Formation of DNA triple helices inhibits DNA unwinding by the SV40 large T-antigen helicase.

AUTOR(ES)

Peleg, M

RESUMO

Previous studies have indicated that d(TC)n.d(GA)n microsatellites may serve as arrest signals for mammalian DNA replication through the ability of such sequences to form DNA triple helices and thereby inhibit replication enzymes. To further test this hypothesis, we examined the ability of d(TC)i.d(GA)i.d(TC)i triplexes to inhibit DNA unwinding in vitro by a model eukaryotic DNA helicase, the SV40 large T-antigen. DNA substrates that were able to form triplexes, and non-triplex-forming control substrates, were tested. We found that the presence of DNA triplexes, as assayed by endonuclease S1 and osmium tetroxide footprinting, significantly inhibited DNA unwinding by T-antigen. Strong inhibition was observed not only at acidic pH values, in which the triplexes were most stable, but also at physiological pH values in the range 6.9-7.2. Little or no inhibition was detected at pH 8.7. Based on these results, and on previous studies of DNA polymerases, we suggest that DNA triplexes may form in vivo and cause replication arrest through a dual inhibition of duplex unwinding by DNA helicases and of nascent strand synthesis by DNA polymerases. DNA triplexes also have the potential to inhibit recombination and repair processes in which helicases and polymerases are involved.

Documentos Relacionados

• Unwinding of the third strand of a DNA triple helix, a novel activity of the SV40 large T-antigen helicase.
• Unwinding of chromatin by the SV40 large T antigen DNA helicase.
• The SV40 large T-antigen helicase can unwind four stranded DNA structures linked by G-quartets.
• Binding studies of SV40 T-antigen to SV40 binding site II.
• Dimerization of simian virus 40 T-antigen hexamers activates T-antigen DNA helicase activity.