Bernard L E, Wood S
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
Genome. 1993 Apr;36(2):302-9. doi: 10.1139/g93-042.
Members of the Alu family of repetitive elements occur frequently in the human genome and are often polymorphic. Techniques involving Alu element mediated polymerase chain reactions (Alu PCR) allow the isolation of region-specific human DNA fragments from mixed DNA sources. Such fragments are a source of region-specific Alu elements useful for the detection of Alu-related polymorphisms. A clone from human chromosome 5, corresponding to locus D5F40S1, was isolated using Alu PCR differential hybridization. Alu elements within this clone were investigated for the presence of potentially polymorphic 3' polyA tails. Primers were devised to amplify the 3' polyA tail of an Alu element present within the clone. One primer, D5F40S1-T, was specific to the DNA flanking the 3' end of the Alu element, and the other primer was homologous to sequences within the element. When these primers were used in PCR reactions, products from chromosomes 2 and 17 (loci D2F40S2 and D17F40S3) were amplified in addition to the expected product from chromosome 5. The most likely explanation for this nonspecific amplification is that the D5F40S1-T primer is located within a low-copy repetitive element that is 3' of the Alu element. This phenomenon presents a potential problem for the identification of region-specific Alu polymorphisms.
重复元件的Alu家族成员在人类基因组中频繁出现,且常常具有多态性。涉及Alu元件介导的聚合酶链反应(Alu PCR)的技术能够从混合DNA来源中分离出区域特异性的人类DNA片段。这些片段是用于检测Alu相关多态性的区域特异性Alu元件的来源。使用Alu PCR差异杂交从人类5号染色体上分离出一个与位点D5F40S1对应的克隆。对该克隆内的Alu元件进行研究,以确定是否存在潜在的多态性3'聚腺苷酸尾。设计引物以扩增该克隆内存在的Alu元件的3'聚腺苷酸尾。一个引物D5F40S1-T对Alu元件3'端侧翼的DNA具有特异性,另一个引物与该元件内的序列同源。当这些引物用于PCR反应时,除了预期的来自5号染色体的产物外,还扩增出了来自2号和17号染色体(位点D2F40S2和D17F40S3)的产物。这种非特异性扩增最可能的解释是D5F40S1-T引物位于Alu元件3'端的一个低拷贝重复元件内。这种现象给区域特异性Alu多态性的鉴定带来了潜在问题。