TY - JOUR
T1 - Cytosolic WPRa4 and Plastoskeletal PMI4 Proteins Mediate Touch Response in a Model Organism Arabidopsis
AU - Wu, Kebin
AU - Yang, Nan
AU - Ren, Jia
AU - Liu, Shichang
AU - Wang, Kai
AU - Dai, Shuaijian
AU - Lu, Yinglin
AU - An, Yuxing
AU - Tian, Fuyun
AU - Gao, Zhaobing
AU - Yang, Zhu
AU - Zhang, Yage
AU - Yu, Weichuan
AU - Li, Ning
N1 - Publisher Copyright:
© 2025 THE AUTHORS.
PY - 2025/7
Y1 - 2025/7
N2 - Plastoskeletal PMI4 Protein is a Key Regulator of ThigmomorphogenesisTo elucidate the early signaling components involved in thigmomorphogenesis in Arabidopsis thaliana, we combined microscopy and proximity-labeling (PL)-based quantitative biotinylproteomics to characterize the touch-responsive putative cytoskeleton-interacting protein WPRa4 (TREPH1). Our findings revealed that WPRa4 localizes near plastids and interacts with cytosolic Plastid Movement-Impaired (PMI) proteins and a plastidic translocon component, suggesting a cytoskeleton-plastid network in mechanosensing. Bioinformatic analysis of PL and cross-linking mass spectrometry (XL-MS) data identified PMI4 as a key mediator, with pmi4 mutants lacking touch-induced bolting delay, rosette size reduction, and Ca2+ oscillations. Transcriptomics further showed that PMI4 regulates touch-responsive and jasmonic acid (JA)associated genes, such as LOX2. We propose a molecular model where interconnected Cytoskeleton-Plastoskeleton Continuum (CPC) proteins act as early mechanosensors, integrating the touch responses of plant aerial organs with calcium signaling and transcriptional reprogramming in Arabidopsis.
AB - Plastoskeletal PMI4 Protein is a Key Regulator of ThigmomorphogenesisTo elucidate the early signaling components involved in thigmomorphogenesis in Arabidopsis thaliana, we combined microscopy and proximity-labeling (PL)-based quantitative biotinylproteomics to characterize the touch-responsive putative cytoskeleton-interacting protein WPRa4 (TREPH1). Our findings revealed that WPRa4 localizes near plastids and interacts with cytosolic Plastid Movement-Impaired (PMI) proteins and a plastidic translocon component, suggesting a cytoskeleton-plastid network in mechanosensing. Bioinformatic analysis of PL and cross-linking mass spectrometry (XL-MS) data identified PMI4 as a key mediator, with pmi4 mutants lacking touch-induced bolting delay, rosette size reduction, and Ca2+ oscillations. Transcriptomics further showed that PMI4 regulates touch-responsive and jasmonic acid (JA)associated genes, such as LOX2. We propose a molecular model where interconnected Cytoskeleton-Plastoskeleton Continuum (CPC) proteins act as early mechanosensors, integrating the touch responses of plant aerial organs with calcium signaling and transcriptional reprogramming in Arabidopsis.
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:001530421000001
UR - https://openalex.org/W4411196802
UR - https://www.scopus.com/pages/publications/105012760444
U2 - 10.1016/j.mcpro.2025.101015
DO - 10.1016/j.mcpro.2025.101015
M3 - Journal Article
C2 - 40513778
AN - SCOPUS:105012760444
SN - 1535-9476
VL - 24
JO - Molecular and Cellular Proteomics
JF - Molecular and Cellular Proteomics
IS - 7
M1 - 101015
ER -