This competitive renewal application requests continued support for a Training Program in Biomolecular Signal Transduction at Thomas Jefferson University. This program was established in 1994 and provides broad interdisciplinary training at the pre-doctoral and post-doctoral levels in the field of signal transduction. Program faculty are drawn from members of three basic science departments (Biochemistry & Molecular Biology, Microbiology & Immunology, and Pathology, Cell Biology, & Anatomy) and two clinical divisions (Endocrinology and Clinical Pharmacology) in the Department of Medicine. Specific training areas include growth factor and G protein-coupled receptor signaling, signal integration, protein targeting and trafficking, cell cycle regulation, and apoptosis. The overall goal of the program is to provide aspiring researchers with the training and experience necessary to establish careers as independent investigators. The pre-doctoral training program is available to students who hold a bachelor degree from an accredited institution who wish to pursue biomedical research careers. Applicants must have a solid background in the biological and chemical sciences. Grade point averages, GRE scores, letters of recommendation, prior research experience, and interviews are the major criteria for acceptance into the program. Pre-doctoral matriculates must complete a rigorous series of graduate courses giving them a thorough background in biochemistry, pharmacology, genetics, cell and molecular biology, bioinformatics, and research ethics. Students are also required to complete a minimum of three laboratory rotations within the first year of matriculation. Students also have ample opportunity to present seminars on their own work and on the current literature to faculty and fellow trainees in both formal and informal settings. The post-doctoral training program is available to individuals who hold the Ph.D., M.D., or equivalent doctoral degree and acceptance depends upon past research and educational experience. Pre-doctoral and post-doctoral trainees are required to actively participate in Research-In-Progress seminars as well as a Cell Signaling seminar series. The goal of this program is to develop highly trained research scientists in the broad area of biomolecular signal transduction.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Institutional National Research Service Award (T32)
Project #
5T32DK007705-14
Application #
7243465
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Hyde, James F
Project Start
1994-06-01
Project End
2009-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
14
Fiscal Year
2007
Total Cost
$305,280
Indirect Cost
Name
Thomas Jefferson University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Donaldson, Joshua M; Zer, Cindy; Avery, Kendra N et al. (2013) Identification and grafting of a unique peptide-binding site in the Fab framework of monoclonal antibodies. Proc Natl Acad Sci U S A 110:17456-61
Siglin, Amanda E; Sun, Shangjin; Moore, Jeffrey K et al. (2013) Dynein and dynactin leverage their bivalent character to form a high-affinity interaction. PLoS One 8:e59453
Montie, Heather L; Pestell, Richard G; Merry, Diane E (2011) SIRT1 modulates aggregation and toxicity through deacetylation of the androgen receptor in cell models of SBMA. J Neurosci 31:17425-36
Barker, Breann L; Benovic, Jeffrey L (2011) G protein-coupled receptor kinase 5 phosphorylation of hip regulates internalization of the chemokine receptor CXCR4. Biochemistry 50:6933-41
Orr, Christopher R; Montie, Heather L; Liu, Yuhong et al. (2010) An interdomain interaction of the androgen receptor is required for its aggregation and toxicity in spinal and bulbar muscular atrophy. J Biol Chem 285:35567-77
Crouthamel, Marykate; Abankwa, Daniel; Zhang, Li et al. (2010) An N-terminal polybasic motif of Gýýq is required for signaling and influences membrane nanodomain distribution. Mol Pharmacol 78:767-77
Shin, Marcus E; Skokotas, Aikaterini; Winter, Edward (2010) The Cdk1 and Ime2 protein kinases trigger exit from meiotic prophase in Saccharomyces cerevisiae by inhibiting the Sum1 transcriptional repressor. Mol Cell Biol 30:2996-3003
Kahle, Kristen M; Steger, H Kirby; Root, Michael J (2009) Asymmetric deactivation of HIV-1 gp41 following fusion inhibitor binding. PLoS Pathog 5:e1000674
McDonald, Christine M; Wagner, Marisa; Dunham, Maitreya J et al. (2009) The Ras/cAMP pathway and the CDK-like kinase Ime2 regulate the MAPK Smk1 and spore morphogenesis in Saccharomyces cerevisiae. Genetics 181:511-23
Xiong, Ling; Chen, Xiaole L; Silver, Hannah R et al. (2009) Deficient SUMO attachment to Flp recombinase leads to homologous recombination-dependent hyperamplification of the yeast 2 microm circle plasmid. Mol Biol Cell 20:1241-51

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