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UA Life Science Research - BioGate
Carol C Gregorio
Contact Information
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Address: 1501 N. Campbell
Tucson, AZ 85724-5044
Phone: (520) 626-8113
E-Mail: gregorio@email.arizona.edu
Degrees
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Ph.D.
Department Affiliations
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Cell Biology & Anatomy, Molecular & Cellular Biology, BIO5 Institute
Program Affiliations
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Cell Biology & Anatomy, Molecular and Cellular Biology, Cancer Biology GIDP
Research Areas
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Developmental Biology, Cancer Biology, Cell Biology, Molecular Biology, Physiological Sciences
Research Interests
The research in my laboratory is focused on identifying the components and molecular mechanisms regulating actin architecture in cardiac and skeletal muscle during normal development and disease. Control of actin filament lengths and dynamics is important for cell motility and architecture and is regulated in part by capping proteins that block elongation and depolymerization at both the fast-growing (barbed) and slow-growing (pointed) ends of the filaments. Striated muscle is an ideal model system to test for the functional properties of various actin regulatory proteins due to the precise organization and polarity of cytoskeletal components within repeating sarcomeric units (for example, the ~1 mm long actin filaments are easily resolved by light microscopy). Using this system we can combine advanced cell biological and biochemical approaches with direct tests of physiological function in live beating muscle cells.
The research objectives of the laboratory can be broadly summarized as follows: 1) understanding the cellular mechanisms involved in the assembly, regulation and maintenance of contractile proteins in cardiac muscle in health and disease; 2) deciphering the mechanisms critical for precisely specifying and maintaining the lengths of actin filaments. Actin is an indispensable structural element of cells and is the major component of heart muscle. Changes in actin, caused by genetic mutations, which have been identified in humans, are a frequent cause of several forms of cardiomyopathy. We are determining how genetic defects in this protein affect muscle force generation and muscle contraction, leading to sudden cardiac death. 3) discovery of novel models of de novo cardiac muscle assembly, with special emphasis on differentiating murine embryonic stem (ES) cells to study all stages of heart muscle development.
Selected Publications
Pappas, C.T., Bhattacharya, N., Cooper J.A., and Gregorio CC. May 2008. Nebulin Interacts with CapZ and Regulates Thin Filament Architecture within the Z-Disc. Mol Biol Cell, 19:1837-47
Gregorio CC, Perry CN, McElhinny AS. Feb 2006. Functional properties of the titin/connectin-associated proteins, the muscle-specific RING finger proteins (MURFs), in striated muscle. J Muscle Res Cell Motil, 1-12
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