Epigenetic regulation of chromatin determines how and when genetic information is used in a heritable way. Specific chromatin modifying proteins have profound effects on the chromatin landscape. Two recent surprises from the cancer genome atlas are of direct importance to this proposal: driver mutations in genes encoding proteins involved in epigenetic processes, and driver mutations in enzymes of central metabolism. Recent studies give us a peek into coordination between metabolism and the activity of histone modifying enzymes, and establish the principle that epigenetic processes are sensitive to changes in the metabolic state of a cell. The scope of this phenomenon and the precise mechanisms involved remain unclear despite its high relevance to cancer development and potential for new therapeutic strategies. Both metabolic and epigenetic dysregulation play a critical role in tumor development. This proposal seeks an understanding of both the scope and mechanism for how metabolism impacts genetic and epigenetic processes. The central hypothesis of this proposal is that changes in metabolism can affect the epigenetic landscape of a cell by altering the level of critical cofactors required by chromatin modifying enzymes and, in turn, the structures of chromatin determined by these modifications.
Three aims are proposed: using Saccharomyces 1) elucidate links between central carbon metabolism and heterochromatin regulation, 2) identify the impact that accumulation of the cancer metabolite D-2-hydroxyglutarate has on gene silencing, and 3) comprehensively identify metabolic pathways that impact epigenetic processes. Results from this research will make a significant impact on our understanding of cellular processes governing epigenetic regulation, a fundamental aspect of genome biology. Of greatest importance, and in line with the goals of the National Institutes of Health, insight from this research will reveal key mechanisms that drive human diseases, particularly cancers, as well as open the door to new potential therapeutic strategies.

Public Health Relevance

Dysregulation of both epigenetic and metabolic processes contribute to the onset and progress of numerous human diseases, and nowhere is this more evident than in cancers. Epigenetic processes are sensitive to changes in metabolism, and despite the high importance of this in human disease, the mechanisms behind this remain very poorly understood. This proposal seeks to better define both the scope and mechanism for how metabolism impacts genetic and epigenetic processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32GM115074-02
Application #
9237115
Study Section
Special Emphasis Panel (ZRG1-F08-B (20)L)
Program Officer
Maas, Stefan
Project Start
2016-02-01
Project End
2018-01-31
Budget Start
2017-02-01
Budget End
2018-01-31
Support Year
2
Fiscal Year
2017
Total Cost
$59,166
Indirect Cost
Name
University of California Berkeley
Department
Miscellaneous
Type
Organized Research Units
DUNS #
124726725
City
Berkeley
State
CA
Country
United States
Zip Code
94704
Janke, Ryan; King, Grant A; Kupiec, Martin et al. (2018) Pivotal roles of PCNA loading and unloading in heterochromatin function. Proc Natl Acad Sci U S A 115:E2030-E2039