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1.
Genetika ; 44(3): 315-22, 2008 Mar.
Artigo em Russo | MEDLINE | ID: mdl-18664134

RESUMO

Two types (MIR and Alu) of short interspersed repeated DNA sequences (SINEs) were used for analysis of genetic relationships among higher primates, and for detection of polymorphism in human genomic DNA. The DNA regions located between the neighboring copies of these SINEs were amplified in polymerase chain reaction with primers complementary to the MIR and Alu consensus sequences (inter-SINE PCR). Comparison of the sets of amplified DNA fragments for different species or individuals provides evaluation of the relationships among them. Using inter-MIR PCR technique, the relationships among the higher primates of the infraorder Catarrhini reported elsewhere were confirmed, pointing to the efficiency of the method for phylogenetic studies. No human DNA polymorphism was revealed with the help of inter-MIR PCR. This polymorphism was detected by means of inter-Alu PCR, which is probably associated with the continuing amplification of Alu elements in human genome.


Assuntos
Genoma , Primatas/genética , Elementos Nucleotídeos Curtos e Dispersos , Elementos Alu , Animais , Genoma Humano , Humanos , Filogenia , Reação em Cadeia da Polimerase
2.
Mol Biol (Mosk) ; 41(5): 839-51, 2007.
Artigo em Russo | MEDLINE | ID: mdl-18240566

RESUMO

A number of populations of genus Darevskia lizards were studied using inter-SINE-PCR (IS-PCR). The number and size of PCR-amplified spacers of genomic DNA flanked by SINE-type repeats were compared in 17 populations of the D. raddei species complex along with several other species from the same genus. Nei and Li's (D(NL)) genetic distances between populations were unequivocal. Individual differences among D. r. nairensis sample specimens and between the samples fall into a range of less than 0.1. Individual variability intra each of the D. r. raddei samples--into a range of 0.1-0.2, but the inter samples differences in this subspecies depends on its geographic localizations. Thus the differences between 10 samples from Armenia and Karabach fall into a range of 0.2-0.3, but between all these and two samples from Talysh (Azerbajdzhan)--of 0.3-0.4. At the same time, the variability between both known subspecies (D. r. raddei and D. r. nairensis) reaches the same values. The differences between "good" species D. raddei and D. rudis were about 0.60-0.7. It may be supposed that D. r. raddei is currently undergoing the speciation process. The population of lizards from Turkey which is considered to be close to D. raddei by some researchers and to D. rudis by others is, according to our molecular data, more closely related to the latter species. The difference of homogeneity between other populations was revealed by comparison of the DNL values. Possible phylogeographic pathways of Darevskia species distribution based on the molecular data were proposed.


Assuntos
Genoma/genética , Lagartos/genética , Filogenia , Sequências Repetitivas de Ácido Nucleico/genética , Animais , Armênia , Azerbaijão , Impressões Digitais de DNA , Marcadores Genéticos , Genética Populacional , Reação em Cadeia da Polimerase , Turquia
3.
Mol Biol (Mosk) ; 40(1): 61-73, 2006.
Artigo em Russo | MEDLINE | ID: mdl-16523693

RESUMO

In order to elucidate the molecular-genetic relations of some Lacerta s. str. lizard populations, subspecies and species in comparison with some other genera we used methods revealing four types of nuclear DNA markers. Among these were taxonprint, RAPD, Inter-MIR-PCR markers and also satellite DNA monomer sequences. The aim was to compare the phylogeny and systematics of this reptilian group based on morphological and molecular criteria. This problem has a general importance for understanding a speciation process. Our results show a good correlation between both approaches when genera and species levels were studied. Systematic status of five subspecies of L. agilis were supported but not in all cases, some subspecies have no meaningful genetic differences by three types of molecular markers, but all of them were differed by RAPD markers. The data confirm the subdivision of L. agilis populations into west and east clades proposed by other authors earlier on the basis of mitochondrial DNA and morphology. The population structure of one of the subspecies--L. agilis exigua, was studied on a number of populations distributed from Ural region up to Kabardino-Balkaria by IMP method. There were no significant differences among these 14 populations investigated. The data testify the rapid distribution of the species after the end of Pleistocene glaciation.


Assuntos
Variação Genética , Lagartos/genética , Animais , Sequência de Bases , DNA Satélite/genética , Evolução Molecular , Marcadores Genéticos , Genética Populacional , Lagartos/classificação , Dados de Sequência Molecular , Filogenia , Técnica de Amplificação ao Acaso de DNA Polimórfico , Especificidade da Espécie
4.
Mol Biol (Mosk) ; 36(2): 296-306, 2002.
Artigo em Russo | MEDLINE | ID: mdl-11969091

RESUMO

The genetic relatedness of several bisexual and of four unisexual "Lacerta saxicola complex" lizards was studied, using monomer sequences of the complex-specific CLsat tandem repeats and anonymous RAPD markers. Genomes of parthenospecies were shown to include different satellite monomers. The structure of each such monomer is specific for a certain pair of bisexual species. This fact might be interpreted in favor of co-dominant inheritance of these markers in bisexual species hybridogenesis. This idea is supported by the results obtained with RAPD markers; i.e., unisexual species genomes include only the loci characteristic of certain bisexual species. At the same time, in neither case parthenospecies possess specific, autoapomorphic loci that were not present in this or that bisexual species.


Assuntos
Evolução Biológica , Marcadores Genéticos , Lagartos/fisiologia , Partenogênese/genética , Sequências de Repetição em Tandem , Animais , Sequência de Bases , Feminino , Masculino , Dados de Sequência Molecular , Técnica de Amplificação ao Acaso de DNA Polimórfico , Homologia de Sequência do Ácido Nucleico
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