Analysis of in-vivo LacR-mediated gene repression based on the mechanics of DNA looping

Abstract

Interactions of E. coli lac repressor (LacR) with a pair of operator sites on the same DNA molecule can load to the formation of looped nucleuprotein complexes both in vitro and in vivo. As a major paradigm for loop-mediated gene regulation, parameters such as operator affinity and spacing, repressor concentration, and DNA bending induced by specific or non-specific DNA-binding proteins (e.g., HU), have been examined extensively. However, a complete and rigorous model that integrates all of these aspects in a systematic and qualitative treatment of experimental data has not been available. Applying our recent statistical-mechanical theory for DNA looping, we calculated repression as a function of operator spacing (58-156 bp) from first principles and obtained excellent agreement with independent sets of in-vivo data, The results suggest that a linear extended as opposed to a closed v-shaped LacR conformation is the dominant form of the tetramer in vivo. Moreover, loop mediated repression in wild-type E coli strains is facilitated by decreased DNA rigidity and high levels of flexibility in the LacR tetramer. In contrast, repression data for strains lacking HU gave a near-normal value of the DNA persistence length. These findings underscore the importance of both protein conformation and elasticity in the formation of small DNA loops widely observed in vivo, and demonstrate the utility of quantitatively analyzing gene regulation based on the mechanics of nucleoprotein complexes. © 2006 Zhang et al.