Wu Meng, Si Min, Li Xieyu, Song Linyan, Liu Jianlong, Zhai Rui, Cong Liu, Yue Rongrong, Yang Chengquan, Ma Fengwang, Xu Lingfei, Wang Zhigang
College of Horticulture, Northwest A&F University, Taicheng Road NO.3, Yangling 712100, China.
Plants (Basel). 2019 Feb 12;8(2):39. doi: 10.3390/plants8020039.
The synthesis of anthocyanin in pear () fruit is regulated by light. However, little is known about the molecular mechanisms of pear fruit coloring mediated by upstream light-signaling regulators. Here, the photoresponse factors CONSTITUTIVE PHOTOMORPHOGENIC (COP) 1.1 and 1.2 were cloned from 'Red Zaosu' peel to study their functions in pear fruit coloring. The overexpression vectors pBI121-PbCOP1.1 and pBI121-PbCOP1.2 were constructed to analyze their effects on anthocyanin synthesis in pear fruit. A protein sequence alignment and phylogenetic tree analysis revealed that PbCOP1 proteins are highly homologous with those of other species. An analysis of tissue differential expression showed that the greatest expression levels of PbCOP1s occurred in the leaves. Their expression levels increased in the leaves during development, when the leaves changed from red to green. The overexpression of PbCOP1s in the peel resulted in reduced anthocyanin synthesis at the injection sites. A quantitative PCR analysis of the injection sites showed that PbCOP1.1 significantly inhibited the expression of the anthocyanin synthesis-related genes CHI, DFR, UFGT2, bHLH3, HY5 and GST. Based on the above results, we hypothesize that PbCOP1.1 is an anthocyanin synthetic inhibitory factor of pear coloration.
梨()果实中花青素的合成受光照调节。然而,关于上游光信号调节因子介导的梨果实着色的分子机制知之甚少。在此,从‘红早酥’果皮中克隆了光响应因子组成型光形态建成(COP)1.1和1.2,以研究它们在梨果实着色中的功能。构建了过表达载体pBI121-PbCOP1.1和pBI121-PbCOP1.2,以分析它们对梨果实花青素合成的影响。蛋白质序列比对和系统发育树分析表明,PbCOP1蛋白与其他物种的蛋白高度同源。组织差异表达分析表明,PbCOP1s在叶片中的表达水平最高。在叶片发育过程中,当叶片从红色变为绿色时,它们的表达水平增加。在果皮中过表达PbCOP1s导致注射部位花青素合成减少。对注射部位进行定量PCR分析表明,PbCOP1.1显著抑制花青素合成相关基因CHI、DFR、UFGT2、bHLH3、HY5和GST的表达。基于上述结果,我们推测PbCOP1.1是梨着色的花青素合成抑制因子。