The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives

被引:676
作者
Pattyn, A [1 ]
Morin, X [1 ]
Cremer, H [1 ]
Goridis, C [1 ]
Brunet, JF [1 ]
机构
[1] Univ Meditterranee, AP Marseille, INSERM, CNRS,Dev Biol Inst Marseille,Lab Genet & Physiol, F-13288 Marseille 9, France
关键词
D O I
10.1038/20700
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The sympathetic, parasympathetic and enteric ganglia are the main components of the peripheral autonomic nervous system(1), and are all derived from the neural crest(2). The factors needed for these structures to develop include the transcription factor Mash 1 (refs 3-5), the glial-derived neurotrophic factor GNDF (refs 6-8) and its receptor subunits(9-12), and the neuregulin signalling system(13), each of which is essential for the differentiation and survival of subsets of autonomic neurons. Here we show that all autonomic ganglia fail to form properly and degenerate in mice lacking the homeodomain transcription factor Phox2b, as do the three cranial sensory ganglia that are part of the autonomic reflex circuits. in the anlagen of the enteric nervous system and the sympathetic ganglia, Phox2b is needed for the expression of the GDNF-receptor subunit Ret and for maintaining Mash1 expression. Mutant ganglionic anlagen also fail to switch on the genes that encode two enzymes needed for the biosynthesis of the neurotransmitter noradrenaline, dopamine-beta-hydroxylase and tyrosine hydroxylase, demonstrating that Phox2b regulates the noradrenergic phenotype in vertebrates.
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页码:366 / 370
页数:5
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