Zhao Le, Zhu Yun-Hao, Wang Min, Ma Li-Gang, Han Yong-Guang, Zhang Meng-Jia, Li Xing-Can, Feng Wei-Sheng, Zheng Xiao-Ke
School of Pharmacy, Henan University of Chinese Medicine, No. 156 Jinshui East Road, Zhengzhou, 450046 Henan China.
Collaborative Innovation Center for Respiratory Disease Diagnosis and Treatment and Chinese Medicine Development of Henan Province, Zhengzhou, 450046 China.
3 Biotech. 2021 Jul;11(7):327. doi: 10.1007/s13205-021-02865-x. Epub 2021 Jun 12.
To study the molecular mechanism of the hyperaccumulator plant against cadmium (Cd) stress, the leaves of treated with 400 μM Cd for 0, 2, 12, and 24 h were harvested for comparative transcriptome analysis. In total, 110.07 Gb of clean data were obtained, and 63,957 unigenes were acquired after being assembled. Due to the lack of genome information, only 24,517 unigenes were annotated by public databases. After Cd treatment, 5054 differentially expressed genes (DEGs) were identified. KEGG pathway enrichment analysis of DEGs showed that genes involved in the flavonoid biosynthesis and antenna proteins of photosynthesis were significantly down-regulated, while genes related to the lignin biosynthesis pathway were remarkably up-regulated, indicating that could synthesize more lignin to cope with Cd stress. Moreover, genes related to heavy metal accumulation, sulfur metabolism and glutathione metabolism were also significantly up-regulated. The gene expression pattern of several key genes related to distinct metabolic pathways was verified by qRT-PCR. The results indicated that the immobilization of lignin in cell wall, chelation, vacuolar compartmentalization, as well as the increase of thiol compounds content may be the important mechanisms of Cd detoxification in hyperaccumulator plant . Accession numbers: the raw data of transcriptome presented in this study are openly available in NCBI SRA database, under the BioProject of PRJNA649785.
The online version contains supplementary material available at 10.1007/s13205-021-02865-x.
为研究超富集植物抵御镉(Cd)胁迫的分子机制,采集经400 μM Cd处理0、2、12和24小时的叶片用于比较转录组分析。共获得110.07 Gb的clean数据,组装后获得63,957个单基因。由于缺乏基因组信息,只有24,517个单基因被公共数据库注释。Cd处理后,鉴定出5054个差异表达基因(DEG)。对DEG进行KEGG通路富集分析表明,参与类黄酮生物合成和光合作用天线蛋白的基因显著下调,而与木质素生物合成途径相关的基因显著上调,表明[植物名称]可以合成更多木质素来应对Cd胁迫。此外,与重金属积累、硫代谢和谷胱甘肽代谢相关的基因也显著上调。通过qRT-PCR验证了与不同代谢途径相关的几个关键基因的基因表达模式。结果表明,木质素在细胞壁中的固定、螯合、液泡区室化以及硫醇化合物含量的增加可能是超富集植物[植物名称]中Cd解毒的重要机制。登录号:本研究中呈现的[植物名称]转录组原始数据在NCBI SRA数据库中公开可用,生物项目编号为PRJNA649785。
在线版本包含可在10.1007/s13205-021-02865-x获取的补充材料。