首页> 美国卫生研究院文献>DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes >Transcriptomic and functional analyses unveil the role of long non-coding RNAs in anthocyanin biosynthesis during sea buckthorn fruit ripening
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Transcriptomic and functional analyses unveil the role of long non-coding RNAs in anthocyanin biosynthesis during sea buckthorn fruit ripening

机译:转录组学和功能分析揭示了沙棘果实成熟过程中长非编码RNA在花色苷生物合成中的作用

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摘要

Fruit ripening is a developmental process regulated by a complex network of endogenous and exogenous cues. Sea buckthorn is an excellent material for fruit ripening studies due to its dramatic ripening process and high contents of nutritional and anti-oxidant compounds in berries. Here, the whole transcriptome of sea buckthorn fruit at three development stages were analysed using multiple high-throughput sequencings. We assembled and annotated 9,008 long non-coding RNAs (lncRNAs) in sea buckthorn fruits, and identified 118 differentially expressed lncRNAs (DE-lncRNAs) and 32 differentially expressed microRNAs in fruit developmental process. In addition, we predicted 1,061 cis-regulated and 782 trans-regulated targets of DE-lncRNAs, and these DE-lncRNAs are specifically enriched in the biosynthesis of ascorbic acid, carotenoids and flavonoids. Moreover, the silencing of two lncRNAs (LNC1 and LNC2) in vivo and expression analysis revealed that LNC1 and LNC2 can act as endogenous target mimics of miR156a and miR828a to reduce SPL9 and induce MYB114 expression, respectively, which lead to increased and decreased anthocyanin content as revealed by high-performance liquid chromatography analysis. Our results present the first global functional analysis of lncRNA in sea buckthorn and provide two essential regulators of anthocyanin biosynthesis, which provides new insights into the regulation of fruit quality.
机译:果实成熟是由内源和外源线索的复杂网络调节的发育过程。沙棘由于其惊人的成熟过程以及浆果中营养和抗氧化化合物的含量高,因此是进行水果成熟研究的极佳材料。在这里,使用多个高通量测序分析了沙棘果实在三个发育阶段的整个转录组。我们在沙棘果实中组装并注释了9,008个长的非编码RNA(lncRNA),并在果实发育过程中鉴定出118个差异表达的lncRNA(DE-lncRNA)和32个差异表达的microRNA。此外,我们预测了DE-lncRNA的1,061个顺式调控靶标和782个反式调控靶标,这些DE-lncRNAs在抗坏血酸,类胡萝卜素和类黄酮的生物合成中特别丰富。此外,体内两个lncRNA(LNC1和LNC2)的沉默和表达分析表明,LNC1和LNC2可以作为miR156a和miR828a的内源靶标模拟物,分别降低SPL9并诱导MYB114表达,从而导致花色苷含量增加和降低。如高效液相色谱分析所示。我们的结果提出了沙棘中lncRNA的首次全球功能分析,并提供了两个主要的花色苷生物合成调节剂,为调节果实品质提供了新见识。

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