| DEVELOPMENTAL NEUROBIOLOGY AND GENE REGULATION |
The vertebrate nervous system includes many different classes of neurons, each exhibiting characteristic neurotransmitter receptors, ion channels, patterns of axonal growth, and synapse formation. Producing this cellular diversity during brain development is, in part, an enormous problem of gene regulation. We are engaged in studies of transcription factors of the homeodomain family that bind to DNA and activate or repress gene expression in specific classes of neurons. We employ a variety of approches to understanding the regulation of brain development. First, we use biochemical methods to characterize the target DNA binding sites of neural transcription factors and coordinate these findings with sequence data from the mouse and human genomes. Second, we manipulate the expression of regulatory genes in living chick embryos using microsurgery and electroporation, and in transgenic mice using targeted gene expression, and study the effects of these manipulations on neural marker genes, axonal growth, and cell survival. Third, we use array-based analysis of gene expression (“GeneChips”) and information from the mouse and human genome projects to understand the coordinated regulation of gene expression in the nervous system. Thus interesting projects are available using methods ranging from biochemistry to embryology. Please visit our lab homepage for more details of our work.
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Eng, SR, Gratwick, K, Rhee, JM, Fedtsova, N, Gan, L and Turner, EE. (2001) Defects in sensory axon growth precede neuronal death in Brn3a-deficient mice. J. Neuroscience, 21, 541-49.
Trieu, M, Ma, A, Eng, SR, Fedstova, N and Turner, EE. (2003) Direct autoregulation and gene dosage compensation by POU-domain transcription factor Brn3a. Development, 130, 111-121.
Fedtsova, N, Perris, R, and Turner, EE. (2003) Sonic hedgehog regulates the position of the trigeminal ganglia. Developmental Biology 261, 456-69.
Eng, SR, Lanier, J, Fedtsova, N, and Turner, EE. (2004) Coordinated regulation of gene expression by Brn3a in developing sensory ganglia. Development 131, 3859-70.
Quina, LA, Pak, W, Lanier, J, Banwait, P, Gratwick, K, Liu, Y, Velasquez, T, O’Leary, DDM, Goulding, M and Turner, EE. (2005) Brn3a-expressing retinal ganglion cells project specifically to thalamocortical and collicular visual pathways. J. Neuroscience 25, 11595-11604
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