Genetic response to selection on reindeer calf weights

Selection response was investigated after 11 years of selection in the herding district of Ruvhten Sijte in Sweden (63°N,12°E) by comparing the weights of calves owned by herders applying selection with the weights of calves owned by herders not applying selection. Three owner groups in Ruvhten Sijte have selected calves at the autumn slaughter every year since 1986 by retaining heavy calves. They own approximately 45% of the reindeer in Ruvhten Sijte. The other owners do not select on recorded weights, and all animals mix during the mating season. The recorded data on calf weights (1986 to 1997) consisted of 12 484 observations, with mean selection differentials of 2.9 kg and 4.6 kg for female and male calves, respectively (phenotypic standard deviation equal to 4.4 kg). The female generation interval was 6.4 years. In 1996 and 1997, autumn live weights of calves owned by herders applying selection (n = 971) were compared with the weights of calves owned by herders not applying selection (n = 1125). The observed difference was 0.67 kg (total mean = 42.6 kg), of which 0.32 kg was due to differences in dam age structure between the two types of herds, therefore the estimated difference in selection response was 0.35 kg. The realized heritability was 0.2. The potential response that would have been realized if the selected part of the herd had been isolated from gene flow was predicted to be 2.0 kg. In conclusion, the introduction of a selection programme applied by all owners in a herding district would result in an increase in calf weights of approximately 2 kg after two generations of selection.&nbsp

Detecting Major Genetic Loci Controlling Phenotypic Variability in Experimental Crosses

Traditional methods for detecting genes that affect complex diseases in humans or animal models, milk production in livestock, or other traits of interest, have asked whether variation in genotype produces a change in that trait’s average value. But focusing on differences in the mean ignores differences in variability about that mean. The robustness, or uniformity, of an individual’s character is not only of great practical importance in medical genetics and food production but is also of scientific and evolutionary interest (e.g., blood pressure in animal models of heart disease, litter size in pigs, flowering time in plants). We describe a method for detecting major genes controlling the phenotypic variance, referring to these as vQTL. Our method uses a double generalized linear model with linear predictors based on probabilities of line origin. We evaluate our method on simulated F2 and collaborative cross data, and on a real F2 intercross, demonstrating its accuracy and robustness to the presence of ordinary mean-controlling QTL. We also illustrate the connection between vQTL and QTL involved in epistasis, explaining how these concepts overlap. Our method can be applied to a wide range of commonly used experimental crosses and may be extended to genetic association more generally

Breeding schemes in reindeer husbandry

The objective of the paper was to investigate annual genetic gain from selection (G), and the influence of selection on the inbreeding effective population size (Ne), for different possible breeding schemes within a reindeer herding district. The breeding schemes were analysed for different proportions of the population within a herding district included in the selection programme. Two different breeding schemes were analysed: an open nucleus scheme where males mix and mate between owner flocks, and a closed nucleus scheme where the males in non-selected owner flocks are culled to maximise G in the whole population. The theory of expected long-term genetic contributions was used and maternal effects were included in the analyses. Realistic parameter values were used for the population, modelled with 5000 reindeer in the population and a sex ratio of 14 adult females per male. The standard deviation of calf weights was 4.1 kg. Four different situations were explored and the results showed: 1. When the population was randomly culled, Ne equalled 2400. 2. When the whole population was selected on calf weights, Ne equalled 1700 and the total annual genetic gain (direct + maternal) in calf weight was 0.42 kg. 3. For the open nucleus scheme, G increased monotonically from 0 to 0.42 kg as the proportion of the population included in the selection programme increased from 0 to 1.0, and Ne decreased correspondingly from 2400 to 1700. 4. In the closed nucleus scheme the lowest value of Ne was 1300. For a given proportion of the population included in the selection programme, the difference in G between a closed nucleus scheme and an open one was up to 0.13 kg. We conclude that for mass selection based on calf weights in herding districts with 2000 animals or more, there are no risks of inbreeding effects caused by selection

Detecting and predicting changes in milk homogeneity using data from automatic milking systems

To ensure milk quality and detect cows with signs of mastitis, visual inspection of milk by prestripping quarters before milking is recommended in many countries. An objective method to find milk changed in homogeneity (i.e., with clots) is to use commercially available inline filters to inspect the milk. Due to the required manual labor, this method is not applicable in automatic milking systems (AMS). We investigated the possibility of detecting and predicting changes in milk homogeneity using data generated by AMS. In total, 21,335 quarter-level milk inspections were performed on 5,424 milkings of 624 unique cows on 4 farms by applying visual inspection of inline filters that assembled clots from the separate quarters during milking. Images of the filters with clots were scored for density, resulting in 892 observations with signs of clots for analysis (77% traces or mild cases, 15% moderate cases, and 8% heavy cases). The quarter density scores were combined into 1 score indicating the presence of clots during a single cow milking and into 2 scores summarizing the density scores in cow milkings during a 30-h sampling period. Data generated from the AMS, such as milk yield, milk flow, conductivity, and online somatic cell counts, were used as input to 4 multilayer perceptron models to detect or predict single milkings with clots and to detect milking periods with clots. All models resulted in high specificity (98-100%), showing that the models correctly classified cow milkings or cow milking periods with no clots observed. The ability to successfully classify cow milkings or cow periods with observed clots had a low sensitivity. The highest sensitivity (26%) was obtained by the model that detected clots in a single milking. The prevalence of clots in the data was low (2.4%), which was reflected in the results. The positive predictive value depends on the prevalence and was relatively high, with the highest positive predictive value (72%) reached in the model that detected clots during the 30-h sampling periods. The misclassification rate for cow milkings that included higher-density scores was lower, indicating that the models that detected or predicted clots in a single milking could better distinguish the heavier cases of clots. Using data from AMS to detect and predict changes in milk homogeneity seems to be possible, although the prediction performance for the definitions of clots used in this study was poor

Family History of Breast Cancer Is Associated with Elevated Risk of Prostate Cancer: Evidence for Shared Genetic Risks

Introduction: Although breast and prostate cancers arise in different organs and are more frequent in the opposite sex, multiple studies have reported an association between their family history. Analysis of single nucleotide polymorphism data, based on distant relatives, has revealed a small positive genetic correlation between these cancers explained by common variants. The estimate of genetic correlation based on close relatives reveals the extent to which shared genetic risks are explained by both common and rare variants. This estimate is unknown for breast and prostate cancer. Method: We estimated the relative risks, heritability, and genetic correlation of breast cancer and prostate cancer based on the Minnesota Breast and Prostate Cancer Study, a family study of 141 families ascertained for breast cancer. Results: Heritability of breast cancer was 0.34 (95% credible interval: 0.23-0.49) and 0.65 (95% credible interval: 0.36-0.97) for prostate cancer, and the genetic correlation was 0.23. In terms of odds ratios, these values correspond to a 1.3 times higher odds of breast cancer among probands, given that the brother has prostate cancer. Conclusion: This study shows the inherent relation between prostate cancer and breast cancer; an incident of one in a family increases the risk of developing the other. The large difference between estimates of genetic correlation from distant and close relatives, if replicated, suggests that rare variants contribute to the shared genetic risk of breast and prostate cancer. However, the difference could stem from genotype-by-family effects shared between the two types of cancers

Современные подходы в формировании прогнозов у больных артериальной гипертензией

ГИПЕРТЕНЗИЯ /ДИАГНКРОВЕНОСНЫХ СОСУДОВ БОЛЕЗНИПРОГНОЗАЛГОРИТМ

2-этилтиобензимидазола гидробромид предупреждает развитие оксидативного стресса и воспалительной реакции при стрессе

ОКСИДАТИВНЫЙ СТРЕСССТРЕСС2-ЭТИЛТИОБЕНЗИМИДАЗОЛА ГИДРОБРОМИДСЕРДЕЧНО-СОСУДИСТАЯ СИСТЕМА /ДЕЙСТВ ПРЕППЕРЕКИСНОЕ ОКИСЛЕНИЕ ЛИПИДОВОКИСЛИТЕЛЬНО-ВОССТАНОВИТЕЛЬНЫЕ РЕАКЦИИБИОМЕДИЦИНСКИЕ ИССЛЕДОВАНИЯЭКСПЕРИМЕНТЫ НА ЖИВОТНЫХКРЫС