Race R E, Graham K, Ernst D, Caughey B, Chesebro B
National Institutes of Health, National Institute of Allergy and Infectious Diseases, Rocky Mountain Laboratories, Hamilton, Montana 59840.
J Gen Virol. 1990 Feb;71 ( Pt 2):493-7. doi: 10.1099/0022-1317-71-2-493.
A single gene is known to have a predominant influence on scrapie incubation period in mice. In crosses between strains that give a short incubation period, such as NZW mice, and those which give a long incubation period, such as I/LnJ mice, long incubation period was dominant using a Chandler scrapie agent isolate. Recently a close linkage was found between the incubation period gene and the prion protein (PrP) structural gene in I/LnJ mice crossed to NZW mice. Because this linkage suggested an important role for PrP in the pathogenesis of scrapie we sought to verify the linkage between these genes and extended the analysis to three additional mouse strains. All four of the mouse strains that we evaluated, I/LnJ, P/J, MA/MyJ, and RIIIS/J, had incubation periods longer than those of the NZW mice to which they were crossed. In addition, all four strains shared an XbaI restriction enzyme polymorphism, which suggested that all four strains might also exhibit linkage between the incubation period and the PrP structural gene. Very strong linkage between PrP and incubation period was found in I/LnJ and P/J mice crossed to NZW mice, whereas less obvious linkage was demonstrated for MA/MyJ mice crossed to NZW mice. In MA/MyJ mice genes other than PrP also had an obvious influence on incubation period. In RIIIS/J mice no linkage was shown. Although linkage between PrP and incubation period was very significant in I/LnJ and P/J mice, a few animals were identified in both crosses that represented potential recombinants in which PrP and incubation period did not segregate together. Therefore, although these phenotypes are certainly linked in I/LnJ and P/J mice, it is possible that PrP and incubation period are controlled by separate genes.
已知单个基因对小鼠痒病潜伏期有主要影响。在潜伏期短的品系(如新西兰白兔(NZW)小鼠)与潜伏期长的品系(如I/LnJ小鼠)之间的杂交中,使用钱德勒痒病病原体分离株时,长潜伏期是显性的。最近,在与NZW小鼠杂交的I/LnJ小鼠中,发现潜伏期基因与朊病毒蛋白(PrP)结构基因之间存在紧密连锁。由于这种连锁表明PrP在痒病发病机制中起重要作用,我们试图验证这些基因之间的连锁,并将分析扩展到另外三个小鼠品系。我们评估的所有四个小鼠品系,即I/LnJ、P/J、MA/MyJ和RIIIS/J,其潜伏期都比与之杂交的NZW小鼠长。此外,所有四个品系都共享一种XbaI限制性内切酶多态性,这表明所有四个品系在潜伏期和PrP结构基因之间可能也存在连锁。在与NZW小鼠杂交的I/LnJ和P/J小鼠中,发现PrP与潜伏期之间有非常强的连锁,而在与NZW小鼠杂交的MA/MyJ小鼠中,连锁不太明显。在MA/MyJ小鼠中,除PrP外的其他基因对潜伏期也有明显影响。在RIIIS/J小鼠中未显示连锁。尽管在I/LnJ和P/J小鼠中PrP与潜伏期之间的连锁非常显著,但在两个杂交组合中都鉴定出了一些可能的重组动物,其中PrP和潜伏期没有一起分离。因此,尽管在I/LnJ和P/J小鼠中这些表型肯定是连锁的,但PrP和潜伏期有可能由不同的基因控制。