Hou Yujun, Wong Darren Chern Jan, Sun Xiaoming, Li Qingyun, Zhou Huimin, Meng Lin, Liao Xiaoli, Liang Zhenchang, Aryal Rishi, Wang Qingfeng, Xin Haiping
CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture/Center of Economic Botany, Core Botanical Gardens/Sino-Africa Joint Research Center, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan 430074, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Plant Physiol. 2024 Dec 2;196(4):2871-2889. doi: 10.1093/plphys/kiae483.
Cold stress is an adverse environmental factor that limits the growth and productivity of horticulture crops such as grapes (Vitis vinifera). In this study, we identified a grapevine cold-induced basic helix-loop-helix (bHLH) transcription factor (VvbHLH036). Overexpression and CRISPR/Cas9-mediated knockout (KO) of VvbHLH036 enhanced and decreased cold tolerance in grapevine roots, respectively. Transcriptome analysis of VvbHLH036-overexpressed roots identified threonine synthase (VvThrC1) as a potential downstream target of VvbHLH036. We confirmed that VvbHLH036 could bind the VvThrC1 promoter and activate its expression. Both the transcripts of VvThrC1 and the content of threonine were significantly induced in the leaves and roots of grapevine under cold treatment compared to controls. Conversely, these dynamics were significantly suppressed in the roots of CRISPR/Cas9-induced KO of VvbHLH036. These observations support the regulation of threonine accumulation by VvbHLH036 through VvThrC1 during cold stress in grapevine. Furthermore, overexpression and CRISPR/Cas9-mediated KO of VvThrC1 also confirmed its role in regulating threonine content and cold tolerance in transgenic roots at low temperature. Exogenous threonine treatment increased cold tolerance and reduced the accumulation of superoxide anions and hydrogen peroxide in grapevine leaves. Together, these findings point to the pivotal role of VvbHLH036 and VvThrC1 in the cold stress response in grapes by regulating threonine biosynthesis.
低温胁迫是一种不利的环境因素,限制了葡萄(Vitis vinifera)等园艺作物的生长和生产力。在本研究中,我们鉴定出一种葡萄低温诱导的碱性螺旋-环-螺旋(bHLH)转录因子(VvbHLH036)。VvbHLH036的过表达和CRISPR/Cas9介导的敲除(KO)分别增强和降低了葡萄根系的耐寒性。对VvbHLH036过表达根系的转录组分析确定苏氨酸合酶(VvThrC1)为VvbHLH036的潜在下游靶点。我们证实VvbHLH036可以结合VvThrC1启动子并激活其表达。与对照相比,低温处理下葡萄叶片和根系中VvThrC1的转录本和苏氨酸含量均显著诱导。相反,在CRISPR/Cas9诱导的VvbHLH036敲除根系中,这些动态变化被显著抑制。这些观察结果支持VvbHLH036在葡萄低温胁迫期间通过VvThrC1调节苏氨酸积累。此外,VvThrC1的过表达和CRISPR/Cas9介导的敲除也证实了其在调节转基因根系低温下苏氨酸含量和耐寒性中的作用。外源苏氨酸处理提高了葡萄叶片的耐寒性,并减少了超氧阴离子和过氧化氢的积累。总之,这些发现表明VvbHLH036和VvThrC1通过调节苏氨酸生物合成在葡萄低温胁迫响应中起关键作用。