Dean J D, Goodwin P H, Hsiang T
Department of Environmental Biology, University of Guelph, Guelph, Ontario N1G 2W1, Canada.
J Exp Bot. 2005 Jun;56(416):1525-33. doi: 10.1093/jxb/eri145. Epub 2005 Apr 18.
Four glutathione S-transferase (GST) genes, NbGSTU1, NbGSTU2, NbGSTU3, and NbGSTF1, were amplified from cDNA of Nicotiana benthamiana leaves infected with Colletotrichum destructivum using primers based on conserved regions of N. tabacum GST sequences. Expression of NbGSTU1 and NbGSTU3 increased progressively during infection by either C. destructivum or Colletotrichum orbiculare, except for a slight decrease by NbGSTU1 late in the infection, whereas NbGSTU2 and NbGSTF1 expression remained relatively constant. Each of the four genes was cloned into a PVX vector for virus-induced gene silencing, and reduced expression of the four genes was detected by RT-PCR. A statistically significant increase in susceptibility of N. benthamiana to infection following gene silencing was found only for NbGSTU1-silenced plants, which had 130% more lesions and 67% more colonization by C. orbiculare compared with control plants. These results demonstrate that the different GST genes respond in different ways to fungal infection, and at least one plant GST gene has an important role in disease development.
从感染毁灭炭疽菌的本氏烟草叶片的cDNA中,使用基于烟草GST序列保守区域设计的引物,扩增出四个谷胱甘肽S-转移酶(GST)基因,即NbGSTU1、NbGSTU2、NbGSTU3和NbGSTF1。在被毁灭炭疽菌或圆形炭疽菌感染期间,NbGSTU1和NbGSTU3的表达逐渐增加,不过NbGSTU1在感染后期略有下降,而NbGSTU2和NbGSTF1的表达则保持相对稳定。将这四个基因分别克隆到PVX载体中用于病毒诱导的基因沉默,并通过RT-PCR检测到这四个基因的表达降低。仅在沉默NbGSTU1的植株中发现,基因沉默后本氏烟草对感染的易感性有统计学意义的增加,与对照植株相比,其病斑多130%,圆形炭疽菌的定殖多67%。这些结果表明,不同的GST基因对真菌感染的反应方式不同,并且至少有一个植物GST基因在病害发展中起重要作用。