Bioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan.
Bioscience and Biotechnology Center, Nagoya University, Nagoya 464-8601, Japan.
Mol Plant. 2017 Apr 3;10(4):590-604. doi: 10.1016/j.molp.2016.12.013. Epub 2017 Jan 6.
Although auxin and brassinosteroid (BR) synergistically control various plant responses, the molecular mechanism underlying the auxin-BR crosstalk is not well understood. We previously identified SMOS1, an auxin-regulated APETALA2-type transcription factor, as the causal gene of the small organ size 1 (smos1) mutant that is characterized by a decreased final size of various organs in rice. In this study, we identified another smos mutant, smos2, which shows the phenotype indistinguishable from smos1. SMOS2 was identical to the previously reported DWARF AND LOW-TILLERING (DLT), which encodes a GRAS protein involved in BR signaling. SMOS1 and SMOS2/DLT physically interact to cooperatively enhance transcriptional transactivation activity in yeast and in rice nuclei. Consistently, the expression of OsPHI-1, a direct target of SMOS1, is upregulated only when SMOS1 and SMOS2/DLT proteins are both present in rice cells. Taken together, our results suggest that SMOS1 and SMOS2/DLT form a keystone complex on auxin-BR signaling crosstalk in rice.
尽管生长素和油菜素内酯(BR)协同控制各种植物反应,但生长素-BR 串扰的分子机制尚不清楚。我们之前鉴定了 SMOS1,一种生长素调节的 APETALA2 型转录因子,作为小器官大小 1(smos1)突变体的因果基因,该突变体的特征是水稻各种器官的最终大小减小。在这项研究中,我们鉴定了另一个 smos 突变体 smos2,其表型与 smos1 无法区分。SMOS2 与先前报道的 DWARF AND LOW-TILLERING (DLT) 相同,它编码一种参与 BR 信号转导的 GRAS 蛋白。SMOS1 和 SMOS2/DLT 物理相互作用,以协同方式增强酵母和水稻核中转录转录激活活性。一致地,OsPHI-1 的表达,SMOS1 的直接靶标,仅在 SMOS1 和 SMOS2/DLT 蛋白都存在于水稻细胞中时才被上调。总之,我们的结果表明,SMOS1 和 SMOS2/DLT 在水稻的生长素-BR 信号转导串扰中形成一个关键复合物。