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	Figure 1. Intercalation inhibits initiation of chromosomal DNA replication. (A) Replication time-courses in the control extract or in the presence of ethidium bromide or doxorubicin at indicated concentrations. (B) Replication was assessed by immunofluorescence of incorporated biotin-dUTP in the absence (Ctl) or presence of 100 μM ethidium (EB), the 45 min time-point is shown. (C) Replication time-course of ssDNA (M13 bacteriophage) in the absence or presence of 100 μM ethidium bromide. (D) Replication time-course of dsDNA in the absence or presence of 100 μM ethidium, added either at the beginning (EB 0′) or at 60 min. (EB 60′). (E) Sperm nuclei were incubated in the presence of Br-dUTP without (Ctl) or with 100 μM ethidium bromide (EB). At 75 min DNA was combed and single fibre analysis was performed. Images represent examples of DNA fibres; ssDNA in red, Br-dUTP in green, bar 10 μm.
	Figure 5. Pre-RC and initiation complexes are present on the chromatin, despite the absence of nuclear membrane and lamina, but replication does not initiate. (A) Assessment by immunofluorescence of the presence of pre-RC (MCM7) and initiation (PCNA, RPA and polymerase ε) complex proteins on the chromatin at 60 min in control (Ctl) extracts or extracts with 100 μM ethidium bromide (EB) or 100 nM recombinant geminin (Gem). DNA replication was monitored by biotin-dUTP incorporation (bio-dUTP). (B) Chromatin was purified from replicating nuclei incubated in the absence (Ctl) or presence of 100 μM ethidium (EB) at indicated time-points, and blotted with antibodies against proteins of the pre-RC, pre-IC, Cdk1/2 (PSTAIR, which recognizes Cdk1, upper band, and Cdk2, lower band), Cyclin E, RCC1 and histone H3; *bottom band, loading control (non-specific chromatin protein band recognized by Cdc6 antibody). For clarity, lanes are assembled electronically but all are from a single exposure of one gel.
	Figure 2. Ethidium does not activate the intra-S phase checkpoint. (A) Replication time-courses in the control extract (Ctl) or in the presence of 100 µM ethidium bromide (EB), 2 µg/ml aphidicolin (Aphi), with or without 5 mM caffeine (Caff). (B) Western blots of nuclei purified at 60 min from control extracts (Ctl), or extracts containing 0.5 μg/ml bleomycin (Bleo), 50 ng/µl double-stranded poly-dA/poly-dT oligonucleotides (pApT), 100 µg/ml aphidicolin (Aphi), 100 µg/ml aphidicolin and 5 mM caffeine (A + C), or 100 µM ethidium bromide (EB). Non-specific bands are shown as loading control. (C) Analysis of H2A.X phosphorylation in 0.5 μg/ml bleomycin (Bleo) or 100 μM ethidium bromide (EB) treated extract by immunofluorescence, at indicated time-points (bar, 10 μm).
	Figure 3. Ethidium inhibits the second phase of chromatin decondensation. (A) Sperm nuclei were incubated for 60 min in control (Ctl) or 100 µM ethidium (EB) treated extracts, and decondensation was monitored by staining DNA with Hoechst 33‱258. (B) Sperm decondensation in the absence (Ctl) or presence of 100 μM ethidium (EB) was monitored by incubating sperm nuclei in IEE, isolating them and staining directly with Hoechst 33‱258, at indicated time-points. (C) Sperm nuclei (or without DNA, lane 3) were incubated in buffer alone (lanes 4 and 7) or in interphase egg extract, in the absence (lanes 2, 3, 4 and 5) or in presence of EB, at 100 μM (lanes 6, 7 and 10), 50 μM (lane 9) or 25 μM (lane 8), without (lanes 2 and 6) or with micrococcal nuclease, for 10 min. Nucleosome assembly was monitored by gel electrophoresis; lane 1:100 bp DNA ladder.
	Figure 4. Intercalation disrupts nuclear membrane and lamina assembly. (A) Sperm nuclei were incubated in IEE with or without 100 μM ethidium bromide, in the presence of the lipid die DHCC, to monitor nuclear membrane assembly, or NLS-GFP, to assess its competence for active transport. Enlargements of nuclear membrane are shown. (B) Replication time-courses of extract treated with increasing concentrations of echinomycin. (C) Nuclear membrane formation and function in the presence of 5 μM echinomycin (Echino) or 100 μM doxorubicin (Doxo) was monitored at 90 min by immunofluorescence, by staining with DHCC, and the ability of nuclei to concentrate NLS-GFP. (D) Assessment of lamina formation by immunofluorescence staining with antibodies against Lamin B3 in nuclei incubated in control (Ctl) or 100 μM ethidium-treated extract (EB), at indicated time-points. Bars, 10 μm. In this figure, for clarity, only individual nuclei are shown, but all nuclei showed this phenotype.
	Figure 6. A nucleus is not required for pre-IC formation on chromatin. (A) Replication time-courses of single-stranded M13 DNA (pM13) or demembranated sperm nuclei (nuclei) in low speed interphase egg extracts (IEE) or high speed supernatants (HSS). (B) Chromatin was purified from control HSS (Ctl) or HSS containing 100 µM ethidium (EB) after incubation with demembranated sperm nuclei for the indicated times, or without DNA (-DNA) and western blotted against the indicated proteins. In the 20 min time-point, more material was recovered as shown by increased MCM7 signal, but the ratio of pre-IC and initiation factors to pre-RC components remained the same. (C) Assessment by immunofluorescence of the presence of pre-RC (MCM7) and initiation (PCNA and polymerase ε) complex proteins on the chromatin at 60 min in control (Ctl) HSS extracts or HSS extracts with 100 μM ethidium bromide (EB).

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