2001/12/31 by Ulrich Gerland, J. David Moroz, Terence Hwa · 9 citations
Biochemistry, Genetics and Molecular Biology · Physics and Astronomy · #Diffusion and Search Dynamics #Genomics and Chromatin Dynamics #RNA and protein synthesis mechanisms #cond-mat.stat-mech #physics.bio-ph #q-bio.BM
paper · pdf · doi:10.1073/pnas.192693599
published as Proc. Natl. Acad. Sci. USA 99 (2002) 12015-20 · 9 pages, 4 figures; revised version as published in PNAS
openalex publication_date 2002/09/06 · arxiv created 2002/09/09 · arxiv updated 2009/11/30 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/28
We study theoretical "design principles" for transcription factor (TF)-DNA interaction in bacteria, focusing particularly on the statistical interaction of the TFs with the genomic background (i.e., the genome without the target sites). We introduce and motivate the concept of programmability, i.e., the ability to set the threshold concentration for TF binding over a wide range merely by mutating the binding sequence of a target site. This functional demand, together with physical constraints arising from the thermodynamics and kinetics of TF-DNA interaction, leads us to a narrow range of "optimal" interaction parameters. We find that this parameter set agrees well with experimental data for the interaction parameters of a few exemplary prokaryotic TFs, which indicates that TF-DNA interaction is indeed programmable. We suggest further experiments to test whether this is a general feature for a large class of TFs.