Enhancer buffering protects dosage-sensitive housekeeping genes during vulnerable developmental transitions
Ni, C.; Ichino, L.; Swigut, T.; Wysocka, J.
Show abstract
Housekeeping genes maintain robust expression across cell types despite dynamic transcription factor fluctuations, yet their haploinsufficiency is associated with many tissue-specific developmental disorders. To understand this paradox, we focus on TCOF1, a broadly expressed regulator of rRNA synthesis, whose haploinsufficiency causes Treacher Collins syndrome (TCS). We show that transitional cranial neural crest cells (tCNCC) undergoing mesenchymal specification exhibit extreme dosage-sensitivity to TCOF1, but not to RNA polymerase I, explaining both cellular origins of TCS and prevalence of TCOF1 mutations in the disease. To maintain robust expression, TCOF1 deploys CNCC-specific enhancers that buffer against fluctuations in promoter-regulating factors, converting sensitive expression responses into threshold-protected outputs. Systematic promoter-enhancer coupling experiments demonstrate this principle generalizes across many dosage-sensitive housekeeping genes, whose promoters operate near saturation and only reveal their enhancer-dependency under suboptimal conditions. Thus, enhancers play a unique role at housekeeping promoters: rather than amplifying expression, they ensure its robustness during vulnerable developmental transitions.
Matching journals
The top 5 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Primordial germ cell DNA demethylation and development require DNA translesion synthesis. 96%
- Nodal is a short-range morphogen with activity that spreads through a relay mechanism in human gastruloids 95%
- Ire1α-Regulated mRNA Translation Rate Controls the Identity and Polarity of Upper Layer Cortical Neurons 95%
Similar papers in this journal
- Postmitotic accumulation of histone variant H3.3 in new cortical neurons establishes neuronal chromatin, transcriptome, and identity 96%
- Induction of Recurrent Break Cluster Genes in Neural Progenitor Cells Differentiated from Embryonic Stem Cells In Culture 96%
- Integrated Genome and Transcriptome Analyses Reveal the Mechanism of Genome Instability in Ataxia with Oculomotor Apraxia 2 96%
Similar papers in this journal
- Primate-restricted KRAB zinc finger proteins and target retrotransposons control gene expression in human neurons 96%
- eIF4A2 targets developmental potency and histone H3.3 transcripts for translational control of stem cell pluripotency 95%
- Gastrulation-stage gene expression in Nipbl+/- mouse embryos foreshadows the development of syndromic birth defects 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.