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1.
Anim Genet ; 50(4): 381-385, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31179563

ABSTRACT

Polledness has been shown to have autosomal Mendelian inheritance, with the polled locus being dominant to the horned locus. This trait was mapped to the BTA1 centromeric end in several breeds. One of the distinctive attributes of Creole cattle, such as the Argentinean Creole, is the presence of long, lyre-shaped horns. However, polled native animals were reported before the introduction of modern selected European breeds. Here, we studied the origin of the polled mutation, either independent or introgressed, in a Creole line from the Creole cattle founder group at the IIACS-INTA Leales Experimental Station (northwest Argentina). The study sample (65 animals: 26 horned and 39 polled) was genotyped using high-density SNP microarrays and three previously reported genetic markers (P202 ID , P80kb ID and PG ). A genome-wide association study, selection signatures, linkage disequilibrium analysis and copy number variations were used to detect the responsible region and the segregating haplotypes/alleles. The interval mapped in the Leales herd (1.23-2.13 Mb) overlapped with the region previously reported in several European cattle breeds, suggesting that the same locus could be segregating in this population. The previously reported variants PF and PG were not detected, thus dismissing the Holstein-Friesian and Nellore origins of the polled phenotype in this native breed. Conversely, the presence of the Celtic variant PC suggests an almost complete co-segregation. The cluster analysis rejected the hypothesis of recent introgression, which is compatible with the historical record of polled Creole cattle in northwest Argentina.


Subject(s)
Cattle/genetics , Horns/physiology , Animals , Argentina , Cattle/classification , Chromosomes, Mammalian , Genome-Wide Association Study , Linkage Disequilibrium , Mutation , Phenotype
2.
Free Radic Biol Med ; 129: 486-491, 2018 12.
Article in English | MEDLINE | ID: mdl-30315934

ABSTRACT

The development of high-throughput technologies in the last decade produced an exponential increase in the amount of biological data available. The case of redox biology and apoptosis is not an exception, and nowadays there is a need to integrate information from multiple "omics" studies. Therefore, validation of proposed discoveries is essential. However, the study in biological systems of the effect of the massive amounts of sequence variation data generated with next-generation sequencing (NGS) technologies can be a very difficult and expensive process. In this context, the present study aimed to demonstrate the advantages of a computational methodology to systematically analyze the structural and functional effects of protein variants, in order to prioritize further studies. This approach stands out for its easy implementation, low costs and low time consumed. First, the possible impact of mutations on protein structure and function was tested by a combination of tools based on evolutionary and structural information. Next, homology modeling was performed to predict and compare the 3D protein structures of unresolved amino acid sequences obtained from genomic resequencing. This analysis applied to the bovine GSTP1 allowed to determine that some of amino acid substitutions may generate important changes in protein structure and function. Moreover, the haplotype analysis highlighted three structure variants worthwhile studying through in vitro or in vivo experiments.


Subject(s)
Amino Acid Substitution , Glutathione S-Transferase pi/chemistry , Mutation , Polymorphism, Single Nucleotide , RNA, Messenger/genetics , Amino Acid Sequence , Animals , Cattle , Computational Biology/methods , Gene Expression , Glutathione S-Transferase pi/genetics , Glutathione S-Transferase pi/metabolism , Haplotypes , Protein Conformation , RNA, Messenger/metabolism , Sequence Analysis, DNA , Structural Homology, Protein , Structure-Activity Relationship
3.
Meat Sci ; 108: 17-20, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26010991

ABSTRACT

The biochemical bases of meat color are determined by the concentration and redox state of myoglobin, hemoglobin, cytochromes, and other pigments. Post-mortem depletion of cellular oxygen results in oxidative stresses that consume NADH and affects reducing activity, while enzymatic detoxification influences the cellular oxidative processes, both affecting meat color. The aim of this work was to study the influence of several genes related to cellular oxidative processes that could affect CIELAB meat color parameters. The study was performed in steers that received a grass-based diet combined with grain, hays and silages. Results suggest a possible link between colorimetric parameters (a*, b* and chroma) and SNPs in the GSTP1 gene (P<0.05). Although the influence of the enzymes, encoded by GSTP1 gene, on meat color has been proposed previously at biochemical level and protein expression level, further association studies in different populations and functional studies of proteins are needed to confirm the genetic determination of that gene on meat color.


Subject(s)
Cattle/genetics , Color , Oxidation-Reduction , Red Meat , Animal Feed , Animals , Diet/veterinary , Glutathione Peroxidase/genetics , Glutathione Peroxidase/metabolism , Glutathione S-Transferase pi/genetics , Glutathione S-Transferase pi/metabolism , Isoenzymes/genetics , Isoenzymes/metabolism , L-Lactate Dehydrogenase/genetics , L-Lactate Dehydrogenase/metabolism , Lactate Dehydrogenase 5 , Molecular Chaperones/genetics , Molecular Chaperones/metabolism , Muscle, Skeletal/metabolism , Myoglobin/metabolism , Phospholipid Hydroperoxide Glutathione Peroxidase , Polymorphism, Single Nucleotide
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