4.6 Article

Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations

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PLOS ONE
卷 8, 期 10, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0077172

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资金

  1. US National Science Foundation [0703273, 1116561]
  2. Direct For Biological Sciences
  3. Division Of Integrative Organismal Systems [1116561, 0703273] Funding Source: National Science Foundation
  4. Direct For Biological Sciences
  5. Div Of Molecular and Cellular Bioscience [1025976] Funding Source: National Science Foundation

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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.

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