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
Ward-Caviness, Cavin K; Huffman, Jennifer E; Everett, Karl et al. (2018) DNA methylation age is associated with an altered hemostatic profile in a multiethnic meta-analysis. Blood 132:1842-1850
Goodarzi, Mark O (2018) Genetics of obesity: what genetic association studies have taught us about the biology of obesity and its complications. Lancet Diabetes Endocrinol 6:223-236
Hevener, Andrea L; Zhou, Zhenqi; Moore, Timothy M et al. (2018) The impact of ER? action on muscle metabolism and insulin sensitivity - Strong enough for a man, made for a woman. Mol Metab 15:20-34
Wong, Jason Y Y; Margolis, Helene G; Machiela, Mitchell et al. (2018) Outdoor air pollution and mosaic loss of chromosome Y in older men from the Cardiovascular Health Study. Environ Int 116:239-247
Rausch, John C; Lavine, Joel E; Chalasani, Naga et al. (2018) Genetic Variants Associated With Obesity and Insulin Resistance in Hispanic Boys With Nonalcoholic Fatty Liver Disease. J Pediatr Gastroenterol Nutr 66:789-796
Dunn, Erin C; Sofer, Tamar; Wang, Min-Jung et al. (2018) Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos. J Psychiatr Res 99:167-176
Chen, Han; Cade, Brian E; Gleason, Kevin J et al. (2018) Multiethnic Meta-Analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea-related Quantitative Trait Locus in Men. Am J Respir Cell Mol Biol 58:391-401
McKeown, Nicola M; Dashti, Hassan S; Ma, Jiantao et al. (2018) Sugar-sweetened beverage intake associations with fasting glucose and insulin concentrations are not modified by selected genetic variants in a ChREBP-FGF21 pathway: a meta-analysis. Diabetologia 61:317-330
Que, Xuchu; Hung, Ming-Yow; Yeang, Calvin et al. (2018) Oxidized phospholipids are proinflammatory and proatherogenic in hypercholesterolaemic mice. Nature 558:301-306
Wang, Y X Rachel; Liu, Ke; Theusch, Elizabeth et al. (2018) Generalized correlation measure using count statistics for gene expression data with ordered samples. Bioinformatics 34:617-624

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