Zhong Ruiqin, Richardson Elizabeth A, Ye Zheng-Hua
Department of Plant Biology, University of Georgia, Athens, GA 30602, USA.
Plant Cell. 2007 Sep;19(9):2776-92. doi: 10.1105/tpc.107.053678. Epub 2007 Sep 21.
We demonstrate that the Arabidopsis thaliana MYB46 transcription factor is a direct target of SECONDARY WALL-ASSOCIATED NAC DOMAIN PROTEIN1 (SND1), which is a key transcriptional activator regulating the developmental program of secondary wall biosynthesis. The MYB46 gene is expressed predominantly in fibers and vessels in stems, and its encoded protein is targeted to the nucleus and can activate transcription. MYB46 gene expression was shown to be regulated by SND1, and transactivation analysis demonstrated that SND1 as well as its close homologs were able to activate the MYB46 promoter. Electrophoretic mobility shift assays and chromatin immunoprecipitation experiments revealed that SND1 binds to the MYB46 promoter. Dominant repression of MYB46 caused a drastic reduction in the secondary wall thickening of fibers and vessels. Overexpression of MYB46 resulted in an activation of the biosynthetic pathways of cellulose, xylan, and lignin and concomitantly led to ectopic deposition of secondary walls in cells that are normally nonsclerenchymatous. In addition, the expression of two secondary wall-associated transcription factors, MYB85 and KNAT7, was highly upregulated by MYB46 overexpression. These results demonstrate that MYB46 is a direct target of SND1 and is another key player in the transcriptional network involved in the regulation of secondary wall biosynthesis in Arabidopsis.
我们证明,拟南芥MYB46转录因子是次生壁相关NAC结构域蛋白1(SND1)的直接靶标,SND1是调控次生壁生物合成发育程序的关键转录激活因子。MYB46基因主要在茎中的纤维和导管中表达,其编码的蛋白定位于细胞核并能激活转录。研究表明,MYB46基因表达受SND1调控,反式激活分析表明SND1及其紧密同源物能够激活MYB46启动子。电泳迁移率变动分析和染色质免疫沉淀实验表明,SND1与MYB46启动子结合。MYB46的显性抑制导致纤维和导管的次生壁加厚大幅减少。MYB46的过表达导致纤维素、木聚糖和木质素生物合成途径的激活,并伴随导致次生壁在通常非厚壁组织的细胞中异位沉积。此外,两个次生壁相关转录因子MYB85和KNAT7的表达在MYB46过表达时被高度上调。这些结果表明,MYB46是SND1的直接靶标,并且是拟南芥中参与调控次生壁生物合成的转录网络中的另一个关键因子。