Protein occupancy landscape of a bacterial genome
Open accessAbstract
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.
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Predicted high-occupancy RNA polymerase regions correspond to highly transcribed rRNAs and tRNAs.
“Consistent with a recent experimental study by Vora et al., 2009, the predicted high-occupancy RNA polymerase regions correspond to highly transcribed rRNAs and tRNAs.”
From A Whole-Cell Computational Model Predicts Phenotype from Genotype (2012) · cites this paper as Vora et al., 2009
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References 29 · Cited by 126
- Authors
- Vora, T., Hottes, A. K., & Tavazoie, S.
- Affiliations
- Princeton University (US)
- Corresponding author
- Tavazoie, Saeed
- ORCID
- Tavazoie, Saeed
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2009-07
- Volume
- 35
- Issue
- 2
- Pages
- 247-253
- ISSN
- 1097-2765 (ISSN-L)
- PMC
- PMC2763621
- OpenAlex
- W2018521934
- Cited by
- 126
- References
- 29
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 10 · 2023: 6 · 2022: 2 · 2021: 9 · 2020: 5 · 2019: 3 · 2018: 7 · 2017: 6 · 2016: 13 · 2015: 8 · 2014: 9 · 2013: 9 · 2012: 11
- FWCI
- 6.34
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (DP1OD003787)
- National Institute of General Medical Sciences (P50GM071508)
- National Center for Chronic Disease Prevention and Health Promotion (1DP10D 003787-01)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
- Keywords
- protein-DNA interactions, bacterial chromosome, Escherichia coli, RNA polymerase, DNA curvature, chromosome organization
- MeSH terms
- Binding Sites, Chromosomes, Bacterial, DNA-Binding Proteins, Escherichia coli, Hybridization, Genetic, DNA-Directed RNA Polymerases, RNA, Messenger, Genome, Bacterial, DNA Footprinting, Gene Expression Profiling, Escherichia coli Proteins
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