Institut National de la Recherche Agronomique and Université de Bordeaux, Unité Mixte de Recherche 1332 Biologie du Fruit et Pathologie, Villenave d'Ornon, France.
Institut National de la Recherche Agronomique US1279 Etude du Polymorphisme des Génomes Végétaux, CEA-Institut de Génomique-CNG, Evry, France.
Nat Protoc. 2016 Dec;11(12):2401-2418. doi: 10.1038/nprot.2016.143. Epub 2016 Nov 3.
The tomato is the model species of choice for fleshy fruit development and for the Solanaceae family. Ethyl methanesulfonate (EMS) mutants of tomato have already proven their utility for analysis of gene function in plants, leading to improved breeding stocks and superior tomato varieties. However, until recently, the identification of causal mutations that underlie particular phenotypes has been a very lengthy task that many laboratories could not afford because of spatial and technical limitations. Here, we describe a simple protocol for identifying causal mutations in tomato using a mapping-by-sequencing strategy. Plants displaying phenotypes of interest are first isolated by screening an EMS mutant collection generated in the miniature cultivar Micro-Tom. A recombinant F population is then produced by crossing the mutant with a wild-type (WT; non-mutagenized) genotype, and F segregants displaying the same phenotype are subsequently pooled. Finally, whole-genome sequencing and analysis of allele distributions in the pools allow for the identification of the causal mutation. The whole process, from the isolation of the tomato mutant to the identification of the causal mutation, takes 6-12 months. This strategy overcomes many previous limitations, is simple to use and can be applied in most laboratories with limited facilities for plant culture and genotyping.
番茄是肉质果实发育和茄科植物的模式物种。乙基磺酸甲酯(EMS)番茄突变体已被证明可用于分析植物中的基因功能,从而培育出改良的品系和更优良的番茄品种。然而,直到最近,确定导致特定表型的因果突变仍然是一项非常漫长的任务,由于空间和技术限制,许多实验室都无法承担这项任务。在这里,我们描述了一种使用基于测序的图谱构建策略鉴定番茄中因果突变的简单方案。首先通过筛选在微型栽培品种 Micro-Tom 中产生的 EMS 突变体库,从表型感兴趣的突变体中分离出来。然后,通过将突变体与野生型(WT;未诱变)基因型杂交产生重组 F1 群体,随后将表现相同表型的 F1 分离体混合在一起。最后,对混合群体中的全基因组测序和等位基因分布分析可鉴定因果突变。从番茄突变体的分离到因果突变的鉴定,整个过程需要 6-12 个月。该策略克服了许多以前的限制,使用简单,并且可以在大多数具有有限植物培养和基因分型设施的实验室中应用。