MO_III_L: Molecular Sciences III. Lectures
Milán Somogyvári1, Csaba Sőti1
1 Department of Molecular Biology at the Institute of Biochemistry and Molecular Biology, Semmelweis University
Obesity is a risk factor for the leading causes of death in our modern societies. Many of the hallmarks of obesity and metabolic syndrome have large overlaps with hallmarks of another important risk factor for various diseases: ageing. The metabolic regulator SIR-2.1 protein deacetylase and the proteostasis regulator heat shock transcription factor HSF-1 are both involved in the regulation of lifespan, ageing and the longevity-promoting effects of diatery restriction.
The aim of this study is to investigate how these important regulators might modulate metabolism through lipid mobilization.
We took use of various C. elegans techniques, such as lipid staining by the dye Oil Red O to monitor the lipid content of animals, quantitative PCR measurements to register changes in lipase expressions, fluorescently labelled nematodes for the same reason and various mutant strains to get a closer look into the underlying mechanisms.
We were able to confirm SIR-2.1’s necessity for lipid mobilization and the induction of lipase expression, but also found that it acts through blocking HSF-1’s inhibitory effect on this metabolic process. We also found this interaction to be tissue specific, since both proteins are required for their effects in the intestine – the place for lipid storage. Furthermore, our results indicate that HSF-1 might exert its influence by utilizing the microRNA gene regulatory system.
Taken together these data point in the direction of an intricate regulatory mechanism linking energy-metabolism to proteostasis and potentially, lifespan.
This work was funded by ÚNKP-20-4-II-SE-6
Semmelweis University, Doctoral School of Molecular Medicine