McKinley M P, Lingappa V R, Prusiner S B
Department of Neurology, University of California, San Francisco 94143.
Ciba Found Symp. 1988;135:101-16. doi: 10.1002/9780470513613.ch7.
During development of the hamster brain, synthesis of the cellular isoform of the scrapie prion protein (PrPC) was found to be regulated. Low levels of PrP poly(A)+ mRNA were detectable one day after birth. PrP poly(A)+ mRNA reached maximal levels between 10 and 20 days post-partum; thereafter, no change in its level could be detected at ages up to 13 months. In contrast, myelin basic protein poly(A)+ mRNA was shown to reach maximal levels by 30 days of age and thereafter steadily declined in adult brain. Using monospecific PrP antisera, immunoprecipitable cell-free translation products were detected at low levels two days after birth and progressively increased up to 10 days of age. How the PrP mRNA participates in brain development and its function in scrapie prion infection are being investigated.
在仓鼠大脑发育过程中,发现瘙痒病朊病毒蛋白(PrPC)的细胞异构体合成受到调控。出生一天后可检测到低水平的PrP多聚腺苷酸(poly(A))+ mRNA。PrP poly(A)+ mRNA在产后10至20天达到最高水平;此后,在长达13个月的年龄段内未检测到其水平变化。相比之下,髓鞘碱性蛋白多聚腺苷酸(poly(A))+ mRNA在30日龄时达到最高水平,此后在成年大脑中稳步下降。使用单特异性PrP抗血清,出生两天后可检测到低水平的免疫沉淀无细胞翻译产物,到10日龄时逐渐增加。目前正在研究PrP mRNA如何参与大脑发育及其在瘙痒病朊病毒感染中的作用。