Aug 2026· Nature Communications· Vol 17· 0 citations· 100 references
Medicine
TL;DR
A single-cell CRISPR screening platform is established in gastruloids to identify Cnot8-dependent mRNA deadenylation as a driver of mesoderm patterning and identify the deadenylase Cnot8 as a fundamental mechanism linking cellular identity with morphogenetic signaling during mammalian body plan formation.
Abstract
The establishment of the body plan during gastrulation represents a hallmark of animal life. It emerges from the interplay of gene-regulatory programs and positional cues, yet how these signals are integrated post-transcriptionally remains largely unexplored. Here, we combine the scalability of mouse gastruloids with a single-cell CRISPR screening platform to functionally dissect germ layer specification at single-cell transcriptomic resolution. Focusing on post-transcriptional regulation, we systematically map drivers of mesodermal and endodermal fate and identify the deadenylase Cnot8. Loss of Cnot8 leads to widespread poly(A) tail elongation and transcript stabilization, shifting mesoderm differentiation toward ectopic notochord fate, thereby profoundly impacting axial patterning. Collectively, our findings identify mRNA deadenylation as a fundamental mechanism linking cellular identity with morphogenetic signaling during mammalian body plan formation. How post-transcriptional mechanisms shape the mammalian body plan remains unclear. Here, the authors establish a single-cell CRISPR screening platform in gastruloids to identify Cnot8-dependent mRNA deadenylation as a driver of mesoderm patterning.
The chromatoid body is established as a dynamic post-transcriptional regulatory compartment that integrates genome surveillance, RNA quality control and selective transcript sorting, uncovering general principles through which biomolecular condensates shape cell-specific transcriptomes.
Lin Ma, A. Ahmedani, Simang Champramary et al.· bioRxiv· 0 citations
The mouse genome encodes two
Lefty
genes that antagonize NODAL signaling to break symmetry during gastrulation. Despite their central regulatory role, accurately describing and comparing their embryonic function remains unclear. Here, we generated high replicate powered single-cell transcriptional atlases of
Lef...
Min-Ming Wang, T. Hou, JoAnne Villagrana et al.· Nature Communications· 0 citations
It is demonstrated that post-transcriptional regulation of the Profilin 2 (Pfn2) transcript is essential for differentiation of embryonic stem cells into the primary germ layer lineages and revealed the Pfn2 microRNA-IRE regulatory axis as a critical post-transcriptional regulatory node governing the switch from plurip...
Carolyn Sangokoya, Isabella R. Rosso, Rana Ghandehari-Alavijeh et al.· PLoS Genetics· 0 citations
Transcriptional shut-off experiments confirmed that m6A has opposing effects on mRNA decay depending on cellular context: it stabilizes transcripts in differentiated cells, while it promotes the degradation of mRNAs associated with neoblasts.
C. Höhn, Andreas Pittroff, Anne-Sophie Gribling-Burrer et al.· Nucleic Acids Research· 0 citations
Ch chromatin polyvalency model is established as a multi-layered, hierarchical repression mechanism that governs temporal control of gene expression during embryogenesis and disrupts temporal control of polyvalent gene activation.
During embryogenesis, morphologically diverse epithelial organs bud from different regions of the embryonic gut. The unique features of each nascent organ result from distinct cell fate specification and morphogenetic events elicited by organ-inducing cues. Retinoic acid is a powerful inducer of the pancreas, yet, how...
Ivan Kulik, Cheng-Lei Tian, Sabina Chubanava et al.· Development· 0 citations
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