Related Experiment Video
Updated: Mar 1, 2026

Infinium Assay for Large-scale SNP Genotyping Applications
Published on: November 19, 2013
Frequency of haplotypes in the beta globin gene cluster in a selected sample of the mexican population
Rosenda Peñaloza1, Alejandro García-Carrancá2, Teresa Ceras3
1Unit of Investigation in Human Genetics, National Medical Center, IMSS, Mexico City 03020.
Abstract:
Five polymorphic restriction enzyme sites in the beta globin gene cluster (HindIII Gγ-Hind III Aγ-, Ava IIINV-2 β-and Hpa I and Bam HI 3'β-globin gene) were studied in individuals from 13 families: 13 homozygote patients for sickle cell anemia, two double heterozygotes (one SC and one S/βThal ), 35 AS heterozygotes (23 parents and 12 siblings), one father (A/βThal ), and three normal siblings. In addition, 17 normal unrelated Mexican subjects were studied. All subjects were from the state of Veracruz on the coast of the Gulf of Mexico. The Southern blot technique was used. Fifteen haplotypes were identified in the 142 chromosomes. Five were the most frequent: two haplotypes, (+-+++) (52.4%) and (--+-+) (19.0%) were associated with βS chromosomes; two haplotypes, (--+++) (38.2%) and (---++) (19.7%), were linked with βA chromosomes, and the fifth (--++-) was present in both types of chromosomes. Haplotype (+-+++) corresponded to the Bantu or Senegal type. With Hinc II analysis after PCR amplification in both the 5' and 3' regions of the ψβ-globin gene, it was possible to distinguish between these African types, as in the former both restriction sites are absent. This analysis was done in 23 βS and 10 βA subjects. All βS chromosomes disclosed the Bantu type, while βA were similar to Caucasians. Bantu and Benin haplotypes have been found with high frequency in African populations, indicating the great influence of African genes in the population of the Mexican coasts. In addition, two previously unidentified haplotypes were found: (++--+) and (-++++). These can be explainded by crossing-over events and/or by new mutations. © 1995 Wiley-Liss, Inc.
Related Concept Videos
Multiple Allele Traits
Genetic Variation
Genes exist in different versions called alleles,...
What is Population Genetics?
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
Single Nucleotide Polymorphisms-SNPs
Human Genetics
The complex relationship between genetics and psychology is observable through common biological components such...

