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CTR1 phosphorylates the central regulator EIN2 to control ethylene hormone signaling from the ER membrane to the nucleus in Arabidopsis

Permanent URL:
http://handle.nal.usda.gov/10113/56698
File:
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Abstract:
The gaseous phytohormone ethylene C(2)H(4) mediates numerous aspects of growth and development. Genetic analysis has identified a number of critical elements in ethylene signaling, but how these elements interact biochemically to transduce the signal from the ethylene receptor complex at the endoplasmic reticulum (ER) membrane to transcription factors in the nucleus is unknown. To close this gap in our understanding of the ethylene signaling pathway, the challenge has been to identify the target of the CONSTITUTIVE TRIPLE RESPONSE1 (CTR1) Raf-like protein kinase, as well as the molecular events surrounding ETHYLENE-INSENSITIVE2 (EIN2), an ER membrane-localized Nramp homolog that positively regulates ethylene responses. Here we demonstrate that CTR1 interacts with and directly phosphorylates the cytosolic C-terminal domain of EIN2. Mutations that block the EIN2 phosphorylation sites result in constitutive nuclear localization of the EIN2 C terminus, concomitant with constitutive activation of ethylene responses in Arabidopsis. Our results suggest that phosphorylation of EIN2 by CTR1 prevents EIN2 from signaling in the absence of ethylene, whereas inhibition of CTR1 upon ethylene perception is a signal for cleavage and nuclear localization of the EIN2 C terminus, allowing the ethylene signal to reach the downstream transcription factors. These findings significantly advance our understanding of the mechanisms underlying ethylene signal transduction.
Author(s):
Chuanli Ju , Gyeong Mee Yoon , Jennifer Marie Shemansky , David Y. Lin , Z Irene Ying , Jianhong Chang , Wesley M. Garrett , Mareike Kessenbrock , Georg Groth , Mark L. Tucker , Bret Cooper , Joseph J. Kieber , Caren Chang
Subject(s):
Arabidopsis , cell membranes , cell nucleus , endoplasmic reticulum , ethylene , genetic techniques and protocols , growth and development , hormones , mutation , plant proteins , protein phosphorylation , protein-serine-threonine kinases , signal transduction , transcription factors
Source:
Proceedings of the National Academy of Sciences 2012 11 20 v.109 no.47
Language:
English
Year:
2012
Collection:
Journal Articles, USDA Authors, Peer-Reviewed
Rights:
Works produced by employees of the U.S. Government as part of their official duties are not copyrighted within the U.S. The content of this document is not copyrighted.