Jeffreys A J, Wilson V, Neumann R, Keyte J
Department of Genetics, University of Leicester, UK.
Nucleic Acids Res. 1988 Dec 9;16(23):10953-71. doi: 10.1093/nar/16.23.10953.
Hypervariable minisatellites can be amplified from human DNA by the polymerase chain reaction, using primers from DNA flanking the minisatellite to amplify the entire block of tandem repeat units. Minisatellite alleles up to 5-10 kb long can be faithfully amplified. At least six minisatellite loci can be co-amplified from the same DNA sample and simultaneously detected to provide a reproducible and highly variable DNA fingerprint which can be obtained from nanogram quantities of human DNA. The polymerase chain reaction can also be used to analyse single target minisatellite molecules and single human cells, despite the appearance of spurious PCR products from some hypervariable loci. DNA fingerprinting at the level of one or a few cells therefore appears possible.
高变微小卫星可通过聚合酶链反应从人类DNA中扩增出来,使用位于微小卫星两侧的DNA引物来扩增整个串联重复单位块。长达5 - 10 kb的微小卫星等位基因能够被如实地扩增。至少六个微小卫星位点可从同一DNA样本中共扩增并同时检测,以提供可重复且高度可变的DNA指纹图谱,该图谱可从纳克量的人类DNA中获得。尽管一些高变位点会出现假PCR产物,但聚合酶链反应也可用于分析单个目标微小卫星分子和单个人类细胞。因此,在一个或几个细胞水平上进行DNA指纹分析似乎是可行的。