This Article Full Text (PDF) Supplemental Research Data All Versions of this Article: gr.070276.107v1 gr.070276.107v2    most recent Alert me when this article is cited Alert me if a correction is posted Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Google Scholar Articles by Cho, B.-K. Articles by Palsson, B. O. PubMed PubMed Citation Articles by Cho, B.-K. Articles by Palsson, B. O. Social Bookmarking                   What's this?

Letter

Genome-wide analysis of Fis binding in Escherichia coli indicates a causative role for A-/AT-tracts

Department of Bioengineering, University of California–San Diego, La Jolla, California 92093-0412, USA

We determined the genome-wide distribution of the nucleoid-associated protein Fis in Escherichia coli using chromatin immunoprecipitation coupled with high-resolution whole genome-tiling microarrays. We identified 894 Fis-associated regions across the E. coli genome. A significant number of these binding sites were found within open reading frames (33%) and between divergently transcribed transcripts (5%). Analysis indicates that A-tracts and AT-tracts are an important signal for preferred Fis-binding sites, and that A₆-tracts in particular constitute a high-affinity signal that dictates Fis phasing in stretches of DNA containing multiple and variably spaced A-tracts and AT-tracts. Furthermore, we find evidence for an average of two Fis-binding regions per supercoiling domain in the chromosome of exponentially growing cells. Transcriptome analysis shows that 21% of genes are affected by the deletion of fis; however, the changes in magnitude are small. To address the differential Fis bindings under growth environment perturbation, ChIP-chip analysis was performed using cells grown under aerobic and anaerobic growth conditions. Interestingly, the Fis-binding regions are almost identical in aerobic and anaerobic growth conditions—indicating that the E. coli genome topology mediated by Fis is superficially identical in the two conditions. These novel results provide new insight into how Fis modulates DNA topology at a genome scale and thus advance our understanding of the architectural bases of the E. coli nucleoid.

² Corresponding author.

E-mail bpalsson{at}bioeng.ucsd.edu; fax (858) 822-3120.

[Supplemental material is available online at www.genome.org.]

Article published online before print. Article and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.070276.107

CiteULike    Connotea    Del.icio.us    Digg    Reddit    Technorati    What's this?