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Transgene copy number estimation and analysis of gene expression levels in Populusspp. transgenic lines
© Donnarumma et al; licensee BioMed Central Ltd. 2011
- Published: 13 September 2011
- Transgenic Plant
- Transgenic Line
- nptII Gene
- Transgenic Poplar
- Copy Number Estimation
The genus Populus has certain important features, such as a relatively small nuclear genome, it can be easily regenerated easily in vitro and genetically transformed by Agrobacterium vector system, which make it ideal for gene transfer and molecular genetic studies in forest trees . Insect-tolerant poplars have been obtained using several types of insecticidal genes coding for Bacillus thuringiensis-toxins. Regenerated plants with insect-resistance were obtained in different studies. Agrobacterium-mediated transformation has been the favored method for the introduction of foreign genes into plants. The effectiveness of insect-resistance in transgenic plants is related to the side effects of gene transfer (site of gene insertion, copy number, gene silencing etc.).Moreover intransgenic plants, transgene copy number can greatly affect the expression level and genetic stability of the target gene, making estimation of transgene copy numbers an important area of genetically modified plant research . Thus molecular biological analysis of transgenic plants, like real time PCR, widely used to detect and quantify DNA and cDNA , could represent an useful tool to investigate the genetic stability of transgenic forest trees having a long life cycleas well as for determining copy number in transformed plants.
The present study was undertaken to investigate Populus alba and P. tremula x P. tremuloides transgenic lines, obtained via Agrobacterium-mediated transformation, carrying cry1Ab and nptII genes in the T-DNA region. The plants were vegetatively propagated in growth chambers over 2 years. Ten individuals from each clone were planted in containers with "forest soil", and grown in a climate chamber.
Extraction of genomic DNA and RNA from leaves was performed for PCR and Real Time PCR (RT-PCR) analysis to estimate the transgene copy number  as well as expression of the inserted gene in transgenic poplar, respectively.
Preliminary results indicate a differential expression of endogenous genes among transgenic lines and towards their isogenic form.
The evaluation of the copy number of the inserted genes has indicated their stability after 2 years of micropropagation. The lower expression level of the nptII inserted gene in one line could suggest that factors like position effects or DNA rearrangements lead to differential expression.
The screening of the transcriptomic variations in transgenic plants carrying the cry gene and the comparison with position effects or DNA rearrangements is in course. The final aim is to unravel possible pleiotropic transcriptomic effects following cry gene expression in P. alba and P. tremula x P. tremuloides transgenic lines.
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