Nobile C, Romeo G
Laboratorio di Genetica, Università di Bologna, Italy.
Genomics. 1988 Oct;3(3):272-4. doi: 10.1016/0888-7543(88)90088-2.
A method for partial digestion of total human DNA with restriction enzymes has been developed on the basis of a principle already utilized by P.A. Whittaker and E. Southern (1986, Gene 41: 129-134) for the analysis of phage lambda recombinants. Total human DNA irradiated with uv light of 254 nm is partially digested by restriction enzymes that recognize sequences containing adjacent thymidines because of TT dimer formation. The products resulting from partial digestion of specific genomic regions are detected in Southern blots by genomic-unique DNA probes with high reproducibility. This procedure is rapid and simple to perform because the same conditions of uv irradiation are used for different enzymes and probes. It is shown that restriction site polymorphisms occurring in the genomic regions analyzed are recognized by the "allelic" partial digest patterns they determine.
基于P.A. 惠特克和E. 萨瑟恩(1986年,《基因》41卷:129 - 134页)已用于分析λ噬菌体重组体的原理,开发了一种用限制性内切酶对人总DNA进行部分消化的方法。用254纳米紫外线照射的人总DNA,由于形成了TT二聚体,会被识别包含相邻胸腺嘧啶序列的限制性内切酶部分消化。通过基因组特异DNA探针在Southern印迹中以高重现性检测特定基因组区域部分消化产生的产物。该方法操作快速且简单,因为对不同的酶和探针使用相同的紫外线照射条件。结果表明,在所分析的基因组区域中出现的限制性酶切位点多态性可通过它们所确定的“等位基因”部分消化模式来识别。