Genetic susceptibility contributes significantly to the development of diabetes and its complications. Recent successes in genome wide association and exome sequencing have demonstrated that the technological capability now exists to identify many of the genes responsible for complex disorders. To be successful in such endeavors, it is necessary to combine expertise in genetic epidemiology, clinical investigation, molecular genotyping, DNA sequencing, and mathematical genetic analysis. The goal of the Human Genetics Core is to offer such expertise to DRC investigators conducting genetic studies. To achieve this objective, the Human Genetics Core will: a) Assist DRC investigators in the development and successful completion of well-designed genetic studies; b) Establish and store EBV-transformed lymphoblastoid cell lines (LCLs), as well as PAXgene tubes; c) Provide access to molecular methodology for genome-wide association studies (GWAS) and specialized (e.g., the exome chip), candidate gene sequencing, whole exome sequencing (WES), whole genome sequencing (WGS), and large-scale gene methylation analysis (by chip); d) Assist with mathematical genetic epidemiologic analysis, including analysis of multi-omics data; e) Make induced pluripotent stem cells (iPSCs), as well as diabetes-relevant cells derived from them, available to investigators as a means of investigating the impact of specific genetic variants on organ development and tissue function; f) Provide training in genetic techniques to DRC investigators and staff; g) Provide access to DRC investigators to a national multi-ethnic (including high-risk minorities) genomics resource for the study of diabetes and diabetes- related phenotypes. In the last cycle, the Human Genetics Core brought GWAS technology to DRC investigators and in this cycle extends the technology available for studying human samples with the addition of specialized genotyping chips, methylation chips, exome and whole genome sequencing, and iPSC technology. The DRC offers a unique opportunity to facilitate research directed at identifying and characterizing the genes responsible for diabetes and related disorders, including both macrovascular and microvascular complications, by providing access to both the expertise and facilities necessary for such genetic research in human populations. In the last cycle, the Human Genetics Core augmented GWAS technology by offering specialized genotyping chips to DRC investigators as well as iPSC technology. In this cycle, the Core will expand the available technologies, including several new specialized genotyping chips (e.g., GSA, 850K methylation), next generation sequencing, and diabetes-relevant tissues derived from iPSCs, complemented by updated multi-omic analysis methods. The DRC facilitates research directed at identifying and characterizing the genes responsible for diabetes and related disorders by providing access to both the expertise and facilities necessary for such genetic research in human populations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Center Core Grants (P30)
Project #
2P30DK063491-18
Application #
9961916
Study Section
Special Emphasis Panel (ZDK1)
Project Start
Project End
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
18
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California, San Diego
Department
Type
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Ahmadian, Maryam; Liu, Sihao; Reilly, Shannon M et al. (2018) ERR? Preserves Brown Fat Innate Thermogenic Activity. Cell Rep 22:2849-2859
Adams, Elizabeth; Genter, Pauline; Keefe, Emma et al. (2018) The GLP-1 response to glucose does not mediate beta and alpha cell dysfunction in Hispanics with abnormal glucose metabolism. Diabetes Res Clin Pract 135:185-191
Petcherski, Anton; Trudeau, Kyle M; Wolf, Dane M et al. (2018) Elamipretide Promotes Mitophagosome Formation and Prevents Its Reduction Induced by Nutrient Excess in INS1 ?-cells. J Mol Biol 430:4823-4833
Sung, Yun J (see original citation for additional authors) (2018) A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Am J Hum Genet 102:375-400
Liesa, Marc; Shirihai, Orian S (2018) Mitochondrial adaptation in obesity is a ClpPicated business. EMBO Rep 19:
Wan, Ma; Bennett, Brian D; Pittman, Gary S et al. (2018) Identification of Smoking-Associated Differentially Methylated Regions Using Reduced Representation Bisulfite Sequencing and Cell type-Specific Enhancer Activation and Gene Expression. Environ Health Perspect 126:047015
Leary, Peter J; Kronmal, Richard A; Bluemke, David A et al. (2018) Histamine H2 Receptor Polymorphisms, Myocardial Transcripts, and Heart Failure (from the Multi-Ethnic Study of Atherosclerosis and Beta-Blocker Effect on Remodeling and Gene Expression Trial). Am J Cardiol 121:256-261
Guo, Y; Moon, J-Y; Laurie, C C et al. (2018) Genetic predisposition to obesity is associated with asthma in US Hispanics/Latinos: Results from the Hispanic Community Health Study/Study of Latinos. Allergy 73:1547-1550
Hoeksema, Marten A; Glass, Christopher K (2018) Nature and nurture of tissue-specific macrophage phenotypes. Atherosclerosis :
Emdin, Connor A; Khera, Amit V; Chaffin, Mark et al. (2018) Analysis of predicted loss-of-function variants in UK Biobank identifies variants protective for disease. Nat Commun 9:1613

Showing the most recent 10 out of 926 publications