Evidence map›Paper›PMID 29133298›Full record

ArticleGenetics2018

Functional Redundancy of Variant and Canonical Histone H3 Lysine 9 Modification in

Taylor J R Penke, Daniel J McKay, Brian D Strahl, A Gregory Matera, Robert J Duronio

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
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  7. SetDB1 and Su(var)3-9 are essential for late stages of larval development of Drosophila melanogaster.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2023
    Article
  8. Lysine-36 ofbioRxiv : the preprint server for biology · 2023
    Article
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  10. Review
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  13. Review
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  18. Article
  19. Sex-specific phenotypes of histone H4 point mutants establish dosage compensation as the critical function of H4K16 acetylation inProceedings of the National Academy of Sciences of the United States of America · 2018
    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

5 authors at 1 institution in 1 country.

Taylor J R PenkeCurriculum in Genetics and Molecular Biology, The University of North Carolina at Chapel Hill, North Carolina 27599.
Daniel J McKayCurriculum in Genetics and Molecular Biology, The University of North Carolina at Chapel Hill, North Carolina 27599.
Brian D StrahlCurriculum in Genetics and Molecular Biology, The University of North Carolina at Chapel Hill, North Carolina 27599.
A Gregory MateraCurriculum in Genetics and Molecular Biology, The University of North Carolina at Chapel Hill, North Carolina 27599.
Robert J DuronioCurriculum in Genetics and Molecular Biology, The University of North Carolina at Chapel Hill, North Carolina 27599 duronio@med.unc.edu.
University of North Carolina at Chapel Hill · US

Funding

NRSA IN GENETICST32GM007092 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SEKELSKY, JEFF J. · 1985 to 2019
$5.9M
Engineering histone genes to interrogate the epigenetic code in space and timeR01DA036897 · NIDA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DURONIO, ROBERT J, MATERA, A. GREGORY · 2013 to 2017
$2.2M
Investigating the Role of Histone Modifications in Heterochromatin FormationF31GM115194 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI PENKE, TAYLOR JOEL RICHARD · 2015 to 2017
$84k
NIDA NIH HHS R01 DA036897NIGMS NIH HHS F31 GM115194NIGMS NIH HHS T32 GM007092
6 · The paper itself

Abstract

Histone post-translational modifications (PTMs) and differential incorporation of variant and canonical histones into chromatin are central modes of epigenetic regulation. Despite similar protein sequences, histone variants are enriched for different suites of PTMs compared to their canonical counterparts. For example, variant histone H3.3 occurs primarily in transcribed regions and is enriched for "active" histone PTMs like Lys9 acetylation (H3.3K9ac), whereas the canonical histone H3 is enriched for Lys9 methylation (H3K9me), which is found in transcriptionally silent heterochromatin. To determine the functions of K9 modification on variant

Indexed as

Genetic VariationAllelesAnimalsAnimals, Genetically ModifiedDrosophilaGenotypeHeterochromatinHistonesLysineMutationPhenotypeTranscription, GeneticHeterochromatinHistonesLysineDrosophilaH3heterochromatinhistone varianttranscription

Identifiers

PMID29133298
PMCPMC5753860
OpenAlexW2751780022

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.