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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.
  • 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
Artículo en Inglés | LILACS | ID: lil-505777
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.
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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Infecciones por VIH / Fármacos Anti-VIH Límite: Humanos País/Región como asunto: America del Sur / Brasil Idioma: Inglés Revista: Genet. mol. biol Asunto de la revista: Genética Año: 2009 Tipo del documento: Artículo País de afiliación: Brasil / Alemania Institución/País de afiliación: Universidade Federal do Paraná/BR / University of Tübingen/DE

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Infecciones por VIH / Fármacos Anti-VIH Límite: Humanos País/Región como asunto: America del Sur / Brasil Idioma: Inglés Revista: Genet. mol. biol Asunto de la revista: Genética Año: 2009 Tipo del documento: Artículo País de afiliación: Brasil / Alemania Institución/País de afiliación: Universidade Federal do Paraná/BR / University of Tübingen/DE