Department of Biology, Duke University, Durham, NC, 27708, USA.
U.S. Department of Agriculture, Agricultural Research Service, Plant Science Research Unit, Raleigh, NC, 27607, USA.
Nat Commun. 2024 Sep 3;15(1):7694. doi: 10.1038/s41467-024-52033-x.
DELLA proteins are conserved master growth regulators that play a central role in controlling plant development in response to internal and environmental cues. DELLAs function as transcription regulators, which are recruited to target promoters by binding to transcription factors (TFs) and histone H2A via their GRAS domain. Recent studies showed that DELLA stability is regulated post-translationally via two mechanisms, phytohormone gibberellin-induced polyubiquitination for its rapid degradation, and Small Ubiquitin-like Modifier (SUMO)-conjugation to increase its accumulation. Moreover, DELLA activity is dynamically modulated by two distinct glycosylations: DELLA-TF interactions are enhanced by O-fucosylation, but inhibited by O-linked N-acetylglucosamine (O-GlcNAc) modification. However, the role of DELLA phosphorylation remains unclear as previous studies showing conflicting results ranging from findings that suggest phosphorylation promotes or reduces DELLA degradation to others indicating it has no effect on its stability. Here, we identify phosphorylation sites in REPRESSOR OF ga1-3 (RGA, an AtDELLA) purified from Arabidopsis by mass spectrometry analysis, and show that phosphorylation of two RGA peptides in the PolyS and PolyS/T regions enhances RGA activity by promoting H2A binding and RGA association with target promoters. Notably, phosphorylation does not affect RGA-TF interactions or RGA stability. Our study has uncovered a molecular mechanism of phosphorylation-induced DELLA activity.
DELLA 蛋白是保守的主要生长调节剂,在响应内部和环境信号控制植物发育方面发挥着核心作用。DELLA 作为转录调节剂发挥作用,通过其 GRAS 结构域与转录因子 (TF) 和组蛋白 H2A 结合,被招募到靶启动子上。最近的研究表明,DELLA 的稳定性通过两种机制进行翻译后调控,即赤霉素诱导的多泛素化使其快速降解,以及通过小泛素样修饰物 (SUMO) 缀合来增加其积累。此外,DELLA 活性通过两种不同的糖基化动态调节:O-岩藻糖基化增强 DELLA-TF 相互作用,但 O-连接的 N-乙酰葡糖胺 (O-GlcNAc) 修饰抑制其相互作用。然而,DELLA 磷酸化的作用仍然不清楚,因为之前的研究结果相互矛盾,从表明磷酸化促进或减少 DELLA 降解的发现到其他表明它对其稳定性没有影响的发现。在这里,我们通过质谱分析鉴定了从拟南芥中纯化的 REPRESSOR OF ga1-3 (RGA,一种 AtDELLA) 中的磷酸化位点,并表明在 PolyS 和 PolyS/T 区域的两个 RGA 肽的磷酸化通过促进 H2A 结合和 RGA 与靶启动子的结合来增强 RGA 活性。值得注意的是,磷酸化不影响 RGA-TF 相互作用或 RGA 稳定性。我们的研究揭示了磷酸化诱导的 DELLA 活性的分子机制。