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Bacterial chromatin proteins, transcription, and DNA topology: Inseparable partners in the control of gene expression.

Christine M HustmyerRobert Landick
Published in: Molecular microbiology (2024)
DNA in bacterial chromosomes is organized into higher-order structures by DNA-binding proteins called nucleoid-associated proteins (NAPs) or bacterial chromatin proteins (BCPs). BCPs often bind to or near DNA loci transcribed by RNA polymerase (RNAP) and can either increase or decrease gene expression. To understand the mechanisms by which BCPs alter transcription, one must consider both steric effects and the topological forces that arise when DNA deviates from its fully relaxed double-helical structure. Transcribing RNAP creates DNA negative (-) supercoils upstream and positive (+) supercoils downstream whenever RNAP and DNA are unable to rotate freely. This (-) and (+) supercoiling generates topological forces that resist forward translocation of DNA through RNAP unless the supercoiling is constrained by BCPs or relieved by topoisomerases. BCPs also may enhance topological stress and overall can either inhibit or aid transcription. Here, we review current understanding of how RNAP, BCPs, and DNA topology interplay to control gene expression.
Keyphrases
  • circulating tumor
  • gene expression
  • cell free
  • single molecule
  • transcription factor
  • dna methylation
  • nucleic acid
  • dna damage
  • genome wide
  • circulating tumor cells
  • hiv infected
  • human immunodeficiency virus