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Ng-Blichfeldt, J.-P.

Publications and source records attributed to Ng-Blichfeldt, J.-P..

3 recordsLinked to original sources

Chromatin priming and co-factor availability shape lineage response to the neuronal pioneer factor ASCL1 in pluripotency

Transcription factors act within defined developmental windows, yet how naive pluripotent cells acquire competence to execute specific transcription factor-driven fate programmes remains unclear. Pioneer transcription factors that engage target sites in closed chromatin to initiate gene expression programmes often act at the top of hierarchies in cell identity transitions. However, we show that the ability of ASCL1 to induce a coherent neuronal programme emerges only after exit from pluripotency, coincident with progressive chromatin remodelling and accumulation of permissive histone marks at neuronal ASCL1 target sites. Binding analysis reveals that although ASCL1 can access a subset of neuronal loci in mESCs and EpiLCs, ASCL1 is preferentially diverted to non-neuronal sites, resulting in divergent transcriptional responses. Increasing global histone acetylation enhances activation of individual neuronal genes but is insufficient to drive full neuronal differentiation. In contrast, co-expression of the homeodomain transcription factor PHOX2B redirects ASCL1 towards neuronal targets while suppressing inappropriate programmes in mESCs. These findings demonstrate that ASCL1 pioneer activity is highly context-dependent and that developmental priming of chromatin is essential for appropriate lineage specification. HIGHLIGHTSO_LIEctopic ASCL1 drives non-neuronal transcriptional responses in naive and formative pluripotent cells C_LIO_LIASCL1 occupies distinct, predominantly non-neuronal genomic targets in pluripotent cells due to differential chromatin accessibility C_LIO_LIASCL1 pioneer activity is locus- and cell type-specific and predicted by histone acetylation status C_LIO_LICo-expression of ASCL1 with Phox2 homeodomain cofactors potentiates neuronal lineage acquisition in pluripotent cells C_LI

developmental biology↗

Hierarchical TBX6-FOXC Regulatory Logic Controls Human Trunk Mesoderm Diversification

Mesoderm forms during gastrulation and diversifies to generate many embryonic tissues, yet the regulatory logic governing early human mesodermal lineage decisions remains poorly defined. We use human iPSC-derived 3D trunk-like structures (hTLS) to model lineage specification during early post-gastrulation development, a stage experimentally inaccessible in humans. Developing hTLS generate neural and mesodermal lineages and recapitulate progressive mesodermal diversification into paraxial (somitic) and intermediate (renal) identities. Using genetic perturbations and temporally controlled transcription factor activation, we identify duration-dependent TBX6 activity as a critical determinant of mesodermal diversification. Downstream, the forkhead box transcription factors FOXC1 and FOXC2 stabilise somitic identity and are required for sclerotome differentiation. These findings reveal a duration-dependent hierarchical regulatory logic in early human mesoderm, in which competence for diversification is established before downstream lineage identities are stabilised, positioning hTLS as a powerful platform to experimentally dissect human developmental programs. HighlightsO_LIHuman trunk-like structures model mesodermal diversification during early post-gastrulation human trunk development C_LIO_LITBX6 duration acts as a temporal gate controlling mesodermal fate potential C_LIO_LIFOXC1/2 function downstream of TBX6 to lock in somitic identity and restrict alternative fates C_LIO_LIDegTrace enables lineage tracing following transient transcription factor activation C_LI

developmental biology↗

PAX8 and transient Wnt signalling are critical for induction and completion of human renal mesenchymal-to-epithelial transition

During kidney development, nephron epithelia arise de novo from fate-committed mesenchymal progenitors through a mesenchymal-to-epithelial transition (MET). Downstream of fate specification, transcriptional mechanisms that drive establishment of epithelial morphology through MET are poorly understood. We used human renal organoids derived from induced pluripotent stem cells, which recapitulate nephrogenesis, to investigate mechanisms controlling the renal MET programme. Multi-ome profiling of organoids revealed dynamic changes in gene expression and chromatin accessibility driven by transcriptional activators and repressors throughout renal MET. CRISPR-interference-based gene perturbation revealed that PAX8 is essential for initiation of MET in human renal organoids, contrary to mouse, by activating a cell adhesion programme. Furthermore, while Wnt/{beta}-Catenin signalling specifies nephron fate, we find that it must be attenuated to allow HNF1B and TEAD transcription factors to drive completion of MET. These results reveal how the developing kidney balances fate-commitment and morphogenesis with implications for understanding both developmental kidney diseases and aberrant epithelial plasticity following adult renal tubular injury.

developmental biology↗