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质体基因组中bar基因的表达赋予了除草剂抗性。

Expression of bar in the plastid genome confers herbicide resistance.

作者信息

Lutz K A, Knapp J E, Maliga P

机构信息

Waksman Institute, Rutgers, State University of New Jersey, 190 Frelinghuysen Road, Piscataway, New Jersey 08854-8020, USA.

出版信息

Plant Physiol. 2001 Apr;125(4):1585-90. doi: 10.1104/pp.125.4.1585.

Abstract

Phosphinothricin (PPT) is the active component of a family of environmentally safe, nonselective herbicides. Resistance to PPT in transgenic crops has been reported by nuclear expression of a bar transgene encoding phosphinothricin acetyltransferase, a detoxifying enzyme. We report here expression of a bacterial bar gene (b-bar1) in tobacco (Nicotiana tabacum cv Petit Havana) plastids that confers field-level tolerance to Liberty, an herbicide containing PPT. We also describe a second bacterial bar gene (b-bar2) and a codon-optimized synthetic bar (s-bar) gene with significantly elevated levels of expression in plastids (>7% of total soluble cellular protein). Although these genes are expressed at a high level, direct selection thus far did not yield transplastomic clones, indicating that subcellular localization rather than the absolute amount of the enzyme is critical for direct selection of transgenic clones. The codon-modified s-bar gene is poorly expressed in Escherichia coli, a common enteric bacterium, due to differences in codon use. We propose to use codon usage differences as a precautionary measure to prevent expression of marker genes in the unlikely event of horizontal gene transfer from plastids to bacteria. Localization of the bar gene in the plastid genome is an attractive alternative to incorporation in the nuclear genome since there is no transmission of plastid-encoded genes via pollen.

摘要

草丁膦(PPT)是一类环境安全的非选择性除草剂的活性成分。通过编码草丁膦乙酰转移酶(一种解毒酶)的bar转基因的核表达,已报道了转基因作物对PPT的抗性。我们在此报道了细菌bar基因(b-bar1)在烟草(Nicotiana tabacum cv Petit Havana)质体中的表达,该基因赋予了对含有PPT的除草剂Liberty的田间水平耐受性。我们还描述了第二个细菌bar基因(b-bar2)和一个密码子优化的合成bar(s-bar)基因,其在质体中的表达水平显著提高(>总可溶性细胞蛋白的7%)。尽管这些基因高水平表达,但迄今为止直接选择并未产生转质体克隆,这表明亚细胞定位而非酶的绝对量对于转基因克隆的直接选择至关重要。由于密码子使用的差异,密码子修饰的s-bar基因在常见肠道细菌大肠杆菌中表达不佳。我们建议将密码子使用差异作为一种预防措施,以防止在不太可能发生的质体向细菌水平基因转移情况下标记基因的表达。bar基因定位于质体基因组是一种比整合到核基因组更具吸引力的选择,因为质体编码的基因不会通过花粉传递。

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