Bacterial chromatin remodeling associated with transcription-induced domains at pathogenicity Islands
Open Access
- 8 January 2026
- journal article
- research article
- Published by Springer Nature in Nature Communications
- Vol. 17 (1) , 161
Abstract
The nucleoid-associated protein H-NS is a bacterial xenogeneic silencer responsible for preventing costly expression of genes acquired through horizontal gene transfer. H-NS silences several Salmonella Pathogenicity Islands (SPIs) essential for host infection. The stochastic expression of SPI-1 is required for invasion of host epithelial cells but complicates investigation of factors involved in SPI-1 chromatin structure and regulation. We performed functional genomics on sorted Salmonella populations expressing SPI-1 or not, to characterize how SPI-1 activation affects chromatin composition, DNA conformation, gene expression and SPI-1 subcellular localization. We show that silent SPIs are associated with spurious antisense transcriptional activity originating from H-NS-free regions. Upon SPI-1 activation, remodeling of H-NS occupancy defines a new chromatin landscape, which together with the master SPI-1 regulator HilD, facilitates transcription of SPI-1 genes. SPI-1 activation promotes formation of Transcription Induced Domains accompanied by repositioning SPI-1 close to the nucleoid periphery. We present a model for tightly regulated chromatin remodeling that minimizes the cost of pathogenicity island activation.Keywords
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Funding Information
- Agence Nationale de la Recherche (ANR-20-CE35-005)
- Agence Nationale de la Recherche (ANR-24-INBS-0005 FBI (BIOGEN))
- 80 Prime CNRS project
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