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

Man WuGuang XuChong HanPeng-Fei LuanYu-Hang XingFang NanLiang-Zhong YangYoukui HuangZheng-Hu YangLin ShanLi YangJiaquan LiuLing-Ling Chen
Published in: Science (New York, N.Y.) (2021)
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.
Keyphrases
  • long noncoding rna
  • transcription factor
  • long non coding rna
  • molecular dynamics simulations
  • heat shock protein
  • oxidative stress