CO2 Response Screen in Grass Brachypodium Reveals Key Role of a MAP Kinase in CO2-Triggered Stomatal Closure.

ABA Bicarbonate CO2 sensor Carbon dioxide Graminacea Guard cell

Journal

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

Informations de publication

Date de publication:
06 May 2024
Historique:
received: 08 03 2024
revised: 15 04 2024
accepted: 16 04 2024
medline: 6 5 2024
pubmed: 6 5 2024
entrez: 6 5 2024
Statut: aheadofprint

Résumé

Plants respond to increased CO2 concentrations through stomatal closure, which can contribute to increased water use efficiency. Grasses display faster stomatal responses than eudicots due to dumbbell-shaped guard cells flanked by subsidiary cells working in opposition. However, forward genetic screening for stomatal CO2 signal transduction mutants in grasses has yet to be reported. The grass model Brachypodium distachyon is closely related to agronomically important cereal crops, sharing largely collinear genomes. To gain insights into CO2 control mechanisms of stomatal movements in grasses, we developed an unbiased forward genetic screen with an EMS-mutagenized Brachypodium distachyon M5 generation population using infrared imaging to identify plants with altered leaf temperatures at elevated CO2. Among isolated mutants, a "chill1" mutant exhibited cooler leaf temperatures than wildtype Bd21-3 parent control plants after exposure to increased [CO2]. chill1 plants showed strongly impaired high CO2-induced stomatal closure despite retaining a robust abscisic acid-induced stomatal closing response. Through bulked segregant whole-genome-sequencing analyses followed by analyses of further backcrossed F4 generation plants and generation and characterization of sodium-azide and CRISPR-cas9 mutants, chill1 was mapped to a protein kinase, Mitogen-Activated Protein Kinase 5 (BdMPK5). The chill1 mutation impaired BdMPK5 protein-mediated CO2/HCO3- sensing together with the High Temperature 1 (HT1) Raf-like kinase in vitro. Furthermore, AlphaFold2-directed structural modeling predicted that the identified BdMPK5-D90N chill1 mutant residue is located at the interface of BdMPK5 with the BdHT1 Raf-like kinase. BdMPK5 is a key signaling component that mediates CO2-induced stomatal movements and is proposed to function as a component of the primary CO2 sensor in grasses.

Identifiants

pubmed: 38709683
pii: 7665566
doi: 10.1093/plphys/kiae262
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. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

Auteurs

Bryn N K Lopez (BNK)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Paulo H O Ceciliato (PHO)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Yohei Takahashi (Y)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.
Institute of Transformative Bio-Molecules (ITbM), Nagoya University, Furocho, Chikusa Ward, Nagoya, Aichi 464-0813, Japan.

Felipe J Rangel (FJ)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Evana A Salem (EA)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Klara Kernig (K)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Kelly Chow (K)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Li Zhang (L)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Morgana A Sidhom (MA)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Christian G Seitz (CG)

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093 USA.

Tingwen Zheng (T)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Richard Sibout (R)

Biopolymères Interactions Assemblages, Equipe Paroi Végétale et Polymères Pariétaux (PVPP), Impasse Y. Cauchois/Site de la Géraudière BP71627, 44316 NANTES cedex 03, FRANCE.

Debbie L Laudencia-Chingcuanco (DL)

Crop Improvement and Genetics Research, USDA, ARS, PWA, WRRC-CIG, 800 BUCHANAN STREET, ALBANY, CA 94710.

Daniel P Woods (DP)

Department of Plant Sciences, University of California, Davis, CA 95616, USA.

James Andrew McCammon (JA)

Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, CA 92093 USA.

John P Vogel (JP)

U.S. Dept. of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720.

Julian I Schroeder (JI)

School of Biological Sciences, Cell and Developmental Biology Department, University of California San Diego, La Jolla, CA 92093-0116, USA.

Classifications MeSH