ARR1 and ARR12 modulate arsenite toxicity responses in Arabidopsis roots by transcriptionally controlling the actions of NIP1;1 and NIP6;1

细胞分裂素 拟南芥 转录组 细胞生物学 拟南芥 侧根 生物 生长素 基因表达 遗传学 基因 突变体
作者
Ping Zhang,Fei Liu,Mostafa Abdelrahman,Qianqian Song,Fei Wu,Ruishan Li,Min Wu,Luís Herrera‐Estrella,Lam‐Son Phan Tran,Jin Xu
出处
期刊:Plant Journal [Wiley]
卷期号:120 (4): 1536-1551
标识
DOI:10.1111/tpj.17065
摘要

SUMMARY Cytokinin is central to coordinating plant adaptation to environmental stresses. Here, we first demonstrated the involvement of cytokinin in Arabidopsis responses to arsenite [As(III)] stress. As(III) treatment reduced cytokinin contents, while cytokinin treatment repressed further primary root growth in Arabidopsis plants under As(III) stress. Subsequently, we revealed that the cytokinin signaling members ARR1 and ARR12, the type‐B ARABIDOPSIS RESPONSE REGULATORs, participate in cytokinin signaling‐mediated As(III) responses in plants as negative regulators. A comprehensive transcriptome analysis of the arr1 and arr12 single and arr1,12 double mutants was then performed to decipher the cytokinin signaling‐mediated mechanisms underlying plant As(III) stress adaptation. Results revealed important roles for ARR1 and ARR12 in ion transport, nutrient responses, and secondary metabolite accumulation. Furthermore, using hierarchical clustering and regulatory network analyses, we identified two NODULIN 26‐LIKE INTRINSIC PROTEIN (NIP)‐encoding genes, NIP1;1 and NIP6;1 , potentially involved in ARR1/12‐mediated As(III) uptake and transport in Arabidopsis . By analyzing various combinations of arr and nip mutants, including high‐order triple and quadruple mutants, we demonstrated that ARR1 and ARR12 redundantly function as negative regulators of As(III) tolerance by acting upstream of NIP1;1 and NIP6;1 to modulate their function in arsenic accumulation. ChIP–qPCR, EMSA, and transient dual‐LUC reporter assays revealed that ARR1 and ARR12 transcriptionally activate the expression of NIP1;1 and NIP6;1 by directly binding to their promoters and upregulating their expression, leading to increased arsenic accumulation under As(III) stress. These findings collectively provide insights into cytokinin signaling‐mediated plant adaptation to excessive As(III), contributing to the development of crops with low arsenic accumulation.
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