Evidence map›Paper›PMID 33689235›Full record

ArticleJournal of experimental zoology. Part B, Molecular and developmental evolution2022

Measuring potential effects of the developmental burden associated with the vertebrate notochord.

Satoko Fujimoto, Kaori Yamanaka, Chiharu Tanegashima, Osamu Nishimura, Shigehiro Kuraku, Shigeru Kuratani, Naoki Irie

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental zoology. Part B, Molecular and developmental evolution, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Article
  3. Measuring potential effects of the developmental burden associated with the vertebrate notochord.Journal of experimental zoology. Part B, Molecular and developmental evolution · 2022
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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

7 authors at 2 institutions in 1 country.

Satoko FujimotoRIKEN, Center for Biosystems Dynamics Research, Kobe, Japan.
Kaori YamanakaRIKEN, Center for Biosystems Dynamics Research, Kobe, Japan.
Chiharu TanegashimaRIKEN, Center for Biosystems Dynamics Research, Kobe, Japan.
Osamu NishimuraRIKEN, Center for Biosystems Dynamics Research, Kobe, Japan.
Shigehiro KurakuRIKEN, Center for Biosystems Dynamics Research, Kobe, Japan.
Shigeru KurataniRIKEN, Center for Biosystems Dynamics Research, Kobe, Japan.ORCID 0000-0001-9717-7221
Naoki IrieDepartment of Biological Sciences, The University of Tokyo, Tokyo, Japan.ORCID 0000-0002-6720-381X
RIKEN Center for Biosystems Dynamics Research · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The notochord functions primarily as a supporting tissue to maintain the anteroposterior axis of primitive chordates, a function that is replaced entirely by the vertebral column in many vertebrates. The notochord still appears during vertebrate embryogenesis and plays a crucial role in the developmental pattern formation of surrounding structures, such as the somites and neural tube, providing the basis for the vertebrate body plan. The indispensable role of the notochord has often been referred to as the developmental burden and used to explain the evolutionary conservation of notochord; however, the existence of this burden has not been successfully exemplified so far. Since the adaptive value of target tissues appears to result in the evolutionary conservation of upstream structures through the developmental burden, we performed comparative gene expression profiling of the notochord, somites, and neural tube during the mid-embryonic stages in turtles and chicken to measure their evolutionary conservation. When compared with the somites and neural tube, overall gene expression profiles in the notochord showed significantly lower or merely comparable levels of conservation. However, genes involved in inductive signalings, such as the sonic hedgehog (Shh) cascade and the formation of functional primary cilia, showed relatively higher levels of conservation in all the three structures analyzed. Collectively, these results suggest that shh signals are critical as the inductive source and receiving structures, possibly constituting the inter-dependencies of developmental burden.

Indexed as

Hedgehog ProteinsNotochordAnimalsGene Expression Regulation, DevelopmentalSignal TransductionSomitesVertebratesHedgehog Proteinsdevelopmental burdenevolutiongene expression profilenotochordphylotypic period

Identifiers

PMID33689235
PMCPMC9291948
OpenAlexW3135864414

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.