Title
Coordinated regulation of Arabidopsis thaliana development by light and gibberellins
Date Issued
24 January 2008
Access level
open access
Resource Type
journal article
Author(s)
Feng S.
Martinez C.
Gusmaroli G.
Wang Y.
Zhou J.
Wang F.
Chen L.
Yu L.
Kircher S.
Schäfer E.
Fu X.
Fan L.M.
Deng X.W.
Universidad Autónoma de Madrid
Publisher(s)
Nature Publishing Group
Abstract
Light and gibberellins (GAs) mediate many essential and partially overlapping plant developmental processes. DELLA proteins are GA-signalling repressors that block GA-induced development. GA induces degradation of DELLA proteins via the ubiquitin/proteasome pathway, but light promotes accumulation of DELLA proteins by reducing GA levels. It was proposed that DELLA proteins restrain plant growth largely through their effect on gene expression. However, the precise mechanism of their function in coordinating GA signalling and gene expression remains unknown. Here we characterize a nuclear protein interaction cascade mediating transduction of GA signals to the activity regulation of a light-responsive transcription factor. In the absence of GA, nuclear-localized DELLA proteins accumulate to higher levels, interact with phytochrome- interacting factor 3 (PIF3, a bHLH-type transcription factor) and prevent PIF3 from binding to its target gene promoters and regulating gene expression, and therefore abrogate PIF3-mediated light control of hypocotyl elongation. In the presence of GA, GID1 proteins (GA receptors) elevate their direct interaction with DELLA proteins in the nucleus, trigger DELLA protein's ubiquitination and proteasome-mediated degradation, and thus release PIF3 from the negative effect of DELLA proteins. ©2008 Nature Publishing Group.
Start page
475
End page
479
Volume
451
Issue
7177
Language
English
OCDE Knowledge area
Ciencias de las plantas, Botánica Bioquímica, Biología molecular
Scopus EID
2-s2.0-38549142539
PubMed ID
Source
Nature
ISSN of the container
00280836
Sponsor(s)
Acknowledgements We thank J. Lee, K. He and I. Lee for providing unpublished results of their ChIP-microarray studies; J. A. Sullivan for MYC-and HA-tag vectors; F. Nagy for the YFP-tag vector; X. P. Wang for the Flag-tag vector; P.H. Quail for the pPIF3-RSETb plasmid; G. Choi for pif3-1 and 35S-PIF3–His–MYC seeds; T. P. Sun for rga-24 and rgl2-13 seeds; N. P. Harberd for gai-t6 seeds; S. P. Dinesh-Kumar for tobacco seeds; and F. Parcy for providing the BiFC vector system. This work was supported by a grant from the National Institutes of Health to X.W.D., by a grant from the Ministry of Science and Technology of China to National Institute of Biological Sciences at Beijing, by a 985 program fund from Peking University and the Ministry of Education of China to the Peking-Yale Joint Center laboratory, and by a grant from Program for New Century Excellent Talents in Peking University to L.-M.F. C.M. is a recipient of a postdoctoral fellowship from the Spanish Ministerio de Educacion y Ciencia. J.M.I.-P. is a recipient of a predoctoral fellowship from the Spanish Ministerio de Educacion y Ciencia. E.S. and S.K. were supported by grants from the Deutsche Forschungsgesellschaft.
Sources of information: Directorio de Producción Científica Scopus