Winichagoon P, Fucharoen S, Wilairat P, Chihara K, Fukumaki Y
Department of Medicine, Faculty of Medicine, Siriraj Hospital, Thailand.
Br J Haematol. 1994 Aug;87(4):797-804. doi: 10.1111/j.1365-2141.1994.tb06740.x.
The beta-globin gene clusters of three unrelated Thai families with a nondeletional type of hereditary persistence of fetal haemoglobin (HPFH) were studied using polymerase chain reaction-related techniques. All appeared to have normal nucleotide sequences from the Cap site to position -400 of both the G gamma- and A gamma-globin genes. Two individuals suspected of having a beta-thalassaemia gene linked to the high HbF condition also had a normal beta-globin gene sequence, spanning from position -108 from the Cap site to the polyadenylation site. Deletion of four nucleotides, AGCA, at positions -225 to -222 of one A gamma-globin allele was detected in one subject and was confirmed by dot-blot hybridization. Restriction fragment length polymorphisms in the beta-globin gene cluster showed that the 5' haplotype (-+-++) and the presence (+) of an Xmm 1 polymorphic site at -158 of the G gamma-globin gene are associated with the high F phenotype in these families. Direct sequencing of the 5' hypersensitive-2 (5' HS-2) site of the locus control region (LCR) showed that this Xmn 1 (+) site is also linked to a specific rearrangement of TA repeats (TA)9CACATATACG(TA)10, in HS-2 segment.
利用聚合酶链反应相关技术对三个不相关的泰国家庭的β-珠蛋白基因簇进行了研究,这些家庭患有非缺失型胎儿血红蛋白遗传性持续存在(HPFH)。从帽位点到Gγ和Aγ珠蛋白基因的-400位,所有序列的核苷酸序列似乎均正常。两名疑似携带与高HbF状况相关的β地中海贫血基因的个体,其β珠蛋白基因序列也正常,从帽位点的-108位到聚腺苷酸化位点。在一名受试者中检测到一个Aγ珠蛋白等位基因的-225至-222位缺失了四个核苷酸AGCA,并通过点杂交得到证实。β珠蛋白基因簇中的限制性片段长度多态性表明,5'单倍型(-+-++)以及Gγ珠蛋白基因-158位Xmm 1多态性位点的存在(+)与这些家庭中的高F表型相关。对基因座控制区(LCR)的5'超敏-2(5'HS-2)位点进行直接测序表明,该Xmn 1(+)位点也与HS-2片段中TA重复序列(TA)9CACATATACG(TA)10的特定重排相关。