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Regulation of mRNA poly(A) tail length governs mammalian body plan formation in gastruloids

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.

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