香蕉抗枯萎病热带小种4的诱导突变。

J. Jankowicz-Cieslak, F. Goessnitzer, S. Datta, A. Viljoen, I. Ingelbrecht, B. Till
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引用次数: 0

摘要

香蕉是4亿多人的主食。此外,出口超过1650万吨,使其成为一种重要的粮食安全和经济作物。卡文迪什型香蕉的产量受到非生物和生物胁迫的威胁。事实上,三倍体香蕉是不育的、单性生殖的和专性无性繁殖的,这使得它们特别容易受到疾病的影响,包括由Fusarium oxysporum f. sp. cubense (Foc)热带小种4 (Foc TR4)引起的枯萎病。这是因为连续的无性繁殖导致了遗传多样性的丧失。此外,减数分裂的缺乏限制了育种方法。Foc TR4对东南亚的卡文迪什香蕉造成了破坏,但最近澳大利亚昆士兰、中东和莫桑比克也报告了这一情况,从而威胁到全球香蕉生产。为了解决这个问题,我们正在对体外繁殖的香蕉进行诱变,以扩大遗传多样性,从而找到新的抗病等位基因。我们已经开发了利用化学诱变剂和电离辐射有效诱导离体茎尖分生组织突变的方法。突变发现方法已经适应于恢复突变,包括单点突变和跨越数百万碱基对的大缺失。我们已经创建了大约5000个突变系用于前向遗传筛选,以鉴定温室评估材料的TR4抗性。约500个试管苗的一个亚群使用毒力强的尖孢镰刀菌分离物进行了基于温室的筛选。迄今为止,已确定23个菌株对Foc TR4表现出改变的耐药反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induced mutations for generating bananas resistant to Fusarium wilt tropical race 4.
Abstract Bananas are a staple for more than 400 million people. Additionally, more than 16.5 million tonnes are exported, making it both an important food security and a cash crop. Productivity of Cavendish-type bananas is threatened by both abiotic and biotic stresses. The fact that triploid bananas are sterile, parthenocarpic and obligate vegetatively propagated makes them particularly susceptible to diseases, including Fusarium wilt caused by Fusarium oxysporum f. sp. cubense (Foc) tropical race 4 (Foc TR4). This is because continual clonal propagation has led to loss of genetic diversity. Additionally, lack of meiosis limits methods for breeding. Foc TR4 has been devastating Cavendish bananas in South-east Asia but has recently also been reported from Queensland in Australia, the Middle East and Mozambique, thus threatening global banana production. To address this, we are performing mutagenesis of in vitro propagated bananas to broaden the genetic diversity in order to find new alleles conferring disease resistance. We have developed methods for efficient induction of mutations in isolated apical meristems from shoot tips using chemical mutagens and ionizing radiation. Mutation discovery methods have been adapted to recover mutations including single point mutations and large deletions spanning millions of base pairs. We have created approximately 5000 mutated lines for forward-genetic screens to identify TR4 resistance in greenhouse- evaluated material. A subset of ca. 500 in vitro plantlets was subjected to glasshouse-based screening using a virulent F. oxysporum isolate. To date, 23 lines showing altered resistance responses to Foc TR4 have been identified.
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