Jones R W, Old J M, Wood W G, Clegg J B, Weatherall D J
Br J Haematol. 1982 Mar;50(3):415-22. doi: 10.1111/j.1365-2141.1982.tb01936.x.
We report here restriction endonuclease maps of the beta-like globin gene cluster for the British form of HPFH and for a case of G gamma beta + HPFH, and also confirm and extend previous reports of the map for the Greek form of HPFH. These results show that all these conditions belong to a group lacking any substantial deletion or rearrangement of DNA sequence in this gene cluster. The absence of any gross disruption of the structure of this region of the genome, together with evidence that the HPFH genotype is either allelic with, or closely linked to, the beta-like globin gene cluster, suggests that the responsible lesions are nearer to being purely regulatory in nature than in forms of HPFH due to substantial deletions. Thus these conditions promise to provide less equivocal evidence about the regulation of beta-like globin gene expression than has so far been available.
我们在此报告了英国型遗传性胎儿血红蛋白持续存在(HPFH)以及一例Gγβ⁺ HPFH患者的类β珠蛋白基因簇的限制性内切酶图谱,同时证实并扩展了先前关于希腊型HPFH图谱的报道。这些结果表明,所有这些情况都属于该基因簇中DNA序列没有任何实质性缺失或重排的一组情况。基因组这一区域结构没有任何明显破坏,以及HPFH基因型与类β珠蛋白基因簇等位或紧密连锁的证据,表明与因大量缺失导致的HPFH形式相比,其致病损伤在本质上更接近纯粹的调节性。因此,与迄今为止所获得的证据相比,这些情况有望为类β珠蛋白基因表达的调控提供不那么模棱两可的证据。