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The role of protein phosphatase 2A (PP2A) in the unfolded protein response (UPR) of plants

Protein phosphatase 2A (PP2A) is a key regulator of plant growth and development, but its role in the endoplasmic reticulum (ER) stress response remains elusive. In this study, we investigated the function of PP2A under ER stress using loss-of-function mutants of ROOTS CURL of NAPHTHYLPHTHALAMIC ACI...

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Published in:Biochemical and biophysical research communications 2023-08, Vol.670, p.94-101
Main Authors: Ko, Ki Seong, Yoo, Jae Yong, Vu, Bich Ngoc, Lee, Young Eun, Choi, Ha Na, Lee, Yoo Na, Fanata, Wahyu Indra Duwi, Harmoko, Rikno, Chung, Woo Sik, Hong, Jong Chan, Lee, Kyun Oh
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Language:English
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Summary:Protein phosphatase 2A (PP2A) is a key regulator of plant growth and development, but its role in the endoplasmic reticulum (ER) stress response remains elusive. In this study, we investigated the function of PP2A under ER stress using loss-of-function mutants of ROOTS CURL of NAPHTHYLPHTHALAMIC ACID1 (RCN1), a regulatory A1 subunit isoform of Arabidopsis PP2A. RCN1 mutants (rcn1-1 and rcn1-2) exhibited reduced sensitivity to tunicamycin (TM), an inhibitor of N-linked glycosylation and inducer of unfolded protein response (UPR) gene expression, resulting in less severe effects compared to wild-type plants (Ws-2 and Col-0). TM negatively impacted PP2A activity in Col-0 plants but did not significantly affect rcn1-2 plants. Additionally, TM treatment did not influence the transcription levels of the PP2AA1(RCN1), 2, and 3 genes in Col-0 plants. Cantharidin, a PP2A inhibitor, exacerbated growth defects in rcn1 plants and alleviated TM-induced growth inhibition in Ws-2 and Col-0 plants. Furthermore, cantharidin treatment mitigated TM hypersensitivity in ire1a&b and bzip28&60 mutants. These findings suggest that PP2A activity is essential for an efficient UPR in Arabidopsis. •PP2A function in ER stress response in plants explored.•rcn1 mutants show reduced sensitivity to ER stress.•PP2A inhibitor cantharidin mitigates plant ER stress.•Findings enhance understanding of UPR signaling pathways.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2023.05.106