Affiliation:
1. Department of Biomedical Science, Program in Biomedical Science and Engineering, Department of Physiology and Biophysics, College of Medicine Inha University Incheon Korea
2. Department of Life Sciences Ewha Womans University Seoul Korea
Abstract
ABSTRACTThis study explores the 24‐h rhythmic cycle of protein O‐GlcNAcylation within the brain and highlights its crucial role in regulating the circadian cycle and neuronal function based on zebrafish as an animal model. In our experiments, disruption of the circadian rhythm, achieved through inversion of the light‐dark cycle or daytime melatonin treatment, not only impaired the rhythmic changes of O‐GlcNAcylation along with altering expression patterns of O‐GlcNAc transferase (OGT) and O‐GlcNAcase (OGA) in zebrafish brain but also significantly impeded learning and memory function. In particular, circadian disruption affected rhythmic expression of protein O‐GlcNAcylation and OGT in the nuclear fraction. Notably, the circadian cycle induces rhythmic alterations in O‐GlcNAcylation of H2B histone protein that correspond to changes in H3 trimethylation. Disruption of the cycle interfered with these periodic histone code alterations. Pharmacological inhibition of OGT with OSMI‐1 disrupted the wake‐sleep patterns of zebrafish without affecting expression of circadian rhythm‐regulating genes. OSMI‐1 inhibited the expression of c‐fos, bdnf, and calm1, key genes associated with brain function and synaptic plasticity, and decreased the binding of O‐GlcNAcylated H2B and OGT to promoter regions of these genes. The collective findings support the potential involvement of circadian cycling of the O‐GlcNAc histone code in regulating synaptic plasticity and brain function. Overall, data from this study provide evidence that protein O‐GlcNAcylation serves as a pivotal posttranslational mechanism integrating circadian signals and neuronal function to regulate rhythmic physiology.