IMR Press / FBL / Volume 17 / Issue 5 / DOI: 10.2741/4015

Frontiers in Bioscience-Landmark (FBL) is published by IMR Press from Volume 26 Issue 5 (2021). Previous articles were published by another publisher on a subscription basis, and they are hosted by IMR Press on imrpress.com as a courtesy and upon agreement with Frontiers in Bioscience.

Article
Architectural roles of long noncoding RNAs in the intranuclear formation of functional paraspeckles
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1 Biomedicinal Information Research Center, National Institute of Advanced Industrial Science and Technology, 2-4-7 Aomi, Koutou 135-0064, Tokyo, Japan
2 Graduate School of Biomedical Sciences, Tokyo Medical and Dental University, 1-5-45, Yushima, Bunkyo 113-8510, Tokyo, Japan
Front. Biosci. (Landmark Ed) 2012, 17(5), 1729–1746; https://doi.org/10.2741/4015
Published: 1 January 2012
Abstract

The eukaryotic nucleus is highly compartmentalized, and this structural complexity allows the regulation of complex gene expression pathways. Some of the subnuclear structures called nuclear bodies are known to contain RNAs. Recently multiple noncoding RNAs (ncRNAs) have been identified as products from regions covering large portions of mammalian genomes. Several abundant ncRNAs were found to localize in nuclear bodies, suggesting new roles for ncRNAs in these nuclear bodies. Paraspeckle, one of these nuclear bodies, contains specific ncRNAs, termed MEN (Multiple Endocrine Neoplasia) epsilon/beta ncRNAs, and characteristic RNA-binding proteins. Paraspeckle is ubiquitously observed in cultured cell lines but is cell type-specific in mouse tissues. Paraspeckle reportedly plays an important role in the nuclear retention of inosine-containing mRNAs and is regulated under stress conditions. Intriguingly, MEN epsilon/beta ncRNAs are prerequisite for the formation of paraspeckles, indicating architectural roles for these ncRNAs and, presumably, significant roles in the nuclear retention of mRNAs as well. This review focuses on known aspects of the paraspeckle structure and its components, and we attempt here to construct a model of the ncRNA-dependent formation of nuclear body structures.

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