Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.01.13.699194

The juvenile-to-adult phase transition in wheat is independent of the winter-spring growth habit regulated by VRN1

Abstract

In plants, the juvenile-to-adult (JA) phase transition occurs during the vegetative stage with drastic morphological and physiological changes. Common wheat (Triticum aestivum L.) has a molecular mechanism regulating the duration of vegetative growth in response to cold accumulation, and its sensitivity varies among varieties (winter-spring growth habit) predominantly due to VRN1 genotypes. However, the association of the growth habit with the JA phase transition remained unclear. Here, we investigated temporal changes in shoot apex and leaf morphology, and in the expression of the JA phase transition regulators miR156 and miR172, in winter and spring varieties and VRN1 near-isogenic lines (NILs) under controlled growth conditions, and leaf morphology under field growth conditions. Under controlled conditions, the results indicated that the timing of JA phase transition completion varied among spring varieties without association with VRN1 genotypes. All NILs underwent the JA phase transition at the same timing, and the expression levels of miR156 and miR172 were unrelated to VRN1 expressions during the vegetative stage. The field evaluation of leaf morphology revealed that the phase transition timing was consistent regardless of the sowing timings. These results suggested that the JA phase transition regulatory pathway and the vernalization regulator VRN1 are independent in wheat. HighlightThis study shows that the timing of the juvenile-to-adult phase transition in wheat is not affected by the expression of VRN1, the master regulator of vernalization.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Senoo, K., Yoshikawa, T., Gorafi, Y. S. A., Nasuda, S.. 2026-01-13. The juvenile-to-adult phase transition in wheat is independent of the winter-spring growth habit regulated by VRN1. https://doi.org/10.64898/2026.01.13.699194

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Spatially resolved transcriptomics of poplar reveals tissue organization across shoot-associated organs

Poplar (Populus spp.) is a model for tree biology and a platform for engineering woody biomass, biofuels, biomaterials, and bioproducts. Many relevant traits depend on tissue position, developmental stage, and cell type, yet these spatial relationships are difficult to recover from bulk or single-cell transcriptomes. Here, we generated a spatial transcriptome atlas of Populus tremula x P. alba INRA 717-1B4 across the shoot apex, axillary bud, stem, and petiole. After quality control, the atlas retained 29,687 spatial spots from 45 tissue sections and detected 58,748 genes. Histology-guided clustering and marker analysis resolved meristematic, epidermal, cortical, vascular, and organ-specific domains. Cross-organ comparisons assessed whether published markers retained tissue-associated expression across different anatomical contexts and developmental stages, while de novo analysis identified additional domain-enriched candidates. As case studies of the utility of the atlas, we examined the emergence of trichome-associated programs in the shoot apex and adaxial - abaxial expression differences in petioles. A trichome identity score based on poplar markers from the single-cell shoot atlas peaked along the inferred meristem-to-primordium trajectory, revealing spatially localized expression of trichome-associated programs during early leaf development. Petiole expression differences were concentrated in the epidermis and cortex and involved polarity-associated, auxin-responsive, and cell-wall-remodeling genes, with distinct expression profiles across leaf positions. Together, these data provide a spatial reference for investigating tissue differentiation and developmental patterning in a transformable poplar genotype.

plant biology↗

Sugarcane's drought memory legacy: how past stress shapes future resilience

Plants frequently experience recurrent drought events separated by periods of rehydration. Although drought imposes strong constraints on plant physiology, prior exposure may alter subsequent stress responsiveness through memory-based mechanisms. Here, we investigated whether recurrent drought at distinct developmental stages establishes stress memory in sugarcane and whether this response persists across vegetative propagation. Two genotypes contrasting in drought tolerance and productivity (IACCTC07-8008 and IACSP95-5000, respectively) were grown under greenhouse conditions and subjected to three drought cycles imposed either at tillering or maturation stage. Gas exchange, photochemical performance, leaf water status, primary metabolite profile, and growth traits were assessed across cycles, and vegetative propagules were subsequently evaluated under renewed drought. The first drought cycle imposed strong limitations on carbon assimilation and photochemistry in both genotypes and developmental stages. However, subsequent cycles resulted in attenuated reductions in A and g, improved intrinsic water use efficiency, and partial stabilization of PSII performance, indicating a modified stress-response trajectory. Young plants displayed earlier improvements (from the second cycle), whereas in mature plants this shift was evident mainly during the third cycle. Recurrent drought promoted sustained reorganization of amino acid, carbohydrate, organic acid and polyol metabolism alongside increased root biomass and higher relative water content during later cycles. Importantly, propagules derived from drought-conditioned plants exhibited faster recovery of photosynthetic performance and reduced cumulative physiological impairment under renewed drought, despite showing similar stress sensitivity at maximum water deficit. This persistence of enhanced recovery capacity across vegetative propagation indicates that drought-induced memory was maintained beyond the initially stressed plants. Together, our findings demonstrate that recurrent drought establishes a metabolically imprinted state in clonal sugarcane, integrating physiological adjustment, metabolic reprogramming, and whole-plant acclimation. These results highlight the potential of stress memory as a mechanism supporting resilience in perennial crops exposed to increasingly recurrent drought events.

plant biology↗

Dim blue light drives reversible fucoxanthin derivative accumulation in the pelagophyte Pelagomonas calceolata

Pigment composition and regulation are critical for efficient photosynthesis in the ocean, where light intensity decreases and the spectrum narrows with depth. Fucoxanthin (Fx), the main carotenoid of several microalgal lineages, harvests the blue-green light prevailing in the deep euphotic zone. In pelagophytes, the acylated derivative 19'-butanoyloxyfucoxanthin (19'-BFx) is abundant, yet its function and regulation remain unclear. Here, we investigated how irradiance and spectral quality shape photoacclimation in Pelagomonas calceolata, an abundant and cosmopolitan low-light pelagophyte. Cultures were grown under blue or white light across 2-60 umol photons m^-2 s^-1. We analysed growth, PSII photophysiology, pigment composition, gene expression levels, and the impact of spectral shifts on the 19'-BFx/Fx ratio. Pelagomonas calceolata grew optimally under dim blue light and displayed low non-photochemical quenching (NPQ) under assay conditions. Transcriptomes revealed broad remodelling driven mainly by irradiance and modulated by light colour, including carotenoid-related processes. Dim blue light progressively increased the 19'-BFx/Fx ratio, whereas white light kept it low and reversed the response after a blue-to-white shift. These results identify reversible, spectrum-dependent 19'-BFx accumulation as a key component of photoacclimation in P. calceolata and separate irradiance-driven from spectrum-dependent cellular responses. This plasticity may explain the ecological success of P. calceolata in low-light oceans.

plant biology↗