Evidence map›Paper›PMID 27257070›Full record

ArticleNucleic acids research2016

ZFP57 maintains the parent-of-origin-specific expression of the imprinted genes and differentially affects non-imprinted targets in mouse embryonic stem cells.

Vincenzo Riso, Marco Cammisa, Harpreet Kukreja, Zahra Anvar, Gaetano Verde, Angela Sparago, Basilia Acurzio, Shraddha Lad, Enza Lonardo, Aditya Sankar and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.9field-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

47 citing papers in PubMed, 76 citations in OpenAlex.

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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 6 institutions in 3 countries.

Vincenzo RisoInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy.
Marco CammisaInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy.
Harpreet KukrejaInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy.
Zahra AnvarInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy.
Gaetano VerdeInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy.
Angela SparagoInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy.
Basilia AcurzioInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy.
Shraddha LadInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy.
Enza LonardoInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy.
Aditya SankarBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark Center for Epigenetics, University of Copenhagen, 2200 Copenhagen, Denmark.
Kristian HelinBiotech Research and Innovation Centre (BRIC), University of Copenhagen, Copenhagen, Denmark The Danish Stem Cell Center (Danstem), University of Copenhagen, 2200 Copenhagen, Denmark.ORCID 0000-0003-1975-6097
Robert FeilInstitute of Molecular Genetics (IGMM), CNRS, 34293 Montpellier, France University of Montpellier, 34090 Montpellier, France.
Annalisa FicoInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy.
Claudia AngeliniIstituto per le Applicazioni del Calcolo 'Mauro Picone' (IAC), CNR, 80131 Naples, Italy.
Giovanna GrimaldiInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Ceinge Biotecnologie Avanzate s.c.a.r.l., 80145 Naples, Italy.
Andrea RiccioInstitute of Genetics and Biophysics 'A. Buzzati-Traverso', CNR, 80131 Naples, Italy Department of Environmental, Biological and Pharmaceutical Sciences and Technologies, Second University of Naples, 81100 Caserta, Italy andrea.riccio@unina2.it.ORCID 0000-0001-7990-3576
University of Campania "Luigi Vanvitelli" · ITInstitute of Genetics and Biophysics · ITUniversity of Copenhagen · DKCeinge Biotecnologie Avanzate (Italy) · ITCentre National de la Recherche Scientifique · FRIstituto per le Applicazioni del Calcolo Mauro Picone · IT

Funding

Telethon GGP15131
6 · The paper itself

Abstract

ZFP57 is necessary for maintaining repressive epigenetic modifications at Imprinting control regions (ICRs). In mouse embryonic stem cells (ESCs), ZFP57 binds ICRs (ICRBS) and many other loci (non-ICRBS). To address the role of ZFP57 on all its target sites, we performed high-throughput and multi-locus analyses of inbred and hybrid mouse ESC lines carrying different gene knockouts. By using an allele-specific RNA-seq approach, we demonstrate that ZFP57 loss results in derepression of the imprinted allele of multiple genes in the imprinted clusters. We also find marked epigenetic differences between ICRBS and non-ICRBS suggesting that different cis-acting regulatory functions are repressed by ZFP57 at these two classes of target loci. Overall, these data demonstrate that ZFP57 is pivotal to maintain the allele-specific epigenetic modifications of ICRs that in turn are necessary for maintaining the imprinted expression over long distances. At non-ICRBS, ZFP57 inactivation results in acquisition of epigenetic features that are characteristic of poised enhancers, suggesting that another function of ZFP57 in early embryogenesis is to repress cis-acting regulatory elements whose activity is not yet required.

Indexed as

Gene Expression Regulation, DevelopmentalGenomic ImprintingAnimalsBinding SitesCell DifferentiationCpG IslandsEpigenesis, GeneticGenetic LociHistonesLysineMethylationMiceModels, GeneticMouse Embryonic Stem CellsNuclear ProteinsRepressor ProteinsHistonesLysineNuclear ProteinsRepressor ProteinsZfp-57 protein, mouse

Identifiers

PMID27257070
PMCPMC5041456
OpenAlexW2418895208

What OpenQuestion holds

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LicenceCC BY-NC
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Registered trials

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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.