An ensemble model of competitive multi-factor binding of the genome. Export

@article{citeulike:5695623, abstract = {Hundreds of different factors adorn the eukaryotic genome, binding to it in large number. These DNA binding factors (DBFs) include nucleosomes, transcription factors (TFs), and other proteins and protein complexes, such as the origin recognition complex (ORC). DBFs compete with one another for binding along the genome, yet many current models of genome binding do not consider different types of DBFs together simultaneously. Additionally, binding is a stochastic process that results in a continuum of binding probabilities at any position along the genome, but many current models tend to consider positions as being either binding sites or not. Here, we present a model that allows a multitude of DBFs, each at different concentrations, to compete with one another for binding sites along the genome. The result is an "occupancy profile," a probabilistic description of the DNA occupancy of each factor at each position. We implement our model efficiently as the software package COMPETE. We demonstrate genome-wide and at specific loci how modeling nucleosome binding alters TF binding, and vice versa, and illustrate how factor concentration influences binding occupancy. Binding cooperativity between nearby TFs arises implicitly via mutual competition with nucleosomes. Our method applies not only to TFs, but also recapitulates known occupancy profiles of a well-studied replication origin with and without ORC binding. Importantly, the sequence preferences our model takes as input are derived from in vitro experiments. This ensures that the calculated occupancy profiles are the result of the forces of competition represented explicitly in our model and the inherent sequence affinities of the constituent DBFs.}, author = {Wasson, Todd and Hartemink, Alexander J.}, citeulike-article-id = {5695623}, citeulike-linkout-0 = {http://dx.doi.org/10.1101/gr.093450.109}, citeulike-linkout-1 = {http://genome.cshlp.org/content/early/2009/08/28/gr.093450.109.abstract}, citeulike-linkout-2 = {http://genome.cshlp.org/content/early/2009/08/28/gr.093450.109.full.pdf}, citeulike-linkout-3 = {http://view.ncbi.nlm.nih.gov/pubmed/19720867}, citeulike-linkout-4 = {http://www.hubmed.org/display.cgi?uids=19720867}, day = {31}, doi = {10.1101/gr.093450.109}, issn = {1549-5469}, journal = {Genome research}, keywords = {motif, proteins, tf}, month = {November}, number = {11}, pages = {2101--2112}, posted-at = {2009-11-02 18:15:45}, priority = {2}, title = {An ensemble model of competitive multi-factor binding of the genome.}, url = {http://dx.doi.org/10.1101/gr.093450.109}, volume = {19}, year = {2009} }

TY - JOUR ID - citeulike:5695623 L3 - citeulike-article-id:5695623 N2 - Hundreds of different factors adorn the eukaryotic genome, binding to it in large number. These DNA binding factors (DBFs) include nucleosomes, transcription factors (TFs), and other proteins and protein complexes, such as the origin recognition complex (ORC). DBFs compete with one another for binding along the genome, yet many current models of genome binding do not consider different types of DBFs together simultaneously. Additionally, binding is a stochastic process that results in a continuum of binding probabilities at any position along the genome, but many current models tend to consider positions as being either binding sites or not. Here, we present a model that allows a multitude of DBFs, each at different concentrations, to compete with one another for binding sites along the genome. The result is an "occupancy profile," a probabilistic description of the DNA occupancy of each factor at each position. We implement our model efficiently as the software package COMPETE. We demonstrate genome-wide and at specific loci how modeling nucleosome binding alters TF binding, and vice versa, and illustrate how factor concentration influences binding occupancy. Binding cooperativity between nearby TFs arises implicitly via mutual competition with nucleosomes. Our method applies not only to TFs, but also recapitulates known occupancy profiles of a well-studied replication origin with and without ORC binding. Importantly, the sequence preferences our model takes as input are derived from in vitro experiments. This ensures that the calculated occupancy profiles are the result of the forces of competition represented explicitly in our model and the inherent sequence affinities of the constituent DBFs. IS - 11 JF - Genome research SN - 1549-5469 EP - 2112 TI - An ensemble model of competitive multi-factor binding of the genome. VL - 19 SP - 2101 KW - motif KW - proteins KW - tf AU - Wasson, Todd AU - Hartemink, Alexander PY - 2009/11/31/ UR - http://dx.doi.org/10.1101/gr.093450.109 ER -