Vos P, Hogers R, Bleeker M, Reijans M, van de Lee T, Hornes M, Frijters A, Pot J, Peleman J, Kuiper M
Keygene N.V., Wageningen, The Netherlands.
Nucleic Acids Res. 1995 Nov 11;23(21):4407-14. doi: 10.1093/nar/23.21.4407.
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.
本文描述了一种名为AFLP的新型DNA指纹技术。AFLP技术基于对基因组DNA完全酶切产生的限制性片段进行选择性PCR扩增。该技术包括三个步骤:(i)DNA酶切及寡核苷酸接头的连接;(ii)对限制性片段组进行选择性扩增;(iii)对扩增片段进行凝胶分析。通过使用接头和限制性酶切位点序列作为引物退火的靶位点来实现限制性片段的PCR扩增。选择性扩增是通过使用延伸至限制性片段内的引物来实现的,仅扩增那些引物延伸与限制性位点侧翼核苷酸匹配的片段。使用这种方法,无需了解核苷酸序列,即可通过PCR观察到限制性片段组。该方法允许对大量限制性片段进行特异性共扩增。然而,可同时分析的片段数量取决于检测系统的分辨率。通常在变性聚丙烯酰胺凝胶上扩增并检测50 - 100个限制性片段。AFLP技术为任何来源或复杂度的DNA提供了一种新颖且非常强大的DNA指纹技术。