565. A study of variation in twin cattle: III. Growth

1955 ◽  
Vol 22 (1) ◽  
pp. 1-9 ◽  
Author(s):  
J. W. B. King ◽  
H. P. Donald

1. Polynomial coefficients have been fitted to data on growth in live weight to 19 months and on height at withers to 27 months of age shown by one-egg (MZ) and two-egg (DZ) twins and pairs of half-sisters (HZ). The coefficients obtained (a0, a2 and a3) have been subjected to analysis of variance.2. For growth in live weight, the ratio of intrapair variances for MZ, DZ and HZ pairs was 1:6·8:10 for a1, which gives the straight line best fitting the observed curve. Unrelated pairs, it is calculated, would have had an intrapair variance 20·9 times as great as MZ pairs. From the point of view of minimizing the intrapair variance, the advantage of the MZ pairs was usually a little less for a0, and considerably less for a2 and a3.3. For height at withers, the results were similar to those for weight.4. The contribution of environmental variance to total intrapair variance increased from a0 to a3, while that due to additive genetic effects diminished. Owing to the wide fiducial limits applicable, the results can be accommodated assuming only additive genetic effects in addition to environmental effects as estimated from one-egg twins. The extent to which HZ pairs exceeded the variance expected, however, suggests that this simple assumption may prove inadequate.

2008 ◽  
Vol 11 (3) ◽  
pp. 257-265 ◽  
Author(s):  
Heather R. Bemmels ◽  
S. Alexandra Burt ◽  
Lisa N. Legrand ◽  
William G. Iacono ◽  
Matt McGue

AbstractAlthough life events are often conceptualized as reflecting exogenous risk factors for psychopathology, twin studies have suggested they are heritable. We undertook a mixed twin/adoption study to further explore genetic and environmental contributions to individual differences in the experience of life events. Specifically, a sample of 618 pairs of like-sex adolescent twins, 244 pairs of like-sex adopted adolescent and young adult siblings, and 128 pairs of like-sex biological siblings completed a life events interview. Events were classified as independent (not likely to have been influenced by respondent's behavior), dependent (likely to have been influenced by respondent's behavior), or familial (experienced by a family member), and then summed to form three life event scales. Variance on the scales was assumed to be a function of four factors: additive genetic effects (a2), shared environmental effects (c2), twin-specific effects (t2), and nonshared environmental effects (e2). Data were analyzed using standard biometrical models. Shared environmental effects were found to be the largest contributor to variance in familial events (c2 = .71; 95% confidence interval of .65, .76); additive genetic effects were the largest contributor to dependent events (a2 = .45; CI = .31, .58); and nonshared environmental effects were found to be the largest contributor independent events (e2 = .57; CI = .51, .64). A significant twin-specific effect was also found for independent life events, indicating that twins are more likely to be exposed to such events than non-twin biological siblings. Findings are discussed in terms of their implication for understanding the nature of psychosocial risk.


1981 ◽  
Vol 30 (1) ◽  
pp. 51-57 ◽  
Author(s):  
C. C. Morton ◽  
R. M. Cantor ◽  
L. A. Corey ◽  
W. E. Nance

Taste threshold for phenylthiocarbamide (PTC) was measured in 393 offspring from the families of 85 monozygotic (MZ) twin pairs. PTC scores were bimodally distributed with modes at one and eight and the antimode at five. Because of the non-normality of the distribution, a jackknife procedure was used to obtain 95% confidence intervals for the estimates of genetic, maternal, and environmental parameters. Analyses which assumed no epistasis and which included additive genetic effects revealed that 37.9% of the observed variation in PTC threshold was due to additive genetic effects, 16.6% was due to dominance effects, 14.2% was due to maternal effects, 13.7% was due to a common sibship environment, and 17.6% was due to random environmental effects, yielding a broad sense heritability of 0.55 for the threshold ability to taste PTC. Analyses which did not include additive genetic effects revealed 26.6% of the observed variance was due to dominance effects, 23.6% to maternal effects, and 49.8% to environmental effects at the 0.67 confidence levels, but that environmental factors accounted for 72.4% and dominance effects for 23.6% of the observed variation at the 95% level.


Twin Research ◽  
2002 ◽  
Vol 5 (4) ◽  
pp. 277-286 ◽  
Author(s):  
Dan A. Svensson ◽  
Bo Larsson ◽  
Elisabet Waldenlind ◽  
Nancy L. Pedersen

AbstractTo explore age-related mechanisms in the expression of recurrent headache, we evaluated whether genetic and environmental influences are a function of the reporting age using questionnaire information that was gathered in 1973 for 15- to 47-year-old Swedish twins (n =12,606 twin pairs). Liability to mixed headache (mild migraine and tension-type headache) was explained by non-additive genetic influences (49%) in men aged from 15 to 30 years and additive genetic plus shared environmental influences (28%) in men aged from 31 to 47 years. In women, the explained proportion of variance, which was mainly due to additive genetic effects, ranged from 61% in adolescent twins to 12% in twins aged from 41 to 47 years, whereas individual specific environmental variance was significantly lower in twins aged from 15 to 20 years than in twins aged from 21 to 30 years. Liability to migrainous headache (more severe migraine) was explained by non-addi-tive genetic influences in men, 32% in young men and 45% in old men, while total phenotypic variance was significantly lower in young men than in old men. In women, the explained proportion of variance ranged from 91% in the youngest age group to 37% in the oldest age group, with major contributions from non-additive effects in young and old women (15–20 years and 41–47 years, respectively) and additive genetic effects in intermediate age groups (21–40 years). While total variance showed a positive age trend, genetic variance tended to be stable across age groups, whereas individual specific environmental variance was significantly lower in adolescent women as compared to older women.


2013 ◽  
Vol 56 (1) ◽  
pp. 497-508
Author(s):  
R. Abdullahpour ◽  
M. M. Shahrbabak ◽  
A. Nejati-Javaremi ◽  
R. V. Torshizi ◽  
R. Mrode

Abstract. Data including 219 105 test day records of 22 569 first parity Holstein cows in 56 herds were analysed for milk yield, fat content and protein content. Legendre polynomials were used in a random regression model to explain traits curves, additive genetic and permanent environmental effects along days in milk (DIM). Legendre polynomials of order 3 were used to describe additive genetic effects on the traits. For permanent environmental effects, for milk the order of 6 and for fat and protein content the order of 4 were used. Heterogeneity of residual variance was considered. Restricted maximum likelihood (REML) methodology was used to estimate the required parameters. Variations in genetic, permanent environment and residual effects and heritability changes along DIM were computed and illustrated. Daily heritability estimates averaged as 0.22, 0.14 and 0.23 for milk, fat and protein contents, respectively. Minimum correlations between DIM for additive genetic effects were as 0.49, −0.01 and 0.34 for milk, fat and protein contents. There were higher genetic correlations between test day milk yield and protein content compared to fat content. The genetic trend of milk yield has increased over the years from 1971 to 2005, while the genetic trend for fat and protein content declined.


2014 ◽  
Vol 59 (No. 4) ◽  
pp. 182-189 ◽  
Author(s):  
I. Nagy ◽  
J. Farkas ◽  
I. Curik ◽  
G. Gorjanc ◽  
P. Gyovai ◽  
...  

Additive, dominance, and permanent environmental variance components were estimated for the number of kits born alive, number of kits born dead, and total number of kits born of a synthetic rabbit line (called Pannon Ka). The data file consisted of 11 582 kindling records of 2620 does collected between the years 1996–2013. The total number of animals in the pedigree files was 4012. The examined traits were evaluated using single-trait and two-trait (number of kits born alive-dead) animal models containing all or part of the following effects: additive genetic effects, permanent environmental effects, dominance effects. Heritability estimates calculated using the basic single-trait and two-trait models were 0.094 ± 0.018 and 0.090 ± 0.016 for number of kits born alive, 0.037 ± 0.010 and 0.041 ± 0.012 for number of kits born dead, and 0.117 ± 0.018 for total number of kits born, respectively. The relative significance of permanent environmental effects was 0.069 ± 0.014 and 0.069 ± 0.012 for number of kits born alive, 0.025 ± 0.011 and 0.023 ± 0.010 for number of kits born dead, and 0.060 ± 0.013 for total number of kits born, respectively. Using the extended single-trait and two-trait models, the ratios of the dominance components compared to the phenotypic variances were 0.048 ± 0.008 and 0.046 ± 0.007 for number of kits born alive, 0.068 ± 0.006 and 0.065 ± 0.006 for number of kits born dead, and 0.005 ± 0.0073 for total number of kits born, respectively. Genetic correlation coefficients between number of kits born alive and number of kits born dead were 0.401 ± 0.171 and 0.521 ± 0.182, respectively. Spearman’s rank correlations between the breeding values of the different single-trait models were close to unity in all traits (0.992–0.990). Much lower breeding value stability was found for two-trait models (0.384–0.898), especially for number of kits born dead. Results showed that the dominance components for number of kits born alive and number of kits born dead were not zero and affected the ranking of the animals (based on the breeding values).  


2015 ◽  
Vol 72 (5) ◽  
pp. 751-758 ◽  
Author(s):  
Aimee Lee S. Houde ◽  
Craig A. Black ◽  
Chris C. Wilson ◽  
Trevor E. Pitcher ◽  
Bryan D. Neff

Although studies addressing natural selection have primarily focused on additive genetic effects because of their direct relationship with responses to selection, nonadditive genetic and maternal effects can also significantly influence phenotypes. We partitioned the phenotypic variance of survival and fitness-related traits in juvenile Atlantic salmon (Salmo salar) from three allopatric populations (LaHave, Sebago, and Saint-Jean) into additive genetic, nonadditive genetic, and maternal environmental effects using a full-factorial breeding design. We also modelled the potential increase in offspring performance if nonrandom mating (e.g., mate choice) is considered instead of random mating. The three populations exhibited significant differences in trait values as well as the genetic architecture of the traits. Nevertheless, nonadditive genetic and maternal environmental effects tended to be larger than the additive genetic effects. There was also a shift from maternal environmental to genetic effects during development in two of the populations. That is, maternal environmental effects were larger at early (egg and alevin) life stages, whereas nonadditive effects were larger at the later (fry) life stage. The amount of additive genetic effects was small, suggesting the traits will respond slowly to selection. We discuss how different maternal environmental effects across years may influence the genetic architecture of offspring traits.


2006 ◽  
Vol 290 (5) ◽  
pp. L1010-L1017 ◽  
Author(s):  
Grith L. Sørensen ◽  
Jacob v. B. Hjelmborg ◽  
Kirsten O. Kyvik ◽  
Mogens Fenger ◽  
Anette Høj ◽  
...  

The collectin surfactant protein D (SP-D) is an important component of the pulmonary innate immune system, but SP-D is also present on extrapulmonary epithelial surfaces and in serum, where it has been used as a biomarker for pulmonary disease states. In this study, we investigate the mechanisms defining the constitutional serum level of SP-D and determine the magnitude of the genetic contribution to serum SP-D in the adult population. Recent studies have demonstrated that serum SP-D concentrations in children are genetically determined and that a single nucleotide polymorphism (SNP) located in the NH2-terminal region (Met11Thr) of the mature protein is significantly associated with the serum SP-D levels. A classic twin study was performed on a twin population including 1,476 self-reported healthy adults. The serum SP-D levels increased with male sex, age, and smoking status. The intraclass correlation was significantly higher for monozygotic (MZ) twin pairs than for dizygotic (DZ) twin pairs. Serum SP-D variance was influenced by nonshared environmental effects and additive genetic effects. Multivariate analysis of MZ and DZ covariance matrixes showed significant genetic correlation among serum SP-D and metabolic variables. The Met11Thr variant explained a significant part of the heritability indicating that serum SP-D variance could be decomposed into non-shared environmental effects (e2 = 0.19), additive genetic effects (h2 = 0.42), and the effect of the Met11Thr variations (q2 = 0.39).


2016 ◽  
Vol 3 (2) ◽  
Author(s):  
SHAILESH CHAND GAUTAM ◽  
MP Chauhan

Line × tester analysis of twenty lines and three testers of Indian mustard (Brassica juncea L. Czern & Coss.) cultivars were used to estimate general combining ability (GCA), specific combining ability (SCA) effects, high parent heterosis and narrow-sense heritability estimate for plant height, yield components and seed yield. Significant variance of line x tester for the traits like pods per plant and seed yield indicating non additive genetic effects have important role for controlling these traits. Significant mean squares of parents v/s crosses which are indicating significant average heterosis were also significant for all the traits except seeds per pod. High narrow-sense heritability estimates for all the traits except seeds per pod exhibited the prime importance of additive genetic effects for these traits except seeds per pod. Most of the crosses with negative SCA effect for plant height had at least one parent with significant negative or negative GCA effect for this trait. For most of the traits except pods per plant, the efficiency of high parent heterosis effect was more than SCA effect for determining superior cross combinations.


BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Akio Onogi ◽  
Toshio Watanabe ◽  
Atsushi Ogino ◽  
Kazuhito Kurogi ◽  
Kenji Togashi

Abstract Background Genomic prediction is now an essential technology for genetic improvement in animal and plant breeding. Whereas emphasis has been placed on predicting the breeding values, the prediction of non-additive genetic effects has also been of interest. In this study, we assessed the potential of genomic prediction using non-additive effects for phenotypic prediction in Japanese Black, a beef cattle breed. In addition, we examined the stability of variance component and genetic effect estimates against population size by subsampling with different sample sizes. Results Records of six carcass traits, namely, carcass weight, rib eye area, rib thickness, subcutaneous fat thickness, yield rate and beef marbling score, for 9850 animals were used for analyses. As the non-additive genetic effects, dominance, additive-by-additive, additive-by-dominance and dominance-by-dominance effects were considered. The covariance structures of these genetic effects were defined using genome-wide SNPs. Using single-trait animal models with different combinations of genetic effects, it was found that 12.6–19.5 % of phenotypic variance were occupied by the additive-by-additive variance, whereas little dominance variance was observed. In cross-validation, adding the additive-by-additive effects had little influence on predictive accuracy and bias. Subsampling analyses showed that estimation of the additive-by-additive effects was highly variable when phenotypes were not available. On the other hand, the estimates of the additive-by-additive variance components were less affected by reduction of the population size. Conclusions The six carcass traits of Japanese Black cattle showed moderate or relatively high levels of additive-by-additive variance components, although incorporating the additive-by-additive effects did not improve the predictive accuracy. Subsampling analysis suggested that estimation of the additive-by-additive effects was highly reliant on the phenotypic values of the animals to be estimated, as supported by low off-diagonal values of the relationship matrix. On the other hand, estimates of the additive-by-additive variance components were relatively stable against reduction of the population size compared with the estimates of the corresponding genetic effects.


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.


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