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Identification of Candidate Anthocyanin-Related Genes by Transcriptomic Analysis of ‘Furongli’ Plum (Prunus salicina Lindl.) during Fruit Ripening Using RNA-Seq

机译:使用RNA-Seq的果实成熟过程中的芙蓉梨(李子)的转录组学分析鉴定候选花色苷相关基因

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摘要

Anthocyanins are important pigments and are responsible for red coloration in plums. However, little is known about the molecular mechanisms underlying anthocyanin accumulation in plum fruits. In this study, the RNA-seq technique was used to analyze the transcriptomic changes during fruit ripening in the red-fleshed plum (Prunus salicina Lindl.) cultivar ‘Furongli’. Over 161 million high-quality reads were assembled into 52,093 unigenes and 49.4% of these were annotated using public databases. Of these, 25,681 unigenes had significant hits to the sequences in the NCBI Nr database, 17,203 unigenes showed significant similarity to known proteins in the Swiss-Prot database and 5816 and 8585 unigenes had significant similarity to existing sequences in the Kyoto Encyclopedia of Genes and Genomes and the Cluster of Orthologous Groups databases, respectively. A total of 3548 unigenes were differentially expressed during fruit ripening and 119 of these were annotated as involved in “biosynthesis of other secondary metabolites.” Biological pathway analysis and gene ontology term enrichment analysis revealed that 13 differentially expressed genes are involved in anthocyanin biosynthesis. Furthermore, transcription factors such as MYB and bHLH, which may control anthocyanin biosynthesis, were identified through coexpression analysis of transcription factors, and structural genes. Real-time qPCR analysis of candidate genes showed good correlation with the transcriptome data. These results contribute to our understanding of the molecular mechanisms underlying anthocyanin biosynthesis in plum flesh. The transcriptomic data generated in this study provide a basis for further studies of fruit ripening in plum.
机译:花青素是重要的色素,对李子呈红色。然而,关于李子花色苷积累的分子机制知之甚少。在这项研究中,RNA-seq技术用于分析红肉李(Prunus salicina Lindl。)品种'Furongli'果实成熟过程中的转录组变化。超过1.61亿个高质量读段被组装成52,093个单基因,其中49.4%使用公共数据库进行注释。其中25,681个单基因对NCBI Nr数据库中的序列有重大影响,17,203个单基因与Swiss-Prot数据库中的已知蛋白质具有显着相似性,而5816和8585个单基因与《京都议定书》中的现有序列具有显着相似性。和直系同源群数据库。共有3548个单基因在果实成熟期间差异表达,其中119个被注释为涉及“其他次生代谢产物的生物合成”。生物途径分析和基因本体术语富集分析表明,花色苷生物合成涉及13个差异表达的基因。此外,通过对转录因子和结构基因的共表达分析,确定了可控制花色苷生物合成的转录因子,如MYB和bHLH。候选基因的实时qPCR分析显示与转录组数据具有良好的相关性。这些结果有助于我们了解梅花肉中花色苷生物合成的分子机制。本研究产生的转录组数据为进一步研究李子果实成熟提供了基础。

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