Wu Yaran, Dai Xufang, Ni Zhenhong, Yan Xiaojing, He Fengtian, Lian Jiqin
Department of Biochemistry and Molecular Biology, College of Basic Medical Sciences, Third Military Medical University, Chongqing 400038, China.
Department of Educational Science College, Chongqing Normal University, Chongqing 400047, China.
Iran J Basic Med Sci. 2017 Oct;20(10):1125-1130. doi: 10.22038/IJBMS.2017.9446.
Autophagy-related 4B (ATG4B) plays an important role in the process of autophagy induction. However, the molecular events that govern the expression of ATG4B in this process are not well known.
Human ATG4B 3'-UTR region (1377 nt) containing miR-34a/miR-34c-5p binding site was amplified by PCR. Luciferase assay was used to assess the activity of reporter genes. Real-time PCR was used to detect the levels of miR-34a and miR-34c-5p. Western blot was used toanalyze the protein levels of ATG4B, LC3 and p62.
Both miR-34a and miR-34c-5p could directly target the 3'-UTR of ATG4B mRNA at same site. Overexpression of either miR-34a or miR-34c-5p significantly down-regulated ATG4B at both mRNA and protein levels and this effect can be reversed by ATG4B overexpression. Moreover, Rapamycin-induced autophagy is accompanied with the upregulation of ATG4B and the downregulation of miR-34a/miR-34c-5p. Ectopic expression of either miR-34a or miR-34c-5p markedly suppressed rapamycin-triggered autophagy.
In the present study, we found that miR34/ATG4B signaling axis involves in rapamycin-triggered autophagy. This study may provide a new insight for understanding the mechanisms of ATG4B regulation and autophagy induction.
自噬相关蛋白4B(ATG4B)在自噬诱导过程中发挥重要作用。然而,在此过程中调控ATG4B表达的分子事件尚不清楚。
通过PCR扩增包含miR-34a/miR-34c-5p结合位点的人ATG4B 3'-UTR区域(1377 nt)。采用荧光素酶报告基因检测法评估报告基因的活性。运用实时PCR检测miR-34a和miR-34c-5p的水平。采用蛋白质免疫印迹法分析ATG4B、LC3和p62的蛋白水平。
miR-34a和miR-34c-5p均可直接靶向ATG4B mRNA的3'-UTR同一区域。miR-34a或miR-34c-5p的过表达均显著下调ATG4B的mRNA和蛋白水平,且这种作用可被ATG4B过表达逆转。此外,雷帕霉素诱导的自噬伴随着ATG4B的上调和miR-34a/miR-34c-5p的下调。miR-34a或miR-34c-5p的异位表达显著抑制雷帕霉素触发的自噬。
在本研究中,我们发现miR34/ATG4B信号轴参与雷帕霉素触发的自噬。本研究可能为理解ATG4B调控机制和自噬诱导提供新的见解。