BRZ-INSENSITIVE-LONG HYPOCOTYL8 inhibits kinase-mediated phosphorylation to regulate brassinosteroid signaling

Author:

Chagan Zhana1ORCID,Nakata Genki23ORCID,Suzuki Shin1ORCID,Yamagami Ayumi1ORCID,Tachibana Ryo1ORCID,Surina Surina1ORCID,Fujioka Shozo2,Matsui Minami2ORCID,Kushiro Tetsuo3ORCID,Miyakawa Takuya1ORCID,Asami Tadao4ORCID,Nakano Takeshi1ORCID

Affiliation:

1. Graduate School of Biostudies, Kyoto University , Kyoto 606-8502 , Japan

2. Center for Sustainable Resource Science , RIKEN, Kanagawa 230-0045 , Japan

3. School of Agriculture, Meiji University , Kanagawa 214-8571 , Japan

4. Department of Applied Biological Chemistry, The University of Tokyo , Tokyo 113-8657 , Japan

Abstract

Abstract Glycogen synthase kinase 3 (GSK3) is an evolutionarily conserved serine/threonine protein kinase in eukaryotes. In plants, the GSK3-like kinase BRASSINOSTEROID-INSENSITIVE 2 (BIN2) functions as a central signaling node through which hormonal and environmental signals are integrated to regulate plant development and stress adaptation. BIN2 plays a major regulatory role in brassinosteroid (BR) signaling and is critical for phosphorylating/inactivating BRASSINAZOLE-RESISTANT 1 (BZR1), also known as BRZ-INSENSITIVE-LONG HYPOCOTYL 1 (BIL1), a master transcription factor of BR signaling, but the detailed regulatory mechanism of BIN2 action has not been fully revealed. In this study, we identified BIL8 as a positive regulator of BR signaling and plant growth in Arabidopsis (Arabidopsis thaliana). Genetic and biochemical analyses showed that BIL8 is downstream of the BR receptor BRASSINOSTEROID-INSENSITIVE 1 (BRI1) and promotes the dephosphorylation of BIL1/BZR1. BIL8 interacts with and inhibits the activity of the BIN2 kinase, leading to the accumulation of dephosphorylated BIL1/BZR1. BIL8 suppresses the cytoplasmic localization of BIL1/BZR1, which is induced via BIN2-mediated phosphorylation. Our study reveals a regulatory factor, BIL8, that positively regulates BR signaling by inhibiting BIN2 activity.

Funder

NARO Bio-oriented Technology Research Advancement Institution

Japan Science and Technology Agency

Publisher

Oxford University Press (OUP)

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