Zhang Heting, Xiao Yu, Deng Xiaojiang, Feng Hongyu, Li Zhe, Zhang Lulu, Chen Huiping
Key Laboratory of Tropical Biological Resources of Ministry of Education, Hainan University, Haikou, 570228, China.
Rice (N Y). 2020 Mar 30;13(1):22. doi: 10.1186/s12284-020-00376-6.
Vacuolar processing enzymes (VPEs) have been identified as the enzymes that regulate vacuole-mediated programmed cell death (PCD) in plants. The mechanism that VPE regulates the PCD in rice aleurone layers remains unknown.
The aleurone layers treated with distilled water exerted caspase-1 and VPE activity, both of which were inhibited by the caspase-1 specific inhibitor Ac-YVAD-CMK but not by the caspase-3 specific inhibitor Ac-DEVD-CHO. However, the caspase-1 and caspase-3 inhibitors weakened the activity of caspase-3. Combined with the effects of endogenous gibberellin (GA) on the induction of OsVPEs, we suggest that the OsVPE3 in the aleurone layers, which exhibits caspase-1-like activity, is a key molecule in GA-induced PCD via regulating the protease with caspase-3-like activity. Many studies have confirmed that vacuolar fusion is an important feature of vacuole-mediated PCD in plants. In this experiment, the process of vacuole fusion was accompanied by changes in the structure of actin filaments (AFs), specifically, their depolymerization and polymerization. The process of vacuolar fusion was accelerated or delayed by the promotion or inhibition of the depolymerization of AFs, respectively. Here, the inhibition of OsVPE3 blocked the depolymerization of AFs and delayed the fusion of vacuoles, indicating that OsVPE3 can regulate the fusion of vacuoles in rice aleurone layers via mediating AFs. Furthermore, the depolymerization of AFs contributed to the up-regulation of OsVPE3 gene expression and VPE activity, resulting in accelerated PCD in rice aleurone layers. However, the inhibitor of VPE reversed the effects of AF depolymerization on the activity of VPE, then postponing the process of PCD, implying that AF can involve in GA-induced PCD of rice aleurone layers by mediating OsVPE3.
Together, activation of OsVPE3 and depolymerization of AFs shortened the process of vacuolation and PCD in rice aleurone layers, and OsVPE3 interacted with AFs during regulation.
液泡加工酶(VPEs)已被鉴定为调节植物液泡介导的程序性细胞死亡(PCD)的酶。VPE调节水稻糊粉层中PCD的机制尚不清楚。
用蒸馏水处理的糊粉层表现出caspase-1和VPE活性,二者均被caspase-1特异性抑制剂Ac-YVAD-CMK抑制,但不被caspase-3特异性抑制剂Ac-DEVD-CHO抑制。然而,caspase-1和caspase-3抑制剂减弱了caspase-3的活性。结合内源赤霉素(GA)对OsVPEs诱导的影响,我们认为糊粉层中具有caspase-1样活性的OsVPE3是GA通过调节具有caspase-3样活性的蛋白酶诱导PCD的关键分子。许多研究证实液泡融合是植物液泡介导的PCD的一个重要特征。在本实验中,液泡融合过程伴随着肌动蛋白丝(AFs)结构的变化,具体而言,是它们的解聚和聚合。液泡融合过程分别因AFs解聚的促进或抑制而加速或延迟。在此,OsVPE3的抑制阻止了AFs的解聚并延迟了液泡的融合,表明OsVPE3可通过介导AFs来调节水稻糊粉层中液泡的融合。此外,AFs的解聚导致OsVPE3基因表达和VPE活性上调,从而加速水稻糊粉层中的PCD。然而,VPE抑制剂逆转了AF解聚对VPE活性的影响,进而推迟了PCD过程,这意味着AF可通过介导OsVPE3参与GA诱导的水稻糊粉层PCD。
总之,OsVPE3的激活和AFs的解聚缩短了水稻糊粉层中液泡化和PCD的过程,且OsVPE3在调节过程中与AFs相互作用。