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To understand the roles of hesC and gcm during larval mesenchyme specification and differentiation in echinoids, we performed perturbation experiments for these genes in two distantly related euechinoids, Hemicentrotus pulcherrimus and Scaphechinus mirabilis. The number of larval mesenchyme cells increased when the translation of hesC was inhibited, thereby suggesting that hesC has a general role in larval mesenchyme development. We confirmed previous results by demonstrating that gcm is involved in pigment cell differentiation. Simultaneous inhibition of the translation of hesC and gcm induced a significant increase in the number of skeletogenic cells, which suggests that gcm functions in skeletogenic fate repression. Based on these observations, we suggest that: (i) hesC participates in some general aspects of mesenchymal cell development; and (ii) gcm is involved in the mechanism responsible for the binary specification of skeletogenic and pigment cell fates.
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http://dx.doi.org/10.1111/dgd.12277 | DOI Listing |
G3 (Bethesda)
August 2025
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
Coffin-Siris syndrome (CSS) is a rare human genetic disorder that is characterized by developmental delay, fifth digit abnormalities, and craniofacial defects. Heterozygous mutations in two SoxC proteins, SOX4 and SOX11, are associated with this disorder. C.
View Article and Find Full Text PDFFish Shellfish Immunol
October 2025
Liaoning Key Laboratory of Marine Animal Immunology and Disease Control, Dalian Ocean University, Dalian, 116023, China; Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao Marine Science and Technology Center, Qingdao, Shandong, 266237, China; Liaoning Key Laboratory of M
The transcription factor Brachyury plays a key role in mesoderm development and notochord formation in most animals. In the present study, a homologue of Brachyury with a conserved Brachyury domain was identified from the Pacific oyster Crassostrea gigas. During the embryogenesis of oyster, CgBrachyury showed high mRNA expression level from the morula to the D-shaped larval stage, with highest level in gastrula stage.
View Article and Find Full Text PDFbioRxiv
July 2025
Department of Biology, Boston University, Boston, MA 02215, United States.
Alizarin Red S (AZ) is an anthraquinone dye that is commonly used in histological studies and textiles. Exposure to AZ results in morphological perturbations in several species, including rats, frogs, and dogs; however, the mechanisms by which AZ has these effects is largely unexplored, and little is known about its effect on development. We have previously shown that AZ is teratogenic to sea urchin larvae, and that AZ was the only calcium-binding mineralization marker among five tested that perturbed skeletal patterning.
View Article and Find Full Text PDFFront Biosci (Landmark Ed)
March 2025
Department of Anatomy and Molecular Embryology, Institute of Anatomy, Ruhr-University, 44801 Bochum, Germany.
Background: The basic helix-loop-helix (bHLH) transcription factor atonal homologue 8 (Atoh8) has been implicated in various developmental and physiological processes by means of transient knockdown and conditional knockout approaches in zebrafish, chick and mouse. Despite its demonstrated involvement in multiple tissues, the role of Atoh8 remains elusive in zebrafish. A recent permanent knockout study in zebrafish investigated the role of Atoh8 on the background of previous morpholino studies which demonstrated various developmental defects but could not find any of the morpholino-based effects in the mutant.
View Article and Find Full Text PDFDev Dyn
March 2025
Department of Genetics, Development and Cell Biology, Iowa State University, Ames, Iowa, USA.
Background: The ability to generate endogenous Cre recombinase drivers using CRISPR-Cas9 knock-in technology allows lineage tracing, cell type-specific gene studies, and in vivo validation of inferred developmental trajectories from phenotypic and gene expression analyses. This report describes endogenous zebrafish hand2 Cre and CreERT2 drivers generated with GeneWeld CRISPR-Cas9 precision targeted integration.
Results: hand2-2A-cre and hand2-2A-creERT2 knock-ins crossed with ubiquitous loxP-based Switch reporters led to broad labeling in expected mesodermal and neural crest-derived lineages in branchial arches, cardiac, fin, liver, intestine, and mesothelial tissues, as well as enteric neurons.