Evidence map›Paper›PMID 33597570›Full record

ArticleScientific reports2021

Using linkage logic theory to control dynamics of a gene regulatory network of a chordate embryo.

Kenji Kobayashi, Kazuki Maeda, Miki Tokuoka, Atsushi Mochizuki, Yutaka Satou

Abstract read
In one paragraph

Article in Scientific reports, 2021. 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. Network topology creates independent control of multiple checkpoints in the cell cycle system.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Mathematical modeling for developmental processes.Development, growth & differentiation · 2023
    Review
  4. Article
  5. Leveraging network structure in nonlinear control.NPJ systems biology and applications · 2022
    Review
  6. NETISCE: a network-based tool for cell fate reprogramming.NPJ systems biology and applications · 2022
    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

5 authors.

Kenji KobayashiDepartment of Zoology, Graduate School of Science, Kyoto University, Sakyo, Kyoto, 606-8502, Japan.
Kazuki MaedaFaculty of Informatics, The University of Fukuchiyama, 3370 Hori, Fukuchiyama, Kyoto, 620-0886, Japan.
Miki TokuokaDepartment of Zoology, Graduate School of Science, Kyoto University, Sakyo, Kyoto, 606-8502, Japan.
Atsushi MochizukiInstitute for Frontier Life and Medical Sciences, Kyoto University, Sakyo, Kyoto, 606-8507, Japan. mochi@infront.kyoto-u.ac.jp.
Yutaka SatouDepartment of Zoology, Graduate School of Science, Kyoto University, Sakyo, Kyoto, 606-8502, Japan. yutaka@ascidian.zool.kyoto-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Linkage logic theory provides a mathematical criterion to control network dynamics by manipulating activities of a subset of network nodes, which are collectively called a feedback vertex set (FVS). Because many biological functions emerge from dynamics of biological networks, this theory provides a promising tool for controlling biological functions. By manipulating the activity of FVS molecules identified in a gene regulatory network (GRN) for fate specification of seven tissues in ascidian embryos, we previously succeeded in reproducing six of the seven cell types. Simultaneously, we discovered that the experimentally reconstituted GRN lacked information sufficient to reproduce muscle cells. Here, we utilized linkage logic theory as a tool to find missing edges in the GRN. Then, we identified a FVS from an updated version of the GRN and confirmed that manipulating the activity of this FVS was sufficient to induce all seven cell types, even in a multi-cellular environment. Thus, linkage logic theory provides tools to find missing edges in experimentally reconstituted networks, to determine whether reconstituted networks contain sufficient information to fulfil expected functions, and to reprogram cell fate.

Indexed as

Models, BiologicalAnimalsCell DifferentiationChordataEmbryonic DevelopmentGene Expression Regulation, DevelopmentalGene Regulatory NetworksHumansMuscle CellsReproductionSignal TransductionSystems Biology

Identifiers

PMID33597570
PMCPMC7889898

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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.