Nonclassic Functions of Human Topoisomerase I: Genome-wide and Pharmacologic Analyses

The biological functions of nuclear topoisomerase I (Top1) have been difficult to study because knocking out TOP1 is lethal in metazoans. To reveal the functions of human Top1, we have generated stable Top1 small interfering RNA (siRNA) cell lines from colon and breast carcinomas (HCT116-siTop1 and MCF-7-siTop1, respectively). In those clones, Top1 is reduced f5-fold and Top2A compensates for Top1 deficiency. A prominent feature of the siTop1 cells is genomic instability, with chromosomal aberrations and histone ;-H2AX foci associated with replication defects. siTop1 cells also show rDNA and nucleolar alterations and increased nuclear volume. Genome-wide transcription profiling revealed 55 genes with consistent changes in siTop1 cells. Among them, asparagine synthetase (ASNS) expression was reduced in siTop1 cells and in cells with transient Top1 down-regulation. Conversely, Top1 complementation increased ASNS, indicating a causal link between Top1 and ASNS expression. Correspondingly, pharmacologic profiling showed L-asparaginase hypersensi-tivity in the siTop1 cells. Resistance to camptothecin, indenoisoquinoline, aphidicolin, hydroxyurea, and stauro-sporine and hypersensitivity to etoposide and actinomycin D show that Top1, in addition to being the target of camptothe-cins, also regulates DNA replication, rDNA stability, and apoptosis. Overall, our studies show the pleiotropic nature of human Top1 activities. In addition to its classic DNA nicking-closing functions, Top1 plays critical nonclassic roles in genomic stability, gene-specific transcription, and response to various anticancer agents. The reported cell lines and approaches described in this article provide new tools to perform detailed functional analyses related to Top1 function.


Introduction
DNA topoisomerase I (Top1) is biologically and pharmacologically important for at least two reasons related to what might be considered its classic activity, enzymatic DNA nicking-closing.First, it is essential for the removal of topological stress in DNA associated with replication, transcription, repair, and recombination (1,2).Second, it is the sole molecular target of camptothecins, which are used to treat human cancers (3)(4)(5).
The essential nature of Top1 is reflected in the fact that animals [e.g., Drosophila (6) and mice (7)] whose TOP1 gene is inactivated die at an early stage of embryogenesis.The survival of budding and fission yeasts without Top1 has been explained by compensation by topoisomerase II (Top2; ref. 2).The enzymatic function of Top1 avoids the accumulation of DNA supercoiling during replication and transcription (1,2).Top1-mediated DNA cleavage-religation proceeds by the formation and resealing of covalent enzyme-DNA intermediates, which are referred to as the cleavage complexes (Top1cc).Top1cc form with broad sequence selectivity, allowing the enzyme to act at a large number of sites in the genome.
The natural alkaloid camptothecin and its therapeutic derivatives, topotecan and the active metabolite of irinotecan, selectively trap Top1cc by binding at the interface of the Top1-DNA cleavage complex (3,5).Top1cc can also be stabilized by promiscuous endogenous DNA modifications (8) such as abasic sites, mismatches, and nicks and by carcinogenic adducts formed by benzo(a)pyrene diol epoxide, vinyl chloride, acetaldehyde, and 4-nitroquinoline-1oxide (4NQO; refs.8,9).Such cleavage complexes are particularly damaging when they produce collisions with replication forks, thereby introducing DNA double-strand breaks that can be detected as histone g-H2AX foci (10).Recently, we also found that Top1cc form early during apoptosis (5,11).
Besides regulating DNA topology, Top1 has been proposed to serve other important functions that might be considered as independent of its classic DNA cleavage-religation activity.First, Top1 may directly interact with many host cell proteins, including DNA repair factors, transcription factors, RNA splicing factors, cell cycle regulators, apoptosis-related proteins, and viral proteins, 6suggesting the involvement of Top1 in a variety of physiologic processes mediated by those factors.Second, Top1 may serve as a general transcription cofactor by binding to the core transcription initiation complex (transcription factor IID; refs.12, 13) to regulate transcription (12,14).Top1 has also been suggested to activate transcription of specific genes [including epidermal growth factor receptor (EGFR)] by binding to c-Jun (15).Finally, Top1 may also regulate transcription by acting as a specific protein kinase for SR proteins, thereby contributing to RNA splicing (16).
The evidence for many of those classic and especially nonclassic functions is fragmentary or indirect.Hence, we wished to establish an experimental system with which to examine the possible functions of vertebrate Top1 in as well controlled a way as possible.Accordingly, we have generated and characterized colon and breast carcinoma cell lines stably transfected with small interfering RNA (siRNA) to down-regulate Top1.

Materials and Methods
Cell culture and establishment of stable siTop1 cell lines.HCT116 (NCI-DTP), MCF-7 (American Type Culture Collection), and the derived siTop1 and siCtrl cell lines were grown in DMEM plus 10% (vol/vol) heatinactivated FCS.
The genetic constructs for the Top1-knockdown cell lines are detailed in Supplementary Fig. S1.Hygromycin B-resistant clones were selected, and the resulting cell lines were designated as HCT116-siTop1, MCF-7-siTop1, HCT116-siCtrl, and MCF-7-siCtrl.The doubling times of the siTop1 and siCtrl cell lines was comparable.
Western blotting.Top1 monoclonal antibody was a kind gift from Dr. Yung-Chi Cheng (Yale University, New Haven, CT).Top2a and Top2h antibodies were from Abcam Inc. and BD, respectively.Top3a and Top3h antibodies were from Santa Cruz Biotechnology, Inc.Western blotting was done using electrochemiluminescent reagents (Pierce) and high-performance Hyperfilm-ECL (Amersham Biosciences).
Cytogenetic analyses and NOR staining.Spectral karyotyping (SKY) analyses were done as described (17).For NOR staining (18), chromosome spreads were stained, and metaphases were digitally recorded in two separate channels: fluorescent 4 ¶,6-diamidino-2-phenylindole (DAPI) to visualize chromosomes and transmitted light to record silver grains.Those gray-scale images were adjusted for contrast, inverted, merged, and pseudocolored.
Micrococcal nuclease digestions.Nuclei were extracted using the TransFactor Extraction Kit (BD Biosciences) and digested with 1 unit/mL micrococcal nuclease (Sigma-Aldrich Co.) under standard conditions.DNA was purified and resolved by 1% agarose gel electrophoresis.
CEL files were analyzed using programs developed in R, a programming language and developer environment for statistical computing and graphics. 7The Robust Multi-array Analysis (RMA) algorithm as implemented in the BioConductor package was employed for data normalization using the quantile method. 8This method aims at making the distribution of probe intensities the same across all arrays in a given set.Gene expression signal calculation was based on Perfect Match values from each probe set.To identify differentially expressed genes, RMA data were subjected to significance analysis of microarrays (SAM) with a false discovery rate (FDR) set to 5%.
Array comparative genomic hybridization analyses.Total DNA was analyzed in duplicate for comparative genomic hybridization (CGH; NimbleGen Systems).The data of all the probes against a given gene based on its chromosome location were extracted and averaged to determine the change in gene copy in the siTop1 cells relative to the corresponding siCtrl cells.

Results
Topoisomerase activities in the siTop1 cell lines.The main steps used to produce the shRNA vectors and siRNA cell lines are described in Supplementary Fig. S1.Cell pairs (siTop1 and siCtrl) were generated by transfection of the construct into human colon carcinoma HCT116 and breast carcinoma MCF-7 cells, followed by selection for resistance to hygromycin B.
When examined by Western blotting, all of the siTop1 clones expressed Top1, albeit at much reduced levels.Two of the clones were selected for further studies based on their consistently low Top1 expression.Top1 protein levels were 10% to 20% of that in their respective control cell lines (Fig. 1A).Top1 down-regulation has been stable for more than 3 months in hygromycin B-free medium, indicating the effectiveness and stability of Top1 knockdown.Western blotting also showed no significant change in global protein levels for Top2a, Top2h, Top3a, or Top3h (Fig. 1B).
To determine whether Top1 down-regulation was accompanied by concurrent changes in topoisomerase activity at the chromatin level, we used camptothecin to trap Top1cc and then detected Top1 bound to cellular DNA by immunoblot following cesium gradient centrifugation (Fig. 1C; refs.9,19,20).Both siTop1 cell lines showed reduced trapping of Top1cc (Fig. 1C and D).Thus, Top1 down-regulation was effective at the chromatin level.Next, we determined whether chromatin-bound Top2 was changed in the siTop1 cell lines.For those studies, we used etoposide (VP-16), a specific Top2 inhibitor.Both of the siTop1 cell lines formed significantly more Top2a cleavage complexes (Fig. 1C and D).In contrast, Top2h cleavage complexes were unchanged in the Top1down-regulated cell lines (Fig. 1C and D).Because etoposide targets both Top2a and Top2h, those experiments indicate a selective increase in the association of Top2a with chromatin in the Top1-down-regulated cell lines and suggest that Top2a compensates for defective Top1 at the chromatin level.
High frequency of genomic reorganizations in Top1-deficient cell lines.MCF-7 cells are notorious for intrinsic genomic instability and fast acquisition of karyotypic differences in culture (21,22).In contrast, HCT116 has a stable, near-diploid chromosome number with only four structural chromosome rearrangements (17,23), making it an ideal model for evaluation of genomic instability.Therefore, to detect the impact of Top1 reduction on genomic stability, we used comprehensive SKY-based karyotypic comparison of the HCT116-siTop1 and HCT116-siCtrl lines.Thirtytwo metaphases each from HCT116-siTop1 and HCT-siCtrl were randomly selected and submitted to spectral karyotyping.The basic karyotype in both cases was the same as reported previously (17) and is best described as: 45, X, der(10)t(10;16), der(16)t(8;16), der(18)t (17;18).The mean chromosome number was comparable in both cell lines (44.9 F 0.8 for the siCtrl cells and 45.0 F 1.8 for the siTop1 cells, P = 0.348).Detailed spectral karyotype analysis, however, revealed increased numerical aberrations in HCT116-siTop1.Thirty-two metaphases from the control cells showed altogether 12 numerical aberrations per pool of 1,436 chromosomes, whereas that value in HCT116-siTop1 cells was increased almost 3-fold to 32 per pool of 1,440 chromosomes (P = 0.0193).Much larger differences between the two cell lines were observed for structural aberrations.Thirty-two metaphases from control cells showed only one [t(10;14)] translocation, whereas corresponding samples from HCT116-siTop1 cells showed 17 deletions, translocations, and inversions (P = 0.0002).When numerical and structural changes were pooled together, the statistical difference was highly significant (P = 0.0008; Fig. 2A).Those data indicate that Top1 knockdown is associated with genomic reorganizations in HCT116 cells.
Because ribosomal DNA (rDNA) alterations are among the most obvious phenotypes of Top1-deficient yeast (24), we used the controlled silver-staining assay to probe nucleolus organizing regions (NOR; ref. 18).NORs are comprised of rDNA sequences tandemly clustered on the short arms of the five acrocentric chromosomes (no.13, 14, 15, 21, and 22).In both HCT116-siTop1 and -siCtrl, almost 100% of chromosomes 13, 15, and 22 were labeled, whereas chromosome 14 often showed only one labeled copy in both samples.The average number of NOR signals per acrocentric chromosome was smaller (0.79 F 0.08) in HCT116-siTop1 cells compared with controls (0.86 F 0.06), and this statistically significant (P V 0.012) difference may have resulted, in part, from the fact that in HCT116-siTop1, only one copy of chromosome 21 exhibited positive NORs, compared with HCT116-siCtrl cells where both copies were labeled (Fig. 2B) in nearly all metaphases (P = 0.0005).Those results suggest that Top1 deficiency may be associated with decreased NOR activity.
To evaluate whether Top1 down-regulation also affected chromatin structure, we used micrococcal assays.Figure 2C shows no detectable difference between HCT116 siCtrl and HCT116 siTop1 cells in the global distribution of nucleosomal arrays.
Top1 deficiency leads to the formation of histone ;-H2AX foci associated with replication.To find factors that contribute to the chromosomal changes observed in the siTop1 cells, we searched for histone g-H2AX foci, which are indicators of genomic instability and DNA double-strand breaks (DSB; refs.25,26).Figure 3A and B shows that both HCT116-and MCF-7-siTop1 cell lines formed more endogenous g-H2AX foci than did their respective control cell lines.Notably, those g-H2AX foci were produced selectively in PCNApositive cells (Fig. 3A), showing their association with DNA replication (10).Moreover, the g-H2AX foci colocalized with the PCNA foci (Fig. 3B).
Nuclear abnormalities in siTop1 cells.Figure 3D shows representative images of nuclei from the HCT116 and MCF-7 pairs.The size of the nuclei and number of nucleoli were greater in the Top1 siRNA cells than in the corresponding controls.The MCF-7-siTop1 showed the largest nuclei (Fig. 3D, bottom).Nucleolar structures were better separated from each other in MCF-7 than in HCT116, and the MCF-7-siTop1 showed clear increased number of nucleoli and heterogeneity in size.The increased number of nucleoli was less in the HCT116-siTop1.Altogether, those observations suggest that Top1 deficiency affects nuclear and nucleolar structures.
Top1 selectively regulates gene transcription.To investigate a possible involvement of Top1 in the regulation of transcription, we studied mRNA levels using Affymetrix U133-plus-2-Genechips.The array contains 54,613 probe sets against more than 47,000 transcripts, including 17,942 different genes with HuGO (Human Genome Organization) names.A list of 308 candidate genes was generated by taking the changes common to two independent experiments on two different clones of the HCT116-derived sublines (Fig. 4A).The changes in mRNA levels of 19 genes chosen from that merged list were validated by quantitative reverse transcription-PCR (QRT-PCR; Supplementary Table S2).Western blotting also showed consistent changes for 14 of 15 genes assessed (Figs.1A and 5B and Supplementary Fig. S2A).In addition, HCT116-siTop1 and HCT116-siCtrl cell lines showed similar mRNA half-lives (Supplementary Fig. S2B), excluding the possibility that differential mRNA degradation had led to the differences between the mRNA levels of those genes.C, representative FACScan analyses following pulse-labeling with BrdUrd (30 min).BrdUrd and PI incorporation are plotted on the Y -and X-axes, respectively.Gated regions defined from the control cells without BrdUrd (data not shown) were used to calculate BrdUrd incorporation relative to total positive signal.Percentages are the mean of two independent determinations for % BrdUrd incorporation.D, top, representative images for nuclei and nucleoli after PI staining.Bottom left, quantitation of nuclear size and nucleoli numbers.Fifteen nuclei were chosen randomly and measured for each cell line.Top, nuclear size (approximated as the product of the long and short diameters of a given nucleus).Bottom, numbers of nucleoli per nucleus.Bottom right, relative increase in mean nuclear size and number of nucleoli in both siTop1 cell lines relative to the respective siCtrl cell lines.Data are the ratio of mean values obtained from the individual measurements derived from the analysis of 60 individual cells (left).
To identify genes transcriptionally regulated by Top1, we did additional microarray analyses on the MCF-7-siTop1 and MCF-7-siCtrl cell lines.The data discussed in this publication have been deposited in the Gene Expression Omnibus9 of the National Center for Biotechnology Information (NCBI) and are accessible through GEO series accession number GSE7161.Taking the genes differentially expressed in three separate experiments (one from the MCF-7-derived cell pair and the other two from replicates of the HCT116-derived pair) produced a list of 55 genes (Fig. 4A and B and Supplementary Table S1).Among those 55 genes, four were up-regulated (7.3%), and 51 were down-regulated (92.7%).Twelve of the genes are related to cellular substance metabolism and transport, nine genes to cellular signal transduction, and nine to nucleic acid or chromosome binding (Fig. 4B and Supplementary Table S1).Notably, expression of the genes coding for Top1interacting proteins was not modulated in siTop1 cells at either the mRNA or protein level.
We next asked by CGH whether the mRNA changes observed in the Top1 siRNA cells were related to alterations in gene structure.Figure 4D shows only minor DNA copy number changes in the HCT116-siTop1 cells.Although the MCF-7-siTop1 showed more abnormalities, there was no correlation between genomic and mRNA alterations (compare in Fig. 4B and D), indicating that the gene dysregulation in siTop1 cells is due to transcription rather than genetic defects.
One of the transcripts down-regulated in the siTop1 cell lines was ASNS (Fig. 4B, green ellipse).To further analyze the relationship between ASNS and Top1, we measured mRNA levels of the genes within f2.3 million bp of the ASNS gene (Fig. 4C).Among the 17 genes located in that region, 10 ASNS was the only one whose mRNA levels were changed by more than 50% in the siTop1 cells compared with their respective controls (Fig. 4C).Those results suggest that the down-regulation of ASNS in the siTop1 cells is not simply a regional genomic effect, and that the regulation of transcription by Top1 is gene specific.
Top1 regulates ASNS expression.The ASNS mRNA downregulation observed by microarray analysis in the Top1 siRNA cell lines was confirmed independently using the Quantigene-Branched-DNA assay (Fig. 5A).Western blotting also showed reduced ASNS protein levels (Fig. 5B).To test the causal role of Top1 reduction in the decreased expression of the ASNS gene, we did Top1 complementation experiments.Because of the endogenously produced Top1 siRNA, we engineered a Top1 transfection vector (pV5-Top1-sm) with silent mutations in the Top1-siRNA target sequence (Fig. 5C, left).Transfection of pV5-Top1-sm effectively enhanced Top1 protein levels and also increased the expression of ASNS mRNA in a time-dependent manner in both HCT116-siTop1 and MCF-7-siTop1 cell lines (Fig. 5C, right), suggesting that Top1 plays a causal role in the regulation of ASNS expression, a conclusion further supported by the decreased expression of ASNS protein following transient transfection with Top1 siRNAs (Fig. 5D).Transfection of ASNS siRNA, on the other hand, had no effect on Top1 expression (Fig. 5D, right).Overall, those results indicate that Top1 positively regulates ASNS at the level of transcription.
Stable Top1 reduction changes drug responsiveness.Besides camptothecins, various DNA-interactive agents can trap Top1cc, including reactive oxygen species, alkylating agents, antimetabolites, and carcinogens (8,9).Staurosporine also leads to the formation of apoptotic Top1cc (11).For many of those agents, however, it has remained unclear whether and to what extent Top1cc contribute to the biological effects.We used the siTop1 cell lines to address that question.More than 20 compounds targeting at least 15 different molecular pathways, as well as ionizing and UV radiations, were investigated (Fig. 6 and Supplementary Tables S3  and S4).Only the agents giving differential responses in the siTop1 and siCtrl cells will be discussed here.
Both siTop1 cell lines were 6-to 8-fold resistant to camptothecin (Fig. 6 and Supplementary Table S3A) and to the indenoisoquinoline NSC 706744 (MJ-III-65; ref. 27), which both target Top1 directly (5).The siTop1 cell lines were also resistant to 4-NQO, which traps Top1cc as it forms carcinogenic DNA adducts (9).Both siTop1 cell lines showed slight resistance to the potent apoptosis inducer staurosporine (28), which may be attributable to the role of Top1 in promoting apoptosis (5,29).Both siTop1 cell lines were also slightly resistant to aphidicolin and hydroxyurea, possibly as a result of a replication slowdown (see Fig. 3C).Chk1 activation by aphidicolin was also attenuated in HCT116 siTop1 cells (Supplementary Fig. S3A).
Conversely, both siTop1 cell lines were 2-fold hypersensitive to etoposide (Fig. 6), consistent with increased Top2a cleavage complexes (see Fig. 1C and D).The siTop1 cells were hypersensitive to L-asparaginase (Fig. 6), an observation consistent with ASNS down-regulation (see Top1 regulates ASNS expression).Both siTop1 cell lines were also hypersensitive to actinomycin D (Fig. 6), which may be related to the importance of Top1 for rDNA transcription.

Discussion
In this study, we designed and introduced Top1 siRNA constructs into human cell lines to establish siTop1 cell lines from two different tissues of origin (colon carcinoma HCT116-siTop1 and breast carcinomas MCF-7-siTop1).Both siTop1 cell lines show a stable f5-fold reduction of Top1 expression.
However, neither of the siTop1 clones lacked Top1, consistent with the idea that, in contrast to yeast (2), human cells require Top1 [as do mouse and fly embryos (6,7)].The studies reported here provide the first direct lines of evidence for nonclassic roles of human Top1 in maintaining genomic stability, regulating gene-specific transcription and determining response to anticancer drugs.
Human Top1 and genomic integrity.Previous studies have shown that Top1 inhibitors can induce deletion mutations (30), chromosomal aberrations (31), and replication double-strand breaks (10).However, using Top1 inhibitors (e.g., CPT) cannot appropriately define the role of Top1 in genomic stability because drug-stabilized Top1cc act as DNA damage lesions.Our finding that both siTop1 cell lines exhibit genomic alterations in the absence of drug treatment (Figs. 2 and 3) indicate that Top1 deficiency in human cells leads to chromosomal rearrangements (Fig. 2A), replication slowdown and replication-associated DNA lesions (Fig. 3A-C), as well as rDNA (Fig. 2B) and nucleolar alterations (Fig. 3D).
Although yeast and human Top1s are relatively conserved (32), genetic and functional insights derived from yeast can be extrapolated to humans only with caution because genetic inactivation of Top1 is not lethal in either budding (33) or fission yeast (34), whereas knocking out the TOP1 gene is lethal in mice (7) and flies (6).The more stringent requirement for Top1 in human cells may be related to the complexity of the human genome, with its developmental and epigenetic controls.In agreement with the fact that Top1 is the major replication swivel in yeast (35), the human siTop1 cells showed replication defects, including replication-associated g-H2AX foci (Fig. 3A and B), reduced nucleotide incorporation (Fig. 3C), and resistance to aphidicolin and hydroxyurea (Fig. 6 and Supplementary Table S3).Top1 deficiency may increase replication fork stalling and collapse because of excess superhelical tension in replicating chromatin domains (35).
The siTop1 cells are also characterized by abnormally high levels of chromosomal structure rearrangement (Fig. 2).Those rearrangements may arise from the replication defects discussed above and/or may be linked to chromatin alterations.Indeed, in Xenopus extracts, Top1 is the dominant actor in chromatin assembly (36).Our micrococcal nuclease analyses showed comparable nucleosomal patterns in siTop1 cells and their normal counterpart (Fig. 2C).Thus, chromatin perturbations resulting from Top1 deficiency may be localized to certain genomic regions and may not be detectable by global analyses.Consistently, in yeast, Top1 deficiency increases negative supercoiling without producing detectable changes in nucleosomal spacing (37).The increase in Top2a in both siTop1 cell lines might correspond to a compensatory mechanism for Top1 deficiency as Top2a has recently been shown to relax positive supercoiling preferentially, whereas Top2h and Top3 are equally effective at removing positive and negative supercoiling (38).However, the compensatory increase of Top2a activity might contribute, together with the Top1 deficiency, to the chromosomal rearrangements observed in the siTop1 cells because Top2 can promote chromosomal translocations (39).
Another characteristic of the siTop1 cells is the presence of structural alterations.Both siTop1 cell lines (particularly the MCF-7-siTop1 cells) showed increased numbers of nucleoli and heterogeneity in nucleolar size (Fig. 3D).Such nucleolar defects may be related to the nucleolar concentration of Top1 in normal Figure 6.Differential sensitivity of the siTop1 cell lines to anticancer agents.Cells were treated with the indicated drugs for 72 h.Cell survival was measured by SRB assays.The resistance factor is the ratio of the IC 50 value obtained from at least three independent experiments for the siTop1 cells to that of the corresponding siCtrl cells (see Supplementary Table S3 for mean IC 50 values FSD).Additional agents tested but giving no significant difference are not shown in the figure (see Supplementary Table S4).
cells and the binding of Top1 to nucleolin (40), which is an important component of the nucleolus.Top1 deficiency also resulted in the lack of NOR staining on one of chromosomes 21 in HCT116-siTop1 cells, consistent with either the loss or reduction in size of rDNA cluster.Top1 deficiency in yeast also increases mitotic recombination in the rDNA cluster (24).An unexpected finding in the siTop1 cells was the apparent increase in nuclear size, especially in the MCF-7-siTop1 cells (Fig. 3D).That finding may be related to previous observations of nuclear abnormalities in TOP1-null yeast (34).Increased supercoiling has been proposed to alter the density of the corresponding chromatin regions because chromatin domains are anchored to the nuclear membrane (34).Thus, the examination of the siTop1 cells shows that human Top1 may regulate both chromatin structure and organization, as well as genomic stability.
Gene-specific transcriptional regulation by human Top1.Top1 regulates gene transcription in at least two ways.One is by way of the enzymatic activity of Top1, which relaxes DNA superhelical tension generated during transcription (1,2,5,32); the other results from the coordination of Top1 with the activities of gene-specific transcriptional activators and general transcriptional factors, independently of Top1 catalytic activity (12)(13)(14)(15).Prior studies on the regulation of transcription by Top1 were conducted in cellular systems focusing on specific genes (15,41,42).However, those observations did not address whether all genes or only some specific genes are under transcriptional regulation by Top1.Answering that question could be crucial to our understanding of the lethal phenotype of Top1 knock-out in mice and flies (6,7) and possibly in human cells.
Profiling mRNA expression with spotted oligonucleotide microarrays showed 55 genes whose expression was altered in both siTop1 cell lines (Fig. 4).Considering that those genes are altered in both cell lines despite their different tissues of origin (i.e., breast and colon), we conclude the involvement of Top1 in the transcriptional regulation of at least some of those 55 genes.The complete data set will be made publicly available at the Discover Web site 11 and has been deposited in the Gene Expression Omnibus of the NCBI (GEO series accession number GSE7161). 9 Our current analysis did not focus on colon-or breast-specific differences.Nevertheless, Top1 has been implicated in tissuespecific transcriptional regulation, for example, in the case of the epidermal growth factor receptor (EGFR) gene, whose expression has been reported to be positively regulated by Top1 in human fibrosarcoma HT-1080 cells (15).However, we find EGFR gene expression to be within normal levels in our colon and breast carcinoma siTop1 cells.Comparison of our microarray gene list (Fig. 4B and Supplementary Table S1) from the siTop1 cell lines with those from camptothecin-treated human cell lines shows no similarity in gene expression changes.The dissimilarities probably reflect the fact that Top1 inhibitors primarily activate DNA damage responses (43) rather than simply reducing Top1 catalytic activity.
Only 4 of the 55 differentially expressed genes were upregulated (Fig. 4 and Supplementary Table S1).Two of those genes belong to the group of nucleic acid and chromatin binding factors, HIST1H2BD (coding for histone H2B type 1-D) and NR2F2, which may compensate for the transcriptional defects resulting from Top1 down-regulation.The two other upregulated genes, CD59 and GIP3, both encode factors that protect cells (44,45).We also found the inactivation in the BAX gene in HCT116-siTop1 cells (data not shown).Thus, the inactivation of death pathways may provide a growth advantage to the siTop1 cells as they accumulate replication-associated DNA damage and genomic lesions.
ASNS is among the 51 genes consistently down-regulated in both siTop1 cell lines (Fig. 4).The fact that the genes immediately flanking the ASNS gene locus in chromosome 7 are not differentially expressed in the siTop1 cells (Fig. 4C) suggests a specific effect of Top1 on the ASNS gene, rather than a regional chromosomal effect.Moreover, the parallel expression of ASNS and Top1 mRNA and protein levels in response to the transient reduction of Top1 protein and to Top1 complementation (Fig. 5) suggests a direct causal relationship between Top1 and ASNS expression.Thus, it is likely that Top1 is specifically involved in the up-regulation of ASNS transcription.However, the reverse is not true; the down-regulation of ASNS by siRNA does not affect Top1 expression (Fig. 5D).ASNS is a housekeeping gene.Its main promoter contains no conventional TATA and CAAT boxes.It contains GC boxes (putative SP1 sites) and multiple transcription start sites and, notably, a nutrient-sensing response unit located within the ASNS main promoter (46,47).In addition to ASNS, 11 metabolism genes (20% of all changed genes) were down-regulated in the siTop1 cells (Supplementary Table S1), suggesting that Top1 may be involved in the regulation of housekeeping genes.The mechanism of such regulation and, more specifically, the role of DNA supercoiling in the regulation of metabolism and transport genes deserve further study.
Roles of human Top1 in responses to anticancer agents and apoptosis.The siTop1 cell lines provided us with a way to test the effect of Top1 on cellular sensitivity to diverse anticancer agents.Staurosporine is a protein kinase inhibitor and a remarkably potent and widely used inducer of apoptosis in a variety of cell lines (28), which also induces apoptotic Top1cc (11).The resistance of both siTop1 cell lines to staurosporine (Fig. 6 and Supplementary Table S1A) provides functional evidence for a role of Top1 in apoptotic cell death.
The drugs showing increased activity in both Top1-downregulated cell lines include L-asparaginase, etoposide (VP-16), and actinomycin D (Fig. 6; Supplementary Table S3B).Because ASNS expression is related to cellular resistance to L-ASP (Fig. 6) and because the reduction of Top1 levels is observed in cells treated with Top1 inhibitors (48), the results presented here open the novel possibility of combining L-ASP with a Top1 inhibitor for cancer treatment.
The pharmacologic experiments discussed above show the utility of the siTop1 cell lines as new tools for studying the role of Top1 as a target for not only therapeutic but also carcinogenic agents.That approach is complementary to the use of yeast cells lacking Top1 (4,49), with the advantage of avoiding cell permeability limitations in yeast and of being closer to human tissues in the case of drugs with therapeutic potential.

Figure 1 .
Figure1.Topoisomerase expression and topoisomerase cleavage complexes in the siTop1 cell lines.A, total cellular Top1 protein levels were detected by Western blotting in HCT116-and MCF-7-derived cells.Quantitation was conducted with Adobe Photoshop 7.0, and the relative Top1 protein levels are expressed as mean F SD, n = 3. B, total protein levels for Top2a, Top2h, Top3a, and Top3h were detected and quantified as in (A ).C, chromatinassociated Top1 was evaluated as cleavage complexes in camptothecin (CPT )-treated cells using the ICE-bioassay.Fractions collected from the cesium chloride gradients are indicated above the immunoblot.Chromatin-associated topoisomerases II (Top2a and Top2b) were evaluated as cleavage complexes in etoposide (VP-16 )-treated cells using the ICE-bioassay.D, quantitation of Top1, Top2a, and Top2h associated with chromatin.Data are from ICE bioassay experiments with 10 Amol/L CPT for Top1 and 20 Amol/L VP-16 for Top2a and Top2h as in (B and D ), and computed with Adobe Photoshop 7.0.The data show two representative independent experiments.

Figure 2 .
Figure 2. Chromosomal abnormalities in siTop1 cells.A, numerical, structural, and total chromosomal aberrations in HCT116-siTop1 cells.Representative karyotypes detected by SKY are shown.Chromosomal aberrations were computed from 32 metaphases for each cell line (right ).B, staining of nucleolar organizing regions (NOR ) in representative mitotic spreads shows nine signals in HCT116-siCtrl cells and eight in HCT116-siTop1 cells.White arrows, unlabeled acrocentric chromosomes.Right, overall distribution of signals per chromosome in both samples.C, global chromatin structure in HCT116-derived cells detected by digestion with 1 unit/mL microccocal nuclease for the indicated times.

Figure 3 .
Figure3.Increased g-H2AX foci, reduced replication rate, increased nuclear size, and nucleolar number in the siTop1 cell lines.A, fractions of g-H2AX-positive cells and PCNA-positive cells.About 400 cells were counted for each cell type.The color code is indicated below the pie charts.B, representative immunofluorescence images for g-H2AXand PCNA-positive siTop1 cells.Green and red, PCNA and g-H2AX foci in the merged images, respectively.Yellow foci, colocalized signals.C, representative FACScan analyses following pulse-labeling with BrdUrd (30 min).BrdUrd and PI incorporation are plotted on the Y -and X-axes, respectively.Gated regions defined from the control cells without BrdUrd (data not shown) were used to calculate BrdUrd incorporation relative to total positive signal.Percentages are the mean of two independent determinations for % BrdUrd incorporation.D, top, representative images for nuclei and nucleoli after PI staining.Bottom left, quantitation of nuclear size and nucleoli numbers.Fifteen nuclei were chosen randomly and measured for each cell line.Top, nuclear size (approximated as the product of the long and short diameters of a given nucleus).Bottom, numbers of nucleoli per nucleus.Bottom right, relative increase in mean nuclear size and number of nucleoli in both siTop1 cell lines relative to the respective siCtrl cell lines.Data are the ratio of mean values obtained from the individual measurements derived from the analysis of 60 individual cells (left).

Figure 4 .
Figure 4. Selective transcription deregulation in the siTop1 cell lines.A, Venn diagrams showing the number of genes with significant changes in mRNA expression in three independent microarray experiments (Exp.).Yellow and blue, HCT116-siTop1 data.Red, MCF-7-siTop1 data.B, relative expression and functional classification of the 55 genes with consistent changes in mRNA level in both siTop1 cell lines.Points, means of eight values from two individual experiments for HCT116-siTop1 cells and the mean of four values from one experiment for MCF-7-siTop1 cells.C, relative expression of ASNS and of the genes flanking ASNS on chromosome 7. Data were collected from the microarray analyses.D, DNA copy numbers for the 55 genes with modified transcripts detected in the siTop1 cells.Analyses were done by array CGH.Points, averages of the data points of all the probes against the given gene in a duplicate experiment.In B-D , black and gray, HCT116-siTop1 and MCF-7-siTop1 cell lines, respectively.

Figure 5 .
Figure 5. Top1 regulates the expression of the ASNS gene.A, levels of ASNS mRNA in the siTop1 cells relative to their respective siCtrl cells measured by Quantigene Branched-DNA assays (superscript a) or by microarray analyses.B, reduced ASNS protein levels in the siTop1 cells (average of two independent experiments giving consistent results in the bar graph; representative Western blot below).C, left, construct used for Top1 complementation.The Top1 cDNA sequence used to avoid siRNA targeting is shown.The corresponding plasmid is referred to as pV5-Top1-sm.Right, pV5-Top1-sm transfection effectively complements Top1 in the siTop1 cells and enhances ASNS expression.ASNS mRNA was measured by Quantigene Branched-DNA assays.Data are normalized to ASNS mRNA in the siTop1 control groups (con, not complemented; average of two independent experiments).D, down-regulation of ASNS protein in HCT116 or MCF-7 transiently transfected with two Top1 siRNAs of different sequences (Top1-1 and Top1-2) for 48 or 72 h.Transient transfection with ASNS siRNA does not change Top1 protein expression.Western blotting images are representative of at least two separate experiments.