Evidence map›Paper›PMID 35338361›Full record

ReviewNature reviews. Genetics2022

Histone post-translational modifications - cause and consequence of genome function.

Gonzalo Millán-Zambrano, Adam Burton, Andrew J Bannister, Robert Schneider

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 665 papers.

0numbers the graph read from it
0cells of the map it votes in
665citing papers in PubMed
–field-weighted citation impact
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

665 citing papers in PubMed.

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605 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

4 authors.

Gonzalo Millán-Zambrano *Centro Andaluz de Biología Molecular y Medicina Regenerativa CABIMER, Universidad de Sevilla-CSIC-Universidad Pablo de Olavide, Seville, Spain.ORCID http://orcid.org/0000-0002-4530-6359
Adam Burton *Institute of Epigenetics and Stem Cells, Helmholtz Center Munich, Munich, Germany.
Andrew J BannisterGurdon Institute and Department of Pathology, University of Cambridge, Cambridge, UK. a.bannister@gurdon.cam.ac.uk.
Robert SchneiderInstitute of Functional Epigenetics, Helmholtz Center Munich, Munich, Germany. robert.schneider@helmholtz-muenchen.de.ORCID http://orcid.org/0000-0001-5303-0973

Funding

Cancer Research UK 27321Cancer Research UK C6946/A24843Cancer Research UK RG96894Wellcome Trust WT203144
6 · The paper itself

Abstract

Much has been learned since the early 1960s about histone post-translational modifications (PTMs) and how they affect DNA-templated processes at the molecular level. This understanding has been bolstered in the past decade by the identification of new types of histone PTM, the advent of new genome-wide mapping approaches and methods to deposit or remove PTMs in a locally and temporally controlled manner. Now, with the availability of vast amounts of data across various biological systems, the functional role of PTMs in important processes (such as transcription, recombination, replication, DNA repair and the modulation of genomic architecture) is slowly emerging. This Review explores the contribution of histone PTMs to the regulation of genome function by discussing when these modifications play a causative (or instructive) role in DNA-templated processes and when they are deposited as a consequence of such processes, to reinforce and record the event. Important advances in the field showing that histone PTMs can exert both direct and indirect effects on genome function are also presented.

Indexed as

HistonesProtein Processing, Post-TranslationalDNADNA RepairDNA ReplicationDNAHistones

Identifiers

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.