Next-Gen Sequencing-Based Mapping and Identification of Ethyl Methanesulfonate-Induced Mutations in Arabidopsis thaliana

Curr Protoc Mol Biol. 2014 Oct 1:108:7.18.1-7.18.16. doi: 10.1002/0471142727.mb0718s108.

Abstract

Forward genetic analysis using ethyl methanesulfonate (EMS) mutagenesis has proven to be a powerful tool in biological research, but identification and cloning of causal mutations by conventional genetic mapping approaches is a painstaking process. Recent advances in next-gen sequencing have greatly invigorated the process of identifying EMS-induced mutations corresponding to a specific phenotype in model genetic hosts, including the plant Arabidopsis thaliana and the nematode Caenorhabditis elegans. Next-gen sequencing of bulked F2 mutant recombinants produces a wealth of high-resolution genetic data, provides enhanced delimitation of the genomic location of mutations, and greatly reduces hands-on time while maintaining high accuracy and reproducibility. In this unit, a detailed procedure to simultaneously map and identify EMS mutations in Arabidopsis is described.

Keywords: ethyl methanesulfonate (EMS); genetic mapping; next-gen sequencing.

MeSH terms

  • Arabidopsis / genetics*
  • DNA Mutational Analysis / methods
  • DNA, Plant / chemistry
  • DNA, Plant / genetics*
  • Ethyl Methanesulfonate / chemistry*
  • High-Throughput Nucleotide Sequencing / methods*
  • Mutagenesis*
  • Mutation*

Substances

  • DNA, Plant
  • Ethyl Methanesulfonate