Satoh C, Takahashi N, Asakawa J, Hiyama K, Kodaira M
Department of Genetics, Radiation Effects Research Foundation, Hiroshima, Japan.
Am J Hum Genet. 1993 Jan;52(1):167-75.
In the course of feasibility studies to examine the efficiencies and practicalities of various techniques for screening for genetic variations, the human coagulation factor IX (F9) genes of 63 Japanese families were examined by PCR-denaturing gradient gel electrophoresis (PCR-DGGE). Four target sequences with lengths of 983-2,891 bp from the F9 genes of 126 unrelated individuals from Hiroshima and their 100 children were amplified by PCR, digested with restriction enzymes to approximately 500-bp fragments, and examined by DGGE--a total of 6,724 bp being examined per individual. GC-rich sequences (GC-clamps) of 40 bp were attached to both ends of the target sequences, as far as was feasible. Eleven types of new nucleotide substitutions were detected in the population, none of which produced RFLPs or caused hemophilia B. By examining two target sequences in a single lane, approximately 8,000 bp in a diploid individual could be examined. This approach is very effective for the detection of variations in DNA and is applicable to large-scale population studies.
在对各种基因变异筛查技术的效率和实用性进行可行性研究的过程中,采用聚合酶链反应-变性梯度凝胶电泳(PCR-DGGE)对63个日本家庭的人类凝血因子IX(F9)基因进行了检测。对来自广岛的126名无关个体及其100名子女的F9基因中长度为983 - 2891 bp的4个靶序列进行PCR扩增,用限制性内切酶消化成约500 bp的片段,然后进行DGGE检测——每人共检测6724 bp。在可行的情况下,在靶序列两端尽可能连接40 bp的富含GC的序列(GC夹)。在该人群中检测到11种新的核苷酸替换,其中没有一种产生限制性片段长度多态性(RFLP)或导致B型血友病。通过在单泳道中检测两个靶序列,二倍体个体中约8000 bp的片段可以被检测。这种方法对于检测DNA变异非常有效,适用于大规模人群研究。