New Low Morphine Opium Poppy Genotype Obtained by TILLING Approach
The opium poppy’s ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and...
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Published in | Plants (Basel) Vol. 12; no. 5; p. 1077 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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28.02.2023
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ISSN | 2223-7747 2223-7747 |
DOI | 10.3390/plants12051077 |
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Abstract | The opium poppy’s ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and single-molecule real-time NGS sequencing, is presented. Verification of the mutants in the TILLING population was obtained using RT-PCR and HPLC methods. Only three of the single-copy genes of the morphine pathway among the eleven genes were used for the identification of mutant genotypes. Point mutations were obtained only in one gene (CNMT) while an insertion was obtained in the other (SalAT). Only a few expected transition SNPs from G:C to A:T were obtained. In the low morphine mutant genotype, the production of morphine was decreased to 0.1% from 1.4% in the original variety. A comprehensive description of the breeding process, a basic characterization of the main alkaloid content, and a gene expression profile for the main alkaloid-producing genes is provided. Difficulties with the TILLING approach are also described and discussed. |
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AbstractList | The opium poppy's ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and single-molecule real-time NGS sequencing, is presented. Verification of the mutants in the TILLING population was obtained using RT-PCR and HPLC methods. Only three of the single-copy genes of the morphine pathway among the eleven genes were used for the identification of mutant genotypes. Point mutations were obtained only in one gene (
) while an insertion was obtained in the other (
). Only a few expected transition SNPs from G:C to A:T were obtained. In the low morphine mutant genotype, the production of morphine was decreased to 0.1% from 1.4% in the original variety. A comprehensive description of the breeding process, a basic characterization of the main alkaloid content, and a gene expression profile for the main alkaloid-producing genes is provided. Difficulties with the TILLING approach are also described and discussed. The opium poppy’s ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and single-molecule real-time NGS sequencing, is presented. Verification of the mutants in the TILLING population was obtained using RT-PCR and HPLC methods. Only three of the single-copy genes of the morphine pathway among the eleven genes were used for the identification of mutant genotypes. Point mutations were obtained only in one gene (CNMT) while an insertion was obtained in the other (SalAT). Only a few expected transition SNPs from G:C to A:T were obtained. In the low morphine mutant genotype, the production of morphine was decreased to 0.1% from 1.4% in the original variety. A comprehensive description of the breeding process, a basic characterization of the main alkaloid content, and a gene expression profile for the main alkaloid-producing genes is provided. Difficulties with the TILLING approach are also described and discussed. The opium poppy's ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and single-molecule real-time NGS sequencing, is presented. Verification of the mutants in the TILLING population was obtained using RT-PCR and HPLC methods. Only three of the single-copy genes of the morphine pathway among the eleven genes were used for the identification of mutant genotypes. Point mutations were obtained only in one gene (CNMT) while an insertion was obtained in the other (SalAT). Only a few expected transition SNPs from G:C to A:T were obtained. In the low morphine mutant genotype, the production of morphine was decreased to 0.1% from 1.4% in the original variety. A comprehensive description of the breeding process, a basic characterization of the main alkaloid content, and a gene expression profile for the main alkaloid-producing genes is provided. Difficulties with the TILLING approach are also described and discussed.The opium poppy's ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and single-molecule real-time NGS sequencing, is presented. Verification of the mutants in the TILLING population was obtained using RT-PCR and HPLC methods. Only three of the single-copy genes of the morphine pathway among the eleven genes were used for the identification of mutant genotypes. Point mutations were obtained only in one gene (CNMT) while an insertion was obtained in the other (SalAT). Only a few expected transition SNPs from G:C to A:T were obtained. In the low morphine mutant genotype, the production of morphine was decreased to 0.1% from 1.4% in the original variety. A comprehensive description of the breeding process, a basic characterization of the main alkaloid content, and a gene expression profile for the main alkaloid-producing genes is provided. Difficulties with the TILLING approach are also described and discussed. The opium poppy’s ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an important task. In this paper, the breeding technology of new low morphine poppy genotypes, based on a combination of a TILLING approach and single-molecule real-time NGS sequencing, is presented. Verification of the mutants in the TILLING population was obtained using RT-PCR and HPLC methods. Only three of the single-copy genes of the morphine pathway among the eleven genes were used for the identification of mutant genotypes. Point mutations were obtained only in one gene ( CNMT ) while an insertion was obtained in the other ( SalAT ). Only a few expected transition SNPs from G:C to A:T were obtained. In the low morphine mutant genotype, the production of morphine was decreased to 0.1% from 1.4% in the original variety. A comprehensive description of the breeding process, a basic characterization of the main alkaloid content, and a gene expression profile for the main alkaloid-producing genes is provided. Difficulties with the TILLING approach are also described and discussed. |
Audience | Academic |
Author | Čurn, Vladislav Endlová, Lenka Červeň, Jiří Bartas, Martin Pečinka, Petr Vrbovský, Viktor Horáček, Jiří |
AuthorAffiliation | 3 Agritec Plant Research, Ltd., Zemědělská 2520/16, 787 01 Šumperk, Czech Republic 2 Research Institute of Oilseed Crops, Development and Research, Purkyňova 10, 764 01 Opava, Czech Republic 4 Department of Genetics and Agricultural Biotechnology, Faculty of Agriculture, University of South Bohemia, Studentská 1668, 370 05 České Budějovice, Czech Republic 1 Department of Biology and Ecology, Faculty of Science, University of Ostrava, Chittussiho 10, 710 00 Ostrava, Czech Republic |
AuthorAffiliation_xml | – name: 4 Department of Genetics and Agricultural Biotechnology, Faculty of Agriculture, University of South Bohemia, Studentská 1668, 370 05 České Budějovice, Czech Republic – name: 2 Research Institute of Oilseed Crops, Development and Research, Purkyňova 10, 764 01 Opava, Czech Republic – name: 3 Agritec Plant Research, Ltd., Zemědělská 2520/16, 787 01 Šumperk, Czech Republic – name: 1 Department of Biology and Ecology, Faculty of Science, University of Ostrava, Chittussiho 10, 710 00 Ostrava, Czech Republic |
Author_xml | – sequence: 1 givenname: Jiří surname: Červeň fullname: Červeň, Jiří – sequence: 2 givenname: Viktor surname: Vrbovský fullname: Vrbovský, Viktor – sequence: 3 givenname: Jiří surname: Horáček fullname: Horáček, Jiří – sequence: 4 givenname: Martin orcidid: 0000-0002-4415-2220 surname: Bartas fullname: Bartas, Martin – sequence: 5 givenname: Lenka surname: Endlová fullname: Endlová, Lenka – sequence: 6 givenname: Petr orcidid: 0000-0003-1270-3646 surname: Pečinka fullname: Pečinka, Petr – sequence: 7 givenname: Vladislav orcidid: 0000-0002-9661-8715 surname: Čurn fullname: Čurn, Vladislav |
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Keywords | morphine content TILLING opium poppy chemical mutagenesis expression profiles new breeding methods |
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Snippet | The opium poppy’s ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an... The opium poppy's ability to produce various alkaloids is both useful and problematic. Breeding of new varieties with varying alkaloid content is therefore an... |
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SubjectTerms | Alkaloids Breeding chemical mutagenesis Communication expression profiles Food Gene expression Gene mutations Genes Genetic aspects Genetic engineering Genomes genotype Genotype & phenotype Genotypes Metabolism Methods Morphine morphine content Mutagenesis Mutants Mutation new breeding methods Opium opium poppy Opium trade Papaver somniferum Poppies Seeds Single-nucleotide polymorphism TILLING |
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Title | New Low Morphine Opium Poppy Genotype Obtained by TILLING Approach |
URI | https://www.ncbi.nlm.nih.gov/pubmed/36903937 https://www.proquest.com/docview/2785212448 https://www.proquest.com/docview/2786093144 https://www.proquest.com/docview/3040444629 https://pubmed.ncbi.nlm.nih.gov/PMC10005565 https://doaj.org/article/8dfab301e2d94ae798794c52918da0be |
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