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1.
J Hum Genet ; 47(2): 95-8, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-11916010

RESUMEN

Human Y-chromosomal binary polymorphisms have been considered to preserve the paternal genetic legacy and provide evidence on human evolution and the genetic relationships among and demographic history of different populations. To reveal the genetic origin and immigration of the Fujian Han, 13 binary markers on the Y chromosome were used to screen Fujian Han by allele-specific polymerase chain reaction. The results indicated that the M9G marker was highly prevalent (96.20%), suggesting a significant genetic drift. In addition, M122C frequency was only 22.78%, and M45A and M103T were default. The distinctive haplogroup frequencies (H1, H5, and H6/7/8) imply that the haplogroup pattern is a relatively ancestral and interim type.


Asunto(s)
Pueblo Asiatico/genética , Marcadores Genéticos , Haplotipos , Cromosoma Y/genética , China , Evolución Molecular , Humanos , Filogenia
2.
Anthropol Anz ; 60(3): 267-71, 2002 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-12378793

RESUMEN

A mutant allele of the chemokine receptor gene CCR5 bearing a 32-basepair deletion (delta 32CCR5) could increase the resistance to HIV-1 infection or delayed progression to AIDS. The frequency of this mutation is higher in Europeans than in Asians. To investigate the distribution of this polymorphism in China, 715 individuals from 11 Chinese populations were screened by PCR, including the Han and 10 other ethnic groups. The delta 32CCR5 gene was found in 16 individuals from 5 ethnic groups. All of them were heterozygous. The frequency of the mutant alleles of delta 32CCR5 is low in China and reflects (or might reflect) ancestral gene flow from Europe to Chinese ethnic groups and recent intermarriage within the ethnic groups.


Asunto(s)
Pueblo Asiatico , Emparejamiento Base/genética , Deleción Cromosómica , Frecuencia de los Genes/genética , Genética de Población , Mutación/genética , Receptores CCR5/genética , Síndrome de Inmunodeficiencia Adquirida/genética , Alelos , China , Progresión de la Enfermedad , Tamización de Portadores Genéticos , Predisposición Genética a la Enfermedad/genética , Infecciones por VIH/genética , VIH-1 , Humanos , Polimorfismo Genético/genética
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