Primary multistep phosphorelay activation comprises both cytokinin and abiotic stress responses: insights from comparative analysis of Brassica type-A response regulators

Author:

Nicolas Mala Katrina Leslie12ORCID,Skalak Jan12ORCID,Zemlyanskaya Elena34ORCID,Dolgikh Vladislav34ORCID,Jedlickova Veronika1,Robert Helene S1ORCID,Havlickova Lenka5ORCID,Panzarova Klara6ORCID,Trtilek Martin6ORCID,Bancroft Ian5ORCID,Hejatko Jan12ORCID

Affiliation:

1. CEITEC - Central European Institute of Technology, Masaryk University , Kamenice 5/A2, 625 00 Brno , Czech Republic

2. National Centre for Biomolecular Research, Faculty of Science, Masaryk University , Kamenice 5/A2, 625 00 Brno , Czech Republic

3. Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences , Novosibirsk, 630090 , Russia

4. Faculty of Natural Sciences, Novosibirsk State University , Novosibirsk, 630090 , Russia

5. Department of Biology, University of York , York , UK

6. PSI (Photon Systems Instruments), Ltd , Drásov, 66424 Drásov , Czech Republic

Abstract

Abstract Multistep phosphorelay (MSP) signaling integrates hormonal and environmental signals to control both plant development and adaptive responses. Type-A RESPONSE REGULATOR (RRA) genes, the downstream members of the MSP cascade and cytokinin primary response genes, are thought to mediate primarily the negative feedback regulation of (cytokinin-induced) MSP signaling. However, transcriptional data also suggest the involvement of RRA genes in stress-related responses. By employing evolutionary conservation with the well-characterized Arabidopsis thaliana RRA genes, we identified five and 38 novel putative RRA genes in Brassica oleracea and Brassica napus, respectively. Our phylogenetic analysis suggests the existence of gene-specific selective pressure, maintaining the homologs of ARR3, ARR6, and ARR16 as singletons during the evolution of Brassicaceae. We categorized RRA genes based on the kinetics of their cytokinin-mediated up-regulation and observed both similarities and specificities in this type of response across Brassicaceae species. Using bioinformatic analysis and experimental data demonstrating the cytokinin and abiotic stress responsiveness of the A. thaliana-derived TCSv2 reporter, we unveil the mechanistic conservation of cytokinin- and stress-mediated up-regulation of RRA genes in B. rapa and B. napus. Notably, we identify partial cytokinin dependency of cold stress-induced RRA transcription, thus further demonstrating the role of cytokinin signaling in crop adaptive responses.

Funder

Ministry of Education

Youth and Sports of the Czech Republic

TowArds Next GENeration Crops

Russian State Budgetary Project

Publisher

Oxford University Press (OUP)

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