Evidence map›Paper›PMID 35322122›Full record

ArticleScientific reports2022

Despite its sequence identity with canonical H4, Drosophila H4r product is enriched at specific chromatin regions.

Andrea Ábrahám, Zoltán Villányi, Nóra Zsindely, Gábor Nagy, Áron Szabó, László Bodai, László Henn, Imre M Boros

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. 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
0.2field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 1 country.

Andrea ÁbrahámInstitute of Biochemistry, Biological Research Centre of Szeged, Szeged, 6726, Hungary.
Zoltán VillányiDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Szeged, 6726, Hungary.
Nóra ZsindelyDepartment of Genetics, Faculty of Science and Informatics, University of Szeged, Szeged, 6726, Hungary.
Gábor NagyDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Szeged, 6726, Hungary.
Áron SzabóDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Szeged, 6726, Hungary.
László BodaiDepartment of Biochemistry and Molecular Biology, Faculty of Science and Informatics, University of Szeged, Szeged, 6726, Hungary.
László HennInstitute of Biochemistry, Biological Research Centre of Szeged, Szeged, 6726, Hungary.
Imre M BorosInstitute of Biochemistry, Biological Research Centre of Szeged, Szeged, 6726, Hungary. imreboros53@gmail.com.
University of Szeged · HUHUN-REN Szegedi Biológiai Kutatóközpont · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone variants are different from their canonical counterparts in structure and are encoded by solitary genes with unique regulation to fulfill tissue or differentiation specific functions. A single H4 variant gene (His4r or H4r) that is located outside of the histone cluster and gives rise to a polyA tailed messenger RNA via replication-independent expression is preserved in Drosophila strains despite that its protein product is identical with canonical H4. In order to reveal information on the possible role of this alternative H4 we epitope tagged endogenous H4r and studied its spatial and temporal expression, and revealed its genome-wide localization to chromatin at the nucleosomal level. RNA and immunohistochemistry analysis of H4r expressed under its cognate regulation indicate expression of the gene throughout zygotic and larval development and presence of the protein product is evident already in the pronuclei of fertilized eggs. In the developing nervous system a slight disequibrium in H4r distribution is observable, cholinergic neurons are the most abundant among H4r-expressing cells. ChIP-seq experiments revealed H4r association with regulatory regions of genes involved in cellular stress response. The data presented here indicate that H4r has a variant histone function.

Indexed as

ChromatinDrosophilaAnimalsHistonesNucleosomesReceptors, Histamine H4ChromatinHistonesNucleosomesReceptors, Histamine H4

Identifiers

PMID35322122
PMCPMC8943024
OpenAlexW4221031163

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.