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Comparative analysis of full-length transcriptomes based on hybrid population reveals regulatory mechanisms of anthocyanin biosynthesis in sweet potato ( Ipomoea batatas (L.) Lam)

机译:基于杂化群的全长转录om对比较分析揭示红薯(Ipomoea Batatas(L.)林的花青素生物合成的调节机制

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Sweet potato (Ipomoea batatas (L.) Lam.) is a highly heterozygous autohexaploid crop with high yield and high anthocyanin content. Purple sweet potato is the main source of anthocyanins, and the mechanism of anthocyanin biosynthesis in storage roots has not been fully revealed. In order to reveal the mechanism of anthocyanin biosynthesis and identify new homologous genes involved in anthocyanin biosynthesis in the storage roots of sweet potato, we used Ningzishu 1 and Jizishu 2 as parents to construct a F1 hybrid population. Seven anthocyanin-containing lines and three anthocyanin-free lines were selected for full-length and second-generation transcriptome analyses. A total of 598,375 circular consensus sequencing reads were identified from full-length transcriptome sequencing. After analysis and correction of second-generation transcriptome data, 41,356 transcripts and 18,176 unigenes were obtained. Through a comparative analysis between anthocyanin-containing and anthocyanin-free groups 2329 unigenes were found to be significantly differentially expressed, of which 1235 were significantly up-regulated and 1094 were significantly down-regulated. GO enrichment analysis showed that the differentially expressed unigenes were significantly enriched in molecular function and biological process. KEGG enrichment analysis showed that the up-regulated unigenes were significantly enriched in the flavonoid biosynthesis and phenylpropanoid biosynthesis pathways, and the down-regulated unigenes were significantly enriched in the plant hormone signal transduction pathway. Weighted gene co-expression network analysis of differentially expressed unigenes revealed that anthocyanin biosynthesis genes were co-expressed with transcription factors such as MYB, bHLH and WRKY at the transcription level. Our study will shed light on the regulatory mechanism of anthocyanin biosynthesis in sweet potato storage roots at the transcriptome level.
机译:甘薯(Ipomoea Batatas(L.)林。)是一种高度杂合的自身清新含量,具有高产量和高的花青素含量。紫色甘薯是花青素的主要来源,并且储存根中的花青素生物合成的机制尚未完全揭示。为了揭示花青素生物合成的机制,并鉴定甘薯储存根部中涉及的新的同源基因,我们使用Ningzishu 1和Jizishu 2作为父母构建F1杂交种群。选择含有七条三核苷酸的线和三条三孔素的不用于全长和第二代转录组分析。从全长转录组测序中鉴定了总共598,375个循环共识测序读数。在分析和校正第二代转录组数据之后,获得了41,356份转录物和18,176个unigenes。通过对比较分析的含沙孔素和无花青素组2329 unigenes显着差异表达,其中1235显着上调,1094%明显下调。富集分析显示,分子功能和生物过程中显着富集了差异表达的unigenes。 KEGG富集分析表明,在黄酮类生物合成和苯丙醇丙胺生物合成途径中显着富集了上调的unigenes,并且在植物激素信号转导途径中显着富集下调的unigenes。差异表达的unigenes的加权基因共表达网络分析显示,在转录水平的转录因子中与诸如MyB,BHLH和Wrky的转录因子(BHLH和Wrky)共同表达血清素生物合成基因。我们的研究将阐明在转录组水平的红薯储存根中花青素生物合成的调节机制。

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