Wang Hong, Chang XiaoXiao, Lin Jing, Chang Youhong, Chen Jen-Chih, Reid Michael S, Jiang Cai-Zhong
1Institute of Pomology/Jiangsu Key Laboratory for Horticultural Crop Genetic Improvement, Jiangsu Academy of Agricultural Sciences, 210014 Nanjing, China.
2Department of Plant Sciences, University of California, Davis, Davis, CA 95616 USA.
Hortic Res. 2018 Apr 1;5:16. doi: 10.1038/s41438-018-0018-1. eCollection 2018.
The genetic regulatory mechanisms that govern natural corolla senescence in petunia are not well understood. To identify key genes and pathways that regulate the process, we performed a transcriptome analysis in petunia corolla at four developmental stages, including corolla fully opening without anther dehiscence (D0), corolla expansion, 2 days after anthesis (D2), corolla with initial signs of senescence (D4), and wilting corolla (D7). We identified large numbers of differentially expressed genes (DEGs), ranging from 4626 between the transition from D0 and D2, 1116 between D2 and D4, a transition to the onset of flower senescence, and 327 between D4 and D7, a developmental stage representing flower senescence. KEGG analysis showed that the auxin- and ethylene-related hormone biosynthesis and signaling transduction pathways were significantly activated during the flower development and highly upregulated at onset of flower senescence. Ethylene emission was detected at the D2 to D4 transition, followed by a large eruption at the D4 to D7 transition. Furthermore, large numbers of transcription factors (TFs) were activated over the course of senescence. Functional analysis by virus-induced gene silencing (VIGS) experiments demonstrated that inhibition of the expression of TFs, such as ethylene-related ERF, auxin-related ARF, bHLH, HB, and MADS-box, significantly extended or shortened flower longevity. Our data suggest that hormonal interaction between auxin and ethylene may play critical regulatory roles in the onset of natural corolla senescence in petunia.
目前,人们对矮牵牛中控制天然花冠衰老的遗传调控机制还了解甚少。为了确定调控这一过程的关键基因和途径,我们对矮牵牛花冠在四个发育阶段进行了转录组分析,这四个阶段包括:花冠完全开放且花药未开裂(D0)、花冠伸展期、开花后2天(D2)、花冠出现衰老初始迹象(D4)以及枯萎的花冠(D7)。我们鉴定出了大量差异表达基因(DEG),其中从D0到D2的转变阶段有4626个,从D2到D4(即向花朵衰老开始的转变阶段)有1116个,以及从D4到D7(代表花朵衰老的发育阶段)有327个。KEGG分析表明,生长素和乙烯相关的激素生物合成及信号转导途径在花朵发育过程中被显著激活,并在花朵衰老开始时高度上调。在从D2到D4的转变阶段检测到乙烯释放,随后在从D4到D7的转变阶段出现大量爆发。此外,在衰老过程中大量转录因子(TF)被激活。通过病毒诱导基因沉默(VIGS)实验进行的功能分析表明,抑制乙烯相关的ERF、生长素相关的ARF、bHLH、HB和MADS-box等转录因子的表达,可显著延长或缩短花朵寿命。我们的数据表明,生长素和乙烯之间的激素相互作用可能在矮牵牛天然花冠衰老的起始过程中发挥关键调控作用。