Nocturnin is an enzyme belonging to the EEP (endonuclease/exonuclease/phosphatase) structural family that is expressed rhythmically under the control of the circadian oscilator. It has been hypothesized to control the stability of other circadian clock controlled transcripts through degradation of their 3' poly(A) tails, and shows deadenylase activity in vitro. Functional studies in cell culture and kockout mice have implicated nocturnin in the regulation of intestinal lipid absorption, dipocyte and osteoblast formation, and lipid and glucose metabolism in hepatocytes. We have discovered that nocturnin's hydrolytic activity is not limited to deadenylation, but it can also act as a phosphatase and dephosphorylate AMP and other substrates, raising the question as to which activity is responsible for its primary cellular function. As nocturnin represents an important target for understanding and modulating the interactions between circadian rhythms and metabolism in homeostasis and disease, the experiments described in this proposal are designed to characterize the steady state kinetics, substrate specificity, and three dimensional structure of nocturnin.

Public Health Relevance

Nocturnin is an enzyme that is controlled by circadian rhythms and involved in the reulation of fat and carbohydrate metabolism and the differentiation of fat cells and bone cells. Itcan trim the ends off of mRNA molecules and is hypothesized to degrade them in cells, and our preliminary experiments have discovered that it also catalyzes removal of phosphate groups. The proposed research will study the three dimensional structure of the nocturnin molecule and the kinetics and molecular mechanism of the enzymatic reactions catalyzed by nocturnin in an effort to help us understan the biochemical basis for nocturnin's cellular effects.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15GM110679-01A1
Application #
8879794
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Sesma, Michael A
Project Start
2015-04-01
Project End
2018-03-31
Budget Start
2015-04-01
Budget End
2018-03-31
Support Year
1
Fiscal Year
2015
Total Cost
$367,275
Indirect Cost
$118,275
Name
University of Toledo
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
051623734
City
Toledo
State
OH
Country
United States
Zip Code
43606