Evidence map›Paper›PMID 23633960›Full record

ArticlePLoS genetics2013

High-resolution mapping of h1 linker histone variants in embryonic stem cells.

Kaixiang Cao, Nathalie Lailler, Yunzhe Zhang, Ashwath Kumar, Karan Uppal, Zheng Liu, Eva K Lee, Hongwei Wu, Magdalena Medrzycki, Chenyi Pan and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

84 citing papers in PubMed, 135 citations in OpenAlex.

  1. Review
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  12. Exploring Intrinsic Disorder in Human Synucleins and Associated Proteins.International journal of molecular sciences · 2024
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  18. Regulation of Chromatin Architecture by Transcription Factor Binding.bioRxiv : the preprint server for biology · 2023
    Article
  19. CSSQ: a ChIP-seq signal quantifier pipeline.Frontiers in cell and developmental biology · 2023
    Article
  20. Article

24 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

16 authors at 3 institutions in 3 countries.

Kaixiang CaoSchool of Biology, Georgia Institute of Technology, Atlanta, Georgia, USA.
Nathalie Lailler
Yunzhe Zhang
Ashwath Kumar
Karan Uppal
Zheng Liu
Eva K Lee
Hongwei Wu
Magdalena Medrzycki
Chenyi Pan
Po-Yi Ho
Guy P Cooper
Xiao Dong
Christoph Bock
Eric E Bouhassira
Yuhong Fan
Georgia Institute of Technology · USAlbert Einstein College of Medicine · USCeMM Research Center for Molecular Medicine · AT

Funding

Role of Linker Histone H1 in Epigenetic Gene RegulationR01GM085261 · NIGMS · GEORGIA INSTITUTE OF TECHNOLOGY · PI FAN, YUHONG · 2008 to 2012
$2.0M
NIGMS NIH HHS GM085261NIGMS NIH HHS R01 GM085261
6 · The paper itself

Abstract

H1 linker histones facilitate higher-order chromatin folding and are essential for mammalian development. To achieve high-resolution mapping of H1 variants H1d and H1c in embryonic stem cells (ESCs), we have established a knock-in system and shown that the N-terminally tagged H1 proteins are functionally interchangeable to their endogenous counterparts in vivo. H1d and H1c are depleted from GC- and gene-rich regions and active promoters, inversely correlated with H3K4me3, but positively correlated with H3K9me3 and associated with characteristic sequence features. Surprisingly, both H1d and H1c are significantly enriched at major satellites, which display increased nucleosome spacing compared with bulk chromatin. While also depleted at active promoters and enriched at major satellites, overexpressed H1(0) displays differential binding patterns in specific repetitive sequences compared with H1d and H1c. Depletion of H1c, H1d, and H1e causes pericentric chromocenter clustering and de-repression of major satellites. These results integrate the localization of an understudied type of chromatin proteins, namely the H1 variants, into the epigenome map of mouse ESCs, and we identify significant changes at pericentric heterochromatin upon depletion of this epigenetic mark.

Indexed as

Embryonic Stem CellsAnimalsChromatinChromatin Assembly and DisassemblyChromosome MappingEpigenesis, GeneticGene Knock-In TechniquesHeterochromatinHistone-Lysine N-MethyltransferaseHistonesMiceChromatinHeterochromatinHistone-Lysine N-MethyltransferaseHistones

Identifiers

PMID23633960
PMCPMC3636266
OpenAlexW2038761741

What OpenQuestion holds

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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.