Evidence map›Paper›PMID 27152625›Full record

ArticlePLoS genetics2016

A Maternal System Initiating the Zygotic Developmental Program through Combinatorial Repression in the Ascidian Embryo.

Izumi Oda-Ishii, Atsushi Kubo, Willi Kari, Nobuhiro Suzuki, Ute Rothbächer, Yutaka Satou

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 49 citations in OpenAlex.

  1. Temporal neuronal differentiation programs safeguard neuronal diversity.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Cell numbers contribute to cell fate during Ciona cardiopharyngeal mesoderm specification.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Ascidian gene regulation and bioadhesion.Genesis (New York, N.Y. : 2000) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Quantitative Dissection of the ProximalFrontiers in cell and developmental biology · 2021
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Outstanding questions in developmental ERK signaling.Development (Cambridge, England) · 2018
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Izumi Oda-IshiiDepartment of Zoology, Graduate School of Science, Kyoto University, Kita-Shirakawa Oiwake-cho, Sakyo, Kyoto, Japan.
Atsushi KuboDepartment of Zoology, Graduate School of Science, Kyoto University, Kita-Shirakawa Oiwake-cho, Sakyo, Kyoto, Japan.
Willi KariDepartment of Evolution and Developmental Biology, Zoological Institute, University Innsbruck, Innsbruck, Austria.
Nobuhiro SuzukiDepartment of Zoology, Graduate School of Science, Kyoto University, Kita-Shirakawa Oiwake-cho, Sakyo, Kyoto, Japan.
Ute RothbächerDepartment of Evolution and Developmental Biology, Zoological Institute, University Innsbruck, Innsbruck, Austria.
Yutaka SatouDepartment of Zoology, Graduate School of Science, Kyoto University, Kita-Shirakawa Oiwake-cho, Sakyo, Kyoto, Japan.ORCID 0000-0001-5193-0708
Kyoto University · JPUniversität Innsbruck · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maternal factors initiate the zygotic developmental program in animal embryos. In embryos of the chordate, Ciona intestinalis, three maternal factors-Gata.a, β-catenin, and Zic-r.a-are required to establish three domains of gene expression at the 16-cell stage; the animal hemisphere, vegetal hemisphere, and posterior vegetal domains. Here, we show how the maternal factors establish these domains. First, only β-catenin and its effector transcription factor, Tcf7, are required to establish the vegetal hemisphere domain. Second, genes specifically expressed in the posterior vegetal domain have additional repressive cis-elements that antagonize the activity of β-catenin/Tcf7. This antagonizing activity is suppressed by Zic-r.a, which is specifically localized in the posterior vegetal domain and binds to DNA indirectly through the interaction with Tcf7. Third, Gata.a directs specific gene expression in the animal hemisphere domain, because β-catenin/Tcf7 weakens the Gata.a-binding activity for target sites through a physical interaction in the vegetal cells. Thus, repressive regulation through protein-protein interactions among the maternal transcription factors is essential to establish the first distinct domains of gene expression in the chordate embryo.

Indexed as

Animalsbeta CateninBlastomeresBody PatterningCiona intestinalisEmbryonic DevelopmentGATA Transcription FactorsGene Expression Regulation, DevelopmentalIn Situ HybridizationProtein Interaction MapsSequence Analysis, DNAT Cell Transcription Factor 1Zygotebeta CateninGATA Transcription FactorsT Cell Transcription Factor 1

Identifiers

PMID27152625
PMCPMC4859511
OpenAlexW2346784459

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.