Atg7 in development and disease: panacea or Pandora's Box?

被引:83
|
作者
Xiong, Jianhua [1 ]
机构
[1] NHLBI, Ctr Mol Med, NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
autophagy; Atg7; mouse model; development; disease; PROGRAMMED CELL-DEATH; LIFE-SPAN EXTENSION; INTESTINAL EPITHELIUM; INDUCED AUTOPHAGY; OXIDATIVE STRESS; PROTEOMICS ANALYSIS; PANETH CELLS; GENE; HOMEOSTASIS; DEFICIENCY;
D O I
10.1007/s13238-015-0195-8
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macroautophagy is an evolutionarily conserved intracellular degradation system used by life ranging from yeasts to mammals. The core autophagic machinery is composed of ATG (autophagy-related) protein constituents. One particular member of the ATG protein family, Atg7, has been the focus of recent research. Atg7 acts as an E1-like activating enzyme facilitating both microtubule-associated protein light chain 3 (LC3)-phosphatidylethanolamine and ATG12 conjugation. Thus, Atg7 stands at the hub of these two ubiquitin-like systems involving LC3 and Atg12 in autophagic vesicle expansion. In this review, I focus on the pleiotropic function of Atg7 in development, maintenance of health, and alternations of such control in disease.
引用
收藏
页码:722 / 734
页数:13
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