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无瓣海桑根响应盐胁迫的转录组分析

Transcriptome Analysis of Sonneratia apetala Root in Response to Salt Stress

  • 摘要:
    目的 初步探究无瓣海桑的耐盐分子机制,筛选出无瓣海桑抗盐候选基因,为后续功能验证实验及林木抗盐性遗传育种奠定分子基础。
    方法 以1年生无瓣海桑幼苗为材料,用500 mmol·L−1 NaCl分别处理0 d(对照组)和10 d(处理组),取不同条件下的根部组织进行转录组测序,并结合三代全长转录组数据进行后续生物信息学分析。
    结果 (1)与对照组相比,NaCl处理10 d后,无瓣海桑幼苗根系中共有14401个差异表达基因,其中,7153个上调,7248个下调。(2)GO分析发现,共有11068个差异基因在47个GO 条目得到注释。(3)在KEGG富集分析中,共有6189个差异基因富集到134条通路,其中,共有14条通路显著富集(P值<0.01,Q值<0.05)。(4)通过进一步对差异基因进行功能注释分析,共筛选出抗盐候选基因89个,其中,抗氧化基因24个,渗透调节物质基因22个,植物激素基因19个,蛋白激酶基因10个,转录因子基因14个。
    结论 活性氧清除、渗透调节、植物激素、蛋白激酶及转录因子相关基因参与调控无瓣海桑盐逆境适应过程。

     

    Abstract:
    Objective To lay a molecular basis for functional verification experiment and genetic breeding of tree salinity tolerance, the genetic mechanisms was explored, and salt-related genes were identified for Sonneratia apetala Buch.-Ham.
    Method In this study, the root tissues were collected from a 1-year-old S. apetala treated with 500 mmol•L−1 NaCl for 0 (control group) and 10 d (treatment group). Then transcriptome sequencing and bioinformatics analysis was performed based on the three-generation full-length transcriptome dataset of S. apetala.
    Result (1) Compared with the control group, 14401 genes were differentially expressed after salt treatment, of which 7153 were up-regulated and 7248 were down-regulated. (2) GO analysis found that a total of 11068 differential genes were annotated in 47 GO items. (3) For KEGG enrichment analysis, a total of 6189 differential expression genes were enriched to 134 pathways, of which 14 were significantly enriched (P-value <0.01, Q-value <0.05). (4) Further functional annotation analysis of the differentially expressed genes revealed a total of 89 genes was potential salt-related candidate genes. Among these, 24, 22, 19, 10 and 14 genes encoded enzymes or functional proteins referred to antioxidation, osmotic adjustment substances, plant hormones, protein kinase and transcription factors, respectively.
    Conclusion Genes relating to active oxygen scavenging, osmotic regulation, plant hormones, protein kinases and transcription factors participate in the regulation of salt stress adaptation in S. apetala.

     

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