酶 6(MdHDA6)进行了表征,该酶通过催化与干旱响应基因相关的组蛋白去乙酰化来负调控苹果的耐旱性。过表达 MdHDA6 的转基因苹果植株耐旱性降低,而下调 MdHDA6 表达的转基因苹果植株比非转基因苹果植株更耐旱。转录组和组蛋白 3 乙酰化(H3ac)染色质免疫沉淀测序分析表明,MdHDA6 可以促进干旱响应基因的组蛋白去乙酰化,抑制基因表达。此外,MdHDA6 与脱落酸(ABA)信号转导转录因子 ABSCISIC ACID-INSENSITIVE 5(MdABI5)相互作用,形成 MdHDA6-MdABI5 复合物。有趣的是,MdHDA6 促进了由 MdABI5 调控的干旱响应基因的组蛋白去乙酰化,导致基因抑制。此外,双荧光素酶实验表明,MdHDA6 可以抑制由 MdABI5 激活的干旱响应基因 RESPONSIVE TO DESICCATION 29A(MdRD29A)的调控。一方面,MdHDA6 可以促进与干旱相关的正调控基因的组蛋白去乙酰化和基因抑制,从而负调控苹果的耐旱性。另一方面,MdHDA6 直接与 MdABI5 相互作用,并通过这些基因周围的组蛋白去乙酰化来抑制 MdABI5 下游基因的表达,从而降低耐旱性。我们的研究揭示了基于 MdHDA6-MdABI5 复合物功能的苹果中不同的干旱响应调控机制,并为提高苹果的抗旱性提供了分子基础。