Transcription factor WOX11 modulates tolerance to cyst nematodes via adventitious lateral root formation.

Heterodera schachtii de novo root organogenesis Adventitious lateral root COI1 ERF109 LBD16 WOX11 damage plasticity root system architecture tolerance

Journal

Plant physiology
ISSN: 1532-2548
Titre abrégé: Plant Physiol
Pays: United States
ID NLM: 0401224

Informations de publication

Date de publication:
08 Feb 2024
Historique:
received: 11 08 2023
revised: 28 11 2023
accepted: 29 12 2023
medline: 8 2 2024
pubmed: 8 2 2024
entrez: 8 2 2024
Statut: aheadofprint

Résumé

The transcription factor WUSCHEL-RELATED HOMEOBOX 11 (WOX11) in Arabidopsis (Arabidopsis thaliana) initiates the formation of adventitious lateral roots upon mechanical injury in primary roots. Root-invading nematodes also induce de novo root organogenesis leading to excessive root branching, but it is not known if this symptom of disease involves mediation by WOX11 and if it benefits the plant. Here, we show with targeted transcriptional repression and reporter gene analyses in Arabidopsis that the beet cyst nematode Heterodera schachtii activates WOX11-mediated adventitious lateral rooting from primary roots close to infection sites. The activation of WOX11 in nematode-infected roots occurs downstream of jasmonic acid-dependent damage signaling via ETHYLENE RESPONSE FACTOR109, linking adventitious lateral root formation to nematode damage to host tissues. By measuring different root system components, we found that WOX11-mediated formation of adventitious lateral roots compensates for nematode-induced inhibition of primary root growth. Our observations further demonstrate that WOX11-mediated rooting reduces the impact of nematode infections on aboveground plant development and growth. Altogether, we conclude that the transcriptional regulation by WOX11 modulates root system plasticity under biotic stress, which is one of the key mechanisms underlying tolerance of Arabidopsis to cyst nematode infections.

Identifiants

pubmed: 38330218
pii: 7603575
doi: 10.1093/plphys/kiae053
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of American Society of Plant Biologists.

Auteurs

Jaap-Jan Willig (JJ)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Nina Guarneri (N)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Thomas van Loon (T)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Sri Wahyuni (S)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Ivan E Astudillo-Estévez (IE)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Lin Xu (L)

National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai 200032, China.

Viola Willemsen (V)

Cluster of Plant Developmental Biology, Cell and Developmental Biology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Aska Goverse (A)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Mark G Sterken (MG)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

José L Lozano-Torres (JL)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Jaap Bakker (J)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Geert Smant (G)

Laboratory of Nematology, Wageningen University & Research, 6708 PB Wageningen, the Netherlands.

Classifications MeSH