Protein occupancy landscape of a bacterial genome.

Protein-DNA interactions are fundamental to core biological processes, including transcription, DNA replication, and chromosomal organization. We have developed in vivo protein occupancy display (IPOD), a technology that reveals protein occupancy across an entire bacterial chromosome at the resolution of individual binding sites. Application to Escherichia coli reveals thousands of protein occupancy peaks, highly enriched within and in close proximity to noncoding regulatory regions. In addition, we discovered extensive (>1 kilobase) protein occupancy domains (EPODs), some of which are localized to highly expressed genes, enriched in RNA-polymerase occupancy. However, the majority are localized to transcriptionally silent loci dominated by conserved hypothetical ORFs. These regions are highly enriched in both predicted and experimentally determined binding sites of nucleoid proteins and exhibit extreme biophysical characteristics such as high intrinsic curvature. Our observations implicate these transcriptionally silent EPODs as the elusive organizing centers, long proposed to topologically isolate chromosomal domains.

[1]  F. Neidhart Escherichia coli and Salmonella. , 1996 .

[2]  C. Dorman H-NS, the genome sentinel , 2007, Nature Reviews Microbiology.

[3]  Julio Collado-Vides,et al.  RegulonDB (version 6.0): gene regulation model of Escherichia coli K-12 beyond transcription, active (experimental) annotated promoters and Textpresso navigation , 2007, Nucleic Acids Res..

[4]  H. Delius,et al.  Electron microscopic studies on the folded chromosome of Escherichia coli. , 1974, Cold Spring Harbor symposia on quantitative biology.

[5]  S. Busby,et al.  Association of nucleoid proteins with coding and non-coding segments of the Escherichia coli genome , 2006, Nucleic acids research.

[6]  John J. Wyrick,et al.  Genome-wide location and function of DNA binding proteins. , 2000, Science.

[7]  Lucy Shapiro,et al.  Genes directly controlled by CtrA, a master regulator of the Caulobacter cell cycle , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[8]  Jolyon Holdstock,et al.  Studies of the distribution of Escherichia coli cAMP-receptor protein and RNA polymerase along the E. coli chromosome. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[9]  Patrick O. Brown,et al.  Genomewide demarcation of RNA polymerase II transcription units revealed by physical fractionation of chromatin , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[10]  A. Segall,et al.  Probing nucleoid structure in bacteria using phage lambda integrase-mediated chromosome rearrangements. , 2007, Methods in enzymology.

[11]  K. Swinger,et al.  IHF and HU: flexible architects of bent DNA. , 2004, Current opinion in structural biology.

[12]  Byung-Kwan Cho,et al.  Genome-wide analysis of Fis binding in Escherichia coli indicates a causative role for A-/AT-tracts. , 2008, Genome research.

[13]  Mark S. Thomas,et al.  Architecture of Fis-activated transcription complexes at the Escherichia coli rrnB P1 and rrnE P1 promoters. , 2002, Journal of molecular biology.

[14]  C. Wyman,et al.  H-NS mediated compaction of DNA visualised by atomic force microscopy. , 2000, Nucleic acids research.

[15]  A. Travers,et al.  A common topology for bacterial and eukaryotic transcription initiation? , 2007, EMBO reports.

[16]  B. J. Hinnebusch,et al.  The bacterial nucleoid visualized by fluorescence microscopy of cells lysed within agarose: comparison of Escherichia coli and spirochetes of the genus Borrelia , 1997, Journal of bacteriology.

[17]  S Brunak,et al.  A DNA structural atlas for Escherichia coli. , 2000, Journal of molecular biology.

[18]  George M. Church,et al.  Quantitative whole-genome analysis of DNA-protein interactions by in vivo methylase protection in E. coli , 1998, Nature Biotechnology.

[19]  M. Rossignol,et al.  Macrodomain organization of the Escherichia coli chromosome , 2004, The EMBO journal.

[20]  A. J. Bendich The form of chromosomal DNA molecules in bacterial cells. , 2001, Biochimie.

[21]  H. Delius,et al.  Electron microscopic visualization of the folded chromosome of Escherichia coli , 1974 .

[22]  C. Gualerzi,et al.  Nature and mechanism of the in vivo oligomerization of nucleoid protein H‐NS , 2005, The EMBO journal.

[23]  Guy Plunkett,et al.  Engineering a reduced Escherichia coli genome. , 2002, Genome research.

[24]  Richard A Stein,et al.  Organization of supercoil domains and their reorganization by transcription , 2005, Molecular microbiology.

[25]  C. D. Hardy,et al.  Topological domain structure of the Escherichia coli chromosome. , 2004, Genes & development.

[26]  S. McLeod,et al.  Mechanism of chromosome compaction and looping by the Escherichia coli nucleoid protein Fis. , 2006, Journal of molecular biology.

[27]  A. Ishihama,et al.  Twelve Species of the Nucleoid-associated Protein from Escherichia coli , 1999, The Journal of Biological Chemistry.

[28]  G. Church,et al.  Preferred analysis methods for Affymetrix GeneChips revealed by a wholly defined control dataset , 2005, Genome Biology.