Circadian clocks drive the 24-hour oscillations in gene expression and behavior that allow an organism to anticipate the day/night cycle, and its disruption has been implicated in the pathogenesis of cancer, metabolic syndrome, and cardiovascular disease. However, our understanding of conditions where the clock fails remains poor, making it crucial to understand how clocks keep accurate timing over a range of physiological conditions. To function effectively, the clock must maintain a consistent period despite being composed of stochastic biochemical reactions. How does the cell achieve noise-free behavior despite being composed of noisy building blocks, and does molecular noise stemming from limited molecular copy number in the cell impose a significant physical constraint on clock robustness? To answer these questions, I will utilize the circadian clock in the model cyanobacterium Synechococcus elongatus, in which core clock behavior is generated post-translationally entirely by three proteins, KaiA, KaiB, and KaiC, allowing for a direct investigation of the effect of molecular noise on clock function by manipulating Kai protein copy numbers in vivo. The central hypothesis of this proposal is that molecular noise constitutes an important physical constraint on the biochemical robustness of circadian clocks, and that reduction of Kai protein copy number will lead to a loss in accuracy of clock timing that ultimately imposes a fitness penalty on the cell. I have engineered a strain of S. elongatus in which Kai protein copy number is tunable, and I have demonstrated with time lapse microscopy that clock noise increases as Kai copy number is reduced. In my first aim, I will investigate the possibility of cell division as a mechanism explaining the observed increase in noise. In my second aim, I will develop a stochastic model of the Kai system that can predict oscillatory performance as a function of Kai protein copy number. Lastly, by measuring single-cell growth rates on the microscope, I will assess whether noisy rhythms induced by low Kai copy number reduce cellular fitness due to more frequent mistiming between the cell and the environment. These three approaches together will elucidate basic principles of the relationship between noise suppression and molecular copy numbers within the cell.

Public Health Relevance

This project will reveal important insights into how the circadian clock is affected by the biological constraint of limited numbers of proteins within the cell. This is critical for enhancing our basic knowledge of how clocks can become dysfunctional, informing future approaches for how we investigate clock-related diseases in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30GM117962-02
Application #
9415989
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Gibbs, Kenneth D
Project Start
2017-01-01
Project End
2018-11-17
Budget Start
2018-01-01
Budget End
2018-11-17
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Chicago
Department
Genetics
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637