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Onecut factors and Pou2f2 regulate the distribution of V2 interneurons in the mouse developing spinal cord

Authors :
Audrey Harris
Gauhar Masgutova
Frédéric Clotman
Lynn M. Corcoran
Benvenuto Jacob
María Hidalgo-Figueroa
Mathilde Toch
Amandine Collin
Cédric Francius
UCL - SSS/IONS/CEMO - Pôle Cellulaire et moléculaire
Source :
Frontiers in Cellular Neuroscience, Vol. 13, no.184, p. 1 (2019), Frontiers in Cellular Neuroscience, Vol 13 (2019), Frontiers in Cellular Neuroscience
Publication Year :
2018
Publisher :
Cold Spring Harbor Laboratory, 2018.

Abstract

Acquisition of proper neuronal identity and position is critical for the formation of neural circuits. In the embryonic spinal cord, cardinal populations of interneurons diversify into specialized subsets and migrate to defined locations within the spinal parenchyma. However, the factors that control interneuron diversification and migration remain poorly characterized. Here, we show that the Onecut transcription factors are necessary for proper diversification and distribution of the V2 interneurons in the developing spinal cord. Furthermore, we uncover that these proteins restrict and moderate the expression of spinal isoforms ofPou2f2, a transcription factor known to regulate B-cell differentiation. By gain- or loss-of-function experiments, we show that Pou2f2 contribute to regulate the position of V2 populations in the developing spinal cord. Thus, we uncovered a genetic pathway that regulates the diversification and the distribution of V2 interneurons during embryonic development.Significance statementIn this study, we identify the Onecut and Pou2f2 transcription factors as regulators of spinal interneuron diversification and migration, two events that are critical for proper CNS development.

Details

Language :
English
Database :
OpenAIRE
Journal :
Frontiers in Cellular Neuroscience, Vol. 13, no.184, p. 1 (2019), Frontiers in Cellular Neuroscience, Vol 13 (2019), Frontiers in Cellular Neuroscience
Accession number :
edsair.doi.dedup.....ccbd55f15a0ee3a12ccf1bcc8ac7e1b9
Full Text :
https://doi.org/10.1101/413054