Evidence map›Paper›PMID 42368449›Full record

ReviewFrontiers in cell and developmental biology2026

Exit from totipotency in mammals: an epigenetic perspective.

Sergio Ruiz

Abstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Sergio RuizLaboratory of Genome Integrity, Center for Cancer Research/National Cancer Institute, National Institutes of Health (CCR/NCI/NIH), Bethesda, MD, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Totipotency is the ability of a single cell to generate a whole organism and is a property restricted to the cells of the earliest embryonic developmental stages. Interestingly, the process of zygotic genome activation (ZGA), which mediates in the embryo the switch from maternal inherited RNAs to embryonic transcripts, has been associated with the loss of totipotency potential. The exit from totipotency correlates with the quick and efficient silencing of a totipotent-associated stage-specific transcriptional program triggered during ZGA. Importantly, the timely and efficient silencing is required for proper embryonic development. However, the molecular mechanisms underlying the activation and subsequent silencing of this program remain elusive. This review will focus on an overlooked aspect associated with ZGA in mice that involves the control over the transient expression of the totipotent-associated transcriptional program. Furthermore, we will discuss the level of conservation of these mechanisms in humans.

Indexed as

ESC (embryonic stem cells)totipotencytotipotent-associated transcriptional programtransposable elements (TEs)ZGA

Identifiers

PMID42368449
PMCPMC13294343

What OpenQuestion holds

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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.