In the developing mammalian brain, directed cell migrations establish the neuronal layers of the cerebellum and the neocortex. While a number of receptor systems have been studied in vertebrate neuronal migrations, an important avenue of discovery of genes that potentially regulate CNS migrations is to search for homologues of genes that function in neuroblast migration in C. elegans and Drosophila. During the prior funding period of this grant, we have begun studies with the laboratory of Dr. Cynthia Kenyon to explore the role of homologues of C. elegans neuroblast migration genes in mammalian brain development. Toward that end, we have cloned homologues of the C. elegans gene mig-13 and initiated studies on the role of Mmig13 in brain development. The overall goal of this Research Plan is to define the function of murine homologues of the C. elegans gene mig-13 in the formation of murine cerebellar and neocortical neural laminae. Our preliminary studies suggest that Mmig13 functions in the formation of the EGL in the embryonic cerebellar anlagen, prior to migration of postmitotic precursors along the Bergmann glial fibers, and in the formation of the cortical plate, the region where young neurons in the neocortex halt their movements along radial glial fibers and assemble into specific layers. The proposed research is aimed at testing and refining this general hypothesis by providing more detailed studies on the timing of expression of Mmig13 in these two brain structures, by imaging living neurons in cells and tissue from Mmig13 BAC transgenic mice, where the Mmig13 gene is marked by EGFP, and by evaluating the effects of either gain of function or loss of function on granule cell migration and/or cortical neuron migration. To better understand the mechanism of action of the gene(s), we will define their extracellular ligands and their intracellular signaling pathways. This information should broaden our view of the mechanisms that control CNS migrations and of the downstream events important to neuronal differentiation within the neural layers.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS015429-25
Application #
6848768
Study Section
Neurogenesis and Cell Fate Study Section (NCF)
Program Officer
Riddle, Robert D
Project Start
1987-09-01
Project End
2008-01-31
Budget Start
2005-02-01
Budget End
2006-01-31
Support Year
25
Fiscal Year
2005
Total Cost
$389,656
Indirect Cost
Name
Rockefeller University
Department
Biology
Type
Other Domestic Higher Education
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
Schneider, Stephanie; Gulacsi, Alexandra; Hatten, Mary E (2011) Lrp12/Mig13a reveals changing patterns of preplate neuronal polarity during corticogenesis that are absent in reeler mutant mice. Cereb Cortex 21:134-44
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Osheroff, Hilleary; Hatten, Mary E (2009) Gene expression profiling of preplate neurons destined for the subplate: genes involved in transcription, axon extension, neurotransmitter regulation, steroid hormone signaling, and neuronal survival. Cereb Cortex 19 Suppl 1:i126-34
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Zhao, Haotian; Ayrault, Olivier; Zindy, Frederique et al. (2008) Post-transcriptional down-regulation of Atoh1/Math1 by bone morphogenic proteins suppresses medulloblastoma development. Genes Dev 22:722-7
Solecki, David J; Govek, Eve-Ellen; Tomoda, Toshifumi et al. (2006) Neuronal polarity in CNS development. Genes Dev 20:2639-47
Solecki, David J; Govek, Eve-Ellen; Hatten, Mary E (2006) mPar6 alpha controls neuronal migration. J Neurosci 26:10624-5
Hatten, Mary E (2005) LIS-less neurons don't even make it to the starting gate. J Cell Biol 170:867-71
Hatten, Mary E; Heintz, Nathaniel (2005) Large-scale genomic approaches to brain development and circuitry. Annu Rev Neurosci 28:89-108
Millen, K J; Millonig, J H; Hatten, M E (2004) Roof plate and dorsal spinal cord dl1 interneuron development in the dreher mutant mouse. Dev Biol 270:382-92

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