Debode, Frédéric
[CRA-W]
Marien, Aline
[CRA-W]
Janssen, Eric
[CRA-W]
Bragard, Claude
[UCL]
Berben, Gilbert
[CRA-W]
Description of the subject. This paper discusses the influence of amplicon length on real-time PCR results. Objectives. The aim of the experiments was to show that amplicon size has an influence on detection. Method. Tests were performed on genomic and plasmid DNA. Double-dye probes and SYBR® Green were used for detection by real-time PCR. Primers were selected in order to produce fragments with increasing sizes. Experiments dealt with two targets: an endogenous target for soybean (part of the lectin gene) and a transgenic target (junction P35S-CTP of the MON40- 3-2 soybean). Results. The results show that the kinetics of amplification curves evolve as a function of amplicon length, and smaller amplicons yield a higher level of fluorescence for the plateau phase. DNA degradation within the sample as well as the principles of fluorescence acquisition as a function of the chemistry used can also be factors. Conclusions. It was experimentally shown that the observed effect is linked to the suboptimal elongation temperature used in real-time PCR. Detection using SYBR® Green is less impacted as the loss of efficiency is partially compensated by the greater integration of SYBR® Green molecules in the larger fragments.
Bibliographic reference |
Debode, Frédéric ; Marien, Aline ; Janssen, Eric ; Bragard, Claude ; Berben, Gilbert . The influence of amplicon length on real-time PCR results
. In: Biotechnologie, Agronomie, Société et Environnement, Vol. 27, no.1, p. 1-9 (2017) |
Permanent URL |
http://hdl.handle.net/2078.1/182859 |