Spring red → Summer green → Autumn scarlet · Anthocyanin & flavan-3-ol pathways
Compare leaf transcriptome profiles (RNA-seq FPKM) and targeted flavonoid metabolite measurements (LC-MS/MS) for Acer palmatum across three seasons: spring, summer and autumn.
Acer palmatum shows a double red-leaf phenotype: young spring leaves flush red-purple, mature summer leaves are green, and senescing autumn leaves turn scarlet. Leaves were sampled in each season (3 biological replicates) for RNA-seq and targeted flavonoid metabolomics — sample groups SPS (spring), SUS (summer), AUS (autumn).
SPS · SpringYoung expanding leaves. Spring-module genes peak (ApCHS5, ApF3′H1, ApANR, ApLAR2); delphinidin and (−)-epiafzelechin reach their seasonal maxima.
SUS · SummerMature green leaves. All 20 flavonoid genes have their lowest seasonal expression in this dataset.
AUS · AutumnApCHS3 expression is 6,435 FPKM and ApANS expression is ~640× its summer value; naringenin chalcone and (−)-epicatechin have their highest seasonal values.
Red leaf color in maples is produced by anthocyanins — glycosylated anthocyanidins accumulating in vacuoles — while the same upstream pathway also feeds flavan-3-ols (catechins), the building blocks of proanthocyanidins. The pathway is conventionally split into early biosynthetic steps (CHS → CHI → F3H → F3′H), which build the dihydroflavonol skeletons, and late biosynthetic steps (DFR → ANS, then ANR/LAR/UFGT), which commit flux to anthocyanidins and their derivatives.
This dataset covers all eight enzyme families with annotated Acer palmatum genes (20 copies) plus nine pathway metabolites. The MYB–bHLH–WD40 regulators that switch the pathway on are not part of this gene set yet; upstream phenylpropanoid genes (PAL, C4H, 4CL) and the glycosyltransferase UFGT are likewise shown in the pathway for context only.
The two red-leaf seasons show higher expression of different members of the same enzyme families. These seasonal expression patterns also appear in the correlation network; they do not establish causal control of leaf colour or transcript isoform switching:
ApCHS5ApCHS8ApCHS9ApF3'H1ApANRApLAR2
Expressed almost exclusively in spring leaves. Correlates positively with delphinidin and (−)-epiafzelechin — the flavan-3-ol / proanthocyanidin branch runs alongside pigmentation in young leaves.
ApCHS3ApCHI2ApF3HApF3'H2ApDFRApANSApLAR1
These genes have higher expression in autumn, moderate expression in spring and low expression in summer. They span the annotated CHS→CHI→F3H→F3′H→DFR→ANS steps.
Data description: leaf transcriptome (Illumina RNA-seq, FPKM) and targeted flavonoid metabolome (LC-MS/MS peak areas) of Acer palmatum leaves in spring (SPS), summer (SUS), and autumn (AUS), three biological replicates each. Gene identifiers follow the Acer palmatum genome assembly (A.palmatum_LGxx_Gxxxxx); enzymes are keyed to KEGG orthology, metabolites to KEGG compound IDs. Data from the Jiangsu Academy of Agricultural Sciences (JAAS).
Search any ApCHS/ApANS/… gene ID for full expression profiles, annotation, and sequences.
ATAC-seq and WGBS tracks for spring leaves are available in the Epigenome browser.
Click a red enzyme label for genes & expression, or an amber-bordered metabolite for measured abundance. Gray dashed items were not measured / not annotated in this dataset.
Mean abundance (LC-MS/MS peak area, n = 3) of the nine quantified flavonoids across the season cycle. Click the chips to toggle metabolites; hover a point for the individual replicate values. Note the log scale — abundances span more than two orders of magnitude.
log₂(FPKM+1) for all 20 annotated flavonoid-pathway genes across the 9 leaf samples (spring SPS · summer SUS · autumn AUS, 3 replicates each). Hover a cell for raw FPKM.
The nine quantified flavonoids, scaled per row (min–max within each metabolite) so seasonal patterns are comparable despite very different absolute abundances. Hover a cell for the raw peak area.
Pearson correlations on log₂-transformed values across the 9 samples: gene–gene edges at |r| ≥ 0.85 and gene–metabolite edges at |r| ≥ 0.80 (67 edges, 21 nodes; unconnected genes/metabolites hidden). Edges are exploratory correlations without a multiple-testing filter. Shared seasonal effects can drive these associations; edges do not establish direct regulation. The layout separates the spring module (CHS5/8/9–F3′H1–ANR–LAR2 + delphinidin, epiafzelechin) from the autumn module (CHS3–CHI–F3H–F3′H2–DFR–ANS–LAR1 + naringenin). Drag nodes; hover an edge for r; click a node for details.
Genome-wide differential expression between spring (SPS) and autumn (AUS) leaves (3 biological replicates per season; thresholds |log₂FC| ≥ 1 and FDR < 0.05; fold change is expressed as AUS relative to SPS). Click a gene ID to open it in the gene module.
| Gene ID | Symbol | SPS FPKM | AUS FPKM | log₂FC | FDR | Description |
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Source: in-house Acer palmatum leaf RNA-seq (SPS-1/2/3 vs AUS-1/2/3). Download the displayed DEG table (JSON). This is the filtered DEG result table; raw reads and the complete tested-gene table are not included in this download.