Australian Research Council Centre of Excellence in Plant Energy Biology, Waite Research Precinct, University of Adelaide, Glen Osmond, SA, Australia; and School of Agriculture, Food and Wine, and Waite Research Institute, Waite Research Precinct, University of Adelaide, Glen Osmond, SA, Australia; and Faculty of Agriculture and Forestry, Tay Nguyen University, 567 Le Duan, BMT, Dak Lak, Vietnam.
Australian Research Council Centre of Excellence in Plant Energy Biology, Waite Research Precinct, University of Adelaide, Glen Osmond, SA, Australia; and School of Agriculture, Food and Wine, and Waite Research Institute, Waite Research Precinct, University of Adelaide, Glen Osmond, SA, Australia.
Funct Plant Biol. 2023 Aug;50(8):633-648. doi: 10.1071/FP22260.
Dynamic changes in aquaporin gene expression occur during seed germination. One example is the ~30-fold increase in Arabidopsis thaliana PIP2;1 transcripts within 24h of seed imbibition. To investigate whether AtPIP2;1 can influence seed germination wild-type Columbia-0, single (Atpip2;1 ) and double (Atpip2;1-Atpip2;2 ) loss-of-function mutants, along with transgenic 2x35S::AtPIP2;1 over-expressing (OE) lines and null-segregant controls, were examined. The various genotypes were germinated in control and saline (75mM NaCl treatment) conditions and tested for germination efficiency, imbibed seed maximum cross sectional (MCS) area, imbibed seed mass, and seed Na+ and K+ content. Seed lacking functional AtPIP2;1 and/or AtPIP2;2 proteins or constitutively over-expressing AtPIP2;1 , had delayed germination in saline conditions relative to wild-type and null-segregant seed, respectively. Exposure to saline germination conditions resulted in Atpip2;1 mutants having greater imbibed seed mass and less accumulated Na+ than wild-type, whereas lines over-expressing AtPIP2;1 had reduced imbibed seed mass and greater seed K+ content than null-segregant control seed. The results imply a role for AtPIP2;1 in seed germination processes, whether directly through its capacity for water and ion transport or H2 O2 signalling, or indirectly through potentially triggering dynamic differential regulation of other aquaporins expressed during germination. Future research will aid in dissecting the aquaporin functions influencing germination and may lead to novel solutions for optimising germination in sub-optimal conditions, such as saline soils.
水通道蛋白基因的表达在种子萌发过程中会发生动态变化。例如,拟南芥 PIP2;1 的转录本在种子吸胀后 24 小时内增加了约 30 倍。为了研究 AtPIP2;1 是否能够影响种子萌发,我们检测了野生型哥伦比亚-0、单个(Atpip2;1)和双(Atpip2;1-Atpip2;2)功能丧失突变体以及过表达 2x35S::AtPIP2;1(OE)的转基因系和纯合缺失突变体的控制种子。在对照和盐(75mM NaCl 处理)条件下对各种基因型进行萌发,并检测其萌发效率、吸胀种子最大横截面积(MCS)、吸胀种子质量以及种子 Na+和 K+含量。缺乏功能性 AtPIP2;1 和/或 AtPIP2;2 蛋白的种子或组成型过表达 AtPIP2;1 的种子在盐条件下的萌发相对于野生型和纯合缺失突变体种子分别延迟。暴露于盐萌发条件下,Atpip2;1 突变体的吸胀种子质量较大,Na+积累较少,而过表达 AtPIP2;1 的系的吸胀种子质量减少,种子 K+含量较高。结果表明,AtPIP2;1 在种子萌发过程中发挥作用,无论是通过其水和离子运输能力或 H2 O2 信号转导直接作用,还是通过潜在触发萌发过程中表达的其他水通道蛋白的动态差异调节间接作用。未来的研究将有助于剖析影响萌发的水通道蛋白功能,并可能为优化在非最佳条件(如盐渍土壤)下的萌发提供新的解决方案。