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1.
PLoS One ; 15(4): e0231009, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32240264

RESUMO

Our study is focused on original and publicly accessible data on the intraspecific variability of the barcoding DNA fragment in ladybirds Harmonia axyridis Pall analysis. The complete dataset consists of 39 haplotypes, 16 of which we identified for the first time. The intra-population and geographical variability of the barcoding fragment was studied for seven populations of the western and eastern groups of the native range and in six invasive populations, in which 25 of the 39 haplotypes are found. Population structure inferred on base of molecular variability and haplotype frequencies showed a high level of differences between the eastern and western groups of native populations and confirm the hypothesis of the origin of all invasive populations from native populations of the eastern group. A comparative analysis of molecular variation indices testifies to various evolutionary scenarios of the formation of the western and eastern groups of native populations and confirms the hypothesis of the microevolutionary history of the species, previously suggested in morphological character based studies of the geographical variability of H. axyridis. A significant decrease in the molecular diversity of invasive populations confirms the hypothesis of a random nature of the primary invasion of this species in North America.


Assuntos
Besouros/genética , Genes Mitocondriais/genética , Variação Genética/genética , Animais , Evolução Biológica , Genética Populacional/métodos , Haplótipos/genética , Espécies Introduzidas , América do Norte
2.
PLoS One ; 7(2): e32179, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22363811

RESUMO

With the aim of uncovering all of the most basal variation in the northern Asian mitochondrial DNA (mtDNA) haplogroups, we have analyzed mtDNA control region and coding region sequence variation in 98 Altaian Kazakhs from southern Siberia and 149 Barghuts from Inner Mongolia, China. Both populations exhibit the prevalence of eastern Eurasian lineages accounting for 91.9% in Barghuts and 60.2% in Altaian Kazakhs. The strong affinity of Altaian Kazakhs and populations of northern and central Asia has been revealed, reflecting both influences of central Asian inhabitants and essential genetic interaction with the Altai region indigenous populations. Statistical analyses data demonstrate a close positioning of all Mongolic-speaking populations (Mongolians, Buryats, Khamnigans, Kalmyks as well as Barghuts studied here) and Turkic-speaking Sojots, thus suggesting their origin from a common maternal ancestral gene pool. In order to achieve a thorough coverage of DNA lineages revealed in the northern Asian matrilineal gene pool, we have completely sequenced the mtDNA of 55 samples representing haplogroups R11b, B4, B5, F2, M9, M10, M11, M13, N9a and R9c1, which were pinpointed from a massive collection (over 5000 individuals) of northern and eastern Asian, as well as European control region mtDNA sequences. Applying the newly updated mtDNA tree to the previously reported northern Asian and eastern Asian mtDNA data sets has resolved the status of the poorly classified mtDNA types and allowed us to obtain the coalescence age estimates of the nodes of interest using different calibrated rates. Our findings confirm our previous conclusion that northern Asian maternal gene pool consists of predominantly post-LGM components of eastern Asian ancestry, though some genetic lineages may have a pre-LGM/LGM origin.


Assuntos
Povo Asiático/genética , DNA Mitocondrial/genética , Etnicidade/genética , Genética Populacional , Haplótipos/genética , População Branca/genética , Ásia , Europa (Continente) , Variação Genética , Humanos , Dados de Sequência Molecular , Filogenia , Filogeografia , Análise de Componente Principal
3.
Ann Hum Genet ; 74(6): 539-46, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20726964

RESUMO

To reconstruct the phylogenetic structure of Y-chromosome haplogroup (hg) C in populations of northern Eurasia, we have analyzed the diversity of microsatellite (STR) loci in a total sample of 413 males from 18 ethnic groups of Siberia, Eastern Asia and Eastern Europe. Analysis of SNP markers revealed that all Y-chromosomes studied belong to hg C3 and its subhaplogroups C3c and C3d, although some populations (such as Mongols and Koryaks) demonstrate a relatively high input (more than 30%) of yet unidentified C3* haplotypes. Median joining network analysis of STR haplotypes demonstrates that Y-chromosome gene pools of populations studied are characterized by the presence of DNA clusters originating from a limited number of frequent founder haplotypes. These are subhaplogroup C3d characteristic for Mongolic-speaking populations, "star cluster" in C3* paragroup, and a set of DYS19 duplicated C3c Y-chromosomes. All these DNA clusters show relatively recent coalescent times (less than 3000 years), so it is probable that founder effects, including social selection resulting in high male fertility associated with a limited number of paternal lineages, may explain the observed distribution of hg C3 lineages.


Assuntos
Cromossomos Humanos Y/genética , Haplótipos , Filogeografia , Etnicidade/genética , Europa Oriental , Ásia Oriental , Variação Genética , Humanos , Masculino , Repetições de Microssatélites , Polimorfismo de Nucleotídeo Único , Sibéria
4.
PLoS One ; 5(12): e15214, 2010 Dec 21.
Artigo em Inglês | MEDLINE | ID: mdl-21203537

RESUMO

More than a half of the northern Asian pool of human mitochondrial DNA (mtDNA) is fragmented into a number of subclades of haplogroups C and D, two of the most frequent haplogroups throughout northern, eastern, central Asia and America. While there has been considerable recent progress in studying mitochondrial variation in eastern Asia and America at the complete genome resolution, little comparable data is available for regions such as southern Siberia--the area where most of northern Asian haplogroups, including C and D, likely diversified. This gap in our knowledge causes a serious barrier for progress in understanding the demographic pre-history of northern Eurasia in general. Here we describe the phylogeography of haplogroups C and D in the populations of northern and eastern Asia. We have analyzed 770 samples from haplogroups C and D (174 and 596, respectively) at high resolution, including 182 novel complete mtDNA sequences representing haplogroups C and D (83 and 99, respectively). The present-day variation of haplogroups C and D suggests that these mtDNA clades expanded before the Last Glacial Maximum (LGM), with their oldest lineages being present in the eastern Asia. Unlike in eastern Asia, most of the northern Asian variants of haplogroups C and D began the expansion after the LGM, thus pointing to post-glacial re-colonization of northern Asia. Our results show that both haplogroups were involved in migrations, from eastern Asia and southern Siberia to eastern and northeastern Europe, likely during the middle Holocene.


Assuntos
DNA Mitocondrial/genética , Filogeografia , Ásia , Povo Asiático/genética , Emigração e Imigração , Feminino , Variação Genética , Genética Populacional , Haplótipos , Humanos , Filogenia , Análise de Sequência de DNA
5.
Am J Hum Genet ; 81(5): 1025-41, 2007 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-17924343

RESUMO

To elucidate the human colonization process of northern Asia and human dispersals to the Americas, a diverse subset of 71 mitochondrial DNA (mtDNA) lineages was chosen for complete genome sequencing from the collection of 1,432 control-region sequences sampled from 18 autochthonous populations of northern, central, eastern, and southwestern Asia. On the basis of complete mtDNA sequencing, we have revised the classification of haplogroups A, D2, G1, M7, and I; identified six new subhaplogroups (I4, N1e, G1c, M7d, M7e, and J1b2a); and fully characterized haplogroups N1a and G1b, which were previously described only by the first hypervariable segment (HVS1) sequencing and coding-region restriction-fragment-length polymorphism analysis. Our findings indicate that the southern Siberian mtDNA pool harbors several lineages associated with the Late Upper Paleolithic and/or early Neolithic dispersals from both eastern Asia and southwestern Asia/southern Caucasus. Moreover, the phylogeography of the D2 lineages suggests that southern Siberia is likely to be a geographical source for the last postglacial maximum spread of this subhaplogroup to northern Siberia and that the expansion of the D2b branch occurred in Beringia ~7,000 years ago. In general, a detailed analysis of mtDNA gene pools of northern Asians provides the additional evidence to rule out the existence of a northern Asian route for the initial human colonization of Asia.


Assuntos
Povo Asiático/genética , DNA Mitocondrial/genética , Geografia , Filogenia , Ásia , Variação Genética , Haplótipos , Humanos , Dados de Sequência Molecular , Análise de Componente Principal , Análise de Sequência de DNA , População Branca/genética
6.
J Hum Genet ; 52(9): 763-770, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17703276

RESUMO

In order to reconstruct the history of Y-chromosome haplogroup (hg) N dispersals in north Eurasia, we have analyzed the diversity of microsatellite (STR) loci within two major hg N clades, N2 and N3, in a total sample of 1,438 males from 17 ethnic groups, mainly of Siberian and Eastern European origin. Based on STR variance analysis we observed that hg N3a is more diverse in Eastern Europe than in south Siberia. However, analysis of median networks showed that there are two STR subclusters of hg N3a, N3a1 and N3a2, that are characterized by different genetic histories. Age calculation of STR variation within subcluster N3a1 indicated that its first expansion occurred in south Siberia [approximately 10,000 years (ky)] and then this subcluster spread into Eastern Europe where its age is around 8 ky ago. Meanwhile, younger subcluster N3a2 originated in south Siberia (probably in the Baikal region) approximately 4 ky ago. Median network and variance analyses of STR haplotypes suggest that south Siberian N3a2 haplotypes spread further into Volga-Ural region undergoing serial bottlenecks. In addition, median network analysis of STR data demonstrates that haplogroup N2-A is represented by two subclusters, showing recent expansion times. The data obtained allow us to suggest Siberian origin of haplogroups N3 and N2 that are currently widespread in some populations of Eastern Europe.


Assuntos
Cromossomos Humanos Y/classificação , Cromossomos Humanos Y/genética , Genética Populacional , Haplótipos , Europa (Continente) , Variação Genética , Humanos , Masculino , Repetições de Microssatélites , Filogenia , Polimorfismo de Nucleotídeo Único , Sibéria
7.
Hum Genet ; 118(5): 591-604, 2006 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-16261343

RESUMO

In order to investigate the genetic history of autochthonous South Siberian populations and to estimate the contribution of distinct patrilineages to their gene pools, we have analyzed 17 Y-chromosomal binary markers (YAP, RPS4Y(711), SRY-8299, M89, M201, M52, M170, 12f2, M9, M20, 92R7, SRY-1532, DYS199, M173, M17, Tat, and LLY22 g) in a total sample of 1,358 males from 14 ethnic groups of Siberia (Altaians-Kizhi, Teleuts, Shors, Tuvinians, Todjins, Tofalars, Sojots, Khakassians, Buryats, Evenks), Central/Eastern Asia (Mongolians and Koreans) and Eastern Europe (Kalmyks and Russians). Based on both, the distribution pattern of Y-chromosomal haplogroups and results on AMOVA analysis we observed the statistically significant genetic differentiation between the populations of Baikal and Altai-Sayan regions. We suggest that these regional differences can be best explained by different contribution of Central/Eastern Asian and Eastern European paternal lineages into gene pools of modern South Siberians. The population of the Baikal region demonstrates the prevalence of Central/Eastern Asian lineages, whereas in the populations of Altai and Sayan regions the highest paternal contribution resulted from Eastern European descent is revealed. Yet, our data on Y-chromosome STRs variation demonstrate the clear differences between the South Siberian and Eastern European R1a1-lineages with the evolutionary ages compatible with divergence time between these two regional groups.


Assuntos
Cromossomos Humanos Y , Etnicidade/genética , Genética Populacional , Haplótipos , Humanos , Masculino , Sibéria
8.
Hum Biol ; 77(3): 355-65, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-16392637

RESUMO

We investigated the frequency of different repeat-length alleles of the trinucleotide CAG microsatellite repeat in the coding sequence of the nuclear gene for the catalytic subunit of mitochondrial DNA polymerase gamma (POLG) in 12 ethnic groups from northern Eurasia. The population sample consisted of 1,330 individuals from 3 large geographic areas: Europe, Southwest Asia, and Siberia/East Asia. We found that the 10-repeat allele of the POLG gene is the most frequent in all analyzed populations, with a frequency of 88-96%. The heterozygosity level ranges from 22% in Europe to 13.6% in Southwest Asia with the lowest value of 7.4% in Siberia/East Asia. The present study provides evidence of clinal distribution of POLG gene heterozygosity in North Eurasian populations. In general, we found an extremely low variability of the trinucleotide CAG microsatellite repeat, suggesting that purifying selection acts against deleterious alleles, although low mutability of the repeated region cannot be ruled out.


Assuntos
DNA Mitocondrial , DNA Polimerase Dirigida por DNA/genética , Variação Genética , Genótipo , Sequências de Repetição em Tandem , Alelos , Ásia , DNA Polimerase gama , Europa (Continente) , Heterozigoto , Humanos , Repetições de Microssatélites/genética
9.
Ann N Y Acad Sci ; 1011: 21-35, 2004 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15126280

RESUMO

The discovery of mtDNA types common to Asians and Amerinds (types A, B, C, and D) forced investigators to search for those nations of Asia which, though not considered the ancestors of the Amerinds, have retained a close genetic resemblance with them. We collected samples and studied the gene pools of the Turkic-speaking nations of South Siberia: Altaians, Khakassians, Shorians, Tuvinians, Todjins, Tofalars, Sojots, as well as Mongolian-speaking Buryats. The data indicate that nearly all Turkic-speaking nations of Siberia and Central Asia, as well as the Buryats, have types A, B, C, and D in their gene pool. The highest total frequency of these types is observed in the Tuvinians and Sojots. They, as well as the Buryats, also have the lowest frequency of the europeoid types. The most mixed Asian-Europeoid gene pool examined turned out to be that of the Shorians. An important finding was the presence of type X in the Altaians, which had not yet been detected in Asia. As shown by computer analysis, this DNA sequence is not a late European admixture. Rather, the Altai variant X is ancient and can be close to the ancestral form of the variants of contemporary Europeans and Amerinds. The presented results prove that of all nations in Asia, the Turkic-speaking nations living between Altai and Baikal along the Sayan mountains are genetically closest to the Amerinds.


Assuntos
Povo Asiático/genética , DNA Mitocondrial/genética , Variação Genética , Genética Populacional , Indígenas Norte-Americanos/genética , América , Ásia Central , Povo Asiático/classificação , Frequência do Gene , Pool Gênico , Humanos , Filogenia , Análise de Sequência de DNA
10.
J Invertebr Pathol ; 79(2): 72-9, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12095235

RESUMO

Ovarioles were found to be infected with Spiroplasma, Wolbachia, and Rickettsia in Adalia bipunctata females with maleless progeny in different natural populations. Ooplasm was infected with few Wolbachia bacteria. In ooplasm infected by Rickettsia, bacteria were present in small foci. Spiroplasmas were found encapsulated into ooplasm from the wider intercellular spaces between epithelial and oocyte cells. The cytoplasm of follicular epithelia infected with Rickettsia was heavily destroyed, but the nucleus was intact and free from bacteria. The essential feature of follicular epithelium cells from Spiroplasma and Wolbachia infected A. bipunctata females was inclusions of three types: crystalline, filaments, and concentric myelin-like lamellae. Observations of smears prepared from ovaries of A. bipunctata from natural populations revealed a low concentration of bacteria within a microscopy field (less 10 bacteria) in more than 90% of specimens, and only a few ovaries were heavily infected. Two different ways of bacterial invasion of the oocyte are suggested: Spiroplasma-like, through the intercellular spaces in the epithelium and Rickettsia-like, through the cytoplasm of follicular epithelium cells. Bacteria were not found in germarium zones and we suggest that each follicle is infected from haemolymph.


Assuntos
Infecções Bacterianas/microbiologia , Besouros/microbiologia , Infecções por Rickettsia/microbiologia , Rickettsia/isolamento & purificação , Spiroplasma/isolamento & purificação , Wolbachia/isolamento & purificação , Animais
11.
Genetics ; 160(3): 1075-86, 2002 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11901123

RESUMO

The two-spot ladybird beetle Adalia bipunctata (Coleoptera: Coccinellidae) is host to four different intracellular maternally inherited bacteria that kill male hosts during embryogenesis: one each of the genus Rickettsia (alpha-Proteobacteria) and Spiroplasma (Mollicutes) and two distinct strains of Wolbachia (alpha-Proteobacteria). The history of infection with these male-killers was explored using host mitochondrial DNA, which is linked with the bacteria due to joint maternal inheritance. Two variable regions, 610 bp of cytochrome oxidase subunit I and 563 bp of NADH dehydrogenase subunit 5, were isolated from 52 A. bipunctata with known infection status and different geographic origin from across Eurasia. Two outgroup taxa were also considered. DNA sequence analysis revealed that the distribution of mitochondrial haplotypes is not associated with geography. Rather, it correlates with infection status, confirming linkage disequilibrium between mitochondria and bacteria. The data strongly suggest that the Rickettsia male-killer invaded the host earlier than the other taxa. Further, the male-killing Spiroplasma is indicated to have undergone a recent and extensive spread through host populations. In general, male-killing in A. bipunctata seems to represent a highly dynamic system, which should prove useful in future studies on the evolutionary dynamics of this peculiar type of symbiont-host association.


Assuntos
Besouros/genética , Besouros/microbiologia , DNA Mitocondrial , Rickettsia/genética , Spiroplasma/genética , Simbiose , Wolbachia/genética , Animais , Evolução Biológica , Complexo IV da Cadeia de Transporte de Elétrons/genética , Genótipo , Masculino , Dados de Sequência Molecular , NADH Desidrogenase/genética , Filogenia , Análise de Sequência de DNA , Simbiose/genética
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