| Literature DB >> 30401432 |
Rotem Ben-Tov Perry1, Hadas Hezroni2, Micah Jonathan Goldrich2, Igor Ulitsky3.
Abstract
In mammals, neurons in the peripheral nervous system (PNS) have regenerative capacity following injury, but it is generally absent in the CNS. This difference is attributed, at least in part, to the intrinsic ability of PNS neurons to activate a unique regenerative transcriptional program following injury. Here, we profiled gene expression following sciatic nerve crush in mice and identified long noncoding RNAs (lncRNAs) that act in the regenerating neurons and which are typically not expressed in other contexts. We show that two of these lncRNAs regulate the extent of neuronal outgrowth. We then focus on one of these, Silc1, and show that it regulates neuroregeneration in cultured cells and in vivo, through cis-acting activation of the transcription factor Sox11.Entities:
Keywords: CRISPR; Norris1; Silc1; Sox11; dorsal root ganglion; long noncoding RNA; regeneration; sciatic nerve injury
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Year: 2018 PMID: 30401432 PMCID: PMC6542662 DOI: 10.1016/j.molcel.2018.09.021
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970