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PRDM12 Is Required for Initiation of the Nociceptive Neuron Lineage during Neurogenesis

Authors :
Luca Bartesaghi
Yiqiao Wang
Paula Fontanet
Simone Wanderoy
Finja Berger
Haohao Wu
Natalia Akkuratova
Filipa Bouçanova
Jean-Jacques Médard
Charles Petitpré
Mark A. Landy
Ming-Dong Zhang
Philip Harrer
Claudia Stendel
Rolf Stucka
Marina Dusl
Maria Eleni Kastriti
Laura Croci
Helen C. Lai
Gian Giacomo Consalez
Alexandre Pattyn
Patrik Ernfors
Jan Senderek
Igor Adameyko
Francois Lallemend
Saida Hadjab
Roman Chrast
Source :
Cell Reports, Vol 26, Iss 13, Pp 3484-3492.e4 (2019)
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

Summary: The sensation of pain is essential for the preservation of the functional integrity of the body. However, the key molecular regulators necessary for the initiation of the development of pain-sensing neurons have remained largely unknown. Here, we report that, in mice, inactivation of the transcriptional regulator PRDM12, which is essential for pain perception in humans, results in a complete absence of the nociceptive lineage, while proprioceptive and touch-sensitive neurons remain. Mechanistically, our data reveal that PRDM12 is required for initiation of neurogenesis and activation of a cascade of downstream pro-neuronal transcription factors, including NEUROD1, BRN3A, and ISL1, in the nociceptive lineage while it represses alternative fates other than nociceptors in progenitor cells. Our results thus demonstrate that PRDM12 is necessary for the generation of the entire lineage of pain-initiating neurons. : The sensation of pain, temperature, and itch by neurons of the nociceptive lineage is essential for animal survival. Bartesaghi et al. report that the transcriptional regulator PRDM12 is indispensable in neural crest cells (NCCs) for the initiation of the sensory neuronal differentiation program that generates the entire nociceptive lineage. Keywords: neurogenesis, pain, nociceptive neurons, Prdm12, neural crest cells

Subjects

Subjects :
Biology (General)
QH301-705.5

Details

Language :
English
ISSN :
22111247
Volume :
26
Issue :
13
Database :
Directory of Open Access Journals
Journal :
Cell Reports
Publication Type :
Academic Journal
Accession number :
edsdoj.8d3c2ac2ef91434cbeb5846bfc9c9928
Document Type :
article
Full Text :
https://doi.org/10.1016/j.celrep.2019.02.098