猴樟叶片转录组测序及盐碱胁迫响应基因表达模式研究

Transcriptome Sequencing and Saline-alkali Stress Response Gene Expression Patterns of Cinnamomun bodinieri Leaves

  • 摘要: 为了解猴樟响应盐碱胁迫机制,以2个耐盐碱猴樟品系和1个盐碱敏感型猴樟品系3年生种苗叶片为材料,利用Illumina HiseqTM平台对其进行转录组测序,对6个精氨酸和脯氨酸通路相关基因进行qRT−PCR分析。结果表明:研究共获得72369条Unigenes,其中39156条Unigenes在NR、NT、KEGG、SwissProt、PFAM、GO、KOG数据库中获得注释;HDHZ vs. HJHZ 组有5415个DEGs,其中4003个得到GO注释;YYHZ vs. HJHZ 组有4665个DEGs,其中331个得到GO注释。此外,KEGG通路分析发现,HDHZ vs. HJHZ组上调基因主要富集在氨基酸代谢和生物碱合成相关通路,下调基因主要富集在倍半萜和三萜的生物合成,以及光合作用相关通路;YYHZ vs. HJHZ组上调基因主要富集在倍半萜和三萜的生物合成及类黄酮生物合成通路;下调基因主要富集在色素代谢和酚类物质代谢相关通路。结合6个差异表达基因的qRT−PCR结果,生物碱类、精氨酸和脯氨酸代谢可能在猴樟响应碱胁迫过程中起主要作用,所得基因的表达模式与RNA−Seq数据结果一致,证实RNA−Seq数据准确。

     

    Abstract: In order to study the mechanism of response to saline-alkali stress, transcriptome sequencing was performed on Illumina HiseqTM on 2 saline-resistant and 1 saline-sensitive 3-year seedlings of Cinnamomun bodinieri. And 6 genes related to arginine and proline pathway were analyzed by qRT-PCR. The results showed that the transcriptional sequencing obtained 72369 Unigenes. Among them, 39156 Unigenes were annotated in NR, NT, KEGG, SwissProt, PFAM, GO and KOG databases.There were 5415 DEGs in the HDHZ vs HJHZ group were founded out and 4003 DEGs were GO annotated, there were 4665 DEGs in the YYHZ vs HJHZ group, of which 331 were GO annotated. KEGG pathway analysis showed that the up-regulated genes in the HDHZ vs HJHZ group were mainly enriched in the pathways related to amino acid metabolism and alkaloid biosynthesis, while the down-regulated genes were mainly enriched in the pathways related to sesquiterpene and triterpene biosynthesis and photosynthesis. The up-regulated genes in YYHZ vs HJHZ group were mainly enriched in sesquiterpene and triterpene biosynthesis and flavonoid biosynthesis pathway. The down-regulated genes were mainly enriched in pigment metabolism and phenolic metabolism-related pathways. Combined with qRT-PCR results of 6 differentially expressed genes, alkaloid, arginine and proline metabolism may play a major role in response to alkali stress, the expression of the obtained genes was consistent with the RNA-Seq data, which confirmed the accuracy of RNA-seq data.

     

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