Datta Sneha, Jankowicz-Cieslak Joanna, Nielen Stephan, Ingelbrecht Ivan, Till Bradley J
Plant Breeding and Genetics Laboratory, Joint FAO/IAEA Division of Nuclear Techniques in Food and Agriculture, IAEA Laboratories Seibersdorf, International Atomic Energy Agency, Vienna International Centre, Vienna, Austria.
Plant Biotechnol J. 2018 Feb 24;16(9):1644-53. doi: 10.1111/pbi.12901.
Traditional breeding methods are hindered in bananas due to the fact that major cultivars are sterile, parthenocarpic, triploid and thus clonally propagated. This has resulted in a narrow genetic base and limited resilience to biotic and abiotic stresses. Mutagenesis of in vitro propagated bananas is one method to introduce novel alleles and broaden genetic diversity. We previously established a method for the induction and recovery of single nucleotide mutations generated with the chemical mutagen EMS. However, officially released mutant banana varieties have been created using gamma rays, a mutagen that can produce large genomic insertions and deletions (indels). Such dosage mutations may be important for generating observable phenotypes in polyploids. In this study, we establish a low-coverage whole-genome sequencing approach in triploid bananas to recover large genomic indels caused by treatment with gamma irradiation. We first evaluated the commercially released mutant cultivar 'Novaria' and found that it harbours multiple predicted deletions, ranging from 0.3 to 3.8 million base pairs (Mbp). In total, predicted deletions span 189 coding regions. To evaluate the feasibility of generating and maintaining new mutations, we developed a pipeline for mutagenesis and screening for copy number variation in Cavendish bananas using the cultivar 'Williams'. Putative mutations were recovered in 70% of lines treated with 20 Gy and 60% of the lines treated with 40 Gy. While deletion events predominate, insertions were identified in 20 Gy-treated material. Based on these results, we believe this approach can be scaled up to support large breeding projects.
由于主要香蕉品种不育、单性结实、三倍体且通过无性繁殖,传统育种方法在香蕉育种中受到阻碍。这导致了遗传基础狭窄,对生物和非生物胁迫的适应能力有限。对离体繁殖的香蕉进行诱变是引入新等位基因和拓宽遗传多样性的一种方法。我们之前建立了一种诱导和恢复由化学诱变剂甲基磺酸乙酯(EMS)产生的单核苷酸突变的方法。然而,已正式发布的突变香蕉品种是利用伽马射线培育出来的,伽马射线这种诱变剂可产生大的基因组插入和缺失(Indel)。这种剂量突变对于在多倍体中产生可观察到的表型可能很重要。在本研究中,我们建立了一种三倍体香蕉低覆盖度全基因组测序方法,以恢复由伽马射线处理导致的大基因组Indel。我们首先评估了已商业化发布的突变品种‘诺瓦里亚’,发现它含有多个预测的缺失,范围从0.3到380万个碱基对(Mbp)。预测的缺失总共跨越189个编码区。为了评估产生和维持新突变的可行性,我们开发了一套流程,用于使用‘威廉姆斯’品种对卡文迪什香蕉进行诱变和筛选拷贝数变异。在用20 Gy处理的株系中,70% 获得了推定突变,在用40 Gy处理的株系中,60% 获得了推定突变。虽然缺失事件占主导,但在20 Gy处理的材料中也鉴定出了插入。基于这些结果,我们认为这种方法可以扩大规模以支持大型育种项目。