Grant: Discovery Grants Program - Individual
University of Windsor
$52,000.00
Structural and Functional Studies of the Regulatory Mechanism of Ubiquitin Enzymes in Stress Response and Gene Expression
EF 2022-23
Résumé
Cells have sophisticated mechanisms to respond to changes in the physiological conditions they live in, such as oxygen or nutrient deprivation or over-supply, imbalances of electrolytes, and deviation from normal body temperatures. To maximize survival under these stresses, cells use different molecular mechanisms to adjust their internal biological processes. In rapid defences, the proteins that carry out cellular functions are modified at certain residues to switch their conformation and interaction partners so that they are activated, deactivated, or tagged for degradation. Over a longer time scale, the expression profile of genes is fundamentally altered to adapt the cells to a changed environment. Ubiquitination, a reversible, dynamic process of tagging a small regulatory protein called ubiquitin to a substrate protein, plays a critical role in many aspects of stress response and collateral gene regulation. Ubiquitin-specific protease 9X (USP9X) is a very large enzyme that removes the ubiquitin tag from ubiquitinated substrates and controls their functions. Three such substrate proteins involved in stress response are ASK1, a kinase that regulates oxidative stress signal transduction; SOX2, a DNA-binding protein that regulates the pluripotency of cells and controls the expression of many other genes; and MCL1, which determines the life and death of cells in response to stress.We will use various biophysical and biochemical techniques that assess the conformation, activity, and interaction of the proteins, including X-ray crystallography, enzymatic assays, thermal change measurement, to find out how USP9X interacts with its substrate at the atomic level, how its removal of the ubiquitin tags is regulated by the intra-molecular interactions of different parts of USP9X, and how other modifications, such as phosphorylation and methylation of the substrate proteins, affect their interaction with USP9X.Stress response is a conserved mechanism for cells to adapt to internal and external challenges. Knowledge of the molecular mechanisms of stress response obtained from this study can be extrapolated to other organisms, such as animals and plants. USP9X is an evolutionarily conserved, multi-functional protein that is crucial for development and stress response, yet not much is known about the molecular details of its functions. The outcome of the proposed research will establish a prototypical model for understanding how ubiquitin enzymes regulate cell stress response and gene regulation. A better understanding of the regulatory mechanisms of ubiquitination and the ability to rationally modulate them is important for the fields of cell reprogramming and drug discovery.
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Ontario, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
RGPIN-2017-06520
Name nom
Tong, Yufeng
Department département
Pharmacology and Toxicology - Pharmacology and Toxicology
Organization id
37
Institution établissement
University of Windsor
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2022
Competition year année de concours
2017
Award amount
52000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
DISCOVERY RESEARCH
Group fr
RECHERCHE AXÉE SUR LA DÉCOUVERTE
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5400
Research subject group en
Biochemistry
Research subject group fr
Biochimie
Research subject en
Biochemistry
Research subject fr
Biochimie
Installment
inst:6;7
Partie
2
Nb partie
7
Application title
Structural and Functional Studies of the Regulatory Mechanism of Ubiquitin Enzymes in Stress Response and Gene Expression
Application summary
Cells have sophisticated mechanisms to respond to changes in the physiological conditions they live in, such as oxygen or nutrient deprivation or over-supply, imbalances of electrolytes, and deviation from normal body temperatures. To maximize survival under these stresses, cells use different molecular mechanisms to adjust their internal biological processes. In rapid defences, the proteins that carry out cellular functions are modified at certain residues to switch their conformation and interaction partners so that they are activated, deactivated, or tagged for degradation. Over a longer time scale, the expression profile of genes is fundamentally altered to adapt the cells to a changed environment. Ubiquitination, a reversible, dynamic process of tagging a small regulatory protein called ubiquitin to a substrate protein, plays a critical role in many aspects of stress response and collateral gene regulation. Ubiquitin-specific protease 9X (USP9X) is a very large enzyme that removes the ubiquitin tag from ubiquitinated substrates and controls their functions. Three such substrate proteins involved in stress response are ASK1, a kinase that regulates oxidative stress signal transduction; SOX2, a DNA-binding protein that regulates the pluripotency of cells and controls the expression of many other genes; and MCL1, which determines the life and death of cells in response to stress.We will use various biophysical and biochemical techniques that assess the conformation, activity, and interaction of the proteins, including X-ray crystallography, enzymatic assays, thermal change measurement, to find out how USP9X interacts with its substrate at the atomic level, how its removal of the ubiquitin tags is regulated by the intra-molecular interactions of different parts of USP9X, and how other modifications, such as phosphorylation and methylation of the substrate proteins, affect their interaction with USP9X.Stress response is a conserved mechanism for cells to adapt to internal and external challenges. Knowledge of the molecular mechanisms of stress response obtained from this study can be extrapolated to other organisms, such as animals and plants. USP9X is an evolutionarily conserved, multi-functional protein that is crucial for development and stress response, yet not much is known about the molecular details of its functions. The outcome of the proposed research will establish a prototypical model for understanding how ubiquitin enzymes regulate cell stress response and gene regulation. A better understanding of the regulatory mechanisms of ubiquitination and the ability to rationally modulate them is important for the fields of cell reprogramming and drug discovery.