Integrative Analysis of Multiomics Data Identified Acetylation as Key Variable of Excessive Energy Metabolism in Hyperthyroidism-induced Osteoporosis Rats

Abstract

Background The results from the previous experiment have demonstrated that there were occurrence of bone loss and excess metabolism in Hyperthyroidism-induced rats. Thus, there was speculation that there may be an underlying relationship between metabolism and bone loss. In addition, there were past studies showing acetylation influencing metabolism in tissues and diseases. The hypothesis from this case study stated that excessive metabolism was induced upon acetylated vital metabolism enzymes. Results In the case study, a HYP-induced osteoporosis rats model was used and the glucose metabolite was tested through the acetylation of proteins by the mass spectrometer. The results showed that pivotal enzymes of Glycolysis-Tricarboxylic acid cycle-Oxidative phosphorylation were acetyled along with upregulated metabolites. All the acetyly-lysine sites of related enzymes were listed in this article.Our results showed that bone loss in HYP rats accompanied by upregulation of CREB-binding protein (Crebbp, CBP). Furthermore, our result indicated that CBP has a close relationship with enhancement of LDHa that promote glucose metabolism. Conclusions Acetylation is the key variable of energy metabolism in hyperthyroid osteoporosis rats, therein, we showed a representation relationship between CBP and LDHa.