Evidence map›Paper›PMID 27300161›Full record

ArticleStem cells (Dayton, Ohio)2016

Characterization of the Epigenetic Changes During Human Gonadal Primordial Germ Cells Reprogramming.

C Eguizabal, L Herrera, L De Oñate, N Montserrat, P Hajkova, J C Izpisua Belmonte

Abstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
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  6. Article
  7. Annelids as models of germ cell and gonad regeneration.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. Current progress onFrontiers in cell and developmental biology · 2023
    Review
  12. Article
  13. Early Gonadal Development and Sex Determination in Mammal.International journal of molecular sciences · 2022
    Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Unique metabolic phenotype and its transition during maturation of juvenile male germ cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    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

6 authors at 3 institutions in 3 countries.

C EguizabalCell Therapy and Stem Cell Group, Basque Center for Transfusion and Human Tissues, Galdakao, Spain.
L HerreraCell Therapy and Stem Cell Group, Basque Center for Transfusion and Human Tissues, Galdakao, Spain.
L De OñatePluripotent Stem Cells and Activation of Endogenous Tissue Programs for Organ Regeneration (PR Lab), Institute for Bioengineering of Catalonia (IBEC), Barcelona, Spain.
N MontserratPluripotent Stem Cells and Activation of Endogenous Tissue Programs for Organ Regeneration (PR Lab), Institute for Bioengineering of Catalonia (IBEC), Barcelona, Spain.
P HajkovaReprogramming and Chromatin Group, Medical Research Council Clinical Sciences Centre, Imperial College London, Hammersmith Hospital Campus, London, United Kingdom.
J C Izpisua BelmonteGene Expression Laboratory, The Salk Institute for Biological Studies, La Jolla, California, USA. belmonte@salk.edu.
Institute for Bioengineering of Catalonia · ESHammersmith Hospital · GBSalk Institute for Biological Studies · US

Funding

Medical Research Council MC_U120092689
6 · The paper itself

Abstract

Epigenetic reprogramming is a central process during mammalian germline development. Genome-wide DNA demethylation in primordial germ cells (PGCs) is a prerequisite for the erasure of epigenetic memory, preventing the transmission of epimutations to the next generation. Apart from DNA demethylation, germline reprogramming has been shown to entail reprogramming of histone marks and chromatin remodelling. Contrary to other animal models, there is limited information about the epigenetic dynamics during early germ cell development in humans. Here, we provide further characterization of the epigenetic configuration of the early human gonadal PGCs. We show that early gonadal human PGCs are DNA hypomethylated and their chromatin is characterized by low H3K9me2 and high H3K27me3 marks. Similarly to previous observations in mice, human gonadal PGCs undergo dynamic chromatin changes concomitant with the erasure of genomic imprints. Interestingly, and contrary to mouse early germ cells, expression of BLIMP1/PRDM1 persists in through all gestational stages in human gonadal PGCs and is associated with nuclear lysine-specific demethylase-1. Our work provides important additional information regarding the chromatin changes associated with human PGCs development between 6 and 13 weeks of gestation in male and female gonads. Stem Cells 2016;34:2418-2428.

Indexed as

Epigenesis, GeneticAnimalsCellular ReprogrammingChromatinDNA MethylationFemaleGerm CellsGonadsHistone DemethylasesHistonesHumansLysineMiceModels, BiologicalPositive Regulatory Domain I-Binding Factor 1Species SpecificityChromatinHistone DemethylasesHistonesKDM1A protein, humanLysinePositive Regulatory Domain I-Binding Factor 1PRDM1 protein, humanTranscription FactorsEpigeneticHuman primordial germ cellsReprograming

Identifiers

PMID27300161
PMCPMC5018215
OpenAlexW2443890241

What OpenQuestion holds

Textmetadata
LicenceTDM
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.