RESUMO
We analyzed 21 paragroup Q* Y chromosomes from South American aboriginal and urban populations. Our aims were to evaluate the phylogenetic status, geographic distribution, and genetic diversity in these groups of chromosomes and compare the degree of genetic variation in relation to Q1a3a haplotypes. All Q* chromosomes from our series and five samples from North American Q* presented the derivate state for M346, that is present upstream to M3, and determined Q1a3* paragroup. We found a restrictive geographic distribution and low frequency of Q1a3* in South America. We assumed that this low frequency could be reflecting extreme drift effects. However, several estimates of gene diversity do not support the existence of a severe bottleneck. The mean haplotype diversity expected was similar to that for South American Q1a3* and Q1a3a (0.478 and 0.501, respectively). The analysis of previous reports from other research groups and this study shows the highest frequencies of Q* for the West Corner and the Grand Chaco regions of South America. At present, there is no information on whether the phylogenetic status of Q* paragoup described in previous reports is similar to that of Q1a3* paragroup though our results support this possibility.
Assuntos
Cromossomos Humanos Y , Variação Genética , Geografia , Indígenas Sul-Americanos/genética , Deriva Genética , Haplótipos , Humanos , Filogenia , América do SulRESUMO
The major histocompatibility complex (MHC) is one of the biological systems of major polymorphisms. The study of HLA class II variability has allowed the identification of several alleles that are characteristic to Amerindian populations, and it is an excellent tool to define the relations and biological affinities among them. In this work, we analyzed the allelic distribution of the HLA-DRB1 class II locus in four Amerindian populations: Mapuche (n = 34) and Tehuelche (n = 23) from the Patagonian region of Argentina, and Wichi SV (n = 24) and Lengua (n = 17) from the Argentinean and Paraguayan Chaco regions, respectively. In all of these groups, relatively high frequencies of Amerindian HLA-DRB1 alleles were observed (DRB1*0403, DRB1*0407, DRB1*0411, DRB1*0417, DRB1*0802, DRB1*0901, DRB1*1402, DRB1*1406 and DRB1*1602). However, we also detected the presence of non-Amerindian variants in Mapuche (35%) and Tehuelche (22%). We compared our data with those obtained in six indigenous groups of the Argentinean Chaco region and in a sample from Buenos Aires City. The genetic distance dendrogram showed a clear-cut division between the Patagonian and Chaco populations, which formed two different clusters. In spite of their linguistic differences, it can be inferred that the biological affinities observed are in concordance with the geographic distributions and interethnic relations established among the groups studied.
RESUMO
As in other Latin American populations, Argentinians are the result of the admixture amongst different continental groups, mainly from America and Europe, and to a lesser extent from Sub-Saharan Africa. However, it is known that the admixture processes did not occur homogeneously throughout the country. Therefore, considering the importance for anthropological, medical and forensic researches, this study aimed to investigate the population genetic structure of the Argentinian Patagonia, through the analysis of 46 ancestry informative markers, in 433 individuals from five different localities. Overall, in the Patagonian sample, the average individual ancestry was estimated as 35.8% Native American (95% CI: 32.2-39.4%), 62.1% European (58.5-65.7%) and 2.1% African (1.7-2.4%). Comparing the five localities studied, statistically significant differences were observed for the Native American and European contributions, but not for the African ancestry. The admixture results combined with the genealogical information revealed intra-regional variations that are consistent with the different geographic origin of the participants and their ancestors. As expected, a high European ancestry was observed for donors with four grandparents born in Europe (96.8%) or in the Central region of Argentina (85%). In contrast, the Native American ancestry increased when the four grandparents were born in the North (71%) or in the South (61.9%) regions of the country, or even in Chile (60.5%). In summary, our results showed that differences on continental ancestry contribution have different origins in each region in Patagonia, and even in each locality, highlighting the importance of knowing the origin of the participants and their ancestors for the correct interpretation and contextualization of the genetic information.
Assuntos
Etnicidade/genética , Genética Populacional/estatística & dados numéricos , Argentina/etnologia , População Negra , Humanos , Indígenas Norte-Americanos , Linhagem , População BrancaRESUMO
The aim of this study is to estimate the gene admixture in the population of Buenos Aires City from samples of blood donors, which come from a public health centre (Hospital de Clínicas). These studies were performed on 218 unrelated people, who donated blood during the year 2002. Eight erythrocyte genetic systems and GM/KM allotypes were analysed. A survey to obtain information about place of birth, present residence and genealogical data of the donors was performed. The gene frequencies were determined using a method of maximum likelihood. The genetic admixture was calculated through the ADMIX program (trihibride). The Amerindian and African contributions were 15.8% and 4.3% respectively. These data were compared with those obtained in a previous study performed in a private centre (Hospital Italiano de Buenos Aires) and significant differences were observed, except in the KM system. The results obtained are in concordance with the demographic and historic information of Buenos Aires City.
Assuntos
Frequência do Gene , Testes Genéticos , África/etnologia , Argentina/etnologia , Emigração e Imigração , Europa (Continente)/etnologia , Feminino , Marcadores Genéticos , Genética Populacional , Humanos , Indígenas Sul-Americanos/genética , MasculinoRESUMO
The population of Argentina today does not have a "visible" black African component. However, censuses conducted during most of the 19th century registered up to 30% of individuals of African origin living in Buenos Aires city. What has happened to this African influence? Have all individuals of African origin died, as lay people believe? Or is it possible that admixture with the European immigrants made the African influence "invisible?" We investigated the African contribution to the genetic pool of the population of Buenos Aires, Argentina, typing 12 unlinked autosomal DNA markers in a sample of 90 individuals. The results of this analysis suggest that 2.2% (SEM=0.9%) of the genetic ancestry of the Buenos Aires population is derived from Africa. Our analysis of individual admixture shows that those alleles that have a high frequency in populations of African origin tend to concentrate among 8 individuals in our sample. Therefore, although the admixture estimate is relatively low, the actual proportion of individuals with at least some African influence is approximately 10%. The evidence we are presenting of African ancestry is consistent with the known historical events that led to the drastic reduction of the Afro-Argentine population during the second half of the 19th century. However, as our results suggest, this reduction did not mean a total disappearance of African genes from the genetic pool of the Buenos Aires population.
Assuntos
População Negra/genética , Etnicidade/genética , Variação Genética/genética , África/etnologia , Argentina/epidemiologia , Frequência do Gene , Genética Populacional/métodos , Humanos , Análise de Sequência de DNARESUMO
The immune response of relatively small, endogamous populations is of special interest, because they may differ from those of large, ethnically diverse, urban groups. As a contribution to this area of investigation, we tested 99 individuals from two Brazilian native populations for two T-cell receptor gene segments (TCRBV3S1 and TCRBV18) and 241 subjects from eight tribes of this ethnic group in relation to the chemokine receptor CCR5delta32 allele. Differences in TCRBV3S1 and TCRBV18 prevalences of the Amerindians in relation to European- and African-derived individuals were not marked. We confirmed the absence of the CCR5delta32 allele in most groups, its presence in the Mura and Kaingang, probably because of European gene introgression.
Assuntos
DNA/genética , Variação Genética , Indígenas Sul-Americanos/genética , Receptores de Antígenos de Linfócitos T/genética , Receptores de Quimiocinas/genética , Idoso , Idoso de 80 Anos ou mais , Alelos , Brasil/etnologia , Frequência do Gene , Marcadores Genéticos , Humanos , Reação em Cadeia da Polimerase , Receptores de Antígenos de Linfócitos T/sangue , Receptores de Quimiocinas/sangueRESUMO
The major histocompatibility complex (MHC) is one of the biological systems of major polymorphisms. The study of HLA class II variability has allowed the identification of several alleles that are characteristic to Amerindian populations, and it is an excellent tool to define the relations and biological affinities among them. In this work, we analyzed the allelic distribution of the HLA-DRB1 class II locus in four Amerindian populations: Mapuche (n = 34) and Tehuelche (n = 23) from the Patagonian region of Argentina, and Wichi SV (n = 24) and Lengua (n = 17) from the Argentinean and Paraguayan Chaco regions, respectively. In all of these groups, relatively high frequencies of Amerindian HLA-DRB1 alleles were observed (DRB1*0403, DRB1*0407, DRB1*0411, DRB1*0417, DRB1*0802, DRB1*0901, DRB1*1402, DRB1*1406 and DRB1*1602). However, we also detected the presence of non-Amerindian variants in Mapuche (35 percent) and Tehuelche (22 percent). We compared our data with those obtained in six indigenous groups of the Argentinean Chaco region and in a sample from Buenos Aires City. The genetic distance dendrogram showed a clear-cut division between the Patagonian and Chaco populations, which formed two different clusters. In spite of their linguistic differences, it can be inferred that the biological affinities observed are in concordance with the geographic distributions and interethnic relations established among the groups studied.
RESUMO
Este estudio tiene como objetivo estimar la mezcla génica en la población de la Ciudad de BuenosAires, a partir de muestras de dadores de sangre provenientes de un centro público de salud (Hospitalde Clínicas). Los estudios se realizaron sobre 218 personas no emparentadas que donaron su sangre duranteel año 2002. Se analizaron 8 sistemas genéticos eritrocitarios y los alotipos GM/KM. Se realizó una encuestacon la finalidad de obtener información sobre lugar de nacimiento, residencia actual y datos genealógicosde los dadores. Las frecuencias génicas se determinaron empleando métodos de máxima verosimilitud. Paracalcular la mezcla génica se aplicó el programa ADMIX (trihíbrido). Se registró un 15.8% de aporte indígena(AI) y 4.3% de africano (AA). Estos datos se compararon con un estudio previo realizado en un centro privado(Hospital Italiano de Buenos Aires), no observándose diferencias significativas salvo en el sistema Km. Los resultadosobtenidos se corresponden con la información histórica y demográfica de la ciudad de Buenos Aires.
The aim of this study is to estimatethe gene admixture in the population of Buenos Aires City from samples of blood donors, whichcome from a public health centre (Hospital de Clínicas). These studies were performed on 218 unrelated people,who donated blood during the year 2002. Eight erythrocyte genetic systems and GM/KM allotypes were analysed.A survey to obtain information about place of birth, present residence and genealogical data of the donors wasperformed. The gene frequencies were determined using a method of maximum likelihood. The genetic admixturewas calculated through the ADMIX program (trihibride). The Amerindian and African contributions were 15.8%and 4.3% respectively. These data were compared with those obtained in a previous study performed in a privatecentre (Hospital Italiano de Buenos Aires) and significant differences were observed, except in the KM system.The results obtained are in concordance with the demographic and historic information of Buenos Aires City.
Assuntos
Humanos , Masculino , Feminino , Frequência do Gene , Testes Genéticos , Hispânico ou Latino/genética , Argentina , África/etnologia , Doadores de Sangue , Europa (Continente)/etnologia , Marcadores Genéticos , Genética Populacional , Indígenas Sul-Americanos/genética , LinhagemRESUMO
The allelic variability of four dinucleotide microsatellites located in the HLA region (MOGc, D6S265, MIB, and TNFa) was analyzed in 67 individuals representing three Amerindian populations of the Argentine Gran Chaco: Toba, Wichi and Chorote. Genomic DNA was prepared from peripheral blood and DNA was extracted using the standard phenol-chloroform procedure. Alleles were identified by PCR, using an end-labelled reverse oligonucleotide primer (fluorescent 6 - Fam labeling). Despite the low number of samples studied, a high level of gene diversity was observed in each population and for each locus. Moreover, the mean number of alleles was 7.7, 5.3, 10.0, and 7.0 at loci MOGc, D6S265, MIB and TNFa, respectively. Differentiation tests between pairs of populations showed a clear differentiation between the Wichi and the other two groups. However, the proportion of the total genetic variability that is due to differences among populations, estimated by the Gst' index, was relatively low (6 percent). Almost all the genetic variation occurred at the intra-population level (96 percent). The high intra-populational genetic variation suggests the existence of an intensive gene flow among the Gran Chaco tribes. Historical information seems to confirm this result.
Assuntos
Humanos , Argentina , DNA , Indígenas Sul-Americanos , Repetições de Microssatélites , Variação Genética , Genética Populacional , Genoma , Reação em Cadeia da PolimeraseRESUMO
Dados relativos a fertilidade, mortalidade e migraçäo de quatro comunidades de índios Mapuche localizadas em uma área linear na direçäo nordeste-sudoeste com 215 km de extensäo na Província de Rio Negro, Argentina, foram associados com a informaçäo genética fornecida por nove sistemas de grupos sangüíneos e os haplogrupos do DNA mitocondrial. Ambos os tipos de informaçäo apontam claramente para uma dicotomia, as quatro populaçöes sendo divididas em grupos de duas. O principal fator responsável por esta separaçäo é provavelmente graus diferentes de mistura com näo-índios. A variabilidade genética total foi muito similar em todos os grupos, aquela entre populações sendo de apenas 10 por cento deste valor. Foi confirmada a baixa prevalência do antígeno Diego(a) entre os Mapuche. O fato de que heterogeneidade genética significativa e conjuntos populacionais diversos foram observados em uma regiäo territorial täo pequena demonstra a sensibilidade dos enfoques demográfico e genético no esclarecimento da história humana.
Assuntos
Humanos , Genética Populacional , Indígenas Sul-Americanos/genética , Argentina , Demografia , Variação Genética , Etnicidade/genética , Haplótipos/genéticaRESUMO
Haplótipos derivados de cinco sítios de restriçäo polimórficos presentes no agrupamento da globina beta foram investigados em 86 cromossomos da populaçäo Mapuche da Argentina. Esses resultados foram analisados em conjunto com os previamente obtidos para dez tribos indígenas brasileiras. Oito haplótipos foram identificados, dos quais os mais freqüêntes foram o 2 (57 por cento) e o 6 (27 por cento). A presença do haplótipo 3 em 2 por cento dos cromossomos dos Mapuches é uma evidência de mistura com indivíduos de ancestralidade africana. Devido ao alto número de haplótipos, a heterozigosidade medida pelo índice Gini-Simpson é mais alta nos Mapuches do que nos índios brasileiros. A distribuçäo haplotípica nos Mapuches é também significativamente diferente da observada nas tribos brasileiras. Essa heterogeneidade poderia ser parcialmente explicada pela mistura com populaçöes näo-indígenas.
Assuntos
Humanos , Globinas/genética , Haplótipos/genética , Indígenas Sul-Americanos , Argentina , Variação Genética , Genética Populacional , Polimorfismo Genético , Reação em Cadeia da PolimeraseRESUMO
Growth in schoolchildren of Villa IAPI--a poor neighborhood placed near Buenos Aires (Argentina)--were cross-sectionally studied. Six hundred and forty five--291 males and 354 females--children from six to twelve years old were weighed (W), and the standing (StH) and sitting (SiH) heights, the head (HC) and the arm (AC) circumferences, and the triceps (TS) an the subscapular (SS) skinfolds were measured. The muscular braquial circumference (MC), and the length of the inferior segment of the body (IS) were also calculated. All of the measurements were transformed to "z" scores. It was observed that in all cases--except for 11 year-old females--both W and StH were diminished. This trend was stronger in males than in females. Both SiH an HC did not show differences with respect to local growth standards. Skinfold values however, were always greater in Villa IAPI children--except SS in 9 to 12 year-old males, and in 12 year-old females--than those of normal standards, Such differential growth pattern suggests that two joined strategies--for protection and adaption to unbalanced environment--actually acted in the Villa IAPI population.