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Combined small RNA and degradome sequencing reveals complex microRNA regulation of catechin biosynthesis in tea (Camellia sinensis)

机译:组合的小RNA和降解组测序揭示了茶(Camellia sinensis)中儿茶素生物合成的复杂microRNA调控。

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摘要

MicroRNAs are endogenous non-coding small RNAs playing crucial regulatory roles in plants. Tea, a globally popular non-alcoholic drink, is rich in health-enhancing catechins. In this study, 69 conserved and 47 novel miRNAs targeting 644 genes were identified by high-throughout sequencing. Predicted target genes of miRNAs were mainly involved in plant growth, signal transduction, morphogenesis and defense. To further identify targets of tea miRNAs, degradome sequencing and RNA ligase-mediated rapid amplification of 5’cDNA ends (RLM-RACE) were applied. Using degradome sequencing, 26 genes mainly involved in transcription factor, resistance protein and signal transduction protein synthesis were identified as potential miRNA targets, with 5 genes subsequently verified. Quantitative real-time PCR (qRT-PCR) revealed that the expression patterns of novel-miR1, novel-miR2, csn-miR160a, csn-miR162a, csn-miR394 and csn-miR396a were negatively correlated with catechin content. The expression of six miRNAs (csn-miRNA167a, csn-miR2593e, csn-miR4380a, csn-miR3444b, csn-miR5251 and csn-miR7777-5p.1) and their target genes involved in catechin biosynthesis were also analyzed by qRT-PCR. Negative and positive correlations were found between these miRNAs and catechin contents, while positive correlations were found between their target genes and catechin content. This result suggests that these miRNAs may negatively regulate catechin biosynthesis by down-regulating their biosynthesis-related target genes. Taken together, our results indicate that miRNAs are crucial regulators in tea, with the results of 5’-RLM-RACE and expression analyses revealing the important role of miRNAs in catechin anabolism. Our findings should facilitate future research to elucidate the function of miRNAs in catechin biosynthesis.
机译:MicroRNA是内源性非编码小RNA,在植物中起着至关重要的调节作用。茶是一种全球流行的非酒精饮料,富含促进健康的儿茶素。在这项研究中,通过高通量测序鉴定了靶向644个基因的69个保守miRNA和47个新颖miRNA。 miRNA的预测靶基因主要参与植物的生长,信号转导,形态发生和防御。为了进一步鉴定茶miRNA的靶标,应用了降解组测序和RNA连接酶介导的5'cDNA末端快速扩增(RLM-RACE)。使用降解基因组测序,主要涉及转录因子,抗性蛋白和信号转导蛋白合成的26个基因被鉴定为潜在的miRNA靶标,随后验证了5个基因。实时定量PCR(qRT-PCR)显示,新型miR1,新型miR2,csn-miR160a,csn-miR162a,csn-miR394和csn-miR396a的表达模式与儿茶素含量呈负相关。还通过qRT-PCR分析了六个miRNA的表达(csn-miRNA167a,csn-miR2593e,csn-miR4380a,csn-miR3444b,csn-miR5251和csn-miR7777-5p.1)及其参与儿茶素生物合成的靶基因。这些miRNA与儿茶素含量之间呈负相关和正相关,而其靶基因与儿茶素含量之间呈正相关。该结果表明这些miRNA可能通过下调其与生物合成相关的靶基因而负调控儿茶素的生物合成。两者合计,我们的结果表明miRNA是茶中的关键调节剂,5'-RLM-RACE的结果和表达分析揭示了miRNA在儿茶素合成代谢中的重要作用。我们的发现应有助于将来的研究,以阐明miRNA在儿茶素生物合成中的功能。

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