Evidence map›Paper›PMID 22897771›Full record

ArticleStem cells and development2013

Functional analysis of Rex1 during preimplantation development.

María Climent, Sonia Alonso-Martin, Raquel Pérez-Palacios, Diana Guallar, Alfredo A Benito, Ana Larraga, Marta Fernández-Juan, Marta Sanz, Alicia de Diego, María T Seisdedos and 2 more

Abstract read
In one paragraph

Article in Stem cells and development, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Rlim/Rnf12, Rex1, and X Chromosome Inactivation.Frontiers in cell and developmental biology · 2019
    Article
  5. Article
  6. Article
  7. Article
  8. Pluripotency Factors on Their Lineage Move.Stem cells international · 2016
    Review
  9. The molecular underpinnings of totipotency.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2014
    Review
  10. Review
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

12 authors at 4 institutions in 1 country.

María ClimentDepartamento de Anatomía, Embriología y Genética Animal, Facultad de Veterinaria, Universidad de Zaragoza, Zaragoza, Spain.
Sonia Alonso-Martin
Raquel Pérez-Palacios
Diana Guallar
Alfredo A Benito
Ana Larraga
Marta Fernández-Juan
Marta Sanz
Alicia de Diego
María T Seisdedos
Pedro Muniesa
Jon Schoorlemmer
Instituto Aragonés de Ciencias de la Salud · ESCentro de Investigaciones Biológicas Margarita Salas · ESUniversidad de Zaragoza · ESFundacion Agencia Aragonesa para la Investigacion y el Desarrollo · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rex1/Zfp42 is a nuclear protein that is highly conserved in mammals, and widely used as an embryonic stem (ES) cell marker. Although Rex1 expression is associated with enhanced pluripotency, loss-of-function models recently described do not exhibit major phenotypes, and both preimplantation development and ES cell derivation appear normal in the absence of Rex1. To better understand the functional role of Rex1, we examined the expression and localization of Rex1 during preimplantation development. Our studies indicated that REX1 is expressed at all stages during mouse preimplantation development, with a mixed pattern of nuclear, perinuclear, and cytoplasmic localization. Chromatin association seemed to be altered in 8-cell embryos, and in the blastocyst, we found REX1 localized almost exclusively in the nucleus. A functional role for Rex1 in vivo was assessed by gain- and loss-of-function approaches. Embryos with attenuated levels of Rex1 after injection of zygotes with siRNAs did not exhibit defects in preimplantation development in vitro. In contrast, overexpression of Rex1 interfered with cleavage divisions and with proper blastocyst development, although we failed to detect alterations in the expression of lineage and pluripotency markers. Rex1 gain- and loss-of-function did alter the expression levels of Zscan4, an important regulator of preimplantation development and pluripotency. Our results suggest that Rex1 plays a role during preimplantation development. They are compatible with a role for Rex1 during acquisition of pluripotency in the blastocyst.

Indexed as

Embryonic DevelopmentAnimalsBlastocystCell NucleusEmbryo Culture TechniquesGene ExpressionGene Expression Regulation, DevelopmentalGene Knockdown TechniquesMiceProtein TransportRNA, Small InterferingTranscription FactorsRNA, Small InterferingTranscription FactorsZfp42 protein, mouse

Identifiers

PMID22897771
PMCPMC3549625
OpenAlexW2020959006

What Socratic holds

Textmetadata
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 Socratic graph.