Nature Communications (Mar 2024)

Transcription-driven DNA supercoiling counteracts H-NS-mediated gene silencing in bacterial chromatin

  • Nara Figueroa-Bossi,
  • Rocío Fernández-Fernández,
  • Patricia Kerboriou,
  • Philippe Bouloc,
  • Josep Casadesús,
  • María Antonia Sánchez-Romero,
  • Lionello Bossi

DOI
https://doi.org/10.1038/s41467-024-47114-w
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 12

Abstract

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Abstract In all living cells, genomic DNA is compacted through interactions with dedicated proteins and/or the formation of plectonemic coils. In bacteria, DNA compaction is achieved dynamically, coordinated with dense and constantly changing transcriptional activity. H-NS, a major bacterial nucleoid structuring protein, is of special interest due to its interplay with RNA polymerase. H-NS:DNA nucleoprotein filaments inhibit transcription initiation by RNA polymerase. However, the discovery that genes silenced by H-NS can be activated by transcription originating from neighboring regions has suggested that elongating RNA polymerases can disassemble H-NS:DNA filaments. In this study, we present evidence that transcription-induced counter-silencing does not require transcription to reach the silenced gene; rather, it exerts its effect at a distance. Counter-silencing is suppressed by introducing a DNA gyrase binding site within the intervening segment, suggesting that the long-range effect results from transcription-driven positive DNA supercoils diffusing toward the silenced gene. We propose a model wherein H-NS:DNA complexes form in vivo on negatively supercoiled DNA, with H-NS bridging the two arms of the plectoneme. Rotational diffusion of positive supercoils generated by neighboring transcription will cause the H-NS-bound negatively-supercoiled plectoneme to “unroll” disrupting the H-NS bridges and releasing H-NS.