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Structural and functional analysis of the HSP90AA1 gene: distribution of polymorphisms among sheep with different responses to scrapie

机译:HSP90AA1基因的结构和功能分析:绵羊对瘙痒病的不同反应之间的多态性分布

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摘要

Scrapie is a transmissible spongiform encephalopathy in sheep and goats. Susceptibility to this neurodegenerative disease is mainly controlled by point mutations at the PRNP locus. Other genes, apart from PRNP, have been reported to modulate resistance/susceptibility to scrapie. On the basis of several studies in Alzheimer and different transmissible spongiform encephalopathy models, HSP90AA1 was chosen as a putative positional and functional candidate gene that might be involved in the polygenic variance mentioned above. In the present work, the ovine HSP90AA1 gene including the promoter and other regulatory regions has been isolated and characterized. Several sequence polymorphisms have also been identified. FISH-mapping localized the HSP90AA1 gene on ovine chromosome OAR19q24dist, which was confirmed by linkage analysis. This chromosome region has been shown to include a quantitative trait loci (QTL) for scrapie incubation period in sheep. Expression analyses were carried out in spleen and cerebellum samples. No differences in the expression of the HSP90AA1 gene were found in any of these tissues (p > 0.05) between control and infected animal samples. Nevertheless, association analyses revealed that several polymorphisms in the 5′ and 3′ regions of the HSP90AA1 gene were differentially distributed among animals with different responses to scrapie infection. Thus, results presented here support the hypothesis that HSP90AA1 could be a positional and functional candidate gene modulating the response to scrapie in sheep.
机译:瘙痒病是绵羊和山羊的传染性海绵状脑病。这种神经退行性疾病的易感性主要由PRNP位点的点突变控制。据报道,除PRNP外,其他基因还可以调节对瘙痒病的抵抗力/敏感性。根据对阿尔茨海默氏症的多种研究和不同的可传播性海绵状脑病模型,选择HSP90AA1作为可能与上述多基因变异有关的位置和功能候选基因。在本工作中,已经分离并鉴定了包括启动子和其他调控区在内的绵羊HSP90AA1基因。还鉴定了几种序列多态性。 FISH映射将HSP90AA1基因定位在绵羊染色体OAR19q24dist上,这已通过连锁分析得到了证实。已显示该染色体区域包括绵羊痒痒病潜伏期的数量性状基因座(QTL)。在脾脏和小脑样本中进行表达分析。在对照和感染动物样品之间的任何这些组织中,均未发现HSP90AA1基因表达的差异(p> 0.05)。然而,关联分析显示,HSP90AA1基因5'和3'区的几种多态性在对瘙痒病感染有不同反应的动物中差异分布。因此,此处给出的结果支持以下假设:HSP90AA1可能是调节绵羊对瘙痒病反应的位置和功能候选基因。

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  • 来源
    《Cell Stress and Chaperones》 |2008年第1期|19-29|共11页
  • 作者单位

    Departamento de Mejora Genética Animal INIA Ctra La Coruña Km 7.5 28040 Madrid Spain;

    Unidad de Tecnología en Producción Animal Avda. Montañana 930 CITA 50059 Zaragoza Spain;

    Departamento de Mejora Genética Animal INIA Ctra La Coruña Km 7.5 28040 Madrid Spain;

    Laboratoire de Génétique biochimique et de Cytogénétique Département de Génétique Animale INRA Centre de Recherche de Jouy 78352 Jouy-en-Josas Cedex France;

    Laboratoire de Génétique biochimique et de Cytogénétique Département de Génétique Animale INRA Centre de Recherche de Jouy 78352 Jouy-en-Josas Cedex France;

    Laboratoire de Génétique biochimique et de Cytogénétique Département de Génétique Animale INRA Centre de Recherche de Jouy 78352 Jouy-en-Josas Cedex France;

    Laboratoire de Génétique biochimique et de Cytogénétique Département de Génétique Animale INRA Centre de Recherche de Jouy 78352 Jouy-en-Josas Cedex France;

    AgResearch Invermay Agricultural Centre Private Bag 50034 Mosgiel New Zealand;

    Laboratorio de Genética Bioquímica Facultad de Veterinaria Universidad de Zaragoza Miguel Servet 177 50013 Zaragoza Spain;

    Laboratorio de Genética Bioquímica Facultad de Veterinaria Universidad de Zaragoza Miguel Servet 177 50013 Zaragoza Spain;

    Laboratorio de Genética Bioquímica Facultad de Veterinaria Universidad de Zaragoza Miguel Servet 177 50013 Zaragoza Spain;

    Departamento de Mejora Genética Animal INIA Ctra La Coruña Km 7.5 28040 Madrid Spain;

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