The role of ALFY in selective autophagy

被引:91
作者
Isakson, P. [1 ]
Holland, P. [1 ]
Simonsen, A. [1 ]
机构
[1] Univ Oslo, Inst Basic Med Sci, Dept Biochem, N-0317 Oslo, Norway
关键词
selective autophagy; ALFY; p62; protein aggregates; BEACH domain; POLYGLUTAMINE-INDUCED NEURODEGENERATION; FAMILY INTERACTING MOTIF; AGGREGATED PROTEINS; MUTANT HUNTINGTIN; ALPHA-MANNOSIDASE; INCLUSION-BODIES; STRUCTURAL BASIS; NUCLEAR-BODIES; BEACH DOMAIN; DEGRADATION;
D O I
10.1038/cdd.2012.66
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Autophagy, a highly conserved lysosomal degradation pathway, was initially characterized as a bulk degradation system induced in response to starvation. In recent years, autophagy has emerged also as a highly selective pathway, targeting various cargoes such as aggregated proteins and damaged organelles for degradation. The key factors involved in selective autophagy are autophagy receptors and adaptor proteins, which connect the cargo to the core autophagy machinery. In this review, we discuss the current knowledge about the only mammalian adaptor protein identified thus far, autophagy-linked FYVE protein (ALFY). ALFY is a large, scaffolding, multidomain protein implicated in the selective degradation of ubiquitinated protein aggregates by autophagy. We also comment on the possible role of ALFY in the context of disease. Cell Death and Differentiation (2013) 20, 12-20; doi:10.1038/cdd.2012.66; published online 1 June 2012
引用
收藏
页码:12 / 20
页数:9
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