Wu Yanyan, Huang Weihua, Tian Qinglan, Liu Jieyun, Xia Xiuzhong, Yang Xinghai, Mou Haifei
Biotechnology Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, Guangxi, China.
Rice Research Institute, Guangxi Academy of Agricultural Sciences, Nanning 530007, Guangxi, China.
PeerJ. 2021 Mar 3;9:e10977. doi: 10.7717/peerj.10977. eCollection 2021.
Chilling stress (CS) is an important limiting factor for the growth and development of passion fruit () in winter in South China. However, little is known about how the passion fruit responds and adapts to CS. In this study, we performed transcriptome sequencing of cold-susceptible cultivar Huangjinguo (HJG) and cold-tolerant cultivar Tainong 1 (TN1) under normal temperature (NT) and CS conditions, and a total of 47,353 unigenes were obtained by seven databases. Using differentially expressed unigenes (DEGs) analysis, 3,248 and 4,340 DEGs were identified at two stages, respectively. The Gene Ontology (GO) enrichment analysis showed that the DEGs were mainly related to phosphorylation, membrane protein, and catalytic activity. In Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway, the unigenes of plant-pathogen interaction, plant hormone signal transduction and fatty acid metabolism were enriched. Then, the 12,471 filtered unigenes were clustered into eight co-expression modules, and two modules were correlated with CS. In this two modules, 32 hub unigenes were obtained. Furthermore, the unigenes related to CS were validated using quantitative real-time PCR (RT-qPCR). This work showed that the expression levels of CS-related unigenes were very different in two passion fruit cultivars. The results provide information for the development of passion fruit with increased chilling tolerance.
低温胁迫是华南地区冬季百香果生长发育的重要限制因素。然而,关于百香果如何响应和适应低温胁迫知之甚少。在本研究中,我们对低温敏感品种黄金果(HJG)和耐寒品种台农1号(TN1)在常温(NT)和低温胁迫条件下进行了转录组测序,通过七个数据库共获得47,353个单基因。利用差异表达单基因(DEG)分析,在两个阶段分别鉴定出3,248个和4,340个DEG。基因本体(GO)富集分析表明,DEG主要与磷酸化、膜蛋白和催化活性有关。在京都基因与基因组百科全书(KEGG)途径中,植物-病原体相互作用、植物激素信号转导和脂肪酸代谢的单基因得到富集。然后,将12,471个筛选后的单基因聚类为八个共表达模块,其中两个模块与低温胁迫相关。在这两个模块中,获得了32个核心单基因。此外,利用定量实时PCR(RT-qPCR)对与低温胁迫相关的单基因进行了验证。这项工作表明,两个百香果品种中与低温胁迫相关的单基因表达水平差异很大。这些结果为培育耐低温性增强的百香果提供了信息。