Li Ji, Wu Zhe, Cui Li, Zhang Tinglin, Guo Qinwei, Xu Jian, Jia Li, Lou Qunfeng, Huang Sanwen, Li Zhengguo, Chen Jinfeng
State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing 210095, ChinaThese authors contributed equally to this work.
State Key Laboratory of Crop Genetics and Germplasm Enhancement, Nanjing Agricultural University, Nanjing 210095, ChinaCollege of Horticulture, Shanxi Agricultural University, Shanxi 030801, ChinaThese authors contributed equally to this work.
Plant Cell Physiol. 2014 Jul;55(7):1325-42. doi: 10.1093/pcp/pcu051. Epub 2014 Apr 14.
Parthenocarpy is an important trait determining yield and quality of fruit crops. However, the understanding of the mechanisms underlying parthenocarpy induction is limited. Cucumber (Cucumis sativus L.) is abundant in parthenocarpic germplasm resources and is an excellent model organism for parthenocarpy studies. In this study, the transcriptome of cucumber fruits was studied using RNA sequencing (RNA-Seq). Differentially expressed genes (DEGs) of set fruits were compared against aborted fruits. Distinctive features of parthenocarpic and pollinated fruits were revealed by combining the analysis of the transcriptome together with cytomorphological and physiological analysis. Cell division and the transcription of cell division genes were found to be more active in parthenocarpic fruit. The study also indicated that parthenocarpic fruit set is a high sugar-consuming process which is achieved via enhanced carbohydrate degradation through transcription of genes that lead to the breakdown of carbohydrates. Furthermore, the evidence provided by this work supports a hypothesis that parthenocarpic fruit set is induced by mimicking the processes of pollination/fertilization at the transcriptional level, i.e. by performing the same transcriptional patterns of genes inducing pollination and gametophyte development as in pollinated fruit. Based on the RNA-Seq and ovary transient expression results, 14 genes were predicted as putative parthenocarpic genes. The transcription analysis of these candidate genes revealed auxin, cytokinin and gibberellin cross-talk at the transcriptional level during parthenocarpic fruit set.
单性结实是决定果树产量和品质的重要性状。然而,对单性结实诱导机制的了解有限。黄瓜(Cucumis sativus L.)拥有丰富的单性结实种质资源,是研究单性结实的优良模式生物。在本研究中,利用RNA测序(RNA-Seq)对黄瓜果实的转录组进行了研究。将坐果的差异表达基因(DEGs)与败育果实进行了比较。通过将转录组分析与细胞形态学和生理学分析相结合,揭示了单性结实果实和授粉果实的显著特征。发现细胞分裂以及细胞分裂基因的转录在单性结实果实中更为活跃。该研究还表明,单性结实坐果是一个高糖消耗过程,这是通过增强碳水化合物降解来实现的,而碳水化合物降解是通过导致碳水化合物分解的基因转录来完成的。此外,这项工作提供的证据支持了一个假设,即单性结实坐果是通过在转录水平上模拟授粉/受精过程来诱导的,即在单性结实果实中表现出与授粉果实中诱导授粉和配子体发育的基因相同的转录模式。基于RNA-Seq和子房瞬时表达结果,预测了14个基因为假定的单性结实基因。对这些候选基因的转录分析揭示了在单性结实坐果过程中生长素、细胞分裂素和赤霉素在转录水平上的相互作用。