Srs2 helicase is known to dismantle nucleofilaments of Rad51 recombinase to prevent spurious recombination events1,2,3,4,5,6 and unwind trinucleotide sequences that are prone to hairpin formation7. Here we document a new, unexpected genome maintenance role of Srs2 in the suppression of mutations arising from mis-insertion of ribonucleoside monophosphates during DNA replication. In cells lacking RNase H2, Srs2 unwinds DNA from the 5′ side of a nick generated by DNA topoisomerase I8 at a ribonucleoside monophosphate residue. In addition, Srs2 interacts with and enhances the activity of the nuclease Exo1, to generate a DNA gap in preparation for repair. Srs2–Exo1 thus functions in a new pathway of nick processing-gap filling that mediates tolerance of ribonucleoside monophosphates in the genome. Our results have implications for understanding the basis of Aicardi–Goutières syndrome, which stems from inactivation of the human RNase H2 complex9.
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We thank S. Jinks-Robertson and T. Kunkel for plasmids used in strain construction, R. Bermejo and M. Foiani for the genome sequencing of the original hpr4 strain, and G.-M. Li and S. Lee for providing hEXO1. This work was supported by National Institutes of Health grants RO1GM053738 (to H.L.K.), RO1ES007061 (to P.S.) and K99ES021441 (to H.N.).
The authors declare no competing financial interests.
Extended data figures and tables
Lists of genes were obtained from the Saccharomyces Genome Database. Genes in grey are synthetically sick or synthetically lethal with either RNH201/RNH202/RNH203 or with SRS2. Genes in black are synthetically sick/lethal with both RNH201/RNH202/RNH203 and SRS2.
Extended Data Figure 2 Full-length srs2-KA shows the same double mutant phenotype with rnh202Δ as do srs2Δ and srs2-KA860.
a, Strains harbouring the helicase null K41A variant at the chromosomal SRS2 locus were constructed. b, Synthetic interaction of rnh202Δ and srs2-KA. c, Dinucleotide slippage rates; plotted are median rates with error bars representing 95% confidence intervals23 (n = 18).
a, Left, percentage cells with spontaneous Rad52–yellow fluorescent protein (YFP) foci formation, with at least ten fields of 50–200 cells counted per strain. Right, representative differential interference contrast and YFP images of a Rad52-YFP focus. b, Log-phase cells were analysed by flow cytometry to determine DNA content and data were quantified using FlowJo software. c, Percentage of large doublet cells in mid-log-phase cultures. Total number of cells and number of large doublet cells were determined for each strain by examining at least ten fields of 50–200 cells per strain. d, Wild-type and rnh202Δ srs2Δ double mutant cells were grown in YPD media, washed and treated for 1 h with 100 mM hydroxyurea. Lysates were extracted and subjected to immunoblotting with an anti-Rad53 antibody26. The higher species represents phosphorylated Rad53. Plotted in a and c are the mean values ± s.d. (n = 3).
Extended Data Figure 4 Mutation spectra at the CAN1 locus for the rnh202Δ single and rnh202Δ srs2Δ double mutant cells.
Independent mutations in the rnh202Δ (blue) and rnh202Δ srs2Δ (red) Canr mutant strains. Base substitutions are written above the wild-type sequence, deletions are represented by ‘ = ’ and insertions are represented by .
Intact duplex DNA (a) and nicked duplex DNA labelled at either the (b) 5′ or (c) 3′ end of the nicked strand were incubated with Srs2 for 10 min at 30 °C with or without ATP. Reactions were run in a polyacrylamide gel and analysed by phosphorimaging analysis. The results are quantified in d. Plotted are the mean values ± s.d. (n = 3).
a, Duplex DNA with or without an embedded rUMP residue (5 nM) was incubated with either E. coli or calf thymus Topo I for 30 min at 37 °C. b, Reactions were analysed by electrophoresis in a polyacrylamide gel followed by phosphorimaging analysis. c, Schematic for the construction of the DNA substrate that harbours a unique nick induced by calf thymus Topo I at a rUMP residue.
a, DNA substrate (5 nM) that harbours a Topo-I-induced nick and radiolabelled on the 3′ side was incubated with Srs2 or Mph1 (20 or 40 nM) in the presence or absence of ATP at 30 °C for 10 min. The reactions were analysed as before. b, (AG)4 dinucleotide slippage rates; plotted are median rates, with error bars representing 95% confidence intervals23 (n = 18). c, Exo1 shows 5′ endo- and exonuclease activities on the 5′ Flap and the nicked duplex DNA, respectively. Radiolabelled 5′ Flap without or with a gap region, nicked duplex DNA, or oligonucleotide dT (5 nM each) was incubated with Exo1 for 10 min at 30 °C. The reactions were analysed as before and the products indicated by the arrows.
Extended Data Figure 8 Stimulation of Exo1-catalysed digestion of a 5′ Flap and a Topo-I-induced nick by Srs2.
a, Radiolabelled 5′ Flap substrate (5 nM) was incubated with Exo1 (0.1 nM) in the absence or presence of Mph1 for 10 min at 30 °C. b, Radiolabelled 5′ Flap substrate (5 nM) was incubated with hEXO1 (4 nM) in the absence or presence of Srs2 (0.4, 2 and 10 nM) for 10 min at 37 °C. c, Radiolabelled DNA substrate harbouring a Topo-I-induced nick (5 nM) was incubated with Exo1 (0.1 nM) in the absence or presence of Srs2 or Mph1 for 10 min at 30 °C. d, Radiolabelled substrate harbouring a Topo-I-induced nick (5 nM) was incubated with increasing amounts of hEXO1 (0.25, 0.5 and 1 nM) in the absence or presence of Srs2 (10 nM) for 10 min at 37 °C. The reactions in a–d were analysed as before. Plotted in b and d are the mean values ± s.d. (n = 3).
Extended Data Figure 9 Model of Srs2–Exo1-mediated processing of a DNA nick induced by Top1 at an embedded ribonucleotide.
RNase H2 normally removes misincorporated rNMPs from DNA (not shown). In the absence of RNase H2, topoisomerase 1 can cleave at the embedded ribonucleotide, leaving 3′ cyclic phosphate and 5′ OH ends that cannot be ligated. Repair starts with unwinding of DNA from the 5′ OH side by Srs2, followed by DNA digestion by Exo1 through its exonuclease or 5′ Flap endonuclease activity to result in a DNA gap, to be filled by a DNA polymerase. Our results show that Srs2 enhances the nuclease activities of Exo1. In the absence of Srs2, re-ligation of ends processed by unknown nuclease activities leads to a deletion mutation.
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Potenski, C., Niu, H., Sung, P. et al. Avoidance of ribonucleotide-induced mutations by RNase H2 and Srs2-Exo1 mechanisms. Nature 511, 251–254 (2014). https://doi.org/10.1038/nature13292
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