Interaction of Mash1 and Phox2b in sympathetic neuron development
- PMID: 15033166
- DOI: 10.1016/j.mcn.2003.10.021
Interaction of Mash1 and Phox2b in sympathetic neuron development
Abstract
The transcription factors Mash1 and Phox2b are both essential for sympathetic neuron development. To understand in more detail their function and interaction, Phox2b and Mash1 were ectopically expressed in vivo, in peripheral nerve precursors. Here, we demonstrate that the Phox2b-induced generation of ectopic noradrenergic neurons in chick peripheral nerve involves the induction of Cash1, the chick homolog of Mash1. All Phox2-induced neurons coexpress the noradrenergic marker genes TH and DBH. Conversely, Mash1 induces neuronal differentiation characterized by the expression of generic neuronal genes SCG10, Hu and NF160; however, only a subpopulation of these neurons also displays an autonomic, noradrenergic phenotype. This context-dependent action of Mash1 implicates autonomic codeterminants, required for noradrenergic differentiation in response to Mash1. In contrast, Phox2b coordinates generic and noradrenergic gene expression, recruiting Mash1/Cash1, which may have a major function in the control of pan-neuronal gene expression during noradrenergic neuron development.
Similar articles
-
Essential role of Gata transcription factors in sympathetic neuron development.Development. 2004 Oct;131(19):4775-86. doi: 10.1242/dev.01370. Epub 2004 Aug 25. Development. 2004. PMID: 15329349
-
Specification of the central noradrenergic phenotype by the homeobox gene Phox2b.Mol Cell Neurosci. 2000 Mar;15(3):235-43. doi: 10.1006/mcne.1999.0826. Mol Cell Neurosci. 2000. PMID: 10736201
-
The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives.Nature. 1999 May 27;399(6734):366-70. doi: 10.1038/20700. Nature. 1999. PMID: 10360575
-
Mechanisms and perspectives on differentiation of autonomic neurons.Dev Biol. 2005 Jan 15;277(2):271-86. doi: 10.1016/j.ydbio.2004.09.034. Dev Biol. 2005. PMID: 15617674 Review.
-
Perspectives on integration of cell extrinsic and cell intrinsic pathways of signaling required for differentiation of noradrenergic sympathetic ganglion neurons.Auton Neurosci. 2006 Jun 30;126-127:225-31. doi: 10.1016/j.autneu.2006.02.029. Epub 2006 May 2. Auton Neurosci. 2006. PMID: 16647305 Review.
Cited by
-
Non ionising radiation as a non chemical strategy in regenerative medicine: Ca(2+)-ICR "In Vitro" effect on neuronal differentiation and tumorigenicity modulation in NT2 cells.PLoS One. 2013 Apr 9;8(4):e61535. doi: 10.1371/journal.pone.0061535. Print 2013. PLoS One. 2013. PMID: 23585910 Free PMC article.
-
From proliferation to target innervation: signaling molecules that direct sympathetic nervous system development.Cell Tissue Res. 2018 May;372(2):171-193. doi: 10.1007/s00441-017-2693-x. Epub 2017 Oct 2. Cell Tissue Res. 2018. PMID: 28971249 Review.
-
Reciprocal gene replacements reveal unique functions for Phox2 genes during neural differentiation.EMBO J. 2005 Dec 21;24(24):4392-403. doi: 10.1038/sj.emboj.7600897. Epub 2005 Dec 1. EMBO J. 2005. PMID: 16319924 Free PMC article.
-
Cholinergic differentiation occurs early in mouse sympathetic neurons and requires Phox2b.Gene Expr. 2006;13(2):133-9. doi: 10.3727/000000006783991854. Gene Expr. 2006. PMID: 17017126 Free PMC article.
-
Distinct neuroblastoma-associated alterations of PHOX2B impair sympathetic neuronal differentiation in zebrafish models.PLoS Genet. 2013 Jun;9(6):e1003533. doi: 10.1371/journal.pgen.1003533. Epub 2013 Jun 6. PLoS Genet. 2013. PMID: 23754957 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Miscellaneous