Wan Liyun, Li Bei, Lei Yong, Yan Liying, Ren Xiaoping, Chen Yuning, Dai Xiaofeng, Jiang Huifang, Zhang Juncheng, Guo Wei, Chen Ao, Liao Boshou
Key Laboratory of Biology and Genetic Improvement of Oil Crops, Ministry of Agriculture, Oil Crops Research Institute of Chinese Academy of Agricultural Sciences, Wuhan, China.
Institute of Food Science and Technology of Chinese Academy of Agricultural Sciences, Beijing, China.
Front Plant Sci. 2017 Nov 9;8:1900. doi: 10.3389/fpls.2017.01900. eCollection 2017.
Pod size is the major yield component and a key target trait that is selected for in peanut breeding. However, although numerous quantitative trait loci (QTLs) for peanut pod size have been described, the molecular mechanisms underlying the development of this characteristic remain elusive. A peanut mutant with a narrower pod was developed in this study using ethyl methanesulfonate (EMS) mutagenesis and designated as the "pod width" mutant line (). The fresh pod weight of was only about 40% of that seen in the wild-type (WT) Zhonghua16, while the hull and seed filling of the mutant both also developed at earlier stages. Pods from both and WT lines were sampled 20, 40, and 60 days after flowering (DAF) and used for RNA-Seq analysis; the results revealed highly differentially expressed lignin metabolic pathway genes at all three stages, but especially at DAF 20 and DAF 40. At the same time, expression of genes related to auxin signal transduction was found to be significantly repressed during the early pod developmental stage. A genome-wide comparative analysis of expression profiles revealed 260 differentially expressed genes (DEGs) across all three stages, and two candidate genes, () and (), responsible for pod width were identified by integrating expression patterns and function annotation of the common DEGs within the three stages. Taken together, the information provided in this study illuminates the processes underlying peanut pod development, and will facilitate further identification of causal genes and the development of improved peanut varieties with higher yields.
荚果大小是花生产量的主要构成因素,也是花生育种中选择的关键目标性状。然而,尽管已经描述了许多与花生荚果大小相关的数量性状位点(QTL),但该性状发育的分子机制仍不清楚。本研究利用甲基磺酸乙酯(EMS)诱变培育出一种荚果较窄的花生突变体,命名为“荚果宽度”突变系()。其新鲜荚果重量仅约为野生型中花16的40%,而突变体的果壳和种子充实也都在较早阶段发育。在开花后20、40和60天(DAF)采集突变系和野生型植株的荚果用于RNA测序分析;结果显示,在所有三个阶段,尤其是在DAF 20和DAF 40时,木质素代谢途径基因存在高度差异表达。同时,发现在荚果发育早期,与生长素信号转导相关的基因表达受到显著抑制。全基因组表达谱比较分析揭示了在所有三个阶段共有260个差异表达基因(DEG),通过整合三个阶段共同DEG的表达模式和功能注释,鉴定出两个与荚果宽度相关的候选基因,即()和()。综上所述,本研究提供的信息阐明了花生荚果发育的过程,将有助于进一步鉴定因果基因并培育出产量更高的改良花生品种。