Honda K, Sugiyama E, Tsuchikane A, Katsuyama Y, Harashima N, Ota M, Fukushima H
Department of Legal Medicine, Shinshu University School of Medicine, Nagano, Japan.
Nihon Hoigaku Zasshi. 1994 Jun;48(3):156-60.
We identified skeletal remains of a highly decomposed body by amplifying the COL2A1 3' variable region. We extracted degraded and contaminated DNA from teeth and bone fragments and amplified the hyper variable regions of COL2A1 by nested PCR. This method is 2,000 times more sensitive than the 27 cycle standard PCR. The sensitivity and specificity of the amplification was extremely improved using nested primer pairs. Using 47 cycles of total amplification by nested PCR, we were able to effectively amplify the target fragment. A total 47 cycles of dual PCR using one pair of primers was not as sensitive as nested PCR, which enabled us to amplify and detect the fragment from 5 pg of template DNA by agarose gel electrophoresis with ethidium bromide staining. We found that the hypersensitive nested PCR was suitable for the forensic identification of old, unidentifiable skeletal remains.
我们通过扩增COL2A1 3'可变区鉴定出一具高度腐败尸体的骨骼遗骸。我们从牙齿和骨碎片中提取了降解和污染的DNA,并通过巢式PCR扩增COL2A1的高变区。该方法比27个循环的标准PCR灵敏2000倍。使用巢式引物对极大地提高了扩增的灵敏度和特异性。通过巢式PCR进行总共47个循环的扩增,我们能够有效地扩增目标片段。使用一对引物进行总共47个循环的双重PCR不如巢式PCR灵敏,巢式PCR使我们能够通过溴化乙锭染色的琼脂糖凝胶电泳从5 pg模板DNA中扩增和检测片段。我们发现超灵敏巢式PCR适用于对陈旧、无法辨认的骨骼遗骸进行法医鉴定。