Baklouti F, Ouazana R, Gonnet C, Lapillonne A, Delaunay J, Godet J
Centre de Génétique Moléculaire et Cellulaire, Villeurbanne, France.
Blood. 1989 Oct;74(5):1817-22.
An atypical sickle cell trait with a very low level of hemoglobin S and features of heterozygous beta-thalassemia was recently described. In vitro globin chain synthesis strongly suggested the presence of the two abnormalities on the same chromosome. We report the corresponding beta S-thal gene. DNA sequence revealed a C----T base substitution in the distal promoter element CACCC, at position-88 from the cap site, in addition to the expected GAG----GTG mutation responsible for the structural variant (beta 6 Glu----Val). Reticulocyte mRNA titration and transient assay of the mutant gene in COS cells showed a defect in beta-mRNA production. Restriction haplotype and DNA sequence analyses revealed that the doubly mutated gene is associated with haplotype 19 (or Benin/Algeria haplotype). In particular, we found the (AT)9(T)4 repeated sequences specifically encountered 5' to the beta S gene of Benin Algeria type. These results support the view that the beta S-thal gene resulted from an independent thalassemic mutation having occurred on a beta S chromosome rather than (a) from a beta S mutation having altered a beta-thalassemic gene or (b) from a recombination event between two chromosomes, each carrying one of the mutations.
最近描述了一种非典型镰状细胞性状,其血红蛋白S水平极低,并具有杂合β地中海贫血的特征。体外珠蛋白链合成强烈提示两条异常存在于同一条染色体上。我们报告了相应的βS-地中海贫血基因。DNA序列显示,除了导致结构变异(β6谷氨酰胺→缬氨酸)的预期GAG→GTG突变外,在距帽位点-88位的远端启动子元件CACCC中存在C→T碱基替换。网织红细胞mRNA滴定和突变基因在COS细胞中的瞬时分析显示β-mRNA产生存在缺陷。限制性单倍型和DNA序列分析表明,双重突变基因与单倍型19(或贝宁/阿尔及利亚单倍型)相关。特别是,我们发现了(AT)9(T)4重复序列,该序列在贝宁阿尔及利亚型βS基因5'端特异性出现。这些结果支持这样的观点,即βS-地中海贫血基因是由βS染色体上发生的独立地中海贫血突变产生的,而不是(a)由改变β地中海贫血基因的βS突变产生的或(b)由两条分别携带一种突变的染色体之间的重组事件产生的。