Rininsland F, Hahn A, Niemann-Seyde S, Slomski R, Hanefeld F, Reiss J
Institut für Humangenetik, Universitätskliniken, Göttingen, Germany.
J Med Genet. 1992 Sep;29(9):647-51. doi: 10.1136/jmg.29.9.647.
The detailed genetic analysis of the Duchenne/Becker muscular dystrophy gene is hindered by the large number of exons involved and their separation by huge introns. These problems can be overcome by the analysis of mRNA rather than genomic DNA and ectopic transcripts derived from peripheral blood lymphocytes provide a convenient source of material. Using reverse transcription and nested PCR, we show here a comprehensive strategy for the rapid and complete analysis of the coding sequences from complex genes and illustrate its potential by the identification of a hitherto undescribed single exon deletion.
杜兴氏/贝克氏肌营养不良基因的详细遗传分析因涉及的外显子数量众多以及它们被巨大的内含子分隔而受到阻碍。通过分析信使核糖核酸(mRNA)而非基因组DNA可以克服这些问题,并且来自外周血淋巴细胞的异位转录本提供了便利的材料来源。利用逆转录和巢式聚合酶链反应(PCR),我们在此展示了一种用于快速、完整分析复杂基因编码序列的综合策略,并通过鉴定一个迄今未描述的单外显子缺失来阐明其潜力。