Type 2 diabetes (T2D) is already placing a major burden on the US healthcare system and projections indicate the problem will get worse. It is therefore of great importance to further our understanding of the molecular mechanisms that contribute to the onset and establishment of T2D and its complications. This application proposes research and training plans for Dr. Leung to become a leading independent investigator in the field of diabetes. While the applicant has had extensive training in molecular biology and simple model organisms, her development and future success as an investigator will require additional practical skills and knowledge regarding advanced mouse models, mouse physiology and metabolism. To attain the necessary skills and knowledge, she has assembled a strong mentoring team comprising of a group of expert senior investigators and proposed a detailed list of career development and training activities. The mentors: Drs. Natarajan, Tontonoz, Rossi, and Lusis, represent a diverse set of investigators with a track record of successful mentoring and diabetes related research. They will provide guidance and assistance with Dr. Leung's research and training in the development of Dr. Leung's academic career as she transitions to an independently funded investigator. Over the course of this award, she will also engage in additional training activities including structured postgraduate courses intended to increase knowledge and skills in mouse metabolism and physiology, grant-writing workshops, laboratory management workshops, and teaching. The research activities proposed in this application will investigate the role of long non-coding RNAs (lncRNAs) in the development of insulin resistance, dysregulation of gluconeogenesis, and ultimately, T2D. This project is based on extensive preliminary data demonstrating that specific lncRNAs are dysregulated in livers of insulin resistant mice. The overarching hypothesis of this application is that lncRNAs are involved in modulating key genes that regulate insulin signaling pathways and hepatic glucose production, and that dysregulation of these lncRNAs can contribute to the development of insulin resistance and dysregulation of hepatic glucose production.
The Specific Aims are: 1) to identify lncRNAs that are dysregulated in livers of diabetic mice, including both genetic and non-genetic mouse models, 2) to determine the functional consequences of altered expression of lncRNAs in the livers of diabetic mice, and 3) to characterize the mechanism of action and regulation of candidate lncRNAs in livers under diabetic conditions. The results from the proposed studies will provide significant new insights into the molecular mechanisms that accompany the development of hepatic insulin resistance and T2D and will form the basis of future grant applications from the applicant. This project will furthermore provide Dr. Leung with the necessary experience for her development into an independent scientist.

Public Health Relevance

While clinical therapies exist, individuals with type 2 diabetes, a growing epidemic that is a major burden on the healthcare system in the US, still display an increase in complications such as neuropathies, nephropathies, and cardiovascular disease. It is therefore imperative to identify novel molecular mechanisms that can be targeted to improve the development of effective treatments. This project will identify such novel mechanisms that function in the development of diabetes which can be therapeutic targets to improve diabetes and its related complications.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
1K01DK104993-01
Application #
8868311
Study Section
Kidney, Urologic and Hematologic Diseases D Subcommittee (DDK)
Program Officer
Spain, Lisa M
Project Start
2015-04-01
Project End
2018-02-28
Budget Start
2015-04-01
Budget End
2016-02-29
Support Year
1
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Beckman Research Institute/City of Hope
Department
Type
DUNS #
027176833
City
Duarte
State
CA
Country
United States
Zip Code
91010
Leung, Amy; Amaram, Vishnu; Natarajan, Rama (2018) Linking diabetic vascular complications with LncRNAs. Vascul Pharmacol :
Leung, Amy; Trac, Candi; Kato, Hiroyuki et al. (2018) LTRs activated by Epstein-Barr virus-induced transformation of B cells alter the transcriptome. Genome Res 28:1791-1798
Das, Sadhan; Senapati, Parijat; Chen, Zhuo et al. (2017) Regulation of angiotensin II actions by enhancers and super-enhancers in vascular smooth muscle cells. Nat Commun 8:1467
Du, Juan; Leung, Amy; Trac, Candi et al. (2016) Chromatin variation associated with liver metabolism is mediated by transposable elements. Epigenetics Chromatin 9:28
Leung, Amy; Trac, Candi; Du, Juan et al. (2016) Persistent Chromatin Modifications Induced by High Fat Diet. J Biol Chem 291:10446-55
Leung, Amy; Stapleton, Kenneth; Natarajan, Rama (2016) Functional Long Non-coding RNAs in Vascular Smooth Muscle Cells. Curr Top Microbiol Immunol 394:127-41
Schones, Dustin E; Leung, Amy; Natarajan, Rama (2015) Chromatin Modifications Associated With Diabetes and Obesity. Arterioscler Thromb Vasc Biol 35:1557-61