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Micro RNA ‐495 regulates starvation‐induced autophagy by targeting ATG 3
Author(s) -
Li Wen,
Yang Yue,
Hou Xiaoyan,
Zhuang Haixia,
Wu Zijun,
Li Zhiyi,
Guo Runmin,
Chen Hao,
Lin Chunxia,
Zhong Wangtao,
Chen Yusen,
Wu Keng,
Zhang Liangqing,
Feng Du
Publication year - 2016
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1002/1873-3468.12108
Subject(s) - autophagy , starvation , rna , chemistry , microbiology and biotechnology , endogeny , viability assay , programmed cell death , cell , biology , apoptosis , gene , biochemistry , endocrinology
The functions of some essential autophagy genes are regulated by micro RNA s. However, an ATG 3‐modulating micro RNA has never been reported. Here we show that the transcription of miR‐495 negatively correlates with the translation of ATG 3 under nutrient‐deprived or rapamycin‐treated conditions. miR‐495 targets ATG 3 and regulates its protein levels under starvation conditions. miR‐495 also inhibits starvation‐induced autophagy by decreasing the number of autophagosomes and by preventing LC 3‐I‐to‐ LC 3‐ II transition and P62 degradation. These processes are reversed by the overexpression of an endogenous miR‐495 inhibitor. Re‐expression of Atg3 without miR‐495 response elements restores miR‐495‐inhibited autophagy. miR‐495 sustains cell viability under starvation conditions but has no effect under hypoxia. Moreover, miR‐495 inhibits etoposide‐induced cell death. In conclusion, miR‐495 is involved in starvation‐induced autophagy by regulating Atg3.