• 中文核心期刊
  • CSCD来源期刊
  • 中国科技核心期刊
  • CA、CABI、ZR收录期刊

千针万线草根转录组测序及黄酮类化合物合成相关基因挖掘

Transcriptome Sequencing and Identification of Genes Associated with Flavonoid Biosynthesis in Stellaria yunnanensis Roots

  • 摘要:
      目的  通过高通量测序获取千针万线草根转录组信息,在分子水平上进一步研究千针万线草根黄酮类的生物合成。
      方法  采用高通量测序技术平台lllumina Novaseq 6000完成千针万线草根的转录组测序,对unigenes进行功能注释和解析黄酮类化合物的生物合成相关基因。
      结果  总共得到34137条Unigenes,平均长度为1093.58 bp。注释到六大功能数据库(NR、egg NOG、Pfam、Swiss-Prot、GO、KEGG)中的Unigenes总数达到22369条。千针万线草根Unigenes匹配至NR数据库的有21510条,与黎科的甜菜、藜麦和菠菜有高度同源性;19414条Unigenes在egg NOG数据库得到19980个注释并划分为23类;19942条Unigenes在GO数据库中获得69356个注释,根据功能划分为细胞组分、分子功能及生物过程三大类,分别对应14、16、23个亚类,其中涉及生物过程较多;6505条Unigenes富集在KEGG数据库的131条通路中,代谢相关的通路占比最大,其中筛选获得80个与黄酮类化合物代谢相关的基因,共编码16个关键酶。同时,有724个Unigenes被注释为转录因子。
      结论  对千针万线草根进行转录组测序及基因功能注释,并筛选到多个与黄酮类化合物合成相关的Unigenes,研究结果丰富了千针万线草根的遗传信息,可以为进一步鉴定该物种药用成分合成的关键基因及其调控机制提供一定的参考依据。

     

    Abstract:
      Objective  Transcriptome of Stellaria yunnanensis root was sequenced and genes associated with the flavonoid biosynthesis identified.
      Method  Transcriptome of S. yunnanensis root was sequenced using the high-throughput Illumina Novaseq 6 000. Functional annotation of the unigenes were conducted and genes related to the biosynthesis identified.
      Result   There were 34 137 unigenes found with an average length of 1 093.58 bp. They annotated to 6 functional databases, including NR, egg NOG, Pfam, Swiss-Prot, GO, and KEGG, that numbered 22 369 in total. There were 21 510 unigenes annotated in NR database, which had high homology with Beta vulgaris, Chenopodium quinoa, and Spinacia oleracea of Chenopodiaceae, while 19 980 from 19 414 unigenes in egg NOG in 23 categories, and 69 356 from 19 942 unigenes in GO in 3 major functional categories of cellular components, molecular functions, and, especially, biological processes with 14, 16, and 23 subcategories, respectively. Of the unigenes, 6 505 were enriched in 131 pathways in KEGG with the largest proportion related to the metabolism pathways, 80 associated with the flavonoid biosynthesis encoding 16 key enzymes, and 724 annotated as transcription factors.
      Conclusion  The high-throughput transcriptome sequencing and gene function annotation on the S. yunnanensis roots were successfully performed. Several unigenes related to the flavonoid synthesis were identified. The information would facilitate further studies on the key genes and mechanisms in the formation of medicinal important functional ingredient in the plant.

     

/

返回文章
返回