Department of Molecular, Cellular, and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-1048, USA.
Mol Plant. 2010 Jan;3(1):260-8. doi: 10.1093/mp/ssp099. Epub 2009 Dec 6.
Brassinosteroids (BRs) are important plant hormones that act synergistically with auxin to regulate a variety of plant developmental and physiological processes. In the past decade, genetic and biochemical studies have revealed a linear signaling pathway that relies on protein phosphorylation to transmit the BR signal into the nucleus, altering expression of hundreds of genes to promote plant growth. We conducted an activation-tagging based suppressor screen to look for Arabidopsis genes that, when overexpressed by inserted 35S enhancer elements, could suppress the dwarf phenotype of a weak BR receptor mutant bri1-301. This screen identified a total of six dominant activation-tagged bri1 suppressors (atbs-Ds). Using a plasmid rescue approach, we discovered that the bri1-301 suppression effect in four atbs-D mutants (atbs3-D to atbs6-D) was caused by overexpression of a YUCCA gene thought to be involved in tryptophan-dependent auxin biosynthesis. Interestingly, the three activation-tagged YUCCA genes belong to the YUCCA IIA subfamily that includes two other members out of 11 known Arabidopsis YUCCA genes. In addition, our molecular studies revealed a T-DNA insertion near a basic helix-loop-helix gene in atbs1-D and a T-DNA insertion in a region carrying a BR biosynthetic gene in atbs2-D. Further studies of these atbs-D mutants could lead to better understanding of the BR signaling process and the BR-auxin interaction.
油菜素内酯(BRs)是重要的植物激素,与生长素协同作用,调节多种植物发育和生理过程。在过去的十年中,遗传和生化研究揭示了一条线性信号通路,该通路依赖于蛋白质磷酸化将 BR 信号传递到细胞核,改变数百个基因的表达,从而促进植物生长。我们进行了基于激活标签的抑制子筛选,以寻找拟南芥基因,当这些基因通过插入的 35S 增强子元件过表达时,能够抑制弱 BR 受体突变体 bri1-301 的矮化表型。该筛选总共鉴定出了 6 个显性激活标签 bri1 抑制子(atbs-Ds)。通过质粒拯救方法,我们发现 4 个 atbs-D 突变体(atbs3-D 至 atbs6-D)中的 bri1-301 抑制效应是由一个被认为参与色氨酸依赖的生长素生物合成的 YUCCA 基因的过表达引起的。有趣的是,这三个激活标签的 YUCCA 基因属于 YUCCA IIA 亚家族,该亚家族包括 11 个已知的拟南芥 YUCCA 基因中的两个其他成员。此外,我们的分子研究揭示了 atbs1-D 中一个 T-DNA 插入位于一个基本螺旋-环-螺旋基因附近,而 atbs2-D 中一个 T-DNA 插入位于一个携带 BR 生物合成基因的区域。对这些 atbs-D 突变体的进一步研究可能有助于更好地理解 BR 信号转导过程和 BR-生长素相互作用。