Cho Lae-Hyeon, Yoon Jinmi, Pasriga Richa, An Gynheung
Crop Biotech Institute, Kyung Hee University, Yongin 446-701, Korea (L.-H.C., J.Y., R.P., G.A.);Department of Life Science, Pohang University of Science and Technology, Pohang 790-784, Korea (L.-H.C., J.Y.); andGraduate School of Biotechnology, Kyung Hee University, Yongin 446-701, Korea (R.P., G.A.).
Crop Biotech Institute, Kyung Hee University, Yongin 446-701, Korea (L.-H.C., J.Y., R.P., G.A.);Department of Life Science, Pohang University of Science and Technology, Pohang 790-784, Korea (L.-H.C., J.Y.); andGraduate School of Biotechnology, Kyung Hee University, Yongin 446-701, Korea (R.P., G.A.)
Plant Physiol. 2016 Apr;170(4):2159-71. doi: 10.1104/pp.15.01723. Epub 2016 Feb 10.
In plants, flowering time is elaborately controlled by various environment factors. Ultimately, florigens such as FLOWERING LOCUS T (FT) or FT-like molecules induce flowering. In rice (Oryza sativa), Early heading date 1 (Ehd1) is a major inducer of florigen gene expression. Although Ehd1 is highly homologous to the type-B response regulator (RR) family in the cytokinin signaling pathway, its precise molecular mechanism is not well understood. In this study, we showed that the C-terminal portion of the protein containing the GARP DNA-binding (G) domain can promote flowering when overexpressed. We also observed that the N-terminal portion of Ehd1, carrying the receiver (R) domain, delays flowering by inhibiting endogenous Ehd1 activity. Ehd1 protein forms a homomer via a 16-amino acid region in the inter domain between R and G. From the site-directed mutagenesis analyses, we demonstrated that phosphorylation of the Asp-63 residue within the R domain induces the homomerization of Ehd1, which is crucial for Ehd1 activity. A type-A RR, OsRR1, physically interacts with Ehd1 to form a heterodimer. In addition, OsRR1-overexpressing plants show a late-flowering phenotype. Based on these observations, we conclude that OsRR1 inhibits Ehd1 activity by binding to form an inactive complex.
在植物中,开花时间受到多种环境因素的精确调控。最终,诸如成花素基因座T(FT)或类FT分子等成花素诱导开花。在水稻(Oryza sativa)中,早抽穗期1(Ehd1)是成花素基因表达的主要诱导因子。尽管Ehd1与细胞分裂素信号通路中的B型响应调节因子(RR)家族高度同源,但其精确的分子机制尚未完全了解。在本研究中,我们发现包含GARP DNA结合(G)结构域的蛋白质C末端部分在过表达时可促进开花。我们还观察到,携带受体(R)结构域的Ehd1 N末端部分通过抑制内源性Ehd1活性来延迟开花。Ehd1蛋白通过R和G之间结构域间的一个16个氨基酸的区域形成同源二聚体。通过定点诱变分析,我们证明R结构域内Asp-63残基的磷酸化诱导Ehd1的同源二聚化,这对Ehd1活性至关重要。一种A型RR,OsRR1,与Ehd1发生物理相互作用形成异源二聚体。此外,过表达OsRR1的植物表现出晚花表型。基于这些观察结果,我们得出结论,OsRR1通过结合形成无活性复合物来抑制Ehd1活性。