Yi So Young, Ku Seong Sub, Sim Hee-Jung, Kim Sang-Kyu, Park Ji Hyun, Lyu Jae Il, So Eun Jin, Choi So Yeon, Kim Jonghyun, Ahn Myung Suk, Kim Suk Weon, Park Hyunwoo, Jeong Won Joong, Lim Yong Pyo, Min Sung Ran, Liu Jang Ryol
Plant Systems Engineering Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Institute of Agricultural Science, Chungnam National University, Daejeon, South Korea.
Front Plant Sci. 2017 Nov 17;8:1965. doi: 10.3389/fpls.2017.01965. eCollection 2017.
salt-responsive gene 1 () was engineered for expression in higher plants, and gene construction was stably incorporated into tobacco plants. We investigated the role of Sysr1 [a member of the alcohol dehydrogenase (ADH) superfamily] by examining the salt tolerance of -overexpressing (-OX) tobacco plants using quantitative real-time polymerase chain reactions, gas chromatography-mass spectrometry, and bioassays. The -OX plants exhibited considerably increased ADH activity and tolerance to salt stress conditions. Additionally, the expression levels of several stress-responsive genes were upregulated. Moreover, airborne signals from salt-stressed -OX plants triggered salinity tolerance in neighboring wild-type (WT) plants. Therefore, Sysr1 enhanced the interconversion of aldehydes to alcohols, and this occurrence might affect the quality of green leaf volatiles (GLVs) in -OX plants. Actually, the -3-hexenol level was approximately twofold higher in -OX plants than in WT plants within 1-2 h of wounding. Furthermore, analyses of WT plants treated with vaporized GLVs indicated that -3-hexenol was a stronger inducer of stress-related gene expression and salt tolerance than -2-hexenal. The results of the study suggested that increased C alcohol (-3-hexenol) induced the expression of resistance genes, thereby enhancing salt tolerance of transgenic plants. Our results revealed a role for ADH in salinity stress responses, and the results provided a genetic engineering strategy that could improve the salt tolerance of crops.
盐响应基因1()被设计用于在高等植物中表达,并且基因构建体被稳定整合到烟草植株中。我们通过使用定量实时聚合酶链反应、气相色谱 - 质谱联用和生物测定法检测过表达(-OX)烟草植株的耐盐性,来研究Sysr1[醇脱氢酶(ADH)超家族的成员之一]的作用。-OX植株表现出ADH活性显著增加以及对盐胁迫条件的耐受性增强。此外,几个胁迫响应基因的表达水平上调。而且,来自盐胁迫的 -OX植株的空气传播信号触发了邻近野生型(WT)植株的耐盐性。因此,Sysr1增强了醛向醇的相互转化,并且这种情况可能会影响 -OX植株中绿叶挥发物(GLVs)的质量。实际上,在受伤后1 - 2小时内,-OX植株中的反 - 3 - 己烯醇水平比WT植株中大约高两倍。此外,对用汽化GLVs处理的WT植株的分析表明,反 - 3 - 己烯醇比反 - 2 - 己烯醛是更强的胁迫相关基因表达和耐盐性诱导剂。该研究结果表明,增加的C醇(反 - 3 - 己烯醇)诱导抗性基因的表达,从而增强转基因植株的耐盐性。我们的结果揭示了ADH在盐胁迫响应中的作用,并且这些结果提供了一种可以提高作物耐盐性的基因工程策略。