Literature DB >> 34326237

lncRNA SLERT controls phase separation of FC/DFCs to facilitate Pol I transcription.

Man Wu1, Guang Xu1, Chong Han1, Peng-Fei Luan1, Yu-Hang Xing1, Fang Nan2, Liang-Zhong Yang1, Youkui Huang1, Zheng-Hu Yang1,3, Lin Shan1, Li Yang2,3, Jiaquan Liu4, Ling-Ling Chen4,3,5.   

Abstract

RNA polymerase I (Pol I) transcription takes place at the border of the fibrillar center (FC) and the dense fibrillar component (DFC) in the nucleolus. Here, we report that individual spherical FC/DFC units are coated by the DEAD-box RNA helicase DDX21 in human cells. The long noncoding RNA (lncRNA) SLERT binds to DDX21 RecA domains to promote DDX21 to adopt a closed conformation at a substoichiometric ratio through a molecular chaperone-like mechanism resulting in the formation of hypomultimerized and loose DDX21 clusters that coat DFCs, which is required for proper FC/DFC liquidity and Pol I processivity. Our results suggest that SLERT is an RNA regulator that controls the biophysical properties of FC/DFCs and thus ribosomal RNA production.
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2021        PMID: 34326237     DOI: 10.1126/science.abf6582

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  10 in total

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7.  rRNA biogenesis regulates mouse 2C-like state by 3D structure reorganization of peri-nucleolar heterochromatin.

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Review 9.  Molecular Mechanisms of lncRNAs in the Dependent Regulation of Cancer and Their Potential Therapeutic Use.

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Review 10.  Long noncoding RNA and protein abundance in lncRNPs.

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Journal:  RNA       Date:  2021-09-15       Impact factor: 4.942

  10 in total

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