Harbaoui Marwa, Ben Romdhane Walid, Ben Hsouna Anis, Brini Faiçal, Ben Saad Rania
Biotechnology and Plant Improvement Laboratory, Center of Biotechnology of Sfax, University of Sfax, B.P "1177", 3018, Sfax, Tunisia.
Plant Production Department, College of Food and Agricultural Sciences, King Saud University, P.O. Box 2460, Riyadh, 11451, Saudi Arabia.
Protoplasma. 2021 Sep;258(5):1047-1059. doi: 10.1007/s00709-021-01622-4. Epub 2021 Feb 16.
TdAnn6 is a gene encoding an annexin protein in durum wheat (Triticum durum). The function of TdAnn6 in plant response to stress is not yet clearly understood. Here, we isolated TdAnn6 and characterized it in genetically modified Arabidopsis thaliana. Expressing TdAnn6 in Arabidopsis coincided with an improvement in stress tolerance at germination and seedling stages. In addition, TdAnn6-expressing seedling antioxidant activities were improved with lower level of malondialdehyde, and enhanced transcript levels of six stress-related genes during salt/osmotic stresses. Under greenhouse conditions, the TdAnn6 plants exhibited increased tolerance to salt or drought stress. To deepen our understanding of TdAnn6 function, we isolated a 1515-bp genomic fragment upstream of its coding sequence, designated as PrTdAnn6. The PrTdAnn6 promoter was fused to the β-glucuronidase reporter gene and transferred to Arabidopsis. By histochemical GUS staining, GUS activity was detected in the roots, leaves, and floral organs, but no activity was detected in the seeds. Furthermore, we noticed a high stimulation of promoter activity when A. thaliana seedlings were exposed to NaCl, mannitol, ABA, GA, and cold conditions. This cross-talk between tissue-specific expression and exogenous stress stimulation may provide additional layers of regulation for salt and osmotic stress responses in crops.
TdAnn6是一个在硬粒小麦(Triticum durum)中编码膜联蛋白的基因。目前尚不清楚TdAnn6在植物应激反应中的功能。在此,我们分离了TdAnn6并在转基因拟南芥中对其进行了表征。在拟南芥中表达TdAnn6与发芽期和幼苗期的胁迫耐受性提高相吻合。此外,表达TdAnn6的幼苗抗氧化活性得到改善,丙二醛水平降低,并且在盐/渗透胁迫期间六个胁迫相关基因的转录水平增强。在温室条件下,表达TdAnn6的植株对盐或干旱胁迫的耐受性增强。为了加深我们对TdAnn6功能的理解,我们分离了其编码序列上游1515 bp的基因组片段,命名为PrTdAnn6。将PrTdAnn6启动子与β-葡萄糖醛酸酶报告基因融合并转入拟南芥。通过组织化学GUS染色,在根、叶和花器官中检测到GUS活性,但在种子中未检测到活性。此外,我们注意到当拟南芥幼苗暴露于NaCl、甘露醇、ABA、GA和低温条件时,启动子活性受到高度刺激。这种组织特异性表达与外源胁迫刺激之间的相互作用可能为作物盐胁迫和渗透胁迫反应提供额外层面的调控。