Kauppinen R, Peltonen L, Palotie A, Mustajoki P
Third Department of Medicine, University Central Hospital of Helsinki, Finland.
Hum Genet. 1990 Jul;85(2):160-4. doi: 10.1007/BF00193189.
Restriction fragment length polymorphism (RFLP) analysis was performed in three Finnish families with different subtypes of acute intermittent porphyria (AIP): 1) cross-reacting immunological material (CRIM)-negative with low erythrocyte porphobilinogen (PBG)-deaminase activity, 2) CRIM-positive with low PBG-deaminase activity and 3) CRIM-negative with normal PBG-deaminase activity. The disease-associated RFLP haplotype (A2B1C2) of the PBG-deaminase gene was the same in each family. In all three families, RFLP linkage analysis resulted in highly positive lod scores. The maximal lod score (4.3) was obtained at the recombinant fraction of zero, thus confirming a tight linkage of AIP to the PBG-deaminase locus. Of the 62 family members tested, 30 had the disease-associated haplotype; in 5 of them, conventional tests for AIP were normal and in one, uncertain. RFLP analysis can thus reveal new gene carriers and help in the diagnosis of individuals with uncertain results in other laboratory tests.
对三个患有不同亚型急性间歇性卟啉症(AIP)的芬兰家庭进行了限制性片段长度多态性(RFLP)分析:1)交叉反应免疫物质(CRIM)阴性且红细胞卟胆原(PBG)脱氨酶活性低;2)CRIM阳性且PBG脱氨酶活性低;3)CRIM阴性且PBG脱氨酶活性正常。每个家庭中,PBG脱氨酶基因与疾病相关的RFLP单倍型(A2B1C2)是相同的。在所有三个家庭中,RFLP连锁分析得出的lod分数均为高度阳性。在重组率为零时获得了最大lod分数(4.3),从而证实AIP与PBG脱氨酶基因座紧密连锁。在接受检测的62名家庭成员中,30人具有与疾病相关的单倍型;其中5人的AIP常规检测结果正常,1人的结果不确定。因此,RFLP分析可以发现新的基因携带者,并有助于诊断其他实验室检测结果不确定的个体。