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首页> 外文期刊>BMC Plant Biology >Functional identification of BpMYB21 and BpMYB61 transcription factors responding to MeJA and SA in birch triterpenoid synthesis
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Functional identification of BpMYB21 and BpMYB61 transcription factors responding to MeJA and SA in birch triterpenoid synthesis

机译:BPMYB21和BPMYB61转录因子的功能鉴定对MEJA和SA在桦木三萜合成中的反应

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摘要

Triterpenoids from birch (Betula platyphylla Suk.) exert antitumor and anti-HIV activities. Due to the complexity of plant secondary metabolic pathways, triterpene compounds in plants is not always determined by a single gene; they may be controlled by polygene quantitative traits. Secondary metabolism related to terpenoids involves tissue specificity and localisation of key biosynthetic enzymes. Terpene synthesis is influenced by light, hormones and other signals, as well as upstream transcription factor regulation. Anchor Herein, we identified and characterised two birch MYB transcription factors (TFs) that regulate triterpenoid biosynthesis. BpMYB21 and BpMYB61 are R2R3 TFs that positively and negatively regulate responses to methyl-jasmonate (MeJA) and salicyclic acid (SA), respectively. Expression of BpMYB21 and BpMYB61 was elevated in leaves and stems more than roots during July/August in Harbin, China. BpMYB21 expression was increased by abscisic acid (ABA), MeJA, SA and gibberellins (GAs). BpMYB61 expression in leaves and BpMYB21 expression in stems was reduced by ABA, MeJA and SA, while GAs, ethylene, and injury increased BpMYB61 expression. BpMYB21 was localised in nuclei, while BpMYB61 was detected in cell membranes and nuclei. Promoters for both BpMYB21 (1302?bp) and BpMYB61 (850?bp) were active. BpMYB21 and BpMYB61 were ligated into pYES3, introduced into AnchorINVScl (yeast strain without exogenous genes), INVScl-pYES2-SSAnchorAnchor (transgenic yeast strain harbouring the SS gene from birch), and INVScl-pYES2-SE (transgenic yeast strain harbouring the SE gene from birch), and the squalene content was highest in AnchorINVScl-pYES-MYB21-SS (transgenic yeast strain harbouring SS and MYB21 genes) and INVScl-pYES3-MYB61 (transgenic yeast strain harbouring the MYB61 gene). In BpMYB21 transgenic birch key triterpenoid synthesis genes were up-regulated, and in BpMYB61 transgenic birch AnchorFPS (farnesyl pyrophosphate synthase) and SS (squalene synthase) were up-regulated, but HMGR (3-hydroxy-3-methylglutaryl coenzyme a reductase), BPWAnchor (lupeol synthase), SE (squalene epoxidase) and BPY (b-amyrin synthase) were down-regulated. Both BpMYB21 and BpMYB61 specifically activate SE and BPX (cycloartenol synthase synthesis) promoters. These findings support further functional characterisation of R2R3-MYB genes, and illuminate the regulatory role of BpMYB21 and BpMYB61 in the synthesis of birch triterpenoids.
机译:来自桦树(Betula platyphylla Suk)的三萜类化合物施用抗肿瘤和抗艾滋病毒活动。由于植物次级代谢途径的复杂性,植物中的三萜化合物并不总是通过单个基因确定;它们可以通过聚乙烯定量性状来控制。与三萜类化合物相关的次生代谢涉及关键生物合成酶的组织特异性和定位。萜烯合成受光,激素和其他信号的影响,以及上游转录因子调节。锚定本文,我们鉴定并表征了调节三萜类化合物生物合成的两个桦木MYB转录因子(TFS)。 BPMYB21和BPMYB61分别是对甲基 - 茉莉酸酯(MEJA)和Salidclic酸(SA)的正面和负面调节响应的R2R3 TFS。 BPMYB21和BPMYB61的表达在叶子和茎中升高,在中国哈尔滨的7月/ 8月期间的茎不止根。 BPMYB21表达由脱落酸(ABA),MEJA,SA和赤霉素(气体)增加。 BPMYB61在茎中的表达和茎中的BPMYB21表达由ABA,Meja和SA减少,而气体,乙烯和损伤增加BPMYB61表达。 BPMYB21在核中定位,而BPMYB61在细胞膜和核中检测到。 BPMYB21(1302磅)和BPMYB61(850?BP)的启动子是活性的。将BPMYB21和BPMYB61连接到PYES3中,引入锚肾上腺症(没有外源基因的酵母菌株),INVSCL-PYES2-SSANCHORANTOR(从桦树携带SS基因的转基因酵母菌株),和INVSCL-PYES2-SE(携带SE基因的转基因酵母菌株从桦树),锚氨基vscl-pyes-myb21-ss(转基因酵母菌菌株含Ss和MyB21基因)和Invscl-pyes3-myb61(含MyB61基因的转基因酵母菌菌株)中,Squalene含量最高。在BPMYB21转基​​因桦木键三萜素合成基因上调,在BPMYB61转基因桦木锚FFP(法牛糖焦磷酸盐合酶)和Ss(Squalene合酶)中进行上调,但HMGR(3-羟基-3-甲基丁酸辅酶还原酶),下调BPWanchor(卢斯合酶),SE(Squalene环氧酶)和BPY(B-淀粉合酶)。 BPMYB21和BPMYB61均特别激活SE和BPX(环丁烯合酶合成)启动子。这些发现支持R2R3-MYB基因的进一步函数表征,并照亮BPMYB21和BPMYB61在桦木三萜的合成中的调节作用。

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