Truernit E, Schmid J, Epple P, Illig J, Sauer N
Lehrstuhl Botanik II, Universität Erlangen-Nürnberg, Germany.
Plant Cell. 1996 Dec;8(12):2169-82. doi: 10.1105/tpc.8.12.2169.
A cDNA for the Arabidopsis STP4 gene (for sugar transport protein 4) was isolated, and the properties of the encoded protein were studied in Schizosaccharomyces pombe. The STP4 monosaccharide H+ symporter is composed of 514 amino acids and has a calculated molecular mass of 57.1 kD. RNA gel blot analyses revealed that STP4 is expressed primarily in roots and flowers of Arabidopsis. This was shown in more detail with STP4 promoter-beta-glucuronidase (GUS) plants yielding strong STP4-driven GUS activity in root tips and anthers. Wounding of plants transformed with STP4-GUS constructs resulted in a rapid increase in GUS activity in cells directly adjacent to the lesion. This was confirmed by RNase protection analyses in Arabidopsis wild-type plants showing a strong, wound-induced increase in STP4 mRNA levels. STP4 expression was induced rapidly in suspension-cultured Arabidopsis cells that were treated with the Pseudomonas syringae elicitor or with chitin or in Arabidopsis plants that were exposed to fungal attacks. Our data suggest that the role of STP4 is to catalyze monosaccharide import into classic sinks, such as root tips and anthers, and, most importantly, to meet the increased carbohydrate demand of cells responding to environmental stress.
分离出了拟南芥STP4基因(糖转运蛋白4)的cDNA,并在粟酒裂殖酵母中研究了其编码蛋白的特性。STP4单糖H⁺同向转运体由514个氨基酸组成,计算分子量为57.1 kD。RNA凝胶印迹分析表明,STP4主要在拟南芥的根和花中表达。这在STP4启动子-β-葡萄糖醛酸酶(GUS)植株中得到了更详细的体现,这些植株在根尖和花药中产生了强烈的由STP4驱动的GUS活性。用STP4-GUS构建体转化的植株受到创伤后,损伤部位相邻细胞中的GUS活性迅速增加。这在拟南芥野生型植株的核糖核酸酶保护分析中得到了证实,该分析表明STP4 mRNA水平在创伤诱导下大幅增加。用丁香假单胞菌激发子或几丁质处理悬浮培养的拟南芥细胞,或使拟南芥植株遭受真菌攻击后,STP4的表达迅速被诱导。我们的数据表明,STP4的作用是催化单糖导入典型的库,如根尖和花药,最重要的是,满足响应环境胁迫的细胞对碳水化合物增加的需求。