Kasai K, Nakamura Y, White R
Department of Human Genetics, University of Utah Health Sciences Center, Salt Lake City.
J Forensic Sci. 1990 Sep;35(5):1196-200.
A genetic locus (D1S58, defined by DNA probe pMCT118) that contains a variable number of tandem repeats (VNTR) has been successfully amplified from a very small amount of genomic deoxyribonucleic acid (DNA) by the polymerase chain reaction (PCR). The DNA sequence of the locus was determined and was found to consist of a 16-base consensus sequence and flanking sequences. Oligonucleotide primers complementary to the flanking sequences were synthesized to serve as primers for amplification of MCT118 by the PCR method. Human genomic DNA isolated from blood (2 ng from each sample) was successfully amplified at the MCT118 locus, and polymorphic bands were detectable by ethidium bromide staining after electrophoresis on polyacrylamide gels. Determination of genotypes at this VNTR locus can now be routinely achieved within 24 h, without the need for Southern blots or radioactive materials. Furthermore, the small size (387 to 723 base pairs) of the DNA fragments produced in the PCR amplification permits good resolution of individual alleles that differ by only one repeat unit. The precise specification of the number of tandem repeats present in each allelic fragment is reproducible from one analysis to another.
一个包含可变数量串联重复序列(VNTR)的基因位点(由DNA探针pMCT118定义的D1S58)已通过聚合酶链反应(PCR)从极少量的基因组脱氧核糖核酸(DNA)中成功扩增出来。该基因位点的DNA序列已被确定,发现其由一个16个碱基的共有序列和侧翼序列组成。合成了与侧翼序列互补的寡核苷酸引物,用作通过PCR方法扩增MCT118的引物。从血液中分离的人类基因组DNA(每个样本2纳克)在MCT118基因位点成功扩增,在聚丙烯酰胺凝胶上电泳后,通过溴化乙锭染色可检测到多态性条带。现在可以在24小时内常规确定该VNTR基因位点的基因型,无需进行Southern印迹或使用放射性材料。此外,PCR扩增产生的DNA片段尺寸较小(387至723个碱基对),能够很好地分辨仅相差一个重复单元的各个等位基因。每个等位基因片段中串联重复序列数量的精确确定在不同分析之间具有可重复性。