Tachi Hiroyuki, Fukuda-Yamada Kumiko, Kojima Toshio, Shiraiwa Masakazu, Takahara Hidenari
Department of Applied Biological Resource Sciences, Ibaraki University, Chuo 3-21-1, Ami-machi, Inashiki-gun, Ibaraki 300-0393, Japan.
Plant Physiol Biochem. 2009 Jan;47(1):73-9. doi: 10.1016/j.plaphy.2008.09.012. Epub 2008 Oct 11.
In this study, we characterized a novel soybean gene encoding a neutral PR-5 protein and compared it to two acidic isoforms of soybean PR-5 protein. This gene, designated as Glycine max osmotin-like protein, b isoform (GmOLPb, accession no. AB370233), encoded a putative protein having the greatest similarity to chickpea PR-5b (89% identity). Unlike the two acidic PR-5, GmOLPa and P21, the protein had a C-terminal elongation responsible for possible vacuolar targeting and after maturation showed a calculated molecular mass of 21.9kDa with pI 6.0. The 3D models, predicted by the homology modeling, contained four alpha-helixes and 16 beta-strands and formed three characteristic domains. The two acidic PR-5 proteins also showed a 3D structure very similar to GmOLPb, although the electrostatic potential on molecular surface of each PR-5 was significantly different. In the study of the gene expression under conditions of high-salt stress, GmOLPb was highly induced in the leaves of the soybean, particularly in the lower part of a leaf. The expression started at 2h after initiation of the stress and was highly induced between 18-72h. Gene expression of P21e (protein homologous to P21) was transiently induced by high-salt stress, but took place earlier than the gene expressions of GmOLPa and GmOLPb. Such differential expression was observed also under investigation with methyl jasmonate and salicylic acid. These results suggested that each soybean PR-5 might play a distinctive role in the defensive system protecting the soybean plant against high-salt stress, particularly in the leaves of the soybean.
在本研究中,我们鉴定了一个编码中性PR-5蛋白的新型大豆基因,并将其与大豆PR-5蛋白的两种酸性同工型进行了比较。该基因被命名为大豆甘氨酸类渗透素样蛋白b同工型(GmOLPb,登录号AB370233),编码一种与鹰嘴豆PR-5b具有最高相似性的假定蛋白(同一性为89%)。与两种酸性PR-5(GmOLPa和P21)不同,该蛋白具有负责可能的液泡靶向的C末端延伸,成熟后计算分子量为21.9kDa,pI为6.0。通过同源建模预测的三维模型包含四个α螺旋和16个β链,并形成三个特征结构域。尽管每种PR-5分子表面的静电势存在显著差异,但两种酸性PR-5蛋白也显示出与GmOLPb非常相似的三维结构。在高盐胁迫条件下的基因表达研究中,GmOLPb在大豆叶片中被高度诱导,特别是在叶片的下部。胁迫开始后2小时开始表达,并在18-72小时之间被高度诱导。P21e(与P21同源的蛋白)的基因表达受到高盐胁迫的瞬时诱导,但比GmOLPa和GmOLPb的基因表达发生得更早。在用茉莉酸甲酯和水杨酸进行的研究中也观察到了这种差异表达。这些结果表明,每种大豆PR-5可能在保护大豆植株免受高盐胁迫的防御系统中发挥独特作用,特别是在大豆叶片中。