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Interplay between small RNA pathways shapes chromatin landscapes in C. elegans.

Ekaterina S Gushchanskaia | Ruben Esse | Qicheng Ma | Nelson C Lau | Alla Grishok
Nucleic acids research | 2019

The nematode Caenorhabditis elegans contains several types of endogenous small interfering RNAs (endo-siRNAs) produced by RNA-dependent RNA polymerase (RdRP) complexes. Both 'silencing' siRNAs bound by Worm-specific Argonautes (WAGO) and 'activating' siRNAs bound by the CSR-1 Argonaute require the DRH-3 helicase, an RdRP component. Here, we show that, in the drh-3(ne4253) mutant deficient in RdRP-produced secondary endo-siRNAs, the silencing histone mark H3K9me3 is largely depleted, whereas in the csr-1 partially rescued null mutant strain (WM193), this mark is ectopically deposited on CSR-1 target genes. Moreover, we observe ectopic H3K9me3 at enhancer elements and an increased number of small RNAs that match enhancers in both drh-3 and csr-1 mutants. Finally, we detect accumulation of H3K27me3 at highly expressed genes in the drh-3(ne4253) mutant, which correlates with their reduced transcription. Our study shows that when abundant RdRP-produced siRNAs are depleted, there is ectopic elevation of noncoding RNAs linked to sites with increased silencing chromatin marks. Moreover, our results suggest that enhancer small RNAs may guide local H3K9 methylation.

Pubmed ID: 31216042

Research resources used in this publication

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Antibodies used in this publication

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Associated grants

  • Agency: NIA NIH HHS, United States
    Id: R01 AG052465
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM107056

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SAMTOOLS (tool)

RRID:SCR_002105

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Bowtie (tool)

RRID:SCR_005476

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RRID:SCR_006646

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edgeR (tool)

RRID:SCR_012802

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RRID:SCR_012931

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