Comparative Transcriptomics of Multi-Stress Responses in Pachycladon cheesemanii and Arabidopsis thaliana

Author:

Dong Yanni1,Gupta Saurabh2ORCID,Wargent Jason J.3,Putterill Joanna4,Macknight Richard C.5,Gechev Tsanko S.67ORCID,Mueller-Roeber Bernd268ORCID,Dijkwel Paul P.1ORCID

Affiliation:

1. School of Natural Sciences, Massey University, Tennent Drive, Palmerston North 4474, New Zealand

2. Department Molecular Biology, Institute of Biochemistry and Biology, University of Potsdam, Karl-Liebknecht-Straße 24–25, Haus 20, 14476 Potsdam, Germany

3. School of Agriculture & Environment, Massey University, Palmerston North 4442, New Zealand

4. School of Biological Sciences, University of Auckland, Auckland 1142, New Zealand

5. Biochemistry Department, School of Biomedical Sciences, University of Otago, Dunedin 9016, New Zealand

6. Center of Plant Systems Biology and Biotechnology (CPSBB), 139 Ruski Blvd., 4000 Plovdiv, Bulgaria

7. Department of Plant Physiology and Plant Molecular Biology, University of Plovdiv, 24 Tsar Assen Str., 4000 Plovdiv, Bulgaria

8. Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476 Potsdam, Germany

Abstract

The environment is seldom optimal for plant growth and changes in abiotic and biotic signals, including temperature, water availability, radiation and pests, induce plant responses to optimise survival. The New Zealand native plant species and close relative to Arabidopsis thaliana, Pachycladon cheesemanii, grows under environmental conditions that are unsustainable for many plant species. Here, we compare the responses of both species to different stressors (low temperature, salt and UV-B radiation) to help understand how P. cheesemanii can grow in such harsh environments. The stress transcriptomes were determined and comparative transcriptome and network analyses discovered similar and unique responses within species, and between the two plant species. A number of widely studied plant stress processes were highly conserved in A. thaliana and P. cheesemanii. However, in response to cold stress, Gene Ontology terms related to glycosinolate metabolism were only enriched in P. cheesemanii. Salt stress was associated with alteration of the cuticle and proline biosynthesis in A. thaliana and P. cheesemanii, respectively. Anthocyanin production may be a more important strategy to contribute to the UV-B radiation tolerance in P. cheesemanii. These results allowed us to define broad stress response pathways in A. thaliana and P. cheesemanii and suggested that regulation of glycosinolate, proline and anthocyanin metabolism are strategies that help mitigate environmental stress.

Funder

European Union’s Horizon 2020 research and innovation programme

PlantaSYST

European Regional Development Fund

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Reference139 articles.

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3. Physiological, biochemical and molecular aspects of water stress responses in plants, and the bio-technological applications;Misra;Proc. Natl. Acad. Sci. India Sect. B,2002

4. Shanker, A., and Venkateswarlu, B. (2011). Abiotic Stress in Plants: Mechanisms and Adaptations, BoD–Books on Demand; IntechOpen.

5. Hasanuzzaman, M., Nahar, K., and Fujit, M. (2013). Abiotic Stress—Plant Responses and Applications in Agriculture, InTechOpen.

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1. ROS and Abiotic Stress in Plants 2.0;International Journal of Molecular Sciences;2023-07-25

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