College of Medicine, Jiaxing University, Jiaxing, 314001, Zhengjiang, People's Republic of China.
Jiaxing Academy of Agricultural Sciences, Jiaxing, 314016, Zhejiang, People's Republic of China.
Mol Biol Rep. 2021 Apr;48(4):3451-3461. doi: 10.1007/s11033-021-06374-1. Epub 2021 May 2.
Saffron is a well-known Chinese traditional herb, and crocin biosynthesis is related to the yield and quality of saffron. This study aimed to screen differentially expressed genes (DEGs) in saffron at different flowering stages and identify cytochrome P450 (CYP) genes involved in crocin biosynthesis. Saffron samples at different flowering stages were used for RNA sequencing, and DEGs between the samples at three days before the flowering stage (- 3da) and two days after the flowering stage (+ 2da) were screened. Thereafter, significantly differentially expressed CYP genes were identified, and CYP gene expression at different flowering stages and in various tissues of saffron was determined using real-time quantitative polymerase chain reaction (RT-qPCR). After sequencing and analysis, 1508 DEGs between the samples at - 3da and + 2da were identified, including 487 upregulated and 1021 downregulated genes, which were enriched in 16 biological processes, 5 cellular components, 3 molecular functions, and 11 KEGG pathways, including protein processing in endoplasmic reticulum, pentose and glucuronate interconversions, starch and sucrose metabolism, estrogen signaling pathway, and mitogen-activated protein kinase signaling pathway. In addition, 12 significantly differentially expressed CYP genes were identified. The RT-qPCR results showed that CYP76C4, CYP72A15, CYP72A219, CYP97B2, CYP714C2, CYP71A1, CYP94C1, and CYP86A8 were all expressed in the pistils, and CYP72A219, CYP72A15, CYP97B2, CYP71A1, and CYP86A8 were highly expressed in the pistils. Our study established a transcriptome library of saffron and found that CYP72A219, CYP72A15, CYP97B2, CYP71A1, and CYP86A8 may be candidates involved crocin biosynthesis in saffron.
藏红花是一种著名的中国传统草药,其藏红花苷的生物合成与藏红花的产量和品质有关。本研究旨在筛选不同花期藏红花中的差异表达基因(DEGs),并鉴定参与藏红花苷生物合成的细胞色素 P450(CYP)基因。使用 RNA 测序对不同花期的藏红花样品进行分析,筛选出在开花前 3 天(-3da)和开花后 2 天(+2da)之间的样品之间的差异表达基因(DEGs)。然后,鉴定出显著差异表达的 CYP 基因,并使用实时定量聚合酶链反应(RT-qPCR)确定藏红花不同花期和不同组织中的 CYP 基因表达。测序和分析后,在-3da 和+2da 之间的样品中鉴定出 1508 个差异表达基因,包括 487 个上调基因和 1021 个下调基因,这些基因富集于 16 个生物过程、5 个细胞组分、3 个分子功能和 11 个 KEGG 途径,包括内质网蛋白质加工、戊糖和葡萄糖醛酸相互转化、淀粉和蔗糖代谢、雌激素信号通路和丝裂原激活蛋白激酶信号通路。此外,鉴定出 12 个差异表达显著的 CYP 基因。RT-qPCR 结果表明,CYP76C4、CYP72A15、CYP72A219、CYP97B2、CYP714C2、CYP71A1、CYP94C1 和 CYP86A8 在雌蕊中均有表达,而 CYP72A219、CYP72A15、CYP97B2、CYP71A1 和 CYP86A8 在雌蕊中表达较高。本研究建立了藏红花转录组文库,并发现 CYP72A219、CYP72A15、CYP97B2、CYP71A1 和 CYP86A8 可能是藏红花藏红花苷生物合成的候选基因。