Posts by Alejandro Berrio Escobar
This work was supported by the National Institutes of Health NIH and to the National Science Foundation
We're grateful for the support that makes long term, data rich developmental biology possible.
#NIH #NSF #FundedScience #DevelopmentalBiology
We'd love to hear what you discover in the data!
#SeaUrchin #WntSignaling #DevelopmentalBiology #GRN #ScienceCommunication
We published this work in the journal @dev-journal.bsky.social
doi.org/10.1242/dev.20...
Want to explore the data yourself?
Check out our Shiny app for hourly scRNA-seq, interactive UMAPs, co-expression, trajectories:
urchinatlas.biology.duke.edu:3838
Nodal isnât just patterning, itâs a gatekeeper of developmental commitment.
And if youâre interested in GRN flexibility, see our earlier paper on embryonic transfating:
đhttps://doi.org/10.1242/dev.203152
This may explain why Nodal was so important in our transfating paper.
When we manipulated nodal signaling, GRN states that are normally stabilized during development became plastic again, allowing cells to reprogram.
When the dance reaches the mouth, a new partner steps in: nodal.
Wnt1 enables anterior wnt8, and wnt8 both directly activates foxA (via ÎČâcatenin/TCF) and induces nodal at the stomodeum.
Nodal then brings in gooscoid, which is required for foxA and brachyury
Despite all the apparent rings, there is only one truly sharp boundary:
Wnt1 outside the blastopore. Wnt6/7/16 inside.
Elsewhere, expression is graded and overlapping
đȘ©wnt1 KD fails to block the pattern of wnt1 expression
đȘ©wnt8 KD reduces but fails to block the pattern of wnt8 expression
đȘ©wnt7 KD inhibits foregut expression of wnt5 but has no effect on wnt5 expression in the ectoderm
đȘ©wnt5 KD reduces foregut-midgut expression of wnt7
And the dancers cue each other.
Wnts donât just pattern tissues, they regulate other Wnts. We tested this by perturbing Wnts with morpholinos and RNAi
Indeed, there is not one signal at a time.
Our temporal scRNAâseq showed that many cells coâexpress multiple Wnts simultaneously, and that coâexpression changes over time. #scRNAseq #bioinformatics
Inside the Wnt1 ring, the choreography calls a figure switch.
At the blastopore, cells momentarily express Wnt6, Wnt7, and Wnt16.
Crossing into the archenteron, they cast off Wnt6 and Wnt16 but retain Wnt7, making moves to the next figure in the GRN.
Before gastrulation, the Wnt1 ring expands outward as neighboring cells activate it and inner cells extinguish it.
During gastrulation, the ring shrinks, tracking the blastopore as Veg1 cells converge, express Wnt1, then turn it off inside
#gastrulation
At start, one ring takes the lead. Wnt1 forms the sharpest boundary just outside the blastopore and every endoderm cell expresses it briefly before entering the gut. This is the embryoâs Ring of Fire.
You pass through once, and you donât come out the same.
#Morphogenesis
We used multiplex HCRâFISH, and mapped six Wnts (Wnt1, 5, 6, 7, 8, 16) across developmental stages.
Each gene turns on at a different time, then appears sequentially in neighboring cells, producing rings of expression around the blastopore. #HCR #FISH
During gastrulation, cells donât just change position they change state.
As endoderm cells move toward and through the blastopore, the signals they receive change over time, advancing their gene regulatory networks (GRNs) step by step. #GRN #WntSignaling
It takes two to tango but gastrulation is a contra dance
Cells move through changing partners and signals, and many Wnts act together to keep the choreography coordinated in space and time.
Thatâs the core idea behind our new paper on gut formation in #seaurchins đ§”
Before gastrulation, the Wnt1 ring expands outward as neighboring cells activate it and inner cells extinguish it.
During gastrulation, the ring shrinks, tracking the blastopore as Veg1 cells converge, express Wnt1, then turn it off inside
The first ring leads the way. Wnt1 forms the sharpest boundary and every endoderm cell expresses it briefly before entering the gut
This is the embryoâs Ring of Fire. You pass through once and you donât come out the same.
We used multiplex HCRâFISH, and mapped six Wnts (Wnt1, 5, 6, 7, 8, 16) across development.
Each gene turns on at a different time, then appears sequentially in neighboring cells, producing rings of expression around the blastopore.
During gastrulation, cells donât just change position, they change state.
As endoderm cells move toward and through the blastopore, the signals they receive change over time, advancing their gene regulatory networks (GRNs) step by step.
Here at #DBSUMI2025 and excited about the new methodologies coming to the community. Automated HCRs, so cool and necessary to screen many genes in parallel
A very appropriate citation report email I got today. Happy Valentine's y'all.
Time-lapsed video of the first cleavage in a Heliocidaris erythrogramma embryo. Taken in my last research trip to Australia.
The best howls are critically endangered Red Wolf howls đș
Dreaming of a world where every wolf is respected đș
Best PPE gift from my bestie at work!
I'll be sharing my passion for sea urchins, science, bicycles, cheese, baking, nature, and standing up against narcissistic personalities from any side in the political compass. For them, I'll be nothing but gray rocks đȘš and đ
Lone wolf and gravel bike in a french beach full of sea urchins, ai generated