Pandey Dhananjay K, Chaudhary Bhupendra
School of Biotechnology, Gautam Buddha University, Greater Noida, 201310, UP, India.
BMC Plant Biol. 2016 May 13;16(1):112. doi: 10.1186/s12870-016-0798-0.
Plant profilin genes encode core cell-wall structural proteins and are evidenced for their up-regulation under cotton domestication. Notwithstanding striking discoveries in the genetics of cell-wall organization in plants, little is explicit about the manner in which profilin-mediated molecular interplay and corresponding networks are altered, especially during cellular signalling of apical meristem determinacy and flower development.
Here we show that the ectopic expression of GhPRF1 gene in tobacco resulted in the hyperactivation of apical meristem and early flowering phenotype with increased flower number in comparison to the control plants. Spatial expression alteration in CLV1, a key meristem-determinacy gene, is induced by the GhPRF1 overexpression in a WUS-dependent manner and mediates cell signalling to promote flowering. But no such expression alterations are recorded in the GhPRF1-RNAi lines. The GhPRF1 transduces key positive flowering regulator AP1 gene via coordinated expression of FT4, SOC1, FLC1 and FT1 genes involved in the apical-to-floral meristem signalling cascade which is consistent with our in silico profilin interaction data. Remarkably, these positive and negative flowering regulators are spatially controlled by the Actin-Related Protein (ARP) genes, specifically ARP4 and ARP6 in proximate association with profilins. This study provides a novel and systematic link between GhPRF1 gene expression and the flower primordium initiation via up-regulation of the ARP genes, and an insight into the functional characterization of GhPRF1 gene acting upstream to the flowering mechanism. Also, the transgenic plants expressing GhPRF1 gene show an increase in the plant height, internode length, leaf size and plant vigor.
Overexpression of GhPRF1 gene induced early and increased flowering in tobacco with enhanced plant vigor. During apical meristem determinacy and flower development, the GhPRF1 gene directly influences key flowering regulators through ARP-genes, indicating for its role upstream in the apical-to-floral meristem signalling cascade.
植物肌动蛋白结合蛋白基因编码核心细胞壁结构蛋白,且有证据表明其在棉花驯化过程中上调。尽管在植物细胞壁组织遗传学方面有惊人发现,但关于肌动蛋白结合蛋白介导的分子相互作用及其相应网络如何改变,尤其是在顶端分生组织确定性和花发育的细胞信号传导过程中,人们了解甚少。
我们在此表明,与对照植株相比,烟草中GhPRF1基因的异位表达导致顶端分生组织过度激活和早期开花表型,花数量增加。关键分生组织确定性基因CLV1的空间表达改变由GhPRF1过表达以WUS依赖的方式诱导,并介导细胞信号传导以促进开花。但在GhPRF1-RNAi株系中未记录到这种表达改变。GhPRF1通过参与顶端到花分生组织信号级联的FT4、SOC1、FLC1和FT1基因的协同表达转导关键正向开花调节因子AP1基因,这与我们的计算机模拟肌动蛋白结合蛋白相互作用数据一致。值得注意的是,这些正向和负向开花调节因子由肌动蛋白相关蛋白(ARP)基因在空间上控制,特别是与肌动蛋白结合蛋白紧密相关的ARP4和ARP6。本研究通过上调ARP基因,在GhPRF1基因表达与花原基起始之间建立了一种新颖而系统的联系,并深入了解了GhPRF1基因在开花机制上游的功能特性。此外,表达GhPRF1基因的转基因植株在株高、节间长度、叶片大小和植株活力方面有所增加。
GhPRF1基因的过表达诱导烟草早期开花并增加花量,同时增强了植株活力。在顶端分生组织确定性和花发育过程中,GhPRF1基因通过ARP基因直接影响关键开花调节因子,表明其在顶端到花分生组织信号级联中的上游作用。