首页> 美国卫生研究院文献>The Plant Cell >Ribozymes targeted to stearoyl-ACP delta9 desaturase mRNA produce heritable increases of stearic acid in transgenic maize leaves.
【2h】

Ribozymes targeted to stearoyl-ACP delta9 desaturase mRNA produce heritable increases of stearic acid in transgenic maize leaves.

机译:靶向硬脂酰-ACP delta9去饱和酶mRNA的核酶在转基因玉米叶片中产生可遗传的硬脂酸增加。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Ribozymes are RNAs that can be designed to catalyze the specific cleavage or ligation of target RNAs. We have explored the possibility of using ribozymes in maize to downregulate the expression of the stearoyl-acyl carrier protein (Delta9) desaturase gene. Based on site accessibility and catalytic activity, several ribozyme constructs were designed and transformed into regenerable maize lines. One of these constructs, a multimer hammerhead ribozyme linked to a selectable marker gene, was shown to increase leaf stearate in two of 13 maize lines. There were concomitant decreases in Delta9 desaturase mRNA and protein. The plants with the altered stearate phenotype were shown to express ribozyme RNA. The ribozyme-mediated trait was heritable, as evidenced by stearate increases in the leaves of the R1 plants derived from a high-stearate line. The increase in stearate correlated with the presence of the ribozyme gene. A catalytically inactive version of this ribozyme did not produce any significant effect in transgenic maize. This is evidence that ribozymes can be used to modulate the expression of endogenous genes in maize.
机译:核酶是可以设计成催化靶RNA特异性切割或连接的RNA。我们已经探索了在玉米中使用核酶下调硬脂酰酰基载体蛋白(Delta9)去饱和酶基因表达的可能性。基于位点可及性和催化活性,设计了几种核酶构建体并将其转化为可再生玉米系。这些构建体之一是与选择标记基因连接的多头锤头状核酶,在13个玉米品系中有2个显示出增加了叶片硬脂酸盐的能力。 Delta9去饱和酶的mRNA和蛋白质也随之减少。显示具有改变的硬脂酸酯表型的植物表达核酶RNA。核酶介导的性状是可遗传的,这是由高硬脂系衍生的R1植物叶片中的硬脂酸盐增加所证明的。硬脂酸的增加与核酶基因的存在有关。这种核酶的无催化活性的形式在转基因玉米中没有产生任何明显的作用。这证明核酶可用于调节玉米中内源基因的表达。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号