The emerging role of acetylation in the regulation of autophagy

被引:151
作者
Banreti, Agnes [1 ,2 ]
Sass, Miklos [1 ]
Graba, Yacine [2 ]
机构
[1] Eotvos Lorand Univ, Dept Anat Cell & Dev Biol, Budapest, Hungary
[2] Aix Marseille Univ, CNRS UMR 7288, Dev Biol Inst Marseille Luminy, Marseille, France
关键词
acetylation; deacetylation; lysine; autophagy; FOXO; ATG genes; post-translational modification; protein aggregates; Huntington disease; FOXO TRANSCRIPTION FACTORS; CREB-BINDING PROTEIN; CELL-DEATH; TUMOR-SUPPRESSOR; HISTONE DEACETYLASES; SELECTIVE AUTOPHAGY; HUNTINGTONS-DISEASE; ALPHA-TUBULIN; HDAC6; DEGRADATION;
D O I
10.4161/auto.23908
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy is an evolutionarily conserved catabolic process through which different components of the cells are sequestered into double-membrane cytosolic vesicles called autophagosomes, and fated to degradation through fusion with lysosomes. Autophagy plays a major function in many physiological processes including response to different stress factors, energy homeostasis, elimination of cellular organelles and tissue remodeling during development. Consequently, autophagy is strictly controlled and post-translational modifications such as phosphorylation and ubiquitination have long been associated with autophagy regulation. In contrast, the importance of acetylation in autophagy control has only emerged in the last few years. In this review, we summarize how previously identified histone acetylases and deacetylases modify key autophagic effector proteins, and discuss how this has an impact on physiological and pathological cellular processes.
引用
收藏
页码:819 / 829
页数:11
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