Transcriptomic Reprogramming in Leaves During Floral Bud Morphogenesis in Blueberry

<b>Background/Objectives</b>: Floral bud morphogenesis is a critical developmental process determining yield potential in blueberry, yet the molecular regulatory mechanisms in leaves during this phase remain poorly understood. <b>Methods:</b> In this study, we employed a time-series transcriptomic approach to investigate leaf gene expression dynamics during floral bud morphogenesis in rabbiteye blueberry. Leaves were sampled at six time points spanning the critical developmental window from the cessation of summer shoot growth to bud swell and dormancy onset. <b>Results:</b> RNA-seq analysis generated 121.68 Gb of clean data, and weighted gene co-expression network analysis (WGCNA) identified four stage-specific modules (brown, red, blue, turquoise) significantly associated with distinct morphogenetic phases. The brown module (0-6W) was enriched in photosynthesis and hormone signaling pathways, while the red (9W) and blue (12W) modules featured protein processing, stress and hormone signaling, and carbohydrate metabolism. The turquoise module (15W) was dominated by carbon metabolism and flavonoid biosynthesis genes. Key flowering-related genes exhibited dynamic expression patterns: <i>FT</i> was specifically upregulated at the late stage (15W), <i>AP2</i> genes peaked at mid-stage (9-12W), and <i>COL9</i> showed early high expression (0-3W). Hormone-related gene analysis revealed extensive involvement of multiple pathways, with brassinosteroid (BR) signaling comprising the largest number of genes (101). Co-expression networks further identified hub genes, including <i>FT</i>, <i>COL9</i>, <i>AP2</i>, <i>ERF1</i>, <i>SR160</i>, <i>LOX3-1</i>, and transcription factor genes like <i>MYB-related</i>, as potential central regulators. <b>Conclusions:</b> Our findings demonstrate that blueberry leaves undergo a phased functional transition from a photosynthetic source to a hub for signal integration and metabolic support during floral bud morphogenesis, actively contributing to reproductive development through systemic signaling. This study provides novel insights into flowering regulation in woody perennials and establishes a foundation for marker-assisted breeding and cropping season management in blueberry.

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Publication Details

Journal
Genes
Published
2026-03-14
DOI
https://doi.org/10.3390/genes17030317
Primary Topic
Plant Molecular Biology Research
Type
article
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article

Transcriptomic Reprogramming in Leaves During Floral Bud Morphogenesis in Blueberry

Dan Sun, Ya Shen, Qin Yang, Biyan Zhou et al.
Genes
Plant Molecular Biology Research
article

Transcriptomic Reprogramming in Leaves During Floral Bud Morphogenesis in Blueberry

Dan Sun, Ya Shen, Qin Yang, Biyan Zhou, Xingyu Lu, Yiyan Yang
article en

Abstract

<b>Background/Objectives</b>: Floral bud morphogenesis is a critical developmental process determining yield potential in blueberry, yet the molecular regulatory mechanisms in leaves during this phase remain poorly understood. <b>Methods:</b> In this study, we employed a time-series transcriptomic approach to investigate leaf gene expression dynamics during floral bud morphogenesis in rabbiteye blueberry. Leaves were sampled at six time points spanning the critical developmental window from the cessation of summer shoot growth to bud swell and dormancy onset. <b>Results:</b> RNA-seq analysis generated 121.68 Gb of clean data, and weighted gene co-expression network analysis (WGCNA) identified four stage-specific modules (brown, red, blue, turquoise) significantly associated with distinct morphogenetic phases. The brown module (0-6W) was enriched in photosynthesis and hormone signaling pathways, while the red (9W) and blue (12W) modules featured protein processing, stress and hormone signaling, and carbohydrate metabolism. The turquoise module (15W) was dominated by carbon metabolism and flavonoid biosynthesis genes. Key flowering-related genes exhibited dynamic expression patterns: <i>FT</i> was specifically upregulated at the late stage (15W), <i>AP2</i> genes peaked at mid-stage (9-12W), and <i>COL9</i> showed early high expression (0-3W). Hormone-related gene analysis revealed extensive involvement of multiple pathways, with brassinosteroid (BR) signaling comprising the largest number of genes (101). Co-expression networks further identified hub genes, including <i>FT</i>, <i>COL9</i>, <i>AP2</i>, <i>ERF1</i>, <i>SR160</i>, <i>LOX3-1</i>, and transcription factor genes like <i>MYB-related</i>, as potential central regulators. <b>Conclusions:</b> Our findings demonstrate that blueberry leaves undergo a phased functional transition from a photosynthetic source to a hub for signal integration and metabolic support during floral bud morphogenesis, actively contributing to reproductive development through systemic signaling. This study provides novel insights into flowering regulation in woody perennials and establishes a foundation for marker-assisted breeding and cropping season management in blueberry.

GenesVol. 17(3)
South China Agricultural University (CN), Kaili University (CN)
Openalex Percentile: Top 20%
Plant Molecular Biology Research
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