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ArticlePlant cell reports2026

Genome-wide identification of MYC transcription factors in Chrysanthemum morifolium and CmMYC25 promotes petal anthocyanin accumulation.

Wenhao Xia, Yuxi Wang, Ge Zhao, Jialin Peng, Xiuge Li, Yukun Li, Yuhe Tian, Aiping Song, Sumei Chen, Fadi Chen and 1 more

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Article in Plant cell reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

11 authors.

Wenhao Xia *State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Yuxi Wang *State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Ge ZhaoState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Jialin PengState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Xiuge LiState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Yukun LiState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Yuhe TianState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Aiping SongState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Sumei ChenState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Fadi ChenState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China.
Li-Jie ZhouState Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, Key Laboratory of Landscaping, Ministry of Agriculture and Rural Affairs, Key Laboratory of State Forestry and Grassland Administration On Biology of Ornamental Plants in East China, College of Horticulture, Nanjing Agricultural University, Nanjing, 210095, China. zhoulijie@njau.edu.cn.ORCID http://orcid.org/0000-0002-5397-2300

Funding

Agriculture Research System of China CARS-23-A18National Natural Science Foundation of China 32372745Natural Science Foundation of Hainan Province 322QN340The "JBGS" Project of Seed Industry Revitalization in Jiangsu Province JBGS[2021]020
6 · The paper itself

Abstract

key messageGenome-wide analysis coupled with spatiotemporal profiling identified CmMYC25 as a key regulator. It functions as a transcriptional co-activator to synergistically enhance CmMYB6-mediated anthocyanin biosynthesis in chrysanthemum petals. Myelocytomatosis (MYC) transcription factors (TFs), belonging to the basic helix-loop-helix (bHLH) superfamily, play a crucial role in regulating various physiological processes in plants. However, research on the MYC gene family in Chrysanthemum morifolium, one of the primary cut flowers, remains scarce. Here, we identified 28 CmMYC genes via genome-wide analysis and classified them into three subfamilies based on phylogenetic relationships. Collinearity analysis suggested expansion driven by both ancient whole-genome duplication (WGD) events and recent segmental duplications. Promoter analysis uncovered a variety of regulatory elements, with hormone-responsive motifs being the most predominant. Phylogenetic clustering indicated that Group B members are orthologous to anthocyanin regulators. Among them, CmMYC25 was prioritized for further analysis, as its expression pattern was perfectly synchronized with anthocyanin accumulation during flower development. CmMYC25 was localized to the nucleus but lacked transcriptional activation activity. Notably, yeast one-hybrid assays indicated that CmMYC25 does not directly bind to the promoters of anthocyanin biosynthetic genes. Instead, it physically interacts with CmMYB6, a central activator of anthocyanin biosynthesis. Dual-luciferase assays confirmed that CmMYC25 functions as a co-activator, synergistically enhancing the transcriptional activity of CmMYB6 on downstream target genes. Functional characterization verified that CmMYC25 acts as a positive regulator of floral pigmentation, as its overexpression significantly increased anthocyanin accumulation, while suppression reduced pigmentation. These findings provide insights into the evolution of CmMYC genes and elucidate the co-activator mechanism of CmMYC25 in regulating flower pigmentation.

Indexed as

AnthocyaninsChrysanthemumFlowersPlant ProteinsTranscription FactorsGene Expression Regulation, PlantPhylogenyPlants, Genetically ModifiedPromoter Regions, GeneticAnthocyaninsPlant ProteinsTranscription FactorsAnthocyanin biosynthesisChrysanthemum morifoliumCmMYC25Genome-wide analysisMYC gene family

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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.