| Literature DB >> 30392800 |
Mateusz C Ambrozkiewicz1, Manuela Schwark2, Mika Kishimoto-Suga2, Ekaterina Borisova3, Kei Hori4, Andrea Salazar-Lázaro5, Alexandra Rusanova3, Bekir Altas6, Lars Piepkorn7, Paraskevi Bessa5, Theres Schaub5, Xin Zhang8, Tamara Rabe9, Silvia Ripamonti2, Marta Rosário5, Haruhiko Akiyama10, Olaf Jahn7, Tatsuya Kobayashi11, Mikio Hoshino4, Victor Tarabykin3, Hiroshi Kawabe12.
Abstract
The establishment of axon-dendrite polarity is fundamental for radial migration of neurons during cortex development of mammals. We demonstrate that the E3 ubiquitin ligases WW-Containing Proteins 1 and 2 (Wwp1 and Wwp2) are indispensable for proper polarization of developing neurons. We show that knockout of Wwp1 and Wwp2 results in defects in axon-dendrite polarity in pyramidal neurons, and their aberrant laminar cortical distribution. Knockout of miR-140, encoded in Wwp2 intron, engenders phenotypic changes analogous to those upon Wwp1 and Wwp2 deletion. Intriguingly, transcription of the Wwp1 and Wwp2/miR-140 loci in neurons is induced by the transcription factor Sox9. Finally, we provide evidence that miR-140 supervises the establishment of axon-dendrite polarity through repression of Fyn kinase mRNA. Our data delineate a novel regulatory pathway that involves Sox9-[Wwp1/Wwp2/miR-140]-Fyn required for axon specification, acquisition of pyramidal morphology, and proper laminar distribution of cortical neurons.Entities:
Keywords: axon formation; host gene; intronic microRNA; neuronal development; neuronal differentiation; neuronal migration; ubiquitin
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Year: 2018 PMID: 30392800 DOI: 10.1016/j.neuron.2018.10.008
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173