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Human cells contain five topoisomerases in the nucleus and cytoplasm, but which one is the major topoisomerase for mRNAs is unclear. To date, Top3β is the only known topoisomerase that possesses RNA topoisomerase activity, binds mRNA translation machinery and interacts with an RNA-binding protein, FMRP, to promote synapse formation; and Top3β gene deletion has been linked to schizophrenia. Here, we show that Top3β is also the most abundant mRNA-binding topoisomerase in cells. Top3β, but not other topoisomerases, contains a distinctive RNA-binding domain; and deletion of this domain diminishes the amount of Top3β that associates with mRNAs, indicating that Top3β is specifically targeted to mRNAs by its RNA binding domain. Moreover, Top3β mutants lacking either its RNA-binding domain or catalytic residue fail to promote synapse formation, suggesting that Top3β requires both its mRNA-binding and catalytic activity to facilitate neurodevelopment. Notably, Top3β proteins bearing point mutations from schizophrenia and autism individuals are defective in association with FMRP; whereas one of the mutants is also deficient in binding mRNAs, catalyzing RNA topoisomerase reaction, and promoting synapse formation. Our data suggest that Top3β is the major topoisomerase for mRNAs, and requires both RNA binding and catalytic activity to promote neurodevelopment and prevent mental dysfunction.
Topoisomerases are ‘magicians of the DNA world’, solving critical topological problems generated in many essential biological processes on DNA, including replication, transcription and segregation (1,2). These enzymes have a unique activity to catalyze DNA strand passage reactions, which enables them to relax supercoils generated during unwinding of duplex DNA by replication and transcription machinery, and to segregate chromosomes during cell division. Topoisomerases are universally present in all species (3), and that their dysfunction can cause genomic instability, defective cell proliferation, abnormal development, shortened life-span, lethality and human diseases (1,4–6). For example, depletion of topoisomerase I (Top1) from human cells can induce DNA breaks, chromosome aberrations and replication defects (7). Inhibition of topoisomerase 2α (Top2α) activity, or disruption of its recruitment to chromatin, can lead to defective chromosome segregation during mitosis (8,9).
Unlike the well-characterized DNA topoisomerases, RNA topoisomerases have received little attention for many years. In fact, the first RNA topoisomerase in eukaryotes was discovered only a few years ago, and it was shown to be capable of catalyzing RNA cleavage (4) as well as RNA strand passage reactions (10). To date, RNA topoisomerase activity has been observed in Type IA topoisomerases from all three domains of life (bacteria, archaea and eukarya) (10–13). This broad prevalence is similar to that of DNA topoisomerases, suggesting that RNA topoisomerase activity could provide growth advantage for its host so that it is retained through millions of years of evolution similarly as DNA topoisomerases. Interestingly, some of the most well-known Type IA topoisomerases, Top1 and Top3 of Escherichia coli and Top3 of yeast, all have dual activities for RNA and DNA (11–13), so that they may solve topological problems for both nucleic acids. In human, only one of the two Type IA enzymes, Top3β, possesses dual activity for both RNA and DNA, whereas its paralog, Top3α, has activity only for DNA (10). This difference in activity for RNA is largely due to a conserved RNA-binding motif, RGG-box, which is present only in Top3β but not Top3α; and deletion of this motif disrupts the RNA topoisomerase activity of Top3β (10).
Increasing evidence has revealed that Top3β regulates translation of mRNAs important for neurodevelopment and mental health together with other RNA binding proteins (RBPs). First, Top3β has been isolated in a complex with TDRD3 (Tudor domain-containing 3) (4,10,14), and this complex biochemically and genetically interacts with FMRP (4,10), an RBP that is inappropriately silenced in Fragile X syndrome and regulates translation of mRNAs important for neuronal function and autism (15). Second, the interaction between Top3β-TDRD3 and FMRP is impaired by a patient-derived FMRP mutation (10,16); and Top3β gene deletion has also been linked to schizophrenia and cognitive defects (4). Moreover, de novo single nucleotide variants (SNVs) of Top3β gene have been identified in schizophrenia and autism patients (17,18). Third, Top3β resembles TDRD3 and FMRP in its association with active-translating polyribosomes (4,10,16), and this association is conserved from human, chicken to fruit flies (12). Fourth, Top3β binds many mRNAs in vivo, and some of them are encoded by genes with neuronal functions related to schizophrenia and autism (10). Expression of one such gene, ptk2/FAK (protein kinase 2/focal adhesion kinase) is reduced in synapses at neuromuscular junctions (NMJs) of Top3β mutant flies. Synapse formation is defective in both flies and mice deleted for Top3β, as observed in FMRP mutant animals. These data suggest that Top3β works with FMRP and TDRD3 to regulate expression of mRNAs important for neurodevelopment and mental health.
Here, we investigate three basic questions regarding RNA topoisomerases in animals. Question one, human cells contain five topoisomerases in nucleus and/or cytoplasm, Top1, Top2α, Top2β, Top3α and Top3β. Which one is the major mRNA-binding topoisomerase in cells? We demonstrate that Top3β is the major mRNA-binding topoisomerase in human cells; and it is targeted to mRNAs mainly by its distinctive RNA-binding domain, which is absent in other topoisomerases. This finding leads to us further investigate the mechanism of how Top3β functions. Question two, is the RNA binding and catalytic activity of Top3β needed for its function in vivo? Question three, do Top3β variants from mental disorder patients disrupt its activities and functions? We show that both RNA-binding and catalytic activity is needed for Top3β to promote synapse formation in Drosophila. Moreover, when the de novo SNV from an autism patient is introduced into Top3β mutant flies, its function in synaptic formation is disrupted, providing evidence that Top3β function is linked to mental health.
HEK293 cells were cultured as described previously (10). The mRNA-binding protein capture assay was performed using HEK 293 cells as described (19). Briefly, HEK 293 cells were transfected with plasmids expressing GFP-Top3β or its variants. After 48 h, the cells were exposed to 300 MJ/cm2 UV254 and harvested. The cells were lysed in lysis buffer (100 mM Tris, pH7.5, 150 mM LiCl, 0.1% lithium dodecyl sulfate (LiDS), 1% NP-40, 10 mM ethylenediaminetetraacetic acid (EDTA), 5 mM dithiothreitol (DTT)) and spun at 17 000 g. The supernatant was added with equal volume binding buffer (100 mM Tris, pH 7.5, 850 mM LiCl, 2% LiDS, 10 mM EDTA, 5 mM DTT) and incubated with Magnetic Oligo(dT) Beads (TAKARA) for 30–60 min at RT. The RNA–protein-captured beads were washed with WB1 buffer (100 mM Tris, pH 7.5, 500 mM LiCl, 1% LiDS, 10 mM EDTA, 5 mM DTT) 3 times and WB2 (20 mM Tris, pH 7.5, 200 mM LiCl, 1 mM EDTA, 1 mM DTT) twice. The RNA–protein complex was eluted with 20 μl EB buffer (20 mM Tris, pH 7.5) at 80°C for 2 min, and RNA was removed by RNase A. Each eluted mixture was then analyzed by immunoblotting together with their corresponding cell lysate.
Human Top3β-R472Q and C666R mutants were made following the protocol of QuikChange II Site-Directed Mutagenesis Kit (Agilent Technologies). The following oligos were used:
Flag-tagged human Top3β and its mutants (R472Q and C666R) were expressed and purified as described previously (10). Briefly, HEK 293 cells were transfected with pcDNA constructs of human Top3β and its mutants using polyethylenimine. Cells were incubated in CO2 incubator shaker at 130 rpm, 5% CO2 for 72 h. Cells were then harvested, washed 2 times with cold phosphate buffered saline (PBS) and lysed in 3.5 volume of lysis buffer containing 20 mM Tris pH 7.5, 500 mM NaCl, 10% glycerol, 0.5% NP40, 10 mM NaF and protease cocktail (Roche) on ice for 30 min. Two volumes of cold 20 mM Tris pH 7.5 were added to the cell lysate, and the diluted lysate was centrifuged at 18 000 rpm at 4°C for 30 min. The supernatant was incubated with the anti-Flag M2-agarose beads (Sigma) at 4°C for 3 h. Beads were washed three times with cold washing buffer (50 mM Tris pH 7.5, 500 mM NaCl, 10% glycerol, 0.5% NP40, 1% EDTA and protease inhibitor cocktail), and once with cold elution buffer (25 mM Tris pH 7.5, 100 mM NaCl and 10% glycerol) for 5–8 min per wash. Flag-tagged proteins were eluted from anti-Flag M2 agarose beads in elution buffer with 200 μg/ml 3X Flag peptide (Sigma).
Subcellular fractionation of HEK293 cell extracts into cytoplasmic and nuclear extracts have been described previously (10). IP using Flag antibody was performed as described earlier (10). Immunoblotting and various antibodies used in this study have also been described (10). Anti-humTop1 antibodies were from Abcam (ab3825); anti-humTop2α and anti-humTop2β antibodies were from Bethyl (A300-054A and A300-950A, respectively); anti-humTop3α antibodies were generated as described early (20). ImageJ software was used to quantify immunoblotting images.
For generation of mutant flies carrying C660 R mutation in Top3β, pMT/V5-Flag-Top3β construct served as template to introduce the required mutation. The template was mutated using QuikChange Lightning Site-Directed Mutagenesis Kit (Agilent Technologies) and a set of primers gTgTATCgCgAgTTCAAgCgCCCgCTggACgACTTTg and gATCAAAgTCgTCCAgCgggCGCTTgAACTCgCg, respectively, following the manufacture's protocol. The mutation was confirmed by sequencing. A Top3β fragment carrying the C660R mutation was excised out from PMT/V5 Vector using NotI and XbaI restriction enzymes (New England Biolab) and sub-cloned into NotI and XbaI digested pBID-UASC vector (Addgene).
The NMJ analysis was performed as described previously (10). Briefly, the third instar wandering Drosophila larvae were dissected in cold Schneider's Drosophila Medium (Invitrogen). Then samples were fixed in 1× PBS with 4% paraformaldehyde (pH 7.4) for 25 min at room temperature. They were then rinsed three times with 1× PBT (phosphate-buffered saline in Triton X-100 (0.2% Triton X-100 in 1× PBS)) and blocked with 1% normal goat serum for 1 h at room temperature. Primary and secondary antibodies were diluted with 1× PBT with 1% normal goat serum and incubated with the samples overnight at 4°C and for 2 h at room temperature, respectively. The primary antibodies used in this study were: anti-DLG (4F3, 1:500 dilution, http://dshb.biology.uiowa.edu/4F3-anti-discs-large) from the Developmental Studies Hybridoma Bank (University of Iowa, IA, USA) and DyLight 549 anti–horseradish peroxidase (1:500 dilution) from Jackson Immuno Research (http://www.jacksonimmuno.com/pdf/lots/98340.pdf). Stained preparations were imaged with the Zeiss confocal microscopy system LSM 710 (Zeiss). The number of synaptic boutons and branches from NMJ4 segments 3–5 (n ≥ 20) of the different genotypes were quantified. The means and the standard errors of means (s.e.m.) of the boutons and branches were calculated. The P-values were obtained using Student's t-test (pairwise). Three independent experiments were performed, and the results are reproducible.
Three of the five known human topoisomerases (Top1, Top2α and Top3β; but not Top2β and Top3α) have been captured as RBPs directly binding to mRNAs in cells by two independent studies using UV-based crosslinking protocols coupled with mass spectrometry (21,22). We investigated which one is the major mRNA-binding topoisomerase in human HEK293 cells by modifying one of the protocols (21): we similarly performed UV-crosslinking of RBPs to mRNAs, captured the mRNA-bound RBPs using oligo-dT beads, but substituted the mass spectrometry with immunoblotting for protein identification (Figure (Figure1A).1A). One advantage of the immunoblotting is that it can detect the levels of an RBP in both the captured mRNA–protein complexes and the input extract on the same gel. The relative ratio between the two levels should correlate with the percentage of the RBP that binds mRNAs in total extract. As positive controls, three known RBPs that have been previously captured by mRNA-binding studies (21,22)—TIA1(23), FMRP (15) and TDRD3 (13)—were all detected by our approach, at relative ratios of greater than 10% (Figure (Figure1B1B and C). As a negative control, RPA32, a subunit of a single-strand DNA binding complex RPA, was absent, with a relative ratio of 0%.
We performed our analyses on all five human topoisomerases. Top3β was detected in mRNA–protein complexes at a relative ratio of about 50% when compared to its level in the input extract (Figure (Figure1B1B and C). In contrast, none of the other topoisomerases was detected in the same complexes (relative ratio is 0), even though their signals in the input were comparable to that of Top3β. These data suggest that Top3β is the major RNA topoisomerase working on mRNAs in human cells. We noted that the relative ratio of Top3β is similar to those of TDRD3 and FMRP, but substantially less than that of TIA1, which are in agreement with the notion that Top3β, TDRD3 and FMRP interact with each other to bind mRNAs (4,10).
We investigated the question why Top3β, but not other topoisomerases, is the most abundant mRNA-binding topoisomerase. A distinguishing feature of Top3β is the presence of an RGG RNA-binding domain, which is not found in Top3α and other human topoisomerases (Figure (Figure1D;1D; data not shown). We therefore investigated whether this domain is required by Top3β to bind mRNAs using the same method described above (Figure (Figure1A).1A). We transfected expression vectors encoding GFP-tagged Top3β wild-type or RGG-box deletion mutant (ΔRGG) protein into HEK293 cells, and found that the mutant protein was present at a substantially reduced level (about 5-fold less) in the mRNA-bound RBPs than that of the wild-type protein (Figure (Figure1E1E and F). As an internal control, the level of TIA1 was comparable in mRNA-bound RBPs isolated from cells transfected with the two vectors. These data indicate that the RGG–RNA binding domain is critical for targeting Top3β mRNAs in vivo.
It should be noted that a putative nuclear localization sequence (NLS), PNPRRPKDK, is present at the C-terminus of RGG-box of Top3β based on a prediction program, PSORT II. This sequence was removed in our RGG-box-deletion construct, raising a possibility that the observed effect may be due to impairment of Top3β nuclear localization. We consider this possibility unlikely because majority of mRNAs are present in the cytoplasm, so that excluding Top3β from the nucleus should not limit its access to mRNAs. In addition, this NLS is absent in Drosophila Top3β, so that the observed phenotype for the Drosophila RGG-deletion mutant should not be due to perturbation of nuclear localization. Moreover, the same prediction program also detected the presence of at least another putative NLS in the middle of Top3β protein (RPRK at amino residue 377). Future experiments are needed to specifically delete these putative NLSs and RGG-box to elucidate their roles in nuclear localization, mRNA binding and other functions.
We also transfected the catalytic-inactive point mutant of Top3β (Y336F), which is completely deficient in both DNA and RNA topoisomerase activity, into the same cell line. We found that this mutant was present at a level similar to that of the wild type, but substantially higher than that of the ΔRGG mutant, in eluted mRNA–protein complexes (Figure (Figure1E1E and F), indicating that the catalytic mutant largely retained the mRNA binding activity.
Top3β has at least two RNA-related biochemical activities: an mRNA binding activity that depends on the RGG-box (as described above), and RNA topoisomerase activity that requires the catalytic Tyr residue (10). We investigated which activity is needed to rescue the abnormal synapse formation at NMJs of Drosophila top3β mutant (10). We generated transgenic flies ectopically expressing Flag-tagged Top3β wildtype, RGG-box deletion and catalytic Tyr mutant proteins in the neurons of top3β deletion background (Figure (Figure2A).2A). Whereas ectopically-expressed Top3β-wildtype protein largely rescued the abnormally higher numbers of synaptic branches and boutons in the top3β mutant, the RGG-box deletion mutant (ΔRGG) and the catalytic mutant Y322F did not (Figure (Figure2B,2B, ,CC and D). These data indicate that Top3β requires both its RNA binding activity and topoisomerase activity to promote synapse formation.
Genomic deletion of Top3β has been linked to schizophrenia (4). In addition, Top3β has been shown to interact with FMRP, a protein silenced in Fragile X syndrome, which is a leading cause of autism. Because autism and schizophrenia share common etiology factors (24,25), we investigated whether Top3β point mutations are similarly associated with mental disorders. Indeed, independent genome-wide sequencing studies have identified two de novo SNVs of Top3β, C666R and R472Q, in autism and schizophrenia patients, respectively (17,18), but absent in their unaffected siblings or parents. The C666R variant substituted a strictly conserved Cys residue in the C-terminal Zn-finger domain with a charged residue, whereas R472Q replaced a positively-charged residue (either R or K) conserved in the core domains of vertebrate Top3β with a non-charged residue (Q) (Figure (Figure3A).3A). Because these variants significantly altered the property of highly conserved amino acid residues, we examined whether they disrupted functions of Top3β using both in vitro and in vivo assays.
First, we expressed and purified flag-tagged recombinant proteins for the wild type and two variants of Top3β (R472Q and C666R) using HEK293 cells (Figure (Figure3B),3B), and then tested their activity using the RNA topoisomerase assay as described previously (10,12). In this assay, a synthetic closed circular RNA substrate is converted to a trefoil knot by the strand-passage activity of an RNA topoisomerase, such as Top3β. The knot produced can be distinguished from the circle substrate by denaturing urea-polyacrylamide gel electrophoresis. Consistent with previous findings, wild-type Top3β converted up to about 30% of the RNA circle to knot (Figure (Figure3C).3C). Similarly, the R472Q mutant exhibited conversion efficiency comparable to that of the wild-type protein (Figure (Figure3D).3D). Notably, the C666R variant converted about 5- to 10-fold less circle to knot at various protein concentrations tested (Figure (Figure3D),3D), indicating that this variant is strongly defective in its RNA topoisomerase activity.
Second, we examined whether C666R and R472Q mutants have reduced mRNA binding activity in vivo using the RBP capture assay described above. We found that the C666R variant showed reduced mRNA binding activity (about 5-fold reduction), whereas the R472Q variant displayed activity similar to that of the wild-type protein (Figure (Figure1E1E and F). Previous studies have shown that Top3β localizes in both nuclear and cytoplasmic fractions (4,10). One possibility for the observed reduction of C666R in binding to mRNAs is that the mutant protein may be misfolded and thus mis-localized in the nucleus, which precludes it from access to the mRNAs in the cytoplasm. To exclude this possibility, we examined the subcellular localization of these mutants by immunoblotting. The two mutant proteins were detected in both nuclear and cytosolic fractions, and their distribution in these fractions was comparable to that of the wild-type protein (Supplementary Figure S1), which argue against this possibility. However, the level of the C666R mutant protein was somewhat lower than that of the wild type (Supplementary Figure S1, and also Figure Figure3E3E below). We therefore cannot rule out a possibility that a small fraction of C666R mutant protein may be misfolded and degraded.
Third, we tested whether the two variants have normal association with FMRP and TDRD3 by transfecting both variants into HEK293 cells and performing co-immunoprecipitation assay as described previously (10). Both variants co-immunoprecipitated with about 5-fold less amounts of FMRP, as well as about 30% less amounts of TDRD3, when compared to the wild-type protein (Figure (Figure3E).3E). These data suggest that the two variants are strongly deficient in association with FMRP, but are only slightly defective in association with TDRD3.
Finally, we generated transgenic flies expressing Drosophila Top3β-C660R variant, which corresponds to the human Top3β-C666R mutant, in the top3β deletion background (Figure (Figure4A).4A). We found that this variant displayed reduced ability to rescue the higher number of synaptic branches and boutons observed at the NMJs of top3β mutant (Figure (Figure4B4B–D). For example, whereas the ectopically-expressed Drosophila Top3β-wild type protein suppressed the mean branch number from 3.9 to 2.4 (lane 2–3), the C660R variant suppressed the number from 3.9 to 3.4; suppression of synaptic boutons was 35 to 21 for the wild type, and 35 to 29 for the C660R mutant. The data provide in vivo evidence that C666R is a partial loss-of-function mutant. We were unable to test the R472Q variant, because this residue is variable in invertebrates, and its corresponding residue in Drosophila Top3β happens to be Q (Figure (Figure3A3A).
Human cells have five topoisomerases that exist in nucleus and/or cytoplasm. One basic question is how many of them can bind mRNAs and function as RNA topoisomerases. We and others have previously shown that Top3β possesses RNA topoisomerase activity in vitro and binds many mRNAs in vivo (4,10). Here, we demonstrate that only Top3β and its two interacting partners (TDRD3 and FMRP) were detected in cellular RBPs that directly bind mRNAs, whereas the other four topoisomerases (Top1, Top2α, Top2β and Top3α) were undetectable. We conclude that Top3β is the major RNA topoisomerase working on mRNAs in human cells.
Our data have similarity and difference when compared to two previous screens using UV-crosslinking coupled with mass spectrometry to identify mRNA-binding RBPs in human cells (21,22). The similarity is that all three studies have identified Top3β and its two partners, TDRD3 and FMRP, but not Top3α and Top2β, in mRNA-binding RBPs. These data together support the proposal that Top3β, but not Top3α, is an RNA topoisomerase that functions in mRNA translation (10). The difference is that the two previous screens, but not the current study, have identified Top1 and Top2α as mRNA-binding RBPs. This raised a possibility that these two enzymes may have RNA topoisomerase activity and work on mRNA, which needs to be addressed in future studies. Nevertheless, our inability to detect Top1 and Top2α implies that the percentage of these two topoisomerases stably associating with mRNAs might be quite low, so that they could not be detected by our immunoblotting-based approach.
Why Top3β differs from the other topoisomerase in mRNA association? We found that the amount of Top3β that binds mRNAs in cells was strongly decreased (about 5-fold) by deletion of its RGG RNA-binding domain. This finding is consistent with our earlier data that the RNA topoisomerase activity of Top3β is severely disrupted by deletion of the same domain (10). Together, these data indicate that the RGG domain plays a crucial role in targeting Top3β to RNA both in vitro and in vivo.
We have examined the protein sequences of all human topoisomerases for the presence of RGG domain and other RNA-binding motifs, and found that Top3β is the only one with a recognizable RNA-binding domain (data not shown) (10). We therefore propose that the main reason for Top3β being the major mRNA-binding topoisomerase is because of its unique RNA-binding domain, which targets the topoisomerase to mRNAs. Other topoisomerases lack such an RNA-targeting domain, so that their main substrate is most likely DNA, but not RNA. We should point out that both interacting partners of Top3β, TDRD3 and FMRP, also possess RNA-binding activity (13,15) and could thus contribute to targeting of Top3β to mRNAs. Moreover, TDRD3 has been shown to directly interact with the exon-junction complex through its EBM motif (exon-junction complex binding motif) (4), and several other mRNA translation factors through its TUDOR domain (4,10,26). Depletion of TDRD3 or mutation of either its EBM or TUDOR domains reduce the amount of TDRD3–Top3β complex that associates with translating polyribosomes (4,12). Thus, Top3β may be targeted to mRNAs by at least three mechanisms: either through its own RGG-box, or its partner's RNA binding domains, or the protein binding motifs of TDRD3 (TUDOR and EBM). Existence of several targeting mechanisms may explain why the Top3β mutant deleted of the RGG-box still has residual mRNA binding activity in cells.
It should be noted that most of Top3β in cells co-fractionates with free mRNAs or mono-ribosomal fractions, whereas only a small amount of Top3β associates with the translating polyribosome fractions (4,10,12). The amount of Top3β associating with polyribosomes is strongly decreased when TDRD3 is depleted, or when the EBM or TUDOR domains of TDRD3 are mutated (4,10,12). The data imply that binding of Top3β to mRNAs through its RGG domain is insufficient for its recruitment to the mRNA translation machinery; and this recruitment requires additional interactions mediated by TUDOR and EBM domains of TDRD3.
We have previously shown that the RGG-domain deletion mutant of Top3β is defective in catalyzing RNA topoisomerase reaction. Our current data that the RGG-domain is required for targeting of Top3β to mRNAs in cells and for promoting neurodevelopment in Drosophila provide in vivo evidence for importance of this RNA-binding domain in Top3β function. Moreover, we demonstrated that the Top3β catalytic Tyr mutant, which had deficient RNA topoisomerase activity but largely normal mRNA binding activity, failed to promote neurodevelopment in flies. Thus, the topoisomerase activity of Top3β is also required for its function in neurodevelopment, whereas the RNA-binding activity alone is insufficient.
It should be pointed out that although Top3β possesses RNA topoisomerase activity in vitro (10), binds mRNAs in cells and requires its RGG RNA-binding domain and catalytic activity to promote neurodevelopment, there is so far no direct evidence to prove that Top3β actually catalyzes topoisomerase reactions on mRNAs in cells. In fact, deletion of the Top3β-RGG domain or mutation of its catalytic residue can impair both RNA and DNA topoisomerase activity of the enzyme (4,10,13,27). Thus, it remains to be determined whether it is the DNA or RNA topoisomerase activity of Top3β that is important for neurodevelopment.
Finally, we demonstrated that two de novo SNVs of human Top3β from schizophrenia and autism patients are both impaired in FMRP association, which are reminiscent of the previous findings that a Fragile X patient-derived mutation disrupts the association between FMRP and Top3β-TDRD3 complex (10,16). Because Fragile X syndrome is a known cause of autism (28,29) and Top3β gene deletion is linked to schizophrenia (4), our data suggest that the association between Top3β-TDRD3 and FMRP is important to prevent both of these mental disorders. Notably, whereas the C666R variant from the autism patient has not been detected in the general population, the R472Q from the schizophrenia patient has been detected, with a frequency of 0.0004 (NCBI SNP database). It will be interesting to study if the individuals carrying this minor allele may have increased risk of developing schizophrenia. Moreover, the C666R variant has additional defects in mRNA binding, in RNA topoisomerase activity, and in promoting synapse formation, suggesting that variants that impair RNA binding and topoisomerase activities of Top3β can lead to abnormal neurodevelopment and increased risk to mental dysfunction. Consistent with this notion, copy number variants of both Top3β and TDRD3 have been reported in individuals with autism spectrum disorders (listed in http://autismkb.cbi.pku.edu.cn). Micro-duplication of the genomic region containing Top3β gene has also been reported for a patient with mental retardation (30). Future studies are needed to identify genes regulated by the Top3β–TDRD3 complex, which could provide targets for therapeutic intervention.
The authors thank Dr T.S. Hsieh for providing Drosophila Top3β flies and antibody, and Dr D. Schlessinger for critical reading of the manuscript. The authors also thank an anonymous reviewer for indicating presence of a putative nuclear localization sequence at the C-terminus of Top3β.
Supplementary Data are available at NAR Online.
Intramural Research Program of the National Institute on Aging, National Institutes of Health [Z01 AG000657-08 in part]; National Basic Research Program of China [2013CB911002]; National Natural Science Foundation of China . Funding for open access charge: National Institute on Aging, NIH [Z01 AG000657-08].
Conflict of interest statement. None declared.