On the possibility of the MN blood group determination in human bones

After a series of preliminary tests on inert substances and on saliva drawn from donors of know MN blood group, 31 right femura from Pisa cemetery buried for 25–30 years and 37 eneolithic femura from Gaudo necropolis near Paestum (2500 – 2000 B.C.) were submitted to 140 assays for the MN system using the standard technique already devised in our Laboratory for ABO blood group determination.Positive and reproducible results were obtained in 18:31 recent femura (58%) and in 24:37 eneolithic bones (65%). The following phenotype and gene frequencies were obtained:

$\text{recent femura:}\text{8.}\text{M}\text{+3.}\text{N}\text{+7.}\text{MN}\text{=18; 0·64m+0.·36n=1}$

$\text{eneolithic femura:}\text{9.}\text{M}\text{+6.}\text{N}\text{+9.}\text{MN}\text{=24; 0·56m+0·44n=1}$

When the ABO and the MN blood group determinations are performed in parallel, a significant positive connection between the two diagnosabilities is observable: P = 0·0387 in the case of the eneolithic bones, $\text{P ? 0·02}$ in the case of the total sample of 59 eneolithic and recent bones tested in parallel. This fact could be reasonably explained considering the similarity of the chemical structure of MN and ABO glycoproteins, which would account for a similar behaviour in preservation.The absence or the very low concentration of M and N substances in tissues and body fluids would on the other hand agree with the percentage of diagnosability: lower in the MN system (60–65%) than in the ABO system (75–80%). The more problematical character of MN blood group typing of bones could be better approached if further research were done.     

A re‐examination of the heritability of fertility in the British peerage

Abstract

The gene and phenotype frequencies for the ABO blood groups system were studied in two socioeconomically different subpopulations of Santiago, Chile. The data were taken from the maternity services and blood banks of two hospitals, one serving mainly low socioeconomic classes and the other serving middle and high socioeconomic groups. Results show a clear difference in gene and phenotype frequencies between the two subpopulations, a difference maintained in two generations (mothers and their children). These results reinforce other studies showing that socioeconomic forces have resulted in assortative mating and different genetic subpopulations in Chile.     

Hierarchical gene diversity and genetic structure of tribal populations of Andhra Pradesh,India

Gene diversity and genetic structure of tribal populations of Andhra Pradesh, India, have been analyzed under a hierarchical model consisting of five regions of the state, tribes within the regions, and local subpopulations within the tribes. Average gene diversity has been estimated from gene frequency data for 15 polymorphic loci by using nested gene diversity analysis of G_ST. The intralocation coefficient of gene diversity was estimated at 96% of the total, whereas the intertribal, within—and between—regional gene diversities were found to be only 1.90, 0.95, and 1.43%, respectively. The estimate of gene diversity was higher for loci with higher degrees of polymorphism such as ABO, MN, ESD, and PTC and lower for loci with low-level polymorphism and extreme gene frequencies such as Hb, Tf, PHI, 6PGD, and Hp. The nature of selective preference or neutrality at the loci seems to be important in this respect. Tribes of the plains exhibit the least gene diversity, apparently because of higher gene flow among them. The contribution of loci with intermediate gene frequencies in intertribal and regional gene diversity was found to be higher than for loci with extreme allelic frequencies. These results suggest that the most significant component of variation is between individuals within locations and that variation between local subpopulations is negligible in the genetic structure of a population. Forces like selection, gene flow and drift also influence the diversity depending upon the nature of the locus. © 1993 Wiley-Liss, Inc.     

Low genetic diversity and lack of population structure in the endangered Galápagos penguin (<Emphasis Type="Italic">Spheniscus mendiculus</Emphasis>)

Long-term monitoring of the endangered Galápagos penguin (Spheniscus mendiculus) has indicated poor reproductive periods and severe population fluctuations in association with El Niño – Southern Oscillation events. An earlier mark and recapture study indicated that adults exhibit some degree of breeding-site and mate fidelity, and that juveniles potentially move more frequently than adults; however, the extent to which migrants and gene flow occur between islands within the Galápagos archipelago is largely unknown. This study tested the hypothesis that geographic isolation and adult breeding philopatry has led to a degree of genetic differentiation between island subpopulations within the archipelago. We examined the genetic diversity within and among different subpopulations and the extent to which gene flow occurs between island subpopulations. Estimates of allelic richness and gene diversity were not significantly different between subpopulations. Tests to detect genetic heterogeneity failed to reject the H ₀ of no difference in allele frequencies for chi-square (P = 0.28) and Fisher’s exact test (P = 0.19). All pairwise values of the F _ST variant θ were not significant, while a power analysis revealed a >99% probability of detecting a biologically true F _ST of 0.05. Migration estimates in BAYESASS+ suggest symmetrical gene flow throughout the species’ distribution. Our results indicate a low level of genetic diversity throughout the population and a seemingly high level of gene flow between subpopulations. We argue that the Galápagos penguin should be managed as one panmictic population and we discuss the risk of disease threats in the archipelago.     

Mixed mating in androdioecious Mercurialis annua inferred using progeny arrays and diploid-acting microsatellite loci in a hexaploid background

Background and Aims

The frequency at which males can be maintained with hermaphrodites in androdioecious populations is predicted to depend on the selfing rate, because self-fertilization by hermaphrodites reduces prospective siring opportunities for males. In particular, high selfing rates by hermaphrodites are expected to exclude males from a population. Here, the first estimates are provided of the mating system from two wild hexaploid populations of the androdioecious European wind-pollinated plant M. annua with contrasting male frequencies.

Methods

Four diploid microsatellite loci were used to genotype 19–20 progeny arrays from two populations of M. annua, one with males and one without. Mating-system parameters were estimated using the program MLTR.

Key Results

Both populations had similar, intermediate outcrossing rates (t_m = 0·64 and 0·52 for the population with and without males, respectively). The population without males showed a lower level of correlated paternity and biparental inbreeding and higher allelic richness and gene diversity than the population with males.

Conclusions

The results demonstrate the utility of new diploid microsatellite loci for mating system analysis in a hexaploid plant. It would appear that androdioecious M. annua has a mixed-mating system in the wild, an uncommon finding for wind-pollinated species. This study sets a foundation for future research to assess the relative importance of the sexual system, plant-density variation and stochastic processes for the regulation of male frequencies in M. annua over space and time.     

Towards a theory of the evolution of modifier genes

The main findings of a study of the evolution of modifier gene frequencies in models of deterministic population genetics are presented. A wide variety of random mating systems are subject to selection with modifiers operating, in different cases, on mutation rates, migration between subpopulations, and linkage between other loci. In all these instances, the modifier frequencies evolve in such a way as to maximize the mean fitness of the population at equilibrium. This is remarkable since, the modifier genes are selectively neutral in the sense that they do not affect the fitness of their individual carriers. In nonrandom mating systems, the mean fitness concept is not well-defined, and there does not appear to be such a simple principle governing the evolution of modifier frequencies. In assortative mating systems, modifiers favoring reduced assortment propensities tend to increase. In contrast, for selfing-outcrossing systems, modifiers favoring increased selfing tend to increase.     

Linkage Disequilibrium in Subdivided Populations

The linkage disequilibrium in a subdivided populaton is shown to be equal to the sum of the average linkage disequilibrium for all subpopulations and the covariance between gene frequencies of the loci concerned. Thus, in a subdivided population the linkage disequilibrium may not be 0 even if the linkage disequilibrium in each subpopulation is 0. If a population is divided into two subpopulations between which migration occurs, the asymptotic rate of approach to linkage equilibrium is equal to either r or 2(m(1) + m(2)) - (m(1) + m(2))(2), whichever is smaller, where r is the recombination value and m(1) and m(2) are the proportions of immigrants in subpopulations 1 and 2, respectively. Thus, if migration rate is high compared with recombination value, the change of linkage disequilibrium in subdivided populations is similar to that of a single random mating population. On the other hand, if migration rate is low, the approach to lnkage equilibrium may be retarded in subdivided populations. If isolated populations begin to exchange genes by migration, linkage disequilibrium may increase temporarily even for neutral loci. If overdominant selection operates and the equilibrium gene frequencies are different in the two subpopulations, a permanent linkage disequilibrium may be produced without epistasis in each subpopulation.     

Multilocus population structure of Tapesia yallundae in Washington State

Population genetic structure of the fungal wheat pathogen Tapesia yallundae in Washington State was determined using genetically characterized amplified fragment length polymorphic (AFLP) markers and mating-type (MAT1-1 or MAT1-2). Segregation and linkage relationships among 164 AFLP markers and MAT were analysed using 59 progeny derived from an in vitro cross. Alleles at 158 AFLP loci and the mating-type locus segregated in a 1:1 ratio. Ten unlinked markers were chosen to determine genetic and genotypic diversity and to test the hypothesis of random mating and population differentiation among five subpopulations of T. yallundae representative of the geographical distribution of wheat production in eastern Washington. Among 228 isolates collected, overall gene diversity was high (h = 0.425) and a total of 91 unique multilocus genotypes (MLG) were identified, with 32 MLG occurring at least twice. The overall population genetic structure was consistent with random mating based on the segregation of mating-type, index of association (IA), parsimony tree length permutation test (PTLPT) and genotypic diversity analyses. However, clonal genotypes were found within each subpopulation and were also distributed among the five subpopulations. No significant differences in allele frequencies were found among the five subpopulations for all 10 loci based on contingency table analysis (G2) and Wier & Cockerham's population differentiation statistic theta (theta = -0.008, P = 0.722). T. yallundae appears to consist of a large homogeneous population throughout eastern Washington with both sexual and asexual reproduction contributing to the observed population genetic structure despite no report of sexual fruiting bodies of T. yallundae occurring under natural field conditions.     

Haplotype inference in crossbred populations without pedigree information

Background

Current methods for haplotype inference without pedigree information assume random mating populations. In animal and plant breeding, however, mating is often not random. A particular form of nonrandom mating occurs when parental individuals of opposite sex originate from distinct populations. In animal breeding this is called crossbreeding and hybridization in plant breeding. In these situations, association between marker and putative gene alleles might differ between the founding populations and origin of alleles should be accounted for in studies which estimate breeding values with marker data. The sequence of alleles from one parent constitutes one haplotype of an individual. Haplotypes thus reveal allele origin in data of crossbred individuals.

Results

We introduce a new method for haplotype inference without pedigree that allows nonrandom mating and that can use genotype data of the parental populations and of a crossbred population. The aim of the method is to estimate line origin of alleles. The method has a Bayesian set up with a Dirichlet Process as prior for the haplotypes in the two parental populations. The basic idea is that only a subset of the complete set of possible haplotypes is present in the population.

Conclusion

Line origin of approximately 95% of the alleles at heterozygous sites was assessed correctly in both simulated and real data. Comparing accuracy of haplotype frequencies inferred with the new algorithm to the accuracy of haplotype frequencies inferred with PHASE, an existing algorithm for haplotype inference, showed that the DP algorithm outperformed PHASE in situations of crossbreeding and that PHASE performed better in situations of random mating.     

Mating system and population genetic structure of Bruguiera gymnorrhiza (Rhizophoraceae), a viviparous mangrove species in China

In order to explain the diversity patterns and develop the conservation strategies, the population genetic structures and the mating systems of Bruguiera gymnorrhiza from the coastlines of south China were investigated in this study. The mating system parameters were analyzed using progeny arrays for allozyme markers. The multilocus outcrossing rates (tm) ranged from 0.845 (Fugong) to 0.267 (Dongzhai harbor). High allozyme variations within the five collected populations were determined and compared with the published data of other plant species with the mixed mating systems. At species level, the percentage of polymorphic loci (P) was 80%, the average number of alleles per locus (A) was 2.440, and the heterozygosity (He) was 0.293. The total gene diversity within each population (H_S = 0.2782) and the coefficient of genetic differentiation (G_ST = 0.0579) among the populations were estimated. On the basis of this population genetic structure, it is suggested that the gene flow (Nm = 3.85) is quite high, which is possibly related to its water-dispersed hypocotyls. It is also suggested that the mating system of this species is of mixed mating.     

Medical genetic study of the population of Turkmenia. VI. Intrapopulation variability from an analysis of marriage migrations and ABO and Hp marker systems

By the sampling procedure, the distribution of phenotypic and genotypic frequencies of ABO and Hp systems and the structure of intermarriage migration in Turkmen population was studied. The geographical subdivision of the Turkmen population coincided with its ethnic divergency. The main Turkmen tribes are highly isolated (the gametic index is 0.965 to 1.0) and the differences in gene frequencies between tribes are significant. The mean gene frequencies for the ABO system in the Turkmen population are: I0-0.5373, IA-0.2601, IB-0.2025, these being Hp1-0.284, Hp2-0.716 for the Hp system.     

安徽省宁国县畲族红细胞血型分布

调查１６０名安徽省宁国县畲族村民的ＡＢＯ、Ｒｈ、Ｐ、ＭＮ系统红细胞血型,结果显示ＡＢＯ血型表型频率分布为Ｏ（０．４６８７）〉Ｂ（０．２３７５）〉Ａ（０．２２５０）〉ＡＢ（０．０６８８）,基因频率ｐ＝０．１５００,ｑ＝０．１５７５,ｒ＝０．６９２５;Ｒｈ血型表型频率分布为ＣＣｄｅｅ（０．５３８５）〉ＣＣＤＥ（０．１６６７）〉ＣｃＤＥ（０．１４７４）〉ＣｃＤｅｅ（０．０９６１）〉ｃｃＤＥ（０．０３２１     

Emergence of Polymorphic Mating Strategies in Robot Colonies

Polymorphism has fascinated evolutionary biologists since the time of Darwin. Biologists have observed discrete alternative mating strategies in many different species. In this study, we demonstrate that polymorphic mating strategies can emerge in a colony of hermaphrodite robots. We used a survival and reproduction task where the robots maintained their energy levels by capturing energy sources and physically exchanged genotypes for the reproduction of offspring. The reproductive success was dependent on the individuals'' energy levels, which created a natural trade-off between the time invested in maintaining a high energy level and the time invested in attracting mating partners. We performed experiments in environments with different density of energy sources and observed a variety in the mating behavior when a robot could see both an energy source and a potential mating partner. The individuals could be classified into two phenotypes: 1) forager, who always chooses to capture energy sources, and 2) tracker, who keeps track of potential mating partners if its energy level is above a threshold. In four out of the seven highest fitness populations in different environments, we found subpopulations with distinct differences in genotype and in behavioral phenotype. We analyzed the fitnesses of the foragers and the trackers by sampling them from each subpopulation and mixing with different ratios in a population. The fitness curves for the two subpopulations crossed at about 25% of foragers in the population, showing the evolutionary stability of the polymorphism. In one of those polymorphic populations, the trackers were further split into two subpopulations: (strong trackers) and (weak trackers). Our analyses show that the population consisting of three phenotypes also constituted several stable polymorphic evolutionarily stable states. To our knowledge, our study is the first to demonstrate the emergence of polymorphic evolutionarily stable strategies within a robot evolution framework.     

A medico-genetic study of the population of Western Pamir. VI. Local genetic differentiation in the populations of Western Pamir]

The article comprises the results on the analysis of the structure of the great Pamirs' population (of a higher rank) and of one of its parts, the subpopulation of the valley of the river Bartang. Wright's F coefficient was used for the statistical treatment of the data obtained in the course of the analysis. The FST estimates were obtained from the variances of the frequencies of the genes located in 5 loci (ABO, MN, P, Rh and P.T.C.) culculated for 23 samples of the great populations of the Pamirs and for 9 samples of the population of the Bartang river valley. The general inbreeding coefficient for the Pamirs FIT=0,0323, its random component FST=0,0017 and the non-random component FIS=0.0306.     

DISRUPTIVE SELECTION ON BODY WEIGHT IN DROSOPHILA MELANOGASTER

Disruptive selection can have two consequences in a population: the rise of polymorphism or the divergence of the population. Divergence creates subpopulations which can be sexually isolated. Previous studies have shown that these consequences depend on the pattern of mate choices by the individuals. We have studied the effects of different patterns of mating (free mating, enforced random mating and enforced assortative mating) in a population of Drosophila melanogaster subjected to disruptive selection on body weight. Disruptive selection increased the weight dispersion in all mating patterns but brought about divergence within the population only when it occurred in association with enforced assortative mating (without complete sexual isolation between the subpopulations). When mating was free, the dispersion, measured by change in the coefficient of variation, was only somewhat larger than with enforced random mating: thus the principal consequence of disruptive selection was the rise of polymorphism in the population.     

ABO Blood Type and Personality Traits in Healthy Japanese Subjects

There is no scientific consensus that a relationship exists between the ABO blood group and personality traits. However, a recent study hypothesized that the dopamine beta-hydroxylase (DBH) gene is in linkage with the ABO gene. The sample population consisted of 1,427 healthy Japanese subjects who completed the Temperament and Character Inventory (TCI). Each subject’s ABO blood type was determined by genotyping the rs8176719 and rs8176746 ABO gene single-nucleotide polymorphisms (SNPs) using a TaqMan genotyping assay. The relationships between the six ABO genotypes or four ABO phenotypes and personality traits were examined using a multivariate analysis of covariance (MANCOVA), controlling for age and sex. The MANCOVA data showed a significant difference in TCI scores among the ABO genotype groups (F [7, 1393] = 3.354, p = 0.001). A subsequent univariate analysis showed a significant difference in the mean scores for Persistence among the genotype groups (F = 2.680, partial η² = 0.010, p = 0.020). Similarly, dividing the ABO blood type into four phenotypes revealed a significant difference among the phenotype groups (F [7, 1397] = 2.529, p = 0.014). A subsequent univariate analysis showed a significant difference among the phenotype groups in the mean scores for Persistence (F = 2.952, partial η²= 0.006, p = 0.032). We observed a significant association between ABO blood group genotypes and personality traits in a large number of healthy Japanese subjects. However, these results should be regarded as preliminary and should be interpreted with caution because it is possible that the association between ABO blood group genotype and the Persistence trait is relatively weak.     

Medicogenetic study of isolates in Uzbekistan. II. Anthropogenetic characteristics, blood groups and serum proteins]

A study is carried out on the distribution of ABO, MN, Rh, P and Le blood groups systems, haptoglobins, and common anthropogenetic features in the population of two villages of the Samarkand district. The examined samples have appeared to be heterogenous for ABO, Rh and P systems. For MN and Le unification is possible. The summary data on the allotment of phenotypes are as follows: (%) 0-30.2, A-35.3, B-26.2, AB-8.3, M-33.9, N-26.2, MN-39.9, Rh- -1.5, P-78.6, Le(a-b+)-33, Le (a+b-)-22.2, Le(a-b-)-34.2, Le(a+b+)-10.6. Gene frequencies have are calculated. The occurrence with regards to haptoglobins in both the villages is the same. The summary data are as follows: Hp1=1-4.8, Hp1=2-36.2, Hp2=2-59%. Gene frequencies have been calculated. In the population of the village Karakent there is a change of the frequency in many features of dermatoglyphics. The frequencies of anthropogenetic features do not differ between the villages. The summary data are the following: the frequency of theelbow type of hand is 86.9%, the right type of "hand clasping"-55.0%, the right type of "arm folding"-50.4%, righthandedness-99.7%. The occurence of square lobe of the ear is 21%, spliced one is 26.2%, the hanging down is 52.7%. The frequency of the gene insensitivity for PTC taste is 0.47 in one village and 0.53 in the other.     

Male-biased dispersal promotes large scale gene flow in a subterranean army ant, Dorylus (Typhlopone) fulvus

Sex-biased dispersal is a widespread phenomenon in the animal kingdom, which strongly influences gene flow and population structure. Particularly army ants, important key-stone predators in tropical ecosystems, are prone to population fragmentation and isolation due to their extraordinary mating system: queens are permanently wingless, propagate via colony fission, and only the males disperse in mating flights. Here we report on sex-biased dispersal and the genetic population structure of an African subterranean army ant, Dorylus (Typhlopone) fulvus. Using maternally inherited mtDNA markers and bi-parentally inherited nuclear microsatellites we found strong geographical structuring of mtDNA haplotypes, whereas the nuclear genetic population structure was less pronounced. Strong mtDNA (Φ _ST = 0.85), but significantly lower nuclear (F _ST = 0.23) genetic differentiation translated into a more than an order of magnitude larger male migration rate compared to that of queens, reflecting the low motility of queens and strong, promiscuous dispersal by males. Thus, the well flying D. fulvus males appear to be the sex to promote large scale gene flow, and D. fulvus is indeed a species in which sex specific dispersal patterns and the mating system profoundly affect the population structure and phylogeography.     

ABO,Rh(D) and haptoglobin distribution in a sample from the sultanate of Oman

The distribution of phenotypic frequencies of ABO, Rh(D) system and Hp polymorphism in a sample from Muscat, Oman, revealed the following gene frequencies: P=0.164, q=0.110, r=0.726; D=0.738, d=0.262; Hp¹=0.289 and Hp²=0.711. These frequencies are in good agreement with the distribution in the Euroasiatic continent.     

Acuity of selective mechanisms operating on ABO, Rh, and MN blood groups

Selection in ABO, Rh, and MN blood groups was studied in 216 matings and their children in an endogamous population. Incompatibility status with respect to these three systems was considered simultaneously. There is no effect of incompatibility on number of pregnancies. Analysis of variance between groups confirms that prenatal loss is associated with incompatibility, and it is greater when the matings are incompatible for any two systems. There is no significant intergenerational change in ABO and Rh polymorphisms. Segregation analysis for the ABO system suggests that there is no significant difference in the proportion of A, B, and O children, based on the compatibility of the parents, while analysis for Rh-D system showed a segregation distortion which is not related to the known antigenic specificities (mother-child incompatibility).