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1.
Proc Natl Acad Sci U S A ; 107(15): 6759-64, 2010 Apr 13.
Artigo em Inglês | MEDLINE | ID: mdl-20351276

RESUMO

The Farming/Language Dispersal Hypothesis posits that prehistoric population expansions, precipitated by the innovation or early adoption of agriculture, played an important role in the uneven distribution of language families recorded across the world. In this case, the most widely spread language families today came to be distributed at the expense of those that have more restricted distributions. In the Americas, Uto-Aztecan is one such language family that may have been spread across Mesoamerica and the American Southwest by ancient farmers. We evaluated this hypothesis with a large-scale study of mitochondrial DNA (mtDNA) and Y-chromosomal DNA variation in indigenous populations from these regions. Partial correlation coefficients, determined with Mantel tests, show that Y-chromosome variation in indigenous populations from the American Southwest and Mesoamerica correlates significantly with linguistic distances (r = 0.33-0.384; P < 0.02), whereas mtDNA diversity correlates significantly with only geographic distance (r = 0.619; P = 0.002). The lack of correlation between mtDNA and Y-chromosome diversity is consistent with differing population histories of males and females in these regions. Although unlikely, if groups of Uto-Aztecan speakers were responsible for the northward spread of agriculture and their languages from Mesoamerica to the Southwest, this migration was possibly biased to males. However, a recent in situ population expansion within the American Southwest (2,105 years before present; 99.5% confidence interval = 1,273-3,773 YBP), one that probably followed the introduction and intensification of maize agriculture in the region, may have blurred ancient mtDNA patterns, which might otherwise have revealed a closer genetic relationship between females in the Southwest and Mesoamerica.


Assuntos
Cromossomos Humanos Y/ultraestrutura , DNA Mitocondrial/ultraestrutura , Variação Genética , Indígenas Norte-Americanos/genética , Idioma , Agricultura/métodos , Evolução Biológica , América Central , Emigração e Imigração , Etnicidade/genética , Feminino , Genética Populacional , História Antiga , Humanos , Indígenas Norte-Americanos/história , Masculino , Dados de Sequência Molecular , Fatores Sexuais , Sudoeste dos Estados Unidos , Zea mays/metabolismo
2.
Genet Mol Res ; 6(2): 461-9, 2007 Jun 30.
Artigo em Inglês | MEDLINE | ID: mdl-17952870

RESUMO

Microdeletions in Yq are associated with defects in spermatogenesis, while those in the AZF region are considered critical for germ cell development. We examined microdeletions in the Y chromosomes of patients attended at the Laboratory of Human Reproduction of the Clinical Hospital of the Federal University of Goiás as part of a screening of patients who plan to undergo assisted reproduction. Analysis was made of the AZF region of the Y chromosome in men who had altered spermograms to detect possible microdeletions in Yq. Twenty-three patients with azoospermia and 40 with severe oligozoospermia were analyzed by PCR for the detection of six sequence-tagged sites: sY84 and sY86 for AZFa, sY127 and sY134 for AZFb, and sY254 and sY255 for AZFc. Microdeletions were detected in 28 patients, including 10 azoospermics and 18 severe oligozoospermics. The patients with azoospermia had 43.4% of their microdeletions in the AZFa region, 8.6% in the AZFb region and 17.4% in the AZFc region. In the severe oligozoospermics, 40% were in the AZFa region, 5% in the AZFb region and 5% in the AZFc region. We conclude that microdeletions can be the cause of idiopathic male infertility, supporting conclusions from previous studies.


Assuntos
Deleção Cromossômica , Cromossomos Humanos Y/ultraestrutura , Deleção de Genes , Infertilidade Masculina/genética , Azoospermia/genética , Brasil , Fertilidade , Células Germinativas/metabolismo , Humanos , Masculino , Reação em Cadeia da Polimerase , Espermatogênese
3.
Genet. mol. res. (Online) ; 6(2): 461-469, 2007. tab, graf, ilus
Artigo em Inglês | LILACS | ID: lil-482023

RESUMO

Microdeletions in Yq are associated with defects in spermatogenesis, while those in the AZF region are considered critical for germ cell development. We examined microdeletions in the Y chromosomes of patients attended at the Laboratory of Human Reproduction of the Clinical Hospital of the Federal University of Goiás as part of a screening of patients who plan to undergo assisted reproduction. Analysis was made of the AZF region of the Y chromosome in men who had altered spermograms to detect possible microdeletions in Yq. Twenty-three patients with azoospermia and 40 with severe oligozoospermia were analyzed by PCR for the detection of six sequence-tagged sites: sY84 and sY86 for AZFa, sY127 and sY134 for AZFb, and sY254 and sY255 for AZFc. Microdeletions were detected in 28 patients, including 10 azoospermics and 18 severe oligozoospermics. The patients with azoospermia had 43.4% of their microdeletions in the AZFa region, 8.6% in the AZFb region and 17.4% in the AZFc region. In the severe oligozoospermics, 40% were in the AZFa region, 5% in the AZFb region and 5% in the AZFc region. We conclude that microdeletions can be the cause of idiopathic male infertility, supporting conclusions from previous studies.


Assuntos
Humanos , Masculino , Cromossomos Humanos Y/ultraestrutura , Deleção Cromossômica , Deleção de Genes , Infertilidade Masculina/genética , Azoospermia/genética , Brasil , Células Germinativas/metabolismo , Espermatogênese , Fertilidade , Reação em Cadeia da Polimerase
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