Evidence map›Paper›PMID 30051891›Full record

ArticleNature2018

Automethylation-induced conformational switch in Clr4 (Suv39h) maintains epigenetic stability.

Nahid Iglesias, Mark A Currie, Gloria Jih, Joao A Paulo, Nertila Siuti, Marian Kalocsay, Steven P Gygi, Danesh Moazed

Open access · greenAbstract read
In one paragraph

Article in Nature, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Clr4Nature communications · 2024
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  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

8 authors at 2 institutions in 1 country.

Nahid Iglesias *Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Mark A Currie *Department of Cell Biology, Harvard Medical School, Boston, MA, USA.
Gloria JihDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Joao A PauloDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Nertila SiutiDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Marian KalocsayDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Steven P GygiDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Danesh MoazedDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA. danesh@hms.harvard.edu.
Harvard University · USHoward Hughes Medical Institute · US

Funding

Overall EvaluationP41GM103403 · NIGMS · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2012 to 2017
$14.3M
TRANSLATIONAL PHARMACOLOGY COREP50GM107618 · NIGMS · HARVARD MEDICAL SCHOOL · PI GOLAN, DAVID E. · 2014 to 2018
$10.8M
New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
RNAi-mediated Targeting of Hetorochromatin AssemblyR01GM072805 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI MOAZED, DANESH · 2005 to 2025
$6.9M
Pixel Array Detector for Macromolecular CrystallographyS10OD021527 · OD · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2016 to 2016
$2.0M
Pixel Array Detector for X-ray CrystallographyS10RR029205 · NCRR · CORNELL UNIVERSITY · PI EALICK, STEVEN E · 2010 to 2010
$1.8M
Resolving the role of nicotine-mediated phosphorylation on pancreatic fibrosisK01DK098285 · NIDDK · HARVARD MEDICAL SCHOOL · PI PAULO, JOAO A · 2013 to 2017
$638k
Howard Hughes Medical InstituteNCRR NIH HHS S10 RR029205NIDDK NIH HHS K01 DK098285NIGMS NIH HHS P41 GM103403NIGMS NIH HHS P50 GM107618NIGMS NIH HHS R01 GM067945NIGMS NIH HHS R01 GM072805NIH HHS S10 OD021527
6 · The paper itself

Abstract

Histone H3 lysine 9 methylation (H3K9me) mediates heterochromatic gene silencing and is important for genome stability and the regulation of gene expression

Indexed as

Epigenesis, GeneticCell Cycle ProteinsEvolution, MolecularGene SilencingHeterochromatinHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHistonesHumansMethylationMethyltransferasesProtein ConformationSchizosaccharomycesSchizosaccharomyces pombe ProteinsCell Cycle Proteinsclr4 protein, S pombeHeterochromatinHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHistonesMethyltransferasesSchizosaccharomyces pombe ProteinsSUV39H2 protein, human

Identifiers

PMID30051891
PMCPMC6287498
OpenAlexW2884613836

What OpenQuestion holds

Textmetadata
LicenceTDM
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.