Fritsch E F, Lawn R M, Maniatis T
Nature. 1979 Jun 14;279(5714):598-603. doi: 10.1038/279598a0.
Deletions in the DNA of individuals with hereditary persistence of fetal haemoglobin (HPFH) and 8 beta-thalassaemia have been mapped as a means of identifying regulatory sequences involved in the switch from fetal to adult globin gene expression. The end points of these deletions have been precisely located with respect to restriction endonuclease cleavage sites within and surrounding the gamma-, delta- and beta-globin genes in normal human DNA and the deletion maps were used to obtain definitive evidence for the physical linkage of the fetal and adult beta-like globin genes in the order 5'Ggamma-Agamma-delta-beta 3'. Correlation of haematological data and the location of deletions in two cases of HPFH and one case of deltabeta-thalassaemia suggest that a region of DNA located near the 5'-end of the delta-globin gene may be involved in the suppression in cis of gamma-globin gene expression in adults. The interpretation of a second case of deltabeta-thalassaemia is complicated by the fact that the deletion removes the Agamma-gene in addition to the region near the 5'-end of the delta-globin gene.
对患有胎儿血红蛋白(HPFH)遗传性持续存在和β地中海贫血的个体的DNA缺失进行了定位,以此作为鉴定参与从胎儿向成人珠蛋白基因表达转换的调控序列的一种手段。相对于正常人DNA中γ、δ和β珠蛋白基因内部及周围的限制性内切酶切割位点,这些缺失的端点已被精确定位,并且利用这些缺失图谱获得了胎儿和成人β样珠蛋白基因按5'Gγ-Aγ-δ-β 3'顺序物理连锁的确凿证据。两例HPFH和一例δβ地中海贫血病例的血液学数据与缺失位置的相关性表明,位于δ珠蛋白基因5'端附近的一个DNA区域可能参与了成人γ珠蛋白基因表达的顺式抑制。第二例δβ地中海贫血病例的解释较为复杂,因为该缺失除了去除δ珠蛋白基因5'端附近的区域外,还去除了Aγ基因。