Claes B, Dekeyser R, Villarroel R, Van den Bulcke M, Bauw G, Van Montagu M, Caplan A
Laboratorium voor Genetica, Rijksuniversiteit Gent, Belgium.
Plant Cell. 1990 Jan;2(1):19-27. doi: 10.1105/tpc.2.1.19.
Protein changes induced by salinity stress were investigated in the roots of the salt-sensitive rice cultivar Taichung native 1. We found eight proteins to be induced and obtained partial sequences of one with a molecular mass of 15 kilodaltons and an isoelectric point of 5.5. Using an oligonucleotide probe based on this information, a cDNA clone, salT, was selected and found to contain an open reading frame coding for a protein of 145 amino acid residues. salT mRNA accumulates very rapidly in sheaths and roots from mature plants and seedlings upon treatment with Murashige and Skoog salts (1%), air drying, abscisic acid (20 microM), polyethylene glycol (5%), sodium chloride (1%), and potassium chloride (1%). Generally, no induction was seen in the leaf lamina even when the stress should affect all parts of the plant uniformly. The organ-specific response of salT is correlatable with the pattern of Na+ accumulation during salt stress.
在盐敏感水稻品种台中本地1号的根部研究了盐胁迫诱导的蛋白质变化。我们发现有8种蛋白质被诱导,并获得了其中一种分子量为15千道尔顿、等电点为5.5的蛋白质的部分序列。基于此信息使用寡核苷酸探针,挑选出一个cDNA克隆salT,发现它含有一个编码145个氨基酸残基蛋白质的开放阅读框。用Murashige和Skoog盐(1%)、空气干燥、脱落酸(20微摩尔)、聚乙二醇(5%)、氯化钠(1%)和氯化钾(1%)处理后,salT mRNA在成熟植株和幼苗的叶鞘和根中迅速积累。通常,即使胁迫应均匀影响植物的所有部分,在叶片中也未观察到诱导现象。salT的器官特异性反应与盐胁迫期间Na+积累模式相关。