Evidence map›Paper›PMID 31122174›Full record

ReviewStem cells and development2019

On Mammalian Totipotency: What Is the Molecular Underpinning for the Totipotency of Zygote?

Kejin Hu

Abstract readReview
In one paragraph

Review in Stem cells and development, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
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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.

Kejin HuDepartment of Biochemistry and Molecular Genetics, University of Alabama at Birmingham, Birmingham, Alabama.

Funding

BET Regulation of Mitosis and Pluripotency EstablishmentR01GM127411 · NIGMS · UNIVERSITY OF NORTH TEXAS HLTH SCI CTR · PI HU, KEJIN · 2018 to 2022
$1.6M
NIGMS NIH HHS R01 GM127411
6 · The paper itself

Abstract

The mammalian zygote is described as a totipotent cell in the literature, but this characterization is elusive ignoring the molecular underpinnings. Totipotency can connote genetic totipotency, epigenetic totipotency, or the reprogramming capacity of a cell to epigenetic totipotency. Here, the implications of these concepts are discussed in the context of the properties of the zygote. Although genetically totipotent as any diploid somatic cell is, a zygote seems not totipotent transcriptionally, epigenetically, or functionally. Yet, a zygote may retain most of the key factors from its parental oocyte to reprogram an implanted differentiated genome or the zygote genome toward totipotency. This totipotent reprogramming process may extend to blastomeres in the two-cell-stage embryo. Thus, a revised alternative model of mammalian cellular totipotency is proposed, in which an epigenetically totipotent cell exists after the major embryonic genome activation and before the separation of the first two embryonic lineages.

Indexed as

AnimalsCell DifferentiationEmbryo, MammalianEpigenesis, GeneticGene Expression Regulation, DevelopmentalHumansZygoteblastomereembryogenesisembryonic stem cellsepigenetic totipotencyreprogrammingtotipotencyzygote

Identifiers

PMID31122174
PMCPMC6648208

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.