Evidence map›Paper›PMID 28239420›Full record

ArticleEpigenetics & chromatin2017

PRC2 is required for extensive reorganization of H3K27me3 during epigenetic reprogramming in mouse fetal germ cells.

Lexie Prokopuk, Jessica M Stringer, Kirsten Hogg, Kirstin D Elgass, Patrick S Western

Abstract read
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Article in Epigenetics & chromatin, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

18 citing papers in PubMed.

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4 · The record

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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.

Lexie ProkopukDepartment of Molecular and Translational Science, Centre for Genetic Diseases, Hudson Institute of Medical Research, Monash University, Clayton, VIC 3168 Australia.
Jessica M StringerDepartment of Molecular and Translational Science, Centre for Genetic Diseases, Hudson Institute of Medical Research, Monash University, Clayton, VIC 3168 Australia.
Kirsten HoggDepartment of Molecular and Translational Science, Centre for Genetic Diseases, Hudson Institute of Medical Research, Monash University, Clayton, VIC 3168 Australia.
Kirstin D ElgassMonash Micro Imaging, Monash University, Clayton, VIC 3800 Australia.
Patrick S WesternDepartment of Molecular and Translational Science, Centre for Genetic Diseases, Hudson Institute of Medical Research, Monash University, Clayton, VIC 3168 Australia.ORCID 0000-0002-7587-8227

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDefining how epigenetic information is established in the germline during fetal development is key to understanding how epigenetic information is inherited and impacts on evolution and human health and disease.

resultsHere, we show that Polycomb Repressive Complex 2 is transiently localized in the nucleus of mouse fetal germ cells, while DNA methylation is removed from the germline. This coincides with significant enrichment of trimethylated lysine 27 on histone 3 near the nuclear lamina that is dependent on activity of the essential PRC2 catalytic proteins, Enhancer of Zeste 1 and/or 2.

conclusionsCombined, these data reveal a role for Polycomb Repressive Complex 2 and trimethylated lysine 27 on histone 3 during germline epigenetic programming that we speculate is required to repress target sequences while DNA methylation is removed.

Indexed as

EpigenomicsAnimalsCell DifferentiationCellular ReprogrammingEnhancer of Zeste Homolog 2 ProteinFemaleFetusGerm CellsGonadsHistonesIndolesMaleMethylationMiceMice, TransgenicMicroscopy, FluorescenceEnhancer of Zeste Homolog 2 ProteinEzh1 protein, mouseEzh2 protein, mouseGSK-2816126HistonesIndolesOctamer Transcription Factor-3Polycomb Repressive Complex 2Pou5f1 protein, mousePyridonesEpigenetic reprogrammingEpigeneticsGerm cellsH3K27me3Histone modifications

Identifiers

PMID28239420
PMCPMC5319108

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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.