Nucleophagy mediators and mechanisms

被引:8
|
作者
Papandreou, Margarita-Elena [1 ,2 ]
Tavernarakis, Nektarios [1 ,2 ]
机构
[1] Fdn Res & Technol Hellas, Inst Mol Biol & Biotechnol, Iraklion, Greece
[2] Univ Crete, Fac Med, Dept Basic Sci, Iraklion, Greece
来源
AUTOPHAGY IN HEALTH AND DISEASE | 2020年 / 172卷
基金
欧洲研究理事会;
关键词
PIECEMEAL MICROAUTOPHAGY; SELECTIVE AUTOPHAGY; NUCLEAR; RECEPTOR; ACCUMULATION; MITOPHAGY; DEGRADES; DNA;
D O I
10.1016/bs.pmbts.2020.01.003
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
Nuclear recycling is essential for cell and organismal homeostasis. Nuclear architecture perturbations, such as nuclear loss or nuclear enlargement, have been observed in several pathological conditions. Apart from proteasomal components which reside in the nucleus, specific autophagic proteins also shuttle between the nucleus and the cytoplasm. Until recently, only the microautophagic degradation of nuclear components had been described. Recent studies, dissecting nuclear material recycling in organisms ranging from yeast to mammals, provide insight relevant to other forms of nucleophagy and the mediators involved. Nucleophagy has also been implicated in pathology. Lamins are degraded in cancer through direct interaction with LC3 in the nucleus. Similarly, in neurodegeneration, Golgi-associated nucleophagy is exacerbated. The physiological role of nucleophagy and its contribution to other pathologies remain to be elucidated. Here we discus recent findings that shed light into the molecular mechanisms and pathways that mediate the autophagic recycling of nuclear material.
引用
收藏
页码:1 / 14
页数:14
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