Unloxing the assembly and activation mechanism of Cre recombinase using Cryo-EM

Abstract

AbstractMechanistic understanding of the structural basis for DNA recombination in the Cre-loxP system has largely been guided by crystallographic structures of tetrameric synaptic complexes (intasomes). These structural and biochemical studies have suggested that conformational changes and DNA bending in presynaptic complexes underlie site-selection and activation mechanisms of Cre recombinase. Here we used protein engineering and various DNA substrates to isolate the Cre-loxP (54 kDa), Cre2-loxP (110 kDa), and Cre4-loxP2 assembly intermediates, and determined their structures using cryo-EM to resolutions of 3.9 Å, 4.5 Å, and 3.2 Å, respectively. Progressive DNA bending along the assembly pathway enables formation of increasingly intimate protein-protein interfaces. Insufficient stabilization of important protein motifs observed during the assembly process provides a compelling explanation for the observed half-the-sites activity, and preferential bottom strand cleavage of loxP sequences. We found that selection of loxP sites is largely dependent on Cre’s ability to bend and stabilize the spacer region between two recombinase binding elements. Application of 3D variability analysis to the tetramer data reveals a propensity for motion along the pathway between protomer activation and Holliday junction isomerization. These findings help us to better understand loxP site specificity, controlled activation of alternating protomers, the basis for the observed bias of strand cleavage order, and the importance of conformational sampling, especially with regards to site-selection and activity among Cre variants. Furthermore, our findings provide invaluable information for the rational development of designer, site-specific recombinases for use as gene editing technologies.HighlightsCryo-EM structures of Cre-loxP assembly intermediates (monomer, dimer, and tetramer) provide insights into mechanisms of site recognition, half-the-sites activity, strand cleavage order, and concerted strand cleavageSelectivity of loxP sites arises from few base-specific contacts made by each protomer and is mainly driven by formation of phosphate contacts and DNA deformations that are maximal in the fully assembled “active” tetramerCis and trans interactions of the β2-3 loop (i) define which sites are “active” and (ii) ensure half-the-sites activityProtein flexibility plays a central role in enabling DNA sequence scanning, recruitment of a second protein to form a dimer, synapsis, control of activity, as well as subsequent recombination stepsConformational sampling within the tetrameric complex was uncovered using 3D variability analysis and revealed the importance of protein-protein interfaces for site- selection and activation of Cre-loxP complexes