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Genes Dev. 2019 Apr 1;33(7-8):436-451. doi: 10.1101/gad.322495.118. Epub 2019 Feb 25.

Synergistic lethality between BRCA1 and H3K9me2 loss reflects satellite derepression.

Author information

1
Friedrich Miescher Institute for Biomedical Research, CH-4058 Basel, Switzerland.
2
Faculty of Natural Sciences, University of Basel, CH-4056 Basel, Switzerland.
#
Contributed equally

Abstract

Caenorhabditis elegans has two histone H3 Lys9 methyltransferases, MET-2 (SETDB1 homolog) and SET-25 (G9a/SUV39H1 related). In worms, we found simple repeat sequences primarily marked by H3K9me2, while transposable elements and silent tissue-specific genes bear H3K9me3. RNA sequencing (RNA-seq) in histone methyltransferase (HMT) mutants shows that MET-2-mediated H3K9me2 is necessary for satellite repeat repression, while SET-25 silences a subset of transposable elements and tissue-specific genes through H3K9me3. A genome-wide synthetic lethality screen showed that RNA processing, nuclear RNA degradation, the BRCA1/BARD1 complex, and factors mediating replication stress survival are necessary for germline viability in worms lacking MET-2 but not SET-25. Unlike set-25 mutants, met-2-null worms accumulated satellite repeat transcripts, which form RNA:DNA hybrids on repetitive sequences, additively with the loss of BRCA1 or BARD1. BRCA1/BARD1-mediated H2A ubiquitination and MET-2 deposited H3K9me2 on satellite repeats are partially interdependent, suggesting both that the loss of silencing generates BRCA-recruiting DNA damage and that BRCA1 recruitment by damage helps silence repeats. The artificial induction of MSAT1 transcripts can itself trigger damage-induced germline lethality in a wild-type background, arguing that the synthetic sterility upon BRCA1/BARD1 and H3K9me2 loss is directly linked to the DNA damage provoked by unscheduled satellite repeat transcription.

KEYWORDS:

BRCA1 complex; DNA repeats; RNA:DNA hybrids; genome instability; heterochromatin; histone H3K9 methylation; satellite repeats; transcriptional silencing

PMID:
30804228
PMCID:
PMC6446544
DOI:
10.1101/gad.322495.118
[Indexed for MEDLINE]
Free PMC Article

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