Abstract
Scrapie is a slow degenerative encephalopathy of animals caused by unusual infectious particles termed prions. A cDNA encoding the only apparent component of the prion, a protein designated PrP 27-30, has recently been cloned and sequenced. By measuring mRNA levels using in situ hybridization with the PrP cDNA, the authors found that prion proteins are synthesized almost exclusively within neurons. The levels of PrP mRNA varied among different types of neurons, but did not change during scrapie infection. A cDNA encoding glial fibrillary acidic protein (GFAP) was a positive control; GFAP mRNA was confined to astrocytes. Our finding of PrP mRNA in neurons may explain the degeneration and vacuolation that occurs in these cells during scrapie infection.
MeSH Terms
Animals
Astrocytes/analysis
Brain/microbiology
Cerebellum/metabolism,microbiology
Cricetinae
DNA
Glial Fibrillary Acidic Protein/genetics
Hippocampus/metabolism,microbiology
Neurons/microbiology
Nucleic Acid Hybridization
Prions/genetics,metabolism
Purkinje Cells/metabolism,microbiology
RNA, Messenger/analysis,genetics
RNA, Viral/analysis,genetics
Scrapie/microbiology
Viral Proteins/biosynthesis,genetics
Chemicals
Glial Fibrillary Acidic Protein
Prions
RNA, Messenger
RNA, Viral
Viral Proteins
DNA
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Kretzschmar H A
Prusiner S B
Stowring L E
DeArmond S J
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