Appleyard V C, Unkles S E, Legg M, Kinghorn J R
Plant Sciences Laboratory, School of Biological and Medical Sciences, University of St. Andrews, Scotland, UK.
Mol Gen Genet. 1995 May 10;247(3):338-42. doi: 10.1007/BF00293201.
We report the potential of differential display technology for the isolation of genes of biotechnological interest. We have assessed the usefulness of the technique for the cloning of genes involved in the production of secondary metabolites, many of which are of industrial use or interest. We have used the complex pathway for the biosynthesis of gibberellins, as well as bikaverin and carotenoids, present in the filamentous fungus Gibberella fujikuroi as a test system. From a total display of approximately 16000 PCR products for each RNA sample, 100 were derived from the derepressed but not the repressed condition. These products were analysed by Northern blotting and a subset of 16 such PCR products showed differential expression at the transcript level. A number of different mRNA species were observed on this basis which varied in their size. Hence, this approach appears suitable for the isolation of genes involved in the complex pathways often required for the synthesis of secondary metabolites in organisms which are genetically intractable. Moreover, the method has the advantage that it is quick, differential displays being obtained after 2 days and DNA clones in 6 days.
我们报道了差异显示技术在分离具有生物技术应用价值基因方面的潜力。我们评估了该技术在克隆参与次生代谢产物合成的基因方面的实用性,其中许多次生代谢产物具有工业用途或价值。我们以丝状真菌藤仓赤霉中存在的赤霉素、比卡维林和类胡萝卜素的生物合成复杂途径作为测试系统。对于每个RNA样本,在总共约16000个PCR产物的显示中,有100个来自去阻遏而非阻遏条件。这些产物通过Northern印迹分析,其中16个这样的PCR产物的一个子集在转录水平上显示出差异表达。在此基础上观察到许多不同大小的mRNA种类。因此,这种方法似乎适用于分离在遗传上难以处理的生物体中次生代谢产物合成通常所需的复杂途径中涉及的基因。此外,该方法的优点是速度快,2天即可获得差异显示,6天即可获得DNA克隆。