ZNF131 suppresses centrosome fragmentation in glioblastoma stem-like cells through regulation of HAUS5

Zinc finger domain genes comprise ∼3% of the human genome, yet many of their functions remain unknown. Here we investigated roles for the vertebrate-specific BTB domain zinc finger gene ZNF131 in the context of human brain tumors. We report that ZNF131 is broadly required for Glioblastoma stem-like cell (GSC) viability, but dispensable for neural progenitor cell (NPC) viability. Examination of gene expression changes after ZNF131 knockdown (kd) revealed that ZNF131 activity notably promotes expression of Joubert Syndrome ciliopathy genes, including KIF7, NPHP1, and TMEM237, as well as HAUS5, a component of Augmin/HAUS complex that facilitates microtubule nucleation along the mitotic spindle. Of these genes only kd of HAUS5 displayed GSC-specific viability loss. Critically, HAUS5 ectopic expression was sufficient to suppress viability defects of ZNF131 kd cells. Moreover, ZNF131 and HAUS5 kd phenocopied each other in GSCs, each causing: mitotic arrest, centrosome fragmentation, loss of Augmin/HAUS complex on the mitotic spindle, and loss of GSC self-renewal and tumor formation capacity. In control NPCs, we observed centrosome fragmentation and lethality only when HAUS5 kd was combined with kd of HAUS2 or HAUS4, demonstrating that the complex is essential in NPCs, but that GSCs have heightened requirement. Our results suggest that GSCs differentially rely on ZNF131-dependent expression of HAUS5 as well as the Augmin/HAUS complex activity to maintain the integrity of centrosome function and viability.


INTRODUCTION
Glioblastoma (GBM) is the most aggressive and common form of brain cancer in adults [1,2]. Both adult and pediatric gliomas and other primary brain tumors appear to be hierarchically organized suggestive of a cancer stem cell origin [3][4][5][6]. Consistent with this notion, GBM stem-like cells (GSCs) have been isolated that retain the development potential and specific genetic alterations found in the patient's tumor [3,4,7,8].
To identify new GBM therapeutic targets, we have previously performed shRNA screens in patient-derived GSC isolates and human neural progenitor cells (NPCs) for genes required for their in vitro expansion [9]. By carrying out control screens in proliferating fetal NPCs,

Priority Research Paper
Oncotarget 48546 www.impactjournals.com/oncotarget which have similar expression profiles and developmental potential but are not transformed [7,8], candidate GSCspecific therapeutic targets can be identified [9][10][11]. Further, by identifying cancer-lethal targets which cross validate in different GSC isolates that contain diverse cancer drivers, cancer therapeutic targets can be identified which may transcend tumor heterogeneity. Here, we validate one such candidate GSC-lethal gene, the putative transcription factor ZNF131 and investigate its GSCrelevant function.

ZNF131 retests as a GSC-lethal screen hits from genome-wide screens in GBM patient isolates
We have previously performed shRNA screens in three patient-derived GSC isolates, including, G166, 0131, and 0827 cells, and a control NPC isolate (CB660 cells [12]), for genes required for in vitro expansion under self-renewal conditions during monolayer outgrowth [9] ( Figure 1A). By comparing GSC and NPC screen results, a list of 162 GSC-specific genes was produced that scored in at least two of the GSC screens, but not NPCs. We initially retested nine genes, six of which retested as being differentially required for GSC in vitro expansion ( Figure  1A). Among these was ZNF131, which encodes a novel BTB domain zinc finger protein and putative transcription factor [13][14][15][16] that appears unique to vertebrates (according to the HomoloGene and UniGene databases). Since very little is known about ZNF131 function, we decided to further characterize its role in promoting GSC self-renewal.
We first examined steady-state ZNF131 expression levels in NPCs and GSCs. Figure 1B shows that ZNF131 is robustly expressed in both NPCs and GSCs in a manner independent of GBM subtype ( Figure 1B). We next examined the impact of ZNF131 knockdown (kd) on GSC and NPC expansion using multiple GBM patient isolates. The results were consistent with ZNF131 kd being generally lethal to GSCs regardless of specific genetic alterations (which were determined by exomeseq and CNV analysis (Supplementary Table S1)). We observed that ZNF131 kd scored similar to an shRNA targeting KIF11 in 7 out of 7 GSCs isolates examined ( Figure 1C). KIF11, which encodes a microtubule motor protein required for mitotic progression in proliferating mammalian cells [17] and also GSC maintenance [18], serves as both a knockdown and proliferation control in our experiments. In contrast to GSCs, ZNF131 kd in two different NPC isolates failed to produce a significant effect ( Figure 1C).
Visual inspection of GSCs experiencing ZNF131 kd revealed significant increases in mitotic cells, consistent with its knockdown causing mitotic arrest or catastrophe ( Figures 1D & 1E). Similar phenotypes were observed with all three shZNF131s examined (not shown; see below). In addition, we observed dramatic induction of apoptosis in three GSC isolates examined after ZNF131 kd, including adult [0131 & 0827] and pediatric [1502] isolates, but not NPCs ( Figure 1F), again suggesting GSCspecific requirement.
Examination of ZNF131 kd in GSCs and NPCs demonstrated similar robust silencing by two independent shRNAs, suggesting that the observed differences were not due to poor silencing in NPCs ( Figure 1G). Moreover, to ensure that the results were due to on-target effects, we performed complementation studies using a mutated ZNF131 ORF resistant to 2 out of 3 effective ZNF131 shRNAs (Materials and Methods) ( Figures. 1H & 1I). For these experiments, cells were first infected with LV containing control or shRNA-resistant-ORF followed by LV-shControl, shKIF11, or shZNF131 and assayed for cell growth. Target sites for ZNF131 shRNAs #1 and #2 where both mutated in the ORF construct and thus made resistant, while the site for shRNA #3 was left unchanged. Expressing this mutant ORF in GSC-0131 cells dramatically rescued lethal effects of ZNF131 kd ( Figures 1H & 1I), demonstrating that the lethality is due to targeting of ZNF131 and not due to an off-target effect. ZNF131 is required for maintaining expression of HAUS5 in GBM stem-like cells ZNF131 encodes a putative transcriptional regulator [13][14][15][16] predominantly expressed in the developing central nervous system and adult brain, testis, and thymus [15]. Despite strong suggestive evidence that ZNF131 is a transcription factor from in vitro and cell-based reporter assays [13][14][15][16] [19] [20], no direct transcriptional regulatory targets of ZNF131 have been identified in cells. And while two studies have suggested ZNF131 transcriptional activities are coordinated with binding partners such as Kaiso/ZBTB33 [19] and human polycomb protein 2 [20], other studies suggest that at least Kaiso functions independently of ZNF131 [21]. Thus, ZNF131's function(s) remains unclear.
To further characterize ZNF131, we first confirmed its cellular localization as exclusively nuclear in GBM cells (Supplementary Figure S1), consistent with previous studies [19,20]. Next, we performed gene expression profiling via mRNA-sequencing after knockdown of ZNF131 in three different GSC isolates (G166, 0131, and 0827 cells) during self-renewal conditions. The goal of these experiments was to identify indirect or direct transcriptional downstream target(s) responsible for maintenance of GBM cell viability. Analyzing RNA-seq results from shControl versus shZNF131 treated cells yielded a surprisingly small set of genes whose expression Oncotarget 48547 www.impactjournals.com/oncotarget Figure 1: ZNF131 is a candidate GSC-lethal gene. A. Overview of GSCs and NPCs shRNA screens that gave rise to ZNF131 as a candidate GSC-lethal gene. B. ZNF131 expression among NPC and GSC isolates. Values are from FPKM normalized RNA-seq data from self-renewing in vitro cultures. C. Short term growth assays showing differential viability requirement for ZNF131 among GSC and NPC isolates. Cell growth assays were performed 7 days after selection for LV-shRNAs in monolayer culture (n ≥ 3). D. Fluorescent micrographs of shRNA transduced cells (GFP+). Arrows show GSC cells displaying mitotic arrest phenotype observed with ZNF131 kd. E. Quantification of mitotic cells from D.. F. Western blot to detect cleavage of PARP protein, an indicator of apoptotic cell death, in NPC-CB660 and three GSC isolates after knockdown of ZNF131. Cells were assayed 48hrs post-selection after LV-shRNA infection (n = 3). G. RT-qPCR analysis of ZNF131 kd in NPCs and GSCs. Cells were assayed 48hrs post-selection after LV-shRNA infection (n = 3). H. Suppression of growth defects caused by shZNF131 using shRNA resistant ZNF131 ORF. Cells were first infected with LV containing control or shRNA resistant ORF followed by LV-shRNA and assayed for cell growth in monolayer culture 7 days post selection (n = 3). Target sites for ZNF131 shRNAs #1 and #2 where both mutated in the ORF construct and thus made resistant, while the site for shRNA #3 was left unchanged. I. Western blots of shRNA resistant ORF expression. *indicates p < .01 student's t-test.
JSRDs represent a group of physiological and developmental disorders, including neurodevelopmental disorders, caused by dysfunction of the primary cilia, which plays key roles in sensory perception and also developmental signaling [23]. Further examination of the list revealed CCDC113, which codes for a centrosomeassociated protein involved in formation of the primary cilium [24], and HAUS5, which encodes a member of the Augmin/HAUS complex and participates in nucleation of microtubules along the mitotic spindle [25][26][27] (Figures  2A and 2B).
Because we observed GSC-specific mitotic arrest after ZNF131 kd and cilium function, centrosome duplication, and mitotic spindle formation are inter-related [28], we wondered whether one or more of these genes are responsible for ZNF131 kd loss viability in GSCs. Thereby, we confirmed ZNF131-dependent regulation of these genes using three independent ZNF131 shRNAs, all of which replicated RNA-seq results and indicated that their change in mRNA levels is not due to an off-target effect ( Figure 1C). We also confirmed the effect in NPCs (Supplementary Figure S3A). We then examined effects of kd on stem cell expansion. Only kd of HAUS5 showed GSC-specific lethality similar to ZNF131 kd ( Figure 2D). In contrast, kd of CCDC113, NPHP1, and TMEM237 triggered GSC-specific enhancements of growth, possibly suggesting that primary cilium functions to limit their in vitro expansion.
This suggested that HAUS5 could be the relevant regulatory target of ZNF131 for maintaining GSC viability. To demonstrate this phenotypically, we performed complementation experiments. Figures 2E &  2F shows that the effects of ZNF131 kd are dramatically reversed in GSC-0131 cells ectopically expressing the HAUS5 ORF. Importantly, HAUS5 expression did not suppress the growth inhibitory effects of KIF11 kd, indicating the effects are specific to ZNF131 activity. Further confirmatory experiments in GSCs and GSCtumors are presented below in Figure 7.
We further examined whether loss of HAUS5 mRNA levels resulting from ZNF131 kd is consistent with transcriptional regulation. To this end, we examined levels of RNA polymerase (RNAP) at the several positions around the HAUS5 transcription start site (TSS) and also in a control gene, GAPDH, whose expression was not changed by ZNF131 kd. Figure 2G shows that RNAP levels drop around the HAUS5 TSS and in its gene body after ZNF131 kd, but remain constant at a distal site (-6 kb from TSS) and at the GAPDH promoter. This suggests that ZNF131 activity promotes RNAP recruitment or helps maintain RNAP steady state levels at the HAUS5 promoter. (Unfortunately, we will unable to perform endogenous ZNF131-ChIP experiments at these same promoters due to lack of suitable commercial ZNF131 antibodies.) Further, although endogenous targets of ZNF131 have not previously been identified, an in vitro DNA binding site screen revealed a 12bp palindrome sequence GTCGCR-(X)n-YGCGAC as potential binding motif [13]. The HAUS5 locus does have partial matches for this sequence, GTCGC-(X)n-GCGAC, at TSS-20bp and TSS+851bp. Regardless, these results demonstrate that ZNF131 expression controls steady state levels of HAUS5 mRNA and that this regulation is sufficient to explain ZNF131's GSC-specific requirement.
To find further support of this notion, we examined the co-expression of ZNF131 and HAUS5 in primary human NPCs and astrocytes and 22 GSC isolates (using data from [29] which includes all of the GSCs used in Figure 1C)(Supplementary Figures 3B & 3C). The results reveal that ZNF131 and HAUS5 significantly co-vary across samples, with a trend toward higher expression of both ZNF131 and HAUS5 in GSCs. This further suggests that the genes are transcriptionally linked.

ZNF131 loss in GSCs, but not NPCs, results in centrosome fragmentation and loss of spindleassociated MT nucleation
The HAUS5 protein is part of an 8-subunit complex Augmin/HAUS complex that has been shown to play critical roles in spindle microtubule (MT) generation Drosophila S2 cells and HeLa cells [25][26][27]. During mitosis, the mitotic spindle is erected via MT nucleation from centrosomes (i.e., spindle poles) and also along the emerging spindle at chromosome proximal regions [31]. The predominant MT nucleation sites are the centrosomes, where γ-tubulin ring complex (γ-TuRC) acts as the major MT nucleation complex [31]. By contrast, the Augmin/HAUS complex is responsible for centrosomeindependent, spindle-based MT nucleation through recruitment of γ-TuRC to pre-existing MTs [25][26][27].
Augmin/HAUS complex members were originally identified from an RNAi screen in Drosophila S2 cells identifying genes required for localization of γ-tubulin along the spindle but not the centrosome [27]. Knockdown of complex members led to reduction in over all spindle MT number, causing relatively mild perturbations in spindle function [27]. However, in combination with kd of genes required for centrosome-specific γ-TuRC recruitment, disruptions in spindle bipolarity and chromosome alignment were more dramatic [27]. www.impactjournals.com/oncotarget A. Examination of spindle polarity and centrosome morphology in NPCs and GSCs with and without ZNF131 kd. Cells were stained for Acetylated-α-Tubulin and γ-Tubulin to reveal changes to spindle and centrosome, respectively, and analyzed using deconvolved 3D images from z-stacked sections (0.2μm intervals). Scale bar indicates 5 μm. B. Quantification of spindle polarity in A. (n > 20). C. Quantification of α-tubulin staining at spindle pole and along spindle in NPCs and GSCs with and without ZNF131 and HAUS5 kd (n = 5).
Oncotarget 48551 www.impactjournals.com/oncotarget Characterization of human orthologs of the complex in HeLa cells, revealed similar, albeit more severe, phenotypes after knockdown of each Augmin/HAUS component [25,26], including centrosome fragmentation and multipolar spindles. Thus, Augmin/HAUS is needed to support construction of the mitotic spindle and, as a result, proper kinetochore-MT attachments.
To further investigate the relationship between ZNF131 and HAUS5 activity, we first examined spindle bipolarity after their kd (Figures 3A & 3B; Supplementary  Figures S4A-S4C). We stained cells for γ-tubulin, which is concentrated at the centrosome during mitosis [32], and α-tubulin, which allows visualization of the entire mitotic spindle. This revealed that ZNF131 kd produces a high proportion of GSC cells ( > 50%) with multipolar spindles and with concentrated γ-tubulin staining at their ends, without affecting NPC mitoses ( Figures  3A & 3B). Staining with pericentrin, which interacts with and likely recruits γ-tubulin to centrosomes [33], produced nearly identical results, as did kd of HAUS5 (Supplementary Figures S4A & S2B). Importantly, similar phenotypes were produced with three different ZNF131 shRNAs (Supplementary Figure 5). Thus, these results are consistent with ZNF131 and HAUS5 kd causing centrosome fragmentation in GSCs.
Since the HAUS5 is presumably rate-limiting for MT-nucleation along the mitotic spindle, we next assayed MT density along the spindle and at the spindle pole, as measured by α-tubulin intensity, in GSCs and NPCs with and without ZNF131 and HAUS5 kd. In NPCs, the results indicated that kd of ZNF131 and HAUS5 results in nearly identical reduction of α-tubulin intensity at both the spindle poles and along the spindle, without resulting in dramatic changes spindle versus pole α-tubulin intensity ratios ( Figure 3C). This suggests that there is a significant, general loss of MT-nucleation at the spindle in NPCs, which does not significantly impact spindle polarity or viability. By contrast, in GSCs both ZNF131 and HAUS5 loss resulted in dramatic increases in α-tubulin intensities around poles and dramatic loss along the spindle ( Figure  3C), skewing intensity ratios, consistent with loss of MT nucleation along the spindle. It is conceivable that the dramatic increases in pole-associated MT staining reflects alterations in feed back regulation of MT nucleation (i.e., γ-TuRC recruitment).
To further investigate consequences of ZNF131 kd, we examined alterations in centrosome size in GSCs and NPCs. To this end, centrosome size was determined by examining the volume of centrosomes based on Pericentrin staining [34] (Supplementary Figures S6A & S6B). This analysis revealed, first, that GSCs have larger centrosomes compared to NPCs, consistent with centrosome alteration and, second, that loss of ZNF131 causes dramatic reduction in centrosome volume only in GSCs, consistent with centrosome fragmentation (Supplementary Figures  S6A). Remarkably, this effect was reversed by ectopic  Figures S6B), further demonstrating that HAUS5 activity is down stream of ZNF131 function. These results are consistent with the notion that ZNF131-dependent regulation of HAUS5 expression is critical in GSCs, but not NPCs, for maintaining integrity of centrosome function and spindle bi-polarity during mitosis.

ZNF131 inhibition results in loss of Augmin/ HAUS complex along the mitotic spindle
To further ensure that ZNF131 kd was impacting Augmin/HAUS complex, we examined staining of HAUS6, which has been previously used assess human Augmin/HAUS complex abundance on along the mitotic spindle [26] (Figures 4A & 4B). Again, ZNF131 and HAUS5 kd phenocopied each other, producing indistinguishable results, showing profound loss of HAUS6 staining along the entire mitotic spindle. GSC-0131 cells showed almost a 4-fold reduction in HAUS6 staining ( Figure 4B). Taken together, these results demonstrate that ZNF131 or HAUS5 inhibition similarly result in GSC-specific centrosome fragmentation, loss of spindle bipolarity, loss of spindle-associated MT nucleation, and loss of Augmin/HAUS complex along the mitotic spindle.

ZNF131 or HAUS5 over-expression stimulates microtubule nucleation in GSCs
One question arising from the above studies is why ZNF131 would only regulate one member of the Augmin complex, especially if other members of the complex appear to make equal contributions to promoting activity [26]. This would seem an inefficient form of regulation unless modulation of expression of HAUS5 is sufficient to affect the overall activity of the Augmin/HAUS complex. To address this question, we examined the changes in MT density along the spindle in GSC-0131 cells with and without ectopic expression of ZNF131 and HAUS5. Remarkably, ectopic expression of either ZNF131 or HAUS5 in GSC-0131 cells dramatically increased MT density both near the spindle poles and along the spindle between 2-3-fold ( Figure 5). This suggests that ZNF131 and HAUS5 activity are rate limiting for MT-nucleation in GSCs.

The Augmin/HAUS complex is essential for suppressing centrosome fragmentation and promoting spindle bipolarity in NPCs
Two questions arising from the above studies include whether the Augmin/HAUS complex is indeed essential for mitosis in non-neoplastic cells and whether the centrosome fragmentation phenotypes require the presence of supernumerary centrosomes (i.e., centrosome amplification) [35]. To address these questions, we used NPCs, since they are diploid and do not have supernumerary centrosomes as judged by pericentrin and γ-tubulin staining. Since kd of HAUS5 has little affect on viability or mitosis of NPCs, we performed combination kd studies of Augmin/HAUS complex members. To this end, we first examined differential effect of kd of single Augmin/HAUS complex members in GSCs and NPCs. We found that HAUS2 and HAUS4 kd showed GSC-specific growth defects similar to HAUS5 kd; kd of HAUS1 and HAUS8 had no effect on GSCs or NPCs; and that HAUS6 kd was growth inhibitory to both GSCs and NPCs (not shown). The latter result suggested that the Augmin/ HAUS complex could be essential in NPCs.
To further examine this in the context of HAUS5 function, we combined kd of HAUS5 with kd of HAUS2 or HAUS4 in NPCs ( Figure 6). We find that either combination of HAUS5+HAUS2 or HAUS5+HAUS4 kd are synthetic lethal in NPCs, producing similar growth inhibition to KIF11 kd when combined, but no significant affect alone ( Figure 6A). We then examined centrosome morphology and spindle bipolarity in these cells. The results exactly mirror the effects of kd of HAUS5 alone in the GSCs. HAUS5+HAUS2 or HAUS5+HAUS4 kd resulted in fragmented centrosomes and multipolar spindles in the majority of cells ( > 70%), without noticeable perturbation in single gene kd cells ( Figures  6B & 6C).
To ensure that these results were not simply the result of differences in expression of different HAUS complex members (for example, perhaps NPCs have more expression and GSCs less), we compared gene expression of the HAUS1-8 genes in NPCs and GSCs used for viability experiments in Figure 1C (Supplementary Figure  7). The results did not show discernable differences, which would explain GSC-specific sensitivity or NPC-specific resistance to their inhibition.
These results demonstrate that the Augmin/HAUS complex is essential for growth of diploid NPCs and that centrosome amplification is not a requirement for centrosome fragmentation resulting from loss of Augmin/ HAUS complex activity.

ZNF131 and HAUS5 knockdown cause similar effects on GSC expansion, self-renewal, and tumor formation
To further ensure that HAUS5 kd phenocopies ZNF131 kd, we examined the effects of HAUS5 kd on cell expansion in four human NPC and three GSC isolates ( Figure 7A). Similar to ZNF131 kd, HAUS5 kd results in significantly diminished expansion capacity similar to shKIF11 in GSCs, but has no effect on expansion of NPCs ( Figure 7A). We next examined effects on tumorisphere formation using a limiting dilution assay, a surrogate assay for stem cell self-renewal [3,30]( Figure  7B). These studies revealed that ZNF131 and HAUS5 kd produce indistinguishable limiting dilution curves showing significant suppression of sphere formation capacity of GSC-0131 and GSC-0827 cells.
Similar results were also obtained by brain tumor formation assays in immunocomprised mice. Knockdown of ZNF131 or HAUS5 each caused similar, profound loss of tumor formation for GSC-0131-derived xenograft tumors, where tumors growth was assayed 7 weeks postinjection ( Figures 7C & 7D). Thus, these results are consistent with the notion that among HAUS5 kd replicates phenotypes produced by ZNF131 loss in GSCs and that loss of their activity compromises GBM tumor formation.

DISCUSSION
Here, we identify ZNF131 as a gene differentially required for patient-derived GSC expansion and determined its primary GSC-relevant activity. We find that GSC-specific requirement for ZNF131 activity arises from regulation of HAUS5 gene expression. Expression of either ZNF131 or HAUS5 could complement the effect of ZNF131 kd in GSCs. HAUS5 protein is a member of the 8 component Augmin/HAUS complex that stimulates MT nucleation along the mitotic spindle [26,27]. In HeLa cells, the Augmin/HAUS complex is required for centrosome and spindle integrity [26]. In our GSC isolates, we find that partial loss of either ZNF131 or HAUS5 caused profound loss of the Augmin/HAUS complex from the spindle, centrosome fragmentation, and spindle multipolarity accompanied by loss of self-renewal and tumorigenesis capacity. However, their kd in NPCs produced little or know effects on spindle or centrosome integrity. Remarkably, we also found that over expression of either ZNF131 or HAUS5 could stimulate increases in MT density along the spindle, further suggesting that both genes are rate-limiting MT nucleation. Taken together, the results demonstrate a novel and unexpected role for www.impactjournals.com/oncotarget One critical question is whether ZNF131-dependent regulation of HAUS5 is an artifact caused by an offtarget RNAi effect, whereby shRNAs designed to target ZNF131 also bind to HAUS5 mRNA. Off target effects of this nature are a cause of concern (e.g., [36]). However, we performed multiple independent experiments that demonstrate our phenotypes are not due to off target effects. First, multiple shRNAs were used to produce kd and phenotypic effects; and second, complementation studies were performed with RNAi resistant ORFs. Both of these controls demonstrated that ZNF131-specific effects cannot be due shZN131s targeting HAUS5.
Previous work has established that ZNF131 encodes a novel BTB (brica-a-brac, tramtrack and broad complex) domain zinc finger protein and putative transcription factor [13][14][15][16]. Our results demonstrate the first down stream targets of ZNF131 in mammals, which include genes associated with Joubert Syndrome and primary cilium function and HAUS5. It is conceivable that ZNF131 evolved as an adaption to promote or maintain Augmin/ HAUS complex activity during key times in development via transcriptional regulation of HAUS5. We were able to show that ZNF131 affects steady-state levels of RNAP at that HAUS5 promoter, consistent with transcriptional regulation. However, we were unable to establish a mechanism for this effect (e.g., is ZNF131 acting as a sequence-specific DNA-binding transcription factor or is it acting through a more exotic mechanism to affect HAUS5 transcription?). Future work will be required to establish a precise mechanism for this regulation.
Another key question arising from this work is why GSC isolates are more sensitive to loss of ZNF131, HAUS5, and the Augmin/HAUS complex activity than NPCs. The 8-subunit complex Augmin/HAUS complex has been shown to play critical roles in spindle microtubule (MT) generation Drosophila S2 cells and HeLa cells [25][26][27]. During mitosis, the mitotic spindle is erected via MT nucleation at spindle poles but also along the emerging spindle at chromosome proximal regions [31]. While the γ-tubulin ring complex (γ-TuRC) acts as the major MT nucleation complex [31] at centrosomes, the Augmin/HAUS complex is responsible for centrosomeindependent, spindle-based MT nucleation through recruitment of γ-TuRC to pre-existing MTs [25][26][27]. Knockdown of Augmin/HAUS complex members leads to reduction in over-all spindle MT number, causing relatively mild perturbations in spindle function [27]. However, in combination with kd of genes required for centrosome-specific γ-TuRC recruitment, disruptions in spindle bipolarity and chromosome alignment were more dramatic [27]. Knockdown of the human orthologs of the complex member genes in HeLa cells, revealed more severe perturbation of spindle function [25,26]. From our results, in non-transformed neural progenitors, we find significant reductions in alpha-tubulin staining both at the spindle pole and along the spindle after ZNF131 and HAUS5 knockdown ( Figure 3C), consistent with loss of MT number. However, these reductions do not lead to loss of spindle integrity (Figures 3A & 3B). In GSCs, both ZNF131 and HAUS5 knockdown also trigger dramatic changes in alpha-tubulin accumulation at the pole and along the spindle, although, in this case, pole accumulation significantly increased while accumulation along the spindle significantly decreased. (This may reflect inherent differences in regulation of the γ-TuRC MT complex at the spindle pole in GSCs.) However, in contrast to NPCs, GSCs displayed dramatic loss of spindle and centrosome integrity (Figures 3A & 3B; Supplementary Figure S6). We assert loss of spindle integrity is the primary cause of lethality after loss of ZNF131 or HAUS5 activity in GSCs.
There is growing evidence that most cancers have numerical or structural alterations in centrosomes [35]. In particular, centrosome amplification, or the presence of supernumerary centrioles caused by their over-replication, failed cytokinesis, or cell fusion, has been documented in multiple cancers [37][38][39][40][41]. Cancer cells compensate for centrosome amplification by "clustering" centrosomes into two poles, in part, via the activity of the kinesin protein Ncd/HSET [42]. Intriguingly, we were able to observe significant increases in centrosome volume in GSCs and observed centrosome fragmentation ZNF131 or HAUS5 kd in GSCs, which is very similar to de-clustering phenotypes for cells with amplified centrosomes. However, we were also able to observe centrosome fragmentation in our NPCs, which are diploid and do not have centrosome amplification (as judged by γ-tubulin and pericentrin staining) with HAUS5+HAUS2 or HAUS5+HAUS4 kd. Thus, it would follow that centrosome fragmentation can occur in the absence of centrosomes amplification when Augmin/HAUS complex activity levels are critically low. One possible explanation is that Augmin/HAUSdependent MT nucleation helps balance forces applied on centrosomes as the spindle is erected, during or after centrosomes separate.
Pelletier and colleagues have suggested that Augmin/HAUS complex activities are opposed by the action of the nonmotor spindle protein NuMA [26]. NuMA plays a functional role in organizing microtubules of the mitotic spindle [43,44]. Intriguingly, inhibition of NuMA can suppress defects in HAUS complex activity [26]. Thus, it is possible that NuMA activity could be higher in GSCs than NPCs, which could explain the difference in ZNF131 and HAUS complex requirement.
Another related possibility is that aneuploidy and genomic alterations have roles in inducing spindle stress (i.e., unbalancing forces) during mitotic spindle erection [45]. For example, it is has been suggested that capture of chromosomes in aneuploid cells can produce additional pulling forces sufficient to cause mother-daughter centrioles to loose integrity during prolonged mitotic delays [45]. In this scenario, ZNF131 and HAUS5 function Oncotarget 48556 www.impactjournals.com/oncotarget Figure 7: HAUS5 kd phenocopies ZNF131 kd in GSC growth, self-renewal, and tumorigenesis assays. A. Short term growth assays showing differential viability requirement for HAUS5 among GSC and NPC isolates, performed as in Figure 1 (n = 3). B. Tumorisphere limiting dilution assays with and without ZNF131 and HAUS5 kd in GSC-131 and GSC-0827 isolates. C. GSC-0131 brain tumorigenesis assays in immunocompromised mice with and without ZNF131 and HAUS5 kd in GSC-0131 (n = 6), seven weeks postinjection. D. Quantification of GFP intensity from (n = 6) C.. *indicates p < .01 student's t-test.
Oncotarget 48557 www.impactjournals.com/oncotarget could help compensate for chromosome alignment defects in GBM cells through maintaining sufficient levels of MT nucleation along the spindle. Supporting this general idea, we have previously reported that GBM cells have RTK-Ras induced chromosome alignment defects that cause added requirement for BuGZ and BubR1 [10,11,46]. However, additional studies focused on alterations of spindle forces in GSCs will be required to address these ideas.
Our studies suggest that the Augmin/HAUS complex activity may represent therapeutic target for GBM. Remarkably, targeting of ZNF131 and HAUS5 resulted in dramatic loss of viability in multiple GSC isolates (7 of 7) with diverse oncogenic drivers ( Figure  1C), without significantly affecting NPCs. The fact that GSCs with different oncogenic drivers could be targeted may bode well for targeting GBM tumors, which are notoriously heterogeneous [47][48][49]. Their knockdown also dramatically reduced GSC self-renewal (i.e., tumor sphere formation) and the formation of GSC-derived tumors ( Figure 7). Thus, the results may have relevance in actual tumors and could suggest a therapeutic window.
However, one related question is whether ZNF131, HAUS5, and the HAUS complex are essential genes. In addition to the synthetic lethal experiments shown in Figure 6, we recently performed a series of CRISPR-Cas9 knockout viability screens in both NPCs and GSCs (e.g., NPC-CB660, GSC-0131, and GSC-0827) [50]. In contrast to RNAi-knockdown screens, which tend to induce hypomorphic gene activities (i.e., partial loss of function), CRISPR-Cas9-based screens can generate highly penetrate insertion-deletion mutations that effectively knockout protein function [51,52]. Critically, from our CRISPR-Cas9 screens we observe that sgRNAs targeting ZNF131 and HAUS complex members (HAUS2, HAUS3, HAUS4, HAUS5, HAUS7, and HAUS8) all scored as essential (being depleted over time during expansion) in both NPCs and GSCs. This is consistent with the notion that the GSC-specific differences presented here are the result of partial loss of gene activities that can be tolerated in NPCs but not GSCs. This certainly does not disqualify the Augmin/HAUS complex as a key GBM target. In fact, it is conceivable that MT nucleation inhibitors could have a better therapeutic window than other spindle targeting agents, like for example, Paclitaxel, owing to lower doselimiting toxicities in non-transformed, proliferative cells. Intriguingly, the Augmin/HAUS complex activity was recently reconstituted in vitro in Xenopus egg extracts [53]. It is possible that this assay could be further refined for small molecule inhibitor screens.
Another important question in the context of patient tumors is whether targeting HAUS complex activity will differentially affect GSCs, non-GSCs (i.e., GSCderived cells) and/or also brain infiltrating tumor cells. Given that all of these cells will share similar features (e.g., oncogenic drivers, levels of aneuploidy, etc) to our HAUS-sensitive GSCs reported here, it seems likely that each population would be sensitive as long as they are traversing mitosis. Taken together, our results reveal a novel regulatory relationship between ZNF131 and the Augmin/HAUS complex that promotes mitotic spindle integrity and cancer cell viability, and suggest that partial inhibition of the Augmin/HAUS complex may represent a new therapeutic strategy for brain tumors.

Lentiviral-mediated ORF expression
RNA was extracted from CB660 cells and reverse transcribed to prepare cDNA library, using SuperScript III RT-PCR kit (Invitrogen). ZNF131 and HAUS5 were PCR www.impactjournals.com/oncotarget amplizied from this cDNA library and cloned into pGUF and pGUM lentiviral expression vectors, which create N-terminal FLAG tag or mCherry fusions (sequence and maps of these vectors are available upon request). We follow above protocol to prepare virus. Expression of each construct was determined by western blot.

Growth assays
For outgrowth assays, post-selection, shRNA transduced cells were harvested, counted, and plated onto a 96-well plate. After 7 days under standard growth conditions, cell proliferative rate was measured using Alamar blue reagent (Invitrogen).

Limiting dilution assays
Cells were infected with shRNA virus for 48 hours followed by selection with puromycin for 72 hours (Day 0). Cells were detached from their respective plate, dissociated into single-cell suspensions, counted, and then plated into non-tissue culture treated 96-well plates not coated with laminin with various seeding densities (0.125-256 cells per well, 10 wells per seeding density). Cells were incubated at 37˚C for 3 weeks and fed with 10X EGF and FGF-2 neural stem cell expansion media every 3-4 days. At the time of quantification, each well was examined for the formation of tumor spheres.

Gene expression (RNA-seq)
Cells were lysed with Trizol reagent (Life Technologies), and RNA was extracted according to manufacture instructions (Life Technologies). Total RNA integrity was checked using an Agilent 2200 TapeStation (Agilent Technologies, Inc., Santa Clara, CA) and quantified using a Trinean DropSense96 spectrophotometer (Caliper Life Sciences, Hopkinton, MA). RNA-seq libraries were prepared from total RNA using the TruSeq RNA Sample Prep Kit (Illumina, Inc., San Diego, CA, USA) and libraries size distributions were validated using an Agilent 2200 TapeStation (Agilent Technologies, Santa Clara, CA, USA). Additional library QC, blending of pooled indexed libraries, and cluster optimization was performed using Life Technologies' Invitrogen Qubit ® 2.0 Fluorometer (Life Technologies-Invitrogen, Carlsbad, CA, USA). RNA-seq libraries were pooled and clustered onto a flow cell lane using an Illumina cBot. Sequencing was performed using an Illumina HiSeq 2000 instrument with a read length of 99 bp. Reads of low quality were discarded prior to alignment to the reference genome (UCSC hg19 assembly) using TopHat v2.0.12 [54]. Counts were generated from TopHat alignments for each gene using the Python package HTSeq v0.6.1 [55]. Genes with counts above threshold equal to at least the number of samples in the smallest group were retained, prior to identification of differentially expressed genes using the Bioconductor package edgeR v3.6.8 [56]. A false discovery rate (FDR) method was employed to correct for multiple testing. This output is contained in Supplementary Table S2. All RNA-seq data including raw data will be deposited on GEO.

RT-qPCR
Quantitect RT-qPCR primer sets and QuantiFast SYBR Green PCR Kits (Qiagen) were used according to the manufacturer's instructions with the ABI Prism 7900 sequence detection system (Genomics Resource, FHCRC). Relative transcript abundance was analyzed using 2−ΔΔCt method. TRIZOL (Invitrogen) extraction was used to collect total RNA from cells.

ChIP-qPCR
Cells were cross-linked with 1% formaldehyde and sonicated to achieve chromosome fragments of 200-400 bp. ChIP was performed using antibodies directed against RNA Polymerase II (Sigma) according to manufactures protocol (Millipore). qPCR was then carried out as described above, using the primers targeting +1K, -1K, or -6K relative to the HAUS5 transcription start site (Qiagen).

Immunofluorescence
Cells were grown on sterile, acid washed coverslips in 35mm cell culture dishes. Cells were rinsed with PHEM (60mM PIPES, 25nM HEPES, 10mM EGTA, 4mM MgSO 4 ) and either immediately treated with 4% paraformaldehyde for 20 minutes at room temperature, or for phosphorylation specific antibodies, treated with lysis buffer (PHEM+1.0%Triton X-100) for 5 minutes at 37°C and then PFA fixed for 20 minutes at room temperature. Fixed cells were washed, blocked for 1 hour at room Oncotarget 48559 www.impactjournals.com/oncotarget temperature in PHEM+10% boiled donkey serum (BDS). Primary antibodies were diluted in PHEM+5% BDS and incubated for 16 hours at 4°C. Coverslips were washed, then incubated with secondary antibodies conjugated to fluorescent dyes (Jackson ImmunoReserach Laboratories) again diluted in PHEM+5% BDS for 45 minutes at room temperature. Coverslips were washed and stained with 2 ng/mL 4′,6-diamidino-2-phenylindole (DAPI) diluted in PHEM then mounted onto microscope slides in an antifade solution containing 90% glycerol and 0.5%N-propyl gallate.

Image acquisition and analysis
Fixed-cell images were acquired using a DeltaVision PersonalDV Imaging System (Applied Precision/GE) on a Photometrics CoolSnap HQ2 camera (Roper Scientific) and a 60x/1.42NA Planapochromat DIC oil immersion lens (Olympus). All immunofluorescence images were collected as z-stacks at 0.2 μm intervals. Kinetochore integrated pixel intensity values were measured on deconvolved images with SoftWorx software (Applied Precision) applying background correction. To measure centrosome volume, the cells were stained with PCM1 antibody and then imaged using Deltavision imaging system. The centrosome volume was determined by centrosomal fluorescence intensity from deconvolved 3D images using Velocity software. An arbitrary threshold was applied to remove the particles with nonspecific staining [34].

Xenografts
GSC-0131 cells were infected with pGIPZ-shRNA virus and selected for 3 days in puromycin (2μg/mL), such that > 80% of cells were GFP+. Cells were then harvested using Accutase (Sigma), counted, resuspended in an appropriate volume of culture media, and kept on ice prior to immediate transplantation. NOD-scid IL2Rgammanull mice (Jackson Labs #005557) were anesthetized by IP injection of 0.2ml/10 grams 1.25% Avertin Solution and kept at 37°C. A small bore hole was made in the skull using a hand drill with a Meisinger #009 steel burr bit (Hager & Meisinger GmbH). 2x10^5 cells were slowly injected by pipet into the right frontal cortex approximately 2mm rostral to Bregma, 2mm lateral and 3mm deep through a 0.2-10ul disposable sterile aerosol barrier tip (Fisher Scientific #02-707-30). The burr hole was closed using SURGIFOAM (Johnson & Johnson) and the skin rejoined using TISSUMEND II (Veterinary Product Laboratories, Phoenix AZ). Seven weeks after initial transplantation mice were injected intravenously with 50μl of 40μM Chlorotoxin: Cy5.5 conjugate [57] 2 hours prior to sacrifice by carbon dioxide inhalation. The brain and tumor were removed from the skull and imaged for Cy5.5 and GFP fluorescence using the Xenogen IVIS Spectrum imaging system (Caliper Life Sciences).