Dierck Robrecht, De Keyser Ellen, De Riek Jan, Dhooghe Emmy, Van Huylenbroeck Johan, Prinsen Els, Van Der Straeten Dominique
Institute for Agricultural and Fisheries Research (ILVO), Caritasstraat 39, Melle, Belgium.
Laboratory of Functional Plant Biology, Department of Physiology, Ghent University, K.L. Ledeganckstraat 35, Ghent, Belgium.
PLoS One. 2016 Aug 24;11(8):e0161732. doi: 10.1371/journal.pone.0161732. eCollection 2016.
In the production and breeding of Chrysanthemum sp., shoot branching is an important quality aspect as the outgrowth of axillary buds determines the final plant shape. Bud outgrowth is mainly controlled by apical dominance and the crosstalk between the plant hormones auxin, cytokinin and strigolactone. In this work the hormonal and genetic regulation of axillary bud outgrowth was studied in two differently branching cut flower Chrysanthemum morifolium (Ramat) genotypes. C17 is a split-type which forms an inflorescence meristem after a certain vegetative period, while C18 remains vegetative under long day conditions. Plant growth of both genotypes was monitored during 5 subsequent weeks starting one week before flower initiation occurred in C17. Axillary bud outgrowth was measured weekly and samples of shoot apex, stem and axillary buds were taken during the first two weeks. We combined auxin and cytokinin measurements by UPLC-MS/MS with RT-qPCR expression analysis of genes involved in shoot branching regulation pathways in chrysanthemum. These included bud development genes (CmBRC1, CmDRM1, CmSTM, CmLsL), auxin pathway genes (CmPIN1, CmTIR3, CmTIR1, CmAXR1, CmAXR6, CmAXR2, CmIAA16, CmIAA12), cytokinin pathway genes (CmIPT3, CmHK3, CmRR1) and strigolactone genes (CmMAX1 and CmMAX2). Genotype C17 showed a release from apical dominance after floral transition coinciding with decreased auxin and increased cytokinin levels in the subapical axillary buds. As opposed to C17, C18 maintained strong apical dominance with vegetative growth throughout the experiment. Here high auxin levels and decreasing cytokinin levels in axillary buds and stem were measured. A differential expression of several branching genes accompanied the different hormonal change and bud outgrowth in C17 and C18. This was clear for the strigolactone biosynthesis gene CmMAX1, the transcription factor CmBRC1 and the dormancy associated gene CmDRM1, that all showed a decreased expression in C17 at floral transition and an increased expression in C18 with continuous vegetative growth. These results offer a case study for Chrysanthemum, showing an altered cytokinin to auxin balance and differential gene expression between vegetative growth with apical dominance and transition to generative growth with loss of apical dominance and axillary bud outgrowth. This suggests a conservation of several aspects of the hormonal and genetical regulation of bud outgrowth in Chrysanthemum. Furthermore, 15 previously uncharacterised genes in chrysanthemum, were described in this study. Of those genes involved in axillary bud outgrowth we identified CmDRM1, CmBRC1 and CmMAX1 as having an altered expression preceding axillary bud outgrowth, which could be useful as markers for bud activity.
在菊花的生产和培育过程中,侧枝生长是一个重要的品质方面,因为腋芽的生长决定了最终的植株形态。芽的生长主要受顶端优势以及植物激素生长素、细胞分裂素和独脚金内酯之间的相互作用控制。在这项研究中,我们在两种分枝方式不同的切花菊(Chrysanthemum morifolium (Ramat))基因型中研究了腋芽生长的激素和遗传调控。C17是一种分裂型,在一定的营养生长阶段后形成花序分生组织,而C18在长日照条件下保持营养生长状态。从C17开始花芽分化前一周起,连续5周监测两种基因型的植株生长情况。每周测量腋芽生长情况,并在最初两周采集茎尖、茎和腋芽样本。我们通过超高效液相色谱-串联质谱联用技术(UPLC-MS/MS)测定生长素和细胞分裂素含量,并对菊花中参与侧枝生长调控途径的基因进行实时定量聚合酶链反应(RT-qPCR)表达分析。这些基因包括芽发育基因(CmBRC1、CmDRM1、CmSTM、CmLsL)、生长素途径基因(CmPIN1、CmTIR3、CmTIR1、CmAXR1、CmAXR6、CmAXR2、CmIAA16、CmIAA12)、细胞分裂素途径基因(CmIPT3、CmHK3、CmRR1)和独脚金内酯基因(CmMAX1和CmMAX2)。基因型C17在花芽分化后顶端优势解除,同时亚顶端腋芽中生长素含量降低,细胞分裂素含量升高。与C17相反,C18在整个实验过程中保持较强的顶端优势并持续营养生长。在此过程中,腋芽和茎中的生长素水平较高,细胞分裂素水平下降。C17和C18中几种分枝基因的差异表达伴随着不同的激素变化和芽的生长。独脚金内酯生物合成基因CmMAX1、转录因子CmBRC1和休眠相关基因CmDRM1表现明显,它们在C17花芽分化时表达降低,而在C18持续营养生长时表达增加。这些结果为菊花提供了一个案例研究,表明在具有顶端优势的营养生长和顶端优势丧失及腋芽生长的生殖生长转变过程中,细胞分裂素与生长素的平衡发生了改变,基因表达也存在差异。这表明菊花芽生长的激素和遗传调控的几个方面具有保守性。此外,本研究还描述了菊花中15个以前未鉴定的基因。在参与腋芽生长的基因中,我们鉴定出CmDRM1、CmBRC1和CmMAX1在腋芽生长之前表达发生改变,可作为芽活动的标记物。