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首页> 外文期刊>Frontiers in Plant Science >A Radish Basic Helix-Loop-Helix Transcription Factor, RsTT8 Acts a Positive Regulator for Anthocyanin Biosynthesis
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A Radish Basic Helix-Loop-Helix Transcription Factor, RsTT8 Acts a Positive Regulator for Anthocyanin Biosynthesis

机译:萝卜基本螺旋-螺旋-螺旋转录因子,RsTT8充当花色素苷生物合成的正向调节剂。

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The MYB-bHLH-WDR (MBW) complex activates anthocyanin biosynthesis through the transcriptional regulation. RsMYB1 has been identified as a key player in anthocyanin biosynthesis in red radish ( Raphanus sativus L.), but its partner bHLH transcription factor (TF) remains to be determined. In this study, we isolated a bHLH TF gene from red radish. Phylogenetic analysis indicated that this gene belongs to the TT8 clade of the IIIF subgroup of bHLH TFs, and we thus designated this gene RsTT8 . Subcellular localization analysis showed that RsTT8-sGFP was localized to the nuclei of Arabidopsis thaliana protoplasts harboring the RsTT8-sGFP construct. We evaluated anthocyanin biosynthesis and RsTT8 expression levels in three radish varieties (N, C, and D) that display different red phenotypes in the leaves, root flesh, and root skins. The root flesh of the C variety and the leaves and skins of the D variety exhibit intense red pigmentation; in these tissues, RsTT8 expression showed totally positive association with the expression of RsMYB1 TF and of five of eight tested anthocyanin biosynthesis genes (i.e., RsCHS, RsCHI, RsF3H, RsDFR , and RsANS ). Heterologous co-expression of both RsTT8 and RsMYB1 in tobacco leaves dramatically increased the expression of endogenous anthocyanin biosynthesis genes and anthocyanin accumulation. Furthermore, a yeast two-hybrid assay showed that RsTT8 interacts with RsMYB1 at the MYB-interacting region (MIR), and a transient transactivation assay indicated that RsTT8 activates the RsCHS and RsDFR promoters when co-expressed with RsMYB1. Complementation of the Arabidopsis tt8-1 mutant, which lacks red pigmentation in the leaves and seeds, with RsTT8 restored red pigmentation, and resulted in high anthocyanin and proanthocyanidin contents in the leaves and seeds, respectively. Together, these results show that RsTT8 functions as a regulatory partner with RsMYB1 during anthocyanin biosynthesis.
机译:MYB-bHLH-WDR(MBW)复合物通过转录调控激活花色苷的生物合成。 RsMYB1已被确定为萝卜红色素(Raphanus sativus L.)中花色苷生物合成的关键参与者,但其伙伴bHLH转录因子(TF)尚待确定。在这项研究中,我们从红萝卜中分离了bHLH TF基因。系统发育分析表明,该基因属于bHLH TFs IIIF亚组的TT8进化枝,因此我们将该基因命名为RsTT8。亚细胞定位分析表明,RsTT8-sGFP位于含有RsTT8-sGFP构建体的拟南芥原生质体核中。我们评估了三个萝卜品种(N,C和D)中的花青素生物合成和RsTT8表达水平,这些萝卜品种在叶,根肉和根皮中表现出不同的红色表型。 C变种的根肉和D变种的叶和皮肤呈现强烈的红色色素沉着。在这些组织中,RsTT8的表达与RsMYB1 TF的表达以及八个测试的花色苷生物合成基因(即RsCHS,RsCHI,RsF3H,RsDFR和RsANS)中的五个表达完全正相关。 RsTT8和RsMYB1在烟草叶片中的异源共表达显着增加了内源性花色苷生物合成基因的表达和花色苷的积累。此外,酵母双杂交试验显示RsTT8在MYB相互作用区域(MIR)与RsMYB1相互作用,瞬时反式激活试验表明RsTT8与RsMYB1共表达时会激活RsCHS和RsDFR启动子。 RsTT8与叶片和种子中缺乏红色色素的拟南芥tt8-1突变体互补,恢复了红色色素沉着,并分别导致叶片和种子中的花色素苷和原花色素含量较高。总之,这些结果表明RsTT8在花色苷生物合成过程中充当RsMYB1的调节伙伴。

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