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Reduced REST expression in neural progenitor cells, adult cortex, and impaired REST nuclear translocation in the prefrontal cortex of Ts1Cje mouse model of Down Syndrome


Citation

Chong, Teik Lim and Lam, Xin Jieh and Crystal, Arthini Arrumugam and Huang, Tan and Jusoh, Norhazlin and Cheah, Pike See and Ling, King Hwa (2024) Reduced REST expression in neural progenitor cells, adult cortex, and impaired REST nuclear translocation in the prefrontal cortex of Ts1Cje mouse model of Down Syndrome. Neurochemical Journal, 18 (1). pp. 147-161. ISSN 1819-7124; eISSN: 1819-7132

Abstract

Abstract—Down syndrome (DS) is a common genetic disorder caused by trisomy of human chromosome 21. DS individuals have neurodevelopmental defects that lead to the manifestation of neurological and neuropsychiatric disorders. Repressor element-1 silencing transcription factor (REST) is the key epigenetic neuronal gene expression regulator. A comprehensive spatiotemporal profiling of REST expression is needed to understand its role in DS brain development. Therefore, we characterised REST targets in this study and profiled its expression using the brain samples from Ts1Cje, a mouse model exhibiting DS neuropathology. Over-representation analysis of Ts1Cje differentially expressed genes (DEGs) with mouse REST targets was performed. The cerebral cortex, hippocampus, and cerebellum of Ts1Cje and wildtype (WT) mice were procured at postnatal—P1, P15, P30, and P84 and embryonic—E14 and P1.5 development timepoints. RNAs from the brain tissues and cultured neurospheres were analysed with qPCR to determine the spatiotemporal profile of Rest expression. Western blot and immunohistochemistry (IHC) staining were performed to assess the level of REST expression and nuclear localisation. Over-representation analysis showed the Ts1Cje DEGs were significantly overlapped with mouse REST target genes. QPCR and Western blot analysis revealed a significant downregulation of Rest transcript in neurospheres and protein in Ts1Cje compared to WT. IHC staining showed REST perinuclear marginalisation and significantly reduced nuclear REST expression in the Ts1Cje prefrontal cortex. Loss of functional REST repression may lead to de-repression of DEGs in the Ts1Cje brain, potentially leading to various neuropathology seen in the Ts1Cje or DS brain.


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Additional Metadata

Item Type: Article
Divisions: Faculty of Medicine and Health Science
Malaysian Research Institute on Ageing
DOI Number: https://doi.org/10.1134/s1819712424010148
Publisher: Pleiades Publishing
Keywords: Down syndrome; REST; Spatiotemporal; Ts1Cje; Nuclear localisation
Depositing User: Ms. Che Wa Zakaria
Date Deposited: 07 Jul 2025 09:32
Last Modified: 07 Jul 2025 09:32
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1134/s1819712424010148
URI: http://psasir.upm.edu.my/id/eprint/117088
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