Marcos-Carcavilla Ane, Calvo Jorge H, González Carmen, Moazami-Goudarzi Katayoun, Laurent Pascal, Bertaud Maud, Hayes Hélène, Beattie Anne E, Serrano Carmen, Lyahyai Jaber, Martín-Burriel Inmaculada, Alves Estefânia, Zaragoza Pilar, Badiola Juan J, Serrano Magdalena
Departamento de Mejora Genética Animal, INIA, Ctra La Coruña Km 7.5, 28040, Madrid, Spain.
Mamm Genome. 2007 Jan;18(1):53-63. doi: 10.1007/s00335-006-0095-6. Epub 2007 Jan 22.
Scrapie (SC) is a transmissible spongiform encephalopathy (TSE) in sheep and goats. Susceptibility to this neurodegenerative disease is controlled mainly by point mutations at the PRNP locus. Other genes, apart from PRNP, have been reported to modulate resistance/susceptibility to SC. On the basis of several studies on Alzheimer's disease and different TSE models, and of requirement for correct homeostasis of cytokines in brain, IL1B and IL1RN were chosen as putative positional and functional candidate genes that might be involved in the polygenic variance mentioned above. In the present work, ovine IL1B and IL1RN genes were partially isolated and characterized, including promoter and other regulatory regions. In addition, several sequence polymorphisms were identified. Furthermore, their cytogenetic positions on sheep chromosomes were determined by FISH and confirmed by linkage analysis, localizing both genes in OAR3p22, a region previously described as carrying a QTL for SC incubation period in sheep. Finally, expression analyses were carried out in eight naturally SC-infected and five uninfected sheep with the same genotype for PRNP (ARQ/ARQ). This comparison was performed using real-time RT-PCR in samples of spleen and cerebellum. Results showed differences in the expression of both cytokines in cerebellum (p < 0.05) but not in spleen (p > 0.05).
羊瘙痒病(SC)是绵羊和山羊的一种传染性海绵状脑病(TSE)。对这种神经退行性疾病的易感性主要由PRNP基因座的点突变控制。除PRNP外,其他基因也被报道可调节对SC的抗性/易感性。基于对阿尔茨海默病和不同TSE模型的多项研究,以及大脑中细胞因子正确稳态的需求,IL1B和IL1RN被选为可能参与上述多基因变异的假定位置和功能候选基因。在本研究中,部分分离并鉴定了绵羊IL1B和IL1RN基因,包括启动子和其他调控区域。此外,还鉴定了几个序列多态性。此外,通过荧光原位杂交(FISH)确定了它们在绵羊染色体上的细胞遗传学位置,并通过连锁分析进行了确认,将这两个基因定位在OAR3p22,该区域先前被描述为携带绵羊SC潜伏期的数量性状位点(QTL)。最后,对8只自然感染SC和5只未感染且PRNP基因型相同(ARQ/ARQ)的绵羊进行了表达分析。使用实时逆转录聚合酶链反应(RT-PCR)对脾脏和小脑样本进行了比较。结果显示,两种细胞因子在小脑(p < 0.05)而非脾脏(p > 0.05)中的表达存在差异。