Department of Biology, Bielefeld University, Universitaetsstrasse 27, D-33615 Bielefeld, Germany.
Gene. 2011 Sep 15;484(1-2):61-8. doi: 10.1016/j.gene.2011.05.031. Epub 2011 Jun 12.
In Arabidopsis thaliana, most mutants impaired in flavonoid accumulation were identified through screens for altered seed pigmentation. Mutations in more than 20 loci have been described that can result in a transparent testa (tt) or tannin deficient seed (tds) phenotype. For some of these mutants it is still unclear if they represent additional loci or if they are allelic to known mutations. In this study, we found that tt17 is allelic to tt11 and tds4 and identified a point mutation in tt17 that affects the gene encoding Leucoanthocyanidin Dioxygenase (LDOX). The mutation results in replacement of a cysteine close to the active site of the enzyme by the hydrophobic amino acid tyrosine. Effects of this mutation on protein structure and activity are discussed in the context of LDOX sequences from various genotypes. Regulation of the LDOX promoter was analyzed and found to be directly controlled by different MYB-BHLH-TTG1 transcription factor complexes containing the BHLH factors EGL3 and TT8. Experiments with single and double loss-of-function mutants identified EGL3 and TT8 as necessary regulators of anthocyanin accumulation in developing A. thaliana seedlings.
在拟南芥中,大多数黄酮类化合物积累受损的突变体是通过改变种子颜色的筛选鉴定出来的。已经描述了 20 多个突变位点,这些突变位点可能导致透明种皮(tt)或单宁缺乏种子(tds)表型。对于其中一些突变体,仍然不清楚它们是否代表额外的基因座,或者它们是否与已知的突变等位。在这项研究中,我们发现 tt17 与 tt11 和 tds4 等位,并在 tt17 中发现了一个影响编码 Leucoanthocyanidin Dioxygenase(LDOX)基因的点突变。该突变导致靠近酶活性位点的半胱氨酸被疏水性氨基酸酪氨酸取代。在不同基因型的 LDOX 序列背景下,讨论了该突变对蛋白质结构和活性的影响。分析了 LDOX 启动子的调控,发现它是由含有 BHLH 因子 EGL3 和 TT8 的不同 MYB-BHLH-TTG1 转录因子复合物直接控制的。用单和双功能丧失突变体进行的实验表明,EGL3 和 TT8 是拟南芥幼苗中花青素积累的必需调控因子。