Evidence map›Paper›PMID 23917692›Full record

ArticleEpigenetics2013

Kinases and chromatin structure: who regulates whom?

Benoit Miotto

Abstract readComment
In one paragraph

Article in Epigenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Benoit MiottoUniversité Paris Diderot; Sorbonne Paris Cité; Epigenetics and Cell Fate; UMR 7216 CNRS; Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromatin structure is regulated by families of proteins that are able to covalently modify the histones and the DNA, as well as to regulate the spacing of nucleosomes along the DNA. Over the years, these chromatin remodeling factors have been proven to be essential to a variety of processes, including gene expression, DNA replication, and chromosome cohesion. The function of these remodeling factors is regulated by a number of chemical and developmental signals and, in turn, changes in the chromatin structure eventually contribute to the response to changes in the cellular environment. Exciting new research findings by the laboratories of Sharon Dent and Steve Jackson indicate, in two different contexts, that changes in the chromatin structure may, in reverse, signal to intracellular signaling pathways to regulate cell fate. The discoveries clearly challenge our traditional view of 'epigenetics', and may have important implications in human health.

Indexed as

Signal TransductionAnimalsCell Cycle ProteinsChromatinDNA-Binding ProteinsHistone AcetyltransferasesHistonesHumansKinetochoresMicrotubule-Associated ProteinsPhosphotyrosineProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsTumor Suppressor ProteinsCell Cycle ProteinsChromatinDNA-Binding ProteinsHistone AcetyltransferasesHistonesMicrotubule-Associated ProteinsPhosphotyrosineProtein Serine-Threonine KinasesSaccharomyces cerevisiae ProteinsTumor Suppressor ProteinschromatinDNA damagehistone tailsJun N-terminal kinasesignaling pathways

Identifiers

PMID23917692
PMCPMC3891680

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.