Journal article

Direct access to millions of mutations by whole genome sequencing of an oilseed rape mutant population


Authors listJhingan, Srijan; Kumar, Avneesh; Harloff, Hans-Joachim; Dreyer, Felix; Abbadi, Amine; Beckmann, Katrin; Obermeier, Christian; Jung, Christian

Publication year2023

Pages866-880

JournalThe Plant Journal

Volume number113

Issue number4

ISSN0960-7412

eISSN1365-313X

Open access statusHybrid

DOI Linkhttps://doi.org/10.1111/tpj.16079

PublisherWiley


Abstract
Induced mutations are an essential source of genetic variation in plant breeding. Ethyl methanesulfonate (EMS) mutagenesis has been frequently applied, and mutants have been detected by phenotypic or genotypic screening of large populations. In the present study, a rapeseed M-2 population was derived from M-1 parent cultivar 'Express' treated with EMS. Whole genomes were sequenced from fourfold (4x) pools of 1988 M-2 plants representing 497 M-2 families. Detected mutations were not evenly distributed and displayed distinct patterns across the 19 chromosomes with lower mutation rates towards the ends. Mutation frequencies ranged from 32/Mb to 48/Mb. On average, 284 442 single nucleotide polymorphisms (SNPs) per M-2 DNA pool were found resulting from EMS mutagenesis. 55% of the SNPs were C -> T and G -> A transitions, characteristic for EMS induced ('canonical') mutations, whereas the remaining SNPs were 'non-canonical' transitions (15%) or transversions (30%). Additionally, we detected 88 725 high confidence insertions and deletions per pool. On average, each M-2 plant carried 39 120 canonical mutations, corresponding to a frequency of one mutation per 23.6 kb. Approximately 82% of such mutations were located either 5 kb upstream or downstream (56%) of gene coding regions or within intergenic regions (26%). The remaining 18% were located within regions coding for genes. All mutations detected by whole genome sequencing could be verified by comparison with known mutations. Furthermore, all sequences are accessible via the online tool 'EMSBrassica' (), which enables direct identification of mutations in any target sequence. The sequence resource described here will further add value for functional gene studies in rapeseed breeding.



Citation Styles

Harvard Citation styleJhingan, S., Kumar, A., Harloff, H., Dreyer, F., Abbadi, A., Beckmann, K., et al. (2023) Direct access to millions of mutations by whole genome sequencing of an oilseed rape mutant population, The Plant Journal, 113(4), pp. 866-880. https://doi.org/10.1111/tpj.16079

APA Citation styleJhingan, S., Kumar, A., Harloff, H., Dreyer, F., Abbadi, A., Beckmann, K., Obermeier, C., & Jung, C. (2023). Direct access to millions of mutations by whole genome sequencing of an oilseed rape mutant population. The Plant Journal. 113(4), 866-880. https://doi.org/10.1111/tpj.16079



Keywords


EMS mutagenesisethyl methanesulfonatePOINT MUTATIONSTILLING

Last updated on 2025-10-06 at 11:48