DNA thermodynamic stability and supercoil dynamics determine the gene expression program during the bacterial growth cycle

• Published in: Molecular bioSystems 2013-01, Vol.9 (7), p.1643-1651
• Main Authors: Sobetzko, Patrick, Glinkowska, Monika, Travers, Andrew, Muskhelishvili, Georgi
• Format: Article
• Language: English
• Subjects: Bacteria; Bacteria - genetics; Bacteria - growth & development; Bacteria - metabolism; Chromosome Mapping; Chromosomes; Chromosomes, Bacterial; DNA, Bacterial - chemistry; DNA, Bacterial - metabolism; DNA, Superhelical - metabolism; Escherichia coli - genetics; Escherichia coli - growth & development; Escherichia coli - metabolism; Gene Expression Profiling; Gene Expression Regulation, Bacterial; Genes, Bacterial; Thermodynamics
• ISSN: 1742-206X; 1742-2051
• DOI: 10.1039/c3mb25515h

The chromosomal DNA polymer constituting the cellular genetic material is primarily a device for coding information. Whilst the gene sequences comprise the digital (discontinuous) linear code, physiological alterations of the DNA superhelical density generate in addition analog (continuous) three-dimensional information essential for regulation of both chromosome compaction and gene expression. Insight into the relationship between the DNA analog information and the digital linear code is of fundamental importance for understanding genetic regulation. Our previous study in the model organism Escherichia coli suggested that the chromosomal gene order and a spatiotemporal gradient of DNA superhelicity associated with DNA replication determine the growth phase-dependent gene transcription. In this study we reveal a general gradient of DNA thermodynamic stability correlated with the polarity of chromosomal replication and manifest in the spatiotemporal pattern of gene transcription during the bacterial growth cycle. Furthermore, by integrating the physical and dynamic features of the transcribed sequences with their functional content we identify spatiotemporal domains of gene expression encompassing different functions. We thus provide both an insight into the organisational principle of the bacterial growth program and a novel holistic methodology for exploring chromosomal dynamics. The chromosomal DNA polymer constituting the cellular genetic material is primarily a device for coding information.