Diabetes mellitus is a highly significant health problem, affecting more than 25 million people in the United States alone. Our understanding of the pathogenesis of diabetes has benefited immensely from the molecular genetic analysis of the disease both in human and in rodent models. Advances in genomics technologies have enabled investigators in the fields of diabetes and endocrinology to simultaneously analyze the expression levels of thousands of genes, and analyze their epigenetic regulation. During the past grant cycle, we have dramatically expanded the capabilities of our well-utilized Functional Genomics Core to serve the DRC's membership needs. We have acquired four next generation sequencing instruments and established multiple applications, including ChIP-Seq for transcription factor occupancy and histone modifications, exome capture and sequencing, RNA-Seq, microRNA-Seq, HITS-CLIP, ATAC-Seq, and methylome analysis. During the next grant cycle, we will offer an expanded repertoire of next generation sequencing services, including library construction and bioinformatics analysis to the DRC's membership. We have recruited Dr. K.-J. Won, an expert computational biologist, to provide advanced bioinformatics analysis exclusively for DRC members. The Core will interact closely with the other DRC cores, for instance in correlating the phenotypic analysis performed on genetically altered or metabolically challenged mice with their expression profiles, including single cell RNAseq, and epigenetic regulation to greatly enhance the power of each individual analysis. Furthermore, similar assessments of the function of control and diabetic human islets from the same donor by the islet biology and functional genomics core will provide valuable functional information that may be integrated with changes in DNA sequence or genome-wide measurements of epigenetic regulation or gene expression. This core, in conjunction with the others, will help measure and understand the normal and pathologic genetic and epigenetic states of islets, adipose tissue, liver, and other important tissues types as it relates to the development and function of these tissues.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
5P30DK019525-43
Application #
9691311
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2019-04-01
Budget End
2020-03-31
Support Year
43
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Pickett-Blakely, Octavia; Young, Kimberly; Carr, Rotonya M (2018) Micronutrients in Nonalcoholic Fatty Liver Disease Pathogenesis. Cell Mol Gastroenterol Hepatol 6:451-462
Kameswaran, Vasumathi; Golson, Maria L; Ramos-Rodríguez, Mireia et al. (2018) The Dysregulation of the DLK1-MEG3 Locus in Islets From Patients With Type 2 Diabetes Is Mimicked by Targeted Epimutation of Its Promoter With TALE-DNMT Constructs. Diabetes 67:1807-1815
Huang, Chen; Walker, Emily M; Dadi, Prasanna K et al. (2018) Synaptotagmin 4 Regulates Pancreatic ? Cell Maturation by Modulating the Ca2+ Sensitivity of Insulin Secretion Vesicles. Dev Cell 45:347-361.e5
Moreira, Leticia; Bakir, Basil; Chatterji, Priya et al. (2018) Pancreas 3D Organoids: Current and Future Aspects as a Research Platform for Personalized Medicine in Pancreatic Cancer. Cell Mol Gastroenterol Hepatol 5:289-298
Pei, Liming; Wallace, Douglas C (2018) Mitochondrial Etiology of Neuropsychiatric Disorders. Biol Psychiatry 83:722-730
Brown, Justin C; Rickels, Michael R; Troxel, Andrea B et al. (2018) Dose-response effects of exercise on insulin among colon cancer survivors. Endocr Relat Cancer 25:11-19
Rickels, M R; Markmann, E; Naji, A (2018) Successful pregnancies after islet transplantation for type 1 diabetes. Am J Transplant :
Friedman, Elliot S; Li, Yun; Shen, Ting-Chin David et al. (2018) FXR-Dependent Modulation of the Human Small Intestinal Microbiome by the Bile Acid Derivative Obeticholic Acid. Gastroenterology 155:1741-1752.e5
Rickels, Michael R; DuBose, Stephanie N; Toschi, Elena et al. (2018) Mini-Dose Glucagon as a Novel Approach to Prevent Exercise-Induced Hypoglycemia in Type 1 Diabetes. Diabetes Care 41:1909-1916
Jang, Cholsoon; Hui, Sheng; Lu, Wenyun et al. (2018) The Small Intestine Converts Dietary Fructose into Glucose and Organic Acids. Cell Metab 27:351-361.e3

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