Linthorst H J, van der Does C, Brederode F T, Bol J F
Department of Biochemistry, Leiden University, Netherlands.
Plant Mol Biol. 1993 Feb;21(4):685-94. doi: 10.1007/BF00014551.
Two sets of clones were isolated from a tobacco cDNA library, utilizing as a probe a PCR fragment obtained from tomato cDNA using a degenerate primer based on the sequence of tomato systemin. Contrary to expectation, the clones did not correspond to tobacco homologues of tomato pro-systemin. However, the cDNAs encoded two highly similar proteins with extensive structural homology to cysteine proteinases from a wide range of plant and animal species. Northern blot analyses showed that in unstressed tobacco leaf the genes for the putative proteinases are expressed according to a circadian rhythm. Furthermore, incision wounding enhances the expression approximately six-fold. Other forms of stress, such as infection with tobacco mosaic virus, treatment with ethephon or UV light do not result in induced expression of the tobacco cysteine proteinase genes.
利用基于番茄系统素序列的简并引物从番茄cDNA中获得的PCR片段作为探针,从烟草cDNA文库中分离出两组克隆。与预期相反,这些克隆与番茄前系统素的烟草同源物不对应。然而,这些cDNA编码了两种高度相似的蛋白质,它们与来自广泛植物和动物物种的半胱氨酸蛋白酶具有广泛的结构同源性。Northern印迹分析表明,在未受胁迫的烟草叶片中,假定蛋白酶的基因按昼夜节律表达。此外,切割伤口可使表达增强约6倍。其他形式的胁迫,如感染烟草花叶病毒、用乙烯利处理或紫外线照射,不会导致烟草半胱氨酸蛋白酶基因的诱导表达。