Heintzman DR et al. (2019), Topoisomerase II Is Crucial for Fork Convergenc...

XB-ART-56348

Cell Rep 2019 Oct 08;292:422-436.e5. doi: 10.1016/j.celrep.2019.08.097.

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Topoisomerase II Is Crucial for Fork Convergence during Vertebrate Replication Termination.

Heintzman DR , Campos LV , Byl JAW , Osheroff N , Dewar JM .

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Termination of DNA replication occurs when two replication forks converge upon the same stretch of DNA. Resolution of topological stress by topoisomerases is crucial for fork convergence in bacteria and viruses, but it is unclear whether similar mechanisms operate during vertebrate termination. Using Xenopus egg extracts, we show that topoisomerase II (Top2) resolves topological stress to prevent converging forks from stalling during termination. Under these conditions, stalling arises due to an inability to unwind the final stretch of DNA ahead of each fork. By promoting fork convergence, Top2 facilitates all downstream events of termination. Converging forks ultimately overcome stalling independently of Top2, indicating that additional mechanisms support fork convergence. Top2 acts throughout replication to prevent the accumulation of topological stress that would otherwise stall converging forks. Thus, termination poses evolutionarily conserved topological problems that can be mitigated by careful execution of the earlier stages of replication.

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Species referenced: Xenopus
Genes referenced: cdc45 cdc7 gmnn mcm6.2 pcna rpa1 top2a
GO keywords: DNA topoisomerase activity [+]

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	Graphical abstract
	Figure 1. Top2Î± Is Important for Decatenation and Fork Merger (A) Schematic of the decatenation assay. (B) Top2Î±-immunodepleted extracts were visualized alongside mock-immunodepleted extracts by western blotting. The dark panel is overexposed. (C) Plasmid DNA was replicated in mock-, Top2Î±-immunodepleted, and rescued (ÎTop2Î±+hTop2Î±) extracts containing [Î±-32P]dATP. Replication intermediates were purified and then separated on an agarose gel and visualized by autoradiography. See also Figures S1EâS1G and S1B. (D) Quantification of decatenation in (C). See also Figure S1C. (E) 500 ng of human Top2Î± was separated on a polyacrylamide gel and visualized by Coomassie staining. (F) DNA synthesis was measured during plasmid DNA replication in mock- and Top2Î±-immunodepleted extracts. Plot depicts mean Â± SD from 4 experiments. (G) Schematic of the fork merger assay. (H) DNA samples from (E) were digested and then separated on an agarose gel and visualized by autoradiography. See also Figure S1H. (I) Quantification of fork merger in (H). See also Figure S1I.
	Figure 2. Fork Merger, but Not Decatenation, Can Occur in the Absence of Top2Î± (A) Schematic of the fork merger assay. (B) Plasmid DNA replication was performed in mock- or Top2Î±-immunodepleted extracts containing [Î±-32P]dATP and either vehicle or Top2-i. Replication intermediates were purified, digested, and then separated on an agarose gel and visualized by autoradiography. See also Figure S2A. (C) Quantification of fork merger in (B). See also Figure S2B. (D) Schematic of the decatenation assay. (E) Replication intermediates from (B) were separated on an agarose gel and visualized by autoradiography. See also Figure S2G. (F) Quantification of Catsâˆ’ and Cats+ in (E). See also Figures S2Iâ€“S2K. (G) Schematic of DNA structures observed by 2D gel analysis of nicked replication intermediates. The source of the Î¸s, Cats, and cm is indicated in (D). Linear monomers (LMs) arise from a double-strand breaks in cm, while Ïƒs arise from double-strand breaks in Î¸s. Each catenated species runs at a discrete location corresponding to the number of catenanes present. Numbers indicate how many catenated linkages are present. (H) Plasmid DNA was replicated in Top2Î±-immunodepleted extracts containing [Î±-32P]dATP and either Vehicle or Top2-i. Replication intermediates were purified, nicked, and then separated by 2D gel electrophoresis and detected by autoradiography. See also Figure S3J. (I and J) Quantification of the number of catenanes present in the catenanted species detected in (Hii), (Hiii), (Hv), and (Hvi). The graphs depict cumulative frequency distribution, and numbers in parentheses indicate the median number of catenanes in each condition. See also Figures S3Kâ€“S3N.
	Figure 3. Loss of Top2Î± Impairs Fork Convergence (A) Schematic of DNA structures observed by 2D gel electrophoresis following restriction digest (as in Figure 1G). Double Ys and Xs arise from intermediates cut behind two forks, while bubbles occur when intermediates are cut between two forks. Ys arise from incision of one fork (see Figure S4B). (B) Plasmid DNA was replicated in mock- and Top2Î±-immunodepleted extracts containing [Î±-32P]dATP. To monitor the DNA structures formed, replication intermediates were digested and then separated by 2D gel electrophoresis and detected by autoradiography. See also Figure S4A. (C) Plasmid DNA was replicated in Mock- and Top2Î±-immunodepleted extracts containing [Î±-32P]dATP. Replication intermediates were purified then denatured. The expected products are shown. Black lines indicate unlabeled parental strands. Dashed lines represent strands that should not be detectable because they are unlabeled or not intertwined with a labeled strand. (D) Schematic depicting the effect of Nb.BssSI treatment on the intermediates shown in (C). (E) Replication intermediates from (C) and (D) were separated on a denaturing agarose gel and visualized by autoradiography. Structures indicated in (C) and (D) are labeled. Linear (3,402) molecules arise from double-stranded monomers that were nicked during DNA purification, prior to Nb.BssSI treatment. Lanes 10â14 are molecular weight standards of the indicated sizes. The numbers in parentheses represent the amount of unreplicated DNA in lanes 2â9 and 15â22 that each standard corresponds to. See also Figures S4C and S4HâS4K. (F) Quantification of the amount of unreplicated DNA in lane 6 of (E) after correcting for the â¼60-bp footprint of the replisome (Dewar et al., 2015). Plot depicts mean Â± SD from 4 experiments. (G) Plasmid DNA containing a LacR-bound 16xlacO array was replicated in mock- and Top2Î±-immunodepleted extracts containing [Î±-32P]dATP. Replication intermediates were purified and then nicked and denatured. (H) Replication intermediates from (G) were separated on a denaturing agarose gel alongside a DNA ladder. Note that lanes 1 and 10 are overexposed. See also Figures S4LâS4Q. (I) Quantification of the size of the nascent strand products from (H) relative to the initial size of the nascent products in mock-immunodepleted extracts. Plot depicts mean Â± SD from 3 experiments. (J) Quantification of the abundance of the leading strand (â¼948) products from (H) relative to the initial abundance in mock-immunodepleted extracts. Plot depicts mean Â± SD from 3 experiments.
	Figure 4. Top2Î± Is Crucial for Ligation and Replisome Unloading (A) Schematic of the ligation assay. Dashed lines represent unlabeled parental strands, which are not detected. (B) Plasmid DNA was replicated in mock-, Top2Î±-immunodepleted, and rescued (Î”Top2Î±+hTop2Î±) extracts containing [Î±-32P]dATP. Replication intermediates were purified, digested, and then separated on a denaturing agarose gel and visualized by autoradiography. See also Figure S5A. (C) Quantification of ligation in (B). See also Figure S5B. (D) Fork merger and ligation were quantified from multiple experiments. Plot depicts mean Â± SD from 4 experiments. See also Figure 1F. (E) Plasmid DNA replication was performed in mock- and Top2Î±-immunodepleted extracts, and chromatin-bound proteins were recovered at different time points by plasmid pull-down. Approximate kinetics of DNA replication are indicated. (F) Chromatin associated proteins from (E) were detected by western blotting. (Gâ€“J) Binding of MCM6 (G), CDC45 (H), RPA70 (I), and RPA30 (J) to chromatin was quantified from (F). See also Figures S5Câ€“S5H.
	Figure 5. Top2Î± Acts throughout Replication to Promote Termination (A) Plasmid DNA containing a LacR-bound 32xlacO array was replicated in mock- and Top2Î±-immunodepleted extracts. To monitor the effect of Top2Î± loss throughout replication, IPTG was added at the onset of replication to mock- and Top2Î±-immunodepleted extracts to allow termination to occur (upper panels). To monitor the effect of Top2Î± loss during termination, replication proceeded in mock-immunodepleted extracts until forks stalled at the LacR array (18 min), then Top2-i was added, and termination was induced by IPTG addition (20 min, lower panels). (B) Replication intermediates from (A) were purified, digested, and then separated on an agarose gel and visualized by autoradiography. See also Figure S6P. (C and D) Quantification of fork merger in (B). See also Figures S6Q and S6R. (E) Schematic of the decatenation assay. (F) Replication intermediates from (E) were separated on an agarose gel and visualized by autoradiography. See also Figure S6S. (G and H) Quantification of decatenation in (F). See also Figures S6T and S6U.
	Figure 6. Top2Î± Binds Pre-catenanes throughout Replication (A) Plasmid DNA was replicated in extracts treated with vehicle, Cdc7-I, or Geminin. Chromatin-bound proteins were recovered at different time points by plasmid pull-down. Approximate kinetics of DNA replication are indicated. (B) Chromatin-associated proteins from (A) were detected by western blotting (C) Binding of Top2Î± was quantified from (B). See also Figure S7A. (D) Replication-dependent binding of Top2Î±, RPA, PCNA, and CDC45 was quantified from (B). See also Figure S7B. (E) Plasmid DNA containing a LacR-bound 16xlacO array was replicated with IPTG added to allow termination (â€œReleaseâ€) or omitted to block termination (â€œBlockâ€). Chromatin-bound proteins were recovered at different time points by plasmid pull-down. Approximate kinetics of DNA replication are indicated. (F) Chromatin-associated proteins from (E) were detected by western blotting. (Gâ€“J) Quantification of replication-dependent CDC45 (G), RPA (H), PCNA (I), and Top2Î± binding in (F). See also Figures S7Câ€“S7I. (K) Plasmid DNA was replicated in extracts treated with vehicle or aphidicolin. Chromatin-bound proteins were recovered at different time points by plasmid pull-down. Red dots indicate RPA binding to nascent single-stranded DNA in aphidicolin-treated extracts. (L) Chromatin-associated proteins from (K) were detected by western blotting. (M and N) Quantification of RPA70 and Top2Î± binding in (L). See also Figures S7Oâ€“S7R.
	Figure 7. Model for the Role of Top2Î± during Vertebrate Termination (A) Under unperturbed conditions, pre-catenanes form prior to termination and are resolved by Top2Î± to facilitate fork convergence (i). Fork convergence occurs when the final stretch of DNA is unwound, and this process is sensitive to topological stress (i and ii). Once replisomes meet, fork merger, final ligation, replisome unloading, and decatenation proceed rapidly (iiâ€“v) as previously described (Dewar et al., 2015). Top2Î± binds prior to termination and remains bound throughout this process. (B) In the absence of Top2Î±, converging replisomes stall with unreplicated DNA between them due to accumulation of topological stress (i). Fork convergence ultimately goes to completion independently of Top2 activity (i and ii), allowing fork merger (ii and iii), ligation (iii and iv), and replisome unloading (iv and v) to occur, likely through the previously described mechanism for termination. Decatenation occurs very slowly (iv and v) using a different Top2 activity (Top2?) that is likely Top2Î².

References [+] :

Baxter, Topoisomerase II inactivation prevents the completion of DNA replication in budding yeast. 2008, Pubmed