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Isolation and Characterization of the Brassinosteroid Receptor Gene (GmBRI1) from Glycine max
AbstractBrassinosteroids (BRs) constitute a group of steroidal phytohormones that contribute to a wide range of plant growth and development functions. The genetic modulation of BR receptor genes, which play major roles in the BR signaling pathway, can create semi-dwarf plants that have great advantages in crop production. In this study, a brassinosteroid insensitive gene homologous with AtBRI1 and other BRIs was isolated from Glycine max and designated as GmBRI1. A bioinformatic analysis revealed that GmBRI1 shares a conserved kinase domain and 25 tandem leucine-rich repeats (LRRs) that are characteristic of a BR receptor for BR reception and reaction and bear a striking similarity in protein tertiary structure to AtBRI1. GmBRI1 transcripts were more abundant in soybean hypocotyls and could be upregulated in response to exogenous BR treatment. The transformation of GmBRI1 into the Arabidopsis dwarf mutant bri1-5 restored the phenotype, especially regarding pod size and plant height. Additionally, this complementation is a consequence of a restored BR signaling pathway demonstrated in the light/dark analysis, root inhibition assay and BR-response gene expression. Therefore, GmBRI1 functions as a BR receptor to alter BR-mediated signaling and is valuable for improving plant architecture and enhancing the yield of soybean.
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Wang, M.; Sun, S.; Wu, C.; Han, T.; Wang, Q. Isolation and Characterization of the Brassinosteroid Receptor Gene (GmBRI1) from Glycine max. Int. J. Mol. Sci. 2014, 15, 3871-3888.View more citation formats
Wang M, Sun S, Wu C, Han T, Wang Q. Isolation and Characterization of the Brassinosteroid Receptor Gene (GmBRI1) from Glycine max. International Journal of Molecular Sciences. 2014; 15(3):3871-3888.Chicago/Turabian Style
Wang, Miao; Sun, Shi; Wu, Cunxiang; Han, Tianfu; Wang, Qingyu. 2014. "Isolation and Characterization of the Brassinosteroid Receptor Gene (GmBRI1) from Glycine max." Int. J. Mol. Sci. 15, no. 3: 3871-3888.
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