The return of the nucleus: transcriptional and epigenetic control of autophagy

被引:384
作者
Fullgrabe, Jens [1 ]
Klionsky, Daniel J. [2 ,3 ]
Joseph, Bertrand [1 ]
机构
[1] Karolinska Inst, Canc Ctr Karolinska, Dept Oncol Pathol, S-17176 Stockholm, Sweden
[2] Univ Michigan, Dept Mol Cellular & Dev Biol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
基金
瑞典研究理事会;
关键词
HISTONE DEACETYLASE INHIBITORS; REGULATES GENE-EXPRESSION; NF-KAPPA-B; SIGNALING PATHWAYS; SUPPRESSES AUTOPHAGY; H4K16; ACETYLATION; MYELOID-LEUKEMIA; MAMMALIAN TARGET; MTOR INHIBITION; CYTOSOLIC FOXO1;
D O I
10.1038/nrm3716
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Autophagy is a conserved process by which cytoplasmic components are degraded by the lysosome. It is commonly seen as a cytoplasmic event and, until now, nuclear events were not considered of primary importance for this process. However, recent studies have unveiled a transcriptional and epigenetic network that regulates autophagy. The identification of tightly controlled transcription factors (such as TFEB and ZKSCAN3), microRNAs and histone marks (especially acetylated Lys16 of histone 4 (H4K16ac) and dimethylated H3K9 (H3K9me2)) associated with the autophagic process offers an attractive conceptual framework to understand the short-term transcriptional response and potential long-term responses to autophagy.
引用
收藏
页码:65 / 74
页数:10
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