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微小 RNA-137 是一种新型的低氧反应性微小 RNA,通过调节两种线粒体自噬受体 FUNDC1 和 NIX 来抑制线粒体自噬。

MicroRNA-137 is a novel hypoxia-responsive microRNA that inhibits mitophagy via regulation of two mitophagy receptors FUNDC1 and NIX.

机构信息

Institute of Neurology, Guangdong Key Laboratory of Age-related Cardiac-cerebral Vascular Disease, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.

Department of Anesthesiology, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong.

出版信息

J Biol Chem. 2014 Apr 11;289(15):10691-10701. doi: 10.1074/jbc.M113.537050. Epub 2014 Feb 26.

Abstract

Mitophagy receptors mediate the selective recognition and targeting of damaged mitochondria by autophagosomes. The mechanism for the regulation of these receptors remains unknown. Here, we demonstrated that a novel hypoxia-responsive microRNA, microRNA-137 (miR-137), markedly inhibits mitochondrial degradation by autophagy without affecting global autophagy. miR-137 targets the expression of two mitophagy receptors NIX and FUNDC1. Impaired mitophagy in response to hypoxia caused by miR-137 is reversed by re-expression of FUNDC1 and NIX expression vectors lacking the miR-137 recognition sites at their 3' UTR. Conversely, miR-137 also suppresses the mitophagy induced by fundc1 (CDS+3'UTR) but not fundc1 (CDS) overexpression. Finally, we found that miR-137 inhibits mitophagy by reducing the expression of the mitophagy receptor thereby leads to inadequate interaction between mitophagy receptor and LC3. Our results demonstrated the regulatory role of miRNA to mitophagy receptors and revealed a novel link between miR-137 and mitophagy.

摘要

线粒体自噬受体介导自噬体对受损线粒体的选择性识别和靶向。这些受体的调节机制尚不清楚。在这里,我们证明了一种新的缺氧反应性 microRNA,microRNA-137(miR-137),在不影响整体自噬的情况下,显著抑制线粒体的自噬降解。miR-137 靶向两种线粒体自噬受体 NIX 和 FUNDC1 的表达。miR-137 对缺氧反应的线粒体自噬受损可通过重新表达 FUNDC1 和 NIX 表达载体来逆转,这些载体在其 3'UTR 中缺乏 miR-137 识别位点。相反,miR-137 也抑制 fundc1(CDS+3'UTR)但不抑制 fundc1(CDS)过表达诱导的线粒体自噬。最后,我们发现 miR-137 通过降低线粒体自噬受体的表达来抑制线粒体自噬,从而导致线粒体自噬受体与 LC3 之间的相互作用不足。我们的结果表明了 miRNA 对线粒体自噬受体的调节作用,并揭示了 miR-137 与线粒体自噬之间的新联系。

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