The CGA1-SNAT regulatory module potentially contributes to cytokinin-mediated melatonin biosynthesis and drought tolerance in wheat
2025 (English)In: BMC Plant Biology, E-ISSN 1471-2229, Vol. 25, no 1, article id 296
Article in journal (Refereed) Published
Abstract [en]
Background: Melatonin plays a pivotal role in alleviating abiotic stresses, yet its biosynthesis regulation in crops, particularly wheat, remains unclear. This study explores regulatory components of melatonin biosynthesis under drought stress using bioinformatic, physiochemical, and molecular approaches in contrasting wheat genotypes.
Results: Bioinformatic analysis identified SNAT, a key melatonin biosynthesis gene, and 88 transcription factors (TFs) from 26 families as potential regulators. The regulatory network for SNAT highlighted CYTOKININ-RESPONSIVE GATA FACTOR 1 (CGA1) as a significant TF. Under drought stress, contrasting wheat genotypes exhibited distinct CGA1-SNAT module expression, melatonin and cytokinin levels, photosynthetic activity, and oxidative damage. Cytokinin treatments regulated the CGA1-SNAT module, altering melatonin content, SPAD values, and chloroplast numbers, particularly in drought-susceptible genotypes.
Conclusions: This study uncovers the pivotal role of the CGA1-SNAT module and its interaction with the cytokinin pathway in regulating melatonin biosynthesis during drought stress. These findings enhance our understanding of the molecular mechanisms underpinning drought tolerance and offer promising targets for genetic and biochemical interventions to improve crop resilience.
Place, publisher, year, edition, pages
BioMed Central (BMC), 2025. Vol. 25, no 1, article id 296
Keywords [en]
Melatonin biosynthesis, Abiotic stress, Gene promoter, Gene regulatory network, Hormones interactions, Cytokinin signaling
National Category
Medical Biotechnology (Focus on Cell Biology, (incl. Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy) Medical Bioinformatics and Systems Biology
Research subject
Bioinformatics
Identifiers
URN: urn:nbn:se:his:diva-24954DOI: 10.1186/s12870-025-06313-3ISI: 001439698400004PubMedID: 40050781Scopus ID: 2-s2.0-86000356062OAI: oai:DiVA.org:his-24954DiVA, id: diva2:1943823
Funder
University of Skövde
Note
CC BY 4.0
© 2025 BioMed Central Ltd unless otherwise stated. Part of Springer Nature.
Correspondence:
Roohollah Shamloo-Dashtpagerdi shamloo.r@gmail.com
Angelica Lindlöf angelica.lindlof@his.se
Open access funding provided by University of Skövde.
2025-03-112025-03-112025-09-29Bibliographically approved