Dynamics of Brassinosteroid Response Modulated by Negative Regulator LIC in Rice

被引:154
作者
Zhang, Cui [1 ,2 ]
Xu, Yunyuan [1 ]
Guo, Siyi [1 ,2 ]
Zhu, Jiaying [1 ,2 ]
Huan, Ging [1 ,2 ]
Liu, Huanhuan [1 ,2 ]
Wang, Lei [1 ]
Luo, Guanzheng [3 ]
Wang, Xiujie [3 ]
Chong, Kang [1 ,4 ]
机构
[1] Chinese Acad Sci, Inst Bot, Key Lab Plant Mol Physiol Photosynth & Environm M, Beijing, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing, Peoples R China
[3] Chinese Acad Sci, Ctr Mol Syst Biol, Inst Genet & Dev Biol, Beijing, Peoples R China
[4] Natl Plant Gene Res Ctr, Beijing, Peoples R China
来源
PLOS GENETICS | 2012年 / 8卷 / 04期
关键词
HETEROTRIMERIC G-PROTEIN; SIGNAL-TRANSDUCTION; GENE-EXPRESSION; PLANT-GROWTH; FUNCTIONAL-ANALYSIS; ENHANCED TOLERANCE; LAMINA INCLINATION; CELL ELONGATION; DWARF MUTANT; ARABIDOPSIS;
D O I
10.1371/journal.pgen.1002686
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Brassinosteroids (BRs) regulate rice plant architecture, including leaf bending, which affects grain yield. Although BR signaling has been investigated in Arabidopsis thaliana, the components negatively regulating this pathway are less well understood. Here, we demonstrate that Oryza sativa LEAF and TILLER ANGLE INCREASED CONTROLLER (LIC) acts as an antagonistic transcription factor of BRASSINAZOLE-RESISTANT 1 (BZR1) to attenuate the BR signaling pathway. The gain-of-function mutant lic-1 and LIC-overexpressing lines showed erect leaves, similar to BZR1-depleted lines, which indicates the opposite roles of LIC and BZR1 in regulating leaf bending. Quantitative PCR revealed LIC transcription rapidly induced by BR treatment. Image analysis and immunoblotting showed that upon BR treatment LIC proteins translocate from the cytoplasm to the nucleus in a phosphorylation-dependent fashion. Phosphorylation assay in vitro revealed LIC phosphorylated by GSK3-like kinases. For negative feedback, LIC bound to the core element CTCGC in the BZR1 promoter on gel-shift and chromatin immunoprecipitation assay and repressed its transcription on transient transformation assay. LIC directly regulated target genes such as INCREASED LEAF INCLINATION 1 (ILI1) to oppose the action of BZR1. Repression of LIC in ILI1 transcription in protoplasts was partially rescued by BZR1. Phenotypic analysis of the crossed lines depleted in both LIC and BZR1 suggested that BZR1 functionally depends on LIC. Molecular and physiology assays revealed that LIC plays a dominant role at high BR levels, whereas BZR1 is dominant at low levels. Thus, LIC regulates rice leaf bending as an antagonistic transcription factor of BZR1. The phenotypes of lic-1 and LIC-overexpressing lines in erect leaves contribute to ideal plant architecture. Improving his phenotype may be a potential approach to molecular breeding for high yield in rice.
引用
收藏
页码:651 / 664
页数:14
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