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Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis

Constitutive expression of the Zea mays L. (maize) morphogenic transcription factors Baby Boom (Bbm) and Wuschel2 (Wus2) in maize can not only greatly increase transformation efficiency but can also induce phenotypic abnormalities and sterility. In an effort to alleviate the pleiotropic effects of c...

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Autores principales: Lowe, Keith, La Rota, Mauricio, Hoerster, George, Hastings, Craig, Wang, Ning, Chamberlin, Mark, Wu, Emily, Jones, Todd, Gordon-Kamm, William
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954046/
https://www.ncbi.nlm.nih.gov/pubmed/29780216
http://dx.doi.org/10.1007/s11627-018-9905-2
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author Lowe, Keith
La Rota, Mauricio
Hoerster, George
Hastings, Craig
Wang, Ning
Chamberlin, Mark
Wu, Emily
Jones, Todd
Gordon-Kamm, William
author_facet Lowe, Keith
La Rota, Mauricio
Hoerster, George
Hastings, Craig
Wang, Ning
Chamberlin, Mark
Wu, Emily
Jones, Todd
Gordon-Kamm, William
author_sort Lowe, Keith
collection PubMed
description Constitutive expression of the Zea mays L. (maize) morphogenic transcription factors Baby Boom (Bbm) and Wuschel2 (Wus2) in maize can not only greatly increase transformation efficiency but can also induce phenotypic abnormalities and sterility. In an effort to alleviate the pleiotropic effects of constitutive expression, a genome wide search was undertaken to find suitable maize promoters to drive tissue and timing-specific expression of the transformation enhancing genes Bbm and Wus2. A promoter from a maize phospholipid transferase protein gene (Zm-PLTP(pro)) was identified based on its expression in leaves, embryos, and callus while being downregulated in roots, meristems, and reproductive tissues. When Zm-PLTP(pro) driving Bbm was transformed into immature maize embryos along with a Wus2 expression cassette driven by the nopaline synthase promoter (Nos(pro)::Wus2) abundant somatic embryos rapidly formed on the scutella. These embryos were individual and uniformly transformed and could be directly germinated into plants without a callus phase. Transformed plants could be sent to the greenhouse in as little as 1 mo and regenerated plants matched the seed-derived phenotype for the inbred and were fertile. However, T1 seed from these plants had poor germination. Replacing Nos(pro) with a maize auxin-inducible promoter (Zm-Axig1(pro)) in combination with Zm-PLTP(pro)::Bbm, allowed healthy, fertile plants to be regenerated. Single-copy T1 seed germinated normally and had a predominantly wild-type inbred phenotype. For maize, this callus-free transformation process has worked in all inbred lines tested.
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spelling pubmed-59540462018-05-18 Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis Lowe, Keith La Rota, Mauricio Hoerster, George Hastings, Craig Wang, Ning Chamberlin, Mark Wu, Emily Jones, Todd Gordon-Kamm, William In Vitro Cell Dev Biol Plant Biotechnology Constitutive expression of the Zea mays L. (maize) morphogenic transcription factors Baby Boom (Bbm) and Wuschel2 (Wus2) in maize can not only greatly increase transformation efficiency but can also induce phenotypic abnormalities and sterility. In an effort to alleviate the pleiotropic effects of constitutive expression, a genome wide search was undertaken to find suitable maize promoters to drive tissue and timing-specific expression of the transformation enhancing genes Bbm and Wus2. A promoter from a maize phospholipid transferase protein gene (Zm-PLTP(pro)) was identified based on its expression in leaves, embryos, and callus while being downregulated in roots, meristems, and reproductive tissues. When Zm-PLTP(pro) driving Bbm was transformed into immature maize embryos along with a Wus2 expression cassette driven by the nopaline synthase promoter (Nos(pro)::Wus2) abundant somatic embryos rapidly formed on the scutella. These embryos were individual and uniformly transformed and could be directly germinated into plants without a callus phase. Transformed plants could be sent to the greenhouse in as little as 1 mo and regenerated plants matched the seed-derived phenotype for the inbred and were fertile. However, T1 seed from these plants had poor germination. Replacing Nos(pro) with a maize auxin-inducible promoter (Zm-Axig1(pro)) in combination with Zm-PLTP(pro)::Bbm, allowed healthy, fertile plants to be regenerated. Single-copy T1 seed germinated normally and had a predominantly wild-type inbred phenotype. For maize, this callus-free transformation process has worked in all inbred lines tested. Springer US 2018-04-30 2018 /pmc/articles/PMC5954046/ /pubmed/29780216 http://dx.doi.org/10.1007/s11627-018-9905-2 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Biotechnology
Lowe, Keith
La Rota, Mauricio
Hoerster, George
Hastings, Craig
Wang, Ning
Chamberlin, Mark
Wu, Emily
Jones, Todd
Gordon-Kamm, William
Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis
title Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis
title_full Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis
title_fullStr Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis
title_full_unstemmed Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis
title_short Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis
title_sort rapid genotype “independent” zea mays l. (maize) transformation via direct somatic embryogenesis
topic Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5954046/
https://www.ncbi.nlm.nih.gov/pubmed/29780216
http://dx.doi.org/10.1007/s11627-018-9905-2
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