Key Laboratory of Biorheological Science and Technology, Ministry of Education, Room 313, Bioengineering College, Chongqing University, Campus A, 174 Shapingba Main Street, Chongqing, 400044, People's Republic of China.
Plant Cell Rep. 2012 Feb;31(2):281-9. doi: 10.1007/s00299-011-1162-3. Epub 2011 Oct 11.
The purple kale (Brassica Oleracea var. acephala f. tricolor) is a mutation in kales, giving the mutant phenotype of brilliant purple color in the interior. Total anthocyanin analysis showed that the amount of anthocyanins in the purple kale was up to 1.73 mg g(-1) while no anthocyanin was detected in the white kale. To elucidate the molecular mechanism of the anthocyanin biosynthesis in the purple kale, we analyzed the expression of structural genes and some transcription factors associated with anthocyanin biosynthesis in the purple cultivar "Red Dove" and the white cultivar "White Dove". The result showed that nearly all the anthocyanin biosynthetic genes showed higher expression levels in the purple cultivar than in the white cultivar, especially for DFR and ANS, they were barely detected in the white cultivar. Interestingly, the fact that a R2R3 MYB transcription factor named BoPAP1 was extremely up-regulated in the purple kale and induced by low temperature attracted our attention. Further sequence analysis showed that BoPAP1 shared high similarity with AtPAP1 and BoMYB1. In addition, the anthocyanin accumulation in the purple kale is strongly induced by the low temperature stress. The total anthocyanin contents in the purple kale under low temperature were about 50-fold higher than the plants grown in the greenhouse. The expression of anthocyanin biosynthetic genes C4H, F3H, DFR, ANS and UFGT were all enhanced under the low temperature. These evidences strongly suggest that BoPAP1 may play an important role in activating the anthocyanin structural genes for the abundant anthocyanin accumulation in the purple kale.
紫甘蓝(Brassica Oleracea var. acephala f. tricolor)是甘蓝的一种突变体,其内部呈现出鲜艳的紫色。总花青素分析表明,紫甘蓝中的花青素含量高达 1.73mg/g,而白甘蓝中则未检测到花青素。为了阐明紫甘蓝中花青素生物合成的分子机制,我们分析了紫色品种“红鸽”和白色品种“白鸽”中与花青素生物合成相关的结构基因和一些转录因子的表达。结果表明,几乎所有的花青素生物合成基因在紫色品种中的表达水平都高于白色品种,特别是 DFR 和 ANS,在白色品种中几乎检测不到。有趣的是,一种名为 BoPAP1 的 R2R3 MYB 转录因子在紫甘蓝中高度上调,且受低温诱导,这一事实引起了我们的注意。进一步的序列分析表明,BoPAP1 与 AtPAP1 和 BoMYB1 具有高度相似性。此外,低温强烈诱导紫甘蓝中的花青素积累。低温下紫甘蓝中的总花青素含量约比温室中生长的植物高 50 倍。花青素生物合成基因 C4H、F3H、DFR、ANS 和 UFGT 的表达在低温下均增强。这些证据强烈表明,BoPAP1 可能在激活花青素结构基因方面发挥重要作用,从而导致紫甘蓝中大量积累花青素。