The DNA Damage Response Pathway Contributes to the Stability of Chromosome III Derivatives Lacking Efficient Replicators

In eukaryotic chromosomes, DNA replication initiates at multiple origins. Large inter-origin gaps arise when several adjacent origins fail to fire. Little is known about how cells cope with this situation. We created a derivative of Saccharomyces cerevisiae chromosome III lacking all efficient origins, the 5ORIΔ-ΔR fragment, as a model for chromosomes with large inter-origin gaps. We used this construct in a modified synthetic genetic array screen to identify genes whose products facilitate replication of long inter-origin gaps. Genes identified are enriched in components of the DNA damage and replication stress signaling pathways. Mrc1p is activated by replication stress and mediates transduction of the replication stress signal to downstream proteins; however, the response-defective mrc1AQ allele did not affect 5ORIΔ-ΔR fragment maintenance, indicating that this pathway does not contribute to its stability. Deletions of genes encoding the DNA-damage-specific mediator, Rad9p, and several components shared between the two signaling pathways preferentially destabilized the 5ORIΔ-ΔR fragment, implicating the DNA damage response pathway in its maintenance. We found unexpected differences between contributions of components of the DNA damage response pathway to maintenance of ORIΔ chromosome derivatives and their contributions to DNA repair. Of the effector kinases encoded by RAD53 and CHK1, Chk1p appears to be more important in wild-type cells for reducing chromosomal instability caused by origin depletion, while Rad53p becomes important in the absence of Chk1p. In contrast, RAD53 plays a more important role than CHK1 in cell survival and replication fork stability following treatment with DNA damaging agents and hydroxyurea. Maintenance of ORIΔ chromosomes does not depend on homologous recombination. These observations suggest that a DNA-damage-independent mechanism enhances ORIΔ chromosome stability. Thus, components of the DNA damage response pathway contribute to genome stability, not simply by detecting and responding to DNA template damage, but also by facilitating replication of large inter-origin gaps.


Introduction
In eukaryotic chromosomes, DNA replication initiates at multiple origins, specified by cis-acting sequences called replicators.In the budding yeast, Saccharomyces cerevisiae, replicators are termed ARS elements and were identified by their ability to promote extrachromosomal maintenance of plasmids.Chromosomal replication origins coincide with ARS elements, which contain the binding site for the six-subunit initiator complex, ORC.During G1, ORC recruits additional proteins to form pre-replicative complexes (pre-RCs) that initiate replication during S phase [1].The average distance between active replication origins in S. cerevisiae is approximately 40 kb, based on both electron microscopic analysis of replicating DNA molecules [2] and whole genome analysis [3,4].In fission yeast, a similar range of estimates was obtained from whole genome analysis and DNA combing [3,5].
The presence of multiple origins on chromosomes raises the question of whether replicators are activated according to a fixed temporal program or whether their use is stochastic, i.e. different replicators are activated in different cells or in successive S phases.In budding yeast, 2D-gel analyses and replication timing studies suggested that replicators are activated according to a program, although some variability is inevitable because some replicators fire inefficiently [3,4,[6][7][8][9][10][11][12].Recent single-molecule studies in budding yeast ( [13,14] Wang and Newlon, manuscript in preparation), and in fission yeast [5,[15][16][17][18] reflect this stochasticity in initiation.
Stochastic activation of replicators should occasionally produce large inter-origin gaps caused by failure of adjacent origins to initiate, referred to as the random gap problem [19].Recent theoretical analysis of the replication dynamics of the fission yeast genome based on data that describe the positions and firing probabilities of replicators and the rate of fork movement suggests that long inter-origin gaps occur frequently in fission yeast [20].In 88% of 2000 simulations using this stochastic hybrid model, at least one region of the genome contained an inter-origin gap more than 6-fold longer than the average inter-origin spacing; replication of such a gap would require about twice the known length of S phase.These results suggest that completion of DNA replication requires most of the normal G2 period of the cell cycle, and in some fraction of the population, regions of the genome would still be replicating at the normal time of mitosis.The problematic regions included about 5% of the genome, and each individual region appeared infrequently in the simulations, making such regions difficult to detect experimentally.It is not known how cells cope with this issue.
One possibility is that ongoing replication activates a checkpoint response to prevent cells from undergoing mitosis prior to completion of S phase.Two intertwined checkpoints function during S phase (Figure 1).The DNA damage response is activated by a signal transduction cascade in response to stalling of replication forks encountering DNA damage (reviewed by Branzei and Foiani [21,22]).Experimentally, this response is activated by treatment with MMS or UV; unperturbed cells probably activate this pathway in response to forks encountering endogenous DNA damage.The replication stress response is activated experimentally by hydroxyurea treatment, which slows replication forks by inhibiting ribonucleotide reductase; it is not known what endogenous signal(s) activate(s) it.
Activation of an S phase response may occur in cells coping with long inter-origin gaps.Rad53p, the ortholog of the mammalian and fission yeast effector kinase, Chk2 (Figure 1), becomes hyperphosphorylated late in S phase in mutants that fail to fire some replication origins, indicating activation of a checkpoint [23,24].In addition the stability of a yeast artificial chromosome (YAC) carrying human DNA sequences from which origins had been deleted depended on RAD9, the mediator in the DNA damage response pathway [25].However, other evidence suggests that cells do not monitor either the initiation or completion of DNA replication.For example, strains carrying tight alleles of cdc6 (cdc18 + in S. pombe), which encodes a pre-RC component, or of dbf4, the regulatory subunit of the Cdc7p kinase required for origin firing, proceed directly from G1 to mitosis despite failing to replicate any DNA [26][27][28].Even ongoing replication may not prevent anaphase entry [29,30].A simplified version of the DNA damage and replication stress checkpoint pathways is shown.The pathways are conceptually divided into sensors, phosphoinosotide-3-kinase-related kinases (PIKKs), mediators and effector kinases.The shared components of the pathways are shown in purple.The pathway-specific mediators, Rad9p, and Mrc1p, are shown in blue and red, respectively.The pathways are activated by sensors.Mec1p and Ddc2p form a complex, homologous to the mammalian ATR-ATRIP complex, which recognizes Replication Protein A (RPA) bound to ssDNA [88].Rad17p, Mec3p, and Ddc1p form a PCNA-like complex, homologous to the 9-1-1 complex, which is loaded onto DNA at 59 junctions adjacent to single-stranded DNA coated with RPA by an alternative clamp loader in which Rad24p replaces Rfc1p in a complex with Rfc2p, Rfc3p, Rfc4p, and Rfc5p [89][90][91][92].Binding of the Rad17p-Ddc1p-Mec3p clamp results in activation of Mec1p kinase activity.Ddc1p is phosphorylated by Mec1p [90].Dpb11 binds to phosphorylated Ddc1p and mediates a more robust activation of Mec1p [93].Signals from the PIKK kinases are transduced to effector kinases with the help of mediators (see text).Components tested are shown in bold type.doi:10.1371/journal.pgen.1001227.g001

Author Summary
Loss of genome integrity underlies aspects of aging and human disease.During DNA replication, two parallel signaling pathways play important roles in the maintenance of genome integrity.One pathway detects DNA damage, while the other senses replication stress.Both pathways activate responses that include arrest of cell cycle progression, giving cells time to cope with the problem.These pathways have been defined by treating cells with compounds that induce either replication stress or DNA damage, but little is known about their roles during unperturbed DNA replication.They may be important when several adjacent replication origins fail to initiate and forks from flanking origins must replicate longer regions of DNA than normal to complete replication.We have used a derivative of budding yeast chromosome III lacking all efficient replication origins to identify mutants that preferentially destabilize this chromosome fragment, which mimics a chromosome with a large inter-origin gap.We found that the DNA damage response pathway, but not the replication stress response pathway, plays an important role in maintaining this fragment.The signal recognized in this case may be replisome failure rather than forks stalled at endogenous DNA damage.
We have created a derivative of yeast chromosome III lacking efficient replicators as a tool to detect mechanisms that contribute to replication of large inter-origin gaps (the 5ORID-DR fragment -Figure 2).This fragment is composed entirely of yeast sequences with the exception of plasmid sequences at the fragmentation point.It replicates efficiently, with a loss rate per division of 2.1610 23 [31] and is much more stable than the YAC [25].We carried out a genetic screen for mutants specifically defective in maintenance of this ORID derivative on the premise that mutations that caused destabilization of the 5ORID-DR derivative, but had little or no effect on maintenance of the corresponding 0ORID-DR derivative (Figure 2) would identify genes required for the replication of long inter-origin gaps, or perhaps new replication initiation mechanisms.This screen identified three originless fragment maintenance (Ofm) mutants, one dominant, OFM1-1, and two recessive, ofm6-1 and ofm14 (an allele of RAD9) [32].The rad9 mutation increased the loss rate of the 5ORID-DR fragment, but did not cause the frequent rearrangement that was seen with the YAC [32].
Here we report the results of a modified synthetic genetic array (SGA) screen [33,34] used to identify additional Ofm mutants.Deletions of several genes in the DNA damage response pathway caused an Ofm phenotype.Further analysis indicated that this pathway contributes to the replication of large inter-origin gaps.In contrast, the replication stress response pathway does not contribute to the stability of the 5ORID-DR fragment.Surprisingly, genes in the homologous recombination pathway, which are believed to contribute to the restart of collapsed replication forks, do not contribute to the maintenance of the fragment.

SGA+Chromoduction-based screen for Ofm mutants
Our previous visual screen for Ofm mutants was labor intensive, during both the initial visual screening of colonies grown from the mutagenized culture and in subsequent attempts to identify mutations responsible for the phenotype.Thus, we adapted synthetic genetic array (SGA) technology [33,34] for use in a colony sectoring screen to identify additional Ofm mutants in the S. cerevisiae viable deletion collection.One limitation of this screen is that essential genes could not be tested.
In the primary screen, as detailed in Methods, we used SGA technology to create ade2D::natR xxxD::kanR haploid MATa progeny.We then used chromoduction [35] to introduce the 5ORID-DR fragment of chromosome III marked with ADE2 into each strain (Figure 2).Chromoductants, each carrying the 5ORID-DR fragment were then streaked on plates with limiting adenine.Loss of the ADE2-marked fragment during growth of a colony results in a red sector.If a mutant has a low 5ORID-DR fragment loss rate, such sectors will be rare; conversely, a mutant with an elevated loss rate will yield highly sectored colonies, providing a semi-quantitative estimate of loss rates.Examples of sectoring patterns are shown in Figure 3.The majority of the 5171 strains screened showed a low rate of sectoring as illustrated by the aro7D mutant used as a control.Ninety strains had an elevated rate of sectoring, as shown by the spe1D and ctf8D strains.
The elevated sectoring observed for the 90 strains selected from the primary screen could reflect either defects in transmission of all chromosomes, e.g. a defect due to the loss of a component of the kinetochore, or defects specific to 5ORID-DR fragment transmission.To distinguish between these possibilities, we identified a colony from each of the 90 strains that had lost the 5ORID-DR fragment, then separately introduced by chromoduction the 0ORID-DR and the 5ORID-DR fragments (Figure 2), and compared the sectoring phenotypes of two independent chromoductants carrying each of these fragments by estimating the number of red sectors per colony seen in chromoductants.Our previous measurements of loss rates of these chromosome III derivatives by fluctuation analysis allowed us to make semiquantitative estimates of loss rates based on sectoring patterns [31,32].The loss rate of the 5ORID-DR derivative is ,2610 23  losses per division in wild type cells, and this loss rate results in 0-3 sectors per colony in the SGA strain background.Colonies of strains carrying the 0ORID-DR derivative, which has a loss rate of about 2610 25 losses per division, rarely have a red sector.Mutant strains with loss rates of the 5ORID-DR fragment in the range of 10 22 losses per division form colonies with 5-10 sectors per colony, and strains with loss rates in the range of 10 21 losses per division form colonies with $10 sectors per colony.The results of this secondary screen are detailed in Table S1.For example, spe1D was classified as an Ofm mutant because cells carrying the 5ORID-DR fragment gave rise to colonies with 5-10 sectors per colony, while those carrying the 0ORID-DR fragment yielded colonies that were rarely sectored; ctf8D was called a non-Ofm mutant because cells carrying either fragment gave rise to colonies with .10sectors per colony (Figure 3).Overall, the 71 deletion strains in which the high sectoring phenotype of the 5ORID-DR fragment was reproduced in the secondary screen were divided into high confidence Ofm mutants (52 strains), possible/probable Ofm mutants (14 strains) and non-Ofm mutants (5 strains) (Table 1).In the high confidence Ofm mutants, the two chromoductants carrying the 5ORID-DR derivative were estimated to have at least 5-10 sectors per colony, and the two chromoductants carrying the 0ORID-DR derivative rarely gave rise to a colony with a sector.In the case of the probable/possible Ofm mutants, either the two 5ORID-DR chromoductants or the two 0ORID-DR chromoductants showed different sectoring patterns.In the non-Ofm mutants, the 0ORID-DR chromoductants all showed a sectoring pattern consistent with at least a 100fold increase in the loss rate of this derivative.
A gene ontology (GO) analysis was performed on the 52 genes whose deletion caused Ofm phenotypes and on the 5 genes whose deletion caused non-Ofm phenotypes (http://db.yeastgenome.org/cgi-bin/GO/goTermFinder.pl).The three highest scoring clusters among the Ofm mutants (P = 8610 25 -4610 23 ) share many genes and correspond to the annotations ''cell cycle checkpoint'', ''DNA damage response, signal transduction'', and ''DNA damage checkpoint''.The cell cycle checkpoint cluster (SGS1, BFA1, MAD2, MAD3, RAD9, RAD17, and RAD24) included all of the genes present in the other two clusters.When the possible/probable Ofm mutants were included in the analysis the highest scoring cluster was still ''cell cycle checkpoint'' (p = 8610 27 ).In addition to the 7 genes above, the cluster included BIM1, BUB1, BUB2, BUB3, CSM3 and TOF1.RAD9, RAD17, and RAD24 function in the DNA damage response pathway while MAD2 and MAD3 function in the spindle checkpoint, though some results have suggested an additional role in the DNA damage checkpoint [36][37][38].BFA1 and BUB2 are required to prevent mitotic exit in both the DNA damage and spindle checkpoint pathways [39].The highest scoring cluster (P = 3610 26 ) among the non-Ofm mutants corresponded to the annotation ''mitotic cell cycle''.This cluster included all five mutants identified as non-Ofm mutants.
Mutations in the DNA damage response pathway, but not the replication stress response pathway, cause an Ofm phenotype Results of the GO analysis and identification of a null allele of RAD9 in our forward mutation screen [32] led us to examine the DNA damage response pathway in more detail.We moved the deletions of interest into the YKN10 strain background (Table S2) as described in Methods.Analysis of these strains allowed us to confirm that each deletion caused an Ofm phenotype and to quantitate the effects of the mutations in the strain background with which we had the most experience.
Our premise in undertaking this screen is that problems with the replication of the 5ORID-DR derivative may be qualitatively different than the problems sustained by the 0ORID-DR derivative by virtue of the presence of a long inter-origin gap.Therefore, we wanted to be able to make a quantitative comparison of loss rates that are very different.We reasoned that a comparison of the number of additional loss events sustained by the 5ORID-DR and 0ORID-DR derivatives in a given mutant would provide a measure of the strength of the Ofm phenotype.We define the ''Ofm index'' as the number of additional loss events per 10 5 divisions for the 5ORID-DR derivative divided by the number of additional losses for the 0ORID-DR derivative (Table 2).Two examples illustrate our reasoning.Suppose that in a wild type cell the loss rate of the 0RID-DR derivative is 1 and the loss rate of the 5ORID-DR derivative is 100.In one case, a mutation causes both derivatives to sustain an additional 400 loss events per 10 5 cell divisions.In this case the Ofm index = (5002100)/(40121) = 1.This is the outcome we might expect for a mutation in a kinetochore component, and we would not consider the mutant to be an Ofm mutant.In another case, a mutation causes the 0ORID-DR derivative to sustain 10 additional loss events and the 5ORID-DR derivative to sustain an additional 900 loss events.In this case the Ofm index = (10002100)/(1121) Figure 3. Examples of sectoring patterns.In the primary screen the 5ORID-DR fragment (marked with ADE2 and LEU2) was introduced into each of the ade2D::natR xxxD::kanR double mutants by chromoduction.Chromoductants were streaked on medium with limiting adenine.Chromosome loss events appear as red sectors due to the accumulation of a pigment in ade2 mutants.For the secondary screen, sectoring colonies from the primary screen were re-streaked.The 5ORID-DR and 0ORID-DR fragments were separately introduced by chromoduction into a Leu 2 Ade 2 colony from these streaks.These chromoductants were then streaked on limiting adenine medium and photographed after 5 days.Left panels: Photographs of mutants carrying the 5ORID-DR fragment: aro7D -wildtype level of sectoring; spe1D -highly elevated sectoring; ctf8D -highly elevated sectoring.Right panels: Photographs of mutants carrying the 0ORID-DR fragment.spe1D was classified as an Ofm mutant because colonies carrying the 0ORID-DR fragment were rarely sectored.ctf8D was classified as a non-Ofm mutant because colonies carrying the 0ORID-DR fragment were highly sectored.See also Table S1.doi:10.1371/journal.pgen.1001227.g003= 90.We would consider this high Ofm index to indicate a specific defect in maintenance of the 5ORID-DR fragment.
We first wished to distinguish the roles of the DNA damage and replication stress response pathways in the maintenance of the 5ORID-DR derivative.In budding yeast, these pathways are best distinguished by the effects of mutations in the mediators because the pathways share both upstream and downstream components (Figure 1).The DNA-damage-specific mediator, Rad9p, an ortholog of mammalian 53BP1, is phosphorylated by the PIKK Mec1.Hyper-phosphorylated Rad9p binds the effector kinase Rad53p, an ortholog of Chk2, and facilitates both phosphorylation of Rad53p by Mec1p and activation of Rad53p kinase activity by autophosphorylation [40][41][42][43][44].We previously found that both our original rad9 allele and the rad9D allele cause Ofm phenotypes, with mutants strains having Ofm indices of 81 and 65, respectively (Table 2 and [32]).These results indicate the DNA damage response pathway contributes to the maintenance of the 5ORID-DR derivative.
The corresponding mediator in the replication stress response pathway is Mrc1p, a homolog of mammalian claspin.Mrc1p plays roles in both the replication stress response and normal replication fork progression [45][46][47][48][49][50].Analysis of the role of MRC1 in the maintenance of the 5ORID-DR derivative was complicated by its location on chromosome III and its dual role in S phase.We constructed both recipient and donor strains carrying the mrc1D allele; the 5ORID-DR mrc1D and 0ORID-DR mrc1D fragments were then separately transferred into the mrc1D recipient strain by chromoduction.Both 5ORID-DR and 0ORID-DR fragments were destabilized in the homozygous mrc1D strain, resulting in a low Ofm index (Table 2); the mrc1D strain is not an Ofm mutant.A deletion that removed the C-terminal half of the MRC1 ORF (the allele included in version 1 of the systematic deletion collection) caused a similar loss rate of the 5ORID-DR fragment, but the 0ORID-DR loss rate was about 10-fold lower than in the complete ORF deletion strain, suggesting that the N-terminus of Mrc1p may contribute to maintenance of the 0ORID-DR fragment (data not shown).
To distinguish between the roles of the replication stress response and fork progression functions of Mrc1p in the maintenance of the 5ORID-DR derivative, we made use of a separation of function allele, mrc1 AQ , made by mutating six consensus Mec1p phosphorylation sites [47]; this allele lacks the replication stress response function of MRC1, but retains the fork progression function.Plasmids carrying either wild type MRC1 or mrc1 AQ complemented the high loss rate of the 5ORID-DR fragment in the mrc1D strain (Table 3).These results indicate that it is the loss of the fork progression function of Mrc1p that destabilizes the 5ORID-DR fragment, not the loss of replication stress signaling.Therefore, mutations that impair DNA damage signaling, but not replication stress signaling, cause an Ofm phenotype.Ofm index = (loss_rate_5ORID-DR mutant 2loss_rate_5ORID-DR wild type )/(loss_rate_0ORID-DR mutant 2loss_rate_0ORID-DR wild type ). 2 Values from [32].Table 1.Genes identified in screen.

2
YOR024W is a dubious ORF upstream of HST3; hst3D was also scored as an Ofm mutant.yor024wD leaves only 52-base-pairs upstream of the HST3 ORF intact, suggesting that this deletion alters HST3 expression.
3 top3 mutants are slow-growing and rapidly accumulate sgs1 mutations which suppress the slow-growth phenotype [94]; the chromoductants screened are likely top3 sgs1 double mutants.sgs1 was scored as an Ofm mutant (see Table S1).doi:10.1371/journal.pgen.1001227.t001 We further tested the role of MRC1 in replication fork progression in our YKN10 background by examining the activation of dormant origins on chromosome III using 2D gel electrophoresis.These origins are inactive in the wild type strain because they are replicated by a fork from an adjacent origin before they can fire.Dormant origins can be activated by deletion of adjacent origins, which causes a delay in the time at which forks from the nearest remaining origins reach them, giving them an opportunity to fire [31,51].The dormant origin ARS304 is also activated in an mrc1D strain [49] in which forks progress slowly [48,49].To explore the generality of this phenomenon, we examined the activation of three dormant origins on chromosome III: ARS301, ARS304 and ARS314.As shown in Figure 4, replication initiation at ARS301 and ARS314, revealed by the presence of bubble-shaped intermediates, was detected in the mrc1D mutant, but not in the MRC1 strain; ARS304 was also active in the mutant (data not shown).Thus, activation of dormant origins is a general phenomenon in mrc1D strains that most likely reflects slow fork progression.
Deletions of other components of the DNA damage and replication stress response pathways also caused Ofm phenotypes.Deletions of genes encoding sensors shared by both pathways, including RAD17, which encodes a subunit of a PCNA-like clamp, and RAD24, which encodes the large subunit of its clamp loader (see Figure 2), caused Ofm phenotypes with Ofm indexes of 100 and 85, respectively (Table 2).Although it was not scored as a potential Ofm mutant in the primary screen, further examination revealed that deletion of DDC1, which encodes another subunit of the clamp, caused colonies of strains carrying the 5ORID-DR fragment to sector similarly to the rad17D strain (Figure S1).Genes encoding other shared sensors were not examined because they are essential, including RFC2, RFC3, RFC4, RFC5, DDC2 and DPB11 (Figure 1).
Sensors activate PIKKs shared by both pathways.In S. cerevisiae, the ATR homolog, Mec1p, plays a more important role in the detection and repair of DNA damage than does the ATM homolog, Tel1p [52].MEC1 is essential and was not in our screen; however the lethality caused by the mec1D allele can be suppressed by deletion of the ribonucleotide reductase inhibitor encoded by SML1 [53].The sml1D mutation did not increase the loss rate of the 5ORID-DR derivative, though it did slightly elevate the loss rate of the 0ORID-DR derivative (Table 2).Since the sml1D strain is not an Ofm mutant, we examined mec1D in the sml1D background.The mec1D allele confers an Ofm phenotype indicating by its Ofm index of 40 (Table 2).The other PIKK, Tel1p, does not contribute to maintenance of the 5ORID-DR fragment.The loss rate of this fragment in the tel1D mutant was 2.360.4610 23per division, similar to its loss rate in the wild type strain, and its loss rate in the mec1D tel1D double mutant was 1.360.2610 22, similar to its loss rate in the mec1D mutant.Downstream of the mediator, Rad9p, are the two effector kinases, Chk1p and Rad53p, homologues of the mammalian kinases, Chk1 and Chk2, respectively.The chk1D strain was not scored as a potential Ofm mutant in the primary screen; however, further examination revealed that this strain had an Ofm phenotype, with an Ofm index of 33 (Table 2).This result implicates Chk1p in transducing the signal from Rad9p to downstream targets.The rad53D mutant was not in the screen because it is inviable, but its inviability is suppressed by deletion of SML1.We found that the rad53D sml1D double mutant did not have an Ofm phenotype (Ofm index = 7) because the rad53D mutation caused an increase in the loss rate of the 0ORID-DR fragment (Table 2).The increased loss rate of the 0ORID-DR fragment in the rad53 strain indicates that Rad53p contributes to the maintenance of chromosomes with a normal complement of replication origins and is consistent with its well-documented role in response to DNA damage [22].However, the loss rate of the 5ORID-DR fragment was increased about 3-fold relative to the sml1D control, raising the possibility that Rad53p also contributes to the maintenance of this fragment.We examined the loss rate of the 5ORID-DR fragment in a sml1D rad53D chk1D strain and found that its loss rate in the triple mutant was 8806140610 25 , approximately equal to the sum of the loss rates in the sml1D rad53D and chk1D mutants and nearly as high as the loss rates in strains carrying deletions of upstream components of the checkpoint pathway (Table 2).The Ofm index of the triple mutant was similar to that of the chk1 strain.Taken together, these results are consistent with the idea that Chk1p is primarily responsible for transducing the signal from Rad9p to downstream  effectors, with Rad53p making a relatively small contribution to the maintenance of the 5ORID-DR fragment as long as Chk1p is active, but becoming important in the absence of Chk1p.

Recombinational repair is not important for maintaining ORID chromosome derivatives
RAD52 is required for virtually all homology-based doublestrand break repair mechanisms, including break-induced replication and single-strand annealing (reviewed by Symington [54]).Our previous work showed that a rad52 mutant does not have an Ofm phenotype [31]; for this analysis we measured the stabilities of the 5ORID-DR and 0ORID-DR fragments (Figure 2) in wild type and rad52 strains in the CF4-16B strain background (Table S2), which differs slightly from the YKN10 background used in experiments summarized in Table 2.The 0ORID-DR fragment was lost at a rate of 7610 25 in the wild type strain and 9.5610 24  in the rad52 strain, while the 5ORID-DR fragment was lost at a rate of 1.5610 23 in the wild type strain and 3.1610 23 in the rad52 strain, leading to an Ofm index of 1.8 [31].Confirming and extending these results, strains carrying deletions of ten genes in the RAD52 epistasis group (RAD50, RAD51, RAD52, RAD54, RAD55, RAD57, RAD59, RDH54, MRE11, and XRS2) all showed wild type sectoring in our primary screen (Figure S2).These results indicate that, in otherwise wild type strains, recombinational repair is not required for maintenance of ORID chromosome derivatives.
Stabilities of chromosome III derivatives with efficient origins and a large inter-origin gap distinguish mec1D and mrc1D mutants from rad9D and rad24D mutants By deleting the five efficient from the 5ORID-DR fragment, we altered both the positions at which replication most likely initiates and the distances that individual replication forks travel.The high loss rates of the 5ORID-DR fragment seen in the DNA damage response mutants could result from difficulty in initiating replication, difficulty in replication fork progression, or both.To address this issue, we examined stabilities of two additional derivatives of chromosome III, the full-length 5ORID chromosome and the DL-6ORID fragment (Figure 2), in these mutants.The 5ORID-DR fragment used in our mutant screen is truncated to the right of the ARS310 deletion.The full-length 5ORID chromosome carries the same deletions of the five efficient origins as the 5ORID-DR fragment, but retains origins distal to the ARS310 deletion; the inefficient origin, ARS313, is located about 20 kb distal to the ARS310 deletion, and the efficient origin, ARS315, is located about 50 kb distal [55].This derivative is as stable as the 0ORID-DR derivative in the wild type strain and the sml1D mutant.The DL-6ORID fragment was derived from the full-length 5ORID chromosome by removing the centromereassociated inefficient origin, ARS308, and fragmenting the chromosome to the right of ARS304, which removed ARS304, the dormant origins associated with HML and the left telomere.This derivative is as stable as the 5ORID-DR derivative in the wild type strain and the sml1D mutant (Table 2).In both 5ORID and DL-6ORID derivatives, the origin-deleted region to the left of ARS313 can be replicated by forks that initiate at ARS313 or at origins further to the right.In 5ORID, but not in DL-6ORID, there also exists the potential for the origin-deleted region to be replicated by forks that initiate at one of the normally-dormant HML-associated origins.
If a mutant has an initiation defect, then the presence of additional origins on 5ORID and DL-6ORID derivatives should suppress the Ofm phenotype.Conversely, if a fork progression defect creates difficulty in completing replication of a large interorigin gap, the presence of additional origins should not suppress the defect.The DL-6ORID fragment provides a particularly stringent test of fork progression and/or fork stability, because a collapsed leftward-moving fork initiated at ARS313 or ARS315 cannot be rescued by a fork initiated at one of the HML-associated dormant origins.
We first examined the stability of these larger gapped constructs in the mrc1D mutant because it has a known fork progression defect [48,49].MRC1 was deleted from the full-length 5ORID chromosome to avoid complementation; MRC1 is distal to ARS304 so, like the dormant origins, it is absent from the DL-6ORID fragment.In mrc1D mutants, loss rates of the full-length 5ORID chromosome and the DL-6ORID fragment were similar, and were about 2.5-fold lower than the loss rate of the 5ORID-DR fragment (Figure 5, Table 2).These results are consistent with our expectation that the additional origins on these two derivatives would not suppress the fork progression defect of mrc1D.Activation of HML-associated dormant origins does not appear to contribute to the stability of the full-length 5ORID chromosome in the absence of Mrc1p, because the DL-6ORID fragment, which lacks HML-associated dormant origins, showed a loss rate similar to 5ORID.The 2.5-fold higher rate of loss of the 5ORID-DR fragment likely reflects the fact that replication of this fragment is at least partially dependent upon activation of HML-associated dormant origins, and that these origins are less efficient than the origins present on the right arm in the full-length 5ORID chromosome and the DL-6ORID fragment (Figure 5).
Consistent with the observation of Cha and Kleckner [56] that Mec1p stabilizes forks in slow replication zones, we found that the mec1D mutant behaved similarly to the mrc1D mutant.The 5ORID chromosome was unstable in a mec1D strain (Figure 5, Table 2), suggesting a fork progression defect.The loss rate of the DL-6ORID fragment was less than three-fold higher than that of the full-length 5ORID chromosome, suggesting that the HML-associated dormant origins make only a small contribution to the stability of the fulllength 5ORID chromosome in the absence of Mec1p.
Results obtained with the rad9 and rad24D mutants contrasted sharply with the mrc1D and mec1D results.The full-length 5ORID chromosome was substantially more stable than 5ORID-DR or DL-6ORID in the absence of Rad9p or Rad24p, with loss rates about 40-fold lower than the 5ORID-DR fragment and only twofold higher than the 0ORID-DR fragment (Table 2 and Figure 5).By contrast, in mrc1D and mec1D strains, the full-length 5ORID chromosome is 10-to 20-fold less stable than 0ORID-DR.The relative stability of 5ORID-DR in rad9 and rad24D mutants might indicate that the presence of efficient origins to the right of the origin-deleted region could suppress the Ofm phenotype of these mutants.If this were the case, then the loss rate of the DL-6ORID fragment should also be low.However, the loss rates of this fragment were as high as or higher than the 5ORID-DR fragment in both mutants.The high loss rates of both the 5ORID-DR fragment and the DL-6ORID fragment indicate that maintenance of the full-length 5ORID chromosome in rad9 and rad24D strains requires the presence of replication origins on both sides of the ORID gap, and suggest that a single fork cannot traverse the gap in these strains.
One explanation for the lower stability of the DL-6ORID fragment in the rad9D strain than in a mec1D sml1D strain is that in the absence of Rad9p, Mec1p kinase activity is deleterious.If this were the case, the loss rate of DL-6ORID fragment in a rad9D mec1D sml1D triple mutant should be the same as in the mec1D sml1D strain.Alternatively, a second pathway, possibly Tel1p-dependent, could activate Rad9p in the absence of Mec1p, or Rad9p could have a DNA-damage-response-independent function that contributes to the maintenance of the DL-6ORID fragment.In both of these cases, the triple mutant should have a loss rate similar to the rad9D strain.The loss rates of the DL-6ORID fragment were 6.960.6610 22in a rad9 sml1D strain and 5.160.4610 22in a rad9 mec1D sml1D strain, suggesting that a second pathway activates Rad9p.Alternatively Rad9p has a function that is independent of its role in the DNA damage response pathway in maintenance of the DL-6ORID fragment (see Discussion).
Finally, the behavior of the DL-6ORID fragment in the effector kinase mutants provides strong support for idea that Rad53p becomes important for the maintenance of ORID chromosomes in the absence of Chk1p.The loss rates of the DL-6ORID derivative in the chk1D and rad53D sml1D strains were similar and elevated approximately 2-fold relative to the 5ORID-DR derivative.The loss rate in the chk1D rad53D sml1D mutant was approximately 10fold higher and was equal to the very high loss rate seen in the rad9D mutant (Table 2).

Activation of dormant origins associated with HML in mec1 and rad53 strains
The loss rate of the full-length 5ORID chromosome was much higher in the mrc1D and mec1D strains than in the rad24D and rad9 strains.It appears that the dormant origins associated with HML near the left end of the full-length 5ORID chromosome contribute to the maintenance of this chromosome in wild-type, because derivatives truncated to remove HML-associated dormant origins showed higher loss rates than derivatives containing them (Figure 5,Table 2 and [31]).Increased activation of these dormant origins in rad9 and rad24D, as compared to in mrc1D and mec1D, could explain the differences in stability of the full-length 5ORID chromosome in these two sets of mutants.Therefore, we examined the activation of the dormant origins ARS301, ARS302/ARS303/ ARS320 (three closely-spaced ARS elements), and ARS304 on the full-length 5ORID fragment by 2D gel analysis (Figure 6).Both bubble-and Y-shaped replication intermediates were detected at ARS301 in mec1D and rad9D strains, indicating that this origin is activated in a subset of the cells in both strains.A fortuitous restriction-site polymorphism allowed us to distinguish the signal arising from the balancer chromosome from that arising from the 5ORID chromosome.Bubble-shaped intermediates were detected only in strains where the 5ORID chromosome was present, indicating that ARS301 fires only on the 5ORID chromosome.Similarly, we found bubble arcs arising from the ARS302/ARS303/ ARS320 cluster in mec1D and rad9D strains, but only when the  4, except that the polymorphic NdeI site is indicated.This site is 5ORID chromosome was present.ARS304 was not detectably active in either mutant (Figure 6).In all cases, the intensity of the bubble arc was less than that of the Y arc, indicating that in the majority of cells each ARS was passively replicated.
We quantitated the percent of bubble-shaped replication intermediates produced by the 5ORID chromosome, using two approaches to quantitate the signal (Methods and Table S3).ARS301 initiated replication in 1.7-6.3% of the population in the rad9D strains, and in 7.4-14.6% of the population in mec1D sml1D strains.The range of values for the ARS302/ARS303/ARS320 cluster was similar, 2.3-7.6% in rad9D strain and 9.4-15.7% in the mec1D sml1D strains.Thus the dormant replicators are 2-to 3-fold more active in mec1D strains than in rad9D strains, indicating that the higher stability of the 5ORID chromosome in rad9D strains cannot be explained by increased activation of dormant origins.
The activation of HML-associated origins in the rad9D strain may account for the differences in stability of the 5ORID chromosome and the DL-6ORID derivative.The HML-associated origins fire only late in S phase [51,57].Leftward-moving forks normally reach them before they are programmed to fire.In the rad9D strain, approximately 10% of cells activate either ARS301 or the ARS302/ARS303/ARS320 cluster in the full length 5ORID chromosome.About 10% of rad9 cells lose the DL-6ORID fragment (Table 2), suggesting that about 10% of the forks initiated to the right of the gap fail to traverse the gap in rad9 mutants.In this situation, the DL-6ORID fragment, which lacks the HML-associated dormant origins, would be lost as a result of incomplete replication.In contrast, only 0.03% of rad9 cells lose the 5ORID chromosome (Table 2) because, in the 10% of cells in which leftward-moving forks fail to traverse the gap, firing of one of the HML-associated dormant origins allows the replication of this chromosome to be completed.
Unlike the 5ORID-DR fragment and the full-length 5ORID chromosome, the DL-6ORID fragment was structurally unstable.Stable derivatives that had lost the cloNAT-resistance marker present at left-hand end of the fragment (Figure 2) arose in the rad9, rad24, and mec1 mutants.The rates of production of these stable derivatives were similar to the loss rates of the DL-6ORID fragment measured in these strains (Table S4).Twelve stable derivatives of the DL-6ORID fragment produced by the rad9 strain migrated on pulsed-field gels with the full-length balancer chromosome, suggesting that chromosome III sequences distal to the fragmentation point had been restored (data not shown).One possible mechanism for the production of these stable derivatives is that replication forks collapse and are processed into double-strand breaks that are repaired by break-induced replication [58] using the balancer chromosome as a template.

Discussion
We employed a novel modification of the SGA method to screen for mutations that preferentially destabilize a chromosome III derivative lacking efficient replication origins.The modification utilized a single chromosome transfer technique, chromoduction, to transfer the 5ORID-DR fragment into an ordered array of the viable ORF deletion collection.Yuen et al. [59] carried out similar colony-sectoring screens of the viable deletion collection using two chromosome fragments.Of the 66 chromosome transmission fidelity (ctf) mutants identified in these screens, 14 were also identified in our screen.As expected, given that the ctf mutants were identified using chromosome fragments carrying a normal complement of replication origins, the majority of the ctf mutants we re-identified were found in the non-Ofm or possible/probable Ofm classes.The two scored as Ofm mutants are ctf18D and mad2.It seems likely that many ctf mutants were not identified in our screen because they caused only small increases in the rate of loss of the 5ORID-DR fragment.Approximately 60% of the loss rates measured for chromosome fragments in ctf mutants are less than or equal to the loss rate of the 5ORID-DR fragment; increases of that magnitude would not have been detected in our visual screen.

Role of the DNA damage response pathway in the maintenance of ORID chromosome derivatives
Our results indicate that the DNA damage signaling pathway, but not the replication stress signaling pathway, contributes to the maintenance of the 5ORID-DR fragment.While the DNA damage and replication stress response pathways share many components (Figure 1), mutation of the DNA-damage-tocheckpoint-signaling mediator, Rad9p, preferentially destabilized the 5ORID-DR fragment, but a checkpoint-deficient mutation in the replication-stress-specific signaling mediator, Mrc1p, did not.Mutations in many of the shared signaling components also caused Ofm phenotypes.
We found unexpected differences in the contributions that the DNA damage signaling pathway makes to maintenance of ORID chromosome derivatives and the contributions that it makes to DNA damage resistance.First, the DNA damage signaling pathway detects and stabilizes forks stalled at sites of damage and facilitates repair or bypass of the damage; studies with DNA damaging agents [60][61][62][63] indicate that this function is more strongly dependent on RAD53 than on CHK1.Based on the results presented here, the DNA damage signaling pathway also contributes to the replication of large inter-origin gaps, which can arise when several adjacent origins fail to fire.Such gaps appear commonly during the replication of the rDNA array [14].The 5ORID-DR fragment, the full-length 5ORID chromosome and the DL-6ORID fragment mimic these large gaps, and the pathways identified by the Ofm mutants may have arisen to facilitate the replication of large inter-origin gaps.Interestingly, this function appears to be facilitated primarily by CHK1 with a contribution from RAD53 evident in the absence of CHK1.
Second, we found that mec1D and mrc1D mutations have different effects than rad9D and rad24D mutations on the stabilities of the DL-6ORID and full-length 5ORID derivatives.Dormant origins near the left end of chromosome III are more strongly activated in a mec1D mutant than in a rad9 mutant (Figure 6), suggesting that in the mec1D strain the HML-associated dormant origins have more time to fire.However, removing the dormant origins, as in the DL-6ORID fragment, caused a 16-fold greater increase in the rate of chromosome loss in the rad9 strain than in the mec1D strain (Table 2), suggesting that forks fail to reach the left end more often in the rad9 strain.One explanation for this disparity is that an alternative pathway activates Rad9p in mec1D cells, which results in stabilization of replication forks and allows them to progress, albeit slowly, in the absence of Mec1p [56].In mec1 mutants, we suggest that slow fork progression through the present on the full-length 5ORID chromosome and absent from the balancer chromosome.The bar below the map indicates the probe.The ARS301 probe also hybridized to a 7.1 kb NdeI fragment from chromosome XI containing the VBA5 gene.B. Southern blots of FspI+SphI+ClaI-cut DNA probed to detect ARS302/ARS303/ARS320 and ARS304 are shown.Bubble-shaped replication intermediates, indicated by the arrows, arise only from ARS302/ARS303/ARS320 in the strain carrying the 5ORID chromosome.Diagrams of the 4.5-kb FspI-ClaI fragment containing ARS302/ARS303/ARS320 and 3.2-kb FspI-SphI fragment containing ARS304 are shown below the blots.ARS elements are indicated by the black boxes, and the bar below each map indicates the probe.doi:10.1371/journal.pgen.1001227.g006long ARS305D -ARS310D gap allows time for the activation of either ARS301 or the ARS302/ARS303/ARS320 cluster in ,20% of the cells (Figure 6).However in the absence of the dormant origins, as in the DL-6ORID fragment, these slow-moving forks are able to complete replication through the gap to the telomere in .99% of the cells (Table 2).Tel1p, which is also a PIKK, is a candidate for activation of Rad9p, in this situation.However, our observation that Tel1p did not contribute to the stability of the 5ORID-DR fragment in either the presence or absence of Mec1p (see Results) suggests that Tel1p does not contribute to this pathway.In the absence of Rad9p, we suggest that forks initiated to the right of the ARS305D -ARS310D gap simply fail to traverse the gap approximately 10% of the time (Table 2), and that, in the absence of the dormant origins, replication of the chromosome is not completed, leading to segregation of the partially replicated molecule and chromosome loss.An alternative explanation for the disparity is that Rad9p has a function that is independent of its role in the DNA damage response pathway.
Finally, we found that strains carrying deletions of ten genes in the RAD52 epistasis group did not show elevated loss rates of the 5ORID-DR fragment.Since genes in this epistasis group are required for all homology-dependent repair processes, including double-strand break repair, break-induced replication and replication fork restart, these results suggest that replication of this ORID derivative does not require repair of DNA damage or double-strand breaks.
Our favored model for the role of the DNA damage response pathway in the replication of ORID chromosome derivatives is based on the idea that replication forks age, i.e. that the probability of fork arrest due to failure of a replisome component increases with the distance the fork has traveled.We refer to these forks as crippled, to distinguish them from forks that are stalled (arrested by DNA damage or nucleotide depletion with replisome intact) or collapsed (replisome disassembled), and to reflect the need for some replisome component to be replaced or modified in order to continue elongation.These crippled forks are then recognized and restored by a RAD9-and CHK1-dependent pathway.The restart of these crippled forks is independent of homologous recombination because there is no DNA damage to be bypassed, and, therefore, double-strand breaks are therefore not formed.If a fork were arrested due to failure of a replisome component, there would be no impediment to elongation once the replisome is reconstituted.
There are alternative models to explain the role of the DNA damage response pathway in maintaining the 5ORID-DR fragment, which has a large inter-origin gap.The simplest is that the DNA damage response monitors the completion of replication.However, the evidence for such a checkpoint is not compelling (see Introduction).Debate over the existence of a replication completion checkpoint is ongoing; our observations provide only circumstantial evidence in favor of such a checkpoint.
Another model to explain the role of the DNA damage response pathway in maintaining fragments with large inter-origin gaps suggests that forks stall at sites of endogenous DNA damage and are stabilized by this pathway.The 5ORID-DR and DL-6ORID fragments would be especially sensitive to such events in the absence of the DNA damage response because the stalled forks would collapse.In the case of the 0ORID-DR fragment, which has a full complement of replication origins, a collapsed fork could be rescued by a converging fork from an adjacent origin.In contrast, the 5ORID-DR fragment has fewer initiation events, so a collapsed fork would be rescued less often by a converging fork, resulting in an elevated loss rate in a DNA damage checkpoint mutant.Consistent with this suggestion, our analysis of individual 5ORID-DR molecules in wild type cells suggests that replication initiates at only one or two places per molecule, but at different places on different molecules (Wang et al., manuscript in preparation).
The enhanced stability of the full-length 5ORID chromosome compared to the DL-6ORID fragment in the rad9 and rad24D mutants is also consistent with this endogenous damage model, as a collapsed leftward-moving fork in the 5ORID chromosome can be rescued by a fork initiating at one of the dormant origins near HML.Our finding that mec1D confers an Ofm phenotype while tel1D does not is also consistent with this model because MEC1 plays a more important role in the tolerance of DNA damage than does TEL1 [52].
However, this endogenous damage model is challenged by findings that fork stabilization at sites of DNA damage and survival are more strongly dependent on RAD53 than on CHK1 [60][61][62][63][64][65][66], whereas CHK1 makes a more important contribution than RAD53 to 5ORID-DR fragment maintenance, suggesting that the DNA damage response is not simply stabilizing forks in response to damage.While Segurado and Diffley [61] have suggested a role for CHK1 in stabilizing replication forks, that function was detected only in the absence of both RAD53 and EXO1, which encodes a nuclease responsible for fork collapse in the absence of RAD53.Thus, it seems unlikely that this explains the contribution of CHK1 to 5ORID-DR fragment maintenance.Another problem is that deletions of genes, whose products are required for mismatch repair, repair of UV damage, and homologous recombination, did not increase the loss rate of the 5ORID-DR fragment in the primary screen, as would have been expected if DNA damage-provoked fork collapse was responsible for loss of this fragment.
Replication fork aging also suggests an explanation for the close spacing of replication origins in S. cerevisiae.A median inter-origin distance of 36 kb was estimated from visualization of replicating molecules by electron microscopy (reviewed by Newlon [67]), and a similar median distance, 34 kb, was estimated using the genomewide replication timing data of Raghuraman et al. [4].Based on a median fork rate of 2.3 kb per minute and an S phase of 55 minutes [4], a single fork from the earliest firing origin would be able to replicate ,120 kb and a fork from an origin activated in the middle of S phase would be able to replicate ,60 kb.Thus, origins are spaced more closely than predicted by the median origin activation time and rate of fork movement.The observed high density of origins may insure that gaps too long to be reliably replicated do not occur, even if several adjacent origins fail to fire.

DNA-replication-linked genes
Pan et al. described a DNA Integrity Network of 78 genes on the basis of synthetic fitness or lethality defects [68].Sixteen of these genes are believed to have roles in S phase checkpoints.Deletions of eight of these genes cause an Ofm phenotype: RAD9, RAD17, RAD24, CTF18, MEC1, DDC1, CHK1, and RAD53.Deletions of two other genes in this group, csm3D and tof1D, were scored possible Ofm mutants.
In addition to the checkpoint genes, our Ofm mutants included deletions of two other genes from the DNA Integrity Network, HST3 and POL32, both of which have links to DNA replication.HST3 encodes a NAD + -dependent histone H3 lysine-56 deacetylase [69][70][71].Our analysis of hst3 mutants will be presented elsewhere; it indicates that the Ofm phenotype of hst3D results from a fork progression defect (Irene et al. manuscript submitted).pol32D mutants, which lack a nonessential subunit of DNA polymerase D, also show fork progression defects, which may explain their Ofm phenotype [72][73][74][75].
In summary, we have identified a set of genes whose products facilitate replication of large inter-origin gaps.This set is enriched in components of the DNA damage and replication stress signaling pathways.Replication of large inter-origin gaps shows several surprising features: Dependence on the DNA-damage-specific mediator, Rad9p, rather than the replication-stress-specific mediator, Mrc1p; a stronger dependence on the effector kinase, Chk1p than Rad53p, and no dependence on homologous recombination

Strains and media
Yeast strains are listed in Table S2.All strains are isogenic with YPH499 [76], except the full-length and fragmented chromosome donor strains, which are in the CF4-16B background [31], and YJT242 (and its parent Y7029) and the viable ORF deletion collection, which are related to S288C [77].SGA selection media were prepared as described in [78].Chromoductants for the SGA screen were selected on -Ade -Leu -Lys -Arg dropout plates containing 60 mg/ml canavanine (Sigma) and 10 mg/ml thialysine (Sigma).Chromoductants in the YKN10 background were selected on -Leu-Trp -Arg dropout plates containing 60 mg/ml canavanine and 10 mg/ml cycloheximide (Sigma), except that chromoductants of the DL-6ORID fragment were selected on -Leu -Ade -Arg dropout plates containing 100 mg/ml CloNAT (Werner Bioagents, Germany), 60 mg/ml canavanine, and 10 mg/ ml cycloheximide.Limiting adenine medium was purchased from US Biologicals.
YJT242 was created by transforming Y7029 with a PCR product carrying the natMX gene, amplified from pAG25 [79], flanked by homology to the ADE2 locus; sequences of primers are available upon request.Individual G418-resistant knockouts were moved into the YKN10 background by transformation with a PCR product amplified from the appropriate strain from the ORF deletion collection (Open Biosystems) using the locus specific A and D primers (www-sequence.stanford.edu/group/yeast_deletion_project/Deletion_primers_PCR_sizes.txt).The mrc1D::NAT allele was introduced into the YKN10 background using primers and a template generously provided by K. Sugimoto (UMDNJ).This allele was converted to mrc1D::KAN by transforming YJT294 with NotI-cut pFA-KanMX4 [80] and selecting for G418-resistance yielding YJT551.The his3-D367 alleles were generated by fusion PCR and introduced by two-step gene replacement [81].Primers are available upon request.The bar1-D1327 allele carries a BglII-BsrGI deletion that removes 1327 bp within the open reading frame.

SGA screen
In our version of the screen, a strain carrying an ade2D::natMX mutation, which causes the accumulation of a red pigment in colonies grown on limiting adenine and confers nourseothricin resistance, was mated to the array of viable deletion mutants, each marked with kanMX, which confers G418 resistance.The resulting diploids were then sporulated, and double mutant ade2D::natR xxxD::kanR haploid MATa progeny were selected.The array of double-mutant strains was mated to F510aA1-4, the donor strain, carrying the 5ORID-DR derivative of chromosome III marked with ADE2 (Figure 2).Because the donor strain carries the kar1-D15 mutation, normal karyogamy is inhibited, resulting in inefficient production of diploid cells [82].During the transient heterokaryon stage, single chromosomes are transferred at low frequency between the two nuclei, a process called chromoduction [35].The strains were marked to allow selection for rare chromoduction events in which the 5ORID-DR fragment was transferred into the ade2D::natR xxxD::kanR nucleus.The 5ORID-DR fragment carries LEU2 at its endogenous locus and an ectopic copy of ADE2 inserted near the ARS307 deletion (Figure 2).The corresponding donor strain carrying the 5ORID-DR fragment is Leu + and Ade + , but canavanine-sensitive and thialysine-sensitive because it carries the wild type CAN1 and LYP1 alleles.The double mutant (ade2D::natR xxxD::kanR) strains generated by SGA analysis are Leu 2 , Ade 2 , canavanine-resistant, and thialysine-resistant. Any diploids that form between the donor strain and the ade2D::natR xxxD::kanR double mutant strains are Leu + and Ade + , but canavanine-sensitive and thialysine-sensitive because the can1D and lyp1D mutations are recessive.The desired chromoduction event results in cells that are Leu + and Ade + , because they carry the 5ORID-DR fragment, and canavanine-and thialysine-resistant, because they carry the can1D and lyp1D mutations.Medium lacking leucine, adenine, arginine, and lysine and containing both canavanine and thialysine selects for these cells.A preliminary screen using approximately 100 strains selected from the viable deletion collection was carried out to determine conditions for the chromoduction.We found that pinning the array of double mutants at the density found in a standard 384 well plate was necessary to ensure efficient mating of the donor strain to the array.
The screen was done in duplicate, and chromoductants from the duplicate arrays were streaked side-by-side on a single plate with limiting adenine for scoring sectoring patterns (see Table S1).This process was completed in less than three months by eight individuals, demonstrating the feasibility of including a chromoduction step in the SGA procedure to transfer a single chromosome or plasmid into the double mutant array.If the phenotype of chromoductants could be scored directly on selective medium, then the entire procedure could be accomplished with robots.

Loss rate measurements
Chromosome loss rates were determined by fluctuation analysis using the colony isolation method [83].Red colonies were tested for leucine and tryptophan auxotrophies to distinguish chromosome losses from gene conversions or mitotic recombination events; leucine auxotrophy and nourseothricin-resistance were used in fluctuations involving the DL-6ORID fragment.The presence of origin deletions was confirmed by PCR.Loss rates were calculated using the method of Lea and Coulson [84].

Analysis of replication intermediates
Genomic DNA was prepared from log-phase cultures as described [85], digested with either NdeI, ClaI+EcoRV, or FspI+ SphI+ClaI, subjected to BND-cellulose (Sigma) chromatography, electrophoresed on neutral-neutral 2D gels, blotted, and hybridized as described [86].The probe for ARS301 was the1.3-kbEcoRI-XhoI fragment from p78_4.6; the probe for ARS302/ARS303/ARS320 was the 1.9-kb EcoRI-HindIII fragment from p78_5.2; the probe for ARS304 was the 3.5-kb PshAI-BamHI fragment from D10B; the probe for ARS314 was the 1.8-kb HindIII fragment from pH 1.8 [55,87].These fragments were labeled with [a-32 P] dATP (Perkin Elmer) using the Megaprime DNA-labeling system (GE Healthcare).Images were acquired on a Molecular Dynamics Typhoon 9410, and the exposure was adjusted using ImageQuant 5.2 software.Quantitations of bubble-shaped and Y-shaped replication intermediates were determined using the polygon tool and the line tool of ImageQuant 5.2.

Photography
Colonies were photographed after ,5 days of growth at 30uC on limiting adenine plates.Images were acquired as TIFF files with a Nikon D-100 camera fitted with an AF Micro-Nikkor 60 mm f/2.8 D lens.Images were cropped and adjusted for color balance and brightness/contrast in Photoshop.csv8.0 (Adobe Systems).

Supporting Information
Figure S1 Sectoring patterns of aro7D, ddc1D, and rad17D strains.The 5ORID-DR fragment was introduced into aro7D, ddc1D and rad17D strains by chromoduction, and the chromoductants were streaked on plates with limiting adenine and photographed after growth for 5 days.Found at: doi:10.1371/journal.pgen.1001227.s001(1.70 MB TIF) Figure S2 Sectoring patterns of mutants in the rad52 epistasis group.Top panels: 5ORID-DR chromoductants of rad50D, rad51D, rad52D, rad54D, rad55D, rad57D, rad59D, rdh54D, mre11D and xrs2D strains isolated in the whole genome screen were streaked on plates with limiting adenine and photographed after growth for 5 days.aro7D and rad9D chromoductants were included as controls.Lower panels: Chromoductants were tested for sensitivity to phleomycin, which induces double-stranded breaks, to confirm that the strains carried the expected deletions.Cultures of the strains shown in the top panels were grown overnight in YEPD, serially diluted and spotted on YEPD plates (control) and plates with 0.1 and 1.0 mg/ml phleomycin.YEPD plates and 0.1 mg/ml phleomycin plates photographed after 3 days, 1.0 g/ml phleomycin plates after 5 days.Each of the strains, with the exception of rad59D and rdh54D, showed sensitivity, indicating that the sensitive strains carried the expected deletions.rad59 mutants have been reported to be 10,000-fold less sensitive to gamma irradiation than rad52 mutants [Bai et al], so the lack of sensitivity of the strain we tested was expected.The sensitivity of rdh54D to gamma irradiation had not been previously tested but it had been shown not to be sensitive to HO-induced double strand breaks [Klein et al]; we found that an authentic rdh54D mutant was also not sensitive to phleomycin.[Bai Y, Symington LS (1996) A Rad52 homolog is required for RAD51-independent mitotic recombination in Saccharomyces cerevisiae.Genes Dev 10: 2025-2037.][Klein HL (1997) RDH54, a RAD54 homolog in Saccharomyces cerevisiae, is required for mitotic diploid-specific recombination and repair and for meiosis.Genetics 147: 1533-1543.]Found at: doi:10.1371/journal.pgen.1001227.s002(6.45 MB TIF)

Figure 1 .
Figure 1.DNA damage and replication stress response pathways.A simplified version of the DNA damage and replication stress checkpoint pathways is shown.The pathways are conceptually divided into sensors, phosphoinosotide-3-kinase-related kinases (PIKKs), mediators and effector kinases.The shared components of the pathways are shown in purple.The pathway-specific mediators, Rad9p, and Mrc1p, are shown in blue and red, respectively.The pathways are activated by sensors.Mec1p and Ddc2p form a complex, homologous to the mammalian ATR-ATRIP complex, which recognizes Replication Protein A (RPA) bound to ssDNA [88].Rad17p, Mec3p, and Ddc1p form a PCNA-like complex, homologous to the 9-1-1 complex, which is loaded onto DNA at 59 junctions adjacent to single-stranded DNA coated with RPA by an alternative clamp loader in which Rad24p replaces Rfc1p in a complex with Rfc2p, Rfc3p, Rfc4p, and Rfc5p [89-92].Binding of the Rad17p-Ddc1p-Mec3p clamp results in activation of Mec1p kinase activity.Ddc1p is phosphorylated by Mec1p [90].Dpb11 binds to phosphorylated Ddc1p and mediates a more robust activation of Mec1p [93].Signals from the PIKK kinases are transduced to effector kinases with the help of mediators (see text).Components tested are shown in bold type.doi:10.1371/journal.pgen.1001227.g001

Figure 2 .
Figure 2. Chromosome III derivatives.The diagram at the top summarizes replicator activity on the wild type (0ORID) chromosome.ARS elements are numbered above the line and color coded to indicate efficiencies: green, active in $90% of cell cycles; yellow, active in 15-25% of cell cycles; red, not detectably active [55].The diagram below shows regions altered in ORID derivatives; individual deletions were made in the ORID region, and the number of deletions present is specified by a number, e.g.0ORID (no origins deleted) or 5ORID (the efficient origins deleted).Additional ORID derivatives were made by fragmenting the chromosome just to the right of ARS304 to remove dormant origins in the 'L' region, or just to the right of ARS310 to remove origins in the 'R' region.We refer to these derivatives as DL-ORID and ORID-DR derivatives.Blue boxes indicate the positions of the HML, MAT and HMR loci.The lavender arrows indicate the position of the LEU2 gene; the red arrows indicate the position of the ADE2 or SUP11-1 insert; the filled black circles indicate CEN3; the green filled circle indicates the CEN4 replacement of CEN3, which removes ARS308; green arrows indicate the positions of TRP1 inserts; the orange arrow indicates the position of the NAT1 insert.doi:10.1371/journal.pgen.1001227.g002

Figure 4 .
Figure 4. Activity of dormant origins in the mrc1D mutant.Genomic DNA was prepared from MRC1 (YDN324) and mrc1D (YDN337), strains lacking ARS305.Southern blots of 2D gels of replicating DNA were probed to detect either ARS301 (left column) or ARS314 (right column).The detection of bubble-shaped replication intermediates, indicated by the arrows, demonstrates that both origins are active in the mrc1D mutant; both origins are inactive in the MRC1 strain.Diagrams of the 4.8 kb NdeI fragment containing ARS301 and the 3.5 kb ClaI-EcoRV fragment containing ARS314 are shown.The black boxes on the map lines indicate the locations of the ARS elements; the bars below the maps indicate the locations of the probes.The ARS301 probe also hybridized to a 7.1 kb NdeI fragment on chromosome XI containing the VBA5 gene.doi:10.1371/journal.pgen.1001227.g004

Figure 5 .
Figure 5. Comparisons of loss rates of ORID derivatives in checkpoint mutants.Selected data from Table 2 are shown.The mec1 data are from the mec1D sml1D strain.doi:10.1371/journal.pgen.1001227.g005

Figure 6 .
Figure 6.Activity of dormant origins on full-length 5ORID chromosome in mec1 and rad9 mutants.Genomic DNA was prepared from mec1D (YIC110) and rad9D (YJT135) strains carrying the full-length 5ORID chromosome (+5ORID) and from strains that had lost the 5ORID chromosome (-5ORID).A. Southern blots of 2D gels were probed to detect ARS301.Replication intermediates of 4.8-kb NdeI fragment from the balancer chromosome and a 4.1-kb NdeI fragment from the full-length 5ORID chromosome are shown.The mec1 gel was run longer in the first dimension than the rad9 gel.Bubble-shaped replication intermediates, indicated by arrows, arise only from the smaller NdeI fragment.Below the blots is a diagram of the ARS301 fragment as in Figure 4, except that the polymorphic NdeI site is indicated.This site is