Plant Cell Culture Technology Section, Nuclear Agriculture and Biotechnology Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085, India.
Plant Cell Culture Technology Section, Nuclear Agriculture and Biotechnology Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400 085, India
AoB Plants. 2014 Jul 4;6:plu037. doi: 10.1093/aobpla/plu037.
In order to feed an ever-increasing world population, there is an urgent need to improve the production of staple food and fruit crops. The productivity of important food and fruit crops is constrained by numerous biotic and abiotic factors. The cultivation of banana, which is an important fruit crop, is severely threatened by Fusarium wilt disease caused by infestation by an ascomycetes fungus Fusarium oxysporum f. sp. cubense (Foc). Since there are no established edible cultivars of banana resistant to all the pathogenic races of Foc, genetic engineering is the only option for the generation of resistant cultivars. Since Foc is a hemibiotrophic fungus, investigations into the roles played by different cell-death-related genes in the progression of Foc infection on host banana plants are important. Towards this goal, three such genes namely MusaDAD1, MusaBAG1 and MusaBI1 were identified in banana. The study of their expression pattern in banana cells in response to Foc inoculation (using Foc cultures or fungal toxins like fusaric acid and beauvericin) indicated that they were indeed differentially regulated by fungal inoculation. Among the three genes studied, MusaBAG1 showed the highest up-regulation upon Foc inoculation. Further, in order to characterize these genes in the context of Foc infection in banana, we generated transgenic banana plants constitutively overexpressing the three genes that were later subjected to Foc bioassays in a contained greenhouse. Among the three groups of transgenics tested, transformed banana plants overexpressing MusaBAG1 demonstrated the best resistance towards Foc infection. Further, these plants also showed the highest relative overexpression of the transgene (MusaBAG1) among the three groups of transformed plants generated. Our study showed for the first time that native genes like MusaBAG1 can be used to develop transgenic banana plants with efficient resistance towards pathogens like Foc.
为了养活不断增长的世界人口,迫切需要提高主食和水果作物的产量。许多生物和非生物因素限制了重要粮食和水果作物的生产力。香蕉是一种重要的水果作物,其种植受到由子囊菌真菌尖孢镰刀菌古巴专化型(Foc)引起的枯萎病的严重威胁。由于没有可食用的香蕉品种对所有 Foc 致病株系都具有抗性,因此遗传工程是培育抗性品种的唯一选择。由于 Foc 是一种半活体真菌,因此研究不同细胞死亡相关基因在 Foc 感染宿主香蕉植物过程中所起的作用非常重要。为此,在香蕉中鉴定了三个这样的基因,即 MusaDAD1、MusaBAG1 和 MusaBI1。研究它们在香蕉细胞中对 Foc 接种(使用 Foc 培养物或真菌毒素,如 Fusaric acid 和 Beauvericin)的响应模式表明,它们确实受到真菌接种的差异调节。在所研究的三个基因中,MusaBAG1 在 Foc 接种后表现出最高的上调。此外,为了在香蕉中 Foc 感染的背景下对这些基因进行表征,我们生成了组成型过表达这三个基因的转基因香蕉植物,随后在封闭温室中对其进行了 Foc 生物测定。在测试的三组转基因中,过表达 MusaBAG1 的转基因香蕉植物对 Foc 感染表现出最好的抗性。此外,这些植物在产生的三组转基因植物中表现出最高的转基因(MusaBAG1)相对过表达。我们的研究首次表明,像 MusaBAG1 这样的天然基因可用于开发对 Foc 等病原体具有高效抗性的转基因香蕉植物。