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Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations
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-through...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806735/ https://www.ncbi.nlm.nih.gov/pubmed/24194867 http://dx.doi.org/10.1371/journal.pone.0077172 |
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author | McCarty, Donald R. Latshaw, Sue Wu, Shan Suzuki, Masaharu Hunter, Charles T. Avigne, Wayne T. Koch, Karen E. |
author_facet | McCarty, Donald R. Latshaw, Sue Wu, Shan Suzuki, Masaharu Hunter, Charles T. Avigne, Wayne T. Koch, Karen E. |
author_sort | McCarty, Donald R. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3806735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38067352013-11-05 Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations McCarty, Donald R. Latshaw, Sue Wu, Shan Suzuki, Masaharu Hunter, Charles T. Avigne, Wayne T. Koch, Karen E. PLoS One Research Article 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. Public Library of Science 2013-10-23 /pmc/articles/PMC3806735/ /pubmed/24194867 http://dx.doi.org/10.1371/journal.pone.0077172 Text en © 2013 McCarty et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article McCarty, Donald R. Latshaw, Sue Wu, Shan Suzuki, Masaharu Hunter, Charles T. Avigne, Wayne T. Koch, Karen E. Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations |
title | Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations |
title_full | Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations |
title_fullStr | Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations |
title_full_unstemmed | Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations |
title_short | Mu-seq: Sequence-Based Mapping and Identification of Transposon Induced Mutations |
title_sort | mu-seq: sequence-based mapping and identification of transposon induced mutations |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3806735/ https://www.ncbi.nlm.nih.gov/pubmed/24194867 http://dx.doi.org/10.1371/journal.pone.0077172 |
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