Fu Chang-Chun, Han Yan-Chao, Qi Xiu-Ye, Shan Wei, Chen Jian-Ye, Lu Wang-Jin, Kuang Jian-Fei
State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources/Guangdong Key Laboratory for Postharvest Science, College of Horticulture, South China Agricultural University, Guangzhou, 510642, China.
Plant Cell Rep. 2016 Nov;35(11):2341-2352. doi: 10.1007/s00299-016-2038-3. Epub 2016 Aug 8.
CpERF9 controls papaya fruit ripening through transcriptional repression of cell-wall-modifying genes CpPME1/2 and CpPG5 by directly binding to their promoters. Papaya fruit ripening is an intricate and highly coordinated developmental process which is controlled by the action of ethylene and expression of numerous ethylene-responsive genes. Ethylene response factors (ERFs) representing the last regulators of ethylene-signaling pathway determine the specificities of ethylene response. However, knowledge concerning the transcriptional controlling mechanism of ERF-mediated papaya fruit ripening is limited. In the present work, a gene-encoding AP2/ERF protein with two ERF-associated amphiphilic repression (EAR) motifs, named CpERF9, was characterized from papaya fruit. CpERF9 was found to localize in nucleus, and possess transcriptional repression ability. CpERF9 expression steadily decreased during papaya fruit ripening, while several genes encoding pectin methylesterases (PMEs) and polygalacturonases (PGs), such as CpPME1/2 and CpPG5, were gradually increased, paralleling the decline of fruit firmness. Electrophoretic mobility shift assay (EMSA) demonstrated a specific binding of CpERF9 to promoters of CpPME1/2 and CpPG5, via the GCC-box motif. Transient expression of CpERF9 in tobacco repressed CpPME1/2 and CpPG5 promoter activities, which was depended on two EAR motifs of CpERF9 protein. Taken together, these findings suggest that papaya CpERF9 may act as a transcriptional repressor of several cell-wall modifying genes, such as CpPME1/2 and CpPG5, via directly binding to their promoters.
CpERF9通过直接结合细胞壁修饰基因CpPME1/2和CpPG5的启动子来转录抑制它们,从而控制番木瓜果实的成熟。番木瓜果实成熟是一个复杂且高度协调的发育过程,受乙烯作用和众多乙烯响应基因表达的调控。乙烯响应因子(ERF)作为乙烯信号通路的最终调节因子,决定了乙烯响应的特异性。然而,关于ERF介导的番木瓜果实成熟转录调控机制的知识有限。在本研究中,从番木瓜果实中鉴定出一个编码具有两个ERF相关两亲性抑制(EAR)基序的AP2/ERF蛋白的基因,命名为CpERF9。发现CpERF9定位于细胞核,并具有转录抑制能力。在番木瓜果实成熟过程中,CpERF9的表达稳步下降,而几个编码果胶甲酯酶(PME)和多聚半乳糖醛酸酶(PG)的基因,如CpPME1/2和CpPG5,则逐渐增加,这与果实硬度的下降平行。电泳迁移率变动分析(EMSA)表明CpERF9通过GCC盒基序与CpPME1/2和CpPG5的启动子特异性结合。CpERF9在烟草中的瞬时表达抑制了CpPME1/2和CpPG5启动子的活性,这依赖于CpERF9蛋白的两个EAR基序。综上所述,这些发现表明番木瓜CpERF9可能通过直接结合其启动子,作为几个细胞壁修饰基因(如CpPME1/2和CpPG5)的转录抑制因子。