Regulation of transcription factor USF2 in cancer by phosphorylation
Thesis event information
Date and time of the thesis defence
Place of the thesis defence
Faculty of Biochemistry and Molecular Medicine, hall F101 Aapistie 7, Zoom link: https://oulu.zoom.us/j/64783814748 C
Topic of the dissertation
Regulation of transcription factor USF2 in cancer by phosphorylation
Doctoral candidate
Master of Science Franklin Chi
Faculty and unit
University of Oulu Graduate School, Faculty of Biochemistry and Molecular Medicine, ECM and Hypoxia
Subject of study
Biochemistry and Molecular Medicine
Opponent
Professor Gerhard P. Püschel, University of Potsdam
Custos
Professor Thomas Kietzmann, University of Oulu
Regulation of transcription factor USF2 in cancer by phosphorylation
In multicellular organisms, the processes of growth, development and function are a result of gene expression. For expression, genes must be turned on and/or off in a coordinated manner in response to diverse stimuli. The coordination of the expression of a group of genes falling into the same functional category is commonly performed by transcription factor(s). These are proteins that bind specific DNA sequences in promoter or enhancer/silencer regions and regulate the transcription into mRNA.
This process of gene regulation is essential for life. In this study, we investigated mechanisms by which the function of the transcription factor USF2 can be regulated in noncancerous and cancer cells as well as the effect of USF2 loss-of-function on the cell fate.
This study provides key results explaining how USF2 can be regulated by phosphorylation and expand our knowledge on how GSK3 and CDK5 affect cell function via USF2 transactivity, DNA binding and protein stability as well as the growth of noncancerous cells by compromising mitochondria.
This process of gene regulation is essential for life. In this study, we investigated mechanisms by which the function of the transcription factor USF2 can be regulated in noncancerous and cancer cells as well as the effect of USF2 loss-of-function on the cell fate.
This study provides key results explaining how USF2 can be regulated by phosphorylation and expand our knowledge on how GSK3 and CDK5 affect cell function via USF2 transactivity, DNA binding and protein stability as well as the growth of noncancerous cells by compromising mitochondria.
Last updated: 1.3.2023