Delich, C. | Search bioRxiv

bioRxiv2025

Wnt5a gain- and loss-of-function present distinctly in craniofacial bone

IntroductionRobinow syndrome has characteristic craniofacial and dental features and can be caused by gain- or loss-of-function variants in Wnt family member 5A (WNT5A) non-canonical signaling. The craniofacial and dental manifestation of Robinow syndrome is heterogenous, as is the effect of altered Wnt5a in animal models. The relationship between Wnt5a and craniofacial and dental phenotypes is not fully understood. MethodsTo investigate the role of Wnt5a in craniofacial and dental development, we utilized a Wnt5a conditional loss-of-function (LOF: Wnt5afl/fl;Ctskcre) and a Wnt5a conditional gain-of-function (GOF: Rosa26-LSL-Wnt5a;Ctskcre) model to determine the effect of both LOF and GOF of Wnt5a in bone cells during craniofacial and dental development. Postnatal day 10 conditional LOF Wnt5a, GOF Wnt5a, and control skulls were scanned by micro-computed tomography and assessed using traditional and geometric morphometrics. Mandibular bone apoptosis was further assessed by TUNEL staining. ResultsConditional Wnt5a LOF resulted in midface hypoplasia, increased maxillary intermolar width, increased rostral basisphenoid width, and delayed molar eruption. Wnt5a LOF mandibles did not have altered bone mineral density or bone microarchitecture unlike our previous study examining Wnt5a LOF femurs. In contrast, conditional Wnt5a GOF results in macrocephaly, shortened hard palate, increased zygomatic length, micrognathia, and mandibular process morphology changes. The micrognathia and mandibular process morphology changes in the Wnt5a GOF mice were not due to increased apoptosis. A partially penetrant snout deviation was present in both the Wnt5a LOF and GOF mice. ConclusionsCraniofacial and dental phenotype differed between mice with conditional GOF and LOF of Wnt5a, consistent with the craniofacial phenotype heterogeneity in Wnt5a-associated Robinow syndrome. We detected tooth eruption delay, mandibular condyle dysmorphology, and facial asymmetry in mice with altered Wnt5a that have not been previously reported in patients. Our data suggest precise regulation of Wnt5a is essential for proper craniofacial and dental development. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=82 SRC="FIGDIR/small/665966v1_ufig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@971284org.highwire.dtl.DTLVardef@40d5f6org.highwire.dtl.DTLVardef@9f0caforg.highwire.dtl.DTLVardef@1f9ba9b_HPS_FORMAT_FIGEXP M_FIG C_FIG

developmental biology↗

bioRxiv2021

Convergent adaptation and ecological speciation result from unique genomic mechanisms in sympatric extremophile fishes

The evolution of independent lineages along replicated environmental gradients frequently results in convergent adaptation, yet the degree to which convergence is present across multiple levels of biological organization is often unclear. Additionally, inherent biases associated with shared ancestry and variation in selective regimes across geographic replicates often pose challenges for confidently identifying patterns of convergence. We investigated a system in which three species of poeciliid fishes sympatrically occur in a toxic spring rich in hydrogen sulfide (H2S) and an adjacent nonsulfidic stream to examine patterns of adaptive evolution across levels of biological organization. We found convergence in morphological and physiological traits and genome-wide patterns of gene expression among all three species. In addition, there were shared signatures of selection on genes encoding H2S toxicity targets in the mitochondrial genomes of each species. However, analyses of nuclear genomes revealed neither evidence for substantial genomic islands of divergence around genes involved in H2S toxicity and detoxification nor substantial congruence of strongly differentiated regions across population pairs. These non-convergent, heterogenous patterns of genomic divergence may indicate that sulfide tolerance is highly polygenic, with shared allele frequency shifts present at many loci with small effects along the genome. Alternatively, H2S tolerance may involve substantial genetic redundancy, with non-convergent lineage-specific variation at multiple loci along the genome underpinning similar changes in phenotypes and gene expression. Overall, we demonstrate variability in the extent of convergence across organizational levels and highlight the challenges of linking patterns of convergence across scales.

evolutionary biology↗