Del Senno L, Pirastu M, Barbieri R, Bernardi F, Buzzoni D, Marchetti G, Perrotta C, Vullo C, Kan Y W, Conconi F
J Med Genet. 1985 Feb;22(1):54-8. doi: 10.1136/jmg.22.1.54.
Six beta(+)-thalassaemic patients from the Po river delta region have been studied. Using synthetic oligonucleotides as specific hybridisation probes, the beta(+) IVS I mutation (G----A at position 108) was demonstrated. This lesion and the enzyme polymorphism pattern in the subjects examined are the same as have been described for other Mediterranean beta(+)-thalassaemias. Antenatal diagnosis through DNA analysis of beta(+)-thalassaemia is therefore possible. The production of beta globin in a beta(+), homozygote and in a beta (+), beta(0) 39 (nonsense mutation at codon 39) double heterozygote is approximately 20% and 10% respectively of total non-alpha globin synthesis. Despite some overlapping of the results, similar beta globin synthesis levels have been obtained in 43 beta(+)-thalassaemia patients. This suggests that in the Po river delta region the most common thalassaemic genes are beta(0) 39 and beta(+) IVS I.
对波河三角洲地区的6名β(+)-地中海贫血患者进行了研究。使用合成寡核苷酸作为特异性杂交探针,证实了β(+)IVS I突变(第108位的G→A)。在所检查的受试者中,这种病变和酶多态性模式与其他地中海β(+)-地中海贫血中所描述的相同。因此,通过对β(+)-地中海贫血进行DNA分析来进行产前诊断是可行的。β(+)纯合子和β(+)、β(0)39(密码子39处的无义突变)双杂合子中β珠蛋白的产生分别约占非α珠蛋白总合成量的20%和10%。尽管结果存在一些重叠,但在43名β(+)-地中海贫血患者中获得了相似的β珠蛋白合成水平。这表明在波河三角洲地区,最常见的地中海贫血基因是β(0)39和β(+)IVS I。