The University of Michigan Center for Gastrointestinal Research (UMCGR) Molecular Biology Core facilitates access to three exceptional Medical School service cores: the Transgenic Rodent, the Viral Vector and Integrated Genomics Programs. In addition, the Genome Editing Program is a new service that is shared with the Diabetes Center for exclusive use by members of our two NIDDK-supported centers. Central to facilitating member access to these molecular-based services is the education and training of new and associate members on the use and application of molecular approaches, a field that is rapidly and continuously shifting. To disseminate the reagents and molecular tools generated by the Molecular Core to as many members as possible in a cost effective manner, databases for all of the core facilities was implemented. During the past funding period, the Molecular Biology Core was used by at least 84% of the membership that generated 132 peer-reviewed publications, of which 36 were collaborative publications among two or more Center members. Drs. Merchant and Samuelson are the core co- directors and are well-trained molecular biologists and gastrointestinal physiologists who use genetically engineered mouse models to study major signal transduction pathways as they apply to homeostasis, inflammation and transformation in the GI tract. The four Specific Aims that underpin the focus of the Molecular Core are: 1) To execute state of the art gene editing and gene profiling techniques in line with evolving member research needs; 2) To support highly trained personnel in the application of genetic technology, organized around four Core Programs: Transgenic Rodent, Genome Editing, Viral Vector and Integrated Genome Analysis; 3) To ensure delivery of high quality services and products and provide technical oversight of all Molecular Core services; 4) To train and educate members, associate members and pilot feasibility recipients in the application and use of molecular techniques for the study of digestive and liver disease. Accomplishment of these aims will allow members to make groundbreaking discoveries from clinical observations to systematic dissection at the molecular level using the most rigorous approaches and technological advances.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK034933-33
Application #
9763571
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2019-06-01
Budget End
2020-05-31
Support Year
33
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Dame, Michael K; Attili, Durga; McClintock, Shannon D et al. (2018) Identification, isolation and characterization of human LGR5-positive colon adenoma cells. Development 145:
Brady, Graham F; Kwan, Raymond; Ulintz, Peter J et al. (2018) Nuclear lamina genetic variants, including a truncated LAP2, in twins and siblings with nonalcoholic fatty liver disease. Hepatology 67:1710-1725
Wang, Zhen; Ocadiz-Ruiz, Ramon; Sundaresan, Sinju et al. (2018) Isolation of Enteric Glial Cells from the Submucosa and Lamina Propria of the Adult Mouse. J Vis Exp :
Kim, D-I; Liao, J; Emont, M P et al. (2018) An OLTAM system for analysis of brown/beige fat thermogenic activity. Int J Obes (Lond) 42:939-945
Park, Min-Jung; Iyer, Sapna; Xue, Xiang et al. (2018) HIF1-alpha Regulates Acinar Cell Function and Response to Injury in Mouse Pancreas. Gastroenterology 154:1630-1634.e3
Cho, Chun-Seok; Park, Hwan-Woo; Ho, Allison et al. (2018) Lipotoxicity induces hepatic protein inclusions through TANK binding kinase 1-mediated p62/sequestosome 1 phosphorylation. Hepatology 68:1331-1346
Tsai, Yu-Hwai; Czerwinski, Michael; Wu, Angeline et al. (2018) A Method for Cryogenic Preservation of Human Biopsy Specimens and Subsequent Organoid Culture. Cell Mol Gastroenterol Hepatol 6:218-222.e7
Morhardt, Tina L; Hayashi, Atsushi; Kao, John Y et al. (2018) Regional control of regulatory immune cells in the intestine. Curr Pathobiol Rep 6:29-34
Zhou, Shi-Yi; Gillilland 3rd, Merritt; Wu, Xiaoyin et al. (2018) FODMAP diet modulates visceral nociception by lipopolysaccharide-mediated intestinal inflammation and barrier dysfunction. J Clin Invest 128:267-280
Perry, Jeffrey W; Chen, Yanhua; Speliotes, Elizabeth et al. (2018) Functional Analysis of the Dengue Virus Genome Using an Insertional Mutagenesis Screen. J Virol 92:

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