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Discovery of induced point mutations in maize genes by TILLING

BACKGROUND: Going from a gene sequence to its function in the context of a whole organism requires a strategy for targeting mutations, referred to as reverse genetics. Reverse genetics is highly desirable in the modern genomics era; however, the most powerful methods are generally restricted to a fe...

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Autores principales: Till, Bradley J, Reynolds, Steven H, Weil, Clifford, Springer, Nathan, Burtner, Chris, Young, Kim, Bowers, Elisabeth, Codomo, Christine A, Enns, Linda C, Odden, Anthony R, Greene, Elizabeth A, Comai, Luca, Henikoff, Steven
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC512284/
https://www.ncbi.nlm.nih.gov/pubmed/15282033
http://dx.doi.org/10.1186/1471-2229-4-12
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author Till, Bradley J
Reynolds, Steven H
Weil, Clifford
Springer, Nathan
Burtner, Chris
Young, Kim
Bowers, Elisabeth
Codomo, Christine A
Enns, Linda C
Odden, Anthony R
Greene, Elizabeth A
Comai, Luca
Henikoff, Steven
author_facet Till, Bradley J
Reynolds, Steven H
Weil, Clifford
Springer, Nathan
Burtner, Chris
Young, Kim
Bowers, Elisabeth
Codomo, Christine A
Enns, Linda C
Odden, Anthony R
Greene, Elizabeth A
Comai, Luca
Henikoff, Steven
author_sort Till, Bradley J
collection PubMed
description BACKGROUND: Going from a gene sequence to its function in the context of a whole organism requires a strategy for targeting mutations, referred to as reverse genetics. Reverse genetics is highly desirable in the modern genomics era; however, the most powerful methods are generally restricted to a few model organisms. Previously, we introduced a reverse-genetic strategy with the potential for general applicability to organisms that lack well-developed genetic tools. Our TILLING (Targeting Induced Local Lesions IN Genomes) method uses chemical mutagenesis followed by screening for single-base changes to discover induced mutations that alter protein function. TILLING was shown to be an effective reverse genetic strategy by the establishment of a high-throughput TILLING facility and the delivery of thousands of point mutations in hundreds of Arabidopsis genes to members of the plant biology community. RESULTS: We demonstrate that high-throughput TILLING is applicable to maize, an important crop plant with a large genome but with limited reverse-genetic resources currently available. We screened pools of DNA samples for mutations in 1-kb segments from 11 different genes, obtaining 17 independent induced mutations from a population of 750 pollen-mutagenized maize plants. One of the genes targeted was the DMT102 chromomethylase gene, for which we obtained an allelic series of three missense mutations that are predicted to be strongly deleterious. CONCLUSIONS: Our findings indicate that TILLING is a broadly applicable and efficient reverse-genetic strategy. We are establishing a public TILLING service for maize modeled on the existing Arabidopsis TILLING Project.
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spelling pubmed-5122842004-08-19 Discovery of induced point mutations in maize genes by TILLING Till, Bradley J Reynolds, Steven H Weil, Clifford Springer, Nathan Burtner, Chris Young, Kim Bowers, Elisabeth Codomo, Christine A Enns, Linda C Odden, Anthony R Greene, Elizabeth A Comai, Luca Henikoff, Steven BMC Plant Biol Methodology Article BACKGROUND: Going from a gene sequence to its function in the context of a whole organism requires a strategy for targeting mutations, referred to as reverse genetics. Reverse genetics is highly desirable in the modern genomics era; however, the most powerful methods are generally restricted to a few model organisms. Previously, we introduced a reverse-genetic strategy with the potential for general applicability to organisms that lack well-developed genetic tools. Our TILLING (Targeting Induced Local Lesions IN Genomes) method uses chemical mutagenesis followed by screening for single-base changes to discover induced mutations that alter protein function. TILLING was shown to be an effective reverse genetic strategy by the establishment of a high-throughput TILLING facility and the delivery of thousands of point mutations in hundreds of Arabidopsis genes to members of the plant biology community. RESULTS: We demonstrate that high-throughput TILLING is applicable to maize, an important crop plant with a large genome but with limited reverse-genetic resources currently available. We screened pools of DNA samples for mutations in 1-kb segments from 11 different genes, obtaining 17 independent induced mutations from a population of 750 pollen-mutagenized maize plants. One of the genes targeted was the DMT102 chromomethylase gene, for which we obtained an allelic series of three missense mutations that are predicted to be strongly deleterious. CONCLUSIONS: Our findings indicate that TILLING is a broadly applicable and efficient reverse-genetic strategy. We are establishing a public TILLING service for maize modeled on the existing Arabidopsis TILLING Project. BioMed Central 2004-07-28 /pmc/articles/PMC512284/ /pubmed/15282033 http://dx.doi.org/10.1186/1471-2229-4-12 Text en Copyright © 2004 Till et al; licensee BioMed Central Ltd.
spellingShingle Methodology Article
Till, Bradley J
Reynolds, Steven H
Weil, Clifford
Springer, Nathan
Burtner, Chris
Young, Kim
Bowers, Elisabeth
Codomo, Christine A
Enns, Linda C
Odden, Anthony R
Greene, Elizabeth A
Comai, Luca
Henikoff, Steven
Discovery of induced point mutations in maize genes by TILLING
title Discovery of induced point mutations in maize genes by TILLING
title_full Discovery of induced point mutations in maize genes by TILLING
title_fullStr Discovery of induced point mutations in maize genes by TILLING
title_full_unstemmed Discovery of induced point mutations in maize genes by TILLING
title_short Discovery of induced point mutations in maize genes by TILLING
title_sort discovery of induced point mutations in maize genes by tilling
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC512284/
https://www.ncbi.nlm.nih.gov/pubmed/15282033
http://dx.doi.org/10.1186/1471-2229-4-12
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