Harteveld Cornelis L, Muglia Maria, Passarino Giuseppe, Kielman Menno F, Bernini Luigi F
Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Br J Haematol. 2002 Dec;119(3):848-54. doi: 10.1046/j.1365-2141.2002.03917.x.
The highly conserved 350-bp major regulatory element HS-40 (or alphaMRE) upstream of the human alpha-globin gene cluster is involved in the regulation of alpha-globin gene expression. The study of alphaMRE differences between human populations and the evolution of alphaMRE sequences in mammals may lead to a better understanding of the function and importance of this element in the regulation of expression of the downstream alpha-cluster. Denaturing gradient gel electrophoresis was used to determine the sequence heterogeneity of the alphaMRE region in 276 unrelated individuals, representing seven different populations. Furthermore, we analysed the alpha major regulatory elements of chimpanzee, orang-utan and rhesus monkeys and compared them with the equivalent human and murine sequences. Six different alphaMRE haplotypes (labelled A to F) were found in humans. Haplotype frequencies between the seven populations showed a gradual shift to a higher haplotype A distribution from west to east, being the highest in Indonesians. The African sample shows the largest divergence in haplotypes. Five out of six different haplotypes were present, three of which were exclusively found in Africans. The high prevalence of the haplotype A in humans, together with the conservation of this haplotype in apes, suggests that it is the ancestral one. The alphaMRE fragment appears to be a highly polymorphic marker, which could be used in combination with the regular markers in the alpha-cluster to extend the haplotype and to follow segregation of alpha-thalassaemia genes in population studies more accurately.
人类α-珠蛋白基因簇上游高度保守的350bp主要调控元件HS-40(或αMRE)参与α-珠蛋白基因表达的调控。对不同人群间αMRE差异以及哺乳动物中αMRE序列进化的研究,可能有助于更好地理解该元件在调控下游α-基因簇表达中的功能和重要性。采用变性梯度凝胶电泳法测定了代表7个不同人群的276名无关个体αMRE区域的序列异质性。此外,我们分析了黑猩猩、猩猩和恒河猴的α主要调控元件,并将它们与相应的人类和小鼠序列进行了比较。在人类中发现了6种不同的αMRE单倍型(标记为A至F)。7个人群之间的单倍型频率呈现出从西到东逐渐向更高的单倍型A分布转变的趋势,在印度尼西亚人中最高。非洲样本的单倍型差异最大。6种不同单倍型中有5种存在,其中3种仅在非洲人中发现。人类中单倍型A的高流行率以及该单倍型在猿类中的保守性,表明它是祖先单倍型。αMRE片段似乎是一个高度多态性的标记,可与α-基因簇中的常规标记结合使用,以扩展单倍型,并在群体研究中更准确地追踪α-地中海贫血基因的分离情况。