Evidence map›Paper›PMID 26889830›Full record

ArticlePLoS genetics2016

A Novel Epigenetic Silencing Pathway Involving the Highly Conserved 5'-3' Exoribonuclease Dhp1/Rat1/Xrn2 in Schizosaccharomyces pombe.

James Franklin Tucker, Corina Ohle, Géza Schermann, Katja Bendrin, Wei Zhang, Tamás Fischer, Ke Zhang

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.5field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Long RNA-Mediated Chromatin Regulation in Fission Yeast and Mammals.International journal of molecular sciences · 2022
    Review
  11. Spreading and epigenetic inheritance of heterochromatin require a critical density of histone H3 lysine 9 tri-methylation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Autonomous Pathway:Plant physiology · 2020
    Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 2 countries.

James Franklin TuckerDepartment of Biology, Wake Forest University, Winston-Salem, North Carolina, United States of America.
Corina OhleBiochemistry Center (BZH), Heidelberg University, Heidelberg, Germany.
Géza SchermannBiochemistry Center (BZH), Heidelberg University, Heidelberg, Germany.
Katja BendrinBiochemistry Center (BZH), Heidelberg University, Heidelberg, Germany.
Wei ZhangDepartment of Microbiology-Immunology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois, United States of America.
Tamás FischerBiochemistry Center (BZH), Heidelberg University, Heidelberg, Germany.
Ke ZhangDepartment of Biology, Wake Forest University, Winston-Salem, North Carolina, United States of America.
Heidelberg University · DEWake Forest University · USNorthwestern University · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
Determination of a Novel Epigenetic Silencing MechanismR15GM119105 · NIGMS · WAKE FOREST UNIVERSITY · PI REID, KE ZHANG · 2016 to 2016
$420k
NCI NIH HHS P30 CA060553NIGMS NIH HHS R15 GM119105
6 · The paper itself

Abstract

Epigenetic gene silencing plays a critical role in regulating gene expression and contributes to organismal development and cell fate acquisition in eukaryotes. In fission yeast, Schizosaccharomyces pombe, heterochromatin-associated gene silencing is known to be mediated by RNA processing pathways including RNA interference (RNAi) and a 3'-5' exoribonuclease complex, the exosome. Here, we report a new RNA-processing pathway that contributes to epigenetic gene silencing and assembly of heterochromatin mediated by 5'-3' exoribonuclease Dhp1/Rat1/Xrn2. Dhp1 mutation causes defective gene silencing both at peri-centromeric regions and at the silent mating type locus. Intriguingly, mutation in either of the two well-characterized Dhp1-interacting proteins, the Din1 pyrophosphohydrolase or the Rhn1 transcription termination factor, does not result in silencing defects at the main heterochromatic regions. We demonstrate that Dhp1 interacts with heterochromatic factors and is essential in the sequential steps of establishing silencing in a manner independent of both RNAi and the exosome. Genomic and genetic analyses suggest that Dhp1 is involved in post-transcriptional silencing of repetitive regions through its RNA processing activity. The results describe the unexpected role of Dhp1/Rat1/Xrn2 in chromatin-based silencing and elucidate how various RNA-processing pathways, acting together or independently, contribute to epigenetic regulation of the eukaryotic genome.

Indexed as

Conserved SequenceEpigenesis, GeneticGene SilencingAmino Acid SequenceBiocatalysisCentromereChromosome SegregationDNA-Directed RNA PolymerasesExoribonucleasesExosomesGenes, Mating Type, FungalGenetic LociHeterochromatinHistonesLysineMethylation5'-exoribonucleaseDNA-Directed RNA PolymerasesExoribonucleasesHeterochromatinHistonesLysineRNA, MessengerSchizosaccharomyces pombe Proteins

Identifiers

PMID26889830
PMCPMC4758730
OpenAlexW2276629228

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.