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1.
Nature ; 511(7507): 46-51, 2014 Jul 03.
Artículo en Inglés | MEDLINE | ID: mdl-24990743

RESUMEN

The large spectrum of limb morphologies reflects the wide evolutionary diversification of the basic pentadactyl pattern in tetrapods. In even-toed ungulates (artiodactyls, including cattle), limbs are adapted for running as a consequence of progressive reduction of their distal skeleton to symmetrical and elongated middle digits with hoofed phalanges. Here we analyse bovine embryos to establish that polarized gene expression is progressively lost during limb development in comparison to the mouse. Notably, the transcriptional upregulation of the Ptch1 gene, which encodes a Sonic hedgehog (SHH) receptor, is disrupted specifically in the bovine limb bud mesenchyme. This is due to evolutionary alteration of a Ptch1 cis-regulatory module, which no longer responds to graded SHH signalling during bovine handplate development. Our study provides a molecular explanation for the loss of digit asymmetry in bovine limb buds and suggests that modifications affecting the Ptch1 cis-regulatory landscape have contributed to evolutionary diversification of artiodactyl limbs.


Asunto(s)
Evolución Biológica , Extremidades/anatomía & histología , Extremidades/embriología , Proteínas Hedgehog/metabolismo , Receptores de Superficie Celular/metabolismo , Animales , Tipificación del Cuerpo , Bovinos , Femenino , Regulación del Desarrollo de la Expresión Génica/genética , Esbozos de los Miembros/anatomía & histología , Esbozos de los Miembros/embriología , Masculino , Mesodermo/metabolismo , Ratones , Ratones Transgénicos , Receptores Patched , Receptor Patched-1 , Receptores de Superficie Celular/genética , Secuencias Reguladoras de Ácidos Nucleicos/genética
2.
PLoS One ; 8(5): e63512, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23717440

RESUMEN

Despite massive research efforts, the molecular etiology of bovine polledness and the developmental pathways involved in horn ontogenesis are still poorly understood. In a recent article, we provided evidence for the existence of at least two different alleles at the Polled locus and identified candidate mutations for each of them. None of these mutations was located in known coding or regulatory regions, thus adding to the complexity of understanding the molecular basis of polledness. We confirm previous results here and exhaustively identify the causative mutation for the Celtic allele (PC) and four candidate mutations for the Friesian allele (PF). We describe a previously unreported eyelash-and-eyelid phenotype associated with regular polledness, and present unique histological and gene expression data on bovine horn bud differentiation in fetuses affected by three different horn defect syndromes, as well as in wild-type controls. We propose the ectopic expression of a lincRNA in PC/p horn buds as a probable cause of horn bud agenesis. In addition, we provide evidence for an involvement of OLIG2, FOXL2 and RXFP2 in horn bud differentiation, and draw a first link between bovine, ovine and caprine Polled loci. Our results represent a first and important step in understanding the genetic pathways and key process involved in horn bud differentiation in Bovidae.


Asunto(s)
Bovinos/crecimiento & desarrollo , Cuernos/crecimiento & desarrollo , Alelos , Animales , Factores de Transcripción con Motivo Hélice-Asa-Hélice Básico/genética , Bovinos/genética , Mapeo Cromosómico/métodos , Factores de Transcripción Forkhead/genética , Regulación del Desarrollo de la Expresión Génica/genética , Variación Genética/genética , Genotipo , Cabras/genética , Cabras/crecimiento & desarrollo , Mutación/genética , Fenotipo , Receptores Acoplados a Proteínas G/genética , Ovinos/genética , Ovinos/crecimiento & desarrollo
3.
PLoS One ; 7(11): e49084, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-23152852

RESUMEN

Polled and Multisystemic Syndrome (PMS) is a novel developmental disorder occurring in the progeny of a single bull. Its clinical spectrum includes polledness (complete agenesis of horns), facial dysmorphism, growth delay, chronic diarrhea, premature ovarian failure, and variable neurological and cardiac anomalies. PMS is also characterized by a deviation of the sex-ratio, suggesting male lethality during pregnancy. Using Mendelian error mapping and whole-genome sequencing, we identified a 3.7 Mb deletion on the paternal bovine chromosome 2 encompassing ARHGAP15, GTDC1 and ZEB2 genes. We then produced control and affected 90-day old fetuses to characterize this syndrome by histological and expression analyses. Compared to wild type individuals, affected animals showed a decreased expression of the three deleted genes. Based on a comparison with human Mowat-Wilson syndrome, we suggest that deletion of ZEB2, is responsible for most of the effects of the mutation. Finally sperm-FISH, embryo genotyping and analysis of reproduction records confirmed somatic mosaicism in the founder bull and male-specific lethality during the first third of gestation. In conclusion, we identified a novel locus involved in bovid horn ontogenesis and suggest that epithelial-to-mesenchymal transition plays a critical role in horn bud differentiation. We also provide new insights into the pathogenicity of ZEB2 loss of heterozygosity in bovine and humans and describe the first case of male-specific lethality associated with an autosomal locus in a non-murine mammalian species. This result sets PMS as a unique model to study sex-specific gene expression/regulation.


Asunto(s)
Anomalías Múltiples/veterinaria , Emparejamiento Base/genética , Enfermedades de los Bovinos/genética , Mosaicismo , Proteínas Represoras/genética , Eliminación de Secuencia/genética , Anomalías Múltiples/genética , Anomalías Múltiples/patología , Animales , Bovinos , Enfermedades de los Bovinos/patología , Mapeo Cromosómico , Femenino , Feto/anomalías , Feto/patología , Cuernos/patología , Humanos , Patrón de Herencia/genética , Masculino , Mutación/genética , Embarazo , Reacción en Cadena en Tiempo Real de la Polimerasa , Proteínas Represoras/metabolismo , Piel/patología , Síndrome
4.
J Sci Food Agric ; 92(4): 975-86, 2012 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-22002664

RESUMEN

BACKGROUND: Improving the hygienic quality of forages for horse nutrition seems to be a reasonable target for decreasing the prevalence of pulmonary diseases. The aim of the experiment was to study the effects of different agricultural practices on the main aero-allergens contained in forages, including breathable dust, fungi, mycotoxins and pollens. RESULTS: Results showed that the late harvest of hay, a second crop or a haylage production provides a good alternative to increase hygienic quality by reducing fungi contamination and breathable dust content. Barn drying of hay, while having no effect on breathable dust, similarly reduced fungi contamination. In contrast, when hay was harvested at a lower dry mass content (750 g DM kg⁻¹ versus 850 g DM kg⁻¹), both breathable dust and fungi contaminations were increased, which could at least be reversed by adding propionic acid just before baling. Zearalenone was detected in different hays, and even in one case, in breathable dust. CONCLUSION: Overall, our data suggest that different approaches can be used to increase forage hygienic quality for horse feeding and thus reduce their exposure to factors involved in equine pulmonary disease.


Asunto(s)
Agricultura/métodos , Alimentación Animal/análisis , Alimentación Animal/microbiología , Contaminación de Alimentos/prevención & control , Enfermedades Transmitidas por los Alimentos/veterinaria , Enfermedades de los Caballos/prevención & control , Enfermedades Pulmonares/veterinaria , Alimentación Animal/efectos adversos , Animales , Polvo/análisis , Polvo/prevención & control , Enfermedades Transmitidas por los Alimentos/inmunología , Enfermedades Transmitidas por los Alimentos/prevención & control , Francia , Hongos/crecimiento & desarrollo , Hongos/inmunología , Hongos/aislamiento & purificación , Enfermedades de los Caballos/inmunología , Caballos , Lactobacillaceae/crecimiento & desarrollo , Lactobacillaceae/aislamiento & purificación , Enfermedades Pulmonares/inmunología , Enfermedades Pulmonares/prevención & control , Enfermedades Pulmonares Fúngicas/inmunología , Enfermedades Pulmonares Fúngicas/prevención & control , Enfermedades Pulmonares Fúngicas/veterinaria , Viabilidad Microbiana , Micotoxinas/análisis , Micotoxinas/toxicidad , Neumoconiosis/inmunología , Neumoconiosis/prevención & control , Neumoconiosis/veterinaria , Polen/efectos adversos , Estaciones del Año , Tiempo (Meteorología)
5.
Reprod Fertil Dev ; 22(7): 1083-91, 2010.
Artículo en Inglés | MEDLINE | ID: mdl-20797346

RESUMEN

In cattle, the embryo production rate after superovulation varies between individuals and is difficult to predict. Recently, we proposed that anti-Müllerian hormone (AMH) plasma levels measured before treatment can help predict superovulatory responses. To establish whether blood measurement of AMH can help predict the number of embryos produced by a given cow after superovulation, data collected over 4 years from 45 dairy cows submitted to repeated embryo production were analysed in a retrospective study. A high within-animal repeatability (0.38 and 0.36) and a strong effect of the father of the donor cow (P < 0.01) were observed for the numbers of collected and transferable embryos, respectively. AMH concentration, measured in the plasma of donor cows during first lactation and several months before the start of the embryo production campaigns, was found to be highly correlated with the maximal number of collected (P < 0.0001) and transferable (P < 0.01) embryos per cow. In conclusion, the capacity of embryo production is a repeatable and probably heritable trait in the cow, and blood measurement of AMH in potential donor cows could be of value in determining a cow's intrinsic capacity to produce transferable embryos.


Asunto(s)
Hormona Antimülleriana/sangre , Bovinos/fisiología , Transferencia de Embrión/veterinaria , Inseminación Artificial/veterinaria , Superovulación/fisiología , Animales , Bovinos/embriología , Femenino , Inseminación Artificial/fisiología , Masculino , Valor Predictivo de las Pruebas , Embarazo , Análisis de Regresión , Estudios Retrospectivos
6.
Pigment Cell Res ; 19(4): 346-55, 2006 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16827753

RESUMEN

Mammalian pigmentation is controlled by the concerted action of Tyr, Tyrp1 and Dct producing eumelanin and/or pheomelanin in melanocytes. The ratio of these two pigments is determined by the agonist alpha-melanocyte stimulating hormone and the antagonist Agouti protein acting on the Mc1r. Here we show that the Agouti gene is over-expressed in Normande breed compared with Prim'Holstein breed. The Normande cattle have a characteristic coat color phenotype with a variable presence of black (eumelanin) hair over a red/brown background. We have found a previously undescribed full-length L1-BT element inserted in the 5'-genomic sequence of the Agouti gene in Normande cattle which promotes the over-expression of alternative transcripts. The variable expression of the alternative transcript directed by the long interspersed nuclear element promoter may be the origin of the brindle coat color pattern of the Normande breed. This new bovine Agouti allele isolated in Normande breed has been named Abr. Finally, as ectopic over-expression of Agouti in Ay mice is responsible for the obesity syndrome, we discuss the possible consequences of Abr for meat and milk production in cattle.


Asunto(s)
Bovinos/genética , Péptidos y Proteínas de Señalización Intercelular/genética , Péptidos y Proteínas de Señalización Intercelular/metabolismo , Elementos de Nucleótido Esparcido Largo/fisiología , Mutagénesis Insercional/fisiología , Transcripción Genética , Proteína de Señalización Agouti , Alelos , Animales , Cruzamiento , Cruzamientos Genéticos , Perfilación de la Expresión Génica , Genotipo , Péptidos y Proteínas de Señalización Intercelular/aislamiento & purificación , Ratones , Datos de Secuencia Molecular , Mutación , Oxidorreductasas/metabolismo , Regiones Promotoras Genéticas , Homología de Secuencia de Ácido Nucleico , Pigmentación de la Piel/genética
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