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首页> 外文期刊>African Journal of Biotechnology >Agrobacterium mediated transformation of banana (Musa sp.) cv. Sukali Ndiizi (ABB) with a modified Carica papaya cystatin (CpCYS) gene
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Agrobacterium mediated transformation of banana (Musa sp.) cv. Sukali Ndiizi (ABB) with a modified Carica papaya cystatin (CpCYS) gene

机译:农杆菌介导的香蕉(Musa sp。)简历的转化。具有修饰的番木瓜半胱氨酸蛋白酶抑制剂(CpCYS)基因的Sukali Ndiizi(ABB)

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Conventional banana breeding for pest and disease resistance is a very difficult and slow process due to the limited sources of resistance, sterility of cultivated banana varieties, high polyploidy levels, long cropping cycle and the lack of rapid screening methods. Molecular breeding using the transgenic approach with candidate genes such as cystatins offers an alternative method to banana improvement. Cystatin proteins inhibit the activity of cysteine proteases responsible for the breakdown of dietary proteins in the gut of many pests including nematodes resulting in protein deficiency. In this study, the papaya cystatin gene was introduced into the banana genome. Embryogenic cell suspension (ECS) cultures of the banana cultivar Sukali Ndiizi (ABB) were used as explants material for the successful transformation of banana. The?Carica papaya?cystatin gene (CpCYS-Mut89) previously modified to improve its inhibitory potential against banana pests was introduced into this cultivar using?Agrobacterium?tumefaciens,?strain LBA4404 and the?gus?reporter gene was used to observe successful transformation process.? We report the successful protocol for routine transformation of this cultivar, which was completed in six months with plant regeneration observed at a frequency of 23%. An additional four months was required to multiply the regenerant lines in order to have at least 20 plants per line for downstream challenging studies. Putatively transgenic plants were analyzed by PCR using?hpt?and?CpCYS-Mut89?specific primers to confirm the presence of transgenes. Out of 28 selected lines, 27 were positive for both?hpt?and?CpCYS-Mut89transgenes giving 96.4% transformation efficiency. Five lines were then selected on the basis of putative PCR positives and a Southern blot analysis gave hybridization signals with 1 to 4 copy number integration patterns characteristic of?Agrobacteriummediated transformation. These results confirm stable gene integration in East African banana cultivar cv. Sukali Ndiizi (genome group ABB) through an efficientAgrobacterium-mediated transformation protocol described for routine use in future improvement of this crop with genes of economic importance.
机译:由于有限的抗性来源,栽培的香蕉品种的不育性,多倍体水平高,种植周期长以及缺乏快速筛选方法,常规的用于病虫害抗性的香蕉育种是非常困难且缓慢的过程。使用转基因方法与候选基因(如胱抑素)进行分子育种为香蕉改良提供了另一种方法。胱抑素蛋白抑制半胱氨酸蛋白酶的活性,该半胱氨酸蛋白酶负责导致包括线虫在内的许多害虫的肠道中的膳食蛋白质分解,从而导致蛋白质缺乏。在这项研究中,木瓜半胱氨酸蛋白酶抑制剂基因被引入到香蕉基因组中。香蕉品种Sukali Ndiizi(ABB)的胚发生细胞悬浮液(ECS)培养用作成功转化香蕉的外植体材料。使用土壤杆菌农杆菌,菌株LBA4404将经过改良以提高其对香蕉害虫的抑制潜力的番木瓜番木瓜半胱氨酸蛋白酶抑制剂基因(CpCYS-Mut89)引入该品种中,并使用gus报道基因进行了成功的转化过程。?我们报告了该品种常规转化的成功方案,该方案在六个月内完成,观察到植物再生的频率为23%。为了使再生品系繁殖,还需要四个月的时间,以便每个品系至少有20株植物用于下游挑战性研究。通过PCR使用“ hpt”和“ CpCYS-Mut89”特异性引物对推定的转基因植物进行分析,以确认转基因的存在。在选定的28个品系中,有27个“ hpt”和“ CpCYS-Mut89”转基因均为阳性,转化效率为96.4%。然后根据推定的PCR阳性结果选择5个品系,进行Southern印迹分析,得到具有农杆菌介导的转化特征的1-4个拷贝数整合模式的杂交信号。这些结果证实了在东非香蕉栽培品种cv中稳定的基因整合。 Sukali Ndiizi(基因组ABB)通过一种高效农杆菌介导的转化方案进行了描述,该方案可常规用于具有经济重要性基因的该作物的未来改良。

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