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首页> 外文期刊>BMC Genomics >Whole-transcriptome analysis of differentially expressed genes in the ray florets and disc florets of Chrysanthemum morifolium
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Whole-transcriptome analysis of differentially expressed genes in the ray florets and disc florets of Chrysanthemum morifolium

机译:菊花射线小花和盘小花中差异表达基因的全转录组分析

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Background Chrysanthemum morifolium is one of the most important global cut flower and pot plants, and has been cultivated worldwide. However, limited genomic resources are available and the molecular mechanisms involved in the two morphologically distinct floret developmental cycles in chrysanthemum remain unclear. Results The transcriptomes of chrysanthemum ray florets, disc florets and leaves were sequenced using Illumina paired-end sequencing technology. In total, 16.9?G reads were assembled into 93,138 unigenes with an average length of 738?bp, of which 44,364 unigenes showed similarity to known proteins in the Swissprot or NCBI non-redundant protein databases. Additionally, 26,320, 22,304 and 13,949 unigenes were assigned to 54 gene ontology (GO) categories, 25 EuKaryotic Orthologous Groups (KOG) categories, and 280 Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, respectively. A total of 1863 differentially expressed genes (DEGs) (1210 up-regulated and 653 down-regulated) were identified between ray florets and disc florets, including genes encoding transcription factors and protein kinases. GO and KEGG pathway enrichment analyses were performed on the DEGs to identify differences in the biological processes and pathways between ray florets and disc florets. The important regulatory genes controlling flower development and flower organ determination, as well as important functional genes in the anthocyanin biosynthetic pathway, were identified, of which two leucoanthocyanidin dioxygenase-encoding genes showed specific expression in ray florets. Lastly, reverse transcription quantitative PCR was conducted to validate the DEGs identified in our study. Conclusions Comparative transcriptome analysis revealed significant differences in patterns of gene expression and signaling pathways between ray florets and disc florets in Chrysanthemum morifolium . This study provided the first step to understanding the molecular mechanism of the differential development of ray florets and disc florets in chrysanthemum, and also provided valuable genomic resources for candidate genes applicable for the breeding of novel varieties in chrysanthemum.
机译:背景菊花是最重要的全球切花和盆栽植物之一,并且已在世界范围内种植。但是,可用的基因组资源有限,并且菊花中两个形态不同的小花发育周期涉及的分子机制仍不清楚。结果采用Illumina双末端测序技术对菊花小花,圆盘小花和叶片的转录组进行了测序。总共将16.9?G读段组装到93,138个单基因中,平均长度为738?bp,其中44,364个单基因显示出与Swissprot或NCBI非冗余蛋白质数据库中的已知蛋白质相似。此外,分别将26,320、22,304和13,949个单基因分配给54个基因本体论(GO)类别,25个真核直系同源族(KOG)类别和280个《京都议定书》。在射线小花和盘状小花之间总共鉴定了1863个差异表达基因(DEG)(上调1210个,下调653个),包括编码转录因子和蛋白激酶的基因。在DEG上进行GO和KEGG途径富集分析,以鉴定射线小花和盘状小花之间生物学过程和途径的差异。确定了控制花发育和花器官测定的重要调控基因,以及花色苷生物合成途径中的重要功能基因,其中两个无色花青素双加氧酶编码基因在射线小花中表达特异性。最后,进行了逆转录定量PCR来验证我们研究中鉴定的DEG。结论对比转录组分析显示菊花的射线小花和盘状小花在基因表达模式和信号转导途径上存在显着差异。该研究为了解菊花射线小花和盘状小花差异发育的分子机制提供了第一步,也为菊花新品种育种的候选基因提供了宝贵的基因组资源。

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