Su(H) Modulates Enhancer Transcriptional Bursting in Prelude to Gastrulation

Cells. 2024 Oct 24;13(21):1759. doi: 10.3390/cells13211759.

Abstract

Transcriptional regulation, orchestrated by the interplay between transcription factors (TFs) and enhancers, governs gene expression dynamics crucial for cellular processes. While gross qualitative fluctuations in transcription factor-dependent gene expression patterning have a long history of characterization, the roles of these factors in the nuclei retaining expression in the presence or absence of these factors are now observable using modern techniques. Our study investigates the impact of Suppressor of Hairless (Su(H)), a broadly expressed transcription factor, on enhancer-driven transcriptional modulation using Drosophila early embryos as a model system. Building upon previous findings, we employ super-resolution microscopy to dissect Su(H)'s influence on sog-Distal (sogD) enhancer activity specifically in nuclei with preserved sogD-driven expression in the absence of Su(H) binding. We demonstrate that Su(H) occupancy perturbations alter expression levels and bursting dynamics. Notably, Su(H) absence during embryonic development exhibits region-specific effects, inhibiting expression dorsally and stabilizing expression ventrally, implying a nuanced role in enhancer regulation. Our findings shed light on the intricate mechanisms that govern transcriptional dynamics and suggest a critical patterning role for Notch/Hairless signaling in sog expression as embryos transition to gastrulation.

Keywords: Notch/Hairless signaling; Su(H); embryogenesis; gene expression dynamics; sog enhancer; transcriptional bursting.

MeSH terms

  • Animals
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster* / embryology
  • Drosophila melanogaster* / genetics
  • Drosophila melanogaster* / metabolism
  • Embryo, Nonmammalian / metabolism
  • Enhancer Elements, Genetic* / genetics
  • Gastrulation* / genetics
  • Gene Expression Regulation, Developmental*
  • Repressor Proteins* / genetics
  • Repressor Proteins* / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Drosophila Proteins
  • Repressor Proteins
  • Su(H) protein, Drosophila
  • Transcription Factors

Grants and funding