Evidence map›Paper›PMID 25897685›Full record

ArticleBMC developmental biology2015

Sprouty gene dosage influences temporal-spatial dynamics of primary enamel knot formation.

Katerina Lochovska, Renata Peterkova, Zuzana Pavlikova, Maria Hovorakova

Open access · hybridAbstract read
In one paragraph

Article in BMC developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Genetic Aspects of Dental Erosive Wear and Dental Caries.International journal of dentistry · 2021
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. From snapshots to movies: Understanding early tooth development in four dimensions.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  10. 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

4 authors at 1 institution in 1 country.

Katerina LochovskaInstitute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, Czech Republic. lochovska@biomed.cas.cz.
Renata PeterkovaInstitute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, Czech Republic. repete@biomed.cas.cz.
Zuzana PavlikovaInstitute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, Czech Republic. pavlikova@biomed.cas.cz.
Maria HovorakovaInstitute of Experimental Medicine, Academy of Sciences of the Czech Republic, Prague, Czech Republic. marhor@biomed.cas.cz.
Czech Academy of Sciences, Institute of Experimental Medicine · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe mouse embryonic mandible comprises two types of tooth primordia in the cheek region: progressive tooth primordia of prospective functional teeth and rudimentary tooth primordia in premolar region - MS and R2. Mice lacking Sprouty genes develop supernumerary tooth in front of the lower M1 (first molar) primordium during embryogenesis. We focused on temporal-spatial dynamics of Sonic Hedgehog expression as a marker of early odontogenesis during supernumerary tooth development.

resultsUsing mouse embryos with different dosages of Spry2 and Spry4 genes, we showed that during the normal development of M1 in the mandible the sooner appearing Shh signaling domain of the R2 bud transiently coexisted with the later appearing Shh expression domain in the early M1 primordium. Both domains subsequently fused together to form the typical signaling center representing primary enamel knot (pEK) of M1 germ at embryonic day (E) 14.5. However, in embryos with lower Spry2;Spry4 gene dosages, we observed a non-fusion of original R2 and M1 Shh signaling domains with consequent formation of a supernumerary tooth primordium from the isolated R2 bud.

conclusionsOur results bring new insight to the development of the first lower molar of mouse embryos and define simple tooth unit capable of individual development, as well as determine its influence on normal and abnormal development of the tooth row which reflect evolutionarily conserved tooth pattern. Our findings contribute significantly to existing knowledge about supernumerary tooth formation.

Indexed as

Gene DosageAnimalsCell LineageDental EnamelEmbryo, MammalianHedgehog ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsMiceMice, KnockoutNerve Tissue ProteinsProtein Serine-Threonine KinasesHedgehog ProteinsIntracellular Signaling Peptides and ProteinsMembrane ProteinsNerve Tissue ProteinsProtein Serine-Threonine KinasesShh protein, mouseSpry2 protein, mouseSpry4 protein, mouse

Identifiers

PMID25897685
PMCPMC4425875
OpenAlexW1990297022

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LicenceCC BY
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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.