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1.
Genet Sel Evol ; 53(1): 12, 2021 Feb 05.
Artigo em Inglês | MEDLINE | ID: mdl-33546581

RESUMO

BACKGROUND: Product quality and production efficiency of Atlantic salmon are, to a large extent, influenced by the deposition and depletion of lipid reserves. Fillet lipid content is a heritable trait and is unfavourably correlated with growth, thus genetic management of fillet lipid content is needed for sustained genetic progress in these two traits. The laboratory-based reference method for recording fillet lipid content is highly accurate and precise but, at the same time, expensive, time-consuming, and destructive. Here, we test the use of rapid and cheaper vibrational spectroscopy methods, namely near-infrared (NIR) and Raman spectroscopy both as individual phenotypes and phenotypic predictors of lipid content in Atlantic salmon. RESULTS: Remarkably, 827 of the 1500 individual Raman variables (i.e. Raman shifts) of the Raman spectrum were significantly heritable (heritability (h2) ranging from 0.15 to 0.65). Similarly, 407 of the 2696 NIR spectral landscape variables (i.e. wavelengths) were significantly heritable (h2 = 0.27-0.40). Both Raman and NIR spectral landscapes had significantly heritable regions, which are also informative in spectroscopic predictions of lipid content. Partial least square predicted lipid content using Raman and NIR spectra were highly concordant and highly genetically correlated with the lipid content values ([Formula: see text] = 0.91-0.98) obtained with the reference method using Lin's concordance correlation coefficient (CCC = 0.63-0.90), and were significantly heritable ([Formula: see text] = 0.52-0.67). CONCLUSIONS: Both NIR and Raman spectral landscapes show substantial additive genetic variation and are highly genetically correlated with the reference method. These findings lay down the foundation for rapid spectroscopic measurement of lipid content in salmonid breeding programmes.


Assuntos
Produtos Pesqueiros/normas , Lipídeos/análise , Característica Quantitativa Herdável , Salmo salar/genética , Análise Espectral Raman/métodos , Animais , Cruzamento/métodos , Cruzamento/normas , Metabolismo dos Lipídeos , Lipídeos/genética , Polimorfismo Genético , Padrões de Referência , Espectroscopia de Luz Próxima ao Infravermelho/métodos , Espectroscopia de Luz Próxima ao Infravermelho/normas , Análise Espectral Raman/normas
2.
Genet Sel Evol ; 48(1): 70, 2016 09 20.
Artigo em Inglês | MEDLINE | ID: mdl-27650044

RESUMO

BACKGROUND: The management of genetic variation in a breeding scheme relies very much on the control of the average relationship between selected parents. Optimum contribution selection is a method that seeks the optimum way to select for genetic improvement while controlling the rate of inbreeding. METHODS: A novel iterative algorithm, Gencont2, for calculating optimum genetic contributions was developed. It was validated by comparing it with a previous program, Gencont, on three datasets that were obtained from practical breeding programs in three species (cattle, pig and sheep). The number of selection candidates was 2929, 3907 and 6875 for the pig, cattle and sheep datasets, respectively. RESULTS: In most cases, both algorithms selected the same candidates and led to very similar results with respect to genetic gain for the cattle and pig datasets. In cases, where the number of animals to select varied, the contributions of the additional selected candidates ranged from 0.006 to 0.08 %. The correlations between assigned contributions were very close to 1 in all cases; however, the iterative algorithm decreased the computation time considerably by 90 to 93 % (13 to 22 times faster) compared to Gencont. For the sheep dataset, only results from the iterative algorithm are reported because Gencont could not handle a large number of selection candidates. CONCLUSIONS: Thus, the new iterative algorithm provides an interesting alternative for the practical implementation of optimal contribution selection on a large scale in order to manage inbreeding and increase the sustainability of animal breeding programs.


Assuntos
Algoritmos , Cruzamento/métodos , Variação Genética/genética , Modelos Genéticos , Animais , Bovinos , Seleção Genética , Ovinos , Suínos
3.
Rev Aquac ; 15(2): 491-535, 2023 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-38504717

RESUMO

Disease and parasitism cause major welfare, environmental and economic concerns for global aquaculture. In this review, we examine the status and potential of technologies that exploit genetic variation in host resistance to tackle this problem. We argue that there is an urgent need to improve understanding of the genetic mechanisms involved, leading to the development of tools that can be applied to boost host resistance and reduce the disease burden. We draw on two pressing global disease problems as case studies-sea lice infestations in salmonids and white spot syndrome in shrimp. We review how the latest genetic technologies can be capitalised upon to determine the mechanisms underlying inter- and intra-species variation in pathogen/parasite resistance, and how the derived knowledge could be applied to boost disease resistance using selective breeding, gene editing and/or with targeted feed treatments and vaccines. Gene editing brings novel opportunities, but also implementation and dissemination challenges, and necessitates new protocols to integrate the technology into aquaculture breeding programmes. There is also an ongoing need to minimise risks of disease agents evolving to overcome genetic improvements to host resistance, and insights from epidemiological and evolutionary models of pathogen infestation in wild and cultured host populations are explored. Ethical issues around the different approaches for achieving genetic resistance are discussed. Application of genetic technologies and approaches has potential to improve fundamental knowledge of mechanisms affecting genetic resistance and provide effective pathways for implementation that could lead to more resistant aquaculture stocks, transforming global aquaculture.

4.
Genet Sel Evol ; 43: 31, 2011 Aug 24.
Artigo em Inglês | MEDLINE | ID: mdl-21864407

RESUMO

BACKGROUND: The four casein proteins in goat milk are encoded by four closely linked casein loci (CSN1S1, CSN2, CSN1S2 and CSN3) within 250 kb on caprine chromosome 6. A deletion in exon 12 of CSN1S1, so far reported only in Norwegian goats, has been found at high frequency (0.73). Such a high frequency is difficult to explain because the national breeding goal selects against the variant's effect. METHODS: In this study, 575 goats were genotyped for 38 Single Nucleotide Polymorphisms (SNP) located within the four casein genes. Milk production records of these goats were obtained from the Norwegian Dairy Goat Control. Test-day mixed models with additive and dominance fixed effects of single SNP were fitted in a model including polygenic effects. RESULTS: Significant additive effects of single SNP within CSN1S1 and CSN3 were found for fat % and protein %, milk yield and milk taste. The allele with the deletion showed additive and dominance effects on protein % and fat %, and overdominance effects on milk quantity (kg) and lactose %. At its current frequency, the observed dominance (overdominance) effects of the deletion allele reduced its substitution effect (and additive genetic variance available for selection) in the population substantially. CONCLUSIONS: The selection pressure of conventional breeding on the allele with the deletion is limited due to the observed dominance (overdominance) effects. Inclusion of molecular information in the national breeding scheme will reduce the frequency of this deletion in the population.


Assuntos
Caseínas/genética , Genes Dominantes , Cabras/genética , Leite/química , Polimorfismo de Nucleotídeo Único , Animais , Cruzamento , Caseínas/metabolismo , Feminino , Deleção de Genes , Genótipo , Cabras/metabolismo , Humanos , Masculino , Leite/metabolismo , Noruega , Paladar
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