Evidence map›Paper›PMID 21598301›Full record

ArticleJournal of cellular biochemistry2011

Cooperative DNA and histone binding by Uhrf2 links the two major repressive epigenetic pathways.

Garwin Pichler, Patricia Wolf, Christine S Schmidt, Daniela Meilinger, Katrin Schneider, Carina Frauer, Karin Fellinger, Andrea Rottach, Heinrich Leonhardt

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cellular biochemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.9field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 75 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. UHRF2 accumulates in early GCell cycle (Georgetown, Tex.) · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Proteins That Read DNA Methylation.Advances in experimental medicine and biology · 2022
    Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Chromatin structure and its chemical modifications regulate the ubiquitin ligase substrate selectivity of UHRF1.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. Article
  18. DNA Methylation and Adult Neurogenesis.Brain plasticity (Amsterdam, Netherlands) · 2017
    Review
  19. 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

9 authors at 1 institution in 1 country.

Garwin PichlerLudwig Maximilians University Munich, Department of Biology II and Center for Integrated Protein Science Munich, Großhaderner Str. 2, 82152 Planegg-Martinsried, Germany.
Patricia Wolf
Christine S Schmidt
Daniela Meilinger
Katrin Schneider
Carina Frauer
Karin Fellinger
Andrea Rottach
Heinrich Leonhardt
Center for Integrated Protein Science Munich · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene expression is regulated by DNA as well as histone modifications but the crosstalk and mechanistic link between these epigenetic signals are still poorly understood. Here we investigate the multi-domain protein Uhrf2 that is similar to Uhrf1, an essential cofactor of maintenance DNA methylation. Binding assays demonstrate a cooperative interplay of Uhrf2 domains that induces preference for hemimethylated DNA, the substrate of maintenance methylation, and enhances binding to H3K9me3 heterochromatin marks. FRAP analyses revealed that localization and binding dynamics of Uhrf2 in vivo require an intact tandem Tudor domain and depend on H3K9 trimethylation but not on DNA methylation. Besides the cooperative DNA and histone binding that is characteristic for Uhrf2, we also found an opposite expression pattern of uhrf1 and uhrf2 during differentiation. While uhrf1 is mainly expressed in pluripotent stem cells, uhrf2 is upregulated during differentiation and highly expressed in differentiated mouse tissues. Ectopic expression of Uhrf2 in uhrf1(-/-) embryonic stem cells did not restore DNA methylation at major satellites indicating functional differences. We propose that the cooperative interplay of Uhrf2 domains may contribute to a tighter epigenetic control of gene expression in differentiated cells.

Indexed as

Gene SilencingAnimalsCCAAT-Enhancer-Binding ProteinsCell DifferentiationCells, CulturedDNADNA MethylationEmbryonic Stem CellsEpigenesis, GeneticGene Knockout TechniquesGreen Fluorescent ProteinsHistonesHumansMethylationMethyltransferasesMiceCCAAT-Enhancer-Binding ProteinsDNAGreen Fluorescent ProteinsHistonesMethyltransferasesRecombinant Fusion ProteinsUbiquitin-Protein LigasesUHRF1 protein, humanUHRF2 protein, humanUHRF2 protein, mouse

Identifiers

PMID21598301
PMCPMC3569875
OpenAlexW2026550542

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.