Landin B, Berglund S, Lindoff B
Department of Clinical Chemistry, University of Lund, Malmö General Hospital, Sweden.
Eur J Haematol. 1994 Jul;53(1):21-5.
Erythrocytosis is sometimes caused by the presence of haemoglobin (Hb) variants with increased oxygen affinity. Here we describe a beta-globin variant found by isoelectric focusing (IEF) of Hb from a 23-year-old Swedish male with moderate erythrocytosis. Amplification of DNA corresponding to the beta-globin gene and subsequent nucleotide sequencing revealed heterozygosity for a GTG-->GAG mutation at codon 20, thus suggesting a Val-->Glu substitution, which was confirmed at the protein level. This mutation occurs at the same position as Hb Olympia [beta 20(B2)Val-->Met], another variant associated with erythrocytosis due to increased oxygen affinity. The novel variant, Hb Trollhättan [beta 20(B2)Val-->Glu], which was also associated with increased oxygen affinity, was shown to be present in three generations of the patient's family.
红细胞增多症有时由具有增加的氧亲和力的血红蛋白(Hb)变体引起。在此,我们描述了通过等电聚焦(IEF)从一名患有中度红细胞增多症的23岁瑞典男性的Hb中发现的一种β-珠蛋白变体。对应于β-珠蛋白基因的DNA扩增及随后的核苷酸测序揭示了密码子20处GTG→GAG突变的杂合性,从而提示缬氨酸→谷氨酸替代,这在蛋白质水平得到证实。该突变发生在与Hb奥林匹亚[β20(B2)缬氨酸→甲硫氨酸]相同的位置,Hb奥林匹亚是另一种因氧亲和力增加而与红细胞增多症相关的变体。这种新型变体Hb特罗尔海坦[β20(B2)缬氨酸→谷氨酸]也与氧亲和力增加相关,在患者家族的三代人中均有发现。