The study of motor neuron differentiation in the developing spinal cord has provided a model system for defining the cellular interactions and molecular nature of inducing factors that control neuronal identify in the vertebrate nervous system. The source and origin of signals that control the diversification of motor neuron subtypes however remains unclear. In this project we will focus on the control of motor neuron diversity in the lateral motor column (LMC), a class of motor neurons that innervates target muscles in the limb. In preliminary studies we have provided evidence that three distinct signaling molecules that have been implicated in cellular differentiation and transformation: retinoids, ETS domain transcription factors and receptor tyrosine kinases of the Eph family are expressed by subsets of motor neurons in the LMC. These studies suggest that the analysis of motor neuron subtype diversity in the LMC may provide novel information on the function of classes of molecules implicated more generally in cellular differentiation and oncogenesis. Using a combination of in vitro assays of motor neuron differentiation and molecular genetic manipulations of gene expression in motor neurons in mouse embryo we will address three main issues: 1. The role of retinoid signaling in the specification of motor neuron columnar subtype identity within the LMC. 2. The role of ETS transcription factors in specifying the identity of motor neuron pool identity within the LMC. 3. The role of Eph kinases and their Ephrin ligands in the organization of motor neurons in the LMC and in the projection of specific subsets of motor axons to their targets in the limb.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA023767-20A1
Application #
6102019
Study Section
Project Start
1998-09-30
Project End
1999-07-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
20
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Qiu, Zhaozhu; Cang, Yong; Goff, Stephen P (2010) c-Abl tyrosine kinase regulates cardiac growth and development. Proc Natl Acad Sci U S A 107:1136-41
Qiu, Zhaozhu; Cang, Yong; Goff, Stephen P (2010) Abl family tyrosine kinases are essential for basement membrane integrity and cortical lamination in the cerebellum. J Neurosci 30:14430-9
Ohno, Nobuhiko; Terada, Nobuo; Komada, Masayuki et al. (2009) Dispensable role of protein 4.1B/DAL-1 in rodent adrenal medulla regarding generation of pheochromocytoma and plasmalemmal localization of TSLC1. Biochim Biophys Acta 1793:506-15
Liberatore, Rachel A; Goff, Stephen P (2009) c-Abl-deficient mice exhibit reduced numbers of peritoneal B-1 cells and defects in BCR-induced B cell activation. Int Immunol 21:403-14
Luria, Victor; Krawchuk, Dayana; Jessell, Thomas M et al. (2008) Specification of motor axon trajectory by ephrin-B:EphB signaling: symmetrical control of axonal patterning in the developing limb. Neuron 60:1039-53
Fleischmann, Alexander; Shykind, Benjamin M; Sosulski, Dara L et al. (2008) Mice with a ""monoclonal nose"": perturbations in an olfactory map impair odor discrimination. Neuron 60:1068-81
Cang, Yong; Zhang, Jianxuan; Nicholas, Sally A et al. (2007) DDB1 is essential for genomic stability in developing epidermis. Proc Natl Acad Sci U S A 104:2733-7
Lomvardas, Stavros; Barnea, Gilad; Pisapia, David J et al. (2006) Interchromosomal interactions and olfactory receptor choice. Cell 126:403-13
Cang, Yong; Zhang, Jianxuan; Nicholas, Sally A et al. (2006) Deletion of DDB1 in mouse brain and lens leads to p53-dependent elimination of proliferating cells. Cell 127:929-40
Heanue, Tiffany A; Pachnis, Vassilis (2006) Expression profiling the developing mammalian enteric nervous system identifies marker and candidate Hirschsprung disease genes. Proc Natl Acad Sci U S A 103:6919-24

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