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Advanced Cell Diagnostics Inc rnascope probe dact2
( A–C ) Representative images of wholemount in situ hybridization showing dact1 , <t>dact2</t> , and wnt11f2 gene expression patterns. ( A ) At 8 hpf, dact2 and wnt11f2 are highly expressed in the dorsal margin and presumptive Nieuwkoop center of the gastrulating embryo, with dact1 being weakly detected (arrowhead). In contrast to wnt11f2 , dact1 , and dact2 are expressed in the presumptive dorsal mesoderm (asterisk). ( B ) Lateral (anterior to the left of page) and anterior (dorsal side toward top of page) views of bud-stage embryos. dact2 and wnt11f2 transcripts are both detected in the tailbud (asterisk) while dact2 is additionally expressed in the axial mesoderm (arrow). dact1 gene expression is concentrated to the paraxial mesoderm and the neuroectoderm (open arrowheads). ( C ) Lateral and flat-mount views of 4 ss embryos. dact2 is expressed in the anterior neural plate and polster (P), notochord (N), paraxial and presomitic mesoderm (PM) and tailbud (TB). In contrast, dact1 is expressed in the midbrain (MB) and the paraxial and presomitic mesoderm. ( D, E ) Representative lateral (anterior to left of page) images of wholemount in situ hybridization showing dact1 and dact2 expression patterns. ( D ) At 24 hpf expression is detected in the developing head. ( E ) At 48 hpf expression is detected in the developing craniofacial structures (arrow). ( F ) Representative images of RNAscope in situ hybridization analysis of dact1 (white) and dact2 (yellow) and irf6 (green) expression in transverse section of 72 hpf embryos. dact1 is expressed in the ethmoid plate (ep) and palatoquadrate (pq) orofacial cartilage, while dact2 is expressed in the oral epithelium (oe). The epithelial marker irf6 is expressed in the oe and surface epithelium (se). Dapi (blue). Scale bar: 100 μm.
Rnascope Probe Dact2, supplied by Advanced Cell Diagnostics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rnascope probe dact2/product/Advanced Cell Diagnostics Inc
Average 90 stars, based on 1 article reviews
rnascope probe dact2 - by Bioz Stars, 2026-05
90/100 stars

Images

1) Product Images from "Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis"

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

Journal: eLife

doi: 10.7554/eLife.91648

( A–C ) Representative images of wholemount in situ hybridization showing dact1 , dact2 , and wnt11f2 gene expression patterns. ( A ) At 8 hpf, dact2 and wnt11f2 are highly expressed in the dorsal margin and presumptive Nieuwkoop center of the gastrulating embryo, with dact1 being weakly detected (arrowhead). In contrast to wnt11f2 , dact1 , and dact2 are expressed in the presumptive dorsal mesoderm (asterisk). ( B ) Lateral (anterior to the left of page) and anterior (dorsal side toward top of page) views of bud-stage embryos. dact2 and wnt11f2 transcripts are both detected in the tailbud (asterisk) while dact2 is additionally expressed in the axial mesoderm (arrow). dact1 gene expression is concentrated to the paraxial mesoderm and the neuroectoderm (open arrowheads). ( C ) Lateral and flat-mount views of 4 ss embryos. dact2 is expressed in the anterior neural plate and polster (P), notochord (N), paraxial and presomitic mesoderm (PM) and tailbud (TB). In contrast, dact1 is expressed in the midbrain (MB) and the paraxial and presomitic mesoderm. ( D, E ) Representative lateral (anterior to left of page) images of wholemount in situ hybridization showing dact1 and dact2 expression patterns. ( D ) At 24 hpf expression is detected in the developing head. ( E ) At 48 hpf expression is detected in the developing craniofacial structures (arrow). ( F ) Representative images of RNAscope in situ hybridization analysis of dact1 (white) and dact2 (yellow) and irf6 (green) expression in transverse section of 72 hpf embryos. dact1 is expressed in the ethmoid plate (ep) and palatoquadrate (pq) orofacial cartilage, while dact2 is expressed in the oral epithelium (oe). The epithelial marker irf6 is expressed in the oe and surface epithelium (se). Dapi (blue). Scale bar: 100 μm.
Figure Legend Snippet: ( A–C ) Representative images of wholemount in situ hybridization showing dact1 , dact2 , and wnt11f2 gene expression patterns. ( A ) At 8 hpf, dact2 and wnt11f2 are highly expressed in the dorsal margin and presumptive Nieuwkoop center of the gastrulating embryo, with dact1 being weakly detected (arrowhead). In contrast to wnt11f2 , dact1 , and dact2 are expressed in the presumptive dorsal mesoderm (asterisk). ( B ) Lateral (anterior to the left of page) and anterior (dorsal side toward top of page) views of bud-stage embryos. dact2 and wnt11f2 transcripts are both detected in the tailbud (asterisk) while dact2 is additionally expressed in the axial mesoderm (arrow). dact1 gene expression is concentrated to the paraxial mesoderm and the neuroectoderm (open arrowheads). ( C ) Lateral and flat-mount views of 4 ss embryos. dact2 is expressed in the anterior neural plate and polster (P), notochord (N), paraxial and presomitic mesoderm (PM) and tailbud (TB). In contrast, dact1 is expressed in the midbrain (MB) and the paraxial and presomitic mesoderm. ( D, E ) Representative lateral (anterior to left of page) images of wholemount in situ hybridization showing dact1 and dact2 expression patterns. ( D ) At 24 hpf expression is detected in the developing head. ( E ) At 48 hpf expression is detected in the developing craniofacial structures (arrow). ( F ) Representative images of RNAscope in situ hybridization analysis of dact1 (white) and dact2 (yellow) and irf6 (green) expression in transverse section of 72 hpf embryos. dact1 is expressed in the ethmoid plate (ep) and palatoquadrate (pq) orofacial cartilage, while dact2 is expressed in the oral epithelium (oe). The epithelial marker irf6 is expressed in the oe and surface epithelium (se). Dapi (blue). Scale bar: 100 μm.

Techniques Used: In Situ Hybridization, Gene Expression, Expressing, RNAscope, Marker

( A ) Schematic representations of dact1 and dact2 exons, positions of guide RNA target site, introduced premature stop codon (arrow), and sequences of mutations. ( B ) DNA fragment analysis of dact1+/- and dact2+/- animals showing wildtype (250 and 387 bp, respectively) and mutant (228 and 380 bp, respectively). ( C ) Expression levels of dact1 and dact2 mRNA by RT-qPCR in 12 hpf dact1−/− mutants, dact2−/− mutants, and dact1/2−/− compound mutants. Eight embryos were pooled for mRNA isolation per sample. ( D ) Injection of dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA rescues the rod-shaped ethmoid plate phenotype in dact1/2−/− compound mutants. Representative images of Alcian blue stained dact1/2−/− double mutant treated with 300 pg dact1 mRNA and 300 pg dact2 mRNA. Arrow highlights normal ethmoid plate (EP). Visceral cartilage (VC) also appeared normal. ( E ) Quantification of the mutant craniofacial phenotype observed in a dact1−/−,dact2+/- breeding in-cross. Without mRNA injection, the mutant phenotype was observed at approximately (35%) the expected Mendelian ratio of 25%. Injection with dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA decreased the frequency that the mutant craniofacial phenotype was observed.
Figure Legend Snippet: ( A ) Schematic representations of dact1 and dact2 exons, positions of guide RNA target site, introduced premature stop codon (arrow), and sequences of mutations. ( B ) DNA fragment analysis of dact1+/- and dact2+/- animals showing wildtype (250 and 387 bp, respectively) and mutant (228 and 380 bp, respectively). ( C ) Expression levels of dact1 and dact2 mRNA by RT-qPCR in 12 hpf dact1−/− mutants, dact2−/− mutants, and dact1/2−/− compound mutants. Eight embryos were pooled for mRNA isolation per sample. ( D ) Injection of dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA rescues the rod-shaped ethmoid plate phenotype in dact1/2−/− compound mutants. Representative images of Alcian blue stained dact1/2−/− double mutant treated with 300 pg dact1 mRNA and 300 pg dact2 mRNA. Arrow highlights normal ethmoid plate (EP). Visceral cartilage (VC) also appeared normal. ( E ) Quantification of the mutant craniofacial phenotype observed in a dact1−/−,dact2+/- breeding in-cross. Without mRNA injection, the mutant phenotype was observed at approximately (35%) the expected Mendelian ratio of 25%. Injection with dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA decreased the frequency that the mutant craniofacial phenotype was observed.

Techniques Used: Mutagenesis, Expressing, Quantitative RT-PCR, Isolation, Injection, Staining

( A ) Inter-cross of compound heterozygotes yield embryos with different degrees of axis extension that correspond to the dact1 and dact2 genotypes. Representative lateral images of embryos at 12 hpf. The yellow line indicates body axis angle measured from the anterior point of the head, the center of the yolk, to the end of the tail. ( B ) Quantification of body axis angle. Numbers represent the difference in angle relative to the average wildtype embryo. Asterisk indicates genotypes with angles significantly different from wildtype. ANOVA p < 0.5 n = 3–21 embryos. Error bars: ± SEM. ( C ) Representative bud stage wildtype and dact1/2−/− mutant embryos stained for gsc (prechordal plate), pax2a (midbrain/hindbrain boundary), and krox20 (rhombomere 3). Asterisk indicates lack of krox20 expression in dact1/2−/− mutant. Scale bar = 200 μm ( D ) Representative flat mounts of 1–2 ss wildtype and dact1/2 mutant embryos stained for zic1 (telencephalon), pax2a and tbx6 (ventrolateral mesoderm). ( E ) Representative flat mounts of 10 ss wildtype and dact1/2−/− mutant embryos stained for ctsl1b (hatching gland), zic1 , pax2a , krox20 , and myo1d (somites).
Figure Legend Snippet: ( A ) Inter-cross of compound heterozygotes yield embryos with different degrees of axis extension that correspond to the dact1 and dact2 genotypes. Representative lateral images of embryos at 12 hpf. The yellow line indicates body axis angle measured from the anterior point of the head, the center of the yolk, to the end of the tail. ( B ) Quantification of body axis angle. Numbers represent the difference in angle relative to the average wildtype embryo. Asterisk indicates genotypes with angles significantly different from wildtype. ANOVA p < 0.5 n = 3–21 embryos. Error bars: ± SEM. ( C ) Representative bud stage wildtype and dact1/2−/− mutant embryos stained for gsc (prechordal plate), pax2a (midbrain/hindbrain boundary), and krox20 (rhombomere 3). Asterisk indicates lack of krox20 expression in dact1/2−/− mutant. Scale bar = 200 μm ( D ) Representative flat mounts of 1–2 ss wildtype and dact1/2 mutant embryos stained for zic1 (telencephalon), pax2a and tbx6 (ventrolateral mesoderm). ( E ) Representative flat mounts of 10 ss wildtype and dact1/2−/− mutant embryos stained for ctsl1b (hatching gland), zic1 , pax2a , krox20 , and myo1d (somites).

Techniques Used: Mutagenesis, Staining, Expressing

( A ) Representative brightfield images of wildtype and dact1/2−/− compound mutants at 4 dpf. 100 individuals were analyzed from a dact1/2 +/- double het cross. Lateral and ventral views show d act1/2−/− compound mutants have a hypoplastic midface, medially displaced eyes, and a displaced lower jaw. ( B ) Representative flat-mount images of Alcian blue stained ethmoid plate (EP) and visceral cartilage (VC) elements from 4 dpf wildtype and d act1/2−/− compound mutants. d act1/2−/− mutants have a rod-shaped EP with no distinct lateral and medial elements. No obvious differences were found in dact1/2 mutant VC. ( C ) Representative brightfield image of 4 dpf wildtype and dact1/2−/− mutant. Bar indicates vertebral spine length. Scale bar: 100 μm. ( D ) Representative images of Alcian blue stained dact1/2−/− , wnt11f2−/− , and wnt11f2−/− , dact1 / 2 −/− compound mutants. Embryos resulted from a dact1+/-,dact2+/-,wnt11f2+/- in-cross. Lateral and ventral views show similar craniofacial phenotypes in each mutant. ( E ) Representative flat-mount images of Alcian blue stained EP show a similar phenotype between dact1/2−/− , wnt11f2−/− , and wnt11f2−/−,dact1/2 −/− compound mutants. Scale bar: 200 μm.
Figure Legend Snippet: ( A ) Representative brightfield images of wildtype and dact1/2−/− compound mutants at 4 dpf. 100 individuals were analyzed from a dact1/2 +/- double het cross. Lateral and ventral views show d act1/2−/− compound mutants have a hypoplastic midface, medially displaced eyes, and a displaced lower jaw. ( B ) Representative flat-mount images of Alcian blue stained ethmoid plate (EP) and visceral cartilage (VC) elements from 4 dpf wildtype and d act1/2−/− compound mutants. d act1/2−/− mutants have a rod-shaped EP with no distinct lateral and medial elements. No obvious differences were found in dact1/2 mutant VC. ( C ) Representative brightfield image of 4 dpf wildtype and dact1/2−/− mutant. Bar indicates vertebral spine length. Scale bar: 100 μm. ( D ) Representative images of Alcian blue stained dact1/2−/− , wnt11f2−/− , and wnt11f2−/− , dact1 / 2 −/− compound mutants. Embryos resulted from a dact1+/-,dact2+/-,wnt11f2+/- in-cross. Lateral and ventral views show similar craniofacial phenotypes in each mutant. ( E ) Representative flat-mount images of Alcian blue stained EP show a similar phenotype between dact1/2−/− , wnt11f2−/− , and wnt11f2−/−,dact1/2 −/− compound mutants. Scale bar: 200 μm.

Techniques Used: Staining, Mutagenesis

( A ) Representative brightfield images of 4 dpf larvae of compound dact1 and dact2 mutant genotypes. Bar represents dact1/2+/+ body length measurement. Scale bar: 100 μm. ( B ) Scatter plot of body length measurement of compound dact1 and dact2 mutant genotypes at 4 dpf. ANOVA p = 0.06. n = 3–4. Error bars: ± SEM.
Figure Legend Snippet: ( A ) Representative brightfield images of 4 dpf larvae of compound dact1 and dact2 mutant genotypes. Bar represents dact1/2+/+ body length measurement. Scale bar: 100 μm. ( B ) Scatter plot of body length measurement of compound dact1 and dact2 mutant genotypes at 4 dpf. ANOVA p = 0.06. n = 3–4. Error bars: ± SEM.

Techniques Used: Mutagenesis

( A ) Representative Alcian blue stained wholemount images of wildtype, dact1/2−/− double mutant, gpc4−/− mutant, and gpc4/dact1/2−/− triple mutants at 4 dpf. Low magnification lateral images of embryos showing tail truncation in dact1/2−/− mutants, shortened and kinked tail in gpc4−/− mutants, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. Higher magnification lateral images show a shortened midface and displaced lower jaw in dact1/2−/− mutants, a shortened midface in gpc4−/− mutant, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. ( B ) Representative flat-mount images of dissected Alcian blue-stained cartilage elements. dact1/2−/− mutants have a narrow rod-shaped ethmoid plate (EP) while gpc4−/− mutants have a broad and shortened EP. dact1/2/gpc4 triple mutants have a combinatorial effect with a short, broad rod-shaped EP. In ventral cartilages (VC), dact1/2−/− mutants have a relatively normal morphology while Meckel’s cartilage in gpc4−/− mutants and gpc4/dact1/2−/− triple mutants is truncated. ( C, D ) Same as above except wls−/− mutant and wls/dact1/2−/− triple mutant, with similar findings. ( E ) Combinatorial genotypes of dact1 , dact2 , and gpc4. dact2 −/− contributed the dact/gpc4 compound phenotype while dact1−/− did not. Scale bar: 200 μm.
Figure Legend Snippet: ( A ) Representative Alcian blue stained wholemount images of wildtype, dact1/2−/− double mutant, gpc4−/− mutant, and gpc4/dact1/2−/− triple mutants at 4 dpf. Low magnification lateral images of embryos showing tail truncation in dact1/2−/− mutants, shortened and kinked tail in gpc4−/− mutants, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. Higher magnification lateral images show a shortened midface and displaced lower jaw in dact1/2−/− mutants, a shortened midface in gpc4−/− mutant, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. ( B ) Representative flat-mount images of dissected Alcian blue-stained cartilage elements. dact1/2−/− mutants have a narrow rod-shaped ethmoid plate (EP) while gpc4−/− mutants have a broad and shortened EP. dact1/2/gpc4 triple mutants have a combinatorial effect with a short, broad rod-shaped EP. In ventral cartilages (VC), dact1/2−/− mutants have a relatively normal morphology while Meckel’s cartilage in gpc4−/− mutants and gpc4/dact1/2−/− triple mutants is truncated. ( C, D ) Same as above except wls−/− mutant and wls/dact1/2−/− triple mutant, with similar findings. ( E ) Combinatorial genotypes of dact1 , dact2 , and gpc4. dact2 −/− contributed the dact/gpc4 compound phenotype while dact1−/− did not. Scale bar: 200 μm.

Techniques Used: Staining, Mutagenesis

( A ) Summary schematic showing similar phenotypes in dact1/2−/− and gpc4−/− mutants at 12 hpf and divergent phenotypes at 4 dpf. Single-cell RNAseq was performed during axis extension to compare and contrast dact1/2−/− and gpc4−/− transcriptional programs. Uniform manifold approximation and projection (UMAP) showing cluster identification. ( B ) UMAP of cell clusters identified by single-cell RNAseq. ( C ) Dot plot showing the most differentially expressed genes between clusters. ( D ) UMAP showing dact1 , dact2 , and gpc4 expression in wildtype embryos.
Figure Legend Snippet: ( A ) Summary schematic showing similar phenotypes in dact1/2−/− and gpc4−/− mutants at 12 hpf and divergent phenotypes at 4 dpf. Single-cell RNAseq was performed during axis extension to compare and contrast dact1/2−/− and gpc4−/− transcriptional programs. Uniform manifold approximation and projection (UMAP) showing cluster identification. ( B ) UMAP of cell clusters identified by single-cell RNAseq. ( C ) Dot plot showing the most differentially expressed genes between clusters. ( D ) UMAP showing dact1 , dact2 , and gpc4 expression in wildtype embryos.

Techniques Used: Expressing

( A ) Single-cell RNAseq gene expression analysis of capn8 in wildtype and dact1/2−/− mutants. In wildtype embryos, capn8 expression is restricted predominantly to the epidermis whereas capn8 is widely expressed throughout the embryo in dact1/2−/− mutants, especially in the mesoderm. ( B ) Wholemount in situ hybridization of capn8 expression in wildtype and dact1/2−/− mutant embryos at 2 ss. Staining corroborates the single-cell RNAseq data, with expanded ectopic expression of capn8 throughout the embryo. Flat mounts are oriented anterior to the left. Scale bar: 100 μm. ( C ) Brightfield images and Alcian blue staining of the ethmoid plate show ectopic expression of capn8 mRNA (200 pg) at the 1 cell stage in dact1+/- , dact2+/- embryos recapitulates the dact1/2−/− compound mutant craniofacial phenotype. The mutant craniofacial phenotype did not manifest in gfp mRNA (200 pg) injected 1 cell-stage dact1+/- , dact2+/- embryos. Scale bar: 100 μm ( D ) Quantification of mutant and normal craniofacial phenotype in 4 dpf larvae after mRNA injection at the 1 cell stage. Larvae were derived from dact1/2+/- interbreeding. Larvae were uninjected or injected with 200 pg gfp control or capn8 mRNA. A Fisher exact test showed a significant effect of capn8 mRNA injecting in the dact1/2 double heterozygotes. Asterisk indicates a significant difference between conditions (p = 0.013).
Figure Legend Snippet: ( A ) Single-cell RNAseq gene expression analysis of capn8 in wildtype and dact1/2−/− mutants. In wildtype embryos, capn8 expression is restricted predominantly to the epidermis whereas capn8 is widely expressed throughout the embryo in dact1/2−/− mutants, especially in the mesoderm. ( B ) Wholemount in situ hybridization of capn8 expression in wildtype and dact1/2−/− mutant embryos at 2 ss. Staining corroborates the single-cell RNAseq data, with expanded ectopic expression of capn8 throughout the embryo. Flat mounts are oriented anterior to the left. Scale bar: 100 μm. ( C ) Brightfield images and Alcian blue staining of the ethmoid plate show ectopic expression of capn8 mRNA (200 pg) at the 1 cell stage in dact1+/- , dact2+/- embryos recapitulates the dact1/2−/− compound mutant craniofacial phenotype. The mutant craniofacial phenotype did not manifest in gfp mRNA (200 pg) injected 1 cell-stage dact1+/- , dact2+/- embryos. Scale bar: 100 μm ( D ) Quantification of mutant and normal craniofacial phenotype in 4 dpf larvae after mRNA injection at the 1 cell stage. Larvae were derived from dact1/2+/- interbreeding. Larvae were uninjected or injected with 200 pg gfp control or capn8 mRNA. A Fisher exact test showed a significant effect of capn8 mRNA injecting in the dact1/2 double heterozygotes. Asterisk indicates a significant difference between conditions (p = 0.013).

Techniques Used: Gene Expression, Expressing, In Situ Hybridization, Mutagenesis, Staining, Injection, Derivative Assay, Control


Figure Legend Snippet:

Techniques Used: CRISPR, Mutagenesis, Reverse Transcription, Gene Expression, Recombinant, Plasmid Preparation, RNAscope, Software



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Advanced Cell Diagnostics Inc rnascope probe dact2
( A–C ) Representative images of wholemount in situ hybridization showing dact1 , <t>dact2</t> , and wnt11f2 gene expression patterns. ( A ) At 8 hpf, dact2 and wnt11f2 are highly expressed in the dorsal margin and presumptive Nieuwkoop center of the gastrulating embryo, with dact1 being weakly detected (arrowhead). In contrast to wnt11f2 , dact1 , and dact2 are expressed in the presumptive dorsal mesoderm (asterisk). ( B ) Lateral (anterior to the left of page) and anterior (dorsal side toward top of page) views of bud-stage embryos. dact2 and wnt11f2 transcripts are both detected in the tailbud (asterisk) while dact2 is additionally expressed in the axial mesoderm (arrow). dact1 gene expression is concentrated to the paraxial mesoderm and the neuroectoderm (open arrowheads). ( C ) Lateral and flat-mount views of 4 ss embryos. dact2 is expressed in the anterior neural plate and polster (P), notochord (N), paraxial and presomitic mesoderm (PM) and tailbud (TB). In contrast, dact1 is expressed in the midbrain (MB) and the paraxial and presomitic mesoderm. ( D, E ) Representative lateral (anterior to left of page) images of wholemount in situ hybridization showing dact1 and dact2 expression patterns. ( D ) At 24 hpf expression is detected in the developing head. ( E ) At 48 hpf expression is detected in the developing craniofacial structures (arrow). ( F ) Representative images of RNAscope in situ hybridization analysis of dact1 (white) and dact2 (yellow) and irf6 (green) expression in transverse section of 72 hpf embryos. dact1 is expressed in the ethmoid plate (ep) and palatoquadrate (pq) orofacial cartilage, while dact2 is expressed in the oral epithelium (oe). The epithelial marker irf6 is expressed in the oe and surface epithelium (se). Dapi (blue). Scale bar: 100 μm.
Rnascope Probe Dact2, supplied by Advanced Cell Diagnostics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rnascope probe dact2/product/Advanced Cell Diagnostics Inc
Average 90 stars, based on 1 article reviews
rnascope probe dact2 - by Bioz Stars, 2026-05
90/100 stars
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( A–C ) Representative images of wholemount in situ hybridization showing dact1 , dact2 , and wnt11f2 gene expression patterns. ( A ) At 8 hpf, dact2 and wnt11f2 are highly expressed in the dorsal margin and presumptive Nieuwkoop center of the gastrulating embryo, with dact1 being weakly detected (arrowhead). In contrast to wnt11f2 , dact1 , and dact2 are expressed in the presumptive dorsal mesoderm (asterisk). ( B ) Lateral (anterior to the left of page) and anterior (dorsal side toward top of page) views of bud-stage embryos. dact2 and wnt11f2 transcripts are both detected in the tailbud (asterisk) while dact2 is additionally expressed in the axial mesoderm (arrow). dact1 gene expression is concentrated to the paraxial mesoderm and the neuroectoderm (open arrowheads). ( C ) Lateral and flat-mount views of 4 ss embryos. dact2 is expressed in the anterior neural plate and polster (P), notochord (N), paraxial and presomitic mesoderm (PM) and tailbud (TB). In contrast, dact1 is expressed in the midbrain (MB) and the paraxial and presomitic mesoderm. ( D, E ) Representative lateral (anterior to left of page) images of wholemount in situ hybridization showing dact1 and dact2 expression patterns. ( D ) At 24 hpf expression is detected in the developing head. ( E ) At 48 hpf expression is detected in the developing craniofacial structures (arrow). ( F ) Representative images of RNAscope in situ hybridization analysis of dact1 (white) and dact2 (yellow) and irf6 (green) expression in transverse section of 72 hpf embryos. dact1 is expressed in the ethmoid plate (ep) and palatoquadrate (pq) orofacial cartilage, while dact2 is expressed in the oral epithelium (oe). The epithelial marker irf6 is expressed in the oe and surface epithelium (se). Dapi (blue). Scale bar: 100 μm.

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A–C ) Representative images of wholemount in situ hybridization showing dact1 , dact2 , and wnt11f2 gene expression patterns. ( A ) At 8 hpf, dact2 and wnt11f2 are highly expressed in the dorsal margin and presumptive Nieuwkoop center of the gastrulating embryo, with dact1 being weakly detected (arrowhead). In contrast to wnt11f2 , dact1 , and dact2 are expressed in the presumptive dorsal mesoderm (asterisk). ( B ) Lateral (anterior to the left of page) and anterior (dorsal side toward top of page) views of bud-stage embryos. dact2 and wnt11f2 transcripts are both detected in the tailbud (asterisk) while dact2 is additionally expressed in the axial mesoderm (arrow). dact1 gene expression is concentrated to the paraxial mesoderm and the neuroectoderm (open arrowheads). ( C ) Lateral and flat-mount views of 4 ss embryos. dact2 is expressed in the anterior neural plate and polster (P), notochord (N), paraxial and presomitic mesoderm (PM) and tailbud (TB). In contrast, dact1 is expressed in the midbrain (MB) and the paraxial and presomitic mesoderm. ( D, E ) Representative lateral (anterior to left of page) images of wholemount in situ hybridization showing dact1 and dact2 expression patterns. ( D ) At 24 hpf expression is detected in the developing head. ( E ) At 48 hpf expression is detected in the developing craniofacial structures (arrow). ( F ) Representative images of RNAscope in situ hybridization analysis of dact1 (white) and dact2 (yellow) and irf6 (green) expression in transverse section of 72 hpf embryos. dact1 is expressed in the ethmoid plate (ep) and palatoquadrate (pq) orofacial cartilage, while dact2 is expressed in the oral epithelium (oe). The epithelial marker irf6 is expressed in the oe and surface epithelium (se). Dapi (blue). Scale bar: 100 μm.

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: In Situ Hybridization, Gene Expression, Expressing, RNAscope, Marker

( A ) Schematic representations of dact1 and dact2 exons, positions of guide RNA target site, introduced premature stop codon (arrow), and sequences of mutations. ( B ) DNA fragment analysis of dact1+/- and dact2+/- animals showing wildtype (250 and 387 bp, respectively) and mutant (228 and 380 bp, respectively). ( C ) Expression levels of dact1 and dact2 mRNA by RT-qPCR in 12 hpf dact1−/− mutants, dact2−/− mutants, and dact1/2−/− compound mutants. Eight embryos were pooled for mRNA isolation per sample. ( D ) Injection of dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA rescues the rod-shaped ethmoid plate phenotype in dact1/2−/− compound mutants. Representative images of Alcian blue stained dact1/2−/− double mutant treated with 300 pg dact1 mRNA and 300 pg dact2 mRNA. Arrow highlights normal ethmoid plate (EP). Visceral cartilage (VC) also appeared normal. ( E ) Quantification of the mutant craniofacial phenotype observed in a dact1−/−,dact2+/- breeding in-cross. Without mRNA injection, the mutant phenotype was observed at approximately (35%) the expected Mendelian ratio of 25%. Injection with dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA decreased the frequency that the mutant craniofacial phenotype was observed.

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Schematic representations of dact1 and dact2 exons, positions of guide RNA target site, introduced premature stop codon (arrow), and sequences of mutations. ( B ) DNA fragment analysis of dact1+/- and dact2+/- animals showing wildtype (250 and 387 bp, respectively) and mutant (228 and 380 bp, respectively). ( C ) Expression levels of dact1 and dact2 mRNA by RT-qPCR in 12 hpf dact1−/− mutants, dact2−/− mutants, and dact1/2−/− compound mutants. Eight embryos were pooled for mRNA isolation per sample. ( D ) Injection of dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA rescues the rod-shaped ethmoid plate phenotype in dact1/2−/− compound mutants. Representative images of Alcian blue stained dact1/2−/− double mutant treated with 300 pg dact1 mRNA and 300 pg dact2 mRNA. Arrow highlights normal ethmoid plate (EP). Visceral cartilage (VC) also appeared normal. ( E ) Quantification of the mutant craniofacial phenotype observed in a dact1−/−,dact2+/- breeding in-cross. Without mRNA injection, the mutant phenotype was observed at approximately (35%) the expected Mendelian ratio of 25%. Injection with dact1 mRNA, dact2 mRNA, or a combination of dact1 and dact2 mRNA decreased the frequency that the mutant craniofacial phenotype was observed.

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Mutagenesis, Expressing, Quantitative RT-PCR, Isolation, Injection, Staining

( A ) Inter-cross of compound heterozygotes yield embryos with different degrees of axis extension that correspond to the dact1 and dact2 genotypes. Representative lateral images of embryos at 12 hpf. The yellow line indicates body axis angle measured from the anterior point of the head, the center of the yolk, to the end of the tail. ( B ) Quantification of body axis angle. Numbers represent the difference in angle relative to the average wildtype embryo. Asterisk indicates genotypes with angles significantly different from wildtype. ANOVA p < 0.5 n = 3–21 embryos. Error bars: ± SEM. ( C ) Representative bud stage wildtype and dact1/2−/− mutant embryos stained for gsc (prechordal plate), pax2a (midbrain/hindbrain boundary), and krox20 (rhombomere 3). Asterisk indicates lack of krox20 expression in dact1/2−/− mutant. Scale bar = 200 μm ( D ) Representative flat mounts of 1–2 ss wildtype and dact1/2 mutant embryos stained for zic1 (telencephalon), pax2a and tbx6 (ventrolateral mesoderm). ( E ) Representative flat mounts of 10 ss wildtype and dact1/2−/− mutant embryos stained for ctsl1b (hatching gland), zic1 , pax2a , krox20 , and myo1d (somites).

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Inter-cross of compound heterozygotes yield embryos with different degrees of axis extension that correspond to the dact1 and dact2 genotypes. Representative lateral images of embryos at 12 hpf. The yellow line indicates body axis angle measured from the anterior point of the head, the center of the yolk, to the end of the tail. ( B ) Quantification of body axis angle. Numbers represent the difference in angle relative to the average wildtype embryo. Asterisk indicates genotypes with angles significantly different from wildtype. ANOVA p < 0.5 n = 3–21 embryos. Error bars: ± SEM. ( C ) Representative bud stage wildtype and dact1/2−/− mutant embryos stained for gsc (prechordal plate), pax2a (midbrain/hindbrain boundary), and krox20 (rhombomere 3). Asterisk indicates lack of krox20 expression in dact1/2−/− mutant. Scale bar = 200 μm ( D ) Representative flat mounts of 1–2 ss wildtype and dact1/2 mutant embryos stained for zic1 (telencephalon), pax2a and tbx6 (ventrolateral mesoderm). ( E ) Representative flat mounts of 10 ss wildtype and dact1/2−/− mutant embryos stained for ctsl1b (hatching gland), zic1 , pax2a , krox20 , and myo1d (somites).

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Mutagenesis, Staining, Expressing

( A ) Representative brightfield images of wildtype and dact1/2−/− compound mutants at 4 dpf. 100 individuals were analyzed from a dact1/2 +/- double het cross. Lateral and ventral views show d act1/2−/− compound mutants have a hypoplastic midface, medially displaced eyes, and a displaced lower jaw. ( B ) Representative flat-mount images of Alcian blue stained ethmoid plate (EP) and visceral cartilage (VC) elements from 4 dpf wildtype and d act1/2−/− compound mutants. d act1/2−/− mutants have a rod-shaped EP with no distinct lateral and medial elements. No obvious differences were found in dact1/2 mutant VC. ( C ) Representative brightfield image of 4 dpf wildtype and dact1/2−/− mutant. Bar indicates vertebral spine length. Scale bar: 100 μm. ( D ) Representative images of Alcian blue stained dact1/2−/− , wnt11f2−/− , and wnt11f2−/− , dact1 / 2 −/− compound mutants. Embryos resulted from a dact1+/-,dact2+/-,wnt11f2+/- in-cross. Lateral and ventral views show similar craniofacial phenotypes in each mutant. ( E ) Representative flat-mount images of Alcian blue stained EP show a similar phenotype between dact1/2−/− , wnt11f2−/− , and wnt11f2−/−,dact1/2 −/− compound mutants. Scale bar: 200 μm.

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Representative brightfield images of wildtype and dact1/2−/− compound mutants at 4 dpf. 100 individuals were analyzed from a dact1/2 +/- double het cross. Lateral and ventral views show d act1/2−/− compound mutants have a hypoplastic midface, medially displaced eyes, and a displaced lower jaw. ( B ) Representative flat-mount images of Alcian blue stained ethmoid plate (EP) and visceral cartilage (VC) elements from 4 dpf wildtype and d act1/2−/− compound mutants. d act1/2−/− mutants have a rod-shaped EP with no distinct lateral and medial elements. No obvious differences were found in dact1/2 mutant VC. ( C ) Representative brightfield image of 4 dpf wildtype and dact1/2−/− mutant. Bar indicates vertebral spine length. Scale bar: 100 μm. ( D ) Representative images of Alcian blue stained dact1/2−/− , wnt11f2−/− , and wnt11f2−/− , dact1 / 2 −/− compound mutants. Embryos resulted from a dact1+/-,dact2+/-,wnt11f2+/- in-cross. Lateral and ventral views show similar craniofacial phenotypes in each mutant. ( E ) Representative flat-mount images of Alcian blue stained EP show a similar phenotype between dact1/2−/− , wnt11f2−/− , and wnt11f2−/−,dact1/2 −/− compound mutants. Scale bar: 200 μm.

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Staining, Mutagenesis

( A ) Representative brightfield images of 4 dpf larvae of compound dact1 and dact2 mutant genotypes. Bar represents dact1/2+/+ body length measurement. Scale bar: 100 μm. ( B ) Scatter plot of body length measurement of compound dact1 and dact2 mutant genotypes at 4 dpf. ANOVA p = 0.06. n = 3–4. Error bars: ± SEM.

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Representative brightfield images of 4 dpf larvae of compound dact1 and dact2 mutant genotypes. Bar represents dact1/2+/+ body length measurement. Scale bar: 100 μm. ( B ) Scatter plot of body length measurement of compound dact1 and dact2 mutant genotypes at 4 dpf. ANOVA p = 0.06. n = 3–4. Error bars: ± SEM.

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Mutagenesis

( A ) Representative Alcian blue stained wholemount images of wildtype, dact1/2−/− double mutant, gpc4−/− mutant, and gpc4/dact1/2−/− triple mutants at 4 dpf. Low magnification lateral images of embryos showing tail truncation in dact1/2−/− mutants, shortened and kinked tail in gpc4−/− mutants, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. Higher magnification lateral images show a shortened midface and displaced lower jaw in dact1/2−/− mutants, a shortened midface in gpc4−/− mutant, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. ( B ) Representative flat-mount images of dissected Alcian blue-stained cartilage elements. dact1/2−/− mutants have a narrow rod-shaped ethmoid plate (EP) while gpc4−/− mutants have a broad and shortened EP. dact1/2/gpc4 triple mutants have a combinatorial effect with a short, broad rod-shaped EP. In ventral cartilages (VC), dact1/2−/− mutants have a relatively normal morphology while Meckel’s cartilage in gpc4−/− mutants and gpc4/dact1/2−/− triple mutants is truncated. ( C, D ) Same as above except wls−/− mutant and wls/dact1/2−/− triple mutant, with similar findings. ( E ) Combinatorial genotypes of dact1 , dact2 , and gpc4. dact2 −/− contributed the dact/gpc4 compound phenotype while dact1−/− did not. Scale bar: 200 μm.

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Representative Alcian blue stained wholemount images of wildtype, dact1/2−/− double mutant, gpc4−/− mutant, and gpc4/dact1/2−/− triple mutants at 4 dpf. Low magnification lateral images of embryos showing tail truncation in dact1/2−/− mutants, shortened and kinked tail in gpc4−/− mutants, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. Higher magnification lateral images show a shortened midface and displaced lower jaw in dact1/2−/− mutants, a shortened midface in gpc4−/− mutant, and a combinatorial effect in gpc4/dact1/2−/− triple mutants. ( B ) Representative flat-mount images of dissected Alcian blue-stained cartilage elements. dact1/2−/− mutants have a narrow rod-shaped ethmoid plate (EP) while gpc4−/− mutants have a broad and shortened EP. dact1/2/gpc4 triple mutants have a combinatorial effect with a short, broad rod-shaped EP. In ventral cartilages (VC), dact1/2−/− mutants have a relatively normal morphology while Meckel’s cartilage in gpc4−/− mutants and gpc4/dact1/2−/− triple mutants is truncated. ( C, D ) Same as above except wls−/− mutant and wls/dact1/2−/− triple mutant, with similar findings. ( E ) Combinatorial genotypes of dact1 , dact2 , and gpc4. dact2 −/− contributed the dact/gpc4 compound phenotype while dact1−/− did not. Scale bar: 200 μm.

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Staining, Mutagenesis

( A ) Summary schematic showing similar phenotypes in dact1/2−/− and gpc4−/− mutants at 12 hpf and divergent phenotypes at 4 dpf. Single-cell RNAseq was performed during axis extension to compare and contrast dact1/2−/− and gpc4−/− transcriptional programs. Uniform manifold approximation and projection (UMAP) showing cluster identification. ( B ) UMAP of cell clusters identified by single-cell RNAseq. ( C ) Dot plot showing the most differentially expressed genes between clusters. ( D ) UMAP showing dact1 , dact2 , and gpc4 expression in wildtype embryos.

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Summary schematic showing similar phenotypes in dact1/2−/− and gpc4−/− mutants at 12 hpf and divergent phenotypes at 4 dpf. Single-cell RNAseq was performed during axis extension to compare and contrast dact1/2−/− and gpc4−/− transcriptional programs. Uniform manifold approximation and projection (UMAP) showing cluster identification. ( B ) UMAP of cell clusters identified by single-cell RNAseq. ( C ) Dot plot showing the most differentially expressed genes between clusters. ( D ) UMAP showing dact1 , dact2 , and gpc4 expression in wildtype embryos.

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Expressing

( A ) Single-cell RNAseq gene expression analysis of capn8 in wildtype and dact1/2−/− mutants. In wildtype embryos, capn8 expression is restricted predominantly to the epidermis whereas capn8 is widely expressed throughout the embryo in dact1/2−/− mutants, especially in the mesoderm. ( B ) Wholemount in situ hybridization of capn8 expression in wildtype and dact1/2−/− mutant embryos at 2 ss. Staining corroborates the single-cell RNAseq data, with expanded ectopic expression of capn8 throughout the embryo. Flat mounts are oriented anterior to the left. Scale bar: 100 μm. ( C ) Brightfield images and Alcian blue staining of the ethmoid plate show ectopic expression of capn8 mRNA (200 pg) at the 1 cell stage in dact1+/- , dact2+/- embryos recapitulates the dact1/2−/− compound mutant craniofacial phenotype. The mutant craniofacial phenotype did not manifest in gfp mRNA (200 pg) injected 1 cell-stage dact1+/- , dact2+/- embryos. Scale bar: 100 μm ( D ) Quantification of mutant and normal craniofacial phenotype in 4 dpf larvae after mRNA injection at the 1 cell stage. Larvae were derived from dact1/2+/- interbreeding. Larvae were uninjected or injected with 200 pg gfp control or capn8 mRNA. A Fisher exact test showed a significant effect of capn8 mRNA injecting in the dact1/2 double heterozygotes. Asterisk indicates a significant difference between conditions (p = 0.013).

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet: ( A ) Single-cell RNAseq gene expression analysis of capn8 in wildtype and dact1/2−/− mutants. In wildtype embryos, capn8 expression is restricted predominantly to the epidermis whereas capn8 is widely expressed throughout the embryo in dact1/2−/− mutants, especially in the mesoderm. ( B ) Wholemount in situ hybridization of capn8 expression in wildtype and dact1/2−/− mutant embryos at 2 ss. Staining corroborates the single-cell RNAseq data, with expanded ectopic expression of capn8 throughout the embryo. Flat mounts are oriented anterior to the left. Scale bar: 100 μm. ( C ) Brightfield images and Alcian blue staining of the ethmoid plate show ectopic expression of capn8 mRNA (200 pg) at the 1 cell stage in dact1+/- , dact2+/- embryos recapitulates the dact1/2−/− compound mutant craniofacial phenotype. The mutant craniofacial phenotype did not manifest in gfp mRNA (200 pg) injected 1 cell-stage dact1+/- , dact2+/- embryos. Scale bar: 100 μm ( D ) Quantification of mutant and normal craniofacial phenotype in 4 dpf larvae after mRNA injection at the 1 cell stage. Larvae were derived from dact1/2+/- interbreeding. Larvae were uninjected or injected with 200 pg gfp control or capn8 mRNA. A Fisher exact test showed a significant effect of capn8 mRNA injecting in the dact1/2 double heterozygotes. Asterisk indicates a significant difference between conditions (p = 0.013).

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: Gene Expression, Expressing, In Situ Hybridization, Mutagenesis, Staining, Injection, Derivative Assay, Control

Journal: eLife

Article Title: Genetic requirement of dact1/2 to regulate noncanonical Wnt signaling and calpain 8 during embryonic convergent extension and craniofacial morphogenesis

doi: 10.7554/eLife.91648

Figure Lengend Snippet:

Article Snippet: Commercial assay or kit , RNAscope probe dact2 , ACDbio , ID_source:identifier 857201-C3 , .

Techniques: CRISPR, Mutagenesis, Reverse Transcription, Gene Expression, Recombinant, Plasmid Preparation, RNAscope, Software