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Identification and Expression of miRNAs Related to Female Flower Induction in Walnut (Juglans regia L.)

机译:核桃(Juglans Regia L.)雌花诱导术的鉴定与表达。

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摘要

Flower induction is an essential stage in walnut (Juglans regia L.) trees, directly affecting yield, yield stability, fruit quality and commodity value. The objective of this study was to identify miRNAs related to female flower induction via high-throughput sequencing and bioinformatics analysis. A total of 123 miRNAs were identified including 51 known miRNAs and 72 novel miRNAs. Differential expression was observed in 19 of the known miRNAs and 34 of the novel miRNAs. Twelve miRNAs were confirmed by RT-qPCR. A total of 1339 target genes were predicted for the differentially expressed miRNAs. The functions of 616 of those target genes had been previously annotated. The target genes of the differentially expressed miRNAs included: (i) floral homeotic protein APETALA 2 (AP2) and ethylene-responsive transcription factor RAP2-7 which were targeted by jre-miRn69; (ii) squamosa promoter-binding protein 1 (SPB1) and various SPLs (squamosa promoter-binding-like protein) which were targeted by jre-miR157a-5p; (iii) various hormone response factors which were targeted by jre-miR160a-5p (ARF18) and jre-miR167a-5p (ARF8) and (iv) transcription factor SCL6 which was targeted by jre-miR171b-3p, jre-miRn46 and jre-miRn49. The KEGG pathway analysis of the target genes indicated that the differentially expressed miRNAs were mainly enriched to ubiquitin mediated proteolysis, RNA degradation and various carbohydrate metabolism pathways. Many miRNAs were detected in J. regia during female flower induction. Some miRNAs (jre-miR157a-5p, jre-miR160a-5p, jre-miR167a-5p, miR171b-3p jre-miRn69 and jre-miRn49) were involved in female flower induction. The results of this experiment will contribute valuable information for further research about the function of miRNAs in flower induction of J. regia and other fruit trees.
机译:花诱导是核桃(Juglans Regia L.)树的重要阶段,直接影响产量,产量稳定,果实质量和商品价值。本研究的目的是通过高通量测序和生物信息学分析鉴定与女性花诱导有关的miRNA。鉴定了总共123个miRNA,包括51名已知的miRNA和72个新的miRNA。在已知的miRNA和新的miRNA的34中观察到差异表达。通过RT-QPCR确认了12个miRNA。差异表达的miRNA预测了总共1339个靶基因。这些靶基因的616的功能先前已被注释。差异表达的miRNA的靶基因包括:(i)由JRE-MiRN69靶向的NaTral Homeot蛋白Apetala 2(AP2)和乙烯响应转录因子Rap2-7; (ii)由JRE-MIR157A-5P靶向的Squamosa启动子结合蛋白1(SPB1)和各种SPL(Squamosa启动子结合蛋白); (iii)由JRE-MIR160A-5P(ARF18)和JRE-MIR167A-5P(ARF8)和(IV)转录因子SCL6靶向的各种激素响应因子,其由JRE-MIR171B-3P,JRE-MIRN46和JRE靶向-mirn49。靶基因的Kegg途径分析表明,差异表达的miRNA主要富集到遍税蛋白介导的蛋白水解,RNA降解和各种碳水化合物代谢途径。在女性花诱导期间,在J. Regia检测到许多miRNA。一些miRNA(JRE-MIR157A-5P,JRE-MIR160A-5P,JRE-MIR167A-5P,MIR171B-3P JRE-MIRN69和JRE-MIRN49)参与了女性花卉诱导。该实验的结果将有助于进一步研究MiRNA在J. Regia和其他果树的花卉诱导中的进一步研究。

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