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FGF-induced loss of the common crus is rescued by RA
E9 paint-filled inner ear of controls (A) and ears implanted with FGF2- (B), RA- (C, E), or both RA- and FGF2- soaked beads (D, F, G) at E5. (B) An inner ear implanted with a bead soaked with FGF2 causes loss of the common crus (A, green arrow). (C,E) Inner ears implanted with beads soaked with a half (E) or standard dose (C) of RA. Only the standard dose of RA results in a widened common crus-like structure (C, green double arrow) and absence of canals. Ears with half dose of RA are largely normal with slightly misshapen canals and thinner common crus (magenta arrows), compared to the control (A). (D) Inner ears implanted with beads soaked with both FGF2 and RA resulted in phenotypes similar to ones treated with RA alone (C). (F, G) Inner ears implanted with beads soaked with FGF2 and the half dosage of RA at E5 exhibit intact canals and common crus with minor defects in canals and common crus (magenta). However, the width of the common crus is wider compared to ones treated with low dose RA alone (E). Abbreviation: A, anterior; aa, anterior ampulla; asc, anterior semicircular canal; cc, common crus; D, dorsal; la, lateral ampulla; lsc, lateral semicircular canal; pa; posterior ampulla; psc, posterior semicircular canal.

FGF-induced loss of the common crus is rescued by RA E9 paint-filled inner ear of controls (A) and ears implanted with FGF2- (B), RA- (C, E), or both RA- and FGF2- soaked beads (D, F, G) at E5. (B) An inner ear implanted with a bead soaked with FGF2 causes loss of the common crus (A, green arrow). (C,E) Inner ears implanted with beads soaked with a half (E) or standard dose (C) of RA. Only the standard dose of RA results in a widened common crus-like structure (C, green double arrow) and absence of canals. Ears with half dose of RA are largely normal with slightly misshapen canals and thinner common crus (magenta arrows), compared to the control (A). (D) Inner ears implanted with beads soaked with both FGF2 and RA resulted in phenotypes similar to ones treated with RA alone (C). (F, G) Inner ears implanted with beads soaked with FGF2 and the half dosage of RA at E5 exhibit intact canals and common crus with minor defects in canals and common crus (magenta). However, the width of the common crus is wider compared to ones treated with low dose RA alone (E). Abbreviation: A, anterior; aa, anterior ampulla; asc, anterior semicircular canal; cc, common crus; D, dorsal; la, lateral ampulla; lsc, lateral semicircular canal; pa; posterior ampulla; psc, posterior semicircular canal.

#DBfeature 👂

Opposing effects between retinoic acid and Fibroblast growth factor in patterning the common crus and semicircular canals of the inner ear

By Weise Chang, John Hopper, Doris K. Wu

tinyurl.com/3pemcrfk

10 2 0 0
Specification of tuberal neurogenic progenitors at early neural plate stages (A–I) Maximum intensity projections of hemi-views (A-C, D-H') or ventral view of isolated neuroectoderm (I) of HH6 (A-C, I) or HH17–18 (D–H') embryos after HCR. (A–C) Hemi-views labelled for SHH and NKX2-1 (A); SHH and PTCH1 (B); FOXG1 and BMP2 (C). White bracket marks HypFP cells. (D-E') Fate mapping of HypFP cells at HH6. (D) Mid-HypFP cells (dorsal view, inset in D) give rise to tuberal gliogenic cells, identified by their position relative to the mammillary pouch (mp arrowhead in D). (E) HH17 embryo after anterior-most HypFP cells labelled at HH6 with DiI, and HCR analysis. DiI is located in the SHH+ neurogenic hypothalamus, the SHH- gliogenic hypothalamus, but not the FOXG1+ telencephalon. Boxed regions in (F, G) shown at high power in (F′, G′). (H′) shows double channel view of FGF10 and FOXA2. Arrowhead points to mammillary pouch (mp) and optic stalk (os). (I) HH6 isolated neuroectoderm after HCR to detect SHH/PTCH1. White bracket marks HypFP cells; white lines represent positions of slices shown in I’. (I′) Explants of regions 1–4, after HCR to detect SHH/PTCH1 confirms accuracy of dissection. (J) Midline sub-dissection from a position 4 explant (yellow boxed region in I′), showing position of DiI-labelling (red circles). MIP shows SHH and PTCH1 are expressed through the explant at 0 h. (K–Q) MIPs of wholemount views of HH6 Hyp explants (regions 3 or 4 in (I′)), cultured for 72 h, then analysed by HCR (right hand panels show single or double channel views) showing expression of SHH/PTCH (L); NKX2-1/POMC/FOXA2 (M); SHH/PTCH1/NKX2-1 (N); ISL1/POMC (O); FGF10 (P); TBX2 (Q). Scale bar = 100 μM.

Specification of tuberal neurogenic progenitors at early neural plate stages (A–I) Maximum intensity projections of hemi-views (A-C, D-H') or ventral view of isolated neuroectoderm (I) of HH6 (A-C, I) or HH17–18 (D–H') embryos after HCR. (A–C) Hemi-views labelled for SHH and NKX2-1 (A); SHH and PTCH1 (B); FOXG1 and BMP2 (C). White bracket marks HypFP cells. (D-E') Fate mapping of HypFP cells at HH6. (D) Mid-HypFP cells (dorsal view, inset in D) give rise to tuberal gliogenic cells, identified by their position relative to the mammillary pouch (mp arrowhead in D). (E) HH17 embryo after anterior-most HypFP cells labelled at HH6 with DiI, and HCR analysis. DiI is located in the SHH+ neurogenic hypothalamus, the SHH- gliogenic hypothalamus, but not the FOXG1+ telencephalon. Boxed regions in (F, G) shown at high power in (F′, G′). (H′) shows double channel view of FGF10 and FOXA2. Arrowhead points to mammillary pouch (mp) and optic stalk (os). (I) HH6 isolated neuroectoderm after HCR to detect SHH/PTCH1. White bracket marks HypFP cells; white lines represent positions of slices shown in I’. (I′) Explants of regions 1–4, after HCR to detect SHH/PTCH1 confirms accuracy of dissection. (J) Midline sub-dissection from a position 4 explant (yellow boxed region in I′), showing position of DiI-labelling (red circles). MIP shows SHH and PTCH1 are expressed through the explant at 0 h. (K–Q) MIPs of wholemount views of HH6 Hyp explants (regions 3 or 4 in (I′)), cultured for 72 h, then analysed by HCR (right hand panels show single or double channel views) showing expression of SHH/PTCH (L); NKX2-1/POMC/FOXA2 (M); SHH/PTCH1/NKX2-1 (N); ISL1/POMC (O); FGF10 (P); TBX2 (Q). Scale bar = 100 μM.

#DBfeature 🧠

FGF10 operates with SHH and BMP to contribute to neurogenic and gliogenic fates in the puberal hypothalamus

By K Chinnaiya, I Groves, E Manning, E Place, C Furley, SE Strawbridge, AG Fletcher, M Placzek

tinyurl.com/muee82sm

5 2 0 0
Dynamic changes of TEADlight signal during myogenic differentiation. Dorsal (A) and front (C) views of a myotome and the overlaying dermomyotome, 48 h after electroporation of the TEADlight reporter (yellow) into the dorsomedial part of the somite. A plasmid driving the constitutive expression of mKate2-NLS (magenta) was used as an electroporation efficiency control (EP control). Image A is a maximal intensity projection of confocal images along the dorsoventral axis, while image C represents a 100 μm-thick virtual transection generated using the Imaris software. The primary myotome territory derived from the DML was arbitrarily divided into a medial half (mMy) and a lateral half (lMy) for quantification. B: Schematics illustrating the morphology of electroporated cells in images A and C. Electroporated cell nuclei are highlighted in magenta. D: Quantification of the TEADlight native signal relative to the mKate2-NLS signal. The TEADlight signal decreases as myofibers migrate laterally. A Friedman test on paired groups revealed significant differences between compartments (p = 0.0115). The insets above each point show TEADlight signal in representative cells.

Dynamic changes of TEADlight signal during myogenic differentiation. Dorsal (A) and front (C) views of a myotome and the overlaying dermomyotome, 48 h after electroporation of the TEADlight reporter (yellow) into the dorsomedial part of the somite. A plasmid driving the constitutive expression of mKate2-NLS (magenta) was used as an electroporation efficiency control (EP control). Image A is a maximal intensity projection of confocal images along the dorsoventral axis, while image C represents a 100 μm-thick virtual transection generated using the Imaris software. The primary myotome territory derived from the DML was arbitrarily divided into a medial half (mMy) and a lateral half (lMy) for quantification. B: Schematics illustrating the morphology of electroporated cells in images A and C. Electroporated cell nuclei are highlighted in magenta. D: Quantification of the TEADlight native signal relative to the mKate2-NLS signal. The TEADlight signal decreases as myofibers migrate laterally. A Friedman test on paired groups revealed significant differences between compartments (p = 0.0115). The insets above each point show TEADlight signal in representative cells.

#DBfeature 💡

The TEADlight reporter dynamics reflects variations in cell density and adhesion in vitro, providing a novel faithful read-out of YAP/TAZ-TEAD signaling.

By Valérie Morin, Yoann Le Toquin, Daria Tepordei, Christophe Marcelle, Emilie Delaune

tinyurl.com/4rhwjy4s

3 1 0 0
VEGF signaling is required for blastema growth and the effect of VEGF inhibition is reversible. (A) schematic of experimental design; (B) representative DMSO-treated limb at 11 dpa (scale bar 100 μm; arrowhead indicates blastema; dashed line indicates amputation plane); (C) representative AV951-treated limb at 11 dpa (scale bar 100 μm; arrowhead indicates blastema; dashed line indicates amputation plane); (D) AV951-treated blastemas are significantly smaller at 11dpa; (E) representative DMSO-treated limb at 22 dpa (scale bar 100 μm); (F) representative AV951-treated limb at 22 dpa (scale bar 100 μm; arrowhead indicates blastema); (G) AV951-treated limbs show no regeneration at 22 dpa; (H) skeletal prep of representative DMSO-treated limb at 22 dpa (scale bar 250 μm); (I) skeletal prep of representative AV95-treated limb at 22 dpa (scale bar 250 μm); (J) AV951-treated blastemas display blocked regeneration compared to controls; (K) AV951-treated blastemas can develop to palette stage upon treatment removal

VEGF signaling is required for blastema growth and the effect of VEGF inhibition is reversible. (A) schematic of experimental design; (B) representative DMSO-treated limb at 11 dpa (scale bar 100 μm; arrowhead indicates blastema; dashed line indicates amputation plane); (C) representative AV951-treated limb at 11 dpa (scale bar 100 μm; arrowhead indicates blastema; dashed line indicates amputation plane); (D) AV951-treated blastemas are significantly smaller at 11dpa; (E) representative DMSO-treated limb at 22 dpa (scale bar 100 μm); (F) representative AV951-treated limb at 22 dpa (scale bar 100 μm; arrowhead indicates blastema); (G) AV951-treated limbs show no regeneration at 22 dpa; (H) skeletal prep of representative DMSO-treated limb at 22 dpa (scale bar 250 μm); (I) skeletal prep of representative AV95-treated limb at 22 dpa (scale bar 250 μm); (J) AV951-treated blastemas display blocked regeneration compared to controls; (K) AV951-treated blastemas can develop to palette stage upon treatment removal

#DBfeature

VEGF signalling promotes blastema growth and proliferation of both vascular and non-vascular cells during axolotl limb regeneration

By Aaron Savage et al.

tinyurl.com/3xs4nffs

3 3 0 0
Deep learning segmentation can be used to quickly segment untrained mutants and quantify new phenotypes. (A) Eyeless mutant (eyD1DA) head. The angle represents optic lobe slope, measured in (I). (B) Manual segmentation of eyD1DA. (C) Deep learning segmentation of eyD1DA using the 43-brain comprehensive model. Arrow highlights region of the lamina called as optic lobe. 3D frontal view of (D) wildtype, (D′) asp, and (D″) eyD1DA. Inferior fiber system defects are seen in eyD1DA and reduced volume of the gnathal ganglion (GNG) in both mutants. 60-degree rotation of the (E) wildtype, (E′) asp, and (E″) eyD1DA brains. Antennal lobes (AL) reduced in size of both mutants. 90-degree rotation of the (F) wildtype, (F′) asp, and (F″) eyD1DA brains. Optic lobe (purple) rotation relative to the central brain (yellow) (red angle line). (G) Quantification of brain volume in wildtype (WT), asp, and eyD1DA mutants. (H) Violin plot showing optic lobe rotation angle, as shown in F-F”. (I) Violin plot showing the optic lobe slope, as shown in (A). Scale bars: 100 μm.

Deep learning segmentation can be used to quickly segment untrained mutants and quantify new phenotypes. (A) Eyeless mutant (eyD1DA) head. The angle represents optic lobe slope, measured in (I). (B) Manual segmentation of eyD1DA. (C) Deep learning segmentation of eyD1DA using the 43-brain comprehensive model. Arrow highlights region of the lamina called as optic lobe. 3D frontal view of (D) wildtype, (D′) asp, and (D″) eyD1DA. Inferior fiber system defects are seen in eyD1DA and reduced volume of the gnathal ganglion (GNG) in both mutants. 60-degree rotation of the (E) wildtype, (E′) asp, and (E″) eyD1DA brains. Antennal lobes (AL) reduced in size of both mutants. 90-degree rotation of the (F) wildtype, (F′) asp, and (F″) eyD1DA brains. Optic lobe (purple) rotation relative to the central brain (yellow) (red angle line). (G) Quantification of brain volume in wildtype (WT), asp, and eyD1DA mutants. (H) Violin plot showing optic lobe rotation angle, as shown in F-F”. (I) Violin plot showing the optic lobe slope, as shown in (A). Scale bars: 100 μm.

#DBfeature 🪰🖥️

A deep learning model for accurate segmentation of the Drosophila melanogaster brain from Micro-CT imaging enables rapid assessment of novel phenotypes.

By Jacob McDaniel, Mike Marsh, Todd Schoborg

tinyurl.com/246czcc8

5 2 0 0
hand1 expression becomes rapidly downregulated in the ventral side of the embryo, similar to that of etv2 expression.
Control embryos were fixed at stage 20, 23 and 25 and probed with dig-labelled antisense mRNA probes against hand1, etv2, spib, globin or ami. Both a side view and ventral view of each embryo is shown above. At stage 25, expression of hand1 is lost along the ventral side of the embryo. When the cleared region begins to form, it corresponds to expression of etv2 in that clear zone. The same phenomenon occurs with Spib expressing cells which are initially in a restricted domain on the ventral midline that tightly corresponds to an area on the ventral midline devoid of hand1 staining starting at stage 23. The Spib expressing cells then migrate throughout the embryo. Both expression of globin and ami are not yet present at these early stages.

hand1 expression becomes rapidly downregulated in the ventral side of the embryo, similar to that of etv2 expression. Control embryos were fixed at stage 20, 23 and 25 and probed with dig-labelled antisense mRNA probes against hand1, etv2, spib, globin or ami. Both a side view and ventral view of each embryo is shown above. At stage 25, expression of hand1 is lost along the ventral side of the embryo. When the cleared region begins to form, it corresponds to expression of etv2 in that clear zone. The same phenomenon occurs with Spib expressing cells which are initially in a restricted domain on the ventral midline that tightly corresponds to an area on the ventral midline devoid of hand1 staining starting at stage 23. The Spib expressing cells then migrate throughout the embryo. Both expression of globin and ami are not yet present at these early stages.

#DBfeature 🐸

Hand1 shows a conserved role of in heart morphogenesis and specific LPM lineages, from Xenopus to mouse

By Victoria Deveau, Jessica Willson, Jennifer Carleton, Thomas Drysdale

tinyurl.com/df8zce7m

2 1 0 0
Fgf signaling inhibitor downregulates mmp1 expression in the articular cartilage during joint regeneration.

Fgf signaling inhibitor downregulates mmp1 expression in the articular cartilage during joint regeneration.

#DBfeature 🐸

Reintegration of blastema and stump by reciprocal interaction for functional joint regeneration in frogs

Fgf-mmp1 axis▶️ cell proliferation

by Haruka Matsubara, Takeshi Inoue, Kiyokazu Agata
www.sciencedirect.com/science/arti...

3 2 0 0
Schematic representation of Slc7a5 regulated TORC1 signaling during limb regeneration in Eriocheir sinensis.
Upregulation of Slc7a5 (left) activates the TORC1 pathway (red arrow) via V-ATPase and Rag GTPases, promoting cell proliferation. Slc7a5 knockdown (right) suppresses TORC1 activation (blue arrow) and reduces regenerative growth.

Schematic representation of Slc7a5 regulated TORC1 signaling during limb regeneration in Eriocheir sinensis. Upregulation of Slc7a5 (left) activates the TORC1 pathway (red arrow) via V-ATPase and Rag GTPases, promoting cell proliferation. Slc7a5 knockdown (right) suppresses TORC1 activation (blue arrow) and reduces regenerative growth.

#DBfeature 🦀

The TORC1 signaling pathway plays an essential role in cell proliferation during limb regeneration in Chinese mitten crab (Eriocheir sinensis).

By Jun Wang, Yangyi Xu, Zhaoyang Guo, Nusrat Hasan Kanika, Xin Hou, Xiaowen Chen, Chenghui Wang

tinyurl.com/mvmmrddv

4 0 0 0
Overview of study design: 15000 protein with 11000 phospho-forms, studied over 11 developmental stages in 3 replicates, from blastula to early juvenile.

Overview of study design: 15000 protein with 11000 phospho-forms, studied over 11 developmental stages in 3 replicates, from blastula to early juvenile.

#DBfeature 🐸

As the Xenopus laevis embryo becomes a tadpole, the transition to functional organ systems coincides with the most dramatic proteome changes.

By Elizabeth Van Itallie, Matthew Sonnett, Marian Kalocsay, Martin Wühr, Leonid Peshkin, Marc Kirschner

tinyurl.com/mv4z88dz

3 2 0 0
Lateral line ganglia have a shared neural crest and placode origin.
Abbreviations are as follows: ov: otic vesicle; gV: trigeminal (Vth nerve) ganglion; gALL: anterior lateral line ganglion; gAD anterodorsal lateral line ganglion; gAV: anteroventral lateral line ganglion; gAV/gVII: anteroventral lateral line ganglion fused with facial ganglion; gVIII: acoustic ganglion; gM: middle lateral line ganglion; gP: posterior lateral line ganglion, gIX: glossopharyngeal ganglion; gX: vagal ganglion.

Lateral line ganglia have a shared neural crest and placode origin. Abbreviations are as follows: ov: otic vesicle; gV: trigeminal (Vth nerve) ganglion; gALL: anterior lateral line ganglion; gAD anterodorsal lateral line ganglion; gAV: anteroventral lateral line ganglion; gAV/gVII: anteroventral lateral line ganglion fused with facial ganglion; gVIII: acoustic ganglion; gM: middle lateral line ganglion; gP: posterior lateral line ganglion, gIX: glossopharyngeal ganglion; gX: vagal ganglion.

#DBfeature 🐠

Development of the zebrafish anterior lateral line system is influenced by underlying cranial neural crest

By Vishruth Venkataraman, Noel McGrory, Theresa Christiansen, Joaquin Navajas Acedo, Michael Coates, Victoria Prince

tinyurl.com/22z6fsbh

10 3 0 1
Comparison of regeneration responses to Wnt signaling perturbation in different species. In both panels, the cladogram indicates phylogenetic relationships. P. fluviatilis and D. lacteum are most closely related to each other and share the same response to canonical Wnt activation and inhibition, so they are represented by one graphic. A(+)/P(+) = anterior and posterior regeneration ability present. A(±)/P(+) = anterior regeneration ability present if cut in anterior 2/3 of body, posterior regeneration ability present. A(−)/P(+) = no anterior regeneration ability, posterior regeneration ability present. Light blue color represents regenerated tissue. (a) Increasing canonical Wnt signaling after amputation results in ectopic posterior axis formation in all species. (b) Decreasing canonical Wnt signaling after amputation results in ectopic head formation in H. miamia and S. mediterranea and rescued anterior regeneration ability in P. fluviatilis and D. lacteum, whereas in C. teleta, no ectopic heads form and anterior regeneration is not rescued.

Comparison of regeneration responses to Wnt signaling perturbation in different species. In both panels, the cladogram indicates phylogenetic relationships. P. fluviatilis and D. lacteum are most closely related to each other and share the same response to canonical Wnt activation and inhibition, so they are represented by one graphic. A(+)/P(+) = anterior and posterior regeneration ability present. A(±)/P(+) = anterior regeneration ability present if cut in anterior 2/3 of body, posterior regeneration ability present. A(−)/P(+) = no anterior regeneration ability, posterior regeneration ability present. Light blue color represents regenerated tissue. (a) Increasing canonical Wnt signaling after amputation results in ectopic posterior axis formation in all species. (b) Decreasing canonical Wnt signaling after amputation results in ectopic head formation in H. miamia and S. mediterranea and rescued anterior regeneration ability in P. fluviatilis and D. lacteum, whereas in C. teleta, no ectopic heads form and anterior regeneration is not rescued.

#DBfeature 🪱

Wnt/β-catenin signaling promotes posterior axial regeneration in non-regenerative tissue of the annelid C. teleta, enabling the prospect of increasing regeneration ability in regeneration-deficient tissues

By Lauren Kunselman, Elaine Seaver

tinyurl.com/2bxpecek

9 3 0 0
Neural fold fusion proceeds bidirectionally from a central “pinch point”

Neural fold fusion proceeds bidirectionally from a central “pinch point”

#DBfeature 🐟

Fold-and-fuse neurulation in zebrafish requires vangl2

Anterior neural tube closure is delayed and abnormal in 🐟embryos lacking PCP gene vangl2

by Jacalyn MacGowan, Mara Cardenas, Margot Kossmann Williams
www.sciencedirect.com/science/arti...

6 3 0 1
A text flow chart about the inclusion of planetary health in developmental biology education. In red: "co-design codevelop a workshop on planetary health" with a double way arrow between students and educators. Red arrow towards purple box "workshop delivered by educator and students", with a contribution in green of an arrow from "consultation with indigenous colleagues". Blue: "pre-class poll" and "post=class poll".

A text flow chart about the inclusion of planetary health in developmental biology education. In red: "co-design codevelop a workshop on planetary health" with a double way arrow between students and educators. Red arrow towards purple box "workshop delivered by educator and students", with a contribution in green of an arrow from "consultation with indigenous colleagues". Blue: "pre-class poll" and "post=class poll".

#DBfeature 🌍

Planetary Health and Indigenous perspectives into the discipline of Developmental Biology exposes students to critical and global challenges that emerging scientists will need to address.

By Sonja McKeown, Marcus Mohr, Tara Moynihan, Beau Cubillo, Liza Barbour

tinyurl.com/yc2m6ncw

3 3 0 0
Timeline of key genetics discoveries in autism spectrum disorder.

Timeline of key genetics discoveries in autism spectrum disorder.

#DBfeature 🧠

In our recent article, researchers explored the intersection of developmental biology and social change, offering strategies to teach autism genetics through a neurodiversity-affirming lens.
-Patra, Aindri H., Katherine Bonefas, Eirene Markenscoff-Papadimitriou.
doi.org/10.1016/j.yd...

4 4 0 0
Neural crest contribution to craniofacial structures and phenotypic variation

Neural crest contribution to craniofacial structures and phenotypic variation

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Bones, brains, and bias—neural crest cell contribution to craniofacial structure

Active Learning Assignments for craniofacial perception & normal phenotypic variation

by Jeffrey Carmichael, Diane Darland et al
www.sciencedirect.com/science/arti...

10 7 1 0
Schematic summary of developmental stages in the formation of amniotic ectoderm and extraembryonic mesoderm in mouse and human

Schematic summary of developmental stages in the formation of amniotic ectoderm and extraembryonic mesoderm in mouse and human

#DBfeature #EvoDevo

Exploring early extraembryonic cells of epiblast origin: Questions on human amniotic ectoderm & extraembryonic mesoderm

How does cellular density regulate the sequential specification of non-neural ectoderm?

by Shota Nakanoh
www.sciencedirect.com/science/arti...

9 4 0 0
Coilin bodies in zebra finch can lie at centromere regions of LBCs and contain cohesin proteins, markers of centromeric protein bodies

Coilin bodies in zebra finch can lie at centromere regions of LBCs and contain cohesin proteins, markers of centromeric protein bodies

#DBfeature 🐦

Coilin-containing nuclear biomolecular condensates in zebra finch Taeniopygia guttata growing oocytes

The coilin condensates reveal components of the nucleoli and centromeric protein bodies

by Svetlana Galkina et al
www.sciencedirect.com/science/arti...

3 1 0 0
Identifying enhancers in the chicken embryo.

Identifying enhancers in the chicken embryo.

#DBfeature 🐣

With the rise of omics data, identifying tissue-specific enhancers is easier than ever—but validation is key. Ruth M. Williams discusses why the chicken embryo is the ideal in vivo sandbox for testing human regulatory elements in our recent review.
www.sciencedirect.com/science/arti...

6 2 0 1
Multiplex fluorescent in situ hybridization gene expression for Col2a1, Bmp2, Bmp4, Wnt2 on untreated tracheas, HH36.5

Multiplex fluorescent in situ hybridization gene expression for Col2a1, Bmp2, Bmp4, Wnt2 on untreated tracheas, HH36.5

#DBfeature 🐣

BMP and WNT signaling are involved in tracheal cartilage development in chicken embryos

COL2A1 co-localises with BMP2 but not with BMP4 in the tracheal cartilages

by Romman Muntzar, Tamara Anne Franz-Odendaal, et al
www.sciencedirect.com/science/arti...

6 2 0 0
AK7 deletion causes an impairment of fluid flow and ciliary function. (A) Representative images of MCCs stained with anti-AK7 (magenta, white) and anti-acetylated tubulin (cyan) antibodies together with phalloidin (green) showing strong ciliary staining in controls (Cas9 alone or gRNA alone) that is missing in AK7 KO cells (Cas9 + gRNAs). Scale is 5 μm.

AK7 deletion causes an impairment of fluid flow and ciliary function. (A) Representative images of MCCs stained with anti-AK7 (magenta, white) and anti-acetylated tubulin (cyan) antibodies together with phalloidin (green) showing strong ciliary staining in controls (Cas9 alone or gRNA alone) that is missing in AK7 KO cells (Cas9 + gRNAs). Scale is 5 μm.

#DBfeature

Centriolar defects underlie a primary ciliary dyskinesia phenotype in an adenylate kinase 7 deficient ciliated epithelium

By Jennifer Sheridan, Aline Grata, Julia Dorr, Eve E. Suva, Enzo Bresteau, Linus R. Mitchell, Osama Hassan, Brian Mitchell

tinyurl.com/c88cax5z

7 3 0 0
Knockdown of centralspindlin results in binucleate anchor cells. LIN-12/Notch reporter lin-12::mNeongreen (yellow) and Notch ligand LAG-2/DSL nuclear reporter lag-2::H2B::::mTurquoise (cyan) expression at mid L2 (A,B), mid L3 (A',B') and late L3 (A",B") in EV(RNAi) (A-A") and zen-4(RNAi) (B-B") treated larvae. White arrowheads denote AC nuclei. Clear arrowheads denote VU nuclei. Asterisks denote primary vulva cell nuclei expressing lag-2::H2B::mTurquoise which is also expressed in some ventral cord neurons.

Knockdown of centralspindlin results in binucleate anchor cells. LIN-12/Notch reporter lin-12::mNeongreen (yellow) and Notch ligand LAG-2/DSL nuclear reporter lag-2::H2B::::mTurquoise (cyan) expression at mid L2 (A,B), mid L3 (A',B') and late L3 (A",B") in EV(RNAi) (A-A") and zen-4(RNAi) (B-B") treated larvae. White arrowheads denote AC nuclei. Clear arrowheads denote VU nuclei. Asterisks denote primary vulva cell nuclei expressing lag-2::H2B::mTurquoise which is also expressed in some ventral cord neurons.

#DBfeature 🪱

Centralspindlin is required for C. elegans anchor cell specification, vulval induction and morphogenesis, with different requirements during postembryonic gonad development compared to early embryogenesis

By Tatsuya Kato, Olga Skorobogata, Christian E. Rocheleau

tinyurl.com/ywjmjsj9

4 1 0 0
(A) The adult Drosophila ovary is composed of 15–20 ovarioles that contain progressively developing egg chambers. Each egg chamber consists of a germline cyst (15 nurse cells and one oocyte; blue) that is surrounded by somatic follicle cells (purple), which is produced in the anterior germarium. (B) Each germarium contains 2-to-3 germline stem cells (GSCs, dark blue) that are maintained by a somatic niche that is primarily composed of cap cells (green). GSCs divide to self-renew and give rise to a cystoblast that will undergo four mitoses with incomplete cytokinesis, generating a germline cyst. GSC and germline cysts are identified by the morphology of the fusome (pink), an ER-like organelle that changes morphology with differentiation. Germline cysts are surrounded by somatic follicle cells (purple) to form a follicle that ultimately buds from the germarium. (C,D) Ovariole (C) and germaria (D) from ERR::GFP.FSTF females showing the expression pattern of ERR::GFP.FSTF based on anti-GFP staining (green). α-Spectrin (magenta), fusome; LamC (magenta), nuclear lamina; DAPI (blue), DNA. Scale bar for (c), 100 μm; scale bar for (d), 10 μm. The germarium (G) and egg chamber stages are labeled in panel (c).

(A) The adult Drosophila ovary is composed of 15–20 ovarioles that contain progressively developing egg chambers. Each egg chamber consists of a germline cyst (15 nurse cells and one oocyte; blue) that is surrounded by somatic follicle cells (purple), which is produced in the anterior germarium. (B) Each germarium contains 2-to-3 germline stem cells (GSCs, dark blue) that are maintained by a somatic niche that is primarily composed of cap cells (green). GSCs divide to self-renew and give rise to a cystoblast that will undergo four mitoses with incomplete cytokinesis, generating a germline cyst. GSC and germline cysts are identified by the morphology of the fusome (pink), an ER-like organelle that changes morphology with differentiation. Germline cysts are surrounded by somatic follicle cells (purple) to form a follicle that ultimately buds from the germarium. (C,D) Ovariole (C) and germaria (D) from ERR::GFP.FSTF females showing the expression pattern of ERR::GFP.FSTF based on anti-GFP staining (green). α-Spectrin (magenta), fusome; LamC (magenta), nuclear lamina; DAPI (blue), DNA. Scale bar for (c), 100 μm; scale bar for (d), 10 μm. The germarium (G) and egg chamber stages are labeled in panel (c).

#DBfeature 🪰

Estrogen-related receptor is required in adult Drosophila females for germline stem cell maintenance

By Anna Zike, Madison Abel, Sophie Fleck, Emily DeWitt, Lesley Weaver

tinyurl.com/3wfmkcfc

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Long-term live imaging of preimplantation embryos expressing endogenously tagged YAP-miRFP670

Long-term live imaging of preimplantation embryos expressing endogenously tagged YAP-miRFP670

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Geometric, cell cycle & maternal-to-zygotic transition-associated YAP dynamics during preimplantation embryo development

YAP behavior depends on cell cycle-nuclei volume dynamics

by Madeleine Chalifoux, Eszter Posfai et al
www.sciencedirect.com/science/arti...

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This illustration indicates the development of the main electric organ in the adult electric eel. Progenitor cells located in the ventral terminus of the main electric organ segregate and migrate dorsally, forming multinuclear syncytium and layer structure. The NKA ion pump begins to be expressed after the layer formation. The syncytia increase the dorsoventral thickness, differentiate into mature electrocytes, and contribute to the generation of high-voltage discharges via ion transporters, including NKA

This illustration indicates the development of the main electric organ in the adult electric eel. Progenitor cells located in the ventral terminus of the main electric organ segregate and migrate dorsally, forming multinuclear syncytium and layer structure. The NKA ion pump begins to be expressed after the layer formation. The syncytia increase the dorsoventral thickness, differentiate into mature electrocytes, and contribute to the generation of high-voltage discharges via ion transporters, including NKA

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Ventral-to-dorsal model for electric organ development of Electrophorus eel

By S Senarat, A Matsumoto, T Nagasawa, S Sakaki, D Tsuzuki, K Uchida, M Kuwahara, M Nikaido, E Hondo, A Iida

tinyurl.com/7c7a266v

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The positions of canal neuromasts, the lateral line canal, and bones of the facial complex are anatomically integrated.

The positions of canal neuromasts, the lateral line canal, and bones of the facial complex are anatomically integrated.

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Review

Integration of the sensory and skeletal systems: A classical perspective on neuromast-bone interactions

Osteogenic potential of neuromast organs

by Alyssa Hamm, Joshua Gross
www.sciencedirect.com/science/arti...

4 2 0 1
Cartoon of a white pregnant mouse being injected with SAG. Diagram of the developing tongue in control conditions, with mesenchymal cell sin blue and myoblasts in red, and in the SAG condition, with a visible cleft between the my blast cells.

Cartoon of a white pregnant mouse being injected with SAG. Diagram of the developing tongue in control conditions, with mesenchymal cell sin blue and myoblasts in red, and in the SAG condition, with a visible cleft between the my blast cells.

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Embryonic exposure to Smoothened Agonist overactivates the Hh signaling pathway, affecting the cell cycle and inhibiting proliferation, leading to cleft tongue

By C Mao, Y Jiang, Z Li, W Zhou, Y Lai, C Wang, M Lu, W Chen

tinyurl.com/zeeb95t8

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RA-deficient DM have a reduction in the number of Nkx2.5+ CMs at 48 hpf

RA-deficient DM have a reduction in the number of Nkx2.5+ CMs at 48 hpf

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Tbx1-dependent and independent pathways promote six gene expression downstream of retinoic acid signaling to determine cardiomyocyte number in zebrafish

by Tiffany Duong, Joshua Waxman et al
www.sciencedirect.com/science/arti...

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Cartoon of Pax9 expression (purple) during facial development in mouse (left) and zebrafish (right).
Text: Mammals. Pax9 is expressed In tooth-forming mesenchyme around the mouth. Required for tooth formation in mouse and human.
Fish. Pax9 is also expressed in oral mesenchyme in fishes. But many fish do not form oral teeth. Vestigial expression or divergent function?
Result: pax9 is required for formation of upper jaw bones and barbels in zebrafish, but dispensable for non-oral teeth.
Support ancestral function in building peri-oral structures from condensed mesenchyme rather than a specific requirement for teeth

Cartoon of Pax9 expression (purple) during facial development in mouse (left) and zebrafish (right). Text: Mammals. Pax9 is expressed In tooth-forming mesenchyme around the mouth. Required for tooth formation in mouse and human. Fish. Pax9 is also expressed in oral mesenchyme in fishes. But many fish do not form oral teeth. Vestigial expression or divergent function? Result: pax9 is required for formation of upper jaw bones and barbels in zebrafish, but dispensable for non-oral teeth. Support ancestral function in building peri-oral structures from condensed mesenchyme rather than a specific requirement for teeth

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Pax9 has a broader role in initiating development of mesenchymal structures around the mouth during zebrafish development

By Sandhya Paudel, Sarah McLeod, Stefani Gjorcheska, Lindsey Barske

tinyurl.com/yc3jfpux

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Shh signaling regulates both sensory and non-sensory development in the cochlea.

Shh signaling regulates both sensory and non-sensory development in the cochlea.

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Review

Multifaceted roles of sonic hedgehog signaling in mammalian inner ear development

Shh confers cochlear apical identity and regulates tonotopy establishment.

by Tianli Qin, Marianne Bronner
www.sciencedirect.com/science/arti...

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Post image

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Wish our authors and readers a Happy Holiday & a fruitful 2026!🥳🥳🥳

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