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意大利南部的δ型地中海贫血:单一突变事件的证据

Delta beta-thalassaemia in southern Italy: evidence for a single mutational event.

作者信息

Carè A, Sposi N M, Giampaolo A, Improta T, Calandrini M, Petrini M, Marinucci M, Tagarelli A, Brancati C

出版信息

J Med Genet. 1984 Apr;21(2):117-20. doi: 10.1136/jmg.21.2.117.

Abstract

Haematological and molecular studies on 32 heterozygotes for G gamma A gamma delta beta(0)-thalassaemia from 15 unrelated families from southern Italy are reported. The haematological features of G gamma A gamma delta beta(0)-thalassaemia carriers are compared with those of beta-thalassaemia and Hb Lepore heterozygotes. Striking similarity exists between the phenotypic expression of beta-thalassaemia and Lepore mutations. Globin gene mapping studies indicated that the molecular lesion underlying delta beta-thalassaemia is a large deletion starting from the large intervening sequence of the delta gene and extending downstream from the beta gene. The possibility that delta beta-thalassaemia haplotypes in southern Italy originated from a single mutational event is discussed.

摘要

报道了对来自意大利南部15个无亲缘关系家庭的32名GγAγδβ(0)-地中海贫血杂合子进行的血液学和分子研究。将GγAγδβ(0)-地中海贫血携带者的血液学特征与β-地中海贫血和Hb Lepore杂合子的特征进行了比较。β-地中海贫血和Lepore突变的表型表达之间存在显著相似性。珠蛋白基因定位研究表明,δβ-地中海贫血的分子病变是一个大的缺失,从δ基因的大间隔序列开始,延伸到β基因的下游。讨论了意大利南部δβ-地中海贫血单倍型起源于单一突变事件的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8ee/1049239/bb9a38ffc050/jmedgene00100-0038-a.jpg

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