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De Novo Transcriptomics Analysis of the Floral Scent of Chinese Narcissus

机译:中国水仙花卉气味的De Novo转录组织分析

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The Chinese narcissus is a well-known monocotyledon plant with a beautiful color, and fresh with a sweet floral scent. Lack of transcriptomic and genomic information hinders understanding of the molecular mechanisms underlying the biosynthesis of narcissus floral scent volatiles. Here we predicted the functions of identified significantly differentially expressed genes (DEGs), according to public protein annotation databases. Using RNA-sequencing (RNA-Seq) on the Illumina HiSeq system and de novo transcriptome assembly, we investigated gene expression in narcissus corona and petal tissues at the early flowering (day 1) and full-bloom (day 7) stages. Significant differences in the expression profiles of 14 fragrance-related genes were further analyzed by qRT-PCR. A total of 62,826,860,514 bases were generated by RNA-seq; clean reads were 210,658,254 bp, and the guanine-cytosine content was 47.7%-48.88%. Transcripts (n = 167,374; 67.27%) and unigenes (n = 81,442; 32.73%) had mean lengths of 1069.70 bp and 813.27 bp, respectively. The total length and N50 length values of transcripts were 179,040,048 bp and 1654 bp, while those of unigenes were 66,234,291 bp and 1406 bp. Assembled genes were annotated by comparison with the non-redundant, Protein family, Clusters of Orthologous Groups of proteins, Swiss-Prot, Kyoto Encyclopedia of Genes and Genomes, and Gene Ontology, public protein databases. Additionally, 46 and 71 significantly differentially expressed genes encoded enzymes and transcription factors, respectively, associated with floral volatiles biosynthesis pathways, were analyzed in-depth. Our findings represent a fundamental step toward better understanding of the mechanisms of narcissus floral volatile biosynthesis.
机译:中国水仙是一家着名的单子叶植物,色彩美丽,新鲜的花香。缺乏转录组和基因组信息妨碍了解水仙花香味挥发物生物合成的分子机制的理解。在这里,我们预测了根据公共蛋白质注释数据库的鉴定显着差异表达基因(DEGS)的功能。使用RNA测序(RNA-SEQ)在Illumina Hiseq系统和De Novo转录组合体中,我们研究了早期开花(第1天)和全绽放(第7天)阶段的Narcissus Corona和Petal组织中的基因表达。通过QRT-PCR进一步分析了14个香料相关基因表达谱的显着差异。 RNA-SEQ共产生62,826,860,514个碱基;清洁读数为210,658,254磅,鸟嘌呤 - 胞嘧啶含量为47.7%-48.88%。转录物(n = 167,374; 67.27%)和unigenes(n = 81,442; 32.73%)分别具有1069.70 bp和813.27 bp的平均长度。转录物的总长度和N50长度值为179,040,048bp和1654 bp,而unigenes的那些是66,234,291bp和1406 bp。通过与非冗余,蛋白质家族,外科蛋白质组,基因和基因组的蛋白质群组,基因本体和基因本体,公共蛋白质数据库的群体,通过对非冗余,蛋白质家族,植物簇进行注释。另外,深入分析了46和71显着表达了与花卉挥发物生物合成途径相关的酶和转录因子的编码和转录因子。我们的研究结果代表了更好地理解水仙花挥发性生物合成机制的基本步骤。

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