Cited by 126Bacterial Genetics and BiotechnologyGenomics and Chromatin DynamicsGenomics and Phylogenetic Studies

Protein occupancy landscape of a bacterial genome

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Vora, Tiffany, Hottes, Alison K., Tavazoie, Saeed·2009·Molecular Cell

Abstract

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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Crossref · 10.1016/j.molcel.2009.06.035

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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
Venue
Molecular Cell
Publisher
Elsevier BV
Published
2009-07
Volume
35
Issue
2
Pages
247-253
ISSN
1097-2765 (ISSN-L)
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
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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