Gelinas R, Yagi M, Endlich B, Lotshaw C, Kazazian H H, Stamatoyannopoulos G
Prog Clin Biol Res. 1985;191:125-39.
Sequencing of the A gamma, G gamma and beta genes of a chromosome containing the A gamma Greek HPFH determinant revealed a mutation in position -117 of the promoter of the A gamma gene. The mutation is located in the distal member of the duplicated CCAAT box of the gamma gene. The finding suggests that the DNA region that includes the CCAAT box may play a role in the developmental control of gamma genes. It is suggested that the CCAAT box or its surroundings are involved in interactions between DNA and regulatory molecules whose binding results in silencing of gamma gene expression. Substitution at -117 of the A gamma gene may inhibit the interaction resulting in an A gamma HPFH phenotype. Sequencing of the beta genes of an A gamma Greek HPFH/beta thalassemia heterozygote was done to test whether beta gene expression takes place in cis to the A gamma HPFH determinant. The beta gene of the HPFH chromosome was found to be structurally normal. The beta thalassemia gene possessed a splicing site mutation known to create a beta thalassemia phenotype. These data provide structural evidence for expression of the beta gene in cis to the HPFH determinant.
对一条含有Aγ希腊遗传性胎儿血红蛋白持续增多症(HPFH)决定簇的染色体的Aγ、Gγ和β基因进行测序,结果显示Aγ基因启动子的-117位存在一个突变。该突变位于γ基因重复的CCAAT框的远端成员中。这一发现表明,包含CCAAT框的DNA区域可能在γ基因的发育调控中发挥作用。有人提出,CCAAT框或其周围区域参与了DNA与调控分子之间的相互作用,这些分子的结合导致γ基因表达沉默。Aγ基因-117位的替换可能会抑制这种相互作用,从而导致Aγ HPFH表型。对一名Aγ希腊HPFH/β地中海贫血杂合子的β基因进行测序,以测试β基因是否在与Aγ HPFH决定簇顺式排列的情况下表达。发现HPFH染色体的β基因结构正常。β地中海贫血基因存在一个已知会导致β地中海贫血表型的剪接位点突变。这些数据为β基因在与HPFH决定簇顺式排列的情况下表达提供了结构证据。