Evidence map›Paper›PMID 41352383›Full record

ArticleDevelopmental biology2026

PRDM paralogs are required for Meckel's cartilage formation during mandibular bone development.

Qootsvenma Denipah-Cook, Bryanna V Saxton, Kristin B Artinger, Lomeli C Shull

Abstract read
In one paragraph

Article in Developmental biology, 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Qootsvenma Denipah-CookDepartment of Biology, University of New Mexico, Albuquerque, NM, USA.
Bryanna V SaxtonDepartment of Biology, University of New Mexico, Albuquerque, NM, USA.
Kristin B ArtingerDepartment of Diagnostic and Biological Sciences, University of Minnesota School of Dentistry, Minneapolis, MN, USA.
Lomeli C ShullDepartment of Biology, University of New Mexico, Albuquerque, NM, USA. Electronic address: lshull1@unm.edu.

Funding

Function of chromatin modifiers in cranial neural crest developmentR01DE024034 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI ARTINGER, KRISTIN, NISWANDER, LEE A. · 2015 to 2019
$3.2M
Functions of PRDM Histone Methyltransferases during Cartilage Development in the Craniofacial SkeletonR00DE031349 · NIDCR · UNIVERSITY OF NEW MEXICO · PI Lomeli Carpio Shull · 2025 to 2026
$455k
Functions of PRDM Histone Methyltransferases during Cartilage Development in the Craniofacial SkeletonK99DE031349 · NIDCR · UNIVERSITY OF NEW MEXICO · PI SHULL, LOMELI CARPIO · 2022 to 2023
$200k
NIDCR NIH HHS K99 DE031349NIDCR NIH HHS R00 DE031349NIDCR NIH HHS R01 DE024034
6 · The paper itself

Abstract

Mandibular bone development depends on the formation of a cartilaginous anlage Meckel's cartilage derived from neural crest cells (NCC) and intramembranous ossification or direct differentiation of NCCs toward osteoblasts. Wnt/β-catenin signaling drives osteogenic vs chondrogenic differentiation and must be tightly controlled during the differentiation of osteochondroprogenitors. Chromatin remodelers add hierarchal regulation to the activation and repression of crucially timed gene regulatory networks and signaling cascades. In this study, we investigated the function of two chromatin remodelers-histone methyltransferases, PRDM3 and PRDM16 during murine craniofacial development. Conditionally ablating both Prdm3 and Prdm16 in the neural crest lineage using the Wnt1-Cre driver resulted in dramatic craniofacial phenotypes, including a severely hypoplastic mandible with complete absence of Meckel's cartilage at E18.5. Focusing on the Meckel's cartilage and mandibular bone phenotype, histological analysis demonstrated a significant increase in RUNX2+ osteoblast precursors, and loss of SOX9+ chondrogenic cells, suggesting an increase in osteoblast progenitors at the expense of chondrocytes that would otherwise form the Meckel's cartilage. This was not due to alterations in proliferation or apoptosis, as we observed no significant changes in the number of phosphoH3+ or cleaved caspase3+ cells in the mandibular process at E11.5, suggesting lack of NCC-derived chondrocytes is due to a change in NCC osteochondroprogenitor fate decisions. mRNA transcripts and protein abundance of Wnt/β-catenin signaling components were elevated in the mandibular process during initial NCC osteochondroprogenitor condensation events, suggesting PRDM3 and PRDM16 normally restrict expression of Wnt/β-catenin signaling components during NCC-derived osteochondroprogenitor differentiation to promote chondrogenesis and Meckel's cartilage formation. Taken together, PRDM3 and PRDM16 are required for NCC differentiation toward chondrocytes during Meckel's cartilage formation by controlling proper spatiotemporal Wnt/β-catenin transcriptional activity and this process is necessary for morphogenesis of the developing mandible.

Indexed as

Bone DevelopmentCartilageDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseMandibleTranscription FactorsAnimalsCell DifferentiationChondrocytesChondrogenesisGene Expression Regulation, DevelopmentalMiceNeural CrestOsteoblastsOsteogenesisWnt Signaling PathwayDNA-Binding ProteinsHistone-Lysine N-MethyltransferasePrdm16 protein, mouseTranscription FactorsCraniofacialMeckel's cartilageMecom/Evi1Prdm16Prdm3Wnt/β-catenin

Identifiers

PMID41352383
PMCPMC12747729

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.