Mamalaki A, Horanyi M, Szelenyi J, Moschonas N K
Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology, Heraklion, Greece.
Hum Genet. 1990 Oct;85(5):509-12. doi: 10.1007/BF00194226.
We have used the powerful methodology of DNA enzymatic amplification in order to assign human alpha-globin structural mutants to one of the two highly homologous alpha-globin genes. Selectively amplified alpha 1 and alpha 2-globin cDNAs were dot-blotted and further hybridized to synthetic oligonucleotides encompassing either the normal or the mutated sequences. The generated signals corresponded specifically to one of the two alpha-globin genes. Using this approach the alpha-globin structural mutants J-Buda and G-Pest were found to be encoded by the alpha 2 and the alpha 1-globin genes, respectively. Furthermore, the exact nucleotide changes were determined. We propose this technique to serve as a simple and definitive method for assigning alpha-globin structural mutants.
我们运用了强大的DNA酶促扩增方法,以便将人类α-珠蛋白结构突变体定位到两个高度同源的α-珠蛋白基因之一。选择性扩增的α1和α2-珠蛋白cDNA进行点杂交,然后进一步与包含正常或突变序列的合成寡核苷酸杂交。产生的信号分别特异性地对应于两个α-珠蛋白基因之一。使用这种方法,发现α-珠蛋白结构突变体J-Buda和G-Pest分别由α2和α1-珠蛋白基因编码。此外,还确定了确切的核苷酸变化。我们提出这项技术可作为一种简单而明确的方法来定位α-珠蛋白结构突变体。