Department of Oncology Pathology, Cancer Centrum Karolinska, Karolinska Institutet, Stockholm 17176, Sweden.
Life Sciences Institute and Departments of Molecular, Cellular and Developmental Biology and Biological Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA.
Nat Rev Mol Cell Biol. 2014 Jan;15(1):65-74. doi: 10.1038/nrm3716. Epub 2013 Dec 11.
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.
自噬是一种保守的过程,通过溶酶体降解细胞质成分。它通常被视为一种细胞质事件,直到现在,核事件并不被认为是这个过程的主要重要因素。然而,最近的研究揭示了一个调节自噬的转录和表观遗传网络。与自噬过程相关的紧密控制的转录因子(如 TFEB 和 ZKSCAN3)、microRNAs 和组蛋白标记(特别是组蛋白 H4 的乙酰化赖氨酸 16(H4K16ac)和 H3K9 的二甲基化(H3K9me2))的鉴定,为理解短期转录反应和自噬的潜在长期反应提供了一个有吸引力的概念框架。