Deciphering lineage specification during early embryogenesis in mouse gastruloids using multilayered proteomics.
Suzan StellooMaria Teresa Alejo-VinogradovaCharlotte A G H van GelderDick W ZijlmansMarek J van OostromJuan Manuel ValverdeLieke A LamersTeja RusPaula Sobrevals AlcarazTilman SchäfersCristina FurlanPascal W T C JansenMarijke P A BaltissenKatharina F SonnenBoudewijn BurgeringMaarten A F M AltelaarHarmjan R VosMichiel VermeulenPublished in: Cell stem cell (2024)
Gastrulation is a critical stage in embryonic development during which the germ layers are established. Advances in sequencing technologies led to the identification of gene regulatory programs that control the emergence of the germ layers and their derivatives. However, proteome-based studies of early mammalian development are scarce. To overcome this, we utilized gastruloids and a multilayered mass spectrometry-based proteomics approach to investigate the global dynamics of (phospho) protein expression during gastruloid differentiation. Our findings revealed many proteins with temporal expression and unique expression profiles for each germ layer, which we also validated using single-cell proteomics technology. Additionally, we profiled enhancer interaction landscapes using P300 proximity labeling, which revealed numerous gastruloid-specific transcription factors and chromatin remodelers. Subsequent degron-based perturbations combined with single-cell RNA sequencing (scRNA-seq) identified a critical role for ZEB2 in mouse and human somitogenesis. Overall, this study provides a rich resource for developmental and synthetic biology communities endeavoring to understand mammalian embryogenesis.
Keyphrases
- single cell
- mass spectrometry
- rna seq
- transcription factor
- liquid chromatography
- high throughput
- label free
- endothelial cells
- gas chromatography
- high performance liquid chromatography
- genome wide identification
- capillary electrophoresis
- poor prognosis
- epithelial mesenchymal transition
- high resolution
- gene expression
- binding protein
- public health
- dna damage
- solar cells
- genome wide
- oxidative stress
- signaling pathway
- induced pluripotent stem cells
- case control
- simultaneous determination