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Published on: October 3, 2012
Evidence that DNA is present in abnormal tubulofilamentous structures found in scrapie
H K Narang1, D M Asher, D C Gajdusek
1Laboratory of Central Nervous System Studies, National Institute of Neurological and Communicative Disorders and Stroke, Bethesda, MD 20892.
Abstract:
Abnormal tubulofilamentous structures have been identified in electron micrographs of thin sections and negatively stained impression grids prepared from brains of animals with scrapie and other spongiform encephalopathies, and we showed that such tubules contain a core of filamentous structures resembling scrapie-associated fibrils (SAF). We treated impression grids from brains of scrapie-infected hamsters with several substances that bind to or cleave proteins and nucleic acids to see if they had any effect on the abnormal tubulofilamentous structures. Treatment with three proteolytic enzymes reduced the caliber of the tubules from about 50 nm to 30 nm; subsequent treatment of the 30-nm tubules with DNase I left many typical SAF as well as transitional forms in which twisted SAF emerged from tubules. DNase treatment of the original thicker tubules had no effect, and no SAF were seen on grids. Treatment of the 30-nm tubules with any of three other nucleases (micrococcal, mung bean, and BAL-31) also produced SAF. However, treatment with RNase A had no effect either on the original 50-nm tubules or on the 30-nm tubules produced by proteolysis. Detergent treatment of any of the preparations produced SAF. Treatment with ethidium bromide resulted in staining of the tubules that was inhibited by magnesium ions. The data suggest that the abnormal tubulofilamentous particles found in spongiform encephalopathies may consist of an outer cylinder of protein, an inner cylinder of DNA, and an innermost core of SAF.
Insights
Abnormal tubulofilamentous structures in spongiform encephalopathies contain protein and DNA. Treatments revealed these structures may consist of an outer protein cylinder, inner DNA cylinder, and a core of scrapie-associated fibrils (SAF).
Area of Science:
- Neuroscience
- Biochemistry
- Molecular Biology
Background:
- Abnormal tubulofilamentous structures are observed in spongiform encephalopathies.
- These structures resemble scrapie-associated fibrils (SAF).
Purpose of the Study:
- To investigate the composition of abnormal tubulofilamentous structures found in spongiform encephalopathies.
- To determine the role of proteins and nucleic acids in these structures.
Main Methods:
- Electron microscopy of brain samples from scrapie-infected hamsters.
- Treatment of structures with proteolytic enzymes, DNase I, other nucleases, RNase A, and detergents.
- Analysis of structural changes and SAF formation post-treatment.
Main Results:
- Proteolytic enzyme treatment reduced tubule diameter and revealed SAF.
- DNase I and other nucleases induced SAF formation from 30-nm tubules.
- RNase A and detergent treatments yielded different results, suggesting specific molecular components.
Conclusions:
- The abnormal tubulofilamentous particles likely comprise an outer protein cylinder, an inner DNA cylinder, and an innermost SAF core.
- This finding provides insight into the molecular architecture of spongiform encephalopathy agents.

