Evidence map›Paper›PMID 39947420›Full record

ArticleDevelopmental biology2025

CMTM4 is an adhesion modulator that regulates skeletal patterning and primary mesenchyme cell migration in sea urchin embryos.

Abigail E Descoteaux, Marko Radulovic, Dona Alburi, Cynthia A Bradham

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Article in Developmental biology, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Abigail E DescoteauxDepartment of Biology, Boston University, Boston, MA, 02215, United States; Program in Molecular Biology, Cell Biology, and Biochemistry, Boston University, Boston, MA, 02215, United States; Biological Design Center, Boston University, Boston, MA, 02215, United States.
Marko RadulovicDepartment of Biology, Boston University, Boston, MA, 02215, United States; Biological Design Center, Boston University, Boston, MA, 02215, United States.
Dona AlburiDepartment of Biology, Boston University, Boston, MA, 02215, United States.
Cynthia A BradhamDepartment of Biology, Boston University, Boston, MA, 02215, United States; Program in Molecular Biology, Cell Biology, and Biochemistry, Boston University, Boston, MA, 02215, United States; Biological Design Center, Boston University, Boston, MA, 02215, United States; Program in Bioinformatics, Boston University, Boston, MA, 02215, United States. Electronic address: cbradham@bu.edu.

Funding

Spatiotemporal Regulation of Developmental Pattern FormationR35GM152180 · NIGMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI CYNTHIA A BRADHAM · 2024 to 2026
$1.3M
NIGMS NIH HHS R35 GM152180
6 · The paper itself

Abstract

MARVEL proteins, including those of the CMTM gene family, are multi-pass transmembrane proteins that play important roles in vesicular trafficking and cell migration; however, little is understood about their role in development, and their role in skeletal patterning is unexplored. CMTM4 is the only CMTM family member found in the developmental transcriptome of the sea urchin Lytechinus variegatus. Here, we validate that LvCMTM4 is a transmembrane protein and show that perturbation of CMTM4 expression via zygotic morpholino or mRNA injection perturbs skeletal patterning, resulting in loss of secondary skeletal elements and rotational defects. We also demonstrate that normal levels of CMTM4 are required for normal PMC migration and filopodial organization, and that these effects are not due to gross mis-specification of the ectoderm. Finally, we show that CMTM4 is sufficient to mediate mesenchymal cell-cell adhesion. Taken together, these data suggest that CMTM4 controls PMC migration and biomineralization via adhesive regulation during sea urchin skeletogenesis. This is the first discovery of a functionally required adhesive gene in this skeletal patterning system.

Indexed as

Body PatterningCell MovementLytechinusMARVEL Domain-Containing ProteinsMesodermSea UrchinsAnimalsCell AdhesionEmbryo, NonmammalianGene Expression Regulation, DevelopmentalMARVEL Domain-Containing ProteinsCMTM4MARVEL domainPMC adhesionPolychrome labelingSea urchinSkeletal patterning

Identifiers

PMID39947420
PMCPMC11909501

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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.