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1.
Animals (Basel) ; 12(19)2022 Oct 06.
Artigo em Inglês | MEDLINE | ID: mdl-36230429

RESUMO

This study investigated the influence of the degree of connectedness on the reliability of the estimated breeding values (EBVs). The focal trait in the study was the number of piglets born alive (NBA) from sows of the highly prolific Large White and Landrace sows. An analysis included total of 58,043 farrowing's during the 2008-2020 period. BLUP procedure was used to estimate the breeding values for NBA for the three herds separately and after merging all three herds into one herd. The model for EBV estimation included the following fixed factors: parity, genotype, seasons, litter sire, herds, sow age at farrowing, weaning-conception interval, length of previous lactation, and the following random effects: common litter environment, permanent litter environment, and direct additive genetic effect of animal. Heritability values for NBA ranged from 0.048 to 0.097, depending on the data included in the analysis. The connectedness between herds was analysed using the connectedness rating (CR) and the gene flow (GF) methods. CR among the observed herds ranged from 0.245 to 0.994%, depending on the data included. The exchange of genetic material between all three herds was determined using GF method. The high degree of connectedness determined by the CR and GF method had a strong effect on EBV reliability. The average EBV reliability ranged from 0.520 to 0.867, depending on the data included. The increase in average reliability was observed in both cases when the data were added, both in the analysis of average reliability for purebred animals and when crossbreeds were added, where an increase in this value was also observed. The increase in average EBV reliability is a consequence of the greater amount of information included in the joint evaluation. In conclusion, we believe that our research will improve EBV reliability and help in further selection work in the Republic of Serbia.

2.
Animals (Basel) ; 11(3)2021 Mar 16.
Artigo em Inglês | MEDLINE | ID: mdl-33809803

RESUMO

This work was aimed at evaluating loin transcriptome and metabolic pathway differences between the two main Serbian local pig breeds with divergent characteristics regarding muscle growth and fatness, as well as exploring nutrigenomic effects of tannin supplementation in Mangalitsa (MA) pigs. The study comprised 24 Mangalitsa and 10 Moravka (MO) males, which were kept under identical management conditions. Mangalitsa animals were divided in two nutritional groups (n = 12) receiving a standard (control) or tannin-supplemented diet (1.5%; MAT). Moravka pigs were fed the standard mixture. All animals were slaughtered at a similar age; 120 kg of average live weight (LW) and loin tissue was used for RNA-seq analysis. Results showed 306 differentially expressed genes (DEGs) according to breed, enriched in genes involved in growth, lipid metabolism, protein metabolism and muscle development, such as PDK4, FABP4, MYOD1 and STAT3, as well as a relevant number of genes involved in mitochondrial respiratory activity (MT-NDs, NDUFAs among others). Oxidative phosphorylation was the most significantly affected pathway, activated in Mangalitsa muscle, revealing the basis of a different muscle metabolism. Also, many other relevant pathways were affected by breed and involved in oxidative stress response, fat accumulation and development of skeletal muscle. Results also allowed the identification of potential regulators and causal networks such as those controlled by FLCN, PPARGC1A or PRKAB1 with relevant regulatory roles on DEGs involved in mitochondrial and lipid metabolism, or IL3 and TRAF2 potentially controlling DEGs involved in muscle development. The Tannin effect on transcriptome was small, with only 23 DEGs, but included interesting ones involved in lipid deposition such as PPARGC1B. The results indicate a significant effect of the breed on muscle tissue gene expression, affecting relevant biological pathways and allowing the identification of strong regulatory candidate genes to underlie the gene expression and phenotypic differences between the compared groups.

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