Journal
MOLECULAR SYSTEMS BIOLOGY
Volume 8, Issue -, Pages -Publisher
WILEY
DOI: 10.1038/msb.2012.42
Keywords
facilitated diffusion; genome organization; single molecule microscopy; transcriptional regulation
Categories
Funding
- National Institutes of Health [GM078591, GM071508]
- Howard Hughes Medical Institute [52005884]
- NIH Ruth Kirschstein NRSA Fellowship [F32GM090568-01A1]
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The diffusion coefficient of the transcription factor LacI within living Escherichia coli has been measured directly by in vivo tracking to be D 0.4 mu m(2)/s. At this rate, simple models of diffusion lead to the expectation that LacI and other proteins will rapidly homogenize throughout the cell. Here, we test this expectation of spatial homogeneity by single-molecule visualization of LacI molecules non-specifically bound to DNA in fixed cells. Contrary to expectation, we find that the distribution depends on the spatial location of its encoding gene. We demonstrate that the spatial distribution of LacI is also determined by the local state of DNA compaction, and that E. coli can dynamically redistribute proteins by modifying the state of its nucleoid. Finally, we show that LacI inhomogeneity increases the strength with which targets located proximally to the LacI gene are regulated. We propose a model for intranucleoid diffusion that can reconcile these results with previous measurements of LacI diffusion, and we discuss the implications of these findings for gene regulation in bacteria and eukaryotes. Molecular Systems Biology 8: 610; published online 11 September 2012; doi:10.1038/msb.2012.42
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