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1.
Genomics ; 112(1): 442-458, 2020 01.
Artigo em Inglês | MEDLINE | ID: mdl-30902755

RESUMO

The Russian Federation is the largest and one of the most ethnically diverse countries in the world, however no centralized reference database of genetic variation exists to date. Such data are crucial for medical genetics and essential for studying population history. The Genome Russia Project aims at filling this gap by performing whole genome sequencing and analysis of peoples of the Russian Federation. Here we report the characterization of genome-wide variation of 264 healthy adults, including 60 newly sequenced samples. People of Russia carry known and novel genetic variants of adaptive, clinical and functional consequence that in many cases show allele frequency divergence from neighboring populations. Population genetics analyses revealed six phylogeographic partitions among indigenous ethnicities corresponding to their geographic locales. This study presents a characterization of population-specific genomic variation in Russia with results important for medical genetics and for understanding the dynamic population history of the world's largest country.


Assuntos
Variação Genética , Adulto , Doenças Transmissíveis/genética , Demografia , Haplótipos , Humanos , Mutação INDEL , Farmacogenética , Fenótipo , Filogeografia , Polimorfismo de Nucleotídeo Único , Federação Russa/etnologia , Seleção Genética , Sequenciamento Completo do Genoma
2.
Mol Biol Evol ; 33(7): 1777-95, 2016 07.
Artigo em Inglês | MEDLINE | ID: mdl-26993256

RESUMO

Although Siberia was inhabited by modern humans at an early stage, there is still debate over whether it remained habitable during the extreme cold of the Last Glacial Maximum or whether it was subsequently repopulated by peoples with recent shared ancestry. Previous studies of the genetic history of Siberian populations were hampered by the extensive admixture that appears to have taken place among these populations, because commonly used methods assume a tree-like population history and at most single admixture events. Here we analyze geogenetic maps and use other approaches to distinguish the effects of shared ancestry from prehistoric migrations and contact, and develop a new method based on the covariance of ancestry components, to investigate the potentially complex admixture history. We furthermore adapt a previously devised method of admixture dating for use with multiple events of gene flow, and apply these methods to whole-genome genotype data from over 500 individuals belonging to 20 different Siberian ethnolinguistic groups. The results of these analyses indicate that there have been multiple layers of admixture detectable in most of the Siberian populations, with considerable differences in the admixture histories of individual populations. Furthermore, most of the populations of Siberia included here, even those settled far to the north, appear to have a southern origin, with the northward expansions of different populations possibly being driven partly by the advent of pastoralism, especially reindeer domestication. These newly developed methods to analyze multiple admixture events should aid in the investigation of similarly complex population histories elsewhere.


Assuntos
Povo Asiático/genética , Genética Populacional/métodos , Evolução Biológica , Evolução Molecular , Fluxo Gênico , Variação Genética , Genômica , Haplótipos , Humanos , Filogenia , Filogeografia/métodos , Polimorfismo de Nucleotídeo Único , Sibéria
3.
J Neurol Sci ; 384: 84-88, 2018 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-29249384

RESUMO

Viliuisk encephalomyelitis (VE) is a neurodegenerative disease that afflicts aboriginal people of Yakutia in Siberia with unknown etiology. Oligoclonal IgG bands (OCBs) were discovered in the VE patients (Green et al., 2003). In this study we analysed the association of OCBs with clinical symptoms in 58 VE patients. Positive oligoclonal IgG are associated with a shorter duration of disease (p=0.002), older age of onset (p=0.023) and high frequency of main neurological VE symptoms such as dementia, frontal dysbasia, bulbar disorders, muscle atrophy and centrally caused pelvic disorders. Our results show that the OCBs in VE patients are associated with more severe central nervous system (CNS) damage and may cause secondary complications in the course of the disease.


Assuntos
Encefalomielite/fisiopatologia , Imunoglobulina G/biossíntese , Imunoglobulina G/líquido cefalorraquidiano , Bandas Oligoclonais/biossíntese , Bandas Oligoclonais/líquido cefalorraquidiano , Adulto , Fatores Etários , Idoso , Encéfalo/diagnóstico por imagem , Doença Crônica , Progressão da Doença , Encefalomielite/diagnóstico por imagem , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Testes de Estado Mental e Demência , Pessoa de Meia-Idade , Índice de Gravidade de Doença
4.
J Neurol Sci ; 212(1-2): 69-73, 2003 Aug 15.
Artigo em Inglês | MEDLINE | ID: mdl-12810001

RESUMO

Viliuisk encephalomyelitis (VE) is a neurodegenerative disorder expressed as subacute meningo-encephalitis progressing to a more prolonged pan-encephalitic syndrome with a fatal outcome within 1 to 10 years. Some patients survive to a steady state of global dementia and severe spasticity that may last for over 20 years. Multiple micronecrotic foci surrounded by inflammatory infiltrates are observed throughout the cerebral cortex and other gray matter areas. Infectious etiology of VE is strongly suspected, but the causative agent has not been identified. We conducted a search for assays that might be helpful for VE diagnosis and established for the first time that the majority of patients with definite VE show evidence for intrathecal IgG synthesis correlating with the clinical manifestations of the disease. This indicates that the detection of oligoclonal IgG banding in the cerebrospinal fluid is a valuable diagnostic assay for VE. Implications of these findings for a possible etiology of VE are discussed.


Assuntos
Encefalomielite/imunologia , Imunoglobulinas/metabolismo , Adulto , Idade de Início , Idoso , Idoso de 80 Anos ou mais , Western Blotting/métodos , Córtex Cerebral/patologia , Encefalomielite/sangue , Encefalomielite/líquido cefalorraquidiano , Feminino , Humanos , Imunoglobulinas/imunologia , Focalização Isoelétrica/métodos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Bandas Oligoclonais , Valores de Referência , Sensibilidade e Especificidade
5.
PLoS One ; 9(2): e84670, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24586232

RESUMO

BACKGROUND: Viliuisk encephalomyelitis (VE) is an endemic neurological disease in Northeast Siberia and generally considered to be a chronic encephalomyelitis of unknown origin actually spreading in the Sakha (Yakutian) Republic. METHODOLOGY AND PRINCIPLE FINDINGS: In search for the pathophysiology and causative agent of VE, we performed a cross-sectional study on clinical, serological and neuroimaging data on chronic VE patients during two medical expeditions to three villages within the Viliuiski river basin in the Republic of Sakha in 2000 and to the capital Yakutsk in 2006. The severity of the core clinical picture with predominant sensory ataxia, gait apraxia, lower limb spasticity, cognitive impairment and bladder dysfunction correlated with the degree of MRI findings showing enlargement of inner ventricular spaces as in communicating hydrocephalus. Laboratory studies revealed transient eosinophilia during the preceding acute meningitis-like phase, but no ongoing inflammatory process in the CSF. We found immune reactions against Toxocara canis in the majority of chronic VE patients but rarely in controls (P = 0.025; Fisher's exact test). Histological analysis of subacute to subchronic VE brain samples showed eosinophilic infiltrations with no signs of persistent Toxocara canis infection. CONCLUSIONS AND SIGNIFICANCE: Our data showed that pressure by the communicating hydrocephalus as a mechanical factor is the major pathogenic mechanism in chronic VE, most likely triggered by eosinophilic meningitis. There are no signs for an ongoing inflammatory process in chronic VE. The past eosinophilic reaction in VE might be caused by Toxocara ssp. infection and might therefore represent the first hint for an initial cause leading to the development of chronic VE. Our data provide a framework for future studies and potential therapeutic interventions for this enigmatic epidemic neurological disease potentially spreading in Sakha Republic.


Assuntos
Encefalomielite/fisiopatologia , Hidrocefalia/fisiopatologia , Meningite/fisiopatologia , Adolescente , Adulto , Idoso , Estudos Transversais , Eletrofisiologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Sibéria , Adulto Jovem
6.
PLoS One ; 8(12): e83570, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24349531

RESUMO

Evenks and Evens, Tungusic-speaking reindeer herders and hunter-gatherers, are spread over a wide area of northern Asia, whereas their linguistic relatives the Udegey, sedentary fishermen and hunter-gatherers, are settled to the south of the lower Amur River. The prehistory and relationships of these Tungusic peoples are as yet poorly investigated, especially with respect to their interactions with neighbouring populations. In this study, we analyse over 500 complete mtDNA genome sequences from nine different Evenk and even subgroups as well as their geographic neighbours from Siberia and their linguistic relatives the Udegey from the Amur-Ussuri region in order to investigate the prehistory of the Tungusic populations. These data are supplemented with analyses of Y-chromosomal haplogroups and STR haplotypes in the Evenks, Evens, and neighbouring Siberian populations. We demonstrate that whereas the North Tungusic Evenks and Evens show evidence of shared ancestry both in the maternal and in the paternal line, this signal has been attenuated by genetic drift and differential gene flow with neighbouring populations, with isolation by distance further shaping the maternal genepool of the Evens. The Udegey, in contrast, appear quite divergent from their linguistic relatives in the maternal line, with a mtDNA haplogroup composition characteristic of populations of the Amur-Ussuri region. Nevertheless, they show affinities with the Evenks, indicating that they might be the result of admixture between local Amur-Ussuri populations and Tungusic populations from the north.


Assuntos
Povo Asiático , Cromossomos Humanos Y/genética , DNA Mitocondrial/genética , Povo Asiático/etnologia , Povo Asiático/genética , Humanos , Masculino , Sibéria/etnologia
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