Wang Liuqiang, Li Zhen, Lu Mengzhu, Wang Yucheng
State Key Laboratory of Tree Genetics and Breeding, Key Laboratory of Tree Breeding and Cultivation of the State Forestry Administration, Research Institute of Forestry, Chinese Academy of ForestryBeijing, China.
Key Laboratory of Biogeography and Bioresource in Arid Land, Xinjiang Institute of Ecology and Geography, Chinese Academy of SciencesUrumqi, China.
Front Plant Sci. 2017 Apr 26;8:635. doi: 10.3389/fpls.2017.00635. eCollection 2017.
NAC (NAM, ATAF1/2, and CUC2) proteins play critical roles in many plant biological processes and environmental stress. However, NAC proteins from have not been functionally characterized. Here, we studied a gene from . , in response to salt and osmotic stresses. ThNAC13 is a nuclear protein with a C-terminal transactivation domain. ThNAC13 can bind to NAC recognized sites and calmodulin-binding NAC (CBNAC) binding element. Overexpression of in improved seed germination rate and increased root growth and fresh weight gain under salt or osmotic stress. Transgenic . plants transiently overexpressing and with RNAi-silenced were generated for gain- and loss-of-function experiments. Following exposure to salt or osmotic stress, overexpression of induced superoxide dismutase (SOD) and peroxidase (POD) activities, chlorophyll and proline contents; decreased the reactive oxygen species (ROS) and malondialdehyde levels; and reduced electrolyte leakage rates in both transgenic and plants. In contrast, RNAi-silenced showed the opposite results in transgenic . Furthermore, induced the expression of s and s in transgenic . These results suggest that ThNAC13 improves salt and osmotic tolerance by enhancing the ROS-scavenging capability and adjusting osmotic potential.
NAC(NAM、ATAF1/2和CUC2)蛋白在许多植物生物学过程和环境胁迫中发挥着关键作用。然而,来自[具体来源未明确]的NAC蛋白尚未进行功能表征。在此,我们研究了来自[具体来源未明确]的一个[具体基因名称未明确]基因。[具体基因名称未明确],响应盐胁迫和渗透胁迫。ThNAC13是一种具有C端反式激活结构域的核蛋白。ThNAC13能与NAC识别位点和钙调蛋白结合NAC(CBNAC)结合元件结合。在[具体植物名称未明确]中过表达[具体基因名称未明确]可提高种子萌发率,并在盐胁迫或渗透胁迫下增加根的生长和鲜重。构建了瞬时过表达[具体基因名称未明确]和RNAi沉默[具体基因名称未明确]的转基因[具体植物名称未明确]植株用于功能获得和功能缺失实验。在盐胁迫或渗透胁迫处理后,过表达[具体基因名称未明确]诱导了超氧化物歧化酶(SOD)和过氧化物酶(POD)活性、叶绿素和脯氨酸含量;降低了活性氧(ROS)和丙二醛水平;并降低了转基因[具体植物名称未明确]和[具体植物名称未明确]植株的电解质渗漏率。相反,RNAi沉默[具体基因名称未明确]在转基因[具体植物名称未明确]中显示出相反的结果。此外,[具体基因名称未明确]诱导了转基因[具体植物名称未明确]中[具体基因名称未明确]和[具体基因名称未明确]的表达。这些结果表明,ThNAC13通过增强ROS清除能力和调节渗透势来提高盐胁迫和渗透胁迫耐受性。