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Clr4SUV39H1 ubiquitination and non-coding RNA mediate transcriptional silencing of heterochromatin via Swi6 phase separation.

Authors :
Kim, Hyun-Soo
Roche, Benjamin
Bhattacharjee, Sonali
Todeschini, Leila
Chang, An-Yun
Hammell, Christopher
Verdel, André
Martienssen, Robert A.
Source :
Nature Communications; 10/30/2024, Vol. 15 Issue 1, p1-14, 14p
Publication Year :
2024

Abstract

Transcriptional silencing by RNAi paradoxically relies on transcription, but how the transition from transcription to silencing is achieved has remained unclear. The Cryptic Loci Regulator complex (CLRC) in Schizosaccharomyces pombe is a cullin-ring E3 ligase required for silencing that is recruited by RNAi. We found that the E2 ubiquitin conjugating enzyme Ubc4 interacts with CLRC and mono-ubiquitinates the histone H3K9 methyltransferase Clr4<superscript>SUV39H1</superscript>, promoting the transition from co-transcriptional gene silencing (H3K9me2) to transcriptional gene silencing (H3K9me3). Ubiquitination of Clr4 occurs in an intrinsically disordered region (Clr4<superscript>IDR</superscript>), which undergoes liquid droplet formation in vitro, along with Swi6<superscript>HP1</superscript> the effector of transcriptional gene silencing. Our data suggests that phase separation is exquisitely sensitive to non-coding RNA (ncRNA) which promotes self-association of Clr4, chromatin association, and di-, but not tri- methylation instead. Ubc4-CLRC also targets the transcriptional co-activator Bdf2<superscript>BRD4</superscript>, down-regulating centromeric transcription and small RNA (sRNA) production. The deubiquitinase Ubp3 counteracts both activities. Here the authors investigate how the E3 ubiquitin ligase Cryptic Loci Regulator Complex mediates the transition from RNAi-dependent co-transcriptional gene silencing to transcriptional gene silencing suggesting the involvement of phase separation in the transition during heterochromatin formation. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20411723
Volume :
15
Issue :
1
Database :
Complementary Index
Journal :
Nature Communications
Publication Type :
Academic Journal
Accession number :
180588876
Full Text :
https://doi.org/10.1038/s41467-024-53417-9