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GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency
Detached organs or differentiated tissues could form a mass of pluripotent cells termed as callus on an auxin-rich medium, the underlying molecular mechanism of which remains elusive in cotton. LATERAL ORGAN BOUNDARIES DOMAIN (LBD) transcription factor is a key regulator of plant cell totipotency/pl...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990305/ https://www.ncbi.nlm.nih.gov/pubmed/35401622 http://dx.doi.org/10.3389/fpls.2022.861706 |
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author | Wang, Ye Yuan, Jiachen Wei, Xi Chen, Yanli Chen, Quanjia Ge, Xiaoyang |
author_facet | Wang, Ye Yuan, Jiachen Wei, Xi Chen, Yanli Chen, Quanjia Ge, Xiaoyang |
author_sort | Wang, Ye |
collection | PubMed |
description | Detached organs or differentiated tissues could form a mass of pluripotent cells termed as callus on an auxin-rich medium, the underlying molecular mechanism of which remains elusive in cotton. LATERAL ORGAN BOUNDARIES DOMAIN (LBD) transcription factor is a key regulator of plant cell totipotency/pluripotency, and a number of cotton GhLBDs with high-level differential expression during the callus induction process have been identified. Their overexpression in cotton calli fostered promotions in and callus induction without exogenous auxin. Expression analysis and histological observation using paraffin sectioning suggested that the first 72 h on culture is a key time point for callus initiation, whereby the GhLBDs showed high transcript abundance and enlarged calli that were rapidly developed from procambium and cambium. GhLBDs’ expression level could be precisely modulated by the gradient concentrations of exogenous auxin, whereas auxin transport inhibitor 2,3,5-triiodobenzoic acid could severely inhibit its expression. The LBD-mediated callus formation was also dependent on the expression levels of GhLBDs. Further, a β-estradiol-inducible promoter pER8 was used to drive GhLBD18-1 expression, which led to rapid callus proliferation, suggesting that pER8/GhLBD18-1 could be used as a selectable marker system to replace the existing antibiotic/herbicide-resistance selectable markers in plant transformation. Our study provides new insights for callus initiation regulatory mechanism and strategies for improving transformation efficiency in cotton. |
format | Online Article Text |
id | pubmed-8990305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89903052022-04-09 GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency Wang, Ye Yuan, Jiachen Wei, Xi Chen, Yanli Chen, Quanjia Ge, Xiaoyang Front Plant Sci Plant Science Detached organs or differentiated tissues could form a mass of pluripotent cells termed as callus on an auxin-rich medium, the underlying molecular mechanism of which remains elusive in cotton. LATERAL ORGAN BOUNDARIES DOMAIN (LBD) transcription factor is a key regulator of plant cell totipotency/pluripotency, and a number of cotton GhLBDs with high-level differential expression during the callus induction process have been identified. Their overexpression in cotton calli fostered promotions in and callus induction without exogenous auxin. Expression analysis and histological observation using paraffin sectioning suggested that the first 72 h on culture is a key time point for callus initiation, whereby the GhLBDs showed high transcript abundance and enlarged calli that were rapidly developed from procambium and cambium. GhLBDs’ expression level could be precisely modulated by the gradient concentrations of exogenous auxin, whereas auxin transport inhibitor 2,3,5-triiodobenzoic acid could severely inhibit its expression. The LBD-mediated callus formation was also dependent on the expression levels of GhLBDs. Further, a β-estradiol-inducible promoter pER8 was used to drive GhLBD18-1 expression, which led to rapid callus proliferation, suggesting that pER8/GhLBD18-1 could be used as a selectable marker system to replace the existing antibiotic/herbicide-resistance selectable markers in plant transformation. Our study provides new insights for callus initiation regulatory mechanism and strategies for improving transformation efficiency in cotton. Frontiers Media S.A. 2022-03-25 /pmc/articles/PMC8990305/ /pubmed/35401622 http://dx.doi.org/10.3389/fpls.2022.861706 Text en Copyright © 2022 Wang, Yuan, Wei, Chen, Chen and Ge. 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 Wang, Ye Yuan, Jiachen Wei, Xi Chen, Yanli Chen, Quanjia Ge, Xiaoyang GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency |
title | GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency |
title_full | GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency |
title_fullStr | GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency |
title_full_unstemmed | GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency |
title_short | GhLBDs Promote Callus Initiation and Act as Selectable Markers to Increase Transformation Efficiency |
title_sort | ghlbds promote callus initiation and act as selectable markers to increase transformation efficiency |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8990305/ https://www.ncbi.nlm.nih.gov/pubmed/35401622 http://dx.doi.org/10.3389/fpls.2022.861706 |
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