| Literature DB >> 29395906 |
Kyung Won Kim1, Ngang Heok Tang1, Matthew G Andrusiak1, Zilu Wu1, Andrew D Chisholm1, Yishi Jin2.
Abstract
The PIWI-interacting RNA (piRNA) pathway has long been thought to function solely in the germline, but evidence for its functions in somatic cells is emerging. Here we report an unexpected role for the piRNA pathway in Caenorhabditis elegans sensory axon regeneration after injury. Loss of function in a subset of components of the piRNA pathway results in enhanced axon regrowth. Two essential piRNA factors, PRDE-1 and PRG-1/PIWI, inhibit axon regeneration in a gonad-independent and cell-autonomous manner. By smFISH analysis we find that prde-1 transcripts are present in neurons, as well as germ cells. The piRNA pathway inhibits axon regrowth independent of nuclear transcriptional silencing but dependent on the slicer domain of PRG-1/PIWI, suggesting that post-transcriptional gene silencing is involved. Our results reveal the neuronal piRNA pathway as a novel intrinsic repressor of axon regeneration.Entities:
Keywords: Argonaute; D-D-H motif; PIWI; PRDE-1; PRG-1; neuronal injury; posttranscriptional gene silencing (PTGS); slicer activity; smFISH; small RNA
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Year: 2018 PMID: 29395906 PMCID: PMC5866297 DOI: 10.1016/j.neuron.2018.01.014
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173