AFLP: a new technique for DNA fingerprinting

AFLP: новый метод генетической дактилоскопии ДНК
Martin Reijans, Marc Zabeau, Martin Kuiper, Pieter Vos, René C. J. Hogers, Marjo Bleeker, Theo van de Lee, Miranda Hornes, Adrie Friters, Jerina Pot, Johan Paleman
1995-01-01

AFLPDNA fingerprintingoligonucleotide adaptersrestriction fragmentsselective PCR amplification
A novel DNA fingerprinting technique called AFLP is described. The AFLP technique is based on the selective PCR amplification of restriction fragments from a total digest of genomic DNA. The technique involves three steps: (i) restriction of the DNA and ligation of oligonucleotide adapters, (ii) selective amplification of sets of restriction fragments, and (iii) gel analysis of the amplified fragments. PCR amplification of restriction fragments is achieved by using the adapter and restriction site sequence as target sites for primer annealing. The selective amplification is achieved by the use of primers that extend into the restriction fragments, amplifying only those fragments in which the primer extensions match the nucleotides flanking the restriction sites. Using this method, sets of restriction fragments may be visualized by PCR without knowledge of nucleotide sequence. The method allows the specific co-amplification of high numbers of restriction fragments. The number of fragments that can be analyzed simultaneously, however, is dependent on the resolution of the detection system. Typically 50-100 restriction fragments are amplified and detected on denaturing polyacrylamide gels. The AFLP technique provides a novel and very powerful DNA fingerprinting technique for DNAs of any origin or complexity.
1
AFLP enables visualization and specific co-amplification of many restriction fragments without prior nucleotide-sequence knowledge.
2
AFLP is a novel DNA fingerprinting method based on selective PCR amplification of restriction fragments from a complete genomic DNA digest.
3
Selective amplification uses primers targeting adapter and restriction-site sequences, with extensions matching flanking nucleotides to determine which fragments are amplified.
4
The technique combines restriction digestion and adapter ligation, selective fragment amplification, and gel-based analysis.
5
Typically, 50–100 restriction fragments can be amplified and detected on denaturing polyacrylamide gels, although capacity depends on detection-system resolution.

genomic DNA restriction fragments

selective PCR amplification and gel-based visualization of restriction-fragment sets for DNA fingerprinting

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1995-01-01
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Authors
Martin Reijans
Marc Zabeau
Martin Kuiper
Pieter Vos
René C. J. Hogers
Marjo Bleeker
Theo van de Lee
Miranda Hornes
Adrie Friters
Jerina Pot
Johan Paleman
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