scholarly journals Genetic correlations between the maternal genetic effect on chick weight and the direct genetic effects on egg composition traits in a White Leghorn line

2003 ◽  
Vol 82 (1) ◽  
pp. 1-8 ◽  
Author(s):  
C Hartmann ◽  
K Johansson ◽  
E Strandberg ◽  
L Rydhmer
2016 ◽  
Vol 56 (5) ◽  
pp. 927 ◽  
Author(s):  
M. G. Jeyaruban ◽  
D. J. Johnston ◽  
B. Tier ◽  
H.-U. Graser

Data on Angus (ANG), Charolais (CHA), Hereford (HER), Limousin (LIM) and Simmental (SIM) cattle were used to estimate genetic parameters for calving difficulty (CD), birthweight (BWT) and gestation length (GL) using threshold-linear models and to examine the effect of inclusion of random effect of sire × herd interaction (SxH) in the models. For models without SxH, estimated heritabilities for direct genetic effect of CD were 0.24 (±0.02), 0.22 (±0.04), 0.31 (±0.02), 0.22 (±0.04) and 0.17 (±0.01) for ANG, CHA, HER, LIM and SIM, respectively, whereas maternal heritabilities ranged from 0.13 to 0.20. Estimated heritabilities for direct genetic effect of BWT were 0.38 (±0.01), 0.37 (±0.03), 0.46 (±0.01), 0.35 (±0.02) and 0.36 (±0.01) for ANG, CHR, HER, LIM and SIM, respectively, whereas maternal heritabilities ranged from 0.08 to 0.11. Estimated heritabilities for direct genetic effect of GL were 0.59 (±0.02), 0.42 (±0.04), 0.50 (±0.03), 0.45 (±0.04) and 0.42 (±0.03) for ANG, CHR, HER, LIM and SIM, respectively, whereas maternal heritabilities ranged from 0.03 to 0.09. Genetic correlations between direct genetic effects of CD with BWT were highly positive and with GL were moderately positive for all five breeds. Estimated genetic correlations between direct genetic effects and maternal genetic effects (rdm) ranged across the five breeds from –0.40 (±0.05) to –0.16 (±0.02), –0.41 (±0.03) to –0.27 (±0.08) and –0.47 (±0.10) to –0.06 (±0.12) for BWT, GL and CD, respectively. Fitting SxH interaction as additional random effect significantly increased the log-likelihood for analyses of BWT, GL and CD of all breeds, except for GL of CHA. The estimated heritabilities were less than or equal to the estimates obtained with models omitting SxH. The rdm increased (i.e. became less negative) for BWT, GL and CD of all five breeds. However, the increase for GL was not substantially high in comparison to the increase observed for BWT and CD. Genetic parameters obtained for BWT, GL and CD, by fitting SxH as an additional random effect, are more appropriate to use in the genetic evaluation of calving ease in BREEDPLAN.


2005 ◽  
Vol 85 (2) ◽  
pp. 139-143 ◽  
Author(s):  
D. P. Rasali ◽  
G. H. Crow ◽  
J. N. B. Shrestha ◽  
A. D. Kennedy ◽  
A. Brûlé-Babel

Bivariate linear animal models were fit using MTDFREML programs for the analysis of cows’ stayability to 3 yr (STAY3, n = 1, 703) as a binary scored trait paired with body weights at birth (BW, n = 6,116), 205-d weaning (WW, n = 5,360,) and 1 yr of age (YW, n = 5250) in Angus cattle. For STAY3, the model included a fixed effect due to herd ×year of cow’s birth along with a random direct genetic effect. For each of BW, WW and YW, the model included fixed effects due to herd ×birth year, birth season, birth type, calf’s sex and the age of dam (as linear and quadratic covariates), while the random effects were direct and maternal genetic effects and permanent maternal environmental effects. Survival analysis revealed that the risk of cows, 10 yr or less in age, being culled from five Canadian Angus herds was highest between 2 and 3 yr of age. The direct heritability (h2) estimates for BW, WW and YW were 0.54, 0.73 and 0.47, respectively, and corresponding maternal heritability estimates were 0.14, 0.33 and 0.13, respectively. Furthermore, the direct h2 estimate for STAY3 from three bivariate analyses was 0.23–0.24. Estimates of direct-maternal genetic correlations of BW, WW and YW were -0.18, -0.70 and -0.39, respectively. The direct genetic correlations of STAY3 with BW, WW and YW were -0.15 to -0.09 indicating that selection for growth would have less detrimental influence on the stayability trait of cows. The correlations of direct genetic effects of STAY3 with maternal genetic effects of BW, WW and YW were between 0.20 and 0.25, indicating their favorable relationships as correlated traits. Key words: Stayability, growth traits, heritability, genetic correlations, beef cattle


2005 ◽  
Vol 56 (8) ◽  
pp. 789 ◽  
Author(s):  
M. Asadi Fozi ◽  
J. H. J. Van der Werf ◽  
A. A. Swan

(Co) variances for greasy fleece weight (GFW), clean fleece weight (CFW), mean fibre diameter (MFD), staple strength (SS), coefficient of variation of fibre diameter (CVFD), birthweight (BW), weaning weight (WW), and yearling weight (YW) were estimated for 5108 Australian Merino sheep from the CSIRO Fine Wool Project, born between 1990 and 1994. Covariances between these traits and number of lambs weaned per ewe joined (NLW) were also estimated. Significant maternal genetic effects were found for GFW, CFW, BW, WW, and YW. Estimates of heritability were biased upwardly when maternal effects were ignored. The maternal heritability estimates for GFW, CFW, BW, WW, and YW were 0.17, 0.15, 0.38, 0.28, and 0.13, respectively. Maternal effects were not important for MFD, CVFD, SS, and NLW. Direct-maternal genetic correlations within each fleece weight and bodyweight trait were estimated to be moderately negative (–0.26 to –0.48). The effect of ignoring maternal genetic effect was explored using selection index theory. Accounting for the maternal effects in both the selection criteria and breeding objective increased the overall response by 14.3%, 4.8%, 2.6%, 1.4%, and 0.0% in 3, 6, 12, 20 and 30% micron premium scenarios, respectively, compared with when the maternal effects were only included in breeding objective. Complete ignorance of the maternal effects led to overestimation in overall response of 2.8–35.7% for different micron premium scenarios in contrast to when the maternal effects were ignored in the selection index weight, but were included in the breeding objective. The results indicate that the maternal genetic effects of fleece weight and bodyweight should be considered in Merino breeding programs.


2002 ◽  
Vol 74 (3) ◽  
pp. 399-408 ◽  
Author(s):  
I. Ap Dewi ◽  
M. Saatci ◽  
Z. Ulutas

AbstractGenetic parameters of weight traits, ultrasonic fat and muscle depths, maternal effects and reproductive traits of Welsh Mountain sheep were estimated based on analyses of data from the nucleus flock of a cooperative breeding scheme. The traits analysed were 12 week weight (TW, no. = 11201), mature weight (MW, no. = 2376), weight at scanning (SW, no. = 1022), muscle depth (SM, no. = 1024), fat depth (SF, no. = 1024), litter weaning weight (LW, no. = 3445) and litter size (LS, no. = 3445). (Co)variance components were estimated in univariate and bivariate animal models. Heritability estimates from univariate analyses were 0.16, 0·49, 0·29, 0·24, 0·22, 0·20 and 0.15 for TW, MW, SW, SF, SM, LW and LS respectively. Genetic correlations among the weight traits were high. There was no detectable correlation between SF and SM. SF and SM were strongly correlated with SW but not with the other weight traits. LW was strongly correlated with MW and SW but not with TW, although the latter analysis was inconclusive. Maternal heritability was similar (0·11) for the univariate analysis of TW and all bivariate analyses involving TW (except for TW v. LW). The permanent environmental effect of dam was generally low (0.02 to 0.04) whilst litter effects were generally high (0·20 to 0·23). The correlation between direct and maternal genetic effects for TW were generally small and non-significant. The maternal genetic effect for TW was moderately correlated with the direct additive effect for MW and SW but was not significantly correlated with the direct additive effect for LS, SM or SF. A very large positive correlation was found between the maternal genetic effect for TW and the direct additive effect for LW. The implications of the results are discussed in the context of selection indices for Welsh Mountain sheep.


1999 ◽  
Vol 79 (3) ◽  
pp. 253-267 ◽  
Author(s):  
L.-E. Liljedahl ◽  
R. W. Fairfull ◽  
R. S. Gowe

White Leghorn strains were crossed reciprocally in a complete factorial mating system producing 6 pure strains and 30 strain-crosses, which were kept in individual cages for two laying cycles, 133–496 and 547–909 d of age. The egg production in the second cycle (C2) of the various genotypes started about 10 – 20% lower and had a more linear and less persistent course than in the first cycle (C1). Strains exhibited very different patterns of age changes in both additive and non-additive genetic effects as well as in cytoplasmic effects. The additive autosomal and sex-linked genes (Ai and Zi) active in one laying cycle were quite different from those active in the other laying cycle as shown by low strain genetic correlations between their effects in C1 and C2. Further, the sets of Ai and Zi genes responded with effects quite opposite to each other in both C1 and C2 as indicated by highly negative strain genetic correlations between the Ai and Zi effects. The average non-additive genetic effect of sire strain i or dam strain j over all its crosses with other strains (hi) and the non-additive genetic effect due to the specific combination of genes occurring in each of the two reciprocal crosses between strain i and strain j (sij), showed very divergent patterns of age changes with a conspicuously greater divergence as age advanced. The overall non-additive genetic effect (mean heterosis) increased significantly with age across the two cycles. The strain crosses that most successfully maintained their rate of lay until the end of C2, also most successfully developed a rising age trend for total heterosis. The non-additive genes active in one laying cycle were significantly different from those active in the other laying cycle as shown by the moderately low strain genetic correlations between their effects in C1 and C2. The genotypic variance and its various components increased markedly with age, however, with a tendency to reach a plateau towards the end of both the first and the second laying cycle. The environmental variance increased parallel to the genotypic variance. Consequently, the phenotypic variance followed the same pattern of age changes. The results are discussed in relation to the theoretical aspects of ageing genetics. A model compatible with all the age trends of the genetic and environmental effects and variances is set up, assuming that ageing is composed of two main opposing forces. Finally, the results are briefly discussed from the animal breeding point of view. Key words: Ageing, fitness, laying hens, genetic effects, variation, expression


2012 ◽  
Vol 34 (5) ◽  
pp. 584-590
Author(s):  
Peng-Yu WANG ◽  
Zha-Xi GUANQUE ◽  
Quan-Qing QI ◽  
Mao DE ◽  
Wen-Guang ZHANG ◽  
...  

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.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Vasiliki Lagou ◽  
◽  
Reedik Mägi ◽  
Jouke- Jan Hottenga ◽  
Harald Grallert ◽  
...  

AbstractDifferences between sexes contribute to variation in the levels of fasting glucose and insulin. Epidemiological studies established a higher prevalence of impaired fasting glucose in men and impaired glucose tolerance in women, however, the genetic component underlying this phenomenon is not established. We assess sex-dimorphic (73,089/50,404 women and 67,506/47,806 men) and sex-combined (151,188/105,056 individuals) fasting glucose/fasting insulin genetic effects via genome-wide association study meta-analyses in individuals of European descent without diabetes. Here we report sex dimorphism in allelic effects on fasting insulin at IRS1 and ZNF12 loci, the latter showing higher RNA expression in whole blood in women compared to men. We also observe sex-homogeneous effects on fasting glucose at seven novel loci. Fasting insulin in women shows stronger genetic correlations than in men with waist-to-hip ratio and anorexia nervosa. Furthermore, waist-to-hip ratio is causally related to insulin resistance in women, but not in men. These results position dissection of metabolic and glycemic health sex dimorphism as a steppingstone for understanding differences in genetic effects between women and men in related phenotypes.


2020 ◽  
Author(s):  
Eshim S Jami ◽  
Anke R Hammerschlag ◽  
Hill F Ip ◽  
Andrea G Allegrini ◽  
Beben Benyamin ◽  
...  

Internalising symptoms in childhood and adolescence are as heritable as adult depression and anxiety, yet little is known of their molecular basis. This genome-wide association meta-analysis of internalising symptoms included repeated observations from 64,641 individuals, aged between 3 and 18. The N-weighted meta-analysis of overall internalising symptoms (INToverall) detected no genome-wide significant hits and showed low SNP heritability (1.66%, 95% confidence intervals 0.84-2.48%, Neffective=132,260). Stratified analyses showed rater-based heterogeneity in genetic effects, with self-reported internalising symptoms showing the highest heritability (5.63%, 95% confidence intervals 3.08-8.18%). Additive genetic effects on internalising symptoms appeared stable over age, with overlapping estimates of SNP heritability from early-childhood to adolescence. Gene-based analyses showed significant associations with three genes: WNT3 (p=1.13×10-06), CCL26 (p=1.88×10-06), and CENPO (p=2.54×10-06). Of these, WNT3 was previously associated with neuroticism, with which INToverall also shared a strong genetic correlation (rg=0.76). Genetic correlations were also observed with adult anxiety, depression, and the wellbeing spectrum (|rg|> 0.70), as well as with insomnia, loneliness, attention-deficit hyperactivity disorder, autism, and childhood aggression (range |rg|=0.42-0.60), whereas there were no robust associations with schizophrenia, bipolar disorder, obsessive-compulsive disorder, or anorexia nervosa. Overall, childhood and adolescent internalising symptoms share substantial genetic vulnerabilities with adult internalising disorders and other childhood psychiatric traits, which could explain both the persistence of internalising symptoms over time, and the high comorbidity amongst childhood psychiatric traits. Reducing phenotypic heterogeneity in childhood samples will be key in paving the way to future GWAS success.


Author(s):  
Ludmila Zavadilová ◽  
Eva Kašná ◽  
Zuzana Krupová

Genomic breeding values (GEBV) were predicted for claw diseases/disorders in Holstein cows. The data sets included 6,498, 6,641 and 16,208 cows for the three groups of analysed disorders. The analysed traits were infectious diseases (ID), including digital and interdigital dermatitis and interdigital phlegmon, and non-infectious diseases (NID), including ulcers, white line disease, horn fissures, and double sole and overall claw disease (OCD), comprising all recorded disorders. Claw diseases/disorders were defined as 0/1 occurrence per lactation. Linear animal models were employed for prediction of conventional breeding values (BV) and genomic breeding values (GEBV), including the random additive genetic effect of animal and the permanent environmental effect of cow and fixed effects of parity, herd, year and month of calving. Both high and intermediate weights (80% and 50%, respectively) of genomic information were employed for GEBV50 and GEBV80 prediction. The estimated heritability for ID was 3.47%, whereas that for NID 4.61% and for OCD was 2.29%. Approximate genetic correlations among claw diseases/disorders traits ranged from 19% (ID x NID) to 81% (NID x OCD). The correlations between predicted BV and GEBV50 (84–99%) were higher than those between BV and GEBV80 (70–98%). Reliability of breeding values was low for each claw disease/disorder (on average, 3.7 to 14.8%) and increased with the weight of genomic information employed.


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