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2.
J Nucl Cardiol ; 24(1): 66-68, 2017 02.
Article in English | MEDLINE | ID: mdl-26715602
3.
Science ; 299(5607): 710-2, 2003 Jan 31.
Article in English | MEDLINE | ID: mdl-12560552

ABSTRACT

mahoganoid is a mouse coat-color mutation whose pigmentary phenotype and genetic interactions resemble those of Attractin (Atrn). Atrn mutations also cause spongiform neurodegeneration. Here, we show that a null mutation for mahoganoid causes a similar age-dependent neuropathology that includes many features of prion diseases but without accumulation of protease-resistant prion protein. The gene mutated in mahoganoid encodes a RING-containing protein with E3 ubiquitin ligase activity in vitro. Similarities in phenotype, expression, and genetic interactions suggest that mahoganoid and Atrn genes are part of a conserved pathway for regulated protein turnover whose function is essential for neuronal viability.


Subject(s)
Brain/pathology , Carrier Proteins/genetics , Carrier Proteins/metabolism , Mutation , Neurodegenerative Diseases/genetics , Neurodegenerative Diseases/pathology , Alleles , Amino Acid Sequence , Animals , Blotting, Northern , Brain/metabolism , Carrier Proteins/chemistry , Crosses, Genetic , Female , Gene Expression , Ligases/metabolism , Male , Membrane Proteins/genetics , Mice , Mice, Inbred C3H , Mice, Mutant Strains , Mice, Transgenic , Models, Biological , Molecular Sequence Data , Neurodegenerative Diseases/metabolism , Neurons/metabolism , Neurons/pathology , Pigmentation , Prions/metabolism , RNA, Messenger/genetics , RNA, Messenger/metabolism , Recombinant Fusion Proteins/metabolism , Transgenes , Ubiquitin/metabolism , Ubiquitin-Protein Ligases , Vacuoles/ultrastructure
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