FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Savvateeva-Popova, E., Popov, A., Grossman, A., Nikitina, E., Medvedeva, A., Peresleni, A., Korochkin, L., Moe, J.G., Davidowitz, E., Pyatkov, K., Myasnyankina, E., Zatsepina, O., Schostak, N., Zelentsova, E., Evgen'ev, M. (2007). Pathogenic chaperone-like RNA induces congophilic aggregates and facilitates neurodegeneration in Drosophila.  Cell Stress Chaperones 12(1): 9--19.
FlyBase ID
FBrf0201942
Publication Type
Research paper
Abstract
Protein aggregation is a hallmark of many neurodegenerative diseases. RNA chaperones have been suggested to play a role in protein misfolding and aggregation. Noncoding, highly structured RNA recently has been demonstrated to facilitate transformation of recombinant and cellular prion protein into proteinase K-resistant, congophilic, insoluble aggregates and to generate cytotoxic oligomers in vitro. Transgenic Drosophila melanogaster strains were developed to express highly structured RNA under control of a heat shock promoter. Expression of a specific construct strongly perturbed fly behavior, caused significant decline in learning and memory retention of adult males, and was coincident with the formation of intracellular congophilic aggregates in the brain and other tissues of adult and larval stages. Additionally, neuronal cell pathology of adult flies was similar to that observed in human Parkinson's and Alzheimer's disease. This novel model demonstrates that expression of a specific highly structured RNA alone is sufficient to trigger neurodegeneration, possibly through chaperone-like facilitation of protein misfolding and aggregation.
PubMed ID
PubMed Central ID
PMC1874921 (PMC) (EuropePMC)
Associated Information
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Cell Stress Chaperones
    Title
    Cell Stress & Chaperones
    Publication Year
    1996-
    ISBN/ISSN
    1355-8145
    Data From Reference
    Alleles (2)
    Genes (1)
    Transgenic Constructs (2)