Zhai Mingming, Ao Zhengxiong, Qu Haoran, Guo Dongwei
College of Agronomy, Northwest A&F University, Yangling, Shaanxi, China.
Front Plant Sci. 2024 Apr 5;15:1347861. doi: 10.3389/fpls.2024.1347861. eCollection 2024.
Plant-specific VQ proteins have crucial functions in the regulation of plant growth and development, as well as in plant abiotic stress responses. Their roles have been well established in the model plant ; however, the functions of the potato VQ proteins have not been adequately investigated. The VQ protein core region contains a short FxxhVQxhTG amino acid motif sequence. In this study, the VQ31 protein from potato was cloned and functionally characterized. The complete open reading frame (ORF) size of StVQ31 is 672 bp, encoding 223 amino acids. Subcellular localization analysis revealed that StVQ31 is located in the nucleus. Transgenic plants overexpressing exhibited enhanced salt tolerance compared to wild-type (WT) plants, as evidenced by increased root length, germination rate, and chlorophyll content under salinity stress. The increased tolerance of transgenic plants was associated with increased osmotic potential (proline and soluble sugars), decreased MDA accumulation, decreased total protein content, and improved membrane integrity. These results implied that overexpression enhanced the osmotic potential of the plants to maintain normal cell growth. Compared to the WT, the transgenic plants exhibited a notable increase in antioxidant enzyme activities, reducing cell membrane damage. Furthermore, the real-time fluorescence quantitative PCR analysis demonstrated that regulated the expression of genes associated with the response to salt stress, including , and . These findings suggest that significantly impacts osmotic and antioxidant cellular homeostasis, thereby enhancing salt tolerance.
植物特有的VQ蛋白在植物生长发育调控以及植物非生物胁迫响应中具有关键作用。它们的作用在模式植物中已得到充分证实;然而,马铃薯VQ蛋白的功能尚未得到充分研究。VQ蛋白核心区域包含一个短的FxxhVQxhTG氨基酸基序序列。在本研究中,克隆了马铃薯的VQ31蛋白并对其进行了功能表征。StVQ31的完整开放阅读框(ORF)大小为672 bp,编码223个氨基酸。亚细胞定位分析表明StVQ31定位于细胞核。与野生型(WT)植物相比,过表达的转基因植物表现出增强的耐盐性,盐胁迫下根长、发芽率和叶绿素含量增加证明了这一点。转基因植物耐受性的提高与渗透势增加(脯氨酸和可溶性糖)、丙二醛积累减少、总蛋白含量降低以及膜完整性改善有关。这些结果表明,过表达增强了植物的渗透势以维持正常细胞生长。与WT相比,转基因植物的抗氧化酶活性显著增加,减少了细胞膜损伤。此外,实时荧光定量PCR分析表明,StVQ31调节了与盐胁迫响应相关基因的表达,包括[具体基因名称缺失]、[具体基因名称缺失]和[具体基因名称缺失]。这些发现表明,StVQ31显著影响渗透和抗氧化细胞内稳态,从而增强耐盐性。