Genetic polymorphism of erythrocytic enzymes in Yakut populations

Polymorphism of the erythrocytic enzymes PGM1, ACP1, ESD, and GLO1 was found in Yakut populations. The allelic frequencies of the polymorphic systems studied varied within the following ranges: PGM1*1+, 0.5833-0.7791; PGM1*1-, 0.0345-0.1176; PGM1*2+, 0.1250-0.2813; ACP1*A, 0.1429-0.3382; ACP1*B, 0.6548-0.8571; ESD*2, 0.1250-0.4643; and GLO1*1, 0.0116-0.2845.     

Genetic analysis of reproduction in the Buryat populations

A complex anthropological survey based on population-genetic methods and a study of a wide spectrum of genetic systems (43 alleles from 17 independent loci) was undertaken among 450 Buryat women of post-reproductive age. The results obtained showed the influence of particular genetic markers and their complex on the formation of peculiarities in the reproduction structure of the Buryat population.A sharp increase in phenotype GC 2-2 frequency and the corresponding GC*2 allele of the group-specific component (GC) was established for women groups with burdened obstetric records. These groups are characterized also by a considerable decrease in the observed geterozygosity (Ho) as compared to its expected value (He). Samples including women with multiple pregnancies in the recorded obstetric anamnesis are characterized by a significant increase in the frequency of the rare alleles TF*C3 of the transferrin system and those of PI*Z belonging to the proteinase inhibitor system (a1-antitrypsin) as compared to the control group.The results obtained widened current knowledge about the influence of genetic and environmental components on reproduction processes in human populations.     

Analysis of Alu-polymorphism in Buryat populations]

Polymorphism of three populations of the Buryat Republic and a population from Aginskii Buryat Autonomous okrug of Chita oblast was examined using a set of five autosomal Alu insertions at the ACE, PLAT, PV92, APOA1, and F13B loci. The allele frequency distribution patterns revealed in Buryat populations were typical to other Asian populations. Buryats were characterized by relatively low level of intrapopulation diversity (0.369 in the pooled population sample). Analysis of autosomal Alu insertions suggests the uniformity of the Buryat gene pool. The coefficient of genetic differentiation in the four populations studied was 0.8%.     

Genetic subdivision of the Buryat population

The results of an estimation of the level of subdivision in the Buryat ethnos (obtained on the basis of data published by a number of research teams) are given. Altogether, information about 34 loci, including 25 diallelic loci and 9 STR loci, was analyzed. The results of the analysis, both for the diallelic polymorphic variants in genes predisposed to multifactorial diseases and for neutral STR markers, indicate the subdivision of the genetic structure of the different territorial groups of Buryats. The peculiarities of the ethnogenesis and heterogeneity of the settlement of Buryat tribes on the territory of residence are considered as one possible (but not the sole) explanation of the genetic heterogeneity of different territorial groups of Buryats. It is indicated that it is important to take into account information about the territorial, ethnic, and tribal affiliation of individuals (included in the studied groups) when planning studies aiming to establish a genetic component of the determination of pathological states in humans.     

Genetic polymorphism in populations of Akodon rodents

By means of starch gel electrophoresis, 16-20 loci coding for enzymes and hemoglobin have been investigated in six population samples of Akodon dolores, captured in a single site of the Córdoba province (Argentina) during a 3-year period and in three samples of an Akodon azarae population. Proportion of polymorphic loci (P) ranged from 0.278 to 0.389 in A. dolores and from 0.166 to 0.300 in A. azarae. Mean heterozygosity (H) ranged from 0.138 to 0.192 in A. dolores and from 0.099 to 0.118 in A. azarae. These values are very high compared with those reported for northern hemisphere rodent populations. The high value is remarkable since the loci sample is biased towards the less variable (group I) enzymes.     

Genetic and chromosomal polymorphism in hybridizing populations of the grasshopper Podisma pedestris

The grasshopper Podisma pedistris occurs in two chromosome races, which have XO/XX and neo-XY sex chromosome systems. We have studied chromosomal and electrophoretic variation in populations where these two races meet and hybridize, in an area near the town of Seyne, Alpes Maritimes, southern France. Allozyme variation, at 21 loci in 11 populations, does not seem to show any relationship to the underlying cline in the frequency of the two chromosome types. This indicates that the chromosomal cline does not offer a strong barrier to the flow of genes at other loci. The XO/XX race in this area occurs on a single plateau, isolated from other populations with the same karyotype. It is suggested that this form is only able to persist here because the introgression of neo-XY chromosomes is inhibited by steep cliffs, which tend to keep the two races apart.     

Genetic distance in inversion polymorphism among natural populations of Drosophila ananassae

Based on the differences in the gene arrangement frequencies average genetic distance has been estimated among natural populations of Drosophila ananassae. Genetic distance obtained by pairwise comparison ranges from 0.002 to 0.371. The most differentiated populations are those from the Andaman and Nicobar Islands. Although the populations from localities separated by a small geographic distance show less genetic distance, the relation between genetic distance and geographic distance does not seem to be positive.     

Genetic structure of Balearic honeybee populations based on microsatellite polymorphism

The genetic variation of honeybee colonies collected in 22 localities on the Balearic Islands (Spain) was analysed using eight polymorphic microsatellite loci. Previous studies have demonstrated that these colonies belong either to the African or west European evolutionary lineages. These populations display low variability estimated from both the number of alleles and heterozygosity values, as expected for the honeybee island populations. Although genetic differentiation within the islands is low, significant heterozygote deficiency is present, indicating a subpopulation genetic structure. According to the genetic differentiation test, the honeybee populations of the Balearic Islands cluster into two groups: Gimnesias (Mallorca and Menorca) and Pitiusas (Ibiza and Formentera), which agrees with the biogeography postulated for this archipelago. The phylogenetic analysis suggests an Iberian origin of the Balearic honeybees, thus confirming the postulated evolutionary scenario for Apis mellifera in the Mediterranean basin. The microsatellite data from Formentera, Ibiza and Menorca show that ancestral populations are threatened by queen importations, indicating that adequate conservation measures should be developed for protecting Balearic bees.     

Genetic variation of esterase D (EsD) polymorphism in Indian populations

Data are presented on the phenotypes and gene frequencies of esterase D (EsD) polymorphism in various endogamous caste groups of Patiala and Faridkot districts of Punjab, north-west India. The frequency of the EsD2 allele in these groups varies from a minimum of 0.157 in Khatris to a maximum of 0.253 in Ramdasia Sikhs, a range quite typical of the north Indian populations. Examination of the available data on esterase D system in indigenous populations demonstrates the existence of a north-south cline in the distribution of the EsD2 allele in India.     

广西4个少数民族17个Y-STR基因座的多态性分析

应用Yfiler复合扩增试剂盒及基因分型技术, 调查了广西瑶、彝、京、壮4个少数民族人群17个Y-STR基因座的多态性分布, 计算等位基因频率和单体型多样性, 并结合国内其他4个群体相应基因座的遗传学资料, 分析其遗传距离和聚类关系。瑶族100名无关男性个体中检出61种单体型, 单体型多样性为0.9784; 彝族105名无关男性个体中检出67种单体型, 单体型多样性为0.9866; 京族103名无关男性个体中检出79种单体型, 单体型多样性为0.9911; 壮族107名无关男性个体中检出91种单体型, 单体型多样性为0.9956。在4个少数民族中, 京族和壮族的遗传距离最小(0.0391), 彝族和瑶族的遗传距离最大(0.3376)。结果表明, 该17个Y-STR基因座在广西4个少数民族人群中均具有较高的多态性, 在法医学、群体遗传学等方面有重要的应用价值。     

Analysis of the genetic and demographic structure of populations from Aginskii Buryat district contrasting in habitation conditions

Genetic and demographic characteristics of populations from two settlements from the Aginskii Buryat district of Trans-Baikal krai (Alkhanai and Orlovskii) were studied. It was demonstrated that the mononational Buryat settlement of Alkhanai, located in the agrarian Dul??durginskii region of the district far from large settlements and transport highways, is characterized by a large prereproductive volume (45%) and by a small share of individuals from the elderly age group (16.4%). A shift in age characteristics in the Buryat group (36.6 and 22.4%, respectively) was detected in the urban settlement of Orlovskii with a population of mixed ethnic composition, located in a densely populated industrialized part of the district. A modified sex ratio was also demonstrated in Alkhanai as opposed to the Buryat part of the Orlovskii population (sex indices were 0.94 and 0.99). Analysis of population mixture was conducted; marriage structure and migrations were described. The endogamy index of the Alkhanai locality was 0.41; in the group of Buryats from Orlovskii, 0.09. A decrease in the amount of pregnancies and births and a larger distribution of family planning practice among Buryats from Orlovskii were detected. The average amount of births of living children per woman in Alkhanai was 5.11; in Buryats from Orlovskii, 3.90. The selection pressure was estimated as low by means of the Crow index (I _tot 0.28?C0.48). In all described groups, a component that characterizes differential fertility (I _f) exceeds the child mortality component (I _m).     

3个山羊群体中4个微卫星DNA多态性及其与杂种优势的关系

利用4个微卫星标记（OarFCB11,OarAE101,McM218,McM38）对波尔山羊、太行山羊和河北奶山羊的等位基因频率、群体多态信息含量、有效等位基因数、杂合度和遗传距离进行了遗传检测,并测定了波尔山羊与河北奶山羊及太行山羊的杂交效果。结果表明：4个微卫星标记在波尔山羊、太行山羊和河北奶山羊3个品种中存在多态性,可以用于山羊遗传多样性的评估;从不同品种来看,太行山羊的遗传变异程度最大,而波尔山羊的遗传变异程度相对较小;波尔山羊与河北奶山羊的遗传距离大于与太行山羊,波尔山羊与河北奶山羊的杂种优势高于与太行山羊,与实际杂种优势测定结果相符。 Abstract: Gene frequency, polymorphism information contents, number of effective alleles, heterozygosity and genetic distances were studied in Boer goat, Taihang goat and Hebei dairy goat using four microsatellite markers（OarFCB11,OarAE101,McM218,McM38）. The crossing effects on Hebei dairy goat and Taihang goat with Boer goat were tested. The results indicated that there are genetic polymorphisms at four microsatellite markers in three goat breeds. Four microsatellite markers can be used for genetic diversity evaluation in goat breeds. The genetic variability of Taihang goat is the highest, and Boer goat is the lowest in three goat breeds. Genetic distances between Boer goat and Hebei dairy goat is bigger than that between Boer goat and Taihang goat. The heterosis between Boer goat and Hebei dairy goat is higher than that between Boer goat and Taihang goat. It accords with testing results on actual heterosis.     

Genetic polymorphism of enzymes of alcohol metabolism and susceptibility to alcoholic liver disease

Differences in the pharmacokinetics of alcohol absorption and elimination are, in part, genetically determined. There are polymorphic variants of the two main enzymes responsible for ethanol oxidation in liver, alcohol dehydrogenase and aldehyde dehydrogenase. The frequency of occurrence of these variants, which have been shown to display strikingly different catalytic properties, differs among different racial populations. Since the activity of alcohol dehydrogenase in liver is a rate-limiting factor for ethanol metabolism in experimental animals, it is likely that the type and content of the polymorphic isoenzyme subunit encoded at ADH2, beta-subunit, and at ADH3, the gamma-subunit, are contributing factors to the genetic variability in ethanol elimination rate. The recent development of methods for genotyping individuals at these loci using white cell DNA will allow us to test this hypothesis as well as any relationship between ADH genotype and the susceptibility to alcoholism or alcohol-related pathology. A polymorphic variant of human liver mitochondrial aldehyde dehydrogenase, ADLH2, which has little or no acetaldehyde oxidizing activity has been identified. Individuals with the deficient ALDH2 phenotype do not have altered ethanol elimination rates but they do exhibit high blood acetaldehyde levels and dysphoric symptoms such as facial flushing, nausea and tachycardia, after drinking alcohol. Because acetaldehyde is so reactive, it binds to free amino groups of proteins including a 37 kilodalton hepatic protein-acetaldehyde adduct and may elicit an antibody response. We would predict that individuals who have low ALDH2 activity because of liver disease or because they have the inactive ALDH2 variant isoenzyme might form more protein-acetaldehyde adducts and elicit a greater immune response. These adducts may represent good biological markers of alcohol abuse and may also play a role in liver injury due to chronic alcohol consumption.     

Genetic relationship among Mongolian native goat populations estimated by blood protein polymorphism

Several local strains and populations of goats distinguished by morphogenetic and performance characteristics are kept by goat breeders in different natural climatic regions of Mongolia, namely Bayandelger, Ulgii Red, Erchim Black, Dorgon and Zavkhan Buural. The genetic relationships among eight native goat populations in Mongolia at 33 biochemical genetic loci was assessed. A total of 440 animals in eight regional zones were studied. Twelve loci, i.e. the serum transferrin, serum amylase, serum alkaline phosphatase, serum prealbumin-3, cell esterase-D, hemoglobin (Hb) β, hemoglobin (Hb) α-II, cell peptidase-B, cell tetrazolium oxidase, cell esterase-1, cell esterase-2 and cell catalase loci, were found to be polymorphic. The data indicated that Mongolian native goats are not highly differentiated (D=0.0002–0.0038) genetically. To set Mongolian native goats in a larger context, the present data were compared with those on other goat breeds and populations in east and southeast Asia that were previously reported. The average heterozygosity in the Mongolian native goats did not significantly differ from those in other Asian goat populations and breeds. A phylogenetic tree of the gene constitution of the Mongolian native goats and other Asian goat breeds and populations was constructed and revealed that genetically the Mongolian native goats had diverged slightly from the group consisting of Chinese, Japanese, Korean and Indonesian native goats, but markedly from the Indian goat group.     

Genetic polymorphism of Baylisascaris procyonis in host infrapopulations and component populations in the Central USA

Baylisascaris procyonis is a nematode of significant concern to public and domestic animal health as well as wildlife management. The population genetics of B. procyonis is poorly understood. To gain insights into patterns of genetic diversity within (infrapopulation level) and among (component population level) raccoon (Procyon lotor) hosts, and specifically to assess the relative importance of indirect and direct transmission of the parasite for explaining observed population structure, we collected 69 B. procyonis from 17 wild raccoons inhabiting five counties in Missouri and Arkansas, USA. Informative regions of mitochondrial (CO1, CO2) and nuclear (28S, ITS2) genes were amplified and the distribution and genetic variability of these genes were assessed within and across raccoons. Concatenation of the CO1 and CO2 mtDNA sequences resulted in 5 unique haplotypes, with haplotype diversity 0.456?±?0.068. The most common haplotype occurred in 94% of raccoons and 72.5% of B. procyonis. Sequences for 28S rDNA revealed four unique nuclear genotypes, the most common found in 100% of raccoons and 82.6% of B. procyonis. ITS2 genotypes were assessed using fragment analysis, and there was a 1:1 correspondence between 28S and ITS-2 genotypes. Infrapopulation variation in haplotypes and genotypes was high and virtually all hosts infected with multiple sequenced nematodes also harbored multiple haplotypes and genotypes. There was a positive relationship between the size of the analyzed infrapopulation (i.e., the number of nematodes analyzed) and the number of haplotypes identified in an individual. Collectively this work emphasizes the importance of indirect transmission in the lifecycle to this parasite.     

Genetic coadaptation in the chromosomal polymorphism of Drosophila subobscura II. Changes of gametic disequilibrium in experimental populations

Experimental populations were examined for temporal changes of gametic disequilibria between allozyme loci (Lap and Pept-1) and gene arrangements of the O chromosome of Drosophila subobscura (O _st and O ₃₊₄₊₇) under several environmental conditions. In the foundation of the experimental populations a genetic perturbation was carried out in order to test the relevance of the current hypotheses used to explain the allozyme-inversion associations observed in natural populations. Differential changes of gametic disequilibria were detected over generations under the different environmental conditions. Mere mechanical or stochastic factors cannot explain the results and natural selection is probably the major agent generating the detected gametic associations. The observations are interpreted as a proof of coadaptation of D. subobscura inversions.     

Migration-selection polymorphism in dioecious populations

Summary Conditions are derived for a protected polymorphism in a dioecious population subdivided into an arbitrary number of demes which exchange migrants. Generations are discrete and nonoverlapping; mutation and random drift are neglected. The analysis is restricted to a diallelic autosomal locus. In contrast to the monoecious case, the protection criteria depend on the order of migration and selection; they become identical for adult and juvenile migration if both the male and female backward migration matrices are symmetric, or the migration or selection patterns in the two sexes are the same. The protection conditions are presented explicitly for the Levene model. A recessive allele is protected in a panmictic dioecious population if the unweighted average of the recessive-to-dominant fitness ratios in the two sexes exceeds unity.Supported by the National Science Foundation (Grant No. DEB77-21494)