Wu Xuexia, Fan Youcun, Li Lanping, Liu Yujiao
State Key Laboratory of Plateau Ecology and Agriculture, Qinghai Academy of Agricultural and Forestry Sciences, Qinghai University, Ningda Road No. 251, Xining, 810016 Qinghai China.
Qinghai Research Station of Crop Gene Resource & Germplasm Enhancement, Ministry of Agriculture, Xining, 810016 Qinghai China.
3 Biotech. 2020 Sep;10(9):381. doi: 10.1007/s13205-020-02374-3. Epub 2020 Aug 7.
Water deficit has a significant impact on growth, development and yield of fava bean ( L.) in arid and semi-arid climates. The aim of this study was to identify differentially expressed genes in the Qinghai 13 genotype under soil drought through leaf transcriptome analysis. A total of 256.95 M clean reads were obtained and assembled into 176334 unigenes, with an average length of 766 bp. A total of 9126 (4439 upregulated and 4687 downregulated) differentially expressed genes (DEGs) were identified in faba bean leaves under soil drought. In total, 324 putative transcription factors were identified and classified as belonging to different transcription factor families. According to GO and KEGG analysis, the soil drought stress-inducible DEGs encoded proteins mainly involved in regulating photosynthesis, osmotic adjustment, detoxification, autophagy and other functions. In addition, a large portion of DEGs appeared to be novel because they could not be annotated in any functional databases, therefore, suggesting a specific response to soil drought in faba bean. Finally, RNA-seq analysis was validated by quantitative reverse-transcription PCR analysis. This work provides comprehensive and valuable information for understanding the molecular mechanisms which faba bean uses to respond to soil drought.
水分亏缺对干旱和半干旱气候条件下蚕豆(L.)的生长、发育和产量有重大影响。本研究的目的是通过叶片转录组分析,鉴定青海13基因型在土壤干旱条件下差异表达的基因。共获得25695万个clean reads,并组装成176334个单基因,平均长度为766 bp。在土壤干旱条件下,蚕豆叶片中共鉴定出9126个差异表达基因(DEGs)(4439个上调,4687个下调)。总共鉴定出324个假定的转录因子,并将其分类为不同的转录因子家族。根据GO和KEGG分析,土壤干旱胁迫诱导的DEGs编码的蛋白质主要参与调节光合作用、渗透调节、解毒、自噬等功能。此外,很大一部分DEGs似乎是新的,因为它们在任何功能数据库中都无法注释,因此表明蚕豆对土壤干旱有特定反应。最后,通过定量逆转录PCR分析验证了RNA-seq分析。这项工作为理解蚕豆应对土壤干旱的分子机制提供了全面而有价值的信息。