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1.
Genet Sel Evol ; 48(1): 78, 2016 10 19.
Artículo en Inglés | MEDLINE | ID: mdl-27760516

RESUMEN

BACKGROUND: The mode of inheritance of horn status in sheep is far more complex than a superficial analysis might suggest. Observations, which were mostly based on crossbreeding experiments, indicated that the allele that results in horns is dominant in males and recessive in females, and some authors even speculated about the involvement of more than two alleles. However, all recent genome-wide association analyses point towards a very strong effect of a single autosomal locus on ovine chromosome 10, which was narrowed down to a putatively causal insertion polymorphism in the 3'-untranslated region of the relaxin/insulin-like family peptide receptor 2 gene (RXFP2). The main objective of this study was to test this insertion polymorphism as the causal mutation in diverse sheep breeds, including breeds with a variable and/or sex-dependent horn status. RESULTS: After re-sequencing a region of about 246 kb that covered the RFXP2 gene and its flanking regions for 24 sheep from six completely horned and six completely polled breeds, we identified the same insertion polymorphism that was previously published as segregating with horn status in these breeds. Multiplex PCR genotyping of 489 sheep from 34 breeds and some crosses between sheep breeds showed a nearly perfect segregation of the insertion polymorphism with horn status in sheep breeds of Central and Western European origin. In these breeds and their crossings, heterozygous males were horned and heterozygous females were polled. However, this segregation pattern was not, or at least not completely, reproducible in breeds with sex-dependent and/or variable horn status, especially in sheep that originated from even more southern European regions and from Africa. In such breeds, we observed almost all possible combinations of genotype, sex and horn status phenotype. CONCLUSIONS: The 1.78-kb insertion polymorphism in the 3'-untranslated region of RXFP2 and SNPs in the 3'-UTR, exon 14 and intron 11 of this gene that we analyzed in this study cannot be considered as the only cause of polledness in sheep and are not useful as a universal marker to define the genetic horn status in sheep.


Asunto(s)
Receptores Acoplados a Proteínas G/genética , Oveja Doméstica/genética , Regiones no Traducidas 3' , Alelos , Animales , Mapeo Cromosómico/métodos , Femenino , Estudios de Asociación Genética , Estudio de Asociación del Genoma Completo , Cuernos/crecimiento & desarrollo , Masculino , Mutagénesis Insercional , Mutación , Polimorfismo de Nucleótido Simple , Selección Artificial/genética , Factores Sexuales
2.
Glycobiology ; 24(6): 488-93, 2014 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-24663385

RESUMEN

Roe deer (Capreolus capreolus) are seasonal breeders and cyclic structural changes of roe bucks' testis come along with a totally arrested (winter) and a highly activated spermatogenesis (summer). For this reason, roe buck represents an interesting model to study general mechanisms of initiation and termination of spermatogenesis. We investigated if polysialic acid (polySia)-a linear homopolymer of α2,8-linked sialic acids, which could act as a negative regulator of cell-cell adhesion-might be involved in the activation and/or inactivation of spermatogenesis. To address this point, testis samples of adult male roe deer were collected at different time point of the year. Intriguingly, we observed that polySia attached to the neural cell adhesion molecule was enhanced during the onset of spermatogenesis in April. In addition, polySia was highly expressed in December. Predominantly, polySia was detectable between Sertoli cells and spermatogonia in the basal regions of testicular tubules and in the adluminal part of Sertoli cells. Interestingly, similar polySia distributions were observed during early testis development of other mammalians when gonocytes (pre-spermatogonia) and Sertoli cells represent the only cell populations in tubuli seminiferi. Thus, polySia is expressed during key steps of the "on/off mechanisms" of spermatogenesis and might represent one mediator of the interaction and communication between Sertoli cells and germ cell precursors.


Asunto(s)
Adhesión Celular , Ciervos/crecimiento & desarrollo , Ácidos Siálicos/metabolismo , Testículo/metabolismo , Animales , Ciervos/metabolismo , Masculino , Moléculas de Adhesión de Célula Nerviosa/metabolismo , Reproducción/genética , Estaciones del Año , Células de Sertoli/metabolismo , Espermatogénesis/genética , Espermatogonias/metabolismo , Testículo/crecimiento & desarrollo
3.
J Dairy Res ; 77(1): 56-62, 2010 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-19889251

RESUMEN

Casein genes have been proved to have an influence on milk properties, and are in addition appropriate for phylogeny studies. A large number of casein polymorphisms exist in goats, making their analysis quite complex. The four casein loci were analyzed by molecular techniques for genetic polymorphism detection in the two dairy goat breeds Bunte Deutsche Edelziege (BDE; n=96), Weisse Deutsche Edelziege (WDE; n=91), and the meat goat breed Buren (n=75). Of the 35 analyzed alleles, 18 were found in BDE, and 17 in Buren goats and WDE. In addition, a new allele was identified at the CSN1S1 locus in the BDE, showing a frequency of 0.05. This variant, named CSN1S1*A', is characterized by a t-->c transversion in intron 9. Linkage disequilibrium was found at the casein haplotype in all three breeds. A total of 30 haplotypes showed frequencies higher than 0.01. In the Buren breed only one haplotype showed a frequency higher than 0.1. The ancestral haplotype B-A-A-B (in the order: CSN1S1-CSN2-CSN1S2-CSN3) occurred in all three breeds, showing a very high frequency (>0.8) in the Buren.


Asunto(s)
Cruzamiento , Caseínas/genética , Industria Lechera , Cabras/genética , Haplotipos/genética , Carne , Animales , Femenino , Frecuencia de los Genes , Genotipo , Desequilibrio de Ligamiento/genética , Leche/química , Reacción en Cadena de la Polimerasa , Polimorfismo Genético/genética , Polimorfismo de Nucleótido Simple/genética , Polimorfismo Conformacional Retorcido-Simple , Sitios de Carácter Cuantitativo/genética , Selección Genética , Especificidad de la Especie
4.
São Paulo; s.n; 2019. 29 p.
Tesis en Portugués | SES-SP, SES SP - Instituto Adolfo Lutz, SES-SP, SESSP-IALACERVO, SESSP-ESPECIALIZACAOSESPROD, SES-SP | ID: biblio-1010358

RESUMEN

A doença renal crônica é uma lesão com perda irreversível da função dos rins. Dentre os tratamentos disponíveis para doenças renais terminais a hemodiálise é o mais utilizado, substituindo parcialmente a função renal, aliviando os sintomas da doença e preservando a vida do paciente. A hemodiálise promove a retirada das substâncias tóxicas, água e sais minerais que estão em excesso no organismo através da passagem do sangue através de um filtro. Seu maior insumo consumido é a água, devendo esta ser amplamente controlada para manter o padrão de segurança e qualidade, obedecendo rigorosamente os padrões normatizados pela Resolução da Diretoria Colegiada ­ RDC Nº 11, 13/03/2014. O monitoramento da água usada é extremamente importante, especialmente por causa do sistema imunológico debilitado dos pacientes que sofrem de insuficiência renal crônica. Se a água não for corretamente tratada, vários contaminantes químicos, bacteriológicos e tóxicos podem ser transferidos para os pacientes, levando ao aparecimento de efeitos adversos que podem ser letais. O objetivo deste trabalho é verificar como está a qualidade microbiológica da água tratada empregada em hemodiálise. Para tanto foi realizada uma revisão sistemática na base de dados BVS e Google Scholar, buscando trabalhos relativos à contaminação microbiológica...(AU)


Asunto(s)
Agua , Microbiología
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