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A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration

Wounding triggers organ regeneration in many plant species, and application of plant hormones, such as auxin and cytokinin, enhances their regenerative capacities in tissue culture. Recent studies have identified several key players mediating wound- and/or plant hormone-induced cellular reprogrammin...

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Autores principales: Ikeuchi, Momoko, Shibata, Michitaro, Rymen, Bart, Iwase, Akira, Bågman, Anne-Maarit, Watt, Lewis, Coleman, Duncan, Favero, David S, Takahashi, Tatsuya, Ahnert, Sebastian E, Brady, Siobhan M, Sugimoto, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018650/
https://www.ncbi.nlm.nih.gov/pubmed/29462363
http://dx.doi.org/10.1093/pcp/pcy013
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author Ikeuchi, Momoko
Shibata, Michitaro
Rymen, Bart
Iwase, Akira
Bågman, Anne-Maarit
Watt, Lewis
Coleman, Duncan
Favero, David S
Takahashi, Tatsuya
Ahnert, Sebastian E
Brady, Siobhan M
Sugimoto, Keiko
author_facet Ikeuchi, Momoko
Shibata, Michitaro
Rymen, Bart
Iwase, Akira
Bågman, Anne-Maarit
Watt, Lewis
Coleman, Duncan
Favero, David S
Takahashi, Tatsuya
Ahnert, Sebastian E
Brady, Siobhan M
Sugimoto, Keiko
author_sort Ikeuchi, Momoko
collection PubMed
description Wounding triggers organ regeneration in many plant species, and application of plant hormones, such as auxin and cytokinin, enhances their regenerative capacities in tissue culture. Recent studies have identified several key players mediating wound- and/or plant hormone-induced cellular reprogramming, but the global architecture of gene regulatory relationships underlying plant cellular reprogramming is still far from clear. In this study, we uncovered a gene regulatory network (GRN) associated with plant cellular reprogramming by using an enhanced yeast one-hybrid (eY1H) screen systematically to identify regulatory relationships between 252 transcription factors (TFs) and 48 promoters. Our network analyses suggest that wound- and/or hormone-invoked signals exhibit extensive cross-talk and regulate many common reprogramming-associated genes via multilayered regulatory cascades. Our data suggest that PLETHORA 3 (PLT3), ENHANCER OF SHOOT REGENERATION 1 (ESR1) and HEAT SHOCK FACTOR B 1 (HSFB1) act as critical nodes that have many overlapping targets and potentially connect upstream stimuli to downstream developmental decisions. Interestingly, a set of wound-inducible APETALA 2/ETHYLENE RESPONSE FACTORs (AP2/ERFs) appear to regulate these key genes, which, in turn, form feed-forward cascades that control downstream targets associated with callus formation and organ regeneration. In addition, we found another regulatory pathway, mediated by LATERAL ORGAN BOUNDARY/ASYMMETRIC LEAVES 2 (LOB/AS2) TFs, which probably plays a distinct but partially overlapping role alongside the AP2/ERFs in the putative gene regulatory cascades. Taken together, our findings provide the first global picture of the GRN governing plant cell reprogramming, which will serve as a valuable resource for future studies.
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spelling pubmed-60186502018-07-10 A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration Ikeuchi, Momoko Shibata, Michitaro Rymen, Bart Iwase, Akira Bågman, Anne-Maarit Watt, Lewis Coleman, Duncan Favero, David S Takahashi, Tatsuya Ahnert, Sebastian E Brady, Siobhan M Sugimoto, Keiko Plant Cell Physiol Special Issue – Regular Papers Wounding triggers organ regeneration in many plant species, and application of plant hormones, such as auxin and cytokinin, enhances their regenerative capacities in tissue culture. Recent studies have identified several key players mediating wound- and/or plant hormone-induced cellular reprogramming, but the global architecture of gene regulatory relationships underlying plant cellular reprogramming is still far from clear. In this study, we uncovered a gene regulatory network (GRN) associated with plant cellular reprogramming by using an enhanced yeast one-hybrid (eY1H) screen systematically to identify regulatory relationships between 252 transcription factors (TFs) and 48 promoters. Our network analyses suggest that wound- and/or hormone-invoked signals exhibit extensive cross-talk and regulate many common reprogramming-associated genes via multilayered regulatory cascades. Our data suggest that PLETHORA 3 (PLT3), ENHANCER OF SHOOT REGENERATION 1 (ESR1) and HEAT SHOCK FACTOR B 1 (HSFB1) act as critical nodes that have many overlapping targets and potentially connect upstream stimuli to downstream developmental decisions. Interestingly, a set of wound-inducible APETALA 2/ETHYLENE RESPONSE FACTORs (AP2/ERFs) appear to regulate these key genes, which, in turn, form feed-forward cascades that control downstream targets associated with callus formation and organ regeneration. In addition, we found another regulatory pathway, mediated by LATERAL ORGAN BOUNDARY/ASYMMETRIC LEAVES 2 (LOB/AS2) TFs, which probably plays a distinct but partially overlapping role alongside the AP2/ERFs in the putative gene regulatory cascades. Taken together, our findings provide the first global picture of the GRN governing plant cell reprogramming, which will serve as a valuable resource for future studies. Oxford University Press 2018-04 2018-02-15 /pmc/articles/PMC6018650/ /pubmed/29462363 http://dx.doi.org/10.1093/pcp/pcy013 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Special Issue – Regular Papers
Ikeuchi, Momoko
Shibata, Michitaro
Rymen, Bart
Iwase, Akira
Bågman, Anne-Maarit
Watt, Lewis
Coleman, Duncan
Favero, David S
Takahashi, Tatsuya
Ahnert, Sebastian E
Brady, Siobhan M
Sugimoto, Keiko
A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration
title A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration
title_full A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration
title_fullStr A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration
title_full_unstemmed A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration
title_short A Gene Regulatory Network for Cellular Reprogramming in Plant Regeneration
title_sort gene regulatory network for cellular reprogramming in plant regeneration
topic Special Issue – Regular Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018650/
https://www.ncbi.nlm.nih.gov/pubmed/29462363
http://dx.doi.org/10.1093/pcp/pcy013
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