Two distinct DNA sequences recognized by transcription factors represent enthalpy and entropy optima

Author:

Morgunova Ekaterina1ORCID,Yin Yimeng1,Das Pratyush K2ORCID,Jolma Arttu1,Zhu Fangjie1,Popov Alexander3,Xu You4,Nilsson Lennart4,Taipale Jussi125ORCID

Affiliation:

1. Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden

2. Genome-Scale Biology Research Program, University of Helsinki, Helsinki, Finland

3. European Synchrotron Radiation Facility, Grenoble, France

4. Department of Bioscience and Nutrition, Karolinska Institutet, Huddinge, Sweden

5. Department of Biochemistry, University of Cambridge, Cambridge, United Kingdom

Abstract

Most transcription factors (TFs) can bind to a population of sequences closely related to a single optimal site. However, some TFs can bind to two distinct sequences that represent two local optima in the Gibbs free energy of binding (ΔG). To determine the molecular mechanism behind this effect, we solved the structures of human HOXB13 and CDX2 bound to their two optimal DNA sequences, CAATAAA and TCGTAAA. Thermodynamic analyses by isothermal titration calorimetry revealed that both sites were bound with similar ΔG. However, the interaction with the CAA sequence was driven by change in enthalpy (ΔH), whereas the TCG site was bound with similar affinity due to smaller loss of entropy (ΔS). This thermodynamic mechanism that leads to at least two local optima likely affects many macromolecular interactions, as ΔG depends on two partially independent variables ΔH and ΔS according to the central equation of thermodynamics, ΔG = ΔH - TΔS.

Funder

Knut och Alice Wallenbergs Stiftelse

Cancerfonden

Karolinska Institutet

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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