Your browser doesn't support javascript.
loading
Analysis of the CCR5 gene coding region diversity in five South American populations reveals two new non-synonymous alleles in Amerindians and high CCR5*D32 frequency in Euro-Brazilians
Boldt, Angelica B. W; Culpi, Lodércio; Tsuneto, Luiza T; Souza, Ilíada R; Kun, Jürgen F. J; Petzl-Erler, Maria Luiza.
Affiliation
  • Boldt, Angelica B. W; Universidade Federal do Paraná. Departamento de Genética. Laboratório de Genética Molecular Humana. Curitiba. BR
  • Culpi, Lodércio; Universidade Federal do Paraná. Departamento de Genética. Laboratório de Polimorfismos e Ligação. Curitiba. BR
  • Tsuneto, Luiza T; Universidade Federal do Paraná. Departamento de Genética. Laboratório de Genética Molecular Humana. Curitiba. BR
  • Souza, Ilíada R; Universidade Federal do Paraná. Departamento de Genética. Laboratório de Genética Molecular Humana. Curitiba. BR
  • Kun, Jürgen F. J; University of Tübingen. Institute of Tropical Medicine. Department of Human Parasitology. Tübingen. DE
  • Petzl-Erler, Maria Luiza; Universidade Federal do Paraná. Departamento de Genética. Laboratório de Genética Molecular Humana. Curitiba. BR
Genet. mol. biol ; 32(1): 12-19, 2009. tab
Article in English | LILACS | ID: lil-505777
Responsible library: BR26.1
ABSTRACT
The CC chemokine receptor 5 (CCR5) molecule is an important co-receptor for HIV. The effect of the CCR5*D32 allele in susceptibility to HIV infection and AIDS disease is well known. Other alleles than CCR5*D32 have not been analysed before, neither in Amerindians nor in the majority of the populations all over the world. We investigated the distribution of the CCR5 coding region alleles in South Brazil and noticed a high CCR5*D32 frequency in the Euro-Brazilian population of the Paraná State (9.3 percent), which is the highest thus far reported for Latin America. The D32 frequency is even higher among the Euro-Brazilian Mennonites (14.2 percent). This allele is uncommon in Afro-Brazilians (2.0 percent), rare in the Guarani Amerindians (0.4 percent) and absent in the Kaingang Amerindians and the Oriental-Brazilians. R223Q is common in the Oriental-Brazilians (7.7 percent) and R60S in the Afro-Brazilians (5.0 percent). A29S and L55Q present an impaired response to beta-chemokines and occurred in Afro- and Euro-Brazilians with cumulative frequencies of 4.4 percent and 2.7 percent, respectively. Two new non-synonymous alleles were found in Amerindians C323F (g.3729G > T) in Guarani (1.4 percent) and Y68C (g.2964A > G) in Kaingang (10.3 percent). The functional characteristics of these alleles should be defined and considered in epidemiological investigations about HIV-1 infection and AIDS incidence in Amerindian populations.
Subject(s)

Full text: Available Collection: International databases Database: LILACS Main subject: HIV Infections / Anti-HIV Agents Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2009 Document type: Article Affiliation country: Brazil / Germany Institution/Affiliation country: Universidade Federal do Paraná/BR / University of Tübingen/DE
Full text: Available Collection: International databases Database: LILACS Main subject: HIV Infections / Anti-HIV Agents Limits: Humans Country/Region as subject: South America / Brazil Language: English Journal: Genet. mol. biol Journal subject: Genetics Year: 2009 Document type: Article Affiliation country: Brazil / Germany Institution/Affiliation country: Universidade Federal do Paraná/BR / University of Tübingen/DE
...