国槐不同器官转录组分析及EST−SSR引物开发应用

Transcriptome Analysis of Different Organs of Sophora japonica and Development and Application of EST−SSR Primers

  • 摘要: 以国槐品种“青云1号”的根、茎、叶3种不同器官为材料,利用高通量测序技术分别对其进行转录组测序,筛选其根、茎、叶差异表达基因,进行生物信息学分析及EST−SSR分析。通过转录组两两对比筛选得到的根 vs. 茎、根 vs. 叶及茎 vs. 叶差异基因数分别为51937、52711和7193条,进一步对其进行GO及KEGG富集分析。结果表明:差异基因显著富集于代谢过程、催化活性、糖酵解和糖质新生等功能。EST−SSR分析表明,国槐根、茎、叶的SSR序列长度均在10~80 bp间变化,主要以10~22 bp的短序列为主,且主要以单核苷酸重复为主,从30对有效性引物中筛选出9对多态性较高的引物,并构建了11个不同国槐无性系的指纹图谱。

     

    Abstract: Using 3 different organs of root, stem and leaf of Sophora japonica cultivar 'Qingyun 1' as materials, the transcriptome was sequenced by high-throughput sequencing technology, and the differentially expressed genes in root, stem and leaf were screened for bioinformatics analysis and EST−SSR analysis. The results showed that there were 51937, 52711 and 7193 differentially expressed genes in root vs stem, root vs leaf and stem vs leaf, respectively. Further enrichment analysis of GO and KEGG showed that the differentially expressed genes were significantly enriched in Metabolic process, catalytic activity, glycolysis and glyconeogenesis. EST−SSR analysis showed that the length of SSR sequences in roots, stems and leaves of S. japonica ranged from 10 bp to 80 bp, mainly 10–22 bp and single nucleotide, 9 pairs of primers with high polymorphism were selected from 30 pairs of effective primers, and the fingerprints of 11 different clones of S. japonica were constructed.

     

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