Carlson G A, Ebeling C, Torchia M, Westaway D, Prusiner S B
McLaughlin Research Institute, Great Falls, Montana 59401.
Genetics. 1993 Apr;133(4):979-88. doi: 10.1093/genetics/133.4.979.
Scrapie is a transmissible neurodegenerative disease caused by unusual pathogens called prions. The interval between inoculation and illness for experimental mouse scrapie is dramatically influenced by an incubation time gene (Prn-i) that is linked to Prn-p, the structural gene for prion protein (PrP). Although prion proteins from mouse strains with short and long scrapie incubation times differ by two amino acids, mice with discordant disease phenotype and Prn-p genotype occur in segregating crosses, suggesting recombination between Prn-p and a distinct incubation time locus. In addition, expression of Prn-pb transgenes from long incubation time mice shortened, rather than prolonged, incubation time. In this study, mice carrying chromosomes with meiotic crossovers near Prn-p were analyzed for scrapie incubation time phenotype. The results indicated that Prn-i (should it exist) must lie within an interval 0.67 cM proximal and 0.22 cM distal to Prn-p. The results also suggest that the cumulative effects of other genes, rather than meiotic recombination, were responsible for the putative recombinants of earlier studies. However, the effect of Prn-pb transgene expression in abbreviating scrapie incubation time was mitigated when the transgenes were transferred to mice with an endogenous long incubation time allele. Thus, Prn-pb transgenes and Prn-i may modulate scrapie pathogenesis by different mechanisms.
羊瘙痒症是一种由名为朊病毒的特殊病原体引起的可传播性神经退行性疾病。实验性小鼠羊瘙痒症的接种与发病间隔受到一个与朊病毒蛋白(PrP)的结构基因Prn-p相关的潜伏期基因(Prn-i)的显著影响。尽管来自短潜伏期和长潜伏期小鼠品系的朊病毒蛋白在两个氨基酸上存在差异,但在分离杂交中会出现疾病表型与Prn-p基因型不一致的小鼠,这表明Prn-p与一个不同的潜伏期基因座之间发生了重组。此外,来自长潜伏期小鼠的Prn-pb转基因的表达缩短而非延长了潜伏期。在本研究中,对携带在Prn-p附近发生减数分裂交叉的染色体的小鼠进行了羊瘙痒症潜伏期表型分析。结果表明,Prn-i(如果存在)必定位于Prn-p近端0.67 cM和远端0.22 cM的区间内。结果还表明,早期研究中假定的重组体是由其他基因的累积效应而非减数分裂重组造成的。然而,当将Prn-pb转基因转移到具有内源性长潜伏期等位基因的小鼠中时,其缩短羊瘙痒症潜伏期的作用会减弱。因此,Prn-pb转基因和Prn-i可能通过不同机制调节羊瘙痒症的发病机制。