Abstract
Heat shock transcription factor 1 (HSF1) is activated by pathophysiologic stresses and activation leads to an increased cellular level of heat shock proteins (Hsp(s)). Although the activation of HSF1 occurs via multiple stress-induced processes such as hyperphosphorylation, the exact cellular mechanism of HSF1 activation is still unclear. Here we show polo-like kinase 1 (PLK1) and HSF1 interact in vivo using the tandem affinity purification system. Although the interaction between HSF1 and PLK1 is increased by thermal stress, overexpression of PLK1 did not affect HSF1 trimerization or DNA binding activity. This interaction results in the phosphorylation of HSF1 on serine 419 by PLK1. Interestingly, mutation of serine 419 to alanine inhibited heat-stress induced HSF1 nuclear translocation. Our results suggest that the phosphorylation of HSF1 by PLK1 is an essential step for HSF1 nuclear translocation by heat stress.
Highlights
One of the most pronounced consequences of heat shock is the unfolding and the misfolding of proteins that leads to cellular damage
Our results suggest that the phosphorylation of Heat shock transcription factor 1 (HSF1) by polo-like kinase 1 (PLK1) is an essential step for HSF1 nuclear translocation by heat stress
Identification of PLK1 as a HSF1-interacting Protein—Previously, we developed a powerful yeast-based assay system to examine the function and regulatory mechanism of human HSF1
Summary
One of the most pronounced consequences of heat shock is the unfolding and the misfolding of proteins that leads to cellular damage. Our results suggest that the phosphorylation of HSF1 by PLK1 is an essential step for HSF1 nuclear translocation by heat stress. Our results suggest PLK1 plays an important role in the nuclear translocation of HSF1 induced by heat stress.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.