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PubMed1986

The interdependence of mating structure and inbreeding depression.

The level of inbreeding depression depends on the genetic structure and composition of a population, and is not a meaningful concept in its own right. Models are presented for the dynamics of alleles governing mating strategy when viability is determined by generalized heterosis or lethal recessive alleles. It is shown that a protected polymorphism for mating strategy may ensue from generalized heterosis, while lethal recessive alleles may favor the common mating strategy. Further, neither model provides the conditions allowing spread of an allele when rare (protection) which are obtained by assuming as constant the level of inbreeding depression associated with the equilibrium genetic structure dictated by the common mating strategy.

Animals↗
PubMed1991

Coevolution of self-fertilization and inbreeding depression. II. Symmetric overdominance in viability.

We describe the evolutionary dynamics of a modifier of selfing coevolving with a locus subject to symmetric overdominance in viability under general levels of reduction in pollination success as a consequence of self-fertilization (pollen discounting). Simple models of the evolution of breeding systems that represent inbreeding depression as a constant parameter do not admit the possibility of stable mixed mating systems involving both inbreeding and random mating. Contrary to this expectation, we find that coevolution between a modifier of selfing and a single overdominant locus situated anywhere in the genome can generate evolutionarily attracting mixed mating systems. Two forms of association between the modifier locus and the viability locus promote the evolution of outcrossing. The favored heterozygous genotype at the viability locus develops positive associations with modifier alleles that enhance outcrossing and with the heterozygous genotype at the modifier locus. Associations between outcrossing and high viability evolve immediately upon the introduction of a rare modifier allele, even in the absence of linkage.

Alleles↗
PubMed1992

Relatedness and inclusive fitness with inbreeding.

Relatedness arising in kin selection theory is measured by a variable taking as values two pedigree indices in populations with inbreeding when selection is weak. This variable reduces to a single pedigree index when inbreeding is caused by partial selfing or partial sib-mating. General inclusive fitness formulations of kin selection models based on such a variable of relatedness are proposed.

Animals↗
PubMed1978

Inbreeding effects: evidence for a genetic system which regulates viability in Drosophila melanogaster populations.

Mating studies on individual couples of Drosophila melanogaster allowed the structure of inbred populations in terms of egg hatchability and egg-to-adult survival to be elucidated. The comparison between inbred (from brother-sister matings) and control (randomly crossed) populations distinguished between couples sensitive and insensitive to inbreeding. Mendelian ratios were observed for this "phenotypic trait" in the progeny of single couples. These ratios and a double mating experiment indicated that a gene or gene complex implicated in morphogenetic events blocked development during embryonic and larvo-pupal stages. The expression of this lethal gene in homozygous embryos depended on the genetic makeup of both parental flies, i.e., on male and female factors which act as regulatory components. Homozygous embryos which survived the first critical phase (from fertilization to hatching) continued to develop normally until the larvo-pupal period, when they died. Lethality was also modulated by the cytoplasmic composition of the parental eggs, as shown by taxonomic analysis and the double mating experiment. The results account for lethality throughout development due to inbreeding. They lead to an estimated genetic load from laying to adult stage of one "lethal equivalent".

Animals↗
PubMed2006

Correlation between incidences of self-inflicted burns and means of inbreeding coefficients, an ecologic study.

PURPOSE: The aim of the study is to obtain more insight into the possible association between consanguinity and the incidence of deliberate self-burning. METHODS: Data were obtained by analysis of medical records of patients hospitalized in two referral burn centers: Chormy Burn Center (Bushehr Province, south of Iran) from March 21, 1998, through March 20, 2004, and Shahid Sadoqi Center of Burns and Injuries (Yazd Province, center of Iran) from March 21, 2000, through March 20, 2004. RESULTS: The incidence of suicidal burns was 6.51 and 2.32/100,000 person-years for Bushehr and Yazd Provinces, respectively. The observed sex ratio of patients in both centers indicated there was a female predominance in patients with self-inflicted burns. Using patients' home addresses, patients were sorted into 16 cities. The incidence of suicide by self-burning ranged from 0.80 (for Tabas, located in Yazd Province) to 12.60/100,000 person-years (for Dilam, located in Bushehr Province). The coefficient of inbreeding defines the probability that an individual received both alleles of a pair from an identical ancestral source. There was a significant correlation between incidences of suicidal burns and mean coefficient of inbreeding (r = 0.782, df = 14, p < 0.001). CONCLUSION: In addition to other factors, consanguineous marriage may be a risk factor that influences the incidence of suicidal burns in a population.

Burns↗
PubMed2006

Inbreeding: when parents transmit more than genes.

Inbreeding in wild populations can have devastating effects on fitness, but the genetic causes should not be transmitted across generations. A new study of song sparrows has revealed a parent-offspring resemblance for inbreeding, resulting from population structuring, with important implications for understanding the genetic causes of phenotypic variation in wild populations.

Animals↗
PubMed2005

Altruism, sex, and inbreeding when the genotype-phenotype map is additive.

Recently published theoretical results suggest that, in a sexual population, when genotypes code for phenotypes in a complex manner, it is possible for altruistic genotypes to spread through a metapopulation (i.e. through a collection of subpopulations). This spread tends to occur during periods when the environment deteriorates throughout the metapopulation. By contrast, under asexual reproduction, non-altruistic genotypes seem to be favoured, at least when subpopulations are substantial in size. The most relevant previous study makes use of Kauffman and Levin's "NK model" as a way to relate genotypes to fitness. Unfortunately, there are both conceptual and technical problems with the application of the NK model to populations that contain many different genotypes (e.g. polymorphic diploid populations with more than a few loci under selection). The present study presents a more tractable and biologically plausible model to study the causal relationship between sexual reproduction and altruism. In particular, phenotypes are determined by additive interactions among alleles at different loci in a diploid genome, with up to 200 loci under selection. In addition, subpopulations are substantially larger than those considered in the most relevant previous work. The results show that, so long as there are multiple "fitness peaks" in "phenotype space", the additive genotype-phenotype map leads to results that are similar to those from the NK model. Various parameters are manipulated in an effort to discover the determinants of altruistic and non-altruistic outcomes. The findings should facilitate further investigations, and they should help to establish the plausibility of the suggested relationship between sexual reproduction and altruism. The results also suggest that inbreeding can lead to a similar result as asexuality. That is, inbreeding seems to enhance the probability that altruistic phenotypes will be eliminated.

Altruism↗
PubMed2004

Kin selection and coefficients of relatedness in family-structured populations with inbreeding.

We consider family specific fitnesses that depend on mixed strategies of two basic phenotypes or behaviours. Pairwise interactions are assumed, but they are restricted to occur between sibs. To study the change in frequency of a rare mutant allele, we consider two different forms of weak selection, one applied through small differences in genotypic values determining individual mixed strategies, the other through small differences in viabilities according to the behaviours chosen by interacting sibs. Under these two specific forms of weak selection, we deduce conditions for initial increase in frequency of a rare mutant allele for autosomal genes in the partial selfing model as well as autosomal and sex-linked genes in the partial sib-mating model with selection before mating or selection after mating. With small differences in mixed strategies, we show that conditions for protection of a mutant allele are tantamount to conditions for initial increase in frequency obtained in additive kin selection models. With particular reference to altruism versus selfishness, we provide explicit ranges of values for the selfing or sib-mating rate based on a fixed cost-benefit ratio and the dominance scheme that allow the spreading of a rare mutant allele into the population. This study confirms that more inbreeding does not necessarily promote the evolution of altruism. Under the hypothesis of small differences in viabilities, the situation is much more intricate unless an additive model is assumed. In general however, conditions for initial increase in frequency of a mutant allele can be obtained in terms of fitness effects that depend on the genotypes of interacting individuals or their mates and generalized conditional coefficients of relatedness according to the inbreeding condition of the interacting individuals.

Animals↗
PubMed1986

Inbreeding of Wistar-Kyoto rat strain with hyperactivity but without hypertension.

A genetic inbreeding program using Wistar-Kyoto rat strains as progenitors was used to combine the hyperactivity trait of the spontaneously hypertensive rat (SHR) with the normotensive trait of the WKY genetic control strain. From an SHR X WKY cross we produced a gene-assorting F2 population from which selected brother-sister matings were carried out through seven successive inbred populations. This program produced a new strain of hyperactive rats with normotensive mean systolic blood pressure levels, and we have designated the new strain as the Wistar-Kyoto hyperactive (WK/HA) rat. Another behavioral characteristic of the SHR rat, poor habituation in a nonreinforcing novel environment, did not appear as a characteristic trait of the new strain of WK/HA rats, suggesting a separate underlying genetic basis for the two traits that had been apparently fortuitously fixed in the SHR genotype as a result of intensive inbreeding of that strain. The new WK/HA strain, together with the WKY control strain, is considered as more suitable for subjects in studying hyperactivity in rats than the original SHR strain with its concomitant hypertension and poor habituation traits.

Animals↗
PubMed2002

Extraordinary haplotype diversity in haplodiploid inbreeders: phylogenetics and evolution of the bark beetle genus Coccotrypes.

Regular inbreeding by sib-mating is one of the most successful ecological strategies in the bark beetle family Scolytinae. Within this family, the many species (119) in Coccotrypes are found breeding in an exceptional variety of untraditional woody tissues different from bark and phloem. Species delineation by morphological criteria is extremely difficult, however, as in most other inbreeding groups of beetles, perhaps due to the unusual evolutionary dynamics characterizing sib-mating organisms. Hence, we here performed a phylogenetic analysis using molecular data in conjunction with morphological data to better understand morphological and ecological evolution in this sib-mating group. We used partial DNA sequences from the nuclear gene EF-alpha and the mitochondrial genes 12S and CO1 to elucidate patterns of morphological evolution, haplotype variation, and evolutionary pathways in resource use. Sequence variation was high among species and far above that expected at the species level (e.g., 19% for CO1 within Coccotrypes advena). The tendency for exhaustive sequence variation at deeper nodes resulted in ambiguous reconstructions of the deepest splits. However, all results suggested that species with the broadest diets were clustered in a single derived position-another piece of evidence against specialization as a derived evolutionary feature.

Animals↗
PubMed2003

Predicted rates of inbreeding with additive maternal effects.

Maternal effects play an important role in fitness and other aspects of individual performance in many species, particularly mammalian, yet their impact on genetic variation within species and its rate of loss during selection has been neglected. In this paper we extend the theory of expected long-term genetic contributions to include maternal effects, and tested the accuracy of predicted rates of inbreeding for populations under mass selection by comparison with simulations. The model includes selective advantages of direct and maternal additive genetic effects, and also the selective advantage of a common maternal environmental effect. The population structures investigated had a fixed number of dams per sire and fixed family size. Most prediction errors of the rate of inbreeding (deltaF) were less than 8% of the simulated means and were lower in magnitude than the prediction errors of genetic gain (deltaG). The predictions of deltaG from contributions equalled previously published predictions. A variation in maternal genetic effects resulted in a much larger deltaF than for an equally sized variation in common maternal environmental effects. For a fixed genetic gain, deltaF increased as the maternal heritability increased. The influence of family size, mating ratio and age structure on deltaF was greater with maternal effects than with only direct genetic effects included. In conclusion, maternal effects can be a very important aspect to consider when predicting deltaF in populations under selection, and the developed methodology gives good predictions.

Animals↗
PubMed1997

Point estimation and graphical inference of marginal dominance for two viability loci controlling inbreeding depression.

A deterministic analysis is conducted to examine marginal dominance for two linked viability loci influencing inbreeding depression and its graphical inferences. Four estimators of marginal dominance are derived, assuming a biallelic marker locus completely linked to one of the viability loci, and the biases in expected estimates due to the other deleterious locus are discussed. Three conditions under which apparent partial dominance or underdominance could occur are found, i.e. when two multiplicative, partially recessive loci are linked in coupling phase and when two synergistic, highly overdominant loci are linked in coupling or repulsion phases. Expected frequencies of the three marker genotypes in selfed progeny are derived, considering two linkage phases, two types of marker locus position with respect to the viability loci, and the multiplicative and synergistic fitness models. Segregation ratios are generated for the marker locus linked to either two overdominant or partially recessive loci and plotted in gene action graphs to examine the robustness of the graphical inferences of gene action due to the presence of an additional linked viability locus. Under a multiplicative fitness model, the presence of an additional partially recessive or overdominant locus in the vicinity of the marker locus does not greatly affect the graphical inferences of the relative role of partially recessive or overdominant genes in expression of inbreeding depression. A marker linked to two synergistic, highly overdominant loci can behave as though linked to a partially recessive, partially dominant or underdominant locus, even with relatively weak synergism.

Genes, Dominant↗
PubMed1993

Inbreeding coefficients from the surnames of grandparents of the schoolchildren in Albanian-speaking Italian villages.

Data on grandparental surnames were obtained from children in 45 Italo-Albanesi villages in nine provinces of southern Italy and Sicily. Concordance of surnames (isonymy) and inbreedding by village were estimated for each province and on the total sample. Total mean isonymy is 0.0251. The weighted mean inbreeding coefficient, and its random and non-random components are 0.0063, 0.0024 and 0.0039, respectively. Isonymy values are similar to those of rural Italian villages except that Alpine and some Appennine villages appear to be more isolated and inbred.

Albania↗
PubMed2003

Sorting out the effects of Wolbachia, genotype and inbreeding on life-history traits of a spider mite.

Wolbachia bacteria manipulate host reproduction by inducing cytoplasmic incompatibility (CI) and sex ratio distortion. Wolbachia are transmitted from mother to offspring through the cytoplasm of the egg. Therefore, reproduction of Wolbachia is tightly coupled to reproduction of its host. Mathematical analysis predicts that in the course of evolution, traits that reduce the physiological costs of the infection will be selectively favored. For a Wolbachia-host system to evolve, traits under selection must have some genetic component and variation must be present in the population. We have previously established that highly inbred isofemale lines of the two-spotted spider mite Tetranychus urticae may differ regarding the effects of infection by Wolbachia, and that at least some of the traits affected had a genetic component. However, the effects measured could have been affected by the fact that the lines were severely inbred prior to the experiments. In this paper we attempt to distinguish between the effects of Wolbachia, isofemale line, and inbreeding. We show that Wolbachia did not affect longevity but infected females produced smaller clutch sizes, more daughter-biased sex ratios and had decreased F1 mortality; between-line variation was found for clutch size, F1 mortality and sex ratio; finally, inbreeding resulted in an overall reduction of clutch sizes, and a change in survival curves and mean longevity.

Animals↗
PubMed1989

Female transfer and inbreeding avoidance in social mammals.

In most social mammals, males leave their natal group to breed in other groups whereas females commonly remain in the same group throughout their lives. In a few species however, females usually transfer between groups during adolescence. The functional significance of sex differences in dispersal and their connection, if any, to the avoidance of inbreeding is disputed. Here I show that in polygynous mammals where females commonly remain to breed in their natal group, their average age at first conception typically exceeds the average period of residence of adult males in breeding groups. In contrast, where females usually transfer to breed in other groups, the average residence of breeding males or of resident male kin groups typically exceeds the average age of females at first conception. These results support the suggestion that female mammals commonly transfer to avoid inbreeding with their father or other close relatives, although female dispersal may also occur for other reasons.

Age Factors↗
PubMed1994

Fluctuating asymmetry does not increase with moderate inbreeding in Drosophila melanogaster.

Fluctuating asymmetry, the unsigned difference between character values on the left and right sides of an individual, is often thought to be highly correlated with the heterozygosity of individuals or populations. A large sample of Drosophila melanogaster individuals with an inbreeding coefficient of F = 0.25 was derived from a laboratory population and compared to a sample of outbred individuals for the fluctuating asymmetry of sternopleural bristle number. Inbred flies were not more asymmetric than outbred flies. There was no evidence for heritability of fluctuating asymmetry, as measured by variance among full-sib lines. Fluctuating asymmetry may not be a reliable measure of the degree of inbreeding at the relatively low levels found in most animal populations and should be used with caution in the management of endangered species.

Animals↗
PubMed2006

Thelytokous parthenogenesis and its consequences on inbreeding in an ant.

Thelytokous parthenogenesis, that is, the production of diploid daughters from unfertilized eggs, may involve various cytological mechanisms, each having a different impact on the genetic structure of populations. Here, we determined the cytological mechanism of thelytokous parthenogenesis and its impact on inbreeding in the ant Cataglyphis cursor, a species where queens use both sexual and asexual reproduction to produce, respectively, workers and new queens. It has been suggested that thelytokous parthenogenesis in C. cursor might have been selected for to face high queen mortality and, originally, to allow workers to replace the queen when she passes away. We first determined the mode of thelytokous parthenogenesis by comparing the rate of transition to homozygosity at four highly polymorphic loci to expectations under the different modes of parthenogenesis. Our data show that thelytoky is achieved through automictic parthenogenesis with central fusion. We then estimated the proportion of colonies headed by worker-produced queens in a natural population. We designed a model linking the observed homozygosity in queens to the proportion of queens produced by workers, based on the assumption that (i) parthenogenesis is automictic with central fusion and (ii) queen lineage is asexually produced, resulting in an increase of the inbreeding over generations, whereas workers are sexually produced and therefore not inbred. Our results indicate that more than 60% of the colonies should be headed by a worker-produced queen, suggesting that queen's lifespan is low in this species.

Animals↗
PubMed2006

Inbreeding reduces power-law scaling in the distribution of fluctuating asymmetry: an explanation of the basis of developmental instability.

The study of fluctuating asymmetry has been controversial because of conflicting results found in much of the primary literature. It has been suggested that the source of this conflict is the fact that the basis of fluctuating asymmetry is poorly understood and that, as a consequence, methodology of fluctuating asymmetry studies may be flawed. A new model for the phenomenological basis of fluctuating asymmetry, that variation in fluctuating asymmetry is in large part due to the random exponential growth of cell populations (geometric Brownian motion) that are terminated randomly around a genetically programmed development time, is presented here. If termination of development has a genetic component, then scaling effects and kurtosis in the distribution of fluctuating asymmetry should increase with genetic redundancy of the population. This model prediction was tested by comparing the distribution of multivariate size and shape fluctuating asymmetry in large samples collected from both wild populations and four moderately inbred lines of Drosophila simulans. It was found that while wild populations were best described by a lognormal distribution with power-law scaled tails, the inbred lines derived from the wild stock were dramatically normalized (half-normal) in three of four cases. As predicted, the scaling exponent of the upper tail of the distribution of fluctuating asymmetry increased with inbreeding while the kurtosis and mean fluctuating asymmetry decreased with inbreeding. The model suggests an additional explanation of leptokurtosis in fluctuating asymmetry. Kurtosis and scaling of the statistical distribution of fluctuating asymmetry in a population is related directly to genetic differences between individuals and these differences affect their ability to buffer the process of development against random perturbations.

Animals↗