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A Phenotyping Protocol for Detailed Evaluation of Apple Root Resistance Responses Utilizing Tissue Culture Micropropagated Apple Plants

机译:利用组织培养微繁苹果植物对苹果根系抗性反应进行详细评估的表型分析方法

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In the post-genomics era, reliable phenotypes are considered the bottleneck for unraveling the genetic control over the biology of interest. Phenotyping resistance response of roots to infection by soilborne pathogen is more challenging compared to that of plant aerial parts. In additional to the hidden nature and small stature of fine roots where infection occurs, extra obstacles exist for rosaceae tree crops such as apple. Due to self-incompatible reproduction and high-level heterozygosity of apple genome, genetically identical apple plants cannot be produced through apple seed germination. Here we report an established phenotyping protocol which includes a streamlined tissue culture procedure for micropropagation of uniform apple plants, standardized inoculation procedure using Pythium ultimum , and multilayered evaluating methods on apple root resistance traits. Because of the implementation of tissue culture based micropropagation procedure, constant availability of the uniform plants with defined genetic background, equivalent age and non-contaminated roots overcame a longstanding barrier of systematic and detailed phenotypic characterization of apple root resistance traits. Repeated infection assays by root-dipping inoculation demonstrated the reproducible and wide-range plant survival rates, from single-digit to over 90% survived plants for a given genotype. Genotype-specific values due to P. ultimum inoculation on shoot and root biomass reduction, maximum root lengths, leaf number and cumulative leaf areas were quantified between mock-inoculated and P. ultimum infected plants. Use of a glass-box container offered enhanced accessibility and minimized invasiveness for continuous and non-disruptive observation on the necrosis progression patterns along inoculated roots. With the assistance of a dissecting microscope, the genotype-specific resistance responses along the infected apple roots were captured and analyzed in detail. This reported phenotyping protocol represents a major development and should be easily adopted for other rosacea tree fruit crops with minor modifications.
机译:在后基因组学时代,可靠的表型被认为是解开对感兴趣生物学的遗传控制的瓶颈。与植物地上部分相比,根对土壤传播的病原体感染的表型抗性响应更具挑战性。除了发生感染的细根的隐蔽性质和矮小的身形外,酒渣鼻科作物(如苹果)还存在其他障碍。由于苹果基因组的自我不相容繁殖和高度杂合性,无法通过苹果种子发芽生产出基因上相同的苹果植物。在这里,我们报告一个已建立的表型方案,包括简化的用于均匀苹果植株微繁的组织培养程序,使用终极腐霉的标准化接种程序以及对苹果根抗性状的多层评估方法。由于基于组织培养的微繁过程的实施,具有确定的遗传背景,同等年龄和未受污染的根的统一植物的持续可用性克服了苹果根抗性性状系统和详细表型表征的长期障碍。通过根浸接种的反复感染试验表明,对于给定的基因型,植物的存活率可重现且范围广泛,从存活到成年的植株从一位数到90%以上。因 P而导致的基因型特定值。在模拟接种和 P之间量化了最终接种对茎和根生物量的减少,最大根长度,叶数和累积叶面积。最终感染的植物。玻璃盒容器的使用提供了更大的可及性,并最大限度地减少了侵袭性,可连续且无中断地观察沿接种根的坏死进展模式。借助解剖显微镜,捕获并详细分析了沿感染苹果根的基因型特异性抗性反应。该报道的表型研究方案代表了一项重大进展,应该对其他酒渣鼻树果实作物进行少量修改即可轻易采用。

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