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质体转基因的诱导型反式激活:真养产碱杆菌聚羟基丁酸酯操纵子在转质体烟草中的表达。

Inducible trans-activation of plastid transgenes: expression of the R. eutropha phb operon in transplastomic tobacco.

作者信息

Lössl Andreas, Bohmert Karen, Harloff Hans, Eibl Christian, Mühlbauer Stefan, Koop Hans-Ulrich

机构信息

Department of Applied Plant Sciences and Plant Biotechnology (DAPP), University of Natural Resources and Applied Life Sciences, Vienna, Gregor-Mendel-Strasse 33, 1180 Vienna, Austria.

出版信息

Plant Cell Physiol. 2005 Sep;46(9):1462-71. doi: 10.1093/pcp/pci157. Epub 2005 Jun 17.

DOI:10.1093/pcp/pci157
PMID:15964903
Abstract

Deleterious effects of constitutive transgene expression can occur if gene products are harmful to the transformed plant. Constraints such as growth inhibition and male sterility have been observed in plastid transformants containing the phb operon encoding the genes required for the production of the polyester polyhydroxybutyric acid (PHB). In order to induce PHB synthesis in tobacco in a well-timed manner, we have constructed a trans-activation system to regulate transcription of the phb operon in plastids. This system consists of a nuclear-located, ethanol-inducible T7RNA polymerase (T7RNAP) which is targeted to plastids harboring the phb operon under control of T7 regulatory elements. Following treatment with 5% ethanol, moderate induction of PHB synthesis was found. PHB amounts reached 1,383 ppm in dry weight, and an overall background activity of 171 ppm was measured in uninduced tissues. On the transcriptional level, T7RNAP induction was proven and we found that the phb operon is transcribed into at least two mRNAs. Without ethanol induction, development of flowers and fertile seeds was possible. Thus, the main problem of inhibitory transgene expression was solved. Our results show that this inducible trans-activation system could serve as an alternative to constitutive expression of transgenes in the plastome.

摘要

如果基因产物对转化植物有害,组成型转基因表达可能会产生有害影响。在含有编码聚羟基丁酸酯(PHB)生产所需基因的phb操纵子的质体转化体中,已观察到生长抑制和雄性不育等限制因素。为了在烟草中适时诱导PHB合成,我们构建了一个反式激活系统来调节质体中phb操纵子的转录。该系统由一个位于细胞核的、乙醇诱导型的T7RNA聚合酶(T7RNAP)组成,该酶靶向含有受T7调控元件控制的phb操纵子的质体。用5%乙醇处理后,发现PHB合成有适度诱导。干重中PHB含量达到1383 ppm,未诱导组织中测得的总体背景活性为171 ppm。在转录水平上,证明了T7RNAP诱导,并且我们发现phb操纵子转录成至少两种mRNA。在没有乙醇诱导的情况下,花和可育种子的发育是可能的。因此,解决了抑制性转基因表达的主要问题。我们的结果表明,这种诱导型反式激活系统可作为质体基因组中转基因组成型表达的替代方案。

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