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TGBp3 触发未折叠蛋白反应和 SKP1 依赖性细胞程序性死亡。

TGBp3 triggers the unfolded protein response and SKP1-dependent programmed cell death.

机构信息

Department of Entomology and Plant Pathology, Oklahoma State University, Stillwater, OK 74078, USA.

出版信息

Mol Plant Pathol. 2013 Apr;14(3):241-55. doi: 10.1111/mpp.12000.

Abstract

The Potato virus X (PVX) triple gene block protein 3 (TGBp3), an 8-kDa membrane binding protein, aids virus movement and induces the unfolded protein response (UPR) during PVX infection. TGBp3 was expressed from the Tobacco mosaic virus (TMV) genome (TMV-p3), and we noted the up-regulation of SKP1 and several endoplasmic reticulum (ER)-resident chaperones, including the ER luminal binding protein (BiP), protein disulphide isomerase (PDI), calreticulin (CRT) and calmodulin (CAM). Local lesions were seen on leaves inoculated with TMV-p3, but not TMV or PVX. Such lesions were the result of TGBp3-elicited programmed cell death (PCD), as shown by an increase in reactive oxygen species, DNA fragmentation and induction of SKP1 expression. UPR-related gene expression occurred within 8 h of TMV-p3 inoculation and declined before the onset of PCD. TGBp3-mediated cell death was suppressed in plants that overexpressed BiP, indicating that UPR induction by TGBp3 is a pro-survival mechanism. Anti-apoptotic genes Bcl-xl, CED-9 and Op-IAP were expressed in transgenic plants and suppressed N gene-mediated resistance to TMV, but failed to alleviate TGBp3-induced PCD. However, TGBp3-mediated cell death was reduced in SKP1-silenced Nicotiana benthamiana plants. The combined data suggest that TGBp3 triggers the UPR and elicits PCD in plants.

摘要

马铃薯 X 病毒(PVX)三基因块蛋白 3(TGBp3)是一种 8kDa 的膜结合蛋白,有助于病毒运动,并在 PVX 感染过程中诱导未折叠蛋白反应(UPR)。TGBp3 由烟草花叶病毒(TMV)基因组(TMV-p3)表达,我们注意到 SKP1 和几种内质网(ER)驻留伴侣蛋白的上调,包括 ER 腔结合蛋白(BiP)、蛋白二硫键异构酶(PDI)、钙网蛋白(CRT)和钙调蛋白(CAM)。用 TMV-p3 接种叶片会出现局部病斑,但用 TMV 或 PVX 接种则不会。这些病斑是 TGBp3 引发的程序性细胞死亡(PCD)的结果,这表现为活性氧增加、DNA 片段化和 SKP1 表达的诱导。在 TMV-p3 接种后 8 小时内发生 UPR 相关基因表达,并在 PCD 发生前下降。在过表达 BiP 的植物中,TGBp3 介导的细胞死亡受到抑制,表明 TGBp3 诱导的 UPR 是一种生存机制。抗凋亡基因 Bcl-xl、CED-9 和 Op-IAP 在转基因植物中表达,并抑制了 N 基因介导的对 TMV 的抗性,但未能减轻 TGBp3 诱导的 PCD。然而,在沉默 SKP1 的 Nicotiana benthamiana 植物中,TGBp3 介导的细胞死亡减少。综合数据表明,TGBp3 在植物中触发 UPR 并引发 PCD。

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