Wang Xinyang, Wang Runfeng, Huo Xing, Zhou Yueni, Umer Muhammad J, Zheng Zihao, Jin Weicai, Huang Lu, Li Haifen, Yu Qianxia, Li Shaoxiong, Varshney Rajeev K, Wang Wenyi, Xiao Yuan, Hong Yanbin, Chen Xiaoping, Lu Qing, Liu Hao
Crops Research Institute, Guangdong Academy of Agricultural Sciences, Guangdong Provincial Key Laboratory of Crop Genetic Improvement, South China Peanut Sub-Center of National Center of Oilseed Crops Improvement, Guangzhou, Guangdong, China.
College of Traditional Chinese Medicine, Bozhou University, Bozhou, Anhui, China.
Plant Biotechnol J. 2025 May;23(5):1814-1831. doi: 10.1111/pbi.70009. Epub 2025 Mar 13.
Peanut stem is a vital organ to provide mechanical support and energy for aerial tissue development. However, the transcriptional regulatory mechanisms underlying stem development at a single-cell resolution remain unclear. Herein, single-nuclei isolation coupled with fluorescent-activated cell sorting was employed to construct a cell atlas of peanut seedling stems using microdroplets-based single-nuclei RNA-sequencing. This approach yielded 29 308 cells with 53 349 expressed genes underlying the identification of five cell types characterized by known marker genes. Additionally, 2053 differentially expressed genes (DEGs) were identified across different cell types. Furthermore, 3306 core-DEGs involved in cell development trajectories were used to construct a transcription factor (TF) interaction network, providing insights into specific biological pathways and transcriptional regulation dynamics underlying cell-type differentiation. Additionally, 1446 DEGs associated with different cell-cycle profile were identified, revealing that peanut stem elongation and cell expansion are closely linked to auxin-responsive pathway. This was supported by the examination of endogenous phytohormones and the identification of 10 hormone-responsive DEGs. Moreover, AhWRKY70 was localized in the nucleus and is highly enriched in stem cortex and xylem cells and exhibits a tissue-specific expression pattern that regulates stem growth. Overexpression of AhWRKY70 in Arabidopsis led to accelerated stem growth by modulating the phytohormone signalling pathway, influencing the expression of sixteen auxin and ethylene-responsive genes as demonstrated by transcriptome sequencing. In conclusion, the single-cell atlas provides a foundational dataset for understanding gene expression heterogeneity in peanut seedling stems. The elucidation of AhWRKY70 function expands our understanding of the roles of WRKY family members in peanut.
花生茎是为地上组织发育提供机械支撑和能量的重要器官。然而,单细胞分辨率下茎发育的转录调控机制仍不清楚。在此,采用单核分离结合荧光激活细胞分选技术,利用基于微滴的单核RNA测序构建花生幼苗茎的细胞图谱。该方法获得了29308个细胞,53349个表达基因,鉴定出了由已知标记基因表征的五种细胞类型。此外,在不同细胞类型中鉴定出2053个差异表达基因(DEG)。此外,利用3306个参与细胞发育轨迹的核心DEG构建转录因子(TF)相互作用网络,为细胞类型分化的特定生物学途径和转录调控动态提供了见解。此外,还鉴定出1446个与不同细胞周期谱相关的DEG,揭示花生茎伸长和细胞扩张与生长素响应途径密切相关。对内源植物激素的检测和10个激素响应DEG的鉴定支持了这一点。此外,AhWRKY70定位于细胞核,在茎皮层和木质部细胞中高度富集,并表现出调节茎生长的组织特异性表达模式。在拟南芥中过表达AhWRKY70通过调节植物激素信号通路促进茎生长,转录组测序表明其影响16个生长素和乙烯响应基因的表达。总之,单细胞图谱为理解花生幼苗茎中的基因表达异质性提供了基础数据集。AhWRKY70功能的阐明扩展了我们对WRKY家族成员在花生中作用的理解。