Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/82011
Title: The Long Noncoding RNA RMST Interacts with SOX2 to Regulate Neurogenesis
Authors: Ng, Shi-Yan
Bogu, Gireesh K.
Soh, Boon Seng
Stanton, Lawrence Walter
Issue Date: 2013
Source: Ng, S.-Y., Bogu, G. K., Soh, B. S., & Stanton, L. W. (2013). The Long Noncoding RNA RMST Interacts with SOX2 to Regulate Neurogenesis. Molecular Cell, 51(3), 349-359.
Series/Report no.: Molecular Cell
Abstract: Long noncoding RNAs (lncRNAs) are abundant in the mammalian transcriptome, and many are specifically expressed in the brain. We have identified a group of lncRNAs, including rhabdomyosarcoma 2-associated transcript (RMST), which are indispensable for neurogenesis. Here, we provide mechanistic insight into the role of human RMST in modulating neurogenesis. RMST expression is specific to the brain, regulated by the transcriptional repressor REST, and increases during neuronal differentiation, indicating a role in neurogenesis. RMST physically interacts with SOX2, a transcription factor known to regulate neural fate. RMST and SOX2 coregulate a large pool of downstream genes implicated in neurogenesis. Through RNA interference and genome-wide SOX2 binding studies, we found that RMST is required for the binding of SOX2 to promoter regions of neurogenic transcription factors. These results establish the role of RMST as a transcriptional coregulator of SOX2 and a key player in the regulation of neural stem cell fate.
URI: https://hdl.handle.net/10356/82011
http://hdl.handle.net/10220/41096
ISSN: 1097-2765
DOI: 10.1016/j.molcel.2013.07.017
Schools: School of Biological Sciences 
Rights: © 2013 Elsevier Inc.
Fulltext Permission: none
Fulltext Availability: No Fulltext
Appears in Collections:SBS Journal Articles

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