Condensin pinches a short negatively supercoiled DNA loop during each round of ATP usage

Abstract

Condensin extrudes DNA loops using an ATP-dependent mechanism that remains to be elucidated. Here, we show how condensin activity alters the topology of the interacting DNA. High condensin concentrations restrain DNA positive supercoils. However, in experimental conditions that sustain DNA loop extrusion, condensin restrains negative supercoils. Namely, upon ATP-mediated loading onto DNA, each condensin constrains a DNA linking number difference (ΔLk) of -0.4. This ΔLk increases to -0.8 during ATP binding and resets to -0.4 upon ATP hydrolysis. These ΔLk values reflect the transient formation of a short lefthanded loop of DNA, which is not the extruding loop. We conclude that, upon condensin ATPase-head engagement, a segment of DNA is pinched to form a short negatively supercoiled loop, which can be subsequently merged with the extruding loop. Such "pinch and merge" mechanism implies that the DNA is transferred between two dynamic DNAbinding sites while anchored at a third site.