Abstract
Mutations tagged by transposon insertions can be readily mapped and identified in organisms with sequenced genomes. Collections of such mutants allow a systematic analysis of gene function, and can be sequence-indexed to build invaluable resources. Here we present Mu-seq (Mutant-seq), a high-throughput NextGen sequencing method for harnessing high-copy transposons. We illustrate the efficacy of Mu-seq by applying it to the Robertson's Mutator system in a large population of maize plants. A single Mu-seq library, for example, constructed from 576 different families (2304 plants), enabled 4, 723 novel, germinal, transposon insertions to be detected, identified, and mapped with single base-pair resolution. In addition to the specificity, efficiency, and reproducibility of Mu-seq, a key feature of this method is its adjustable scale that can accomodate simultaneous profiling of transposons in thousands of individuals. We also describe a Mu-seq bioinformatics framework tailored to high-throughput, genome-wide, and population-wide analysis of transposon insertions. © 2013 McCarty et al.
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CITATION STYLE
McCarty, D. R., Latshaw, S., Wu, S., Suzuki, M., Hunter, C. T., Avigne, W. T., & Koch, K. E. (2013). Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations. PLoS ONE, 8(10). https://doi.org/10.1371/journal.pone.0077172
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