Please use this identifier to cite or link to this item:
|Title:||?-Thalassemia and ?(A) globin gene haplotypes in Mexican mestizos|
|Abstract:||?-globin haplotypes of 20 -thalassemia (?-thal) and 87 ?(A) Mexican mestizo chromosomes were analyzed to ascertain the origin of the ?-thal alleles and the frequencies and distribution of the ?(A) haplotypes among northwestern Mexican mestizos. Sixteen ?-thal chromosomes carried six Mediterranean alleles [five codon 39 C?T; two IVS1:1 G?A; two IVS1:5 G A: three IVS1:110 G(A; one codon 11 (-T) and three (deltabeta)zero-thal]; the remaining four were linked to three rare alleles (two -28 A?C and one each: -87 C T and initiation codon ATG?GTG). Among the 87 ?(A) chromosomes, 17 different 5' haplotypes with frequencies for 1, 3, 2 and 5 of 39.0%, 17.2%, 9.2% and 6.9%, respectively, were observed. The ?-haplotype analysis showed that 13 out of 16 Mediterranean chromosomes could easily be explained by gene migration; however, one codon 39 associated with haplotype 4 (----+ +-), one IVS1:1 with haplotype 1(+----++) and one IVS1:5 G?A, may represent separate mutational events. Analysis of the rare alleles showed that the -28 A?C mutation was associated with the commonest ?(A) haplotype in Mexican mestizos, Mediterraneans and the total world population; therefore an independent origin cannot be ruled out. The -87 C?T and initiation codon ATG?GTG were found with ?-haplotypes different from the reported ones, suggesting an indigenous origin.|
|Appears in Collections:||Producción científica UdeG|
Files in This Item:
There are no files associated with this item.
Items in RIUdeG are protected by copyright, with all rights reserved, unless otherwise indicated.