scholarly journals Mitochondrial genetic effects on reproductive success: signatures of positive intra-sexual, but negative inter-sexual pleiotropy

2017 ◽  
Author(s):  
M. Florencia Camus ◽  
Damian K. Dowling

AbstractMitochondria contain their own DNA, and numerous studies have reported that genetic variation in this (mt)DNA sequence modifies the expression of life-history phenotypes. Maternal inheritance of mitochondria adds a layer of complexity to trajectories of mtDNA evolution, because theory predicts the accumulation of mtDNA mutations that are male-biased in effect. While it is clear that mitochondrial genomes routinely harbor genetic variation that affects components of reproductive performance, the extent to which this variation is sex-biased, or even sex-specific in effect, remains elusive. This is because nearly all previous studies have failed to examine mitochondrial genetic effects on both male and female reproductive performance within the one-and-the-same study. Here, we show that variation across naturally-occurring mitochondrial haplotypes affects components of reproductive success in both sexes, in Drosophila melanogaster. However, while we uncovered evidence for positive pleiotropy, across haplotypes, in effects on separate components of reproductive success when measured within the same sex, such patterns were not evident across sexes. Rather, we found a pattern of sexual antagonism across haplotypes on some reproductive parameters. This suggests the pool of polymorphisms that delineate global mtDNA haplotypes is likely to have been partly shaped by maternal transmission of mtDNA and its evolutionary consequences.

2018 ◽  
Vol 285 (1879) ◽  
pp. 20180187 ◽  
Author(s):  
M. Florencia Camus ◽  
Damian K. Dowling

Theory predicts that maternal inheritance of mitochondria will facilitate the accumulation of mtDNA mutations that are male biased, or even sexually antagonistic, in effect. While there are many reported cases of mtDNA mutations conferring cytoplasmic male sterility in plants, historically it was assumed such mutations would not persist in the streamlined mitochondrial genomes of bilaterian metazoans. Intriguingly, recent cases of mitochondrial variants exerting male biases in effect have come to light in bilaterians. These cases aside, it remains unknown whether the mitochondrial genetic variation affecting phenotypic expression, and in particular reproductive performance, in bilaterians is routinely composed of sex-biased or sex-specific variation. If selection consistently favours mtDNA variants that augment female fitness, but at cost to males, this could shape patterns of pleiotropy and lead to negative intersexual correlations across mtDNA haplotypes. Here, we show that genetic variation across naturally occurring mitochondrial haplotypes affects components of reproductive success in both sexes, in the fruit fly Drosophila melanogaster . We find that intrasexual correlations across mitochondrial haplotypes, for components of reproductive success, are generally positive, while intersexual correlations are negative. These results accord with theoretical predictions, suggesting that maternal inheritance has led to the fixation of numerous mutations of sexually antagonistic effect.


Genetics ◽  
1995 ◽  
Vol 140 (3) ◽  
pp. 1149-1159
Author(s):  
M W Blows ◽  
M B Sokolowski

Abstract Experimental lines of Drosophila melanogaster derived from a natural population, which had been isolated in the laboratory for approximately 70 generations, were crossed to determine if the expression of additive, dominance and epistatic genetic variation in development time and viability was associated with the environment. No association was found between the level of additive genetic effects and environmental value for either trait, but nonadditive genetic effects increased at both extremes of the environmental range for development time. The expression of high levels of dominance and epistatic genetic variation at environmental extremes may be a general expectation for some traits. The disruption of the epistatic gene complexes in the parental lines resulted in hybrid breakdown toward faster development and there was some indication of hybrid breakdown toward higher viability. A combination of genetic drift and natural selection had therefore resulted in different epistatic gene complexes being selected after approximately 70 generations from a common genetic base. After crossing, the hybrid populations were observed for 10 generations. Epistasis contributed on average 12 hr in development time. Fluctuating asymmetry in sternopleural bristle number also evolved in the hybrid populations, decreasing by > 18% in the first seven generations after hybridization.


2021 ◽  
Author(s):  
Laurence Howe ◽  
David Evans ◽  
Gibran Hemani ◽  
George Davey Smith ◽  
Neil Martin Davies

Estimating effects of parental and sibling genotypes (indirect genetic effects) can provide insight into how the family environment influences phenotypic variation. There is growing molecular genetic evidence for effects of parental phenotypes on their offspring (e.g. parental educational attainment), but the extent to which siblings affect each other is currently unclear.Here we used data from samples of unrelated individuals, without (singletons) and with biological full-siblings (non-singletons), to investigate and estimate sibling effects. Indirect genetic effects of siblings increase (or decrease) the covariance between genetic variation and a phenotype. It follows that differences in genetic association estimates between singletons and non-singletons could indicate indirect genetic effects of siblings.We used UK Biobank data to estimate polygenic risk score (PRS) associations for height, BMI and educational attainment in singletons (N = 50,143) and non-singletons (N = 328,549). The educational attainment PRS association estimate was 12% larger (95% C.I. 3%, 21%) in the non-singleton sample than in the singleton sample, but the height and BMI PRS associations were consistent. Birth order data suggested that the difference in educational attainment PRS associations was driven by individuals with older siblings rather than firstborns. The relationship between number of siblings and educational attainment PRS associations was non-linear; PRS associations were 24% smaller in individuals with 6 or more siblings compared to the rest of the sample (95% C.I. 11%, 38%). We estimate that a 1 SD increase in sibling educational attainment PRS corresponds to a 0.025 year increase in the index individual’s years in schooling (95% C.I. 0.013, 0.036).Our results suggest that older siblings influence the educational attainment of younger siblings, adding to the growing evidence that effects of the environment on phenotypic variation partially reflect social effects of germline genetic variation in relatives.


2017 ◽  
Vol 114 (14) ◽  
pp. 3690-3695 ◽  
Author(s):  
Eija Lonn ◽  
Esa Koskela ◽  
Tapio Mappes ◽  
Mikael Mokkonen ◽  
Angela M. Sims ◽  
...  

Most variation in behavior has a genetic basis, but the processes determining the level of diversity at behavioral loci are largely unknown for natural populations. Expression of arginine vasopressin receptor 1a (Avpr1a) and oxytocin receptor (Oxtr) in specific regions of the brain regulates diverse social and reproductive behaviors in mammals, including humans. That these genes have important fitness consequences and that natural populations contain extensive diversity at these loci implies the action of balancing selection. In Myodes glareolus, Avpr1a and Oxtr each contain a polymorphic microsatellite locus located in their 5′ regulatory region (the regulatory region-associated microsatellite, RRAM) that likely regulates gene expression. To test the hypothesis that balancing selection maintains diversity at behavioral loci, we released artificially bred females and males with different RRAM allele lengths into field enclosures that differed in population density. The length of Avpr1a and Oxtr RRAMs was associated with reproductive success, but population density and the sex interacted to determine the optimal genotype. In general, longer Avpr1a RRAMs were more beneficial for males, and shorter RRAMs were more beneficial for females; the opposite was true for Oxtr RRAMs. Moreover, Avpr1a RRAM allele length is correlated with the reproductive success of the sexes during different phases of reproduction; for males, RRAM length correlated with the numbers of newborn offspring, but for females selection was evident on the number of weaned offspring. This report of density-dependence and sexual antagonism acting on loci within the arginine vasopressin–oxytocin pathway explains how genetic diversity at Avpr1a and Oxtr could be maintained in natural populations.


Animals ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 37
Author(s):  
John McGlone ◽  
Arlene Garcia ◽  
Anoosh Rakhshandeh

The objective of this study was to examine the effectiveness of a novel 3-molecule boar pheromone (BOARBETTER®, BB,) to improve sow reproductive performance (breeding, conception, farrowing rates, pigs born alive, stillborn, mummies and total born). Data from 12 commercial farm sites were used to evaluate the effectiveness of BB. Each farm was used as the experimental unit in the meta-analyses. Individual sows records were collected, merged and analyzed in overall analyses. Relative to CON, BB increased the number of total born pigs per litter (13.81 ± 0.11 vs. 14.30 ± 0.11 pigs/litter, respectively; p < 0.01) and the number of pigs born alive (12.76 ± 0.14 vs. 13.13 ± 0.14 pigs/litter, respectively; p < 0.05). In the merged dataset analyses, the parity by treatment interaction was significant for total pigs and pigs born alive per litter (p < 0.01). In parities one through three, treatment with BB increased total pigs born by 0.88 per litter, and pigs born alive per litter by 0.73 pigs per litter (p < 0.05). However, BB had no effect on these parameters in sows from parities four through six. BOARBETTER® increased reproductive success, is cost effective, safe, and can meaningfully improve sow reproductive success and performance.


1971 ◽  
Vol 51 (1) ◽  
pp. 191-201 ◽  
Author(s):  
A. D. STEWART

SUMMARY The possibility of genetic variation in the amino acid composition of neurohypophysial hormones of the mouse was investigated. Acetic acid extracts from acetone-dried neurohypophyses from six strains of mice were subjected to thin-layer chromatography. Extracts from two strains were tested for natriferic potency on a toad bladder preparation. Extracts from three strains of mice were purified on a carboxymethylcellulose column, and the amino acid composition determined by paper electrophoresis at pH 2. All six strains of mice were found to elaborate an oxytocic principle with the chromatographic properties of oxytocin. All results were compatible with the view that five of the strains elaborate the usual mammalian vasopressin, [8-arginine]-vasopressin. However, chromatography, natriferic assays and analyses of amino acid composition indicated that the Peru strain of mice elaborated [8-lysine]-vasopressin. These mice would be the first mammals outside the Suina which possess this hormone, and the difference between the strains of mice is almost certainly genetic in origin. The significance of genetic variation within a species in the structure of a hormone is discussed in terms of its physiological and evolutionary consequences.


2015 ◽  
Vol 282 (1806) ◽  
pp. 20142422 ◽  
Author(s):  
S. Eryn McFarlane ◽  
Jamieson C. Gorrell ◽  
David W. Coltman ◽  
Murray M. Humphries ◽  
Stan Boutin ◽  
...  

Genetic variation in fitness is required for the adaptive evolution of any trait but natural selection is thought to erode genetic variance in fitness. This paradox has motivated the search for mechanisms that might maintain a population's adaptive potential. Mothers make many contributions to the attributes of their developing offspring and these maternal effects can influence responses to natural selection if maternal effects are themselves heritable. Maternal genetic effects (MGEs) on fitness might, therefore, represent an underappreciated source of adaptive potential in wild populations. Here we used two decades of data from a pedigreed wild population of North American red squirrels to show that MGEs on offspring fitness increased the population's evolvability by over two orders of magnitude relative to expectations from direct genetic effects alone. MGEs are predicted to maintain more variation than direct genetic effects in the face of selection, but we also found evidence of maternal effect trade-offs. Mothers that raised high-fitness offspring in one environment raised low-fitness offspring in another environment. Such a fitness trade-off is expected to maintain maternal genetic variation in fitness, which provided additional capacity for adaptive evolution beyond that provided by direct genetic effects on fitness.


2019 ◽  
Vol 81 (2) ◽  
pp. 115-119
Author(s):  
Jay Y. S. Hodgson

Students often have difficulty understanding the underpinning mechanisms of natural selection because they lack the means to directly test hypotheses within the classroom. Computer simulations are ideal platforms to allow students to manipulate variables and observe evolutionary outcomes; however, many available models solve the scenario for the users without revealing the evolutionarily significant calculations. I developed a simplified bioenergetics model of a hammerhead shark for teaching natural selection that allows the users to manipulate variables and see the impacts of modeling while solving for the evolutionary consequences. Students generate variation within the population by controlling cephalofoil widths and swimming speeds of an individual, which affect its ability to detect and capture prey at the expense of energy lost as drag from swimming. The trade-off between energy gained from successful predation and energy lost from metabolic expenditures dictates rates of reproduction. By manipulating a subset of factors that influence differential reproductive success, students gain an improved understanding of natural selection.


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