Zhang Heng, Chen Mingjun, Luo Xiaobo, Song Li, Li Fei
Key Laboratory of Plant Resource Conservation and Germplasm Innovation in Mountainous Region (Ministry of Education), Collaborative Innovation Center for Mountain Ecology & Agro-Bioengineering (CICMEAB), College of Life Sciences/Institute of Agro-Bioengineering, Guizhou University, Guiyang 550025, China.
Guizhou Institute of Biotechnology, Guizhou Provincial Academy of Agricultural Sciences, Guiyang 550003, China.
Plants (Basel). 2024 Dec 25;14(1):18. doi: 10.3390/plants14010018.
Potato ( L.) is an important food crop, but low temperature affects the potato growth and yield. In this study, the expression level of was significantly increased over 1 h and then gradually decreased under cold stress. The subcellular localization of the StBBX14 protein took place in the nucleus. The transgenic lines showed less leaf damage and significantly lower electrolyte leakage compared with the WT under cold stress, indicating that the overexpression of in the potato enhanced the cold resistance. A transcriptome analysis showed that a total of 2449 and 6274 differentially expressed genes were identified in WT-1 h and WT-12 h, respectively, when compared with WT-0h. A Gene Ontology enrichment analysis revealed that photosynthesis, cell wall, thylakoid, transcription regulator activity, oxidoreductase activity and glucosyltransferase activity were significantly enriched in and WT. A total of 14 distinct modules were generated by a WGCNA analysis based on all differentially expressed genes (DEGs). Four major modules with cold-related genes were isolated. RT-qPCR analysis showed that the expression patterns of eight DEGs were consistent between the qPCR and RNA-seq. These findings illustrate that the played an important role in cold stress in potato and provided a data basis for the genetic improvement of cold resistance traits of potato.
马铃薯(L.)是一种重要的粮食作物,但低温会影响马铃薯的生长和产量。在本研究中,[此处原文缺失相关基因名称]的表达水平在冷胁迫下1小时内显著升高,然后逐渐下降。StBBX14蛋白的亚细胞定位发生在细胞核中。与野生型相比,[此处原文缺失相关基因名称]转基因株系在冷胁迫下叶片损伤较轻,电解质渗漏显著降低,表明[此处原文缺失相关基因名称]在马铃薯中的过表达增强了其抗寒性。转录组分析表明,与WT-0h相比,在WT-1h和WT-12h中分别鉴定出2449个和6274个差异表达基因。基因本体富集分析显示,光合作用、细胞壁、类囊体、转录调节活性、氧化还原酶活性和糖基转移酶活性在[此处原文缺失相关基因名称]和野生型中显著富集。基于所有差异表达基因(DEG)通过加权基因共表达网络分析(WGCNA)生成了总共14个不同的模块。分离出四个与冷相关基因的主要模块。RT-qPCR分析表明,八个DEG的表达模式在qPCR和RNA-seq之间是一致的。这些发现表明[此处原文缺失相关基因名称]在马铃薯冷胁迫中起重要作用,并为马铃薯抗寒性状的遗传改良提供了数据基础。