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Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration

Somatic cells of higher plants possess the remarkable ability to regenerate new individuals via reestablishing apical meristems. Reconstitution of shoot meristem is the vital process and is required for application of plant biotechnology. Under in vitro culture condition, shoot meristem can be forme...

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Autores principales: Liu, Jiong Hui, Dong, Wan Chen, Fei, Fang Fang, Li, Xiao Tong, Zhang, Xiao Hang, Zhou, Yangyan, Zhang, Xian Sheng, Sang, Ya Lin, Cheng, Zhi Juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931721/
https://www.ncbi.nlm.nih.gov/pubmed/35310629
http://dx.doi.org/10.3389/fpls.2022.850726
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author Liu, Jiong Hui
Dong, Wan Chen
Fei, Fang Fang
Li, Xiao Tong
Zhang, Xiao Hang
Zhou, Yangyan
Zhang, Xian Sheng
Sang, Ya Lin
Cheng, Zhi Juan
author_facet Liu, Jiong Hui
Dong, Wan Chen
Fei, Fang Fang
Li, Xiao Tong
Zhang, Xiao Hang
Zhou, Yangyan
Zhang, Xian Sheng
Sang, Ya Lin
Cheng, Zhi Juan
author_sort Liu, Jiong Hui
collection PubMed
description Somatic cells of higher plants possess the remarkable ability to regenerate new individuals via reestablishing apical meristems. Reconstitution of shoot meristem is the vital process and is required for application of plant biotechnology. Under in vitro culture condition, shoot meristem can be formed directly or indirectly, depending on the absence or presence of callus as the intermediate status. However, the difference of regulatory mechanisms between the two regeneration types remains unknown. In this study, we established a bi-directional system in which shoots regenerated directly from lateral root primordia (LRP) and indirectly from hypocotyl-derived callus simultaneously. The results based on this system revealed that regulation of WOX11 expression represents the difference between the two regeneration types in two aspects. Firstly, number of founder cells expressing WOX11 is tightly associated with regeneration types. Relatively more founder cells gave rise to callus and produce larger meristem, whereas less founder cells produce LRP that regenerate smaller meristem. Secondly, non-CG DNA methylation specifically regulated WOX11 transcription in LRP and promoted direct shoot regeneration, but had no influence on indirect regeneration. The results provide new insights for understanding the regulatory mechanisms of cell fate transition during de novo organogenesis.
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spelling pubmed-89317212022-03-19 Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration Liu, Jiong Hui Dong, Wan Chen Fei, Fang Fang Li, Xiao Tong Zhang, Xiao Hang Zhou, Yangyan Zhang, Xian Sheng Sang, Ya Lin Cheng, Zhi Juan Front Plant Sci Plant Science Somatic cells of higher plants possess the remarkable ability to regenerate new individuals via reestablishing apical meristems. Reconstitution of shoot meristem is the vital process and is required for application of plant biotechnology. Under in vitro culture condition, shoot meristem can be formed directly or indirectly, depending on the absence or presence of callus as the intermediate status. However, the difference of regulatory mechanisms between the two regeneration types remains unknown. In this study, we established a bi-directional system in which shoots regenerated directly from lateral root primordia (LRP) and indirectly from hypocotyl-derived callus simultaneously. The results based on this system revealed that regulation of WOX11 expression represents the difference between the two regeneration types in two aspects. Firstly, number of founder cells expressing WOX11 is tightly associated with regeneration types. Relatively more founder cells gave rise to callus and produce larger meristem, whereas less founder cells produce LRP that regenerate smaller meristem. Secondly, non-CG DNA methylation specifically regulated WOX11 transcription in LRP and promoted direct shoot regeneration, but had no influence on indirect regeneration. The results provide new insights for understanding the regulatory mechanisms of cell fate transition during de novo organogenesis. Frontiers Media S.A. 2022-03-04 /pmc/articles/PMC8931721/ /pubmed/35310629 http://dx.doi.org/10.3389/fpls.2022.850726 Text en Copyright © 2022 Liu, Dong, Fei, Li, Zhang, Zhou, Zhang, Sang and Cheng. 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
Liu, Jiong Hui
Dong, Wan Chen
Fei, Fang Fang
Li, Xiao Tong
Zhang, Xiao Hang
Zhou, Yangyan
Zhang, Xian Sheng
Sang, Ya Lin
Cheng, Zhi Juan
Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration
title Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration
title_full Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration
title_fullStr Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration
title_full_unstemmed Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration
title_short Regulation of WOX11 Expression Represents the Difference Between Direct and Indirect Shoot Regeneration
title_sort regulation of wox11 expression represents the difference between direct and indirect shoot regeneration
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8931721/
https://www.ncbi.nlm.nih.gov/pubmed/35310629
http://dx.doi.org/10.3389/fpls.2022.850726
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