Unknown

Dataset Information

0

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


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.

SUBMITTER: Ye CM 

PROVIDER: S-EPMC6638746 | biostudies-literature | 2013 Apr

REPOSITORIES: biostudies-literature

altmetric image

Publications

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

Ye Chang-Ming CM   Chen Shaorong S   Payton Mark M   Dickman Martin B MB   Verchot Jeanmarie J  

Molecular plant pathology 20130401 3


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 we  ...[more]

Similar Datasets

| S-EPMC3103370 | biostudies-literature
| S-EPMC7028150 | biostudies-literature
| S-EPMC7369648 | biostudies-literature
| S-EPMC6629704 | biostudies-literature
| S-EPMC9426425 | biostudies-literature
| S-EPMC9249674 | biostudies-literature
| S-EPMC6639181 | biostudies-literature
| S-EPMC7147660 | biostudies-literature
| S-EPMC3196518 | biostudies-literature
| S-EPMC6180055 | biostudies-literature