Literature DB >> 12948444

Met signaling is required for recruitment of motor neurons to PEA3-positive motor pools.

Françoise Helmbacher1, Eric Dessaud, Silvia Arber, Odile deLapeyrière, Christopher E Henderson, Rüdiger Klein, Flavio Maina.   

Abstract

Motor neurons in the spinal cord are grouped into motor pools, each of which innervates a single muscle. The ETS transcription factor PEA3 is a marker of a few such motor pools. Here, we show that pea3 is first induced by GDNF in a caudal subset of the motor neurons that will constitute the pea3+ population. Expansion of the pea3 domain subsequently occurs by recruitment of neurons from more anterior segments. Signaling by Met, the HGF receptor, is required for the rostral expansion of the pea3 domain, while the onset of pea3 expression is independent of met function. met expression is observed in pioneer neurons but does not precede that of pea3 in recruited neurons. We provide genetic evidence for a non-cell-autonomous function of met during the recruitment process. We propose the presence of a relay mechanism allowing cells induced by peripheral signals to recruit more anterior neurons to adopt the same motor pool-related phenotype.

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Year:  2003        PMID: 12948444     DOI: 10.1016/s0896-6273(03)00493-8

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  29 in total

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Review 5.  Stochastic mechanisms of cell fate specification that yield random or robust outcomes.

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6.  Tissue-specific activities of the Fat1 cadherin cooperate to control neuromuscular morphogenesis.

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9.  Laminar patterning in the developing neocortex by temporally coordinated fibroblast growth factor signaling.

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10.  Etv4 and Etv5 are required downstream of GDNF and Ret for kidney branching morphogenesis.

Authors:  Benson C Lu; Cristina Cebrian; Xuan Chi; Satu Kuure; Richard Kuo; Carlton M Bates; Silvia Arber; John Hassell; Lesley MacNeil; Masato Hoshi; Sanjay Jain; Naoya Asai; Masahide Takahashi; Kai M Schmidt-Ott; Jonathan Barasch; Vivette D'Agati; Frank Costantini
Journal:  Nat Genet       Date:  2009-11-08       Impact factor: 38.330

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