Hdira Sabrine, Haddoudi Loua, Hanana Mohsen, Romero Irene, Mahjoub Asma, Ben Jouira Hatem, Ludidi Ndiko, Sanchez-Ballesta Maria Teresa, Abdelly Chedly, Badri Mounawer
Laboratory of Extremophile Plants, Centre of Biotechnology of Borj Cedria, B.P. 901, Hammam-Lif 2050, Tunisia.
Faculty of Mathematical, Physical and Natural Sciences of Tunis, Campus Universitaire El-Manar, University of Tunis El Manar, El Manar 2092, Tunisia.
Plants (Basel). 2021 Apr 20;10(4):808. doi: 10.3390/plants10040808.
We used an integrated morpho-physiological, biochemical, and genetic approach to investigate the salt responses of four lines (TN1.11, TN6.18, JA17, and A10) of . Results showed that TN1.11 exhibited a high tolerance to salinity, compared with the other lines, recording a salinity induced an increase in soluble sugars and soluble proteins, a slight decrease in malondialdehyde (MDA) accumulation, and less reduction in plant biomass. TN6.18 was the most susceptible to salinity as it showed less plant weight, had elevated levels of MDA, and lower levels of soluble sugars and soluble proteins under salt stress. As transcription factors of the APETALA2/ethylene responsive factor (AP2/ERF) family play important roles in plant growth, development, and responses to biotic and abiotic stresses, we performed a functional characterization of gene. Real-time PCR analysis revealed that is mainly expressed in roots and is inducible by NaCl and low temperature. Additionally, under salt stress, a greater increase in the expression of was found in TN1.11 plants than that in TN6.18. Therefore, the pattern of expression may provide a useful marker for discriminating among lines of and can be used as a tool in breeding programs aiming at obtaining lines with improved salt tolerance.
我们采用综合的形态生理、生化和遗传方法来研究[植物名称]的四个品系(TN1.11、TN6.18、JA17和A10)的盐胁迫响应。结果表明,与其他品系相比,TN1.11对盐胁迫表现出较高的耐受性,盐胁迫诱导其可溶性糖和可溶性蛋白增加,丙二醛(MDA)积累略有减少,植物生物量减少较少。TN6.18对盐胁迫最为敏感,因为在盐胁迫下它的植株重量较轻,MDA水平升高,可溶性糖和可溶性蛋白水平较低。由于APETALA2/乙烯响应因子(AP2/ERF)家族的转录因子在植物生长、发育以及对生物和非生物胁迫的响应中发挥重要作用,我们对[基因名称]进行了功能鉴定。实时定量PCR分析表明,[基因名称]主要在根中表达,且受NaCl和低温诱导。此外,在盐胁迫下,TN1.11植株中[基因名称]的表达增幅大于TN6.18。因此,[基因名称]的表达模式可能为区分[植物名称]的不同品系提供有用的标记,并可作为旨在获得耐盐性提高的[植物名称]品系的育种计划中的一种工具。