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Impact of nonrandom mating on genetic variance and gene flow in populations with mass selection.

The mechanisms by which nonrandom mating affects selected populations are not completely understood and remain a subject of scientific debate in the development of tractable predictors of population characteristics. The main objective of this study was to provide a predictive model for the genetic variance and covariance among mates for traits subjected to directional selection in populations with nonrandom mating based on the pedigree. Stochastic simulations were used to check the validity of this model. Our predictions indicate that the positive covariance among mates that is expected to result with preferential mating of relatives can be severely overpredicted from neutral expectations. The covariance expected from neutral theory is offset by an opposing covariance between the genetic mean of an individual's family and the Mendelian sampling term of its mate. This mechanism was able to predict the reduction in covariance among mates that we observed in the simulated populations and, in consequence, the equilibrium genetic variance and expected long-term genetic contributions. Additionally, this study provided confirmatory evidence on the postulated relationships of long-term genetic contributions with both the rate of genetic gain and the rate of inbreeding (deltaF) with nonrandom mating. The coefficient of variation of the expected gene flow among individuals and deltaF was sensitive to nonrandom mating when heritability was low, but less so as heritability increased, and the theory developed in the study was sufficient to explain this phenomenon.

Genetic Variation↗

Use of computerized mate selection programs to control inbreeding of Holstein and Jersey cattle in the next generation.

The expected role of computerized mate selection programs with regard to inbreeding and lifetime profitability of Holstein and Jersey cattle was examined using data from 25 large registered herds of each breed. Sire selection and mate allocation were carried out using linear programming with the following objectives: 1) minimum inbreeding, 2) maximum net merit subject to a fixed inbreeding threshold, and 3) maximum expected lifetime profit after adjustment for inbreeding depression. Inbreeding of actual matings was similar to inbreeding from random matings, indicating that current inbreeding avoidance programs in these herds are ineffective. Inbreeding was reduced by 1.6 and 1.9% in Holsteins and Jerseys, respectively, when a mate allocation program was applied with service sires and usage levels fixed at the actual values. Benefits of mate selection programs increased when both sire selection and mate pair allocation were considered. Maximization of mean net merit with inbreeding restricted to a fixed level (5% in Holsteins and 8% in Jerseys) led to decreases in inbreeding of 0.9 and 1.4% and increases in lifetime profit of $16.66 and $26.86 in Holsteins and Jerseys, respectively, relative to programs that ignored inbreeding. Maximization of mean expected lifetime profit after adjustment for inbreeding depression decreased inbreeding by 1.8 and 2.8% and increased lifetime profit by $37.37 and $59.77 in Holsteins and Jerseys, respectively. Inbreeding coefficients estimated with pedigree traced to 1985 were inadequate predictors of inbreeding coefficients estimated with pedigrees traced to 1960. Mate selection programs cannot function optimally unless extensive historical pedigree data are available, particularly for service sires. Computerized mate selection programs can reduce inbreeding in the next generation, which will lead to an increase in farm profitability. However, if genetic diversity is to be maintained in the long term, procedures for selecting parents of AI sires must also be considered.

Algorithms↗

Mate selection by groups.

The two key components in a breeding program can be described as the development of an objective function and the implementation of an algorithm for mate selection to target the objective function. However, mate selection is unacceptably slow for objective functions that involve longer term aims, such as engineering a good connection between herds. This paper proposes animal clustering to facilitate group mate selection, plus a step to refine mate selection for individual animals. Cluster analysis is used to form groups of animals within each sex based on nominated factors such as breed, herd, age, and EBV. Mate selection is then performed on groups, reducing the size of the problem considerably. The example used involved a three-breed crossbred population with a simple objective function to maximize predicted progeny merit. Twenty sires and 500 dams were to be selected from 816 and 1784 candidates. Group mate selection achieved 96.9% efficiency (random selection, 0%; full mate selection, 100%) and took 0.28 s to compute (394.2 s for full mate selection). Permitting more candidates to reach the individual mate selection stage increased efficiency to, for example, 98.9% at the cost of an extra 1.15 s. Efficiency was also improved by permitting more clusters.

Algorithms↗

Influences of social learning on mate-choice decisions.

Evidence from both field and laboratory is consistent with the hypothesis that animals can acquire mate preferences by observing the mating behavior of others. It is difficult, however, to distinguish social learning about mates from a host of other social effects on mating that do not produce changes in preferences. Examples are drawn from laboratory studies on mate choice in female and male Japanese quail that illustrate ways in which social cues influence mating decisions. Quail of both sexes use social cues to modify their mate choices, but the sexes use the information to serve different purposes. Female quail gain preferences for males seen mating with other females, whereas males avoid females that they had observed mating with other males. This sex difference in social learning provides an example of how costs and benefits of sexual behavior can shape decision-making processes. Implications of the influence of social learning on sexual selection are briefly discussed.

Adaptation, Psychological↗

Mitochondrial inheritance patterns in Didymium iridis are not influenced by stage of mating competency.

To test whether the timing of transition to mating competency affected mitochondrial transmission patterns in D. iridis. Reciprocal crosses were made by combining mating compatible strains that differed in their competency to mate. The results were compared to crosses where both mating strains were competent at the time of combining and crosses where somatic fusion of plasmodia was allowed. The results show that the mating competency of the parental strains at the time of confronting a compatible mate does not affect mitochondrial transmission patterns, mating efficiency or the likelihood of biparental inheritance. However the timing of plasmodial formation is delayed when precompetent and competent strains are mated compared to when both strains are competent at the time of mixing. We also observed that somatic fusion of plasmodia did not appreciably increase the incidence of biparental inheritance compared to crosses where individual plasmodia were isolated. These results provide additional evidence of the variable nature of mitochondrial inheritance in D. iridis within crosses and between mating trials.

Animals↗

Ram mating behavior after long-term selection for reproductive rate in Rambouillet ewes.

Mating behavior is known to be heritable in several species, but it is not known if selection schemes for ewe reproductive traits affect mating behavior of rams. Therefore, our objectives were to determine if divergent (high vs low index) selection of a female reproductive trait (lambs born divided by age of ewe minus one) affects mating behavior patterns of male offspring during training to service an artificial vagina (AV) in a less than natural setting (Exp. 1) or during serving capacity tests (SCT) in simulated natural mating conditions (Exp. 2). The method for evaluating male mating behavior was a series of serving capacity tests to estimate sexual performance. For Exp. 1, five, 30-min observations were conducted to assess the mating behavior of 29 rams (22 mo old) being trained to service an AV. In Exp. 1, percentages of rams mounting (73 vs 36%) and ejaculating (67 vs 29%) differed (P < 0.05) between rams from high and low Rambouillet ewe selection lines, respectively. In Exp. 2, ram classification consisted of exposing each 22- to 24-mo-old ram (n = 48) to three unrestrained ewes in estrus for 18, 30-min tests. Any ram that had not mounted or ejaculated during SCT was evaluated for sexual orientation in a 30-min preference test in which each ram had access to both restrained estrual ewes and restrained rams. In Exp. 2, there was no difference (P > 0.2) in percentages of rams mounting (92 vs 78%) and ejaculating (88 vs 74%) between rams from high and low Rambouillet ewe selection lines, respectively. There was no difference (P > 0.33) between high and low ewe selection line rams for mounts or ejaculations for 18 SCT. Only one male-oriented ram was identified, which was from the high line. In Exp. 2, six SCT were necessary to obtain 95% reliability in sexual performance scores. Results of these studies indicate that long-term selection of ewes for litter size did not alter ram sexual performance after SCT under simulated natural mating conditions or affect incidence of male-oriented rams. Mating behavior observed during training to service an AV was lower for rams from ewes of the low selection line than for rams from ewes of the high selection line. We concluded that long-term selection for reproductive rate in ewes did not alter mating behavior patterns of male offspring; however, test conditions, such as restrained and unrestrained ewes and number of serving capacity tests, may affect conclusions in studies that evaluate sexual performance of rams.

Animals↗

No evidence for minority male mating advantage in wild type strains of Drosophila ananassae tested in multiple-choice experiments.

Minority male mating advantage was tested in wild type strains of Drosophila ananassae through multiple-choice experiments. Mating success of two types of flies present in five different ratios was scored by direct observation in an Elens-Wattiaux mating chamber. We found no evidence for minority male mating advantage in wild type strains of D. ananassae. The relative mating success of two types of females was also compared in the multiple-choice experiments at different ratios; there was no evidence for a rare female effect. Further, there was similarity in the results of experiments employing different methods. The total number of homogamic and heterogamic matings was obtained by combining the data (all five ratios) from each experiment. Homogamic matings were significantly more frequent than heterogamic ones, which demonstrates preferential mating between males and females of the same strain; this was also supported by a lower isolation estimate. There was also a significant difference in the degree of mating preference between the two strains.

Animals↗

The evolution of intratetrad mating rates.

Intratetrad mating, the fusion of gametes formed in a single meiosis, has unusual consequences for genetic diversity, especially in genome regions linked to mating type loci. Here we investigate the fate of modifier alleles that alter the rate of intratetrad mating, under models of heterozygote advantage and of genetic load resulting from recurrent mutation. In both cases, intratetrad mating is favored if the recombination rate between the selected locus and mating type is less than the frequency of lethal recessive alleles at that locus in the population. Positive feedback often accelerates the invasion of modifiers to the intratetrad mating rate. Recombination rate and intratetrad mating rate exert indirect selection on one another, resulting in a cascading decline in outcrossing, even in the absence of any cost of sex. However, under recurrent mutation, alleles for obligate intratetrad mating invade only very slowly, perhaps explaining why outcrossing can persist at low frequencies in a largely intratetrad mating population.

Biological Evolution↗

[Biology of the volcano mouse (N. a. alstone). XVI. Comparison of the reproductive capacity of wild females in the laboratory, following 3 mating systems].

The aim of the present work was the comparison of the reproductive capacity of the wild volcano mouse (Neotomodon alstoni alstoni) in the laboratory, using 3 mating systems: pair, harem and collective. The mice were captured in the Sierra del Volcán Ajusco (Cerro Pelado, Parres, D. F.) The animals were kept in plastic cages with sawdust bedding under room conditions of light, humidity and temperature. They were fed with ALBI-LAB Pellets and tap water, supplemented with carrots and lettuce. All mice were under quarantine for 30 days before the matings begun. These were done in 2 series: pair versus harem (1 male with 4 females), and pair versus collective (2 males with 4 females). Each system had initially 25 females; 4 consecutive pairings were done with each mating system used in both series, with a duration of 12 days each mating. Statistical analysis of the results was done using the square chi test. The data registered in the 4 matings of each pairing system used in the 2 series were: number of mated females, number and percentage of pregnant females, total of offspring born, mean litter number, number and percentage of live offspring at the and of the first week after birth and at weaning, and relation and proportion males-females. The comparative tables of the reproductive records of all the 4 matings of each pairing system used in the 2 series, were analyzed separately and as a whole; the global comparative table (totals of the 2 series) of the reproductive record of neotomodon, according to the 3 systems of mating, i. e., pair (P), harem (H) and collective (C) showed the following results: P = number of mated females, 189; number of pregnant females, 94; percentage of pregnant females, 49.7; total of offspring born, 286; mean litter number, 3.04; number of offsprings alive at the end of the first week after birth, 173; percentage of offsprings alive at the end of the first week after birth, 60.5; number of offsprings alive at weaning, 172; percentage of offsprings alive at weaning, 60.1.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

Assortative mating in somatic traits and its consequences.

The problem of assortative mating embraces non-random mating of spouses. However, it is often discussed together with its consequences, which results from the fact that when we study similarities between spouses at various stages of their acquaintance and/or living together we must take into consideration not only the criteria of mating but also the consequences like, for instance, "resembling" (synchronous changes in husband and wife) and perhaps compensation of one's traits. This problem has not been sufficiently examined so far and further studies are necessary (Wolaánski 1970c, Nikityuk and Filipov 1975, Kasprzak and Wolański 1977, Thiessen and Gregg 1980, James 1989). The problem of assortative mating involves both the reasons principally genetic-evolutionary problems (Pearson 1896, Wolański and Siniarska 1983, 1984)--and the consequences as well, like, for instance homosis, that is transmitting to the offspring similar genes from defined loci, and heterosis, that is transmitting the different genes. Thus problem constitutes genetic foundations of auxology. Also an ecological problem is added, namely a synchronous resemble changes of spouses connected with similar living conditions and life style. Assortative mating seems to be a simple problem but in fact it is a scientific problem in which genetic, ecological and auxological approaches are combined. Below we will discuss assortative mating from these angles with reference to some anthropological traits. As a matter of fact, assortative mating is concerned with such a fundamental problem in the biomedical and social sciences as development the traits of the offspring (organism level) and of the whole future generations (population level). This is a problem of great importance by no means theoretical only. In our studies the main emphasis has been on spouses similarities in the morphological, physiological and psychomotor traits and also on some changes in the successive generations (which was connected with the lasting of marriage before the moment of investigations). The variations of traits of the populations were also taken into consideration as well as the effects of assortative mating of spouses on the development of their children. The above mentioned problems will constitute the contents of the present chapter. Studies on assortative mating have had a long tradition in Poland and most probably are one of the earliest in the world, apart from those conducted by Pearson (1896) in Great Britain and the Anonymous ones from 1903. This pertains mostly to B. Rosiński's (1923, 1925, 1926, 1929) investigations conducted in Poland in 1918 and on Polish immigrants to Brazil in 1931 and USA in 1929-30 (Stołyhwo 1931, Rosiński 1934).

Anthropometry↗

The alpha-factor receptor C-terminus is important for mating projection formation and orientation in Saccharomyces cerevisiae.

Successful mating of MATa Saccharomyces cerevisiae cells is dependent on Ste2p, the alpha-factor receptor. Besides receiving the pheromone signal and transducing it through the G-protein coupled MAP kinase pathway, Ste2p is active in the establishment and orientation of the mating projection. We investigated the role of the carboxyl terminus of the receptor in mating projection formation and orientation using a spatial gradient assay. Cells carrying the ste2-T326 mutation, truncating 105 of the 135 amino acids in the receptor tail including a motif necessary for its ligand-mediated internalization, display slow onset of projection formation, abnormal shmoo morphology, and reduced ability to orient the mating projection toward a pheromone source. This reduction was due to the increased loss of mating projection orientation in a pheromone gradient. Cells with a mutated endocytosis motif were defective in reorientation in a pheromone gradient. ste2-Delta296 cells, which carry a complete truncation of the Ste2p tail, exhibit a severe defect in projection formation, and those projections that do form are unable to orient in a pheromone gradient. These results suggest a complex role for the Ste2p carboxy-terminal tail in the formation, orientation, and directional adjustment of the mating projection, and that endocytosis of the receptor is important for this process. In addition, mutations in RSR1/BUD1 and SPA2, genes necessary for budding polarity, exhibited little or no defect in formation or orientation of mating projections. We conclude that mating projection orientation depends upon the carboxyl terminus of the pheromone receptor and not the directional machinery used in budding.

Cell Differentiation↗

Mating-type locus control of killer toxins from Kluyveromyces lactis and Pichia acaciae.

Killer-toxin complexes produced by Kluyveromyces lactis and Pichia acaciae inhibit cell proliferation of Saccharomyces cerevisiae. Analysis of their actions in haploid MATalpha cells revealed that introduction of the opposite mating-type locus (MATa) significantly suppressed antizymosis. Together with resistance expressed by MATa/MATalpha diploids, the reciprocal action of MATa or MATalpha in haploids of opposite mating types suggests that these killer toxins may be subject to MAT locus control. Congruently, derepressing the silent mating-type loci, HMR and HML, by removing individual components of the histone deacetylase complex Sir1-4, either by transposon-tagging or by chemically inactivating the histone deacetylase catalytic subunit Sir2, yields toxin resistance. Consistent with MAT control of toxin action, killer-toxin-insensitive S. cerevisiae mutants (kti) become mating-compromised despite resisting the toxins' cell-cycle effects. Mating inhibition largely depends on the time point of toxin application to the mating mixtures and is less pronounced in Elongator mutants, whose resistance to the toxins' cell-cycle effects is the result of toxin-target process deficiencies. In striking contrast, non-Elongator mutants defective in early-response events such as toxin import/activation hardly recover from toxin-induced mating inhibition. This study reveals a novel effect of yeast killer toxins on mating and sexual reproduction that is independent of their impact on cellular proliferation and cell-cycle progression.

Genes, Mating Type, Fungal↗

Mating-type locus of Cryptococcus neoformans: a step in the evolution of sex chromosomes.

The sexual development and virulence of the fungal pathogen Cryptococcus neoformans is controlled by a bipolar mating system determined by a single locus that exists in two alleles, alpha and a. The alpha and a mating-type alleles from two divergent varieties were cloned and sequenced. The C. neoformans mating-type locus is unique, spans >100 kb, and contains more than 20 genes. MAT-encoded products include homologs of regulators of sexual development in other fungi, pheromone and pheromone receptors, divergent components of a MAP kinase cascade, and other proteins with no obvious function in mating. The alpha and a alleles of the mating-type locus have extensively rearranged during evolution and strain divergence but are stable during genetic crosses and in the population. The C. neoformans mating-type locus is strikingly different from the other known fungal mating-type loci, sharing features with the self-incompatibility systems and sex chromosomes of algae, plants, and animals. Our study establishes a new paradigm for mating-type loci in fungi with implications for the evolution of cell identity and self/nonself recognition.

Alleles↗

Identification of mating-type dependent genes by non-radioactive, arbitrarily primed PCR in Schizophyllum commune.

Using arbitrary primers for a PCR reaction on cDNA from different mating interactions, genes differentially expressed in a mating-type dependent manner have been identified. The cDNAs were prepared from mRNA extracted from liquid grown cultures of the fungus in order to prevent further steps in development and increase the possibility of identifying genes directly under control of the mating type system. A reaction using a monokaryotic strain was compared to a semicompatible mating reaction induced for B-regulated development and a reaction using a fully compatible mating. In the comparison of silver-stained, non-denaturing polyacrylamide gel separation of the PCR products bands differentially detected between the samples were cloned and subjected to further analysis. Bands were characterized which were present in both mating reactions but absent in the monokaryon while the third band was specifically absent in the fully compatible mating interaction. Sequence analysis allowed design of specific primers for verification of differential expression in a semi-quantitative PCR. Thus, use of radioactivity was not necessary for the fast and reproducible method identifying genes specifically regulated by mating reactions.

Cloning, Molecular↗

Heterozygosity at the b mating-type locus attenuates fusion in Ustilago maydis.

Mating and pathogenesis of the corn smut fungus, Ustilago maydis, are controlled by two unlinked mating-type loci, a and b. Yeast-like haploids that differ at both loci are compatible and fuse to establish a pathogenic dikaryon. Mating is assayed in vitro by co-inoculation on culture medium containing activated charcoal; compatible combinations have a characteristic "fuzzy" appearance caused by the growth of aerial hyphae. In general, this test has not been useful for assaying the mating ability of strains that are already mycelial (e.g., those heterozygous at b or at both mating-type loci). Using an assay for cytoduction involving transfer of a mitochondrial marker during transient cell fusion, and engineered strains with defined genotypes, we examined the mating abilities of strains heterozygous or hemizygous at the mating-type loci. The data (which have not been available from conventional pathogenicity or plate mating tests) show that heterozygosity at b attenuates fusion in haploid and diploid strains, whereas strains heterozygous at a retain the ability to fuse with a compatible haploid partner. It appears, therefore, that subsequent fusion events are attenuated once fusion has occurred to establish the U. maydis dikaryon.

Cell Fusion↗

Mating system of the filamentous ascomycete, Glomerella cingulata.

Mating in heterothallic filamentous ascomycetes is typically controlled by a single mating-type locus with two alternate alleles or idiomorphs. In this study, five self-sterile strains of Glomerella cingulata from pecan were crossed in all possible combinations. Four of the five strains could be placed into two mating-type groups, but the fifth strain was sexually compatible with all of the other strains. Single ascospore progeny were isolated from each of the successful crosses, tested for self-fertility, and backcrossed with both parents. In addition, subsets of F1 isolates were crossed with all five of the original strains from pecan and in all possible combinations with each other. Results from the crosses showed that the ascospore progeny had stably inherited the mating pattern of one of the parental strains and that the mating type had segregated 1:1 among the F1 isolates. Furthermore, the five strains from pecan were sexually compatible with five additional heterothallic strains in all but one combination. Data from these experiments are consistent with a mating system composed of a single mating-type locus with multiple alternate alleles. We believe that this is the first report of this type of mating system for an ascomycete species.

Alleles↗

Cloning and analysis of the mating-type idiomorphs from the barley pathogen Septoria passerinii.

The genus Septoria contains more than 1000 species of plant pathogenic fungi, most of which have no known sexual stage. Species of Septoria without a known sexual stage could be recent derivatives of sexual species that have lost the ability to mate. To test this hypothesis, the mating-type region of S. passerinii, a species with no known sexual stage, was cloned, sequenced, and compared to that of its close relative S. tritici (sexual stage: Mycosphaerella graminicola). Both of the S. passerinii mating-type idiomorphs were approximately 3 kb in size and contained a single reading frame interrupted by one (MAT-2) or two (MAT-1) putative introns. The putative products of MAT-1 and MAT-2 are characterized by alpha-box and high-mobility-group sequences, respectively, similar to those in the mating-type genes of M. graminicolaand other fungi. The mating-type genes of S. passerinii and M. graminicolaare evolving rapidly, approximately ten times faster than the internal transcribed spacer region of the ribosomal DNA, and are not closely related to those from Cochliobolusor other loculoascomycetes in the order Pleosporales. Therefore, the class Loculoascomycetes may be polyphyletic. Furthermore, differences between the phylogenetic trees may indicate separate evolutionary histories for the MAT-1 and MAT-2 idiomorphs. A three-primer multiplex-PCR technique was developed that allowed rapid identification of the mating types of isolates of S. passerinii. Both mating types were present in approximately equal frequencies and often on the same leaf in fields in Minnesota and North Dakota. Analyses with isozyme and random amplified polymorphic DNA markers revealed that each isolate had a unique genotype. The common occurrence of both mating types on the same leaf and the high levels of genotypic diversity indicate that S. passerinii is almost certainly not an asexual derivative of a sexual fungus. Instead, sexual reproduction probably plays an integral role in the life cycle of S. passerinii and may be much more important than previously believed in this (and possibly other) "asexual" species of Septoria.

Amino Acid Sequence↗

Reconciling sexual selection to species recognition: a process-based model of mating decision.

Mating signals often encode information important for both species recognition and mate quality assessment and endure selection pressures that combine both stabilizing and directional components. Here, we present a family of models of mate preference for multiple-message signals. Our models are process based rather than purely normative, they assume the existence of one (or more) "utility function" that order signals along a scale of perceived appropriateness, and interpret preferences either as the differential probability of signals recognition or as the combined effect of differential recognition and direct comparison between signal alternatives. These models show the critical role played by the proximate mechanisms of information processing in influencing the ultimate function of female mate choice. They show that if preferences are an emergent property of the way animals recognize signals then species recognition and mate quality assessment are expected to constrain each other severely and to limit the overall discrimination power of the system. In contrast, if preferences result from two computational processes, recognition and comparison, the constraining effects of species recognition and mate quality assessment are sensibly reduced. In these cases, females may improve discrimination in mate quality by adopting permissive recognition rules and limiting the risks of heterospecific mating.

Animals↗