Travi M, Cremonesi L, Primignani P, Di Benedetto S, Testa R, Schilirò G, Ferrari M
Istituti Clinici di Perfezionamento, Laboratorio di Ricerche Cliniche, Milan, Italy.
Am J Hematol. 1992 Jan;39(1):5-8. doi: 10.1002/ajh.2830390103.
Analysis of polymorphisms of the beta-globin gene cluster was performed on 12 families and on one unrelated individual of Sicilian origin who carried hemoglobin C (Hb C). Two different haplotypes were found in association with beta c Sicilian alleles, corresponding to haplotypes I and II previously described in American blacks. In our population, the more frequent one (haplotype I) was linked to the lack of a polymorphic HpaI site 3' to the beta gene (13.0-kb fragment), similarly to haplotype I in blacks, while the less frequent one was linked to a 7.0-kb HpaI fragment attributable to a site that had never been previously described in linkage with beta c alleles. In Italy, these two haplotypes have been found in rare cases in association with beta A alleles. These findings provide new insights into the origin of Hb C present in Sicily, suggesting that (1) the beta c mutation detected in Sicily derived from African black chromosomes and does not represent a new mutation; and (2) Hb C may have originated either by multiple mutational events on separate chromosomes or by mutation in the HpaI site 3' to the beta gene in a pre-existing beta c chromosome.
对12个家庭以及一名携带血红蛋白C(Hb C)的西西里岛裔无关个体进行了β-珠蛋白基因簇多态性分析。发现与βc西西里岛等位基因相关的两种不同单倍型,分别对应于先前在美国黑人中描述的单倍型I和II。在我们的人群中,较常见的一种(单倍型I)与β基因3'端缺乏多态性HpaI位点(13.0 kb片段)相关,与黑人中的单倍型I类似,而较罕见的一种与一个7.0 kb的HpaI片段相关,该片段归因于一个先前从未与βc等位基因连锁描述过的位点。在意大利,这两种单倍型已在罕见情况下与βA等位基因相关联被发现。这些发现为西西里岛存在的Hb C的起源提供了新见解,表明:(1)在西西里岛检测到的βc突变源自非洲黑人染色体,并非新突变;(2)Hb C可能要么起源于不同染色体上的多个突变事件,要么起源于预先存在的βc染色体中β基因3'端HpaI位点的突变。