Park Sunchung, Han Kyung-Hwan
Department of Forestry, 126 Natural Resources Building, Michigan State University, East Lansing, MI 48824-1222, USA.
Tree Physiol. 2003 Aug;23(12):815-23. doi: 10.1093/treephys/23.12.815.
The plant hormone auxin regulates various growth and developmental processes by controlling the expression of auxin-response genes. While many genes up-regulated by auxin have been characterized, less is known about the genes that are down-regulated by auxin. We isolated and characterized an auxin-repressed gene (RpARP) from the tree legume, Robinia pseudoacacia L. A sequence similarity search in public databases showed that the RpARP gene has homologs in various higher plants including monocots and dicots. The deduced amino acid sequences are highly conserved among these homologs (up to 85% identity). Northern blot analysis showed that auxin repressed RpARP gene expression and that repression was dependent on the presence of metabolizable sugar and on protein synthesis. In addition, cold treatment abolished the auxin-mediated repression of RpARP gene expression. Results from transgenic plant analyses suggest that RpARP gene expression is posttranscriptionally regulated by auxin and by the untranslated regions. Sequence analysis of the promoter region (-70 and -500 bp upstream of the putative transcription initiation site) of the RpARP gene identified four sucrose-repressible response elements (TATCCAT-motifs; Huang et al. 1990), suggesting that the cis-elements responsible for regulation by sucrose are located in the promoter region. In fact, the expression of the transgenic RpARP gene was unaffected by sucrose when driven by a CaMV 35S promoter. We present evidence that RpARP gene expression is negatively associated with hypocotyl elongation.
植物激素生长素通过控制生长素应答基因的表达来调节各种生长和发育过程。虽然许多受生长素上调的基因已得到表征,但对于受生长素下调的基因了解较少。我们从豆科树木刺槐中分离并表征了一个受生长素抑制的基因(RpARP)。在公共数据库中进行的序列相似性搜索表明,RpARP基因在包括单子叶植物和双子叶植物在内的各种高等植物中都有同源物。这些同源物之间推导的氨基酸序列高度保守(同一性高达85%)。Northern印迹分析表明,生长素抑制RpARP基因的表达,且这种抑制依赖于可代谢糖的存在和蛋白质合成。此外,冷处理消除了生长素介导的RpARP基因表达的抑制作用。转基因植物分析结果表明,RpARP基因的表达在转录后受到生长素和非翻译区的调控。对RpARP基因启动子区域(假定转录起始位点上游-70和-500 bp)的序列分析鉴定出四个蔗糖可抑制的应答元件(TATCCAT基序;Huang等人,1990年),这表明负责蔗糖调控的顺式元件位于启动子区域。事实上,当由CaMV 35S启动子驱动时,转基因RpARP基因的表达不受蔗糖的影响。我们提供的证据表明,RpARP基因的表达与下胚轴伸长呈负相关。