Tengs Torstein, Kristoffersen Anja B, Berdal Knut G, Thorstensen Tage, Butenko Melinka A, Nesvold Håvard, Holst-Jensen Arne
National Veterinary Institute, Section of Feed and Food Microbiology, PO Box 8156 Dep, 0033 Oslo, Norway.
BMC Biotechnol. 2007 Dec 18;7:91. doi: 10.1186/1472-6750-7-91.
Due to the increased use of genetic modifications in crop improvement, there is a need to develop effective methods for the detection of both known and unknown transgene constructs in plants. We have developed a strategy for detection and characterization of unknown genetic modifications and we present a proof of concept for this method using Arabidopsis thaliana and Oryza sativa (rice). The approach relies on direct hybridization of total genomic DNA to high density microarrays designed to have probes tiled throughout a set of reference sequences.
We show that by using arrays with 25 basepair probes covering both strands of a set of 235 vectors (2 million basepairs) we can detect transgene sequences in transformed lines of A. thaliana and rice without prior knowledge about the transformation vectors or the T-DNA constructs used to generate the studied plants.
The approach should allow the user to detect the presence of transgene sequences and get sufficient information for further characterization of unknown genetic constructs in plants. The only requirements are access to a small amount of pure transgene plant material, that the genetic construct in question is above a certain size (here >/= 140 basepairs) and that parts of the construct shows some degree of sequence similarity with published genetic elements.
由于在作物改良中基因修饰的使用增加,需要开发有效的方法来检测植物中已知和未知的转基因构建体。我们已经开发了一种检测和表征未知基因修饰的策略,并使用拟南芥和水稻展示了该方法的概念验证。该方法依赖于将总基因组DNA直接与高密度微阵列杂交,这些微阵列设计有覆盖一组参考序列的探针。
我们表明,通过使用具有覆盖235个载体(200万个碱基对)两条链的25个碱基对探针的阵列,我们可以在拟南芥和水稻的转化系中检测转基因序列,而无需事先了解用于产生所研究植物的转化载体或T-DNA构建体。
该方法应允许用户检测转基因序列的存在,并获得足够的信息以进一步表征植物中未知的基因构建体。唯一的要求是能够获得少量纯转基因植物材料,所讨论的基因构建体大于一定大小(此处≥140个碱基对),并且构建体的部分与已发表的遗传元件具有一定程度的序列相似性。