Oranab Sadaf, Ghaffar Abdul, Kiran Shumaila, Yameen Muhammad, Munir Bushra, Zulfiqar Saman, Abbas Shakeel, Batool Fatima, Umar Farooq Muhammad, Ahmad Bilal, Ilyas Hafsa, Ahmad Aftab
Department of Biochemistry, Government College University, Faisalabad 38000, Pakistan.
Department of Applied Chemistry, Government College University, Faisalabad 38000, Pakistan.
Saudi J Biol Sci. 2021 Oct;28(10):5800-5807. doi: 10.1016/j.sjbs.2021.06.027. Epub 2021 Jun 17.
Cyclic nucleotide gated ion channels (CNGCs) in plants have very important role in signaling and development. The study reports role of CNGC19 and CNGC20 in salt stress in genome wide analysis showed that and are related to salt stress with maximum expression after 6 h in . The position of inserted T-DNA was determined ( through TAIL-PCR for activation tagged mutants of and under salt stress. The expression of and after cloning under 35S promoter of expression vectors pBCH1 and pEarleyGate100 was determined in by real-time PCR analysis. Genome wide analysis showed that AtCNGC11 had lowest and AtCNGC20 highest molecular weight as well as number of amino acid residues. expression of and was enhanced through T-DNA insertion and 35S promoter in over-expressed plants under high salt concentration. was activated twice in control and about five times under 150 mM NaCl stress level, and expression value was also higher than . Phenotypically, over-expressed plants and calli were healthier while knock-out plants and calli showed retarded growth under salinity stress. The study provides new insight for the role of AtCNGC19 and AtCNGC20 under salt stress regulation in and will be helpful for improvement of crop plants for salt stress to combat food shortage and security.
植物中的环核苷酸门控离子通道(CNGCs)在信号传导和发育过程中发挥着非常重要的作用。该研究报告了CNGC19和CNGC20在盐胁迫中的作用,全基因组分析表明,它们与盐胁迫相关,在拟南芥中6小时后表达量最高。通过热不对称交错PCR(TAIL-PCR)确定了盐胁迫下AtCNGC19和AtCNGC20激活标签突变体中插入的T-DNA的位置。通过实时PCR分析,在拟南芥中测定了AtCNGC19和AtCNGC20在表达载体pBCH1和pEarleyGate100的35S启动子下克隆后的表达情况。全基因组分析表明,AtCNGC11的分子量和氨基酸残基数最低,AtCNGC20最高。在高盐浓度下,过表达植株中AtCNGC19和AtCNGC20的表达通过T-DNA插入和35S启动子得到增强。AtCNGC19在对照中被激活两次,在150 mM NaCl胁迫水平下被激活约五次,其表达值也高于AtCNGC20。从表型上看,过表达植株和愈伤组织更健康,而敲除植株和愈伤组织在盐胁迫下生长受阻。该研究为拟南芥中AtCNGC19和AtCNGC20在盐胁迫调控中的作用提供了新的见解,将有助于改良作物以应对盐胁迫,解决粮食短缺和安全问题。