Literature DB >> 28820282

Mir505-3p regulates axonal development via inhibiting the autophagy pathway by targeting Atg12.

Kan Yang1,2,3, Bin Yu3, Cheng Cheng3, Tianlin Cheng3, Bo Yuan3, Kai Li1, Junhua Xiao1,2, Zilong Qiu3, Yuxun Zhou1.   

Abstract

In addition to the canonical role in protein homeostasis, autophagy has recently been found to be involved in axonal dystrophy and neurodegeneration. Whether autophagy may also be involved in neural development remains largely unclear. Here we report that Mir505-3p is a crucial regulator for axonal elongation and branching in vitro and in vivo, through modulating autophagy in neurons. We identify that the key target gene of Mir505-3p in neurons is Atg12, encoding ATG12 (autophagy-related 12) which is an essential component of the autophagy machinery during the initiation and expansion steps of autophagosome formation. Importantly, axonal development is compromised in brains of mir505 knockout mice, in which autophagy signaling and formation of autophagosomes are consistently enhanced. These results define Mir505-3p-ATG12 as a vital signaling cascade for axonal development via the autophagy pathway, further suggesting the critical role of autophagy in neural development.

Entities:  

Keywords:  ATG12; Mir505–3p; autophagy; axonal development; microRNA

Mesh:

Substances:

Year:  2017        PMID: 28820282      PMCID: PMC5640177          DOI: 10.1080/15548627.2017.1353841

Source DB:  PubMed          Journal:  Autophagy        ISSN: 1554-8627            Impact factor:   16.016


  69 in total

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