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Ubiquitin C-terminal hydrolase L1 (UCH-L1): structure, distribution and roles in brain function and dysfunction.
Bishop, Paul; Rocca, Dan; Henley, Jeremy M.
Afiliación
  • Bishop P; School of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, U.K.
  • Rocca D; School of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, U.K.
  • Henley JM; School of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol BS8 1TD, U.K. j.m.henley@bristol.ac.uk.
Biochem J ; 473(16): 2453-62, 2016 08 15.
Article en En | MEDLINE | ID: mdl-27515257
ABSTRACT
Ubiquitin C-terminal hydrolase L1 (UCH-L1) is an extremely abundant protein in the brain where, remarkably, it is estimated to make up 1-5% of total neuronal protein. Although it comprises only 223 amino acids it has one of the most complicated 3D knotted structures yet discovered. Beyond its expression in neurons UCH-L1 has only very limited expression in other healthy tissues but it is highly expressed in several forms of cancer. Although UCH-L1 is classed as a deubiquitinating enzyme (DUB) the direct functions of UCH-L1 remain enigmatic and a wide array of alternative functions has been proposed. UCH-L1 is not essential for neuronal development but it is absolutely required for the maintenance of axonal integrity and UCH-L1 dysfunction is implicated in neurodegenerative disease. Here we review the properties of UCH-L1, and how understanding its complex structure can provide new insights into its roles in neuronal function and pathology.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Encéfalo / Ubiquitina Tiolesterasa Límite: Animals / Humans Idioma: En Revista: Biochem J Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Asunto principal: Encéfalo / Ubiquitina Tiolesterasa Límite: Animals / Humans Idioma: En Revista: Biochem J Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido