Mechanical force antagonizes the inhibitory effects of RecX on RecA filament formation in Mycobacterium tuberculosis

• Published in: Nucleic acids research Vol. 42; no. 19; pp. 11992 - 11999
• Main Authors: Le, Shimin, Chen, Hu, Zhang, Xinghua, Chen, Jin, Patil, K Neelakanteshwar, Muniyappa, Kalappa, Yan, Jie
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 29-10-2014
• Subjects: Adenosine Triphosphate - metabolism; Bacterial Proteins - metabolism; Biomechanical Phenomena; DNA, Single-Stranded; Genome Integrity, Repair and; Mycobacterium tuberculosis; Mycobacterium tuberculosis - metabolism; Polymerization; Rec A Recombinases - metabolism
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gku899

Efficient bacterial recombinational DNA repair involves rapid cycles of RecA filament assembly and disassembly. The RecX protein plays a crucial inhibitory role in RecA filament formation and stability. As the broken ends of DNA are tethered during homologous search, RecA filaments assembled at the ends are likely subject to force. In this work, we investigated the interplay between RecX and force on RecA filament formation and stability. Using magnetic tweezers, at single molecular level, we found that Mycobacterium tuberculosis (Mt) RecX could catalyze stepwise de-polymerization of preformed MtRecA filament in the presence of ATP hydrolysis at low forces (<7 pN). However, applying larger forces antagonized the inhibitory effects of MtRecX, and a partially de-polymerized MtRecA filament could re-polymerize in the presence of MtRecX, which cannot be explained by previous models. Theoretical analysis of force-dependent conformational free energies of naked ssDNA and RecA nucleoprotein filament suggests that mechanical force stabilizes RecA filament, which provides a possible mechanism for the observation. As the antagonizing effect of force on the inhibitory function of RecX takes place in a physiological range; these findings broadly suggest a potential mechanosensitive regulation during homologous recombination.