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![]() | Torres,
Gonzalo E. Assistant Professor, Neurobiology Ph.D., St. Louis University (1999) Address: 6061 BST3 Telephone: 412-383-8983 Fax: 412-383-5267 E-mail: gtorres@pitt.edu The work in our laboratory is focused along two main research areas: | |||||||||||||
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Cellular
and Molecular Regulation of Monoamine Transporters:
We are interested in the function and regulation of monoamine transporters
in the brain. The transporter-mediated uptake system is the primary mechanism
involved in the termination of monoaminergic signaling, and thus determines
the intensity and duration of monoamine transmission at synapses. Despite
the importance of biogenic amine transporters in controlling brain function,
very little information is available regarding the cellular and molecular
regulation of these proteins. This information is essential to understand
their contribution to psychiatric disorders and drug addiction. Recently,
results from our lab suggest that monoamine transporters are highly regulated
proteins and indicate a more complex degree of organization for these transporters
than previously anticipated. Findings include the elucidation of the oligomeric
nature of DAT, the identification of domains involved in assembly and trafficking,
and the identification and characterization of interacting proteins. Based
on these results, we hypothesize that monoamine transporters exist as highly
regulated macromolecular complexes and that these new regulatory mechanisms
might have important implications as novel therapeutic targets.
Neurobiology of the Dystonia-Linked TorsinA Protein: Early-onset torsion dystonia (EOTD) is the most common and severe form of a group of diseases known as dystonias. EOTD is an autosomal dominant movement disorder characterized by involuntary and sustained muscle contractions affecting several parts of the body and resulting in twisting, abnormal postures, and in many cases severe disability. The disease has been recently linked to a three-base pair deletion in the DYT1 gene that results in a single glutamate deletion near the carboxyl terminus of the product of the DYT1 gene, a protein termed torsinA. The mutation causes the protein to aggregate in perinuclear inclusions as opposed to the endoplasmic reticulum localization of the wild-type protein. Although there is increasing evidence that dysfunction of the dopamine system is implicated in the development of EOTD, the biological function of torsinA and its relation to dopaminergic neurotransmission has remained unexplored. We are using biochemical, molecular, and genetic approaches to elucidate the normal biological function of torsinA as well as the relationship between the torsinA mutation and EOTD. Trainees in the laboratory have the opportunity to participate in a number of research projects related to the function and regulation of monoamine transporters and the neurobiology of torsinA. Specific projects include :
Sample Publications: Torres GE, Sweeney AL, Beaulieu JM, Shashidharan P, Caron MG. Effect of torsinA on membrane proteins reveals a loss of function and a dominant-negative phenotype of the dystonia-associated DeltaE-torsinA mutant. Proc Natl Acad Sci U S A. 2004 Nov 2;101(44):15650-5. Epub 2004 Oct 25.
Yao, W-D., Gainetdinov, R.R., Arbuckle, M.I., Sotnikova, T.D., Cyr, M., Beaulieu, J-M., Torres, G.E., Grant, S.G.N., and Caron, M.G. (2004) Identification of PSD-95 as a regulator of dopamine-mediated synaptic and behavioral plasticity. Neuron 41, 625-638. Gainetdinov, R.R., Bohn, L.M., Sotnikova, T.D., Cyr, M., Laakso, A., Macrae, A., Kim, K., Torres, G.E., Lefkowitz, R.J., Caron, M.G., and Premont, R.T. (2003) Dopaminergic supersentivity in G protein-coupled receptor kinase 6-deficient mice. Neuron 38, 291-303. Torres, G.E., Gainetdinov, R.R., and Caron, M.G. (2003) Plasma membrane monoamine transporters: structure, regulation and function. Nat. Rev. Neurosci. 4, 13-25. Torres, G. E., Carneiro, A., Sweeney, A., Yao, W. D. and Caron, M. G. (2003) Oligomerization and trafficking of the human dopamine transporter. Mutational analysis identifies critical domains important for the functional expression of the transporter. J. Biol. Chem. 278, 2731-2739.
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Copyright 2001 - University
of Pittsburgh Department of Neurobiology | |||||||||||||