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Sinc 同源小鼠品系中不同毒株瘙痒病的疾病特征:对病原体本质及发病机制宿主控制的启示

The disease characteristics of different strains of scrapie in Sinc congenic mouse lines: implications for the nature of the agent and host control of pathogenesis.

作者信息

Bruce M E, McConnell I, Fraser H, Dickinson A G

机构信息

Institute for Animal Health, AFRC & MRC Neuropathogenesis Unit, Edinburgh, U.K.

出版信息

J Gen Virol. 1991 Mar;72 ( Pt 3):595-603. doi: 10.1099/0022-1317-72-3-595.

Abstract

Mouse lines which are congenic for Sinc, the major gene controlling scrapie incubation period, have been produced by selective breeding from the inbred C57BL(Sincs7) and VM(Sincp7) strains; the s7 allele of Sinc has been introduced into a VM background by 18 serial backcrosses, at each generation selecting on the basis of the incubation period with the ME7 scrapie strain. The characteristics of the disease produced by seven scrapie strains have been compared in Sincs7 and Sincp7 congenic mice and in the F1 cross between them. As previously found in non-congenic mice, each scrapie strain has a characteristic, precisely reproducible incubation period pattern in the three Sinc genotypes. The Sinc gene controls the incubation period for all scrapie strains tested but the direction of allelic action and the apparent dominance pattern differs between scrapie strains. Comparison with non-congenic mice shows that other genes also have a minor effect on incubation period. The distribution of vacuolar degeneration in the brain depends mainly on the scrapie strain but is also influenced by Sinc and other unspecified mouse genes. Restriction fragment length polymorphism analysis has already shown that the close linkage between Sinc and the gene encoding PrP has been maintained in the Sinc congenic lines, strengthening the possibility that PrP is the Sinc gene product. The present study confirms that scrapie strains carry information which is independent of the host but nevertheless suggests that host PrP protein interacts with this information to regulate the progression of the disease.

摘要

通过从近交系C57BL(Sincs7)和VM(Sincp7)品系进行选择性育种,培育出了与控制羊瘙痒病潜伏期的主要基因Sinc同基因的小鼠品系;通过18次连续回交,已将Sinc的s7等位基因导入VM背景中,每一代均根据与ME7羊瘙痒病株的潜伏期进行选择。在Sincs7和Sincp7同基因小鼠及其F1杂交后代中,比较了7种羊瘙痒病株所引发疾病的特征。正如先前在非同基因小鼠中所发现的那样,每种羊瘙痒病株在三种Sinc基因型中都有独特的、可精确重复的潜伏期模式。Sinc基因控制着所有测试羊瘙痒病株的潜伏期,但等位基因作用方向和明显的显性模式在不同病株间有所不同。与非同基因小鼠的比较表明,其他基因对潜伏期也有较小影响。脑中空泡变性的分布主要取决于羊瘙痒病株,但也受Sinc和其他未明确的小鼠基因影响。限制性片段长度多态性分析已经表明,在Sinc同基因系中,Sinc与编码PrP的基因之间的紧密连锁得以维持,这增强了PrP是Sinc基因产物的可能性。本研究证实,羊瘙痒病株携带的信息独立于宿主,但仍表明宿主PrP蛋白与该信息相互作用以调节疾病进程。

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