Evidence map›Paper›PMID 12773576›Full record

ArticleMolecular and cellular biology2003

A novel jmjC domain protein modulates heterochromatization in fission yeast.

Nabieh Ayoub, Ken-ichi Noma, Sara Isaac, Tamar Kahan, Shiv I S Grewal, Amikam Cohen

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

97 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Characterization of the Swi6/HP1 binding motif in its partner protein reveals the basis for the functional divergence of the HP1 family proteins in fission yeast.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. The Fission Yeast Mating-Type Switching Motto: "One-for-Two" and "Two-for-One".Microbiology and molecular biology reviews : MMBR · 2023
    Review
  18. Review
  19. Article
  20. Article

37 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Nabieh AyoubDepartment of Molecular Biology, The Hebrew University-Hadassah Medical School, Jerusalem, Israel 91010.
Ken-ichi Noma
Sara Isaac
Tamar Kahan
Shiv I S Grewal
Amikam Cohen
Cold Spring Harbor Laboratory · USHebrew University of Jerusalem · IL

Funding

EPIGENETIC CONTROL OF GENE EXPRESSIONR01GM059772 · NIGMS · COLD SPRING HARBOR LABORATORY · PI XU, RUI-MING · 2000 to 2003
$929k
NIGMS NIH HHS GM59772NIGMS NIH HHS R01 GM059772
6 · The paper itself

Abstract

The heterochromatin domain at the mat locus of Schizosaccharomyces pombe is bounded by the IR-L and IR-R barriers. A genetic screen for mutations that promote silencing beyond IR-L revealed a novel gene named epe1, encoding a conserved nuclear protein with a jmjC domain. Disruption of epe1 promotes continuous spreading of heterochromatin-associated histone modifications and Swi6 binding to chromatin across heterochromatic barriers. It also enhances position effect variegation at heterochromatic domains, suppresses mutations in silencing genes, and stabilizes the repressed epigenetic state at the mat locus. However, it does not enhance silencing establishment. Our analysis suggests that the jmjC domain is essential for Epe1 activity and that Epe1 counteracts transcriptional silencing by negatively affecting heterochromatin stability. Consistent with this proposition, the meiotic stability of established heterochromatin beyond IR-L is diminished by Epe1 activity, and overexpression of Epe1 disrupts heterochromatin through acetylation of H3-K9 and H3-K14 and methylation of H3-K4. Furthermore, overexpression of Epe1 elevates the rate of chromosome loss. We propose that Epe1 helps control chromatin organization by down-regulating the stability of epigenetic marks that govern heterochromatization.

Indexed as

Amino Acid SequenceCell NucleusChromatinCodon, NonsenseGene SilencingGenotypeGreen Fluorescent ProteinsHeterochromatinHistonesLuminescent ProteinsMicroscopy, FluorescenceModels, GeneticMolecular Sequence DataMutationNuclear ProteinsPhenotypeChromatinCodon, Nonsenseepe1 protein, S pombeGreen Fluorescent ProteinsHeterochromatinHistonesLuminescent ProteinsNuclear ProteinsSchizosaccharomyces pombe Proteins

Identifiers

PMID12773576
PMCPMC156127
OpenAlexW2101089041

What OpenQuestion holds

Textmetadata
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.