De Angioletti M, Lacerra G, Castaldo C, Cutolo R, de Bonis C, Buonanno G, Carestia C
International Institute of Genetics and Biophysics, CNR, Naples, Italy.
Hum Genet. 1992 Apr;89(1):37-41. doi: 10.1007/BF00207039.
We report here a new human alpha-globin gene rearrangement carrying the two normal, alpha 2 and alpha 1, and two hybrid, alpha 1/alpha 2, globin genes in the order 5'-alpha 2-alpha 1/alpha 2-alpha 1/alpha 2-alpha 1-3'. Both the hybrid genes, subtyped with ApaI and RsaI restriction enzymes, were found to be of the uncommon anti 3.7 type II. The hybrid genes were expressed at the biosynthetic level and their interaction with the beta-thalassaemia IVS 1 nt 1 G----A mutation caused thalassaemia intermedia. We also report a case of an alpha alpha alpha-globin gene rearrangement in the twin of one of the alpha alpha alpha alpha-globin gene carriers; the duplicated gene was of the anti 4.2 type and was associated with the absence of RsaI polymorphism. The singular finding of an alpha alpha alpha alpha-anti 3.7 cluster with two identical rare hybrid genes suggests that the reciprocal unequal recombination causing the alpha-globin gene rearrangements could be of the intrachromosomal rather than the interchromosomal type.
我们在此报告一种新的人类α-珠蛋白基因重排,其携带两个正常的α2和α1珠蛋白基因,以及两个杂合的α1/α2珠蛋白基因,顺序为5'-α2-α1/α2-α1/α2-α1-3'。用ApaI和RsaI限制性内切酶分型的两个杂合基因均为罕见的反3.7 II型。杂合基因在生物合成水平上表达,它们与β地中海贫血IVS 1 nt 1 G→A突变的相互作用导致中间型地中海贫血。我们还报告了一例ααα-珠蛋白基因重排在一名αααα-珠蛋白基因携带者的双胞胎中的情况;重复的基因是反4.2型,且与RsaI多态性缺失相关。一个具有两个相同罕见杂合基因的αααα-反3.7基因簇的独特发现表明,导致α-珠蛋白基因重排的相互不等位重组可能是染色体内而非染色体间类型。