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首页> 外文期刊>World Journal of Microbiology & Biotechnology >Development of Agrobacterium-mediated transformation of highly valued hill banana cultivar Virupakshi (AAB) for resistance to BBTV disease
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Development of Agrobacterium-mediated transformation of highly valued hill banana cultivar Virupakshi (AAB) for resistance to BBTV disease

机译:农杆菌介导的高价值山香蕉品种Virupakshi(AAB)对BBTV病的抗性转化

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摘要

One of the most severe viral diseases of hill banana is caused by banana bunchy top virus (BBTV), a nanovirus transmitted by the aphid Pentalonia nigronervosa. In this study, we reported the Agrobacterium-mediated transformation on a highly valued hill banana cultivar Virupakshi (AAB) for resistance to BBTV disease. The target of the RNA interference (RNAi) is the rep gene, encoded by the BBTV-DNA1. In order to develop RNAi construct targeting the BBTV rep gene, the full-length rep gene of 870 bp was polymerase chain reaction amplified from BBTV infected hill banana sample DNA, cloned and confirmed by DNA sequencing. The partial rep gene fragment was cloned in sense and anti sense orientation in the RNAi intermediate vector, pSTARLING-A. After cloning in pSTARLING-A, the cloned RNAi gene cassette was released by NotI enzyme digestion and cloned into the NotI site of binary vector, pART27. Two different explants, embryogenic cells and embryogenic cell suspension derived microcalli were used for co-cultivation. Selection was done in presence of 100 mg/L kanamycin. In total, 143 putative transgenic hill banana lines were generated and established in green house condition. The presence of the transgenes was confirmed in the selected putative transgenic hill banana lines by PCR and reverse transcription PCR analyses. Transgenic hill banana plants expressing RNAi-BBTV rep were obtained and shown to resist infection by BBTV. The transformed plants are symptomless, and the replication of challenge BBTV almost completely suppressed. Hence, the RNAi mediating resistances were shown to be effective management of BBTV in hill banana.
机译:香蕉山最严重的病毒性疾病之一是由香蕉束顶病毒(BBTV)引起的,该病毒是由蚜虫Pentalonia nigronervosa传播的一种纳米病毒。在这项研究中,我们报道了农杆菌介导的对高价值山香蕉品种Virupakshi(AAB)的抗BBTV疾病的转化。 RNA干扰(RNAi)的目标是rep基因,由BBTV-DNA1编码。为了开发针对BBTV rep基因的RNAi构建体,从BBTV感染的山香蕉样品DNA中扩增了870 bp的全长rep基因,进行了聚合酶链反应,克隆并通过DNA测序确认。将部分rep基因片段以有义和反义方向克隆到RNAi中间载体pSTARLING-A中。克隆到pSTARLING-A中后,通过NotI酶消化释放出克隆的RNAi基因盒,并将其克隆到二元载体pART27的NotI位点中。将两种不同的外植体,胚发生细胞和胚发生细胞悬浮液衍生的微愈伤组织用于共培养。在100 mg / L卡那霉素存在下进行选择。总共在温室条件下产生并建立了143个推定的转基因山香蕉品系。通过PCR和逆转录PCR分析,在选择的推定的转基因山香蕉品系中证实了转基因的存在。获得了表达RNAi-BBTV rep的转基因山香蕉植物,并显示出抵抗BBTV的感染。转化的植物是无症状的,挑战性BBTV的复制几乎被完全抑制。因此,RNAi介导的抗药性被证明是对香蕉山中BBTV的有效管理。

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