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1.
Nature ; 596(7873): 543-547, 2021 08.
Artigo em Inglês | MEDLINE | ID: mdl-34433944

RESUMO

Much remains unknown about the population history of early modern humans in southeast Asia, where the archaeological record is sparse and the tropical climate is inimical to the preservation of ancient human DNA1. So far, only two low-coverage pre-Neolithic human genomes have been sequenced from this region. Both are from mainland Hòabìnhian hunter-gatherer sites: Pha Faen in Laos, dated to 7939-7751 calibrated years before present (yr cal BP; present taken as AD 1950), and Gua Cha in Malaysia (4.4-4.2 kyr cal BP)1. Here we report, to our knowledge, the first ancient human genome from Wallacea, the oceanic island zone between the Sunda Shelf (comprising mainland southeast Asia and the continental islands of western Indonesia) and Pleistocene Sahul (Australia-New Guinea). We extracted DNA from the petrous bone of a young female hunter-gatherer buried 7.3-7.2 kyr cal BP at the limestone cave of Leang Panninge2 in South Sulawesi, Indonesia. Genetic analyses show that this pre-Neolithic forager, who is associated with the 'Toalean' technocomplex3,4, shares most genetic drift and morphological similarities with present-day Papuan and Indigenous Australian groups, yet represents a previously unknown divergent human lineage that branched off around the time of the split between these populations approximately 37,000 years ago5. We also describe Denisovan and deep Asian-related ancestries in the Leang Panninge genome, and infer their large-scale displacement from the region today.


Assuntos
DNA Antigo/análise , Fósseis , Genoma Humano/genética , Genômica , Ilhas/etnologia , Filogenia , Sudeste Asiático , Austrália , Osso e Ossos/metabolismo , Cavernas , Feminino , História Antiga , Migração Humana/história , Humanos , Indonésia/etnologia , Nova Guiné
2.
Int J Lang Commun Disord ; 53(3): 643-655, 2018 05.
Artigo em Inglês | MEDLINE | ID: mdl-29575355

RESUMO

BACKGROUND: It has been reported that the inhabitants of the Chilean Robinson Crusoe Island have an increased frequency of specific language impairment (SLI) or developmental language disorder (DLD). AIMS: To explore the familial aggregation of DLD in this community. METHODS & PROCEDURES: We assessed the frequency of DLD amongst colonial children between the ages of 3 and 8;11 years (50 individuals from 45 nuclear families). Familial aggregation rates of language disorder were calculated by assessing all available first-degree relatives (n = 107, 77 parents, 25 siblings, five half-siblings) of the probands. OUTCOMES & RESULTS: We found that 71% of the child population performed significantly below expected in measures of phonological production or expressive and receptive morphology. The majority of these children presented with severe expressive and/or receptive language difficulties. One-quarter of language-disordered probands primarily had phonological difficulties. Family members of affected probands experienced a higher risk of language disorder than those of typically developing probands. This increased risk was apparent regardless of non-verbal IQ. CONCLUSIONS & IMPLICATIONS: The study substantiates the existence of a familial form of speech and language disorder on Robinson Crusoe Island. Furthermore, we find that the familiarity is stable regardless of non-verbal IQ, supporting the recent movement to reduce the importance of non-verbal IQ criterion in DLD diagnoses.


Assuntos
Transtornos do Desenvolvimento da Linguagem/epidemiologia , Criança , Pré-Escolar , Chile/epidemiologia , Chile/etnologia , Feminino , Humanos , Ilhas/epidemiologia , Ilhas/etnologia , Transtornos do Desenvolvimento da Linguagem/etnologia , Transtornos do Desenvolvimento da Linguagem/genética , Masculino , Linhagem , Irmãos , Isolamento Social
3.
PLoS Genet ; 14(1): e1007152, 2018 01.
Artigo em Inglês | MEDLINE | ID: mdl-29370172

RESUMO

Previous studies of the genetic landscape of Ireland have suggested homogeneity, with population substructure undetectable using single-marker methods. Here we have harnessed the haplotype-based method fineSTRUCTURE in an Irish genome-wide SNP dataset, identifying 23 discrete genetic clusters which segregate with geographical provenance. Cluster diversity is pronounced in the west of Ireland but reduced in the east where older structure has been eroded by historical migrations. Accordingly, when populations from the neighbouring island of Britain are included, a west-east cline of Celtic-British ancestry is revealed along with a particularly striking correlation between haplotypes and geography across both islands. A strong relationship is revealed between subsets of Northern Irish and Scottish populations, where discordant genetic and geographic affinities reflect major migrations in recent centuries. Additionally, Irish genetic proximity of all Scottish samples likely reflects older strata of communication across the narrowest inter-island crossing. Using GLOBETROTTER we detected Irish admixture signals from Britain and Europe and estimated dates for events consistent with the historical migrations of the Norse-Vikings, the Anglo-Normans and the British Plantations. The influence of the former is greater than previously estimated from Y chromosome haplotypes. In all, we paint a new picture of the genetic landscape of Ireland, revealing structure which should be considered in the design of studies examining rare genetic variation and its association with traits.


Assuntos
Variação Genética , Migração Humana , População Branca/genética , Etnicidade/genética , Etnicidade/história , Genética Populacional , Estudo de Associação Genômica Ampla , Genômica , História Antiga , Migração Humana/história , Humanos , Irlanda , Ilhas/etnologia , Dinâmica Populacional , Migrantes , Reino Unido , População Branca/história
4.
Ann Hum Biol ; 44(5): 467-474, 2017 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-27670224

RESUMO

BACKGROUND: Investigation of allele and genotype frequencies of microsatellite loci in various populations is an essential pre-requisite in forensic application. AIM: The present study obtained population genetic data and forensic parameters of 39 autosomal Short Tandem Repeats (STRs) loci from a Chinese Li ethnic group and estimated the genetic relationships between Li and other reference populations. SUBJECTS AND METHODS: Thirty-nine STR loci, which include D19S433, D5S818, D21S11, D18S51, D6S1043, D3S1358, D13S317, D7S820, D16S539, CSF1PO, Penta D, D2S441, vWA, D8S1179, TPOX, Penta E, TH01, D12S391, D2S1338, FGA, D6S477, D18S535, D19S253, D15S659, D11S2368, D20S470, D1S1656, D22-GATA198B05, D8S1132, D4S2366, D21S1270, D13S325, D9S925, D3S3045, D14S608, D10S1435, D7S3048, D17S1290 and D5S2500, were amplified in two multiplex DNA-STR fluorescence detection systems for 189 unrelated healthy individuals of the Chinese Li ethnic group. The allele frequency distribution and several parameters commonly used in forensic science were statistically analysed. RESULTS: A total of 378 alleles were observed with corresponding allelic frequencies ranging from 0.0026-0.5899. The power of discrimination and power of exclusion ranged from 0.7569-0.9672 and 0.2513-0.7355, respectively. The power of exclusion (PE) ranged from 0.2580-0.7943 for trio paternity cases and 0.1693-0.5940 for duo paternity cases. The polymorphism information content (PIC) ranged from 0.5001-0.8611. The cumulative match probability across these 39 loci was 2.4242 × 10-38. CONCLUSION: The results indicate that 39 STR loci are polymorphic among the Li ethnic group in Hainan Island in the South China Sea. This set of polymorphic STR loci provide highly polymorphic information and forensic efficiency for forensic individual identification and paternity testing, as well as basic population data for population genetics and anthropological research.


Assuntos
Etnicidade/genética , Frequência do Gene , Genótipo , Ilhas/etnologia , Repetições de Microssatélites/genética , Polimorfismo Genético/genética , China/etnologia , Humanos
5.
Coll Antropol ; 36(4): 1139-42, 2012 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23390803

RESUMO

Although Croatia is divided into continental and insular subpopulation which practice different dietary habits, a general shift in nutritional habits has been observed in the direction of globalization, including considerably higher intake of red meat, saturated fatty acids, milk, dairies etc. and accompanied by a decrease in physical activity. These relatively abrupt changes have had an especially significant impact on the insular populations, known for their traditional Mediterranean diet and have led to the increased prevalence of hypertension, metabolic syndrome, diabetes mellitus, coronary heart diseases etc. on Croatian islands. Since the expression of genes responsible for the occurrence of complex diseases can be enhanced in isolated populations due to the effect of evolutionary forces, genetic-epidemiological research in population isolates is of great importance, giving us insight into the interplay between intrinsic (genes) and extrinsic risk factors (diet) for disease development.


Assuntos
Doença Crônica/etnologia , Dieta Mediterrânea/etnologia , Comportamento Alimentar/etnologia , Internacionalidade , Ilhas/etnologia , Doença Crônica/prevenção & controle , Croácia , Humanos , Fatores de Risco
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