| Literature DB >> 2873895 |
K Basler, B Oesch, M Scott, D Westaway, M Wälchli, D F Groth, M P McKinley, S B Prusiner, C Weissmann.
Abstract
PrP 27-30 is the major protein in purified preparations of scrapie agent. An almost complete PrP cDNA was used to select PrP-related genomic clones from normal hamster DNA. The gene contains a noncoding exon of 56 to 82 bp and a 2 kb coding exon, separated by a 10 kb intron. Transcription initiates at the same multiple sites in vivo and in vitro. The promoter lacks a TATA box and contains three repeats of the sequence GCCCCGCCC, which resembles the Sp1 binding site found in "housekeeping" genes. The PrP coding sequence encodes a presumptive amino-terminal signal peptide. The primary structure of PrP encoded by the gene of a healthy animal does not differ from that encoded by a cDNA from a scrapie-infected animal, suggesting that the different properties of PrP from normal and scrapie-infected brains are due to post-translational events.Entities:
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Year: 1986 PMID: 2873895 DOI: 10.1016/0092-8674(86)90662-8
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582