Cargando…
The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants
Plants have the potency to regenerate adventitious roots from aerial organs after detachment. In Arabidopsis thaliana, de novo root regeneration (DNRR) from leaf explants is triggered by wounding signaling that rapidly induces the expression of the ETHYLENE RESPONSE FACTOR (ERF) transcription factor...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746478/ https://www.ncbi.nlm.nih.gov/pubmed/35164655 http://dx.doi.org/10.1080/15592324.2022.2031784 |
_version_ | 1784849369871155200 |
---|---|
author | Tian, Jingjing Xing, Qian Jing, Tingting Fan, Xing Zhang, Qingzhu Müller-Xing, Ralf |
author_facet | Tian, Jingjing Xing, Qian Jing, Tingting Fan, Xing Zhang, Qingzhu Müller-Xing, Ralf |
author_sort | Tian, Jingjing |
collection | PubMed |
description | Plants have the potency to regenerate adventitious roots from aerial organs after detachment. In Arabidopsis thaliana, de novo root regeneration (DNRR) from leaf explants is triggered by wounding signaling that rapidly induces the expression of the ETHYLENE RESPONSE FACTOR (ERF) transcription factors ERF109 and ABR1 (ERF111). In turn, the ERFs promote the expression of ASA1, an essential enzyme of auxin biosynthesis, which contributes to rooting by providing high levels of auxin near the wounding side of the leaf. Here, we show that the loss of the epigenetic regulator ULTRAPETALA1 (ULT1), which interacts with Polycomb and Trithorax Group proteins, accelerates and reinforces adventitious root formation. Expression of ERF109 and ASA1 was increased in ult1 mutants, whereas ABR1 was not significantly changed. Cultivation of explants on media with exogenous auxin equates adventitious root formation in wild-type with ult1 mutants, suggesting that ULT1 negatively regulates DNRR by suppressing auxin biosynthesis. Based on these findings, we propose that ULT1 is involved in a novel mechanism that prevents overproliferation of adventitious roots during DNRR. |
format | Online Article Text |
id | pubmed-9746478 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-97464782022-12-14 The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants Tian, Jingjing Xing, Qian Jing, Tingting Fan, Xing Zhang, Qingzhu Müller-Xing, Ralf Plant Signal Behav Short Communication Plants have the potency to regenerate adventitious roots from aerial organs after detachment. In Arabidopsis thaliana, de novo root regeneration (DNRR) from leaf explants is triggered by wounding signaling that rapidly induces the expression of the ETHYLENE RESPONSE FACTOR (ERF) transcription factors ERF109 and ABR1 (ERF111). In turn, the ERFs promote the expression of ASA1, an essential enzyme of auxin biosynthesis, which contributes to rooting by providing high levels of auxin near the wounding side of the leaf. Here, we show that the loss of the epigenetic regulator ULTRAPETALA1 (ULT1), which interacts with Polycomb and Trithorax Group proteins, accelerates and reinforces adventitious root formation. Expression of ERF109 and ASA1 was increased in ult1 mutants, whereas ABR1 was not significantly changed. Cultivation of explants on media with exogenous auxin equates adventitious root formation in wild-type with ult1 mutants, suggesting that ULT1 negatively regulates DNRR by suppressing auxin biosynthesis. Based on these findings, we propose that ULT1 is involved in a novel mechanism that prevents overproliferation of adventitious roots during DNRR. Taylor & Francis 2022-02-15 /pmc/articles/PMC9746478/ /pubmed/35164655 http://dx.doi.org/10.1080/15592324.2022.2031784 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Tian, Jingjing Xing, Qian Jing, Tingting Fan, Xing Zhang, Qingzhu Müller-Xing, Ralf The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants |
title | The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants |
title_full | The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants |
title_fullStr | The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants |
title_full_unstemmed | The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants |
title_short | The epigenetic regulator ULTRAPETALA1 suppresses de novo root regeneration from Arabidopsis leaf explants |
title_sort | epigenetic regulator ultrapetala1 suppresses de novo root regeneration from arabidopsis leaf explants |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746478/ https://www.ncbi.nlm.nih.gov/pubmed/35164655 http://dx.doi.org/10.1080/15592324.2022.2031784 |
work_keys_str_mv | AT tianjingjing theepigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT xingqian theepigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT jingtingting theepigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT fanxing theepigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT zhangqingzhu theepigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT mullerxingralf theepigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT tianjingjing epigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT xingqian epigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT jingtingting epigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT fanxing epigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT zhangqingzhu epigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants AT mullerxingralf epigeneticregulatorultrapetala1suppressesdenovorootregenerationfromarabidopsisleafexplants |