Ikeda K, Nakayashiki H, Takagi M, Tosa Y, Mayama S
Laboratory of Plant Pathology, Faculty of Agriculture, Kobe University, Nada, Japan.
Mol Genet Genomics. 2001 Oct;266(2):318-25. doi: 10.1007/s004380100560.
MAGGY is a gypsy-like retrotransposon isolated from the plant pathogenic fungus Magnaporthe grisea. The ability of various stresses to activate MAGGY was tested in the original and in a heterologous host (Colletotrichum lagenarium), using beta-glucuronidase (GUS) as a reporter. The MAGGY promoter was activated in M. grisea by either heat shock, copper sulfate, or oxidative stress, but not by the antifungal substance p-coumaric acid. Transcriptional up-regulation of MAGGY RNA was also observed following heat shock and oxidative stress. The MAGGY promoter remained responsive to the above-mentioned stresses when transformed into a M. grisea isolate that had no endogenous MAGGY elements. In C. lagenarium, however, the MAGGY promoter showed only basal expression of GUS and no further up-regulation was induced by any of the stress treatments, suggesting that the stress-responding cis-element(s) in the MAGGY promoter is not functional in a wider range of fungi. The relationship between the activation of MAGGY by stress and phenotypic diversification in M. grisea, including variations in pathogenicity, is discussed.
MAGGY是从植物病原真菌稻瘟病菌中分离出的一种类吉普赛逆转座子。利用β-葡萄糖醛酸酶(GUS)作为报告基因,在原始宿主和异源宿主(葫芦炭疽菌)中测试了各种胁迫激活MAGGY的能力。MAGGY启动子在稻瘟病菌中可被热激、硫酸铜或氧化胁迫激活,但不能被抗真菌物质对香豆酸激活。热激和氧化胁迫后也观察到MAGGY RNA的转录上调。当将MAGGY启动子转化到无内源性MAGGY元件的稻瘟病菌分离株中时,它仍然对上述胁迫有反应。然而,在葫芦炭疽菌中,MAGGY启动子仅显示GUS的基础表达,任何胁迫处理均未诱导其进一步上调,这表明MAGGY启动子中的胁迫响应顺式元件在更广泛的真菌中不起作用。本文还讨论了胁迫激活MAGGY与稻瘟病菌表型多样化(包括致病性变异)之间的关系。