TRF2 and Apollo Cooperate with Topoisomerase 2α to Protect Human Telomeres from Replicative Damage

SummaryHuman telomeres are protected from DNA damage by a nucleoprotein complex that includes the repeat-binding factor TRF2. Here, we report that TRF2 regulates the 5′ exonuclease activity of its binding partner, Apollo, a member of the metallo-β-lactamase family that is required for telomere integrity during S phase. TRF2 and Apollo also suppress damage to engineered interstitial telomere repeat tracts that were inserted far away from chromosome ends. Genetic data indicate that DNA topoisomerase 2α acts in the same pathway of telomere protection as TRF2 and Apollo. Moreover, TRF2, which binds preferentially to positively supercoiled DNA substrates, together with Apollo, negatively regulates the amount of TOP1, TOP2α, and TOP2β at telomeres. Our data are consistent with a model in which TRF2 and Apollo relieve topological stress during telomere replication. Our work also suggests that cellular senescence may be caused by topological problems that occur during the replication of the inner portion of telomeres.

Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (149 K)Download as PowerPoint slideHighlights▸ Replication through telomeric DNA requires TRF2 and the nuclease domain of Apollo ▸ DNA topoisomerase 2α protects telomeres in the same pathway as TRF2 and Apollo ▸ TRF2 preferentially binds positive supercoiled DNA ▸ Apollo and TRF2 control the amount of topoisomerase needed for telomere replication