Evidence map›Paper›PMID 17984965›Full record

ReviewNature structural & molecular biology2007

How chromatin-binding modules interpret histone modifications: lessons from professional pocket pickers.

Sean D Taverna, Haitao Li, Alexander J Ruthenburg, C David Allis, Dinshaw J Patel

Open access · greenAbstract readReview
In one paragraph

Review in Nature structural & molecular biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 759 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
759citing papers in PubMed, 1 pooled it
39.5field-weighted citation impact, top 1% 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

759 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,389 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Linking cellular metabolism to chromatin modifications in plants.Journal of integrative plant biology · 2026
    Review
  7. Review
  8. Review
  9. Article
  10. A Chromatin Biology Assessment of AlphaFold3.bioRxiv : the preprint server for biology · 2026
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Generative design of intrinsically disordered protein regions with IDiom.bioRxiv : the preprint server for biology · 2026
    Article
  16. Review
  17. Review
  18. Article
  19. Development of Dimethylsulfonium Probes for Broad Profiling of Methyllysine Reader Proteins.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  20. Review

699 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

5 authors at 2 institutions in 1 country.

Sean D Taverna *Laboratory of Chromatin Biology, The Rockefeller University, New York, New York 10021, USA.
Haitao Li *Structural Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Alexander J RuthenburgLaboratory of Chromatin Biology, The Rockefeller University, New York, New York 10021, USA.
C David AllisLaboratory of Chromatin Biology, The Rockefeller University, New York, New York 10021, USA.
Dinshaw J PatelStructural Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Rockefeller University · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
ENZYMOLOGY &BIOLOGICAL FUNC OF HISTONE ACETYLATIONR37GM053512 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ALLIS, CHARLES DAVID · 1999 to 2008
$4.2M
Chromatin Remodeling and Programmed DNA EliminationR01GM063959 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ALLIS, CHARLES DAVID · 2001 to 2008
$3.1M
NUCLEAR DETERMINATION AND DIFFERENTIATION IN DEVELOPMENTR01GM053512 · NIGMS · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ALLIS, CHARLES DAVID · 1995 to 1998
–
NCI NIH HHS P30 CA008748NIGMS NIH HHS GM53512NIGMS NIH HHS GM63959NIGMS NIH HHS R01 GM063959NIGMS NIH HHS R37 GM053512
6 · The paper itself

Abstract

Histones comprise the major protein component of chromatin, the scaffold in which the eukaryotic genome is packaged, and are subject to many types of post-translational modifications (PTMs), especially on their flexible tails. These modifications may constitute a 'histone code' and could be used to manage epigenetic information that helps extend the genetic message beyond DNA sequences. This proposed code, read in part by histone PTM-binding 'effector' modules and their associated complexes, is predicted to define unique functional states of chromatin and/or regulate various chromatin-templated processes. A wealth of structural and functional data show how chromatin effector modules target their cognate covalent histone modifications. Here we summarize key features in molecular recognition of histone PTMs by a diverse family of 'reader pockets', highlighting specific readout mechanisms for individual marks, common themes and insights into the downstream functional consequences of the interactions. Changes in these interactions may have far-reaching implications for human biology and disease, notably cancer.

Indexed as

HistonesProtein Processing, Post-Translational14-3-3 ProteinsAdaptor Proteins, Signal TransducingAmino AcidsCell Cycle ProteinsChromatinDNA-Binding ProteinsEpigenesis, GeneticHistone AcetyltransferasesHumansModels, MolecularNuclear Proteinsp300-CBP-Associated Factorp300-CBP Transcription FactorsProtein Conformation14-3-3 ProteinsAdaptor Proteins, Signal TransducingAmino AcidsCell Cycle ProteinsChromatinDNA-Binding ProteinsH2AX protein, humanHistone AcetyltransferasesHistonesMDC1 protein, humanNuclear Proteinsp300-CBP-Associated Factorp300-CBP Transcription FactorsTATA-binding protein associated factor 250 kDaTATA-Binding Protein Associated FactorsTrans-ActivatorsTranscription Factor TFIID

Identifiers

PMID17984965
PMCPMC4691843
OpenAlexW2036158314

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.