Phase separation of SGS3 drives siRNA body formation and promotes endogenous gene silencing

Huijuan Tan, Wentao Luo, Wei Yan, Jie Liu, Yalikunjiang Aizezi, Ruixue Cui, Ruijun Tian, Jinbiao Ma, Hongwei Guo*

*Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

33 Citations (Scopus)

Abstract

The generation of small interfering RNA (siRNA) involves many RNA processing components, including SUPPRESSOR OF GENE SILENCING 3 (SGS3), RNA-DEPENDENT RNA POLYMERASE 6 (RDR6), and DICER-LIKE proteins (DCLs). Nonetheless, how these components are coordinated to produce siRNAs is unclear. Here, we show that SGS3 forms condensates via phase separation in vivo and in vitro. SGS3 interacts with RDR6 and drives it to form siRNA bodies in cytoplasm, which is promoted by SGS3-targeted RNAs. Disrupting SGS3 phase separation abrogates siRNA body assembly and siRNA biogenesis, whereas coexpression of SGS3 and RDR6 induces siRNA body formation in tobacco and yeast cells. Dysfunction in translation and mRNA decay increases the number of siRNA bodies, whereas DCL2/4 mutations enhance their size. Purification of SGS3 condensates identifies numerous RNA-binding proteins and siRNA processing components. Together, our findings reveal that SGS3 phase separation-mediated formation of siRNA bodies is essential for siRNA production and gene silencing.

Original languageEnglish
Article number111985
JournalCell Reports
Volume42
Issue number1
DOIs
Publication statusPublished - 31 Jan 2023

User-Defined Keywords

  • CP: Molecular biology
  • DCL2/4
  • phase separation
  • RDR6
  • SGS3
  • siRNA biogenesis
  • siRNA-body

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