Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/163613
Title: Nuclear omics of mouse forebrain excitatory neurons in pilocarpine-induced seizures
Authors: Soon, Hui Rong
Keywords: Science::Biological sciences::Human anatomy and physiology::Neurobiology
Science::Biological sciences::Molecular biology
Issue Date: 2022
Publisher: Nanyang Technological University
Source: Soon, H. R. (2022). Nuclear omics of mouse forebrain excitatory neurons in pilocarpine-induced seizures. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/163613
Abstract: An epileptic seizure generates massive neuronal activity in the brain which induces de novo transcription and translation, bringing about cellular changes which may contribute to epileptogenesis. To understand the cell-type-specific molecular changes brought about by seizures, I isolated nuclei from forebrain excitatory neurons of a pilocarpine-induced transgenic mouse and profiled the nuclear transcriptome and proteome. My nuclear transcriptome analyses show that expression of genes related to MAPK signalling are upregulated while a major class of C2H2-type zinc finger proteins, including those containing KRAB domains, are downregulated in seizure-induced animals. In parallel, nuclear proteome analyses uncovered AP-1 complex components and post-translational modifications such as SUMOylation and ubiquitin-like conjugation to be enriched in the seizure group. Finally, I show that changes in nuclear TEF levels are activity-dependent in forebrain excitatory neurons of seizure-induced mice, as well as in cultured hippocampal neurons after stimulation with convulsant drugs. These findings further our understanding of seizure-induced nuclear events in neurons which are relevant to epileptogenesis. My study also demonstrates a robust nuclear profiling method amenable to different sequencing platforms for other cell types.
URI: https://hdl.handle.net/10356/163613
DOI: 10.32657/10356/163613
Schools: School of Biological Sciences 
Rights: This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).
Fulltext Permission: embargo_20241212
Fulltext Availability: With Fulltext
Appears in Collections:SBS Theses

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