Evidence map›Paper›PMID 42848847›Full record

ArticleG3 (Bethesda, Md.)2026

Genetic analysis of bone morphometry and ivory vertebrae in threespine stickleback.

Veronica C Behrens, David Lee, Julia I Wucherpfennig, David M Kingsley

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Article in G3 (Bethesda, Md.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Veronica C BehrensDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.ORCID 0000-0002-2006-9350
David LeeDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.
Julia I WucherpfennigDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.
David M KingsleyDepartment of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.ORCID 0000-0002-6401-6461

Funding

Howard Hughes Medical InstituteNIH HHS 2T32GM007790Stanford Vice Provost for Undergraduate Education Developmental Biology Departmental
6 · The paper itself

Abstract

Previous genetic studies of skeletal variation in threespine stickleback fish (Gasterosteus aculeatus) have focused primarily on striking morphological differences. Here, we examine the largely unexplored genetic architecture of internal bone microstructural variation between marine and freshwater stickleback. Micro-computed tomography X-ray analysis revealed differences in the porosity, bone thickness, and bone volume fraction within armor plates and vertebrae from a marine and freshwater stickleback. Quantitative trait locus mapping in F2 progeny from a marine × freshwater stickleback cross identified a significant locus on chromosome 4 influencing multiple aspects of armor plate internal microstructure. This locus overlaps the well-characterized Eda region previously known to control armor plate number and size. Co-mapping of bone microstructure could be due to pleiotropic effects of Eda on multiple aspects of plate development or to changes in closely linked genes including Itm2a, which also plays a role in bone formation. Most bone microstructure traits in vertebrae showed weak or no genetic signal, consistent with a polygenic architecture. However, we identified a highly significant locus on chromosome 17 that is strongly associated with abnormally thickened "ivory vertebrae" that occurred in 8.4% of F2 offspring. This phenotype resembles Paget's disease in humans, and the major locus region contains Tnfrsf1b, the stickleback ortholog of a human Paget's disease susceptibility gene TNFRSF11A. Together, our findings identify genetic loci underlying natural variation in bone microstructure in wild fish and reveal a candidate gene associated with a disease-like skeletal phenotype, highlighting stickleback as a model for studying both evolutionary and pathological bone biology.

Indexed as

bone microstructurebone morphometryEdaevolutionItm2aivory vertebraePaget’s diseaseQTL mappingsupergenesthreespine sticklebackTNFRSF11ATnfrsf1b

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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.