Evidence map›Paper›PMID 41735885›Full record

ArticleBMC plant biology2026

De novo transcriptome and tissue-specific gene expression analysis in three types of barley following exploring the mechanism of quercetin content in purple barley (Hordeum vulgare).

Md Mahmudul Hasan, Md Sohel Mia, Jiazhen Yang, Tao Yang, Yawen Zeng

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Article in BMC plant biology, 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 authors.

Md Mahmudul HasanBiotechnology and Germplasm Resources Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650205, China.
Md Sohel MiaDepartment of Nutrition and Food Technology, Jashore University of Science and Technology, Jashore, 7408, Bangladesh.
Jiazhen YangBiotechnology and Germplasm Resources Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650205, China.
Tao YangBiotechnology and Germplasm Resources Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650205, China. yt52279076@163.com.
Yawen ZengBiotechnology and Germplasm Resources Institute, Yunnan Academy of Agricultural Sciences, Kunming, 650205, China. zengyw1967@126.com.

Funding

China Agriculture Research System CARS-05-01A-04National Natural Science Foundation of China Grant No.32160453
6 · The paper itself

Abstract

backgroundBarley (Hordeum vulgare L.) is a major cereal crop and an important source of bioactive compounds, including flavonoids. Among these, quercetin is a biologically active flavonol with antioxidant, anti-inflammatory, and anticancer properties. Quercetin accumulation in barley is type-dependent and was detected exclusively in purple barley compared with yellow and black barley. However, the molecular mechanisms underlying quercetin biosynthesis and accumulation in purple barley remain unclear.

resultsIn this study, comparative transcriptome analysis was performed on yellow, black, and purple barley grains at the grain-filling stage to elucidate the transcriptional regulation of quercetin biosynthesis. RNA sequencing followed by de novo assembly resulted in the structural optimization of 6,393 genes, of which 4,986 were functionally annotated. A total of 12 alternative splicing event types and 561,743 putative single-nucleotide polymorphisms were identified. Differential expression analysis revealed 4,540 differentially expressed genes, with purple barley exhibiting the highest number of upregulated genes. Many of these genes were enriched in biological process, cellular component, and molecular function categories and formed dense protein–protein interaction networks. KEGG pathway analysis showed significant enrichment of phenylpropanoid and flavonoid biosynthesis pathways in purple barley. Furthermore, significantly higher expression of key quercetin biosynthesis genes, F3ʹH, F3ʹ5ʹH, FLS1, and FLS2, during grain maturation than the grain-filling stage might guide their regulatory roles in upward transition of quercetin accumulation into the seed along with maturity.

conclusionsThis study provides the first transcriptome-level comparison of quercetin-associated gene regulation among three tyeps of barley. The results reveal a coordinated transcriptional framework underlying quercetin biosynthesis in purple barley and offer valuable genetic resources for future functional studies and breeding strategies aimed at enhancing quercetin content in purple barley.

Indexed as

HordeumQuercetinTranscriptomeGene Expression ProfilingGene Expression Regulation, PlantQuercetinDEGsFunctional annotationsPurple barley (H. vulgare)QRT-PCRQuercetin

Identifiers

PMID41735885
PMCPMC13001208

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