Evidence map›Paper›PMID 41121748›Full record

ReviewJournal of morphology2025

Investigating the Morphogenesis and Replacement of Lamprey Toothlets Using Synchrotron Imaging.

Madleen Grohganz, Jake Leyhr, Zerina Johanson, Tatjana Haitina, Sophie Sanchez, Kathleen Dollman, Jan Stundl, Marianne E Bronner, Gareth J Fraser, Philip C J Donoghue

Abstract readReview
In one paragraph

Review in Journal of morphology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Madleen GrohganzBristol Palaeobiology Group, School of Earth Sciences, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-2021-2882
Jake LeyhrDepartment of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0003-1815-7818
Zerina JohansonNatural History Museum, London, UK.ORCID https://orcid.org/0000-0002-8444-6776
Tatjana HaitinaDepartment of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-8754-5534
Sophie SanchezDepartment of Organismal Biology, Uppsala University, Uppsala, Sweden.ORCID https://orcid.org/0000-0002-3611-6836
Kathleen DollmanEuropean Synchrotron Radiation Facility, Grenoble, France.ORCID https://orcid.org/0000-0002-5468-4896
Jan StundlDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.ORCID https://orcid.org/0000-0002-3740-3378
Marianne E BronnerDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, USA.ORCID https://orcid.org/0000-0003-4274-1862
Gareth J FraserDepartment of Biology, University of Florida, Gainesville, FL, USA.ORCID https://orcid.org/0000-0002-7376-0962
Philip C J DonoghueBristol Palaeobiology Group, School of Earth Sciences, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0003-3116-7463

Funding

M.G. was supported by the Natural Environment Research Council (NE/S007504/1); T.H. was supported by the Swedish Research Council (2022-04988) and Magnus Bergvalls Stiftelse (2022-441); S.S. was awarded a grant from the Swedish research Council-Vetenskaprådet (2019-04595) to fund the workstation and software used for 3D virtual microanatomy and histology investigations; P.C.J.D. was supported by the Natural Environment Research Council (NE/G016623/1; NE/P013678/1), the Biotechnology and Biological Sciences Research Council (BB/T012773/1) and the Leverhulme Trust Research Fellowship (RF-2022-167).
6 · The paper itself

Abstract

Teeth are a key innovation that underpinned the adaptive radiation of jawed vertebrates; however, their evolutionary origin must lie with the diverse tooth-like structures of living and fossil jawless vertebrates. Most previous studies have focussed on the extinct stem-gnathostomes that phylogenetically intercalate the living jawed and jawless vertebrates. The only two extant jawless cyclostome lineages, the lampreys and hagfish bearing keratinous toothlets, have long been overlooked, though they possess complex (but unmineralised) toothlets that some have interpreted as precursors to the teeth of jawed vertebrates. Regardless of whether the toothlets of cyclostomes are homologous or convergent on the teeth of jawed vertebrates, they have the potential to offer unparalleled molecular developmental insights into the evolutionary origin of teeth. To that end, we provide a synthesis of classical literature on cyclostome toothlet structure and development, as a basis for informing future molecular studies, to which we add new insights from X-ray microtomography of three parasitic lamprey species spanning the breadth of the lamprey crown group. Based on detailed morphological analysis we describe their toothlet replacement mechanism at tissue level and uncover a relationship between toothlet size and the number of replacement cones. All examined species reveal the presence of replacement toothlets, suggesting this replacement mode is a conserved feature of the lamprey crown group. We discuss these results in comparison to hagfish, and conclude that toothlet replacement is a symplesiomorphy of cyclostomes. By describing lamprey toothlet development and replacement and comparing it with gnathostome teeth, this study lays the foundation for research into the development and evolution of teeth and tooth-like structures across vertebrate lineages.

Indexed as

LampreysMorphogenesisToothAnimalsBiological EvolutionPhylogenySynchrotronsX-Ray Microtomography

Identifiers

PMID41121748
PMCPMC12541293

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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.