Department of Postharvest Science, The Volcani Center, ARO, Rishon LeZion, Israel.
Institute of Plant Sciences and Genetics in Agriculture, the Robert H. Smith Faculty of Agriculture, Food and Environment, The Hebrew University of Jerusalem, Rehovot Israel.
Autophagy. 2021 Oct;17(10):3109-3123. doi: 10.1080/15548627.2020.1856492. Epub 2020 Dec 19.
The caspase-like vacuolar processing enzyme (VPE) is a key factor in programmed cell death (PCD) associated with plant stress responses. Growth medium lacking a carbon source and dark conditions caused punctate labeling of 35S::VPE1-GFP (StVPE1-GFP) in potato leaves. Under conditions of carbon starvation, VPE activity and PCD symptoms strongly increased in BY-2 cells, but to a much lesser extent in -RNAi BY-2 cells. During extended exposure to carbon starvation, VPE expression and activity levels peaked, with a gradual increase in BY-2 cell death. Histological analysis of StVPE1-GFP in BY-2 cells showed that carbon starvation induces its translocation from the endoplasmic reticulum to the central vacuole through tonoplast engulfment. Exposure of BY-2 culture to the macroautophagy/autophagy inhibitor concanamycin A led to, along with an accumulation of autophagic bodies, accumulation of StVPE1-GFP in the cell vacuole. This accumulation did not occur in the presence of 3-methyladenine, an inhibitor of early-stage autophagy. BY-2 cells constitutively expressing RFP-StATG8IL, an autophagosome marker, showed colocalization with the StVPE1-GFP protein in the cytoplasm and vacuole. RNAi silencing of the core autophagy component in BY-2 cells reduced VPE activity and cell death. These results are the first to suggest that VPE translocates to the cell vacuole through the autophagy pathway, leading to PCD.: ATG: autophagy related; CLP: caspase-like protease; HR: hypersensitive response; PCD: programmed cell death; St: ; VPE: vacuolar processing enzyme.
半胱氨酸天冬氨酸蛋白酶样液泡加工酶 (VPE) 是与植物应激反应相关的程序性细胞死亡 (PCD) 的关键因素。在缺乏碳源的生长培养基和黑暗条件下,马铃薯叶片中的 35S::VPE1-GFP (StVPE1-GFP) 呈现点状标记。在碳饥饿条件下,VPE 活性和 PCD 症状在 BY-2 细胞中强烈增加,但在 -RNAi BY-2 细胞中增加的程度要小得多。在长时间暴露于碳饥饿时,VPE 表达和活性水平达到峰值,BY-2 细胞死亡逐渐增加。对 BY-2 细胞中 StVPE1-GFP 的组织学分析表明,碳饥饿通过液泡吞噬作用诱导其从内质网向中央液泡易位。将 BY-2 培养物暴露于巨自噬/自噬抑制剂康那霉素 A 会导致自噬体的积累,同时 StVPE1-GFP 在细胞液泡中积累。在存在 3-甲基腺嘌呤(早期自噬抑制剂)的情况下,不会发生这种积累。组成型表达自噬体标记物 RFP-StATG8IL 的 BY-2 细胞在细胞质和液泡中与 StVPE1-GFP 蛋白发生共定位。在 BY-2 细胞中沉默核心自噬成分 会降低 VPE 活性和细胞死亡。这些结果首次表明,VPE 通过自噬途径易位到细胞液泡,导致 PCD。ATG:自噬相关;CLP:半胱氨酸天冬氨酸蛋白酶样蛋白酶;HR:过敏反应;PCD:程序性细胞死亡;St:;VPE:液泡加工酶。