Muradov A, Petrasovits L, Davidson A, Scott K J
Department of Biochemistry, University of Queensland, Brisbane, Australia.
Plant Mol Biol. 1993 Oct;23(2):439-42. doi: 10.1007/BF00029021.
A barley cDNA clone (PRb-1) corresponding to an mRNA differentially induced in resistant compared to susceptible barley cultivars by powdery mildew infection was isolated and characterised. The deduced amino acid sequence revealed 24 amino acids comprising the signal peptide and 140 amino acids of the mature peptide (15 kDa). This showed close homology to PR-1-like proteins, which have been isolated from maize, tobacco, tomato and Arabidopsis thaliana. Northern blot analysis showed accumulation of the corresponding mRNA 12 h after inoculation of resistant barley cultivars with Erysiphe graminis. Increased expression of the PRb-1 gene was also observed in resistant compared with near-isogenic susceptible barley plants following treatment with ethylene, salicylic acid, methyl jasmonate and 2,6-dichloro-isonicotinic acid.
分离并鉴定了一个大麦cDNA克隆(PRb - 1),该克隆对应于一种mRNA,在白粉病感染后,与感病大麦品种相比,抗病大麦品种中该mRNA被差异诱导。推导的氨基酸序列显示,其包含由24个氨基酸组成的信号肽和140个氨基酸的成熟肽(15 kDa)。这显示出与从玉米、烟草、番茄和拟南芥中分离出的类PR - 1蛋白具有高度同源性。Northern杂交分析表明,用禾本科布氏白粉菌接种抗病大麦品种12小时后,相应的mRNA开始积累。在用乙烯、水杨酸、茉莉酸甲酯和2,6 - 二氯异烟酸处理后,与近等基因感病大麦植株相比,抗病大麦植株中PRb - 1基因的表达也增加了。