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 #
5P30DK034933-34
Application #
9978785
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
34
Fiscal Year
2020
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
Brady, Graham F; Kwan, Raymond; Bragazzi Cunha, Juliana et al. (2018) Lamins and Lamin-Associated Proteins in Gastrointestinal Health and Disease. Gastroenterology 154:1602-1619.e1
Hu, Yongjun; Song, Feifeng; Jiang, Huidi et al. (2018) SLC15A2 and SLC15A4 Mediate the Transport of Bacterially Derived Di/Tripeptides To Enhance the Nucleotide-Binding Oligomerization Domain-Dependent Immune Response in Mouse Bone Marrow-Derived Macrophages. J Immunol 201:652-662
McClintock, Shannon D; Colacino, Justin A; Attili, Durga et al. (2018) Calcium-Induced Differentiation of Human Colon Adenomas in Colonoid Culture: Calcium Alone versus Calcium with Additional Trace Elements. Cancer Prev Res (Phila) 11:413-428
Kim, Geun Hyang; Shi, Guojun; Somlo, Diane Rm et al. (2018) Hypothalamic ER-associated degradation regulates POMC maturation, feeding, and age-associated obesity. J Clin Invest 128:1125-1140
Wang, Xuexiang; Dande, Ranadheer R; Yu, Hao et al. (2018) TRPC5 Does Not Cause or Aggravate Glomerular Disease. J Am Soc Nephrol 29:409-415
Bhattacharya, Asmita; Sun, Shengyi; Wang, Heting et al. (2018) Hepatic Sel1L-Hrd1 ER-associated degradation (ERAD) manages FGF21 levels and systemic metabolism via CREBH. EMBO J 37:
Perry, Jeffrey W; Tai, Andrew W (2018) Random Insertional Mutagenesis of a Serotype 2 Dengue Virus Clone. Bio Protoc 8:
El-Zaatari, Mohamad; Bass, Adam J; Bowlby, Reanne et al. (2018) Indoleamine 2,3-Dioxygenase 1, Increased in Human Gastric Pre-Neoplasia, Promotes Inflammation and Metaplasia in Mice and Is Associated With Type II Hypersensitivity/Autoimmunity. Gastroenterology 154:140-153.e17
Sze, Marc A; Schloss, Patrick D (2018) Leveraging Existing 16S rRNA Gene Surveys To Identify Reproducible Biomarkers in Individuals with Colorectal Tumors. MBio 9:
Schofield, Heather K; Tandon, Manuj; Park, Min-Jung et al. (2018) Pancreatic HIF2? Stabilization Leads to Chronic Pancreatitis and Predisposes to Mucinous Cystic Neoplasm. Cell Mol Gastroenterol Hepatol 5:169-185.e2

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