Arabidopsis G-Protein β Subunit AGB1 Negatively Regulates DNA Binding of MYB62, a Suppressor in the Gibberellin Pathway

被引:16
作者
Qi, Xin [1 ,2 ]
Tang, Wensi [1 ]
Li, Weiwei [3 ]
He, Zhang [1 ]
Xu, Weiya [1 ]
Fan, Zhijin [2 ]
Zhou, Yongbin [1 ]
Wang, Chunxiao [1 ]
Xu, Zhaoshi [1 ]
Chen, Jun [1 ]
Gao, Shiqin [4 ]
Ma, Youzhi [1 ]
Chen, Ming [1 ]
机构
[1] Chinese Acad Agr Sci CAAS, Inst Crop Sci, Natl Key Facil Crop Gene Resources & Genet Improv, Minist Agr,Key Lab Biol & Genet Improvement Triti, Beijing 100081, Peoples R China
[2] Nankai Univ, Coll Chem, State Key Lab Elementoorgan Chem, Tianjin 300071, Peoples R China
[3] Beijing Technol & Business Univ BTBU, Beijing Adv Innovat Ctr Food Nutr & Human Hlth, Beijing 100048, Peoples R China
[4] Beijing Acad Agr & Forestry Sci, Beijing Engn Res Ctr Hybrid Wheat, Beijing 100097, Peoples R China
关键词
Arabidopsis; GA signaling; AGB1; MYB62; protein interaction; HETEROTRIMERIC G-PROTEIN; TRANSCRIPTION FACTOR; GENE; BIOSYNTHESIS; RECEPTOR; RECOGNITION; RESPONSES; MUTANTS; ENCODES; GREEN;
D O I
10.3390/ijms22158270
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plant G proteins are versatile components of transmembrane signaling transduction pathways. The deficient mutant of heterotrimeric G protein leads to defects in plant growth and development, suggesting that it regulates the GA pathway in Arabidopsis. However, the molecular mechanism of G protein regulation of the GA pathway is not understood in plants. In this study, two G protein beta subunit (AGB1) mutants, agb1-2 and N692967, were dwarfed after exogenous application of GA(3). AGB1 interacts with the DNA-binding domain MYB62, a GA pathway suppressor. Transgenic plants were obtained through overexpression of MYB62 in two backgrounds including the wild-type (MYB62/WT Col-0) and agb1 mutants (MYB62/agb1) in Arabidopsis. Genetic analysis showed that under GA(3) treatment, the height of the transgenic plants MYB62/WT and MYB62/agb1 was lower than that of WT. The height of MYB62/agb1 plants was closer to MYB62/WT plants and higher than that of mutants agb1-2 and N692967, suggesting that MYB62 is downstream of AGB1 in the GA pathway. qRT-PCR and competitive DNA binding assays indicated that MYB62 can bind MYB elements in the promoter of GA2ox7, a GA degradation gene, to activate GA2ox7 transcription. AGB1 affected binding of MYB62 on the promoter of GA2ox7, thereby negatively regulating th eactivity of MYB62.
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页数:17
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