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首页> 外文期刊>Plant Biotechnology Journal >Transcriptional activation of Brassica napus ???2?¢????ketoacyl?¢????ACP synthase II with an engineered zinc finger protein transcription factor
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Transcriptional activation of Brassica napus ???2?¢????ketoacyl?¢????ACP synthase II with an engineered zinc finger protein transcription factor

机译:利用工程化的锌指蛋白转录因子激活甘蓝型油菜2 ???????酮酰基???? ACP合酶II的转录激活

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摘要

Targeted gene regulation via designed transcription factors has great potential for precise phenotypic modification and acceleration of novel crop trait development. Canola seed oil composition is dictated largely by the expression of genes encoding enzymes in the fatty acid biosynthetic pathway. In the present study, zinc finger proteins (ZFPs) were designed to bind DNA sequences common to two canola ???2?¢????ketoacyl?¢????ACP Synthase II (KASII) genes downstream of their transcription start site. Transcriptional activators (ZFP?¢????TFs) were constructed by fusing these ZFP DNA?¢????binding domains to the VP16 transcriptional activation domain. Following transformation using Agrobacterium , transgenic events expressing ZFP?¢????TFs were generated and shown to have elevated KASII transcript levels in the leaves of transgenic T 0 plants when compared to ?¢????selectable marker only?¢???? controls as well as of T 1 progeny plants when compared to null segregants. In addition, leaves of ZFP?¢????TF?¢????expressing T 1 plants contained statistically significant decreases in palmitic acid (consistent with increased KASII activity) and increased total C18. Similarly, T 2 seed displayed statistically significant decreases in palmitic acid, increased total C18 and reduced total saturated fatty acid contents. These results demonstrate that designed ZFP?¢????TFs can be used to regulate the expression of endogenous genes to elicit specific phenotypic modifications of agronomically relevant traits in a crop species.
机译:通过设计的转录因子进行有针对性的基因调控,对于精确的表型修饰和促进新的作物性状发展具有巨大的潜力。菜籽油的组成主要由脂肪酸生物合成途径中编码酶的基因表达决定。在本研究中,锌指蛋白(ZFP)被设计为结合两个芥花油菜在转录开始下游的两个芥菜油菜素2α-β-酮酰基α-β-ACP合酶II(KASII)基因共有的DNA序列。现场。通过将这些ZFP DNA→β结合域与VP16转录激活域融合来构建转录激活因子(ZFP→TFTF)。用农杆菌转化后,产生了表达ZFPα-βTFs的转基因事件,当与仅β-β选择标记物相比时,表明其在转基因T 0植物的叶片中具有升高的KASII转录水平。 ??与无效的分离子相比,对照和T 1后代植物。另外,表达T 1植物的ZFP-TF-TF-的叶子统计上棕榈酸显着降低(与增加的KASII活性一致)和总C 18升高。类似地,T 2种子显示出棕榈酸的统计学显着降低,总C18的增加和总饱和脂肪酸含量的减少。这些结果表明,设计的ZFPΔβ-TFs可用于调节内源基因的表达,以引发农作物中农学相关性状的特定表型修饰。

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