State Key Laboratory of Plant Environmental Resilience, Frontiers Science Center for Molecular Design Breeding, College of Biological Sciences, China Agricultural University, Beijing, 100193, China.
Center for Crop Functional Genomics and Molecular Breeding, China Agricultural University, Beijing, 100193, China.
J Integr Plant Biol. 2024 Jul;66(7):1334-1350. doi: 10.1111/jipb.13677. Epub 2024 May 28.
Drought stress has negative effects on crop growth and production. Characterization of transcription factors that regulate the expression of drought-responsive genes is critical for understanding the transcriptional regulatory networks in response to drought, which facilitates the improvement of crop drought tolerance. Here, we identified an Alfin-like (AL) family gene ZmAL14 that negatively regulates drought resistance. Overexpression of ZmAL14 exhibits susceptibility to drought while mutation of ZmAL14 enhances drought resistance. An abscisic acid (ABA)-activated protein kinase ZmSnRK2.2 interacts and phosphorylates ZmAL14 at T38 residue. Knockout of ZmSnRK2.2 gene decreases drought resistance of maize. A dehydration-induced Rho-like small guanosine triphosphatase gene ZmROP8 is directly targeted and repressed by ZmAL14. Phosphorylation of ZmAL14 by ZmSnRK2.2 prevents its binding to the ZmROP8 promoter, thereby releasing the repression of ZmROP8 transcription. Overexpression of ZmROP8 stimulates peroxidase activity and reduces hydrogen peroxide accumulation after drought treatment. Collectively, our study indicates that ZmAL14 is a negative regulator of drought resistance, which can be phosphorylated by ZmSnRK2.2 through the ABA signaling pathway, thus preventing its suppression on ZmROP8 transcription during drought stress response.
干旱胁迫对作物生长和产量有负面影响。鉴定调控干旱响应基因表达的转录因子对于理解转录调控网络应对干旱至关重要,这有助于提高作物的抗旱性。在这里,我们鉴定了一个 Alfin 样(AL)家族基因 ZmAL14,它负调控抗旱性。ZmAL14 的过表达表现出对干旱的敏感性,而 ZmAL14 的突变增强了抗旱性。一种脱落酸(ABA)激活的蛋白激酶 ZmSnRK2.2 与 ZmAL14 相互作用,并在 T38 残基处磷酸化 ZmAL14。ZmSnRK2.2 基因的敲除降低了玉米的抗旱性。一个脱水诱导的 Rho 样小分子 GTP 酶基因 ZmROP8 被 ZmAL14 直接靶向并抑制。ZmSnRK2.2 对 ZmAL14 的磷酸化防止其与 ZmROP8 启动子结合,从而解除 ZmROP8 转录的抑制。ZmROP8 的过表达刺激过氧化物酶活性,并减少干旱处理后过氧化氢的积累。总之,我们的研究表明,ZmAL14 是抗旱性的负调控因子,它可以通过 ABA 信号通路被 ZmSnRK2.2 磷酸化,从而防止其在干旱胁迫响应过程中抑制 ZmROP8 的转录。