| Registro completo |
| Provedor de dados: |
Genet. Mol. Biol.
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| País: |
Brazil
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| Título: |
Homo sapiens, Homo neanderthalensis and the Denisova specimen: new insights on their evolutionary histories using whole-genome comparisons
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| Autores: |
Paixão-Côrtes,Vanessa Rodrigues
Viscardi,Lucas Henrique
Salzano,Francisco Mauro
Hünemeier,Tábita
Bortolini,Maria Cátira
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| Data: |
2012-01-01
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| Ano: |
2012
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| Palavras-chave: |
Human evolution
Comparative genomics
Positive selection
Neanderthal
Denisova
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| Resumo: |
After a brief review of the most recent findings in the study of human evolution, an extensive comparison of the complete genomes of our nearest relative, the chimpanzee (Pan troglodytes), of extant Homo sapiens, archaic Homo neanderthalensis and the Denisova specimen were made. The focus was on non-synonymous mutations, which consequently had an impact on protein levels and these changes were classified according to degree of effect. A total of 10,447 non-synonymous substitutions were found in which the derived allele is fixed or nearly fixed in humans as compared to chimpanzee. Their most frequent location was on chromosome 21. Their presence was then searched in the two archaic genomes. Mutations in 381 genes would imply radical amino acid changes, with a fraction of these related to olfaction and other important physiological processes. Eight new alleles were identified in the Neanderthal and/or Denisova genetic pools. Four others, possibly affecting cognition, occured both in the sapiens and two other archaic genomes. The selective sweep that gave rise to Homo sapiens could, therefore, have initiated before the modern/archaic human divergence.
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| Tipo: |
Info:eu-repo/semantics/article
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| Idioma: |
Inglês
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| Identificador: |
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572012000600003
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| Editor: |
Sociedade Brasileira de Genética
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| Relação: |
10.1590/S1415-47572012000600003
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| Formato: |
text/html
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| Fonte: |
Genetics and Molecular Biology v.35 n.4 suppl.1 2012
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| Direitos: |
info:eu-repo/semantics/openAccess
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