Gene expression in scrapie -: Cloning a new scrapie-responsive gene and the identification of increased levels of seven other mRNA transcripts

被引:131
作者
Dandoy-Dron, F
Guillo, F
Benboudjema, L
Deslys, JP
Lasmézas, C
Dormont, D
Tovey, MG
Dron, M
机构
[1] IFC1, CNRS, UPR 9045, Lab Oncol Virale, F-94801 Villejuif, France
[2] CEA, Lab Neurovirol, F-92265 Fontenay Aux Roses, France
关键词
D O I
10.1074/jbc.273.13.7691
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To define genes associated with or responsible for the neurodegenerative changes observed in transmissible spongiform encephalopathies, we analyzed gene expression in scrapie-infected mouse brain using "mRNA differential display." The RNA transcripts of eight genes were increased 3-8-fold in the brains of scrapie-infected animals, Five of these genes have not previously been reported to exhibit increased expression in this disease: cathepsin S, the C1q B-chain of complement, apolipoprotein D, and two previously unidentified genes denominated scrapie-responsive gene (ScRG)-1 and ScRG-2, which are preferentially expressed in brain tissue, Increased expression of the three remaining genes, beta 2 microglobulin, F4/80, and metallothionein II, has previously been reported to occur in experimental scrapie, Kinetic analysis revealed a concomitant increase in the levels of ScRG-1, cathepsin S, the C1q B-chain of complement, and beta 2 microglobulin mRNA as well as glial fibrillary acidic protein and F4/80 transcripts, markers of astrocytosis and microglial activation, respectively, In contrast, the level of ScRG-2, apolipoprotein D, and metallothionein II mRNA was only increased at the terminal stage of the disease. ScRG-1 mRNA was found to be preferentially expressed in glial cells and to code for a short protein of 47 amino acids with a strong hydrophobic N-terminal region.
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页码:7691 / 7697
页数:7
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