Literature DB >> 26021608

Architectural RNAs (arcRNAs): A class of long noncoding RNAs that function as the scaffold of nuclear bodies.

Takeshi Chujo1, Tomohiro Yamazaki1, Tetsuro Hirose2.   

Abstract

Mammalian transcriptome analyses elucidated the presence of thousands of unannotated long noncoding RNAs (lncRNAs) with distinct transcriptional units. Molecular characterization and functional classification of these lncRNAs are important challenges in the next decade. A subset of these lncRNAs is the core of nuclear bodies, which are the sites of the biogenesis, maturation, storage, and sequestration of specific RNAs, proteins, and ribonucleoprotein complexes. Here, we define a class of lncRNAs termed architectural RNAs (arcRNAs) that function as the essential scaffold or platform of nuclear bodies. Presently, five lncRNAs from mammals, insects, and yeast are classified as arcRNAs. These arcRNAs are temporarily upregulated upon specific cellular stresses, in developmental stages, or in various disease conditions, and sequestrate specific regulatory proteins, thereby changing gene expression patterns. In this review, we introduce common aspects of these arcRNAs and discuss why RNA is used as the architectural component of nuclear bodies. This article is part of a Special Issue entitled: Clues to long noncoding RNA taxonomy1, edited by Dr. Tetsuro Hirose and Dr. Shinichi Nakagawa.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Architectural RNA; Long noncoding RNA; Nuclear body

Mesh:

Substances:

Year:  2015        PMID: 26021608     DOI: 10.1016/j.bbagrm.2015.05.007

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  53 in total

Review 1.  Divergent actions of long noncoding RNAs on X-chromosome remodelling in mammals and Drosophila achieve the same end result: dosage compensation.

Authors:  Subhash C Lakhotia
Journal:  J Genet       Date:  2015-12       Impact factor: 1.166

2.  Chromatin remodeling complexes in the assembly of long noncoding RNA-dependent nuclear bodies.

Authors:  Tetsuya Kawaguchi; Tetsuro Hirose
Journal:  Nucleus       Date:  2015-12-28       Impact factor: 4.197

Review 3.  Specific genomic cues regulate Cajal body assembly.

Authors:  Iain A Sawyer; Gordon L Hager; Miroslav Dundr
Journal:  RNA Biol       Date:  2016-10-07       Impact factor: 4.652

4.  Unusual semi-extractability as a hallmark of nuclear body-associated architectural noncoding RNAs.

Authors:  Takeshi Chujo; Tomohiro Yamazaki; Tetsuya Kawaguchi; Satoshi Kurosaka; Toru Takumi; Shinichi Nakagawa; Tetsuro Hirose
Journal:  EMBO J       Date:  2017-04-12       Impact factor: 11.598

Review 5.  Non-coding RNAs in chromatin folding and nuclear organization.

Authors:  Sergey V Razin; Alexey A Gavrilov
Journal:  Cell Mol Life Sci       Date:  2021-06-11       Impact factor: 9.261

6.  Protein complex scaffolding predicted as a prevalent function of long non-coding RNAs.

Authors:  Diogo M Ribeiro; Andreas Zanzoni; Andrea Cipriano; Riccardo Delli Ponti; Lionel Spinelli; Monica Ballarino; Irene Bozzoni; Gian Gaetano Tartaglia; Christine Brun
Journal:  Nucleic Acids Res       Date:  2018-01-25       Impact factor: 16.971

Review 7.  Noncoding RNAs in protein clearance pathways: implications in neurodegenerative diseases.

Authors:  Sonali Sengupta
Journal:  J Genet       Date:  2017-03       Impact factor: 1.166

8.  Cellular, physiological and pathological aspects of the long non-coding RNA NEAT1.

Authors:  Pang-Kuo Lo; Benjamin Wolfson; Qun Zhou
Journal:  Front Biol (Beijing)       Date:  2016-01-04

Review 9.  Noncoding RNAs in breast cancer.

Authors:  Pang-Kuo Lo; Benjamin Wolfson; Xipeng Zhou; Nadire Duru; Ramkishore Gernapudi; Qun Zhou
Journal:  Brief Funct Genomics       Date:  2015-12-18       Impact factor: 4.241

10.  HyPR-MS for Multiplexed Discovery of MALAT1, NEAT1, and NORAD lncRNA Protein Interactomes.

Authors:  Michele Spiniello; Rachel A Knoener; Maisie I Steinbrink; Bing Yang; Anthony J Cesnik; Katherine E Buxton; Mark Scalf; David F Jarrard; Lloyd M Smith
Journal:  J Proteome Res       Date:  2018-07-31       Impact factor: 4.466

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