This competitive renewal is for the now 10-year old Signal Transduction Training Program (STTP) at the University of Illinois at Chicago. The STTP provides interdisciplinary predoctoral training in signal transduction, gene transcription and translation, and cellular endocrinology, with strong emphasis on cellular and molecular mechanisms that transduce signals and regulate cell, tissue and organismal development, and environmental and immunologic responses. The goal is the training of predoctoral candidates in broad aspects of signal transduction and cellular endocrinology to develop independent basic scientists and clinical investigators. An STTP theme for the past ten years is the promotion of training environment interactions between faculty researchers and programs that are using different experimental systems and approaches to understand signal transduction mechanisms at various levels of biological organization including molecular, cellular and integrative whole organism biology. The STTP crosses disciplinary, departmental and college lines, drawing upon the expertise of 35 faculty from six basic science departments (anatomy &cell biology, biochemistry &molecular genetics, microbiology &immunology, pharmacology, physiology &biophysics and bioengineering), and four clinical sections (hematology-oncology, endocrinology and metabolism, pulmonary and critical care, urology), offering training opportunities in wide ranging problems in signal transduction and allied areas using a broad spectrum of molecular, biochemical, physiologic, genetic, structural and animal model integrative biology approaches. Signal transduction, membrane receptors, second messengers, cell cycle regulation, gene transcription, cancer biology, mammalian development, endocrine and neurohumoral signaling are major strengths of the STTP faculty. Predoctoral training includes theory, techniques and research perspectives through didactic courses, research presentations, seminars, research rotations and informal interactions. Specialized courses in signal transduction, endocrinology, and a core curriculum in the interdisciplinary Graduate Education in Medical Sciences (GEMS) program at UIC in molecular and cellular biology, biochemistry, genetics, structural biology, physiology, pharmacology, scientific communication and responsible conduct of research provide the foundation for an intensive research training environment. Faculty trainer research interests range from neurohumoral signaling, membrane receptors and second messengers, cell cycle control, transcriptional, translational and epigenetic gene regulation, developmental and structural biology. The STTP emphasizes the interdisciplinary nature of contemporary research in signal transduction and cellular endocrinology in an environment fostering independent and creative thinking, and is contributing to the generation of independent investigators who are now making significant contributions in this broad area, and who beginning to enrich scientific progress and the scientific research community.

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 #
5T32DK007739-15
Application #
8107875
Study Section
Diabetes, Endocrinology and Metabolic Diseases B Subcommittee (DDK)
Program Officer
Castle, Arthur
Project Start
1997-07-01
Project End
2012-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
15
Fiscal Year
2011
Total Cost
$123,500
Indirect Cost
Name
University of Illinois at Chicago
Department
Biochemistry
Type
Schools of Medicine
DUNS #
098987217
City
Chicago
State
IL
Country
United States
Zip Code
60612
Choi, J S; Kim, K-H; Lau, L F (2015) The matricellular protein CCN1 promotes mucosal healing in murine colitis through IL-6. Mucosal Immunol 8:1285-96
Gierut, Jessica J; Mathur, Priya S; Bie, Wenjun et al. (2012) Targeting protein tyrosine kinase 6 enhances apoptosis of colon cancer cells following DNA damage. Mol Cancer Ther 11:2311-20
Nogueira, Veronique; Sundararajan, Deepa; Kwan, Jennifer M et al. (2012) Akt-dependent Skp2 mRNA translation is required for exiting contact inhibition, oncogenesis, and adipogenesis. EMBO J 31:1134-46
Le, Jamie A; Wilson, Heather M; Shehu, Aurora et al. (2012) Generation of mice expressing only the long form of the prolactin receptor reveals that both isoforms of the receptor are required for normal ovarian function. Biol Reprod 86:86
Zimnicka, Adriana M; Ivy, Kristin; Kaplan, Jack H (2011) Acquisition of dietary copper: a role for anion transporters in intestinal apical copper uptake. Am J Physiol Cell Physiol 300:C588-99
Gierut, Jessica; Zheng, Yu; Bie, Wenjun et al. (2011) Disruption of the mouse protein tyrosine kinase 6 gene prevents STAT3 activation and confers resistance to azoxymethane. Gastroenterology 141:1371-80, 1380.e1-2
Ellis, Anne K; Ackerman, Steven J; Crawford, Lynn et al. (2010) Cord blood molecular biomarkers of eosinophilopoiesis: kinetic analysis of GATA-1, MBP1 and IL-5R alpha mRNA expression. Pediatr Allergy Immunol 21:640-8
Lye, Ming F; Fanning, Alan S; Su, Ying et al. (2010) Insights into regulated ligand binding sites from the structure of ZO-1 Src homology 3-guanylate kinase module. J Biol Chem 285:13907-17
Palka-Hamblin, Helena L; Gierut, Jessica J; Bie, Wenjun et al. (2010) Identification of beta-catenin as a target of the intracellular tyrosine kinase PTK6. J Cell Sci 123:236-45
Song, J; Sandoval, R; Pilkinton, M A et al. (2010) ARF-induced downregulation of Mip130/LIN-9 protein levels mediates a positive feedback that leads to increased expression of p16Ink4a and p19Arf. Oncogene 29:1976-86

Showing the most recent 10 out of 37 publications