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An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants

A highly efficient Agrobacterium-mediated transformation method is needed for the molecular study of model tree species such as hybrid poplar 84K (Populus alba × P. glandulosa cv. ‘84K’). In this study, we report a callus-based transformation method that exhibits high efficiency and reproducibility....

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Detalles Bibliográficos
Autores principales: Wen, Shuang-Shuang, Ge, Xiao-Lan, Wang, Rui, Yang, Hai-Feng, Bai, Yu-E., Guo, Ying-Hua, Zhang, Jin, Lu, Meng-Zhu, Zhao, Shu-Tang, Wang, Liu-Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879841/
https://www.ncbi.nlm.nih.gov/pubmed/35216331
http://dx.doi.org/10.3390/ijms23042216
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author Wen, Shuang-Shuang
Ge, Xiao-Lan
Wang, Rui
Yang, Hai-Feng
Bai, Yu-E.
Guo, Ying-Hua
Zhang, Jin
Lu, Meng-Zhu
Zhao, Shu-Tang
Wang, Liu-Qiang
author_facet Wen, Shuang-Shuang
Ge, Xiao-Lan
Wang, Rui
Yang, Hai-Feng
Bai, Yu-E.
Guo, Ying-Hua
Zhang, Jin
Lu, Meng-Zhu
Zhao, Shu-Tang
Wang, Liu-Qiang
author_sort Wen, Shuang-Shuang
collection PubMed
description A highly efficient Agrobacterium-mediated transformation method is needed for the molecular study of model tree species such as hybrid poplar 84K (Populus alba × P. glandulosa cv. ‘84K’). In this study, we report a callus-based transformation method that exhibits high efficiency and reproducibility. The optimized callus induction medium (CIM1) induced the development of calli from leaves with high efficiency, and multiple shoots were induced from calli growing on the optimized shoot induction medium (SIM1). Factors affecting the transformation frequency of calli were optimized as follows: Agrobacterium concentration sets at an OD(600) of 0.6, Agrobacterium infective suspension with an acetosyringone (AS) concentration of 100 µM, infection time of 15 min, cocultivation duration of 2 days and precultivation duration of 6 days. Using this method, transgenic plants are obtained within approximately 2 months with a transformation frequency greater than 50%. Polymerase chain reaction (PCR), reverse transcription-PCR (RT-PCR) and β-galactosidase (GUS) histochemical staining analyses confirmed the successful generation of stable transformants. Additionally, the calli from leaves were subcultured and used to obtain new explants; the high transformation efficiency was still maintained in subcultured calli after 6 cycles. This method provides a reference for developing effective transformation protocols for other poplar species.
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spelling pubmed-88798412022-02-26 An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants Wen, Shuang-Shuang Ge, Xiao-Lan Wang, Rui Yang, Hai-Feng Bai, Yu-E. Guo, Ying-Hua Zhang, Jin Lu, Meng-Zhu Zhao, Shu-Tang Wang, Liu-Qiang Int J Mol Sci Article A highly efficient Agrobacterium-mediated transformation method is needed for the molecular study of model tree species such as hybrid poplar 84K (Populus alba × P. glandulosa cv. ‘84K’). In this study, we report a callus-based transformation method that exhibits high efficiency and reproducibility. The optimized callus induction medium (CIM1) induced the development of calli from leaves with high efficiency, and multiple shoots were induced from calli growing on the optimized shoot induction medium (SIM1). Factors affecting the transformation frequency of calli were optimized as follows: Agrobacterium concentration sets at an OD(600) of 0.6, Agrobacterium infective suspension with an acetosyringone (AS) concentration of 100 µM, infection time of 15 min, cocultivation duration of 2 days and precultivation duration of 6 days. Using this method, transgenic plants are obtained within approximately 2 months with a transformation frequency greater than 50%. Polymerase chain reaction (PCR), reverse transcription-PCR (RT-PCR) and β-galactosidase (GUS) histochemical staining analyses confirmed the successful generation of stable transformants. Additionally, the calli from leaves were subcultured and used to obtain new explants; the high transformation efficiency was still maintained in subcultured calli after 6 cycles. This method provides a reference for developing effective transformation protocols for other poplar species. MDPI 2022-02-17 /pmc/articles/PMC8879841/ /pubmed/35216331 http://dx.doi.org/10.3390/ijms23042216 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wen, Shuang-Shuang
Ge, Xiao-Lan
Wang, Rui
Yang, Hai-Feng
Bai, Yu-E.
Guo, Ying-Hua
Zhang, Jin
Lu, Meng-Zhu
Zhao, Shu-Tang
Wang, Liu-Qiang
An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants
title An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants
title_full An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants
title_fullStr An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants
title_full_unstemmed An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants
title_short An Efficient Agrobacterium-Mediated Transformation Method for Hybrid Poplar 84K (Populus alba × P. glandulosa) Using Calli as Explants
title_sort efficient agrobacterium-mediated transformation method for hybrid poplar 84k (populus alba × p. glandulosa) using calli as explants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8879841/
https://www.ncbi.nlm.nih.gov/pubmed/35216331
http://dx.doi.org/10.3390/ijms23042216
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