Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation

<p>Abstract</p> <p>The transcription factor Brn3a, product of the <it>pou4f1 </it>gene, is expressed in most sensory neurons throughout embryogenesis. Prior work has demonstrated a role for Brn3a in the repression of early neurogenic genes; here we describe a second maj...

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Main Authors: Raisa Eng S, Lanier Jason, Dykes Iain M, Turner Eric E
Format: Article
Language:English
Published: BMC 2010-01-01
Series:Neural Development
Online Access:http://www.neuraldevelopment.com/content/5/1/3
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spelling doaj-0794e8a5ee4a438ca82314654d0623da2020-11-24T20:59:03ZengBMCNeural Development1749-81042010-01-0151310.1186/1749-8104-5-3Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiationRaisa Eng SLanier JasonDykes Iain MTurner Eric E<p>Abstract</p> <p>The transcription factor Brn3a, product of the <it>pou4f1 </it>gene, is expressed in most sensory neurons throughout embryogenesis. Prior work has demonstrated a role for Brn3a in the repression of early neurogenic genes; here we describe a second major role for Brn3a in the specification of sensory subtypes in the trigeminal ganglion (TG). Sensory neurons initially co-express multiple Trk-family neurotrophin receptors, but are later marked by the unique expression of TrkA, TrkB or TrkC. Maturation of these sensory subtypes is known to depend on the expression of Runx transcription factors. Newborn Brn3a knockout mice fail to express TrkC, which is associated in the TG with mechanoreceptors, plus a set of functional genes associated with nociceptor subtypes. In embryonic Brn3a<sup>-/- </sup>ganglia, the normal expression of Runx3 is never initiated in TrkC<sup>+ </sup>neurons, and Runx1 expression is greatly attenuated in TrkA<sup>+ </sup>nociceptors. These changes are accompanied by expanded expression of TrkB in neurons that abnormally express multiple Trks, followed by the loss of TrkC and TrkA expression. In transgenic embryos expressing a Brn3a-VP16 dominant transactivator, Runx3 mRNA expression is increased, suggesting that it is a direct regulatory target of Brn3a. Chromatin immunoprecipitation confirms that Brn3a binds <it>in vivo </it>to a conserved upstream enhancer element within histone H3-acetylated chromatin in the <it>Runx3 </it>locus. Together these data show that Brn3a acts upstream of the Runx factors, which then repress TrkB expression to allow establishment of the non-overlapping Trk receptor profiles and correct terminally differentiated phenotypes.</p> http://www.neuraldevelopment.com/content/5/1/3
collection DOAJ
language English
format Article
sources DOAJ
author Raisa Eng S
Lanier Jason
Dykes Iain M
Turner Eric E
spellingShingle Raisa Eng S
Lanier Jason
Dykes Iain M
Turner Eric E
Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation
Neural Development
author_facet Raisa Eng S
Lanier Jason
Dykes Iain M
Turner Eric E
author_sort Raisa Eng S
title Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation
title_short Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation
title_full Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation
title_fullStr Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation
title_full_unstemmed Brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting Runx expression during sensory differentiation
title_sort brn3a regulates neuronal subtype specification in the trigeminal ganglion by promoting runx expression during sensory differentiation
publisher BMC
series Neural Development
issn 1749-8104
publishDate 2010-01-01
description <p>Abstract</p> <p>The transcription factor Brn3a, product of the <it>pou4f1 </it>gene, is expressed in most sensory neurons throughout embryogenesis. Prior work has demonstrated a role for Brn3a in the repression of early neurogenic genes; here we describe a second major role for Brn3a in the specification of sensory subtypes in the trigeminal ganglion (TG). Sensory neurons initially co-express multiple Trk-family neurotrophin receptors, but are later marked by the unique expression of TrkA, TrkB or TrkC. Maturation of these sensory subtypes is known to depend on the expression of Runx transcription factors. Newborn Brn3a knockout mice fail to express TrkC, which is associated in the TG with mechanoreceptors, plus a set of functional genes associated with nociceptor subtypes. In embryonic Brn3a<sup>-/- </sup>ganglia, the normal expression of Runx3 is never initiated in TrkC<sup>+ </sup>neurons, and Runx1 expression is greatly attenuated in TrkA<sup>+ </sup>nociceptors. These changes are accompanied by expanded expression of TrkB in neurons that abnormally express multiple Trks, followed by the loss of TrkC and TrkA expression. In transgenic embryos expressing a Brn3a-VP16 dominant transactivator, Runx3 mRNA expression is increased, suggesting that it is a direct regulatory target of Brn3a. Chromatin immunoprecipitation confirms that Brn3a binds <it>in vivo </it>to a conserved upstream enhancer element within histone H3-acetylated chromatin in the <it>Runx3 </it>locus. Together these data show that Brn3a acts upstream of the Runx factors, which then repress TrkB expression to allow establishment of the non-overlapping Trk receptor profiles and correct terminally differentiated phenotypes.</p>
url http://www.neuraldevelopment.com/content/5/1/3
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