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A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development
Cytokinin fulfills its diverse roles in planta through a series of transcriptional responses. We identify the in vivo DNA binding site profiles for three genetically redundant type-B ARABIDOPSIS RESPONSE REGULATORS (B-ARRs): ARR1, ARR10, and ARR12. The expression and genome-wide DNA binding location...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913131/ https://www.ncbi.nlm.nih.gov/pubmed/29686312 http://dx.doi.org/10.1038/s41467-018-03921-6 |
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author | Xie, Mingtang Chen, Hongyu Huang, Ling O’Neil, Ryan C. Shokhirev, Maxim N. Ecker, Joseph R. |
author_facet | Xie, Mingtang Chen, Hongyu Huang, Ling O’Neil, Ryan C. Shokhirev, Maxim N. Ecker, Joseph R. |
author_sort | Xie, Mingtang |
collection | PubMed |
description | Cytokinin fulfills its diverse roles in planta through a series of transcriptional responses. We identify the in vivo DNA binding site profiles for three genetically redundant type-B ARABIDOPSIS RESPONSE REGULATORS (B-ARRs): ARR1, ARR10, and ARR12. The expression and genome-wide DNA binding locations of the three B-ARRs extensively overlap. Constructing a primary cytokinin response transcriptional network reveals a recurring theme of widespread cross-regulation between the components of the cytokinin pathway and other plant hormone pathways. The B-ARRs are found to have similar DNA binding motifs, though sequences flanking the core motif were degenerate. Cytokinin treatments amalgamate the three different B-ARRs motifs to identical DNA binding signatures (AGATHY, H(a/t/c), Y(t/c)) which suggests cytokinin may regulate binding activity of B-ARR family members. Furthermore, we find that WUSCHEL, a key gene required for apical meristem maintenance, is a cytokinin-dependent B-ARR target gene, demonstrating the importance of the cytokinin transcription factor network in shoot development. |
format | Online Article Text |
id | pubmed-5913131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59131312018-04-25 A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development Xie, Mingtang Chen, Hongyu Huang, Ling O’Neil, Ryan C. Shokhirev, Maxim N. Ecker, Joseph R. Nat Commun Article Cytokinin fulfills its diverse roles in planta through a series of transcriptional responses. We identify the in vivo DNA binding site profiles for three genetically redundant type-B ARABIDOPSIS RESPONSE REGULATORS (B-ARRs): ARR1, ARR10, and ARR12. The expression and genome-wide DNA binding locations of the three B-ARRs extensively overlap. Constructing a primary cytokinin response transcriptional network reveals a recurring theme of widespread cross-regulation between the components of the cytokinin pathway and other plant hormone pathways. The B-ARRs are found to have similar DNA binding motifs, though sequences flanking the core motif were degenerate. Cytokinin treatments amalgamate the three different B-ARRs motifs to identical DNA binding signatures (AGATHY, H(a/t/c), Y(t/c)) which suggests cytokinin may regulate binding activity of B-ARR family members. Furthermore, we find that WUSCHEL, a key gene required for apical meristem maintenance, is a cytokinin-dependent B-ARR target gene, demonstrating the importance of the cytokinin transcription factor network in shoot development. Nature Publishing Group UK 2018-04-23 /pmc/articles/PMC5913131/ /pubmed/29686312 http://dx.doi.org/10.1038/s41467-018-03921-6 Text en © The Author(s) 2018, last corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Xie, Mingtang Chen, Hongyu Huang, Ling O’Neil, Ryan C. Shokhirev, Maxim N. Ecker, Joseph R. A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
title | A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
title_full | A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
title_fullStr | A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
title_full_unstemmed | A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
title_short | A B-ARR-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
title_sort | b-arr-mediated cytokinin transcriptional network directs hormone cross-regulation and shoot development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5913131/ https://www.ncbi.nlm.nih.gov/pubmed/29686312 http://dx.doi.org/10.1038/s41467-018-03921-6 |
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