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转录组和靶向代谢物关联分析鉴定参与花色苷生物合成的关键基因。

Association Analysis of Transcriptome and Targeted Metabolites Identifies Key Genes Involved in Anthocyanin Biosynthesis.

机构信息

Department of Landscape Architecture, Hebei Agricultural University, 2596 Lekai South Street, Baoding 071001, China.

出版信息

Int J Mol Sci. 2023 Nov 17;24(22):16462. doi: 10.3390/ijms242216462.

Abstract

The anthocyanin biosynthetic pathway is the main pathway regulating floral coloration in , a well-known ornamental plant. We investigated the transcriptome profiles and targeted metabolites to elucidate the relationship between genes and metabolites in anthocyanin biosynthesis in the bitone flower cultivar 'Clarence', which has a deep blue outer perianth and nearly white inner perianth. In this study, delphinidin-, pelargonidin-, and cyanidin-based anthocyanins were detected in the flowers. The content of delphinidin-based anthocyanins increased with the development of the flower. At full bloom (stage 3), delphinidin-based anthocyanins accounted for most of the total anthocyanin metabolites, whereas the content of pelargonidin- and cyanidin-based anthocyanins was relatively low. Based on functional annotations, a number of novel genes in the anthocyanin pathway were identified, which included early biosynthetic genes , and and late biosynthetic genes , and . The expression of key structural genes encoding enzymes, such as , , and , was significantly upregulated in the outer perianth compared to the inner perianth. In addition, most structural genes exhibited their highest expression at the half-color stage rather than at the full-bloom stage, which indicates that these genes function ahead of anthocyanins synthesis. Moreover, transcription factors (TFs) of plant R2R3-myeloblastosis (R2R3-MYB) related to the regulation of anthocyanin biosynthesis were identified. Among 56 R2R3-MYB genes, 2 members belonged to subgroup 4, with them regulating the expression of late biosynthetic genes in the anthocyanin biosynthetic pathway, and 4 members belonged to subgroup 7, with them regulating the expression of early biosynthetic genes in the anthocyanin biosynthetic pathway. Quantitative real-time PCR (qRT-PCR) analysis was used to validate the data of RNA sequencing (RNA-Seq). The relative expression profiles of most candidate genes were consistent with the FPKM of RNA-seq. This study identified the key structural genes encoding enzymes and TFs that affect anthocyanin biosynthesis, which provides a basis and reference for the regulation of plant anthocyanin biosynthesis in

摘要

双色茉莉的花色主要由花色素苷生物合成途径调控,双色茉莉是一种著名的观赏植物。本研究以花色为深紫蓝色外花瓣、近白色内花瓣的双色茉莉品种‘Clarence’为试材,通过转录组和靶向代谢组学分析,阐明花色素苷生物合成途径中基因与代谢物的关系。研究检测到飞燕草色素、天竺葵色素和矢车菊色素型花色素苷。花色随花的发育而变化,在盛花期(第 3 期),飞燕草色素型花色素苷占总花色素苷代谢物的大部分,而天竺葵色素和矢车菊色素型花色素苷的含量相对较低。基于功能注释,鉴定到花色苷途径中的一些新基因,包括早期生物合成基因和晚期生物合成基因。与内花瓣相比,外花瓣中编码酶的关键结构基因如、和的表达显著上调。此外,大多数结构基因在半显色期表达最高,而不是在盛花期,这表明这些基因在花色素苷合成之前起作用。此外,还鉴定到与花色苷生物合成调控相关的植物 R2R3-髓细胞瘤(R2R3-MYB)转录因子(TFs)。在 56 个 R2R3-MYB 基因中,有 2 个成员属于第 4 亚组,它们调节花色苷生物合成途径中晚期生物合成基因的表达,有 4 个成员属于第 7 亚组,它们调节花色苷生物合成途径中早期生物合成基因的表达。实时荧光定量 PCR(qRT-PCR)分析用于验证 RNA 测序(RNA-Seq)的数据。大多数候选基因的相对表达谱与 RNA-seq 的 FPKM 一致。本研究鉴定了影响花色素苷生物合成的关键结构基因编码酶和 TFs,为调控植物花色素苷生物合成提供了基础和参考。

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