Chang Hongping, Chen Dandan, Kam Jason, Richardson Terese, Drenth Janneke, Guo Xinhong, McIntyre C Lynne, Chai Shoucheng, Rae Anne L, Xue Gang-Ping
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Biology, Hunan University, Changsha 410082, PR China; CSIRO Agriculture, 306 Carmody Rd., St Lucia, QLD 4067, Australia.
College of Agronomy, Northwest Agriculture and Forestry University, Yangling, Shaanxi 712100, PR China; CSIRO Agriculture, 306 Carmody Rd., St Lucia, QLD 4067, Australia.
Plant Sci. 2016 Nov;252:88-102. doi: 10.1016/j.plantsci.2016.07.011. Epub 2016 Jul 19.
Q-type CH zinc finger proteins (ZFPs) are plant-specific DNA-binding proteins containing a conserved QALGGH motif. This study investigated the function of abiotic stress-inducible and predominantly root-expressed Triticum aestivum ZFPs (TaZFP22, TaZFP34 and TaZFP46) with a focus on TaZFP34. Expression of TaZFP34 in roots was upregulated by high salinity, dehydration, oxidative and cold stresses. Overexpression of TaZFP34 in wheat roots resulted in an increased root-to-shoot ratio, a phenomenon observed during plant adaptation to drying soil. Expression of a number of genes which are potentially involved in modulating root growth was significantly altered in the roots of TaZFP34 overexpressing lines. In particular, the transcript levels of TaRR12B, TaRR12D and TaSHY2 that are homologues of known negative regulators of root growth were significantly reduced. Expression of shoot growth-related genes, such as GA3-ox and expansins, was downregulated in the transgenic shoots. TaZFP34 bound to (C/G)AGT(G/A)-like elements in the promoters of TaZFP34 down-regulated TaRR12D and TaSHY2 and transrepressed the reporter gene expression driven by TaRR12D and TaSHY2 promoters. Expression of the above reporter genes was also repressed by TaZFP46 and TaZFP22. These data suggest that TaZFP34 is a transcriptional repressor and is involved in modulating the root-to-shoot ratio.
Q型CH锌指蛋白(ZFPs)是植物特有的DNA结合蛋白,含有保守的QALGGH基序。本研究调查了非生物胁迫诱导且主要在根中表达的普通小麦ZFPs(TaZFP22、TaZFP34和TaZFP46)的功能,重点研究TaZFP34。高盐、脱水、氧化和低温胁迫均可上调TaZFP34在根中的表达。在小麦根中过表达TaZFP34导致根冠比增加,这是植物适应干旱土壤时观察到的一种现象。在TaZFP34过表达株系的根中,一些可能参与调节根生长的基因的表达发生了显著变化。特别是,与已知根生长负调控因子同源的TaRR12B、TaRR12D和TaSHY2的转录水平显著降低。在转基因地上部中,与地上部生长相关的基因如GA3-氧化酶和扩张蛋白的表达下调。TaZFP34与TaZFP34启动子中的(C/G)AGT(G/A)样元件结合,下调TaRR12D和TaSHY2,并反式抑制由TaRR12D和TaSHY2启动子驱动的报告基因表达。TaZFP46和TaZFP22也抑制上述报告基因的表达。这些数据表明TaZFP34是一种转录抑制因子,参与调节根冠比。