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Transcriptome and Flavonoids Metabolomic Analysis Identifies Regulatory Networks and Hub Genes in Black and White Fruits of Lycium ruthenicum Murray

机译:转录组和黄酮类化合物代谢物分析鉴定了枸杞毛雷氏菌黑白果实中的监管网络和枢纽基因

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摘要

Lycium ruthenicum Murry. is a highly nutritional cash crop due to its fruit abundant anthocyanins. To understand the complex metabolic networks underlying the color formation in black and white fruits of L. ruthenicum, we conducted transcriptome and flavonoid metabolic profiling to identify the candidate genes possibly involved in flavonoid biosynthesis. As a result, 147 flavonoids were identified and there was almost no anthocyanin in white fruits, while luteolin, kaempferol, and quercetin derivatives showed markedly higher abundance. Furthermore, applying weighted gene co-expression network analyses, 3 MYB, 2 bHLH, 1WRKY and 1 NAC transcription factor, associated with anthocyanin biosynthesis were identified. A bHLH transcription factor, LrAN1b showed the greatest correlations with anthocyanin accumulation with no expression in white fruits. In addition, gene function analysis and qRT-PCR experiments identified a new activated anthocyanin MYB transcription factor designed as LrAN2-like. Yeast two-hybrid and transient tobacco overexpression experiments showed that LrAN1b could interact with LrAN2-like and LrAN11 to form MBW complex to activate the anthocyanin pathway. The yeast one-hybrid experiment indicated that LrAN2-like bonded anthocyanin structural gene LrDFR and LrANS promoters. Heterologous expression of LrAN1b in tobacco can significantly increase the anthocyanin content of tobacco florals and capsules, and activate anthocyanin synthesis related genes. Taken together, an anthocyanin regulatory network model in L. ruthenicum fruit was proposed firstly and we speculate that the white fruit phenotype was due to abnormal expression of LrAN1b. The findings provide new insight into the underlying mechanism of flavonoids, laying the foundation for future functional and molecular biological research in L. ruthenicum.
机译:枸杞ruthenicum murry。由于其果实丰富的花青素是一种高度营养的现金作物。为了了解L. ruthenicum的黑白果实中的复杂代谢网络,我们进行了转录组和黄酮类药物代谢谱,以鉴定可能参与黄酮类生物合成的候选基因。结果,鉴定了147种黄酮类化合物,白色果实中几乎没有花青素,而叶黄素,kaempferol和槲皮素衍生物显示出明显高的丰富。此外,鉴定了施用加权基因共表达网络分析,3μb,2bhlh,1wrgy和1nac转录因子与花青素生物合成相关。 LRAN1B的BHLH转录因子显示出与花青素积累的最大相关性,在白色水果中没有表达。此外,基因功能分析和QRT-PCR实验鉴定了设计为Lran2样的新型活化的花青素MYB转录因子。酵母双杂化和瞬时烟草过度表达实验表明,LRAn1B可以与Lran2样和Lran11相互作用以形成MBW复合物以激活花青素途径。酵母单杂交实验表明,Lran2样键合的花青素结构基因LRDFR和溶液启动子。 Lran1b在烟草中的异源表达可以显着增加烟草植物和胶囊的花青素含量,并激活花青素合成相关基因。连胜,首先提出了L.钌果实中的花青素调节网络模型,我们推测了白色果实表型是由于Lran1b的异常表达。调查结果为黄酮类化合物的潜在机制提供了新的洞察力,奠定了L. Ruthenicum的未来功能和分子生物学研究的基础。

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