Evidence map›Paper›PMID 41214521›Full record

ArticleBMC plant biology2025

Integrative analysis of the transcriptome and metabolome reveals the peel coloration mechanism of Zanthoxylum armatum.

Yun Ren, Jiamin Liu, Liangping He, Jinjue Jiang, Ting Gong, Qian Zhou, Qiang Li, Jing Liu, Ning Tang, Zexiong Chen

Abstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Yun RenChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China. reny1989@sina.com.
Jiamin LiuChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Liangping HeChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Jinjue JiangChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Ting GongChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Qian ZhouChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Qiang LiChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Jing LiuChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Ning TangChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China.
Zexiong ChenChongqing Key Laboratory for Germplasm Innovation for Special Aromatic Spice Plants/ Chongqing Key Laboratory of Economic Plant Biotechnology/ Collaborative Innovation Center of Special Plant Industry in Chongqing, College of Smart Agriculture/ Institute of Special Plants, Chongqing University of Arts and Sciences, Yongchuan, Chongqing, China. chenzexiong1979@163.com.

Funding

the Natural Science Foundation of Chongqing CSTB2024NSCQ-MSX1109the Projects for Innovative Research Groups of Chongqing Universities CXQT21028the Science and Technology Research Program of Chongqing Municipal Education Commission KJZD-K202401308
6 · The paper itself

Abstract

backgroundZanthoxylum armatum is a globally recognized medicinal and edible plant, the fruit peel color of which is considered an important trait that influences its economic value. In this study, Z. armatum fruits were used at five different stages of development to explore the law of metabolite biosynthesis and its potential molecular mechanism.

resultsUsing transcriptomic and widely-targeted metabolomic analyses, 23 differentially accumulated metabolites, 274 differentially expressed structural genes, and 230 differentially expressed transcription factor genes associated with anthocyanin synthesis were identified. Based on co-expression network analysis, key structural genes positively associated with anthocyanin biosynthesis were identified and the corresponding hub transcription factor genes were predicted. Cyanidin-3-O-arabinoside, cyanidin-3-O-glucoside, cyanidin-3-O-(2''-O-glucosyl)glucoside, cyanidin-3-O-(6''-O-malonyl)glucoside, cyanidin-3-O-rutinoside, cyanidin-3-O-galactoside, and petunidin-3-O-glucoside-5-O-arabinoside were identified as key anthocyanins accumulated in the peel of mature Z. armatum fruits, the synthesis of which appeared to involve the structural genes PAL5, PAL8, PAL9, PAL11, PAL13, PAL14, C4H2, CHS17, F3'H2, DFR1, ANS2, and ANS4 as candidate catalysts. Furthermore, dual-luciferase reporter assays indicated that bHLH-MYC9 and MYB19 may trans-activate the promoters of ANS2 and ANS4, respectively.

conclusionsOur findings in this study provide new perspectives regarding the regulation of peel color development during the ripening of Z. armatum fruit.

Indexed as

FruitMetabolomePigmentationTranscriptomeZanthoxylumAnthocyaninsGene Expression Regulation, PlantTranscription FactorsAnthocyaninsTranscription FactorsAnthocyanin biosynthesisMetabolomePeel colorationTranscriptomeZanthoxylum armatum

Identifiers

PMID41214521
PMCPMC12604241

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.