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Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries

To accelerate functional genomic research in tomato, we developed a Micro-Tom TILLING (Targeting Induced Local Lesions In Genomes) platform. DNA pools were constructed from 3,052 ethyl methanesulfonate (EMS) mutant lines treated with 0.5 or 1.0% EMS. The mutation frequency was calculated by screenin...

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Autores principales: Okabe, Yoshihiro, Asamizu, Erika, Saito, Takeshi, Matsukura, Chiaki, Ariizumi, Tohru, Brès, Cécile, Rothan, Christophe, Mizoguchi, Tsuyoshi, Ezura, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212723/
https://www.ncbi.nlm.nih.gov/pubmed/21965606
http://dx.doi.org/10.1093/pcp/pcr134
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author Okabe, Yoshihiro
Asamizu, Erika
Saito, Takeshi
Matsukura, Chiaki
Ariizumi, Tohru
Brès, Cécile
Rothan, Christophe
Mizoguchi, Tsuyoshi
Ezura, Hiroshi
author_facet Okabe, Yoshihiro
Asamizu, Erika
Saito, Takeshi
Matsukura, Chiaki
Ariizumi, Tohru
Brès, Cécile
Rothan, Christophe
Mizoguchi, Tsuyoshi
Ezura, Hiroshi
author_sort Okabe, Yoshihiro
collection PubMed
description To accelerate functional genomic research in tomato, we developed a Micro-Tom TILLING (Targeting Induced Local Lesions In Genomes) platform. DNA pools were constructed from 3,052 ethyl methanesulfonate (EMS) mutant lines treated with 0.5 or 1.0% EMS. The mutation frequency was calculated by screening 10 genes. The 0.5% EMS population had a mild mutation frequency of one mutation per 1,710 kb, whereas the 1.0% EMS population had a frequency of one mutation per 737 kb, a frequency suitable for producing an allelic series of mutations in the target genes. The overall mutation frequency was one mutation per 1,237 kb, which affected an average of three alleles per kilobase screened. To assess whether a Micro-Tom TILLING platform could be used for efficient mutant isolation, six ethylene receptor genes in tomato (SlETR1–SlETR6) were screened. Two allelic mutants of SlETR1 (Sletr1-1 and Sletr1-2) that resulted in reduced ethylene responses were identified, indicating that our Micro-Tom TILLING platform provides a powerful tool for the rapid detection of mutations in an EMS mutant library. This work provides a practical and publicly accessible tool for the study of fruit biology and for obtaining novel genetic material that can be used to improve important agronomic traits in tomato.
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spelling pubmed-32127232011-11-10 Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries Okabe, Yoshihiro Asamizu, Erika Saito, Takeshi Matsukura, Chiaki Ariizumi, Tohru Brès, Cécile Rothan, Christophe Mizoguchi, Tsuyoshi Ezura, Hiroshi Plant Cell Physiol Regular Papers To accelerate functional genomic research in tomato, we developed a Micro-Tom TILLING (Targeting Induced Local Lesions In Genomes) platform. DNA pools were constructed from 3,052 ethyl methanesulfonate (EMS) mutant lines treated with 0.5 or 1.0% EMS. The mutation frequency was calculated by screening 10 genes. The 0.5% EMS population had a mild mutation frequency of one mutation per 1,710 kb, whereas the 1.0% EMS population had a frequency of one mutation per 737 kb, a frequency suitable for producing an allelic series of mutations in the target genes. The overall mutation frequency was one mutation per 1,237 kb, which affected an average of three alleles per kilobase screened. To assess whether a Micro-Tom TILLING platform could be used for efficient mutant isolation, six ethylene receptor genes in tomato (SlETR1–SlETR6) were screened. Two allelic mutants of SlETR1 (Sletr1-1 and Sletr1-2) that resulted in reduced ethylene responses were identified, indicating that our Micro-Tom TILLING platform provides a powerful tool for the rapid detection of mutations in an EMS mutant library. This work provides a practical and publicly accessible tool for the study of fruit biology and for obtaining novel genetic material that can be used to improve important agronomic traits in tomato. Oxford University Press 2011-11 2011-09-30 /pmc/articles/PMC3212723/ /pubmed/21965606 http://dx.doi.org/10.1093/pcp/pcr134 Text en © The Author 2011. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. http://creativecommons.org/licenses/by-nc/2.5 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Regular Papers
Okabe, Yoshihiro
Asamizu, Erika
Saito, Takeshi
Matsukura, Chiaki
Ariizumi, Tohru
Brès, Cécile
Rothan, Christophe
Mizoguchi, Tsuyoshi
Ezura, Hiroshi
Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries
title Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries
title_full Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries
title_fullStr Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries
title_full_unstemmed Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries
title_short Tomato TILLING Technology: Development of a Reverse Genetics Tool for the Efficient Isolation of Mutants from Micro-Tom Mutant Libraries
title_sort tomato tilling technology: development of a reverse genetics tool for the efficient isolation of mutants from micro-tom mutant libraries
topic Regular Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3212723/
https://www.ncbi.nlm.nih.gov/pubmed/21965606
http://dx.doi.org/10.1093/pcp/pcr134
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