Riess O, Michel A, Speer A, Meiske W, Cobet G, Coutelle C
Abteilung für Medizinische Genetik, Humboldt Universität, Berlin, German Democratic Republic.
Hum Genet. 1988 Apr;78(4):343-6. doi: 10.1007/BF00291732.
Probands from 26 PKU-affected families of the Berlin area were analyzed with respect to the allele frequency distribution of six RFLPs in linkage with the normal and the PKU alleles of the phenylalanine hydroxylase gene. These investigations confirm most of the RFLP haplotypes observed by Güttler and colleagues in the Danish population and describe two additional ones. They detect no significant differences in the single RFLP or RFLP haplotype distribution on the normal chromosomes in comparison with the Danish families and confirm a prevalent association of the RFLP haplotypes 1, 4, and 7 with the normal PAH allele. In contrast to the Danish investigations, in our study the PKU allele is found most frequently linked to haplotype 2, rather then to haplotype 3. In one of our patients we found a substitution of the normal 19-kb MspI fragment by a 13.5- and a 5.5-kb fragment, reported up to now only in one other German family.
对来自柏林地区26个苯丙酮尿症(PKU)患者家庭的先证者,就与苯丙氨酸羟化酶基因的正常和PKU等位基因连锁的6种限制性片段长度多态性(RFLP)的等位基因频率分布进行了分析。这些研究证实了Güttler及其同事在丹麦人群中观察到的大多数RFLP单倍型,并描述了另外两种。与丹麦家庭相比,他们在正常染色体上未检测到单个RFLP或RFLP单倍型分布的显著差异,并证实了RFLP单倍型1、4和7与正常苯丙氨酸羟化酶(PAH)等位基因的普遍关联。与丹麦的研究相反,在我们的研究中,PKU等位基因最常与单倍型2连锁,而不是与单倍型3连锁。在我们的一名患者中,我们发现正常的19kb MspI片段被一个13.5kb和一个5.5kb的片段取代,迄今为止仅在另一个德国家庭中报道过。