| Literature DB >> 27809315 |
Virginie Garcia1, Cécile Bres1, Daniel Just1, Lucie Fernandez1, Fabienne Wong Jun Tai1, Jean-Philippe Mauxion1, Marie-Christine Le Paslier2, Aurélie Bérard2, Dominique Brunel2, Koh Aoki3, Saleh Alseekh4, Alisdair R Fernie4, Paul D Fraser5, Christophe Rothan1.
Abstract
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 F2 population is then produced by crossing the mutant with a wild-type (WT; non-mutagenized) genotype, and F2 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.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27809315 DOI: 10.1038/nprot.2016.143
Source DB: PubMed Journal: Nat Protoc ISSN: 1750-2799 Impact factor: 13.491