Key Laboratory of Saline-Alkali Vegetation Ecology Restoration (SAVER), Ministry of Education, Alkali Soil Natural Environmental Science Center (ASNESC), Northeast Forestry University, Harbin 150040, China.
State Key Laboratory of Subtropical Silviculture, Zhejiang A&F University, Hangzhou 311300, China.
Plant Sci. 2019 Apr;281:213-222. doi: 10.1016/j.plantsci.2018.12.007. Epub 2018 Dec 12.
Eukaryotic nucleases are involved in processes such as DNA restriction digestion, repair, recombination, transposition, and programmed cell death (PCD). Studies on the role of nucleases have mostly focused on PCD during plant development, while the information on nucleases involved in responses to different abiotic stress conditions remains limited. Here, we identified a Ca-dependent nuclease, AtCaN2, in Arabidopsis thaliana and characterized its activity, expression patterns, and involvement in plant responses to salt stress. AtCaN2 showed a dual endonuclease and exonuclease activity, being able to degrade circular plasmids, RNA, single-stranded DNA, and double-stranded DNA. Expression analysis showed that AtCaN2 was strongly induced in senescent siliques and by salt stress. Overexpression of AtCaN2 decreased the plant tolerance to salt stress conditions, leading to an excessive HO accumulation. However, an atcan2 mutant showed better tolerance to salt stress and a lower level of HO accumulation. Moreover, the expression of several genes (AtAPX1, AtGPX8, and AtSOD1), encoding reactive oxygen species-scavenging enzymes (ascorbate peroxidase 1, glutathione peroxidase 8, and superoxide dismutase 1, respectively), was highly induced in the atcan2 mutant under salt stress conditions. In addition, salt-stress-induced cell death was increased in the AtCaN2-overexpressing transgenic plant but decreased in the atcan2 mutant. On the basis of these findings, we conclude that AtCaN2 plays a negative role in plant tolerance to salt stress. A AtCaN2 knock out could reduce ROS accumulation, decrease ROS-induced PCD, and improve overall plant tolerance.
真核核酸酶参与 DNA 限制消化、修复、重组、转座和程序性细胞死亡 (PCD) 等过程。关于核酸酶作用的研究主要集中在植物发育过程中的 PCD 上,而关于参与应对不同非生物胁迫条件的核酸酶的信息仍然有限。在这里,我们在拟南芥中鉴定了一种 Ca 依赖性核酸酶 AtCaN2,并对其活性、表达模式及其在植物对盐胁迫反应中的参与进行了表征。AtCaN2 表现出双重内切酶和外切酶活性,能够降解环状质粒、RNA、单链 DNA 和双链 DNA。表达分析表明,AtCaN2 在衰老的蒴果和盐胁迫下强烈诱导。AtCaN2 的过表达降低了植物对盐胁迫条件的耐受性,导致 HO 积累过多。然而,atcan2 突变体对盐胁迫的耐受性更好,HO 积累水平更低。此外,在盐胁迫条件下,编码活性氧清除酶(抗坏血酸过氧化物酶 1、谷胱甘肽过氧化物酶 8 和超氧化物歧化酶 1)的几种基因(AtAPX1、AtGPX8 和 AtSOD1)的表达在 atcan2 突变体中高度诱导。此外,在 AtCaN2 过表达转基因植物中,盐胁迫诱导的细胞死亡增加,但在 atcan2 突变体中减少。基于这些发现,我们得出结论,AtCaN2 在植物对盐胁迫的耐受性中起负作用。AtCaN2 敲除可以减少 ROS 积累,减少 ROS 诱导的 PCD,并提高植物整体耐受性。