Evidence map›Paper›PMID 23893501›Full record

ReviewMolecular reproduction and development2014

Epigenetic control of cell fate in mouse blastocysts: the role of covalent histone modifications and chromatin remodeling.

Soumen Paul, Jason G Knott

Open access · bronzeAbstract readReview
In one paragraph

Review in Molecular reproduction and development, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

32 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Early embryonic lethality of mice lacking POLD2.Molecular reproduction and development · 2023
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. SUV39H2 controls trophoblast stem cell fate.Biochimica et biophysica acta. General subjects · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

2 authors at 2 institutions in 1 country.

Soumen PaulDepartment of Pathology and Laboratory Medicine, University of Kansas Medical Center, Kansas City, Kansas; Institute of Reproductive Health and Regenerative Medicine, University of Kansas Medical Center, Kansas City, Kansas.
Jason G Knott
Michigan State University · USUniversity of Kansas · US

Funding

GATA Factor Function in TrophoblastR01HD062546 · NICHD · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Soumen Paul, Geetu Tuteja · 2010 to 2026
$4.9M
Role of Brg1 in Embryo Development and PluripotencyR01GM095347 · NIGMS · MICHIGAN STATE UNIVERSITY · PI KNOTT, JASON GLENN · 2010 to 2013
$1.1M
Protein Kinase C Signaling and Pluripotent Stem CellR21HL104322 · NHLBI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI PAUL, SOUMEN · 2011 to 2012
$413k
Histone Chaperones in AngiogenesisR21HL106311 · NHLBI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI PAUL, SOUMEN · 2011 to 2012
$413k
NHLBI NIH HHS HL104322NHLBI NIH HHS HL106311NHLBI NIH HHS R21 HL104322NHLBI NIH HHS R21 HL106311NICHD NIH HHS HD062546NICHD NIH HHS R01 HD062546NIGMS NIH HHS GM095347NIGMS NIH HHS R01 GM095347
6 · The paper itself

Abstract

The first cell-fate decision in mammalian preimplantation embryos is the segregation of the inner cell mass (ICM) and trophectoderm (TE) cell lineages. The ICM develops into the embryo proper, whereas the TE ensures embryo implantation and is the source of the extra-embryonic trophoblast cell lineages, which contribute to the functional components of the placenta. The development of a totipotent zygote into a multi-lineage blastocyst is associated with the generation of distinct transcriptional programs. Several key transcription factors participate in the ICM and TE-specific transcriptional networks, and recent studies indicate that post-translational histone modifications as well as ATP-dependent chromatin remodeling complexes converge with these transcriptional networks to regulate ICM and TE lineage specification. This review will discuss our current understanding and future perspectives related to transcriptional and epigenetic regulatory mechanisms that are implicated in the initial mammalian lineage commitment steps, with a focus on events in mice.

Indexed as

BlastocystCell LineageChromatin Assembly and DisassemblyEpigenesis, GeneticAnimalsCell DifferentiationGene Expression Regulation, DevelopmentalHistonesMiceHistoneschromatin remodelinghistone modificationsinner cell masslineage commitmenttrophectoderm

Identifiers

PMID23893501
PMCPMC4276566
OpenAlexW1495384791

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.