| Literature DB >> 25271717 |
Xue-Cheng Zhang1, Yves Millet, Frederick M Ausubel, Mark Borowsky.
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.Entities:
Keywords: ethyl methanesulfonate (EMS); genetic mapping; next-gen sequencing
Mesh:
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Year: 2014 PMID: 25271717 DOI: 10.1002/0471142727.mb0718s108
Source DB: PubMed Journal: Curr Protoc Mol Biol ISSN: 1934-3647