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The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation
Induction of a pluripotent cell mass, called callus, from detached organs is an initial step in in vitro plant regeneration, during which phytohormone auxin-induced ectopic activation of a root developmental program has been shown to be required for subsequent de novo regeneration of shoots and root...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271181/ https://www.ncbi.nlm.nih.gov/pubmed/35763576 http://dx.doi.org/10.1073/pnas.2202669119 |
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author | Zhang, Shiqi Yu, Ruixue Yu, Dongxue Chang, Pengjie Guo, Shiqi Yang, Xiaona Liu, Xinchun Xu, Chongyi Hu, Yuxin |
author_facet | Zhang, Shiqi Yu, Ruixue Yu, Dongxue Chang, Pengjie Guo, Shiqi Yang, Xiaona Liu, Xinchun Xu, Chongyi Hu, Yuxin |
author_sort | Zhang, Shiqi |
collection | PubMed |
description | Induction of a pluripotent cell mass, called callus, from detached organs is an initial step in in vitro plant regeneration, during which phytohormone auxin-induced ectopic activation of a root developmental program has been shown to be required for subsequent de novo regeneration of shoots and roots. However, whether other signals are involved in governing callus formation, and thus plant regeneration capability, remains largely unclear. Here, we report that the Arabidopsis calcium (Ca(2+)) signaling module CALMODULIN IQ-MOTIF CONTAINING PROTEIN (CaM–IQM) interacts with auxin signaling to regulate callus and lateral root formation. We show that disruption of IQMs or CaMs retards auxin-induced callus and lateral root formation by dampening auxin responsiveness, and that CaM–IQM complexes physically interact with the auxin signaling repressors INDOLE-3-ACETIC ACID INDUCIBLE (IAA) proteins in a Ca(2+)-dependent manner. We further provide evidence that the physical interaction of CaM6 with IAA19 destabilizes the repressive interaction of IAA19 with AUXIN RESPONSE FACTOR 7 (ARF7), and thus regulates auxin-induced callus formation. These findings not only define a critical role of CaM–IQM-mediated Ca(2+) signaling in callus and lateral root formation, but also provide insight into the interplay of Ca(2+) signaling and auxin actions during plant regeneration and development. |
format | Online Article Text |
id | pubmed-9271181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-92711812022-12-28 The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation Zhang, Shiqi Yu, Ruixue Yu, Dongxue Chang, Pengjie Guo, Shiqi Yang, Xiaona Liu, Xinchun Xu, Chongyi Hu, Yuxin Proc Natl Acad Sci U S A Biological Sciences Induction of a pluripotent cell mass, called callus, from detached organs is an initial step in in vitro plant regeneration, during which phytohormone auxin-induced ectopic activation of a root developmental program has been shown to be required for subsequent de novo regeneration of shoots and roots. However, whether other signals are involved in governing callus formation, and thus plant regeneration capability, remains largely unclear. Here, we report that the Arabidopsis calcium (Ca(2+)) signaling module CALMODULIN IQ-MOTIF CONTAINING PROTEIN (CaM–IQM) interacts with auxin signaling to regulate callus and lateral root formation. We show that disruption of IQMs or CaMs retards auxin-induced callus and lateral root formation by dampening auxin responsiveness, and that CaM–IQM complexes physically interact with the auxin signaling repressors INDOLE-3-ACETIC ACID INDUCIBLE (IAA) proteins in a Ca(2+)-dependent manner. We further provide evidence that the physical interaction of CaM6 with IAA19 destabilizes the repressive interaction of IAA19 with AUXIN RESPONSE FACTOR 7 (ARF7), and thus regulates auxin-induced callus formation. These findings not only define a critical role of CaM–IQM-mediated Ca(2+) signaling in callus and lateral root formation, but also provide insight into the interplay of Ca(2+) signaling and auxin actions during plant regeneration and development. National Academy of Sciences 2022-06-28 2022-07-05 /pmc/articles/PMC9271181/ /pubmed/35763576 http://dx.doi.org/10.1073/pnas.2202669119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Zhang, Shiqi Yu, Ruixue Yu, Dongxue Chang, Pengjie Guo, Shiqi Yang, Xiaona Liu, Xinchun Xu, Chongyi Hu, Yuxin The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation |
title | The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation |
title_full | The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation |
title_fullStr | The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation |
title_full_unstemmed | The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation |
title_short | The calcium signaling module CaM–IQM destabilizes IAA–ARF interaction to regulate callus and lateral root formation |
title_sort | calcium signaling module cam–iqm destabilizes iaa–arf interaction to regulate callus and lateral root formation |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9271181/ https://www.ncbi.nlm.nih.gov/pubmed/35763576 http://dx.doi.org/10.1073/pnas.2202669119 |
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