ArticleNature communications2025
Cytokinin depends on GA biosynthesis and signaling to regulate different aspects of vegetative phase change in Arabidopsis.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed.
- miR172-AP2 Controls Age-Dependent Regeneration Competence in Populus.Plant biotechnology journal · 2026Article
- Seed priming with Streptomyces griseoviridis culture filtrate: species-specific enhancement of legume germination and seedling vigor through hormonal and metabolic signaling.BMC plant biology · 2026Article
- Comparative Transcriptomic Analysis of Two Apple Cultivars in Response to Dual Cytokinin Applied In Vitro.Plants (Basel, Switzerland) · 2026Article
- Volatiles Released by the Endophytic FungusMicroorganisms · 2026Article
Corrections and comments
- Erratum issued
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The vegetative juvenile-to-adult transition (vegetative phase change) is a critical phase in plant development, the timing of which is controlled by the highly conserved age pathway, comprising the miR156/miR157-SPL module and the downstream miR172-AP2-like module, and is modulated by exogenous and endogenous cues. The phytohormones cytokinin (CK) and gibberellin (GA) have been described to both alter miR172 levels, most probably by regulating SPL activity. In this study, we establish an epistatic relation between CK and GA, in which CK action depends on GA, contrasting with the antagonistic nature described previously for CK-GA crosstalk. We show that CK positively affects GA biosynthesis during Arabidopsis vegetative development and depends on the GA biosynthetic enzymes GA3ox1 and GA3ox2 to modify the appearance of abaxial trichomes as well as leaf shape, both hallmarks of vegetative phase change. Downstream of CK, epidermal identity is regulated in dependence of SPL transcription factors, the GA signaling repressors GAI and RGA and the miR172-targets TOE1 and TOE2. Notably, genetic analysis revealed that GA regulates this process also CK-independently. Furthermore, our data from genetic analyses suggests that CK affects leaf shape through other GA signaling components and AP2-like transcription factors rather than SPLs. Hence, CK differentially regulates several aspects of vegetative phase change. The work contributes to the understanding of vegetative phase change regulation as well as phytohormone crosstalk in general.
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