Department of Biochemistry, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.
Cell Death Differ. 2013 Jan;20(1):12-20. doi: 10.1038/cdd.2012.66. Epub 2012 Jun 1.
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.
自噬是一种高度保守的溶酶体降解途径,最初被描述为一种在饥饿时诱导的批量降解系统。近年来,自噬也被认为是一种高度选择性的途径,能够靶向降解各种物质,如聚集的蛋白质和受损的细胞器。参与选择性自噬的关键因素是自噬受体和衔接蛋白,它们将货物连接到核心自噬机制上。在这篇综述中,我们讨论了目前关于迄今为止唯一鉴定出的哺乳动物衔接蛋白,即自噬相关 FYVE 蛋白(ALFY)的知识。ALFY 是一种大型的支架多结构域蛋白,参与自噬介导的泛素化蛋白聚集体的选择性降解。我们还评论了 AIFY 在疾病背景下的可能作用。