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pmid:37449137
Transcriptome analysis identifies the role of Class I histone deacetylase in Alzheimer's disease.
Fan Geng · Na Zhao · Xiu Chen · XueTing Liu · MengMeng Zhu · Ying Jiang · QingGuo Ren
Heliyon · 2023 doi:10.1016/j.heliyon.2023.e18008
Paper
complete
Experiment
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Data
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Analysis
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Execution
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Complete file
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In this study, we deployed the weighted gene co-expression network analysis (WGCNA) to explore the role of Class I histone deacetylases (HDACs) in AD, which included HDAC1, HDAC2, HDAC3, and HDAC8. The aim of the study was to find how Class I HDACs affected AD pathology by analyzing the Gene Expression Omnibus (GEO) microarray datasets GSE33000. We found that HDAC1 and HDAC8 were more highly expressed in the cortex of AD patients than in Controls, while HDAC2 and HDAC3 were lower expressed. By WGCNA analysis, we found the blue module was associated with HDAC1 and HDAC8, and the turquoise module was related to HDAC2 and HDAC3. Functional enrichment analysis revealed that the Wnt signaling pathway and synaptic plasticity played an important role in the modification of HDAC1 and HDAC8 while gap junction and cell-cell junction were involved in the regulation of HDAC2 and HDAC3 in the disease progression of AD. 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