Literature DB >> 1899270

Search for a putative scrapie genome in purified prion fractions reveals a paucity of nucleic acids.

N Meyer1, V Rosenbaum, B Schmidt, K Gilles, C Mirenda, D Groth, S B Prusiner, D Riesner.   

Abstract

Scrapie can be transmitted by novel infectious pathogens termed prions. No evidence for a scrapie-specific nucleic acid has been detected to date. To investigate amounts, types and sizes of nucleic acid molecules associated with prions in purified preparations, aliquots were deproteinized, and the nucleic acids analysed by PAGE and silver staining. Digestion with nucleases and exposure to Zn2+ prior to analysis substantially diminished the content of nucleic acids, but did not alter the prion titre indicating that those nucleic acids which were removed are not essential for infectivity. Since a single species of scrapie-specific nucleic acid could not be identified, we explored the unprecedented possibility of scrapie-specific nucleic acids of variable length which are biologically active. If such molecules of variable length exist then they might be hidden within the background smear on silver-stained gels after PAGE. A new procedure designated return refocusing gel electrophoresis (RRGE) was developed to identify heterogeneous nucleic acids in purified prion fractions. The content of variable length nucleic acids was reduced by a factor of 10 by exhaustive Bal 31 exonuclease digestion after dispersion of purified prions into detergent-lipid-protein complexes. For example, a typical sample after Bal 31 digestion contained approximately 4 ng of nucleic acid of variable length and 10(8.7) ID50 units of scrapie prion infectivity. Consideration of different models for a hypothetical scrapie-specific nucleic acid suggests that such a molecule would have to be: (i) quite small (less than 100 nucleotides), (ii) possess a particle-to-infectivity ratio near unity or (iii) heterogeneous in size. Although our results do not eliminate the possibility that prions possess a scrapie-specific nucleic acid of variable length, they narrow considerably the spectrum of features specifying such a candidate molecule.

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Year:  1991        PMID: 1899270     DOI: 10.1099/0022-1317-72-1-37

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  16 in total

Review 1.  The spongiform encephalopathies.

Authors:  R G Will
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-09       Impact factor: 10.154

2.  Solid-state NMR studies of the prion protein H1 fragment.

Authors:  J Heller; A C Kolbert; R Larsen; M Ernst; T Bekker; M Baldwin; S B Prusiner; A Pines; D E Wemmer
Journal:  Protein Sci       Date:  1996-08       Impact factor: 6.725

Review 3.  Etiology and pathogenesis of prion diseases.

Authors:  S J DeArmond; S B Prusiner
Journal:  Am J Pathol       Date:  1995-04       Impact factor: 4.307

4.  Nucleic acid binding proteins in highly purified Creutzfeldt-Jakob disease preparations.

Authors:  T Sklaviadis; A Akowitz; E E Manuelidis; L Manuelidis
Journal:  Proc Natl Acad Sci U S A       Date:  1993-06-15       Impact factor: 11.205

5.  Sequence analysis of the PrP protein from two species of antelope susceptible to transmissible spongiform encephalopathy.

Authors:  M Poidinger; J Kirkwood; W Almond
Journal:  Arch Virol       Date:  1993       Impact factor: 2.574

6.  Distinct PrP properties suggest the molecular basis of strain variation in transmissible mink encephalopathy.

Authors:  R A Bessen; R F Marsh
Journal:  J Virol       Date:  1994-12       Impact factor: 5.103

7.  T-lymphocyte activation and the cellular form of the prion protein.

Authors:  N A Mabbott; K L Brown; J Manson; M E Bruce
Journal:  Immunology       Date:  1997-10       Impact factor: 7.397

8.  Search for a prion-specific nucleic acid.

Authors:  Jiri G Safar; Klaus Kellings; Ana Serban; Darlene Groth; James E Cleaver; Stanley B Prusiner; Detlev Riesner
Journal:  J Virol       Date:  2005-08       Impact factor: 5.103

9.  Biological and biochemical characterization of sheep scrapie in Japan.

Authors:  Motohiro Horiuchi; Takuya Nemoto; Naotaka Ishiguro; Hidefumi Furuoka; Shirou Mohri; Morikazu Shinagawa
Journal:  J Clin Microbiol       Date:  2002-09       Impact factor: 5.948

10.  Attempts to convert the cellular prion protein into the scrapie isoform in cell-free systems.

Authors:  A J Raeber; D R Borchelt; M Scott; S B Prusiner
Journal:  J Virol       Date:  1992-10       Impact factor: 5.103

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