| Literature DB >> 28132840 |
Alexandra M Amen1, Claudia R Ruiz-Garzon1, Jay Shi2, Megha Subramanian1, Daniel L Pham1, Mollie K Meffert3.
Abstract
Environmental cues provoke rapid transitions in gene expression to support growth and cellular plasticity through incompletely understood mechanisms. Lin28 RNA-binding proteins have evolutionarily conserved roles in post-transcriptional coordination of pro-growth gene expression, but signaling pathways allowing trophic stimuli to induce Lin28 have remained uncharacterized. We find that Lin28a protein exhibits rapid basal turnover in neurons and that mitogen-activated protein kinase (MAPK)-dependent phosphorylation of the RNA-silencing factor HIV TAR-RNA-binding protein (TRBP) promotes binding and stabilization of Lin28a, but not Lin28b, with an accompanying reduction in Lin28-regulated miRNAs, downstream of brain-derived neurotrophic factor (BDNF). Binding of Lin28a to TRBP in vitro is also enhanced by phospho-mimic TRBP. Further, phospho-TRBP recapitulates BDNF-induced neuronal dendritic spine growth in a Lin28a-dependent manner. Finally, we demonstrate MAPK-dependent TRBP and Lin28a induction, with physiological function in growth and survival, downstream of diverse growth factors in multiple primary cell types, supporting a broad role for this pathway in trophic responses.Entities:
Keywords: BDNF; Dicer; Let-7 microRNA; Lin28; MAPK; TRBP; dendritic spine; microRNA biogenesis; synaptic plasticity; trophic response
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Year: 2017 PMID: 28132840 PMCID: PMC5325678 DOI: 10.1016/j.molcel.2016.12.025
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970