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Roles of the pepper JAZ protein CaJAZ1-03 and its interacting partner RING-type E3 ligase CaASRF1 in regulating ABA signaling and drought responses

Authors
Koh, HaejiJoo, HyunheeLim, Chae WooLee, Sung Chul
Issue Date
Nov-2023
Publisher
WILEY
Keywords
abscisic acid; drought; jasmonic acid; protein stability; ubiquitination
Citation
PLANT CELL AND ENVIRONMENT, v.46, no.11, pp 3242 - 3257
Pages
16
Journal Title
PLANT CELL AND ENVIRONMENT
Volume
46
Number
11
Start Page
3242
End Page
3257
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/67888
DOI
10.1111/pce.14692
ISSN
0140-7791
1365-3040
Abstract
Plants have developed various defense mechanisms against environmental stresses by regulating hormone signaling. Jasmonic acid (JA) is a major phytohormone associated with plant defense responses. JASMONATE ZIM-DOMAIN (JAZ) proteins play a regulatory role in repressing JA signaling, impacting plant responses to both biotic and abiotic stresses. Here, we isolated 7 JAZ genes in pepper and selected CA03g31030, a Capsicum annuum JAZ1-03 (CaJAZ1-03) gene, for further study based on its expression level in response to abiotic stresses. Through virus-induced gene silencing (VIGS) in pepper and overexpression in transgenic Arabidopsis plants, we established the functional role of CaJAZ1-03. Functional studies revealed that CaJAZ1-03 dampens abscisic acid (ABA) signaling and drought stress responses. The cell-free degradation assay showed faster degradation of CaJAZ1-03 in drought- or ABA-treated pepper leaves compared to healthy leaves. Conversely, CaJAZ1-03 was completely preserved under MG132 treatment, indicating that CaJAZ1-03 stability is modulated via the ubiquitin-26s proteasome pathway. We also found that the pepper RING-type E3 ligase CaASRF1 interacts with and ubiquitinates CaJAZ1-03. Additional cell-free degradation assays revealed a negative correlation between CaJAZ1-03 and CaASRF1 expression levels. Collectively, these findings suggest that CaJAZ1-03 negatively regulates ABA signaling and drought responses and that its protein stability is modulated by CaASRF1.
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자연과학대학 (생명과학과)
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