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Discovery of chemically induced mutations in rice by TILLING
BACKGROUND: Rice is both a food source for a majority of the world's population and an important model system. Available functional genomics resources include targeted insertion mutagenesis and transgenic tools. While these can be powerful, a non-transgenic, unbiased targeted mutagenesis method...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1858691/ https://www.ncbi.nlm.nih.gov/pubmed/17428339 http://dx.doi.org/10.1186/1471-2229-7-19 |
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author | Till, Bradley J Cooper, Jennifer Tai, Thomas H Colowit, Peter Greene, Elizabeth A Henikoff, Steven Comai, Luca |
author_facet | Till, Bradley J Cooper, Jennifer Tai, Thomas H Colowit, Peter Greene, Elizabeth A Henikoff, Steven Comai, Luca |
author_sort | Till, Bradley J |
collection | PubMed |
description | BACKGROUND: Rice is both a food source for a majority of the world's population and an important model system. Available functional genomics resources include targeted insertion mutagenesis and transgenic tools. While these can be powerful, a non-transgenic, unbiased targeted mutagenesis method that can generate a range of allele types would add considerably to the analysis of the rice genome. TILLING (Targeting Induced Local Lesions in Genomes), a general reverse genetic technique that combines traditional mutagenesis with high throughput methods for mutation discovery, is such a method. RESULTS: To apply TILLING to rice, we developed two mutagenized rice populations. One population was developed by treatment with the chemical mutagen ethyl methanesulphonate (EMS), and the other with a combination of sodium azide plus methyl-nitrosourea (Az-MNU). To find induced mutations, target regions of 0.7–1.5 kilobases were PCR amplified using gene specific primers labeled with fluorescent dyes. Heteroduplexes were formed through denaturation and annealing of PCR products, mismatches digested with a crude preparation of CEL I nuclease and cleaved fragments visualized using denaturing polyacrylamide gel electrophoresis. In 10 target genes screened, we identified 27 nucleotide changes in the EMS-treated population and 30 in the Az-MNU population. CONCLUSION: We estimate that the density of induced mutations is two- to threefold higher than previously reported rice populations (about 1/300 kb). By comparison to other plants used in public TILLING services, we conclude that the populations described here would be suitable for use in a large scale TILLING project. |
format | Text |
id | pubmed-1858691 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-18586912007-04-28 Discovery of chemically induced mutations in rice by TILLING Till, Bradley J Cooper, Jennifer Tai, Thomas H Colowit, Peter Greene, Elizabeth A Henikoff, Steven Comai, Luca BMC Plant Biol Methodology Article BACKGROUND: Rice is both a food source for a majority of the world's population and an important model system. Available functional genomics resources include targeted insertion mutagenesis and transgenic tools. While these can be powerful, a non-transgenic, unbiased targeted mutagenesis method that can generate a range of allele types would add considerably to the analysis of the rice genome. TILLING (Targeting Induced Local Lesions in Genomes), a general reverse genetic technique that combines traditional mutagenesis with high throughput methods for mutation discovery, is such a method. RESULTS: To apply TILLING to rice, we developed two mutagenized rice populations. One population was developed by treatment with the chemical mutagen ethyl methanesulphonate (EMS), and the other with a combination of sodium azide plus methyl-nitrosourea (Az-MNU). To find induced mutations, target regions of 0.7–1.5 kilobases were PCR amplified using gene specific primers labeled with fluorescent dyes. Heteroduplexes were formed through denaturation and annealing of PCR products, mismatches digested with a crude preparation of CEL I nuclease and cleaved fragments visualized using denaturing polyacrylamide gel electrophoresis. In 10 target genes screened, we identified 27 nucleotide changes in the EMS-treated population and 30 in the Az-MNU population. CONCLUSION: We estimate that the density of induced mutations is two- to threefold higher than previously reported rice populations (about 1/300 kb). By comparison to other plants used in public TILLING services, we conclude that the populations described here would be suitable for use in a large scale TILLING project. BioMed Central 2007-04-11 /pmc/articles/PMC1858691/ /pubmed/17428339 http://dx.doi.org/10.1186/1471-2229-7-19 Text en Copyright © 2007 Till et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Till, Bradley J Cooper, Jennifer Tai, Thomas H Colowit, Peter Greene, Elizabeth A Henikoff, Steven Comai, Luca Discovery of chemically induced mutations in rice by TILLING |
title | Discovery of chemically induced mutations in rice by TILLING |
title_full | Discovery of chemically induced mutations in rice by TILLING |
title_fullStr | Discovery of chemically induced mutations in rice by TILLING |
title_full_unstemmed | Discovery of chemically induced mutations in rice by TILLING |
title_short | Discovery of chemically induced mutations in rice by TILLING |
title_sort | discovery of chemically induced mutations in rice by tilling |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1858691/ https://www.ncbi.nlm.nih.gov/pubmed/17428339 http://dx.doi.org/10.1186/1471-2229-7-19 |
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