| Literature DB >> 12560552 |
Lin He1, Xin-Yun Lu, Aaron F Jolly, Adam G Eldridge, Stanley J Watson, Peter K Jackson, Gregory S Barsh, Teresa M Gunn.
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.Entities:
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Year: 2003 PMID: 12560552 DOI: 10.1126/science.1079694
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728