Cargando…

The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis

To reveal the mechanisms underlying root adaptation to drought stress, we isolated and characterized an Arabidopsis mutant, dig5 (drought inhibition of lateral root growth 5), which exhibited increased sensitivity to the phytohormone abscisic acid (ABA) for the inhibition of lateral root growth. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Wei, Chen, Tao, Liu, Yajie, Le, Quang Tri, Wang, Ruigang, Lee, Hojoung, Xiong, Liming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501241/
https://www.ncbi.nlm.nih.gov/pubmed/36142550
http://dx.doi.org/10.3390/ijms231810642
_version_ 1784795425562165248
author Liu, Wei
Chen, Tao
Liu, Yajie
Le, Quang Tri
Wang, Ruigang
Lee, Hojoung
Xiong, Liming
author_facet Liu, Wei
Chen, Tao
Liu, Yajie
Le, Quang Tri
Wang, Ruigang
Lee, Hojoung
Xiong, Liming
author_sort Liu, Wei
collection PubMed
description To reveal the mechanisms underlying root adaptation to drought stress, we isolated and characterized an Arabidopsis mutant, dig5 (drought inhibition of lateral root growth 5), which exhibited increased sensitivity to the phytohormone abscisic acid (ABA) for the inhibition of lateral root growth. The dig5 mutant also had fewer lateral roots under normal conditions and the aerial parts were yellowish with a lower level of chlorophylls. The mutant seedlings also displayed phenotypes indicative of impaired auxin transport, such as abnormal root curling, leaf venation defects, absence of apical hook formation, and reduced hypocotyl elongation in darkness. Auxin transport assays with [(3)H]-labeled indole acetic acid (IAA) confirmed that dig5 roots were impaired in polar auxin transport. Map-based cloning and complementation assays indicated that the DIG5 locus encodes a chloroplast-localized tRNA adenosine deaminase arginine (TADA) that is involved in chloroplast protein translation. The levels of flavonoids, which are naturally occurring auxin transport inhibitors in plants, were significantly higher in dig5 roots than in the wild type roots. Further investigation showed that flavonoid biosynthetic genes were upregulated in dig5. Introduction of the flavonoid biosynthetic mutation transparent testa 4 (tt4) into dig5 restored the lateral root growth of dig5. Our study uncovers an important role of DIG5/TADA in retrogradely controlling flavonoid biosynthesis and lateral root development. We suggest that the DIG5-related signaling pathways, triggered likely by drought-induced chlorophyll breakdown and leaf senescence, may potentially help the plants to adapt to drought stress through optimizing the root system architecture.
format Online
Article
Text
id pubmed-9501241
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-95012412022-09-24 The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis Liu, Wei Chen, Tao Liu, Yajie Le, Quang Tri Wang, Ruigang Lee, Hojoung Xiong, Liming Int J Mol Sci Article To reveal the mechanisms underlying root adaptation to drought stress, we isolated and characterized an Arabidopsis mutant, dig5 (drought inhibition of lateral root growth 5), which exhibited increased sensitivity to the phytohormone abscisic acid (ABA) for the inhibition of lateral root growth. The dig5 mutant also had fewer lateral roots under normal conditions and the aerial parts were yellowish with a lower level of chlorophylls. The mutant seedlings also displayed phenotypes indicative of impaired auxin transport, such as abnormal root curling, leaf venation defects, absence of apical hook formation, and reduced hypocotyl elongation in darkness. Auxin transport assays with [(3)H]-labeled indole acetic acid (IAA) confirmed that dig5 roots were impaired in polar auxin transport. Map-based cloning and complementation assays indicated that the DIG5 locus encodes a chloroplast-localized tRNA adenosine deaminase arginine (TADA) that is involved in chloroplast protein translation. The levels of flavonoids, which are naturally occurring auxin transport inhibitors in plants, were significantly higher in dig5 roots than in the wild type roots. Further investigation showed that flavonoid biosynthetic genes were upregulated in dig5. Introduction of the flavonoid biosynthetic mutation transparent testa 4 (tt4) into dig5 restored the lateral root growth of dig5. Our study uncovers an important role of DIG5/TADA in retrogradely controlling flavonoid biosynthesis and lateral root development. We suggest that the DIG5-related signaling pathways, triggered likely by drought-induced chlorophyll breakdown and leaf senescence, may potentially help the plants to adapt to drought stress through optimizing the root system architecture. MDPI 2022-09-13 /pmc/articles/PMC9501241/ /pubmed/36142550 http://dx.doi.org/10.3390/ijms231810642 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Wei
Chen, Tao
Liu, Yajie
Le, Quang Tri
Wang, Ruigang
Lee, Hojoung
Xiong, Liming
The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis
title The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis
title_full The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis
title_fullStr The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis
title_full_unstemmed The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis
title_short The Plastidial DIG5 Protein Affects Lateral Root Development by Regulating Flavonoid Biosynthesis and Auxin Transport in Arabidopsis
title_sort plastidial dig5 protein affects lateral root development by regulating flavonoid biosynthesis and auxin transport in arabidopsis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501241/
https://www.ncbi.nlm.nih.gov/pubmed/36142550
http://dx.doi.org/10.3390/ijms231810642
work_keys_str_mv AT liuwei theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT chentao theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT liuyajie theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT lequangtri theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT wangruigang theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT leehojoung theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT xiongliming theplastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT liuwei plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT chentao plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT liuyajie plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT lequangtri plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT wangruigang plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT leehojoung plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis
AT xiongliming plastidialdig5proteinaffectslateralrootdevelopmentbyregulatingflavonoidbiosynthesisandauxintransportinarabidopsis