- Research article
- Open Access
Transcription factor ZNF25 is associated with osteoblast differentiation of human skeletal stem cells
BMC Genomicsvolume 17, Article number: 872 (2016)
The differentiation of human bone marrow derived skeletal stem cells (known as human bone marrow stromal or mesenchymal stem cells, hMSCs) into osteoblasts involves the activation of a small number of well-described transcription factors. To identify additional osteoblastic transcription factors, we studied gene expression of hMSCs during ex vivo osteoblast differentiation.
Clustering of gene expression, and literature investigation, revealed three transcription factors of interest – ZNF25, ZNF608 and ZBTB38. siRNA knockdown of ZNF25 resulted in significant suppression of alkaline phosphatase (ALP) activity. This effect was not present for ZNF608 and ZBTB38. To identify possible target genes of ZNF25, we analyzed gene expression following ZNF25 siRNA knockdown. This revealed a 23-fold upregulation of matrix metallopeptidase 1 and an 18-fold upregulation of leucine-rich repeat containing G protein-coupled receptor 5 and RAN-binding protein 3-like. We also observed enrichment in extracellular matrix organization, skeletal system development and regulation of ossification in the entire upregulated set of genes. Consistent with its function as a transcription factor during osteoblast differentiation of hMSC, we showed that the ZNF25 protein exhibits nuclear localization and is expressed in osteoblastic and osteocytic cells in vivo. ZNF25 is conserved in tetrapod vertebrates and contains a KRAB (Krueppel-associated box) transcriptional repressor domain.
This study shows that the uncharacterized transcription factor, ZNF25, is associated with differentiation of hMSC to osteoblasts.
Adult human skeletal stem cells (also known as bone marrow stromal or mesenchymal stem cells, hMSCs) are present in the bone marrow stroma. They are defined by their ability to both self-renew and differentiate into mesoderm-specific lineage cells including osteoblasts, adipocytes and chondrocytes [1, 2]. These two characteristics make hMSCs a valuable resource in the fields of cellular therapeutics and regenerative medicine [3, 4]. The potential clinical use of hMSC therapy has been examined in an increasing number of clinical conditions, including treating children with osteogenesis imperfecta [5–7] as well as bone repair of non-healed fractures and large bone defects [4, 8, 9].
Lineage-specific differentiation of hMSCs into osteoblasts (OBs) is dependent on a number of microenvironmental cues [1, 10]. In vitro OB differentiation of hMSCs is induced by a mixture of hormones (e.g. dexamethasone, calcitriol) and chemicals (e.g. organic phosphate donors such as β-glycerophosphate) and the expression of mature OB phenotype takes place through a series of developmental stages: cell expansion and proliferation, cell commitment to OB, and differentiation into pre-osteoblasts followed by maturation of osteoblasts which synthesize the bone matrix and promote mineralization [10, 11]. Phases of OB differentiation and establishment of the osteoblastic phenotype are controlled by a set of transcription factors.
A number of transcription factors (TFs) have been demonstrated to play important roles in OB differentiation and function. Runt domain-containing transcription factor (RUNX2) is the major TF in both osteoblast commitment and differentiation [10–12]. Homozygous deletion of this gene in mice resulted in a complete absence of osteoblasts and bone formation . Another TF, Osterix (OSX or SP7), specifically expressed by osteoblasts, is positively regulated by and acts downstream of RUNX2 . Activating transcription factor 4 (ATF4) plays an important role in mature osteoblasts, and it interacts with RUNX2 to regulate the expression of osteocalcin . Other TFs that have been shown to regulate osteoblast differentiation include: the AP1 family of proteins; LEF/TCF (via Wnt signalling); homeobox proteins MSX2, HOXA2 and DLX5; helix-loop-helix (bHLH) proteins HES, HEY, TWIST and HAND2; and CCAAT/enhancer-binding proteins (C/EBPs) . Although a number of TFs have been identified to be important in osteoblastic differentiation, this is a very small subset of all documented human TFs. Vaquerizas et al.  have generated a list of 1391 manually curated, sequence-specific DNA-binding human TFs.
Many reported human transcription factors are uncharacterized in terms of their biological functions . It is plausible that some of the uncharacterized TFs are important regulators of osteoblast differentiation. In this study, we employed genome-wide expression profiling to identify TFs which were differentially expressed between undifferentiated hMSCs and their differentiated osteoblastic cell progeny. By clustering these TFs using self-organizing maps (SOMs), and by literature analysis, we identified three TFs as novel candidates with possible regulatory functions in osteoblast differentiation. We further explored the role of one of these candidates, ZNF25. siZNF25 knockdown experiments showed regulatory effects on osteoblast differentiation. Microarray analysis of siZNF25 deficient osteoblastic cells, identified three highly up-regulated genes, LGR5, MMP1 and RANBP3L, and we propose these as possible targets of ZNF25. We also report that ZNF25 has a KRAB domain, a transcriptional repressor, which is conserved in tetrapod vertebrates.
As a model for primary hMSCs, we employed hMSC-TERT cells (subclone hMSC-TERT4). The source and generation of hMSC-TERT cells are described in . These exhibit a stable cellular and molecular phenotype comparable to that of primary hMSCs . hMSC-TERT cells were routinely cultured in standard media (SM) (MEM (Invitrogen) with 10 % v/v FBS (PAA, Pasching, Austria). The generation and characterization of hMSC-TERT cells were as described in detail in .
Ex vivo osteoblast differentiation was performed using osteoblast induction medium containing β-glycerophosphate (10 mM; Calbiochem-Merck), L-ascorbic acid-2-phosphate (50 μg/ml; Sigma-Aldrich, Brøndby, Denmark), dexamathasone (10nM; Sigma-Aldrich) and calcitriol (1,25 hydroxy-vitamin D3; 10nM) in standard medium (SM). Media were changed every 3 days until day 15.
Alkaline phosphatase activity measurements
Alkaline phosphatase (ALP) activity was quantified as previously described , using a 1 mg/ml solution of P-nitrophenylphosphate (Sigma-Aldrich, Brøndby, Denmark) in 50 mM NaHCO3 with 1 mM MgCl2, pH 9.6, at 37 °C for 20 min. Activity was stopped using 3 M NaOH and the absorbance of each reaction (max = 405 nm) was measured using a FLUOstar Omega plate reader (BMG Laboratories, Ramcon A/S, Birkerod, Denmark). ALP activity was normalized to cell number, as determined using a CellTiter-Blue Cell Viability assay, according to manufacturer’s instructions (Promega, Nacka, Sweden).
Cells undergoing osteogenic differentiation were stained at days 6, 10 and 15 for ALP and days 10 and 15 for alizarin red (AZR) as previously described . Elution of AZR staining was performed using 10 % cetylpyridium for 1 h at room temperature; 25–100 μl was then removed to a 96 well plate and read on a FLUOstar Omega plate reader at 595 nm emission wavelength.
Routine protocols  were used to stain for ZNF25 (Novus Biologics antibody H00219749-B01). Briefly, immunocyto-chemical staining was performed using DAKO PowerVision + HRP according to manufacturer’s instructions. The primary antibody was diluted in ChemMate Antibody diluent (S2022, Dako, Glostrup, Denmark) and processed on an automatic slide processor (Techmate500, Dako, Glostrup, Denmark). DAB was used as the chromogen and the slides were counterstained with haematoxylin. Analysis was carried out on an IX50 Olympus microscope using OlympusDP Software v3.1 (Olympus, Essex, UK) or a Leica DM4500 (Leica, Wetzlar, Germany) using the Surveyor Turboscan Mosaic acquisition imaging analysis system v5.04.01 (Objective Imaging Ltd, Cambridge, UK). To assess localization of the ZNF25 protein, cells undergoing OB induction were passaged and replated 2 days prior to fixation (4 % formalin) in osteoblast induction medium. This ensured that both the cytoplasm and nuclear localization could be easily visualised. Following fixation, cells were blocked and permeabilised (1 % FBS, 0.1 % Triton X-100 in PBS) before overnight incubation with ZNF25 antibody. Anti-rabbit alexa-fluor 488 (Invitrogen) was utilized as a secondary antibody and cells were counterstained with Phalloidin pre-conjugated with TRITC (5nM, Sigma) and Hoechst H33342 (0.1ug/ml, Sigma). Image acquisition was performed on a Perkin Elmer Operetta High Content Imaging System.
Matrix mineralisation assay
Deposition of hydroxyapatite was measured using the OsteoImage™ Bone Mineralization Assay (Lonza) according to manufacturer’s instructions. Briefly, cells were plated in 96 well plates at 20,000/cm2 and induced in osteoblast induction medium for 15 days with media changed every third day. Following fixation (4 % formalin for 10 min at RT), wells were washed in Lonza wash buffer before staining with OsteoImageTM staining reagent conjugated to 488 for 30 min at RT. Post-staining, wells were washed in wash buffer before being read on a FLUOstar Omega plate reader set at 488 nm emission wavelength.
In vivo heterotopic bone formation
hMSC-TERT (0.5 × 106) were suspended into single cells and combined with 40 mg hydroxy-apatite tricalcium phosphate as previously reported (HA/TCP, 0.5–1 mm granules, Biomatlante/Zimmer, Vigneux de Bretagne, France) [19–21]. Non-induced cells were incubated overnight in HA/TCP before implantation into the dorsolateral area of immune compromised mice (NOD.CB17-Prkdc scid/J) for 8 weeks. After retrieval, implants were fixed overnight in 4 % formalin, washed in PBS before decalcification in formic acid for 3–5 days. Following embedding in wax, four serial sections were cut at three depths with 100um between each group and sections from each group were stained with haematoxylin and eosin, or human specific-vimentin antibody (AbCam).
siRNA-based knock down experiments
LNA-modified Silencer® Select siRNAs targeting the desired genes (ZNF608, ZBTB38 and ZNF25) and non-targeted negative controls 1 and 2 were purchased from Ambion (Invitrogen). Validation of siRNA data was done using a second Silencer® Select siRNA for ZBTB38 and ZNF608, and one Mission siRNA (Sigma-Aldrich) for ZNF25. Reverse transfection of siRNA was performed using LipofectamineTM 2000 (Invitrogen) according to the manufacturer’s instructions. siRNA transfections were carried at as described in [3, 16].
Affymetrix microarray gene expression analysis
hMSC-TERT cells were cultured and induced to differentiate into osteoblasts as described . At 0, 3, 6, 9 and 12 days after induction, total RNA was extracted using TRIzol (Invitrogen) as previously reported . Five hundred ng of total RNA from each sample were used for biotin-labeled cRNA production using a linear amplification kit (Ambion). First- and second-strand cDNA syntheses were performed from 8 μg total RNA using the SuperScript Choice System (Life-Technologies, Carlsbad, CA, USA) according to the manufacturer’s instructions. Subsequent hybridization and scanning of the Affymetrix arrays were performed as described previously . The biotinylated targets were hybridized to HuGene 1.0ST v 1 Affymetrix oligonucleotide arrays. Expression measures were generated and normalized using the RMA procedure implemented in the Partek Genomics Suite version 6.12.0307. Values were then log2 transformed before further analysis. Affymetrix HuGene 2.0ST arrays were used for siZNF25 knock down and corresponding control samples. Partek Genomics Suite version 6.6 was used to analyse the resultant microarray data.
Illumina bead chip microarray
hMSC-TERT cells were cultured and induced to differentiate into osteoblasts as described . At days 0, 1, 7 and 13 after induction, total RNA was extracted from each of three independent cell cultures. At 90–100 % confluence, highly purified total cellular RNA was isolated using an RNeasy Kit (QIAGEN Nordic, West Sussex, UK) according to the manufacturer’s instructions. A total of 500 ng of total RNA from each sample was used for biotin-labeled cRNA production using a linear amplification kit (Ambion).
Hybridization, washing, Cy3-streptavidin staining and scanning were performed on the Illumina BeadStation 500 platform (Illumina) according to the manufacturer’s instruction. cRNA samples were hybridized onto Illumina HT12 V4 BeadChips. Analyses of gene expression data were carried out using the GenomeStudio software (v2011.1). Raw data were normalized using the quantile normalisation and then filtered for significant expression on the basis of negative control beads. A p-value of < 0.01 was used as a cut-off for detection of significance.
Differential gene expression analysis and significance testing was done using the ‘lumi’ BioConductor package . After being checked for quality, data was transformed using the ‘variance stabilizing transform’. Data was quantile normalized and probes that passed the detection p-value threshold (p < 0.01), for at least one time point, were selected for further analysis. Differentially expressed genes were identified by a 2-way ANOVA, and Benjamini-Hochberg multiple testing correction.
Extraction of curated transcription factors
Transcription factors were extracted from Illumina and Affymetrix datasets using the list of 1391 curated TFs detailed in . This was done using Partek Genomics Suite (v 6.12.0307). Some TFs on the list were updated to their current Ensembl Identifiers. A small number of TFs were not present on the Affymetrix Gene ST array, and were thus excluded from the analysis.
Self organising map-based cluster analysis
Self organising map (SOM) cluster analysis was performed using Partek Genomics Suite (v 6.12.0307). For the Illumina array dataset, the average gene expression of the three replicates at each time point was used as the gene expression measure. Gene expression data was shifted to a mean of zero before cluster generation to aid in the viewing of cluster profiles. The number of clusters in each map was varied between 25 and 81, in order to identify the optimum number of clusters for a particular dataset. The optimum number of clusters was achieved when each cluster displayed a single gene expression trend across the time course. For the Affymetrix array dataset, this was 64 clusters and for the Illumina array dataset it was 36.
RNA isolation and real-time quantitative PCR
Total RNA was isolated using TRIzol (Invitrogen) as previously reported (15). For real-time quantitative PCR, data were normalised to the geometric mean of four reference genes (β-Actin, B2M, HPRT, UBC1) and analysed using a comparative Ct method. Primer sequences were designed using the Primer-BLAST tool (http://www.ncbi.nlm.nih.gov/tools/primer-blast/). Primer sequences are listed below in Table 1.
Western blot analysis
Western blot analyses were carried out on control and differentiated OB cells as previously reported . The antibodies used were ZNF25 (Novus Biologics antibody H00219749-B01) and alpha-tubulin (Sigma-Aldrich) whereas goat anti Rabbit IgG-HRP (SantaCruz Biotechnology, Inc, Heidelberg, Germany) was used as the secondary antibody.
BLAST analysis and domain alignment
Evolutionary analysis of ZNF25 protein sequence was performed using the blastp program available at http://blast.ncbi.nlm.nih.gov/Blast.cgi. Domain alignments of ZNF25 orthologs were generated using the ‘Illustrator for Biological Sequences’ tool (version 1) .
hMSC-TERT differentiate into osteoblastic cells in vitro and form heterotopic bone in vivo
hMSC-TERT differentiate readily into osteoblastic cells, evidenced by enhanced expression of osteoblast marker genes (ALPL, BGLAP, COL1A1) (Fig. 1a), increased alkaline phosphatase activity and formation of in vitro mineralized matrix stained positive for Alizarin red during differentiation (Fig. 1b). hMSC-TERT cells are also able to form heterotopic bone when implanted subcutaneously, with hydroxyapatite tricalcium phosphate (HA/TCP), in immune deficient mice (Fig. 1c).
Transcription factors associated with in vitro osteoblast differentiation
Two microarray datasets were generated during in vitro osteoblast differentiation of hMSC-TERT: Illumina HT12-v4 arrays at four time points (days 0, 1, 7, 13) and Affymetrix HuGene 1.0 STv1 arrays at six time points (days 0, 3, 6, 9, 12). These datasets will be referred to as the ‘Illumina’ and ‘Affymetrix’ datasets. The Illumina time course dataset was filtered to extract expression patterns for 1391 Human TFs, as curated by Vaquerizas et al. . This produced a list of 1141 probes, mapping to 738 unique TFs. One hundred and forty nine TFs showed expression changes of 0.71 > FC > 1.40 between day 0 and day 13 post OB induction, with an adjusted p value of 0.20. This threshold was used because RUNX2 and ATF4, the major regulators of osteoblastogenesis, displayed a fold change of 1.48 (p adj = 0.141, p unadj = 0.048) and 1.48 (p adj = 0.18, p unadj = 0.065) in the Illumina dataset, respectively. For the Affymetrix dataset, 1380 TFs were extracted, using the same curated set from Vaquerizas et al. .
Transcription factors cluster according to temporal expression during in vitro osteoblast differentiation
To identify groups of genes that showed similar temporal expression patterns during in vitro osteoblastic differentiation, self-organizing maps (SOMs) were used (Fig. 2). For the Affymetrix TF dataset, six clusters showed distinct up or down regulation across the time-course (Fig. 2a). The up-regulated clusters i, ii and iii contained 17, 8 and 13 genes respectively whereas the down-regulated clusters iv, v and vi contained 16, 17 and 9 genes, respectively. Interestingly, another cluster showed a decrease in gene expression from day 0 to day 3, followed by an increase in gene expression to day 12. The TFs contained within all clusters are listed in Table 2.
We examined all the clusters containing upregulated genes, for the presence of TFs that have known roles in osteoblast differentiation. Cluster i contained 17 TFs, of which seven have been previously documented to be involved in osteoblastogenesis in mouse and rat models. These include AHR, DDIT3, EGR2, RORA, SALL4, ZEB2 and ZNF385A  [27–30]. Cluster ii contained RUNX2, along with TFs EPAS1, HES1,NR4A3, PRDM1, STAT4 and ZBTB16; these are known to either be involved in osteoblastic differentiation or bone homeostasis, as direct regulators or via an interaction with a regulator [31–36]. Cluster iii contained 13 TFs, all of which have previously been documented to be involved in hMSC differentiation into either osteoblasts, adipocytes or chondrocytes (e.g. BCL6, EBF1, FOXO1, KLF15, KLF5, MKX, NFIA, NPAS2, OSR2, SIX1, STAT2, THRB and TSC22D3)  [37–44].
We further examined the upregulated clusters for TFs that are currently not associated with differentiation and development. This revealed a total of 11 TFs of interest; ten of which were in cluster i. The majority of these are zinc finger proteins (ZNF25, ZNF117, ZNF235, ZNF345, ZNF354A, ZNF 449, ZNF493, ZNF566) and two are zinc finger and BTB domain-containing proteins, ZBTB1 and ZBTB38. The final TF was in cluster ii, which was zinc finger protein ZNF608.
The Illumina TF dataset was also subjected to the same process of SOM clustering as described for the Affymetrix dataset. In this case, this produced 36 clusters of TF expression profiles. Each cluster contained between 3 and 44 genes. Five clusters showed up-regulation of TFs across the time-course (labeled i-v in Fig. 2b), while three clusters showed a distinct down-regulation (labeled vi, vii and viii in Fig. 2b). The TF content and gene expression information of each labeled cluster is detailed in Table 3. The total of 77 TFs in clusters i to v were examined to identify which TFs have previously been implicated in MSC differentiation, bone formation or related mesodermal differentiation processes such as adipogenesis. Fifty nine of the TFs were found to be differentiation-associated, whereas 16 TFs were identified as potentially novel osteoblast-differentiation associated TF candidates. These included ZNF181, ZNF697, ZNF295, ZNF22, ZNF532, ZNF302, ZNF217, ZNF721, ZNF25, ZNF608, ZNF419, ZNF558 and ZNF627, along with two zinc finger- and BTB-domain containing proteins ZBTB38 and ZBTB40 and zz-type zinc finger-containing protein ZZZ3.
Identification of three novel TFs associated with in vitro osteoblast differentiation
We employed a number of criteria to select TFs for further analysis. As shown in Fig. 3, the TFs had to be present in up-regulated SOM clusters in both Affymetrix and Illumina analyses, the TFs had to be previously unreported in association with hMSC differentiation, bone formation or related processes and, finally, the TFs had to exhibit a statistically significant increase in expression during in vitro OB differentiation. Three TFs satisfied these criteria, namely zinc finger protein 25 (ZNF25), zinc finger- and BTB-domain containing protein 38 (ZBTB38) and zinc finger protein 608 (ZNF608). The fold change increase in gene expression and p-values showed by these during differentiation for day 13 versus day 0 were ZNF25 (1.55 FC, p = 0.067), ZBTB38 (1.66 FC, p = 0.025) and ZNF608 (1.41 FC, p = 0.0013) in the Illumina dataset (Fig. 2c). We further validated gene expression profiles of ZNF25, ZNF608 and ZBTB38, employing quantitative RT-PCR in independent biological experiments (Fig. 4a–c). Similar to the microarray data, all three TFs displayed a temporal increase in gene expression with maximal expression during the late phase (days 10–15) of in vitro osteoblast differentiation (Fig. 4a–c). There was also a statistically significant difference in qPCR expression measurements between day 0 and day 15 for ZNF25 and ZNF608. However, ZBTB38 did not display a significant difference. (Student’s t-test, ZNF25 p = 0.0027, ZNF608 p = 0.0089 and ZBTB38 p = 0.3353).
siRNA knock-down of ZNF25 affects osteoblast differentiation
The temporal gene expression pattern of the candidate TFs suggested a role in osteoblast differentiation of hMSC. To test this hypothesis, we examined the effects of siRNA-mediated knockdown of each of the TFs on ALP activity, as a marker of the osteoblastic phenotype. A statistically significant decrease in ALP activity was seen on knockdown of ZNF25 (p < 0.005, Fig. 4d), relative to that of the scrambled siRNA control. By contrast, siRNA-mediated knockdown of ZNF608 and ZBTB38 did not show a reduction on ALP activity. On the other hand, knockdown of ZNF608 actually showed a statistically significant increase (p = 0.00002) in ALP activity. For the purposes of this study we further focused our analyses only on ZNF25.
ZNF25 protein expression increases during osteoblast differentiation
We investigated the temporal expression of the ZNF25 protein and its localization in cells and in human bone tissue biopsies. Similar to ZNF25 gene expression, the production of the ZNF25 protein was found to increase during in vitro osteoblast differentiation, at days 6, 10 and 15 (Fig. 5a). In keeping with its role as a transcription factor, in vitro staining of hMSC-TERT revealed it to have nuclear and perinuclear localization (Fig. 5b). In human femoral neck bone biopsies, immunostaining localized the ZNF25 protein to active osteoblastic surfaces as well as osteocytes (Fig. 5c).
ZNF25 siRNA knockdown causes increase in expression of genes relevant to osteoblast differentiation
ZNF25 contains a KRAB domain, and is therefore likely to act as a transcriptional repressor . To gain insight into the possible targets of ZNF25 and confirm its repressor activity, we used microarrays to analyse the gene expression of control and ZNF25 knockdown cells (siZNF25) at days 0 and day 14, post-osteoblast differentiation (Fig. 6). At day 0, 50 genes were identified as differentially expressed between siZNF25 and control samples (3 upregulated and 47 downregulated using two - fold change and FDR <0.05 as threshold). At day 14, by contrast, 520 genes were identified as differentially expressed between siZNF25 and control samples (347 upregulated, 173 downregulated and using two - fold change and FDR < 0.05 as threshold). Since ZNF25 contains a KRAB domain and is likely to be a transcriptional repressor, any genes that show marked upregulation could be of functional significance. At day 0, there were no genes that showed dramatic upregulation in siZNF25 cells. However at day 14 there were four genes that showed 18-fold to 26-fold upregulation. The most significantly upregulated gene in differentiated siZNF25 cells relative to control was matrix metallopeptidase 1 (MMP1, FC = 23.00, pval = 6.09 × 10−6). The next most upregulated genes were leucine-rich repeat containing G protein-coupled receptor 5 (LGR5, FC = 18.59, pval = 5.77 × 10−7) and RAN binding protein 3-like (RANBP3L, FC = 18.08, pval = 1.81 × 10−9). We also observed a very high upregulation in unannotated transcript cluster, 17118303 (FC = 26.05, pval = 7.49 × 10−6). On further investigation it was found that this transcript cluster maps to chromosomal location: chr7:94058513–94060553. This chromosomal location corresponds to exon 52 of the COL1A2 gene, however no other probes for this gene were upregulated to this level.
DAVID functional enrichment analysis [46, 47] of the 520 genes differentially expressed at day 14 post-OB induction showed enrichment for: ‘extracellular matrix organisation’ (p value = 2.9 × 10−11, FDR = 4.6 × 10–8), ‘ossification’ (p value = 2.08 × 10−5, FDR = 0.035), ‘bone development’ (p value = 3.9 × 10−5, FDR = 0.06), ‘skeletal system development’ (p value = 2.69 × 10−4, FDR = 0.459) and ‘regulation of ossification’ (p value = 0.0049, but with a higher FDR of 8.08). The genes involved in these enrichment categories are all upregulated (Fig. 6). Analyses of the same gene sets by ReviGO  and GOrilla  yielded functionally similar results (data not shown). Background used for all enrichment analyses was the Affymetrix Human Gene 2.0 ST array gene set.
ZNF25 is conserved but found only in tetrapod vertebrates
The evolutionary conservation of ZNF25 was then investigated. ZNF25 was highly conserved amongst mammals, with the top 250 top-ranked proteins from BLAST analysis being from mammalian species. The mouse protein ZFP9, for example, showed 79 % sequence identity with an E value = 0.0 and appeared as a true ortholog of ZNF25 via a reciprocal BLAST with all human proteins. Use of the GABLAM tool  also identified ZNF25 mammalian homologs in seven species. These observations are consistent with results in the NCBI homologene database, that details ZNF25 orthologs for mammalian species, including Pan troglodytes, Macaca mulatta, Canis lupus, Bos taurus, Mus musculus and Rattus norvegicus. For other species, we observed full length matches to the chicken protein ZFP302 (44 % sequence identity, E value = 8 × 10-126) and Xenopus tropicalus zinc finger protein 180 (44 % sequence identity, E value = 7 × 10−137). However these are unlikely to be true orthologs as they did not identify ZNF25 via reciprocal BLAST. Whilst a single KRAB domain was present in each protein, different numbers of C2H2 domains were present, with 12 in human but 11 in chicken and Xenopus. In zebrafish, there was partial homology to the ZNF25 C2H2 domain found in gastrula zinc finger protein XICGF57.1-like (49 % sequence identity, E value = 6 × 10−126). In the fruit fly, there was also partial homology to the ZNF25 C2H2 domain in the crooked legs protein, isoform B (44 % sequence identity, E value = 1 × 10−86). The KRAB domain was not present in these two proteins. These results indicate that the KRAB domain of ZNF25 protein is conserved in tetrapod vertebrates. Figure 7 shows a domain alignment of ZNF25 and homologs identified by the BLAST analysis.
This study has shown that a novel transcription factor, ZNF25, has a role in the differentiation of hMSCs to osteoblastic cells. We observed that expression of the transcription factor ZNF25 increased steadily during OB differentiation of hMSCs, and its deficiency significantly decreased alkaline phosphatase levels in differentiating osteoblastic cells. The ZNF25 protein is present in the nuclei of mature osteoblastic cells and osteocytes in human bone. These results suggest that ZNF25 plays a role in in osteoblast differentiation of hMSCs.
ZNF25 belongs to the Krueppel C2H2-type zinc-finger protein family and contains 12 C2H2-type zinc fingers and one KRAB domain . The Krueppel-associated box (KRAB) is a domain of around 75 amino acids that is found in the N-terminal part of about one third of eukaryotic Krueppel-type C2H2 zinc finger proteins (KRAB-ZFPs). These KRAB-ZFPs make up the largest family of zinc finger transcription factors in mammals and are only found in tetrapod vertebrates . The KRAB-ZFP family has expanded greatly to include hundreds of members in mammals . The KRAB domain acts as a transcriptional repressor by binding to corepressor proteins, whereas the C2H2 zinc-finger domains bind DNA. The function of proteins in the KRAB family include repression of RNA polymerase II and III promoters and binding and splicing of RNA .
KRAB-zinc finger proteins are known to play important roles during cell differentiation and development. Individual members of one subfamily of KRAB zinc finger genes (ZNF91) are restricted to specific hematopoietic cell lineages and may play a role in lineage commitment, possibly silencing transcription from nonlineage-expressed genes . One of the other KRAB zinc finger proteins is involved in osteoblast differentiation. AJ18 (ZFP354C) was identified by Jhoen et al. as a repressor of osteoblast differentiation in rat embryonic tibia and calvariae . Overexpression of AJ18 suppressed RUNX2 activity and repressed the markers of osteoblast differentiation ALP and, BGLAP. Our BLAST analysis confirmed the KRAB domain is only found in tetrapod vertebrates. Previous studies have reported that KRAB-ZFPs have expanded to a large degree in mammals [52, 55].
The temporal expression profile of ZNF25 clustered with profiles of other transcription factors known to be involved in osteogenesis. These transcription factors include SMAD5, FOS, and SNAI2. SMAD5 functions synergistically with SMAD1 and RUNX2 to induce osteoblast-specific gene expression in C2C12 cells . FOS proteins heterodimerize with JUN proteins to form the AP1 transcription factor complex, which is an important regulator of bone formation . SNAI2 binds to RUNX2 promoters in vivo and acts as a positive transcriptional regulator in human osteoblasts . Whilst the profile of ZNF25 expression does not allow us to understand its exact timing in any transcription factor cascade, its co-expression with the transcription factors, above, emphasizes its association with ostoegenesis.
To discover putative genes that are targets of ZNF25, and thus suggest possible molecular mechanisms by which ZNF25 affects osteoblast differentiation, we identified the genes that are differentially regulated following siRNA-mediated knock down. Given that ZNF25 has a KRAB domain, and is likely to be a transcriptional repressor, we anticipated the upregulation of a number of osteogenic genes. MMP1, RANBP3L and LGR5 showed striking upregulation and are functionally related to osteoblast differentiation.
MMP1 was initially described as a collagenase to degrade fibrillary collagen (type I, II and III)  and other extracellular matrix proteins: fibronectin, aggrecan, laminin, perlecan, and vitronectin . MMP1 has also non-extracellular matrix substrates (pro-TNFa, IGF, SDF1a and MCP 1–4). Degradation of these substrates, such as COL1A1, by increased MMP1 may lead to impaired extracelluar matrix levels and/or organization. Since ECM abundance, structure and/or content may be important triggers for mineralization, this may explain the apparent impairment of in vitro formation of mineralized matrix. RANBP3L has recently  been reported to be a nuclear export factor for Smad1/5/8, which are effectors of canonical BMP signaling. Canonical BMP signalling is tightly regulated through reversible phosphorylation and nucleocytoplasmic shuttling of Smad1/5 and 8. Interestingly, Chen et al.  showed that overexpression of RANBP3L blocks BMP-induced osteogenesis of mouse BM-MSCs, while depletion of RANBP3L expression enhances BMP-dependent MSC differentiation activity and transcriptional responses. Further to this, the overexpression of RANBP3L in BM-MSCs was shown to result in reduced ALP activity and alizarin red staining, a phenotype which is consistent to what we observed on knockdown of ZNF25 and its resulting increase in RANBP3L expression. However, Chen et al.  reported that RANBP3L overexpression compromised the BMP-induced expression of the preosteoblast marker RUNX2, whereas we did not detect any changes in expression of RUNX2. Thus it is likely that RANBP3L acts earlier in the differentiation process than ZNF25. LGR5 is an orphan G-protein coupled receptor and is a direct target of canonical Wnt signaling. LGR5 potentiates the canonical Wnt signaling pathway by binding to R-spondins . LGR5 also a mouse marker of stem cells in small intestine and colon . Its relationship to osteoblast differentiation is currently unknown.
In this study we have shown that the uncharacterized transcription factor, ZNF25, has a role in the differentiation of hMSCs to osteoblasts. ZNF25 appears to act as a transcriptional repressor via a KRAB domain and we identified three potential targets of ZNF25, matrix metallopeptidase 1, leucine-rich repeat containing G protein-coupled receptor 5 and RAN-binding protein 3-like. Future studies will determine the role of this transcription factor in the in vivo bone formation.
Basic local alignment search tool
Database for annotation, visualization and integrated discovery
False discovery rate
Hydroxyapatite tricalcium phosphate
Human mesenchymal stem cell
Telomerised human mesenchymal stem cell line
Runt domain-containing transcription factor
Single nucleotide polymorphism
Self organising map
Zinc finger- and BTB-domain containing protein 38
Zinc finger protein 25
Zinc finger protein 608
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MK acknowledges funding from Odense University Hospital, Denmark and King Abdulah City for Science and Technology (KACST) (10-BIO1308-02), Kingdom of Saudi Arabia. NAT acknowledges funding from the University of New South Wales (UNSW) IPRS scheme. MRW and MK acknowledge funding from the UNSW Visiting Fellow Scheme. MRW acknowledges funding from the Australian Government EIF Super Science Scheme and the New South Wales State Government Science Leveraging Fund scheme. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
Availability of data and materials
The datasets generated during and analysed during the current study are available in the NCBI GEO repository. Links to the GEO accession numbers are:
NAT, MRW, MK conceived and designed the experiments, performed data analysis and interpretation and wrote the manuscript. LH performed the experiments. All authors reviewed and approved the final version of the manuscript. MK, MRW, NAT accept responsibility for the integrity of the data analysis.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
This study used an hMSC-TERT immortalized cell line, as described previously . Use of the cells in this study did not require approval from an ethics committee.