Complete Genomic Sequence and Analysis of the Prion Protein Gene Region from Three Mammalian Species

  1. Inyoul Y. Lee1,
  2. David Westaway4,
  3. Arian F.A. Smit1,6,
  4. Kai Wang1,7,
  5. Jason Seto1,8,
  6. Lei Chen1,7,
  7. Chetana Acharya1,
  8. Mike Ankener1,
  9. Dale Baskin1,9,
  10. Carol Cooper2,
  11. Hong Yao4,
  12. Stanley B. Prusiner2,3, and
  13. Leroy E. Hood1,5
  1. 1Department of Molecular Biotechnology, University of Washington, Seattle, Washington 98195-7730 USA; Departments of 2Neurology and 3Biochemistry and Biophysics, University of California, San Francisco, California 94143-0518 USA; 4Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario M5S 3H2, Canada

Abstract

The prion protein (PrP), first identified in scrapie-infected rodents, is encoded by a single exon of a single-copy chromosomal gene. In addition to the protein-coding exon, PrP genes in mammals contain one or two 5′-noncoding exons. To learn more about the genomic organization of regions surrounding the PrP exons, we sequenced 105 bp of DNA from clones containing human, sheep, and mouse PrP genes isolated in cosmids or λ phage. Our findings are as follows: (1) Although the human PrP transcript does not include the untranslated exon 2 found in its mouse and sheep counterparts, the large intron of the human PrP gene contains an exon 2-like sequence flanked by consensus splice acceptor and donor sites. (2) The mouse Prnpa but not thePrnpb allele found in 44 inbred lines contains a 6593 nucleotide retroviral genome inserted into the anticoding strand of intron 2. This intracisternal A-particle element is flanked by duplications of an AAGGCT nucleotide motif. (3) We found that thePrP gene regions contain from 40% to 57% genome-wide repetitive elements that independently increased the size of the locus in all three species by numerous mutations. The unusually long sheepPrP 3′-untranslated region contains a “fossil” 1.2-kb mariner transposable element. (4) We identified sequences in noncoding DNA that are conserved between the three species and may represent biologically functional sites.

[The nucleotide sequence data reported in this paper have been submitted to the GenBank sequence database and have been assigned the accession numbers U29185(human), U29186 (mouse), and U67922 (sheep).]

Footnotes

  • Present addresses: 6Axys Pharmaceuticals, La Jolla, California 92087 USA; 7Chiroscience, Bothell, Washington 98021 USA; 8Institute of Biosciences, Bioinformatics, and Biotechnology, Manassass, Virginia 20110 USA; 9PE Applied Biosystems, Foster City, California 94404 USA

  • 5 Corresponding author.

  • E-MAIL leehood{at}u.washington.edu; FAX (206) 616-5197.

    • Received June 17, 1998.
    • Accepted August 28, 1998.
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