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An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta

The all-red A. arguta (Actinidia arguta) is an anthocyanin-rich and excellent hardy fruit. Many studies have focused on the green-fleshed A. arguta, and fewer studies have been conducted on the all-red A. arguta. Here we reported a regeneration and Agrobacterium-mediated transformation protocol by u...

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Autores principales: Yao, Wantian, Kong, Lingling, Lei, Diya, Zhao, Bing, Tang, Honglan, Zhou, Xuan, Lin, Yuanxiu, Zhang, Yunting, Wang, Yan, He, Wen, Li, Mengyao, Chen, Qing, Luo, Ya, Wang, Xiaorong, Tang, Haoru, Zhang, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425222/
https://www.ncbi.nlm.nih.gov/pubmed/37583592
http://dx.doi.org/10.3389/fpls.2023.1204267
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author Yao, Wantian
Kong, Lingling
Lei, Diya
Zhao, Bing
Tang, Honglan
Zhou, Xuan
Lin, Yuanxiu
Zhang, Yunting
Wang, Yan
He, Wen
Li, Mengyao
Chen, Qing
Luo, Ya
Wang, Xiaorong
Tang, Haoru
Zhang, Yong
author_facet Yao, Wantian
Kong, Lingling
Lei, Diya
Zhao, Bing
Tang, Honglan
Zhou, Xuan
Lin, Yuanxiu
Zhang, Yunting
Wang, Yan
He, Wen
Li, Mengyao
Chen, Qing
Luo, Ya
Wang, Xiaorong
Tang, Haoru
Zhang, Yong
author_sort Yao, Wantian
collection PubMed
description The all-red A. arguta (Actinidia arguta) is an anthocyanin-rich and excellent hardy fruit. Many studies have focused on the green-fleshed A. arguta, and fewer studies have been conducted on the all-red A. arguta. Here we reported a regeneration and Agrobacterium-mediated transformation protocol by using leaves of all-red A. arguta as explants. Aseptic seedling leaves of A. arguta were used as callus-inducing materials. MS medium supplemented with 0.3 mg·L(-1) 2,4-D and 1.0 mg·L(-1) BA was the optimal medium for callus induction of leaves, and medium supplemented with 3 mg·L(-1) tZ and 0.5 mg·L(-1) IAA was optimal for adventitious shoot regeneration. The best proliferation medium for adventitious buds was MS + 1.0 mg·L(-1) BA + 0.3 mg·L(-1) NAA. The best rooting medium was 1/2MS + 0.7 mg·L(-1) IBA with a 100% rooting rate. For the red flesh hardy kiwi variety ‘Purpurna Saduwa’ (A. arguta var. purpurea), leaves are receptors for Agrobacterium (EHA105)-mediated transformation. The orthogonal experiment was used for the optimization of each genetic transformation parameter and the genetic transformation of the leaves was 21% under optimal conditions. Our study provides technical parameters for applying genetic resources and molecular breeding of kiwifruit with red flesh.
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spelling pubmed-104252222023-08-15 An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta Yao, Wantian Kong, Lingling Lei, Diya Zhao, Bing Tang, Honglan Zhou, Xuan Lin, Yuanxiu Zhang, Yunting Wang, Yan He, Wen Li, Mengyao Chen, Qing Luo, Ya Wang, Xiaorong Tang, Haoru Zhang, Yong Front Plant Sci Plant Science The all-red A. arguta (Actinidia arguta) is an anthocyanin-rich and excellent hardy fruit. Many studies have focused on the green-fleshed A. arguta, and fewer studies have been conducted on the all-red A. arguta. Here we reported a regeneration and Agrobacterium-mediated transformation protocol by using leaves of all-red A. arguta as explants. Aseptic seedling leaves of A. arguta were used as callus-inducing materials. MS medium supplemented with 0.3 mg·L(-1) 2,4-D and 1.0 mg·L(-1) BA was the optimal medium for callus induction of leaves, and medium supplemented with 3 mg·L(-1) tZ and 0.5 mg·L(-1) IAA was optimal for adventitious shoot regeneration. The best proliferation medium for adventitious buds was MS + 1.0 mg·L(-1) BA + 0.3 mg·L(-1) NAA. The best rooting medium was 1/2MS + 0.7 mg·L(-1) IBA with a 100% rooting rate. For the red flesh hardy kiwi variety ‘Purpurna Saduwa’ (A. arguta var. purpurea), leaves are receptors for Agrobacterium (EHA105)-mediated transformation. The orthogonal experiment was used for the optimization of each genetic transformation parameter and the genetic transformation of the leaves was 21% under optimal conditions. Our study provides technical parameters for applying genetic resources and molecular breeding of kiwifruit with red flesh. Frontiers Media S.A. 2023-07-31 /pmc/articles/PMC10425222/ /pubmed/37583592 http://dx.doi.org/10.3389/fpls.2023.1204267 Text en Copyright © 2023 Yao, Kong, Lei, Zhao, Tang, Zhou, Lin, Zhang, Wang, He, Li, Chen, Luo, Wang, Tang and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Yao, Wantian
Kong, Lingling
Lei, Diya
Zhao, Bing
Tang, Honglan
Zhou, Xuan
Lin, Yuanxiu
Zhang, Yunting
Wang, Yan
He, Wen
Li, Mengyao
Chen, Qing
Luo, Ya
Wang, Xiaorong
Tang, Haoru
Zhang, Yong
An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta
title An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta
title_full An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta
title_fullStr An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta
title_full_unstemmed An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta
title_short An effective method for establishing a regeneration and genetic transformation system for Actinidia arguta
title_sort effective method for establishing a regeneration and genetic transformation system for actinidia arguta
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425222/
https://www.ncbi.nlm.nih.gov/pubmed/37583592
http://dx.doi.org/10.3389/fpls.2023.1204267
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