Grompe M, Muzny D M, Caskey C T
Institute for Molecular Genetics, Baylor College of Medicine, Houston, TX 77030.
Proc Natl Acad Sci U S A. 1989 Aug;86(15):5888-92. doi: 10.1073/pnas.86.15.5888.
The mutations in X chromosome-linked diseases are frequently heterogeneous, and yet only a small fraction can be detected by Southern analysis. We therefore adapted the chemical cleavage method of Cotton et al. [Cotton, R. G. H., Rodrigues, N. R. & Campbell, R. D. (1988) Proc. Natl. Acad. Sci. USA 85, 4397-4401] and the polymerase chain reaction to rapidly scan for point mutations in X chromosome-linked ornithine transcarbamoylase (carbamoyl-phosphate: L-ornithine carbamoyltransferase, EC 2.1.3.3.) deficiency. This simple heteroduplex mapping method identified different mismatch sites in polymerase chain reaction-amplified liver cDNA from five unrelated ornithine transcarbamoylase-deficient patients. The predicted sequence alteration was confirmed by DNA sequencing in all five patients and indicated a likely disease-causing mutation in four of these patients. In one atypical ornithine transcarbamoylase-deficient patient a sequence alteration compatible with a cDNA polymorphism was found. One family was studied in detail. Female-carrier detection was performed by chemical cleavage of amplified genomic DNA and verified by allele-specific oligonucleotide hybridization. This mutation scanning approach is simple, sensitive, and applicable to many genetic loci.
X染色体连锁疾病中的突变常常具有异质性,但通过Southern分析只能检测到一小部分。因此,我们采用了Cotton等人[Cotton, R. G. H., Rodrigues, N. R. & Campbell, R. D. (1988) Proc. Natl. Acad. Sci. USA 85, 4397 - 4401]的化学切割方法及聚合酶链反应,以快速筛查X染色体连锁的鸟氨酸转氨甲酰酶(氨甲酰磷酸:L-鸟氨酸氨甲酰转移酶,EC 2.1.3.3.)缺乏症中的点突变。这种简单的异源双链图谱法在5名无亲缘关系的鸟氨酸转氨甲酰酶缺乏症患者的聚合酶链反应扩增的肝脏cDNA中鉴定出了不同的错配位点。通过DNA测序在所有5名患者中证实了预测的序列改变,并表明其中4名患者可能存在致病突变。在1名非典型鸟氨酸转氨甲酰酶缺乏症患者中,发现了与cDNA多态性相符的序列改变。对1个家系进行了详细研究。通过对扩增的基因组DNA进行化学切割来检测女性携带者,并通过等位基因特异性寡核苷酸杂交进行验证。这种突变扫描方法简单、灵敏,适用于许多基因位点。