miR-2909-mediated regulation of KLF4: a novel molecular mechanism for differentiating between B-cell and T-cell pediatric acute lymphoblastic leukemias
© Malik et al.; licensee BioMed Central Ltd. 2014
Received: 8 October 2013
Accepted: 10 July 2014
Published: 18 July 2014
microRNAs (miRNAs) play both oncogenic and oncostatic roles in leukemia. However, the molecular details underlying miRNA-mediated regulation of their target genes in pediatric B- and T-cell acute lymphoblastic leukemias (ALLs) remain unclear. The present study investigated the relationship between miR-2909 and Kruppel-like factor 4 (KLF4), and its functional relevance to cell cycle progression and immortalization in patients with pediatric ALL.
Elevated levels of miR-2909 targeted the tumor suppressor gene KLF4 in pediatric B-cell, but not pediatric T-cell ALL, as detected by pMIR-GFP reporter assay. Expression levels of genes including apoptosis-antagonizing transcription factor (AATF), MYC, B-cell lymphoma (BCL3), P21 CIP , CCND1 and SP1 in B- and T-cells from patients with pediatric ALL were compared with control levels using real-time quantitative reverse transcription polymerase chain reaction, western blotting, and reporter assays.
We identified two novel mutations in KLF4 in pediatric T-ALL. A mutation in the 3′ untranslated region of the KLF4 gene resulted in loss of miR-2909-mediated regulation, while mutation in its first or third zinc-finger motif (Zf1/Zf3) rendered KLF4 transcriptionally inactive. This mutation was a frameshift mutation resulting in alteration of the Zf3 motif sequence in the mutant KLF4 protein in all pediatric T-ALL samples. Homology models, docking studies and promoter activity of its target gene P21 CIP confirmed the lack of function of the mutant KLF4 protein in pediatric T-ALL. Moreover, the inability of miR-2909 to regulate KLF4 and its downstream genes controlling cell cycle and apoptosis in T-cell but not in B-ALL was verified by antagomiR-2909 transfection. Comprehensive sequence analysis of KLF4 identified the predominance of isoform 1 (~55 kDa) in most patients with pediatric B-ALL, while those with pediatric T-ALL expressed isoform 2 (~51 kDa).
This study identified a novel miR-2909-KLF4 molecular axis able to differentiate between the pathogeneses of pediatric B- and T-cell ALLs, and which may represent a new diagnostic/prognostic marker.
KeywordsAcute lymphoblastic leukemia miR-2909 Kruppel-like factor 4 Homology modeling Cell cycle
Acute lymphoblastic leukemia (ALL) is widely recognized as the most prevalent pediatric leukemia ; however, the genomic mechanisms responsible for the uncontrolled cell proliferation coupled with cell immortalization remain unknown . In this context, the genes for apoptosis-antagonizing transcription factor (AATF) and Kruppel like factor 4 (KLF4) have assumed importance. AATF provides a critical link between cell cycle progression, check-point control, and apoptosis , and also encodes the novel microRNA (miRNA) miR-2909, which regulates genes involved in inflammation, cell cycle, and immune response [4–6]. KLF4, a member of the SP1/KLF transcription factor family, is characterized by three highly conserved C2H2-type zinc-finger motifs at its carboxyl terminus, which are crucial for its interaction with its target DNA . The KLF4 gene acts as both an oncogene and a tumor suppressor, depending on its genetic and cellular contexts . The tumor-suppressive role of KLF4 and its involvement in regulating apoptosis, proliferation, and differentiation in B-cell malignancies suggest that KLF4 may play a critical role in leukemogenesis . Furthermore, KLF4 mRNA has been shown to be targeted by miR-130a and 135b in M1 acute myeloid leukemic blasts, and silencing of KLF4 arrested the maturation of blood cells at an early progenitor stage .
The discovery of miRNAs has opened a new epigenomic dimension in terms of the understanding of oncogenesis in general and leukemogenesis in particular . Alterations in miRNA expression patterns and their respective targets have been documented in various tumors  including different types of leukemias such as chronic lymphocytic leukemia , acute myeloid leukemia  and ALL , thus suggesting a possible correlation between miRNA expression status and the development of hematological malignancies.
The present study aimed to identify the expression status of AATF-encoded miR-2909 in B- and T-cells from patients with pediatric ALL and explore the possible relationship between miR-2909 and KLF4 in these cells. We also investigated the functional importance of this relationship in the regulation of genes involved in cell cycle progression (BCL3, CCND1, MYC) and apoptosis (AATF). To the best of our knowledge, the results of this study provide the first evidence for miR-2909-dependent regulatory pathway as the possible underlying mechanism responsible for the initiation of ALL in humans.
miR-2909 targets KLF4
Sequence analysis of KLF4
We further explored if T-ALL patients expressed isoform 3 of KLF-4. Sequencing failed to identify any deletion of the first 50 amino acids in any of the T-ALL samples in the present study, confirming the absence of isoform 3 in these blast cells (Figure 3C). Interestingly, most T-ALL samples showed insertion/deletion of nucleotides in the region corresponding to the third zinc-finger (Zf3) motif of KLF4, while deletion of nucleotides in the first zinc-finger (Zf1) motif was identified in some T-ALL samples (Figure 3D, Additional file 1: Figure S1). These genetic aberrations changed the entire reading frame, altering the sequence of the KLF4 zinc-finger motif and potentially destroying its DNA-binding affinity (Additional file 1: Figure S1G). Modeling/docking studies were performed using mutant KLF4 lacking the Zf3 motif but with intact Zf1 and Zf2 motifs derived from pediatric T-ALL samples (Figure 3E). In addition, we also sequenced the KLF4 coding region corresponding to the three zinc-finger motifs in B-ALL samples to detect the presence of any genetic aberration(s) in this region in pediatric B-ALL. Sequence analysis revealed no genetic aberrations in any of the three zinc-fingers regions of KLF4 in samples from pediatric patients with B-ALL, suggesting that the conformation of KLF4 was unaffected in these patients (Additional file 2: Figure S2).
Molecular modeling and docking studies of KLF4 protein
Loss of transcriptional activity of mutant KLF4 protein
To confirm the bioinformatics result suggesting that mutant KLF4 was unable to interact with its 10-bp target sequence in the P21 CIP gene promoter in pediatric T-ALL, we transfected a β-galactosidase (β-gal) construct under the control of the P21 CIP promoter and harboring a KLF4 site into control and T-lymphoblasts and subsequently incubated for 72 h at 37°C in humidified 5% CO2 atmosphere. Transfected control cells displayed increased transcriptional activity of the reporter construct containing the P21 CIP promoter compared with T-lymphoblasts (Figure 4I), suggesting that mutant KLF4 protein in T-ALL loses its ability to bind to the KLF4-binding site present in the P21 CIP promoter, and is thus unable to induce P21 CIP . In contrast, wild-type KLF4 protein bound to its putative site in the P21 CIP promoter and induced its expression in control T-cells.
Role of SP1 in KLF4-mediated gene expression
miR-2909 regulates cell cycle and apoptosis in B- but not T-lymphoblasts from patients with pediatric ALL
Overexpression of miR-2909 in HeLa cells induces the expression of oncogenes
Mounting evidence has established KLF4 as a transcriptional activator, repressor, tumor suppressor and an oncogene, depending on its genetic context . However, the exact molecular mechanisms whereby KLF4 fulfills these roles remain unknown. Moreover, the pathway regulating KLF4 expression has not been well studied. The present study therefore aimed to investigate the miR-2909-mediated regulation of KLF4 and its downstream functions, especially cell cycle regulation and apoptosis, in both patients with B- and T-ALL. To the best of our knowledge, the results provide the first evidence for two novel mutations in the KLF4 gene in T-ALL: a mutation in the 3′UTR resulted in loss of miR-2909-mediated regulation, and mutation in the Zf1/Zf3 motif rendered KLF4 transcriptionally inactive. In contrast, KLF4 is regulated post-transcriptionally by miR-2909, and suppression of its expression resulted in loss of KLF4 tumor suppressor activity in pediatric B-ALL.
Previous studies involving a variety of epithelial tumors have shown that the expression of the zinc-finger transcription factor KLF4 is silenced by promoter hypermethylation . KLF4 is also known to be inactivated by methylation in adult T-cell leukemia . Recent studies have revealed direct correlations between altered miRNA levels and progression of hematological malignancies, such as the effects of downregulation of miR-15a and miR-16-1 in chronic lymphocytic leukemia  and amplification of miR-155 in B-cell lymphoma, Hodgkin’s lymphoma , Burkitt’s lymphoma  and in human breast cancer cell lines . However, the role of miRNAs in the pathogeneses of pediatric B- and T-cell ALL remains unknown. Earlier studies from our laboratory reported that the AATF gene encodes miR-2909, the functional importance of which remains unexplored in terms of the pathogeneses of B- and T-cell ALLs. We therefore investigated the expression of miR-2909 and its regulation of its target gene KLF4. miR-2909 levels were significantly elevated in both B- and T-ALL compared with corresponding age-matched control subjects. Moreover, we found a reciprocal relationship between miR-2909 and KLF4 expression in B-ALL, but not in T-ALL, which displayed significantly higher levels of KLF4 expression despite elevated levels of miR-2909. The observed low levels of KLF4 in B-ALL compared with healthy subjects were in accordance with a previous report .
We subsequently explored the possibility that patients with T-ALL may harbor mutations in the KLF4 3′UTR, which includes the miR-2909 binding site. Sequence analysis of the 3′UTR revealed altered nucleotides in the ‘seed region’, which is important for target specificity, in T-ALL but not in B-ALL patients. We further demonstrated that miR-2909 targeted the KLF4 3′UTR isolated from B-ALL patients, resulting in repression of KLF4 protein, but not that isolated from T-ALL patients with the mutated miR-2909 binding site, leading to increased levels of KLF4 protein. Using an miRNASelect pMIR-GFP reporter assay, we confirmed that miR-2909 targeted KLF4 in B-ALL but not in T-ALL by constructing plasmids containing the 3′UTR and the miR-2909 target site from the B-cell (pGFP-KLF4-3′UTR-B) and T-cell lineages (pGFP-KLF4-3′UTR-T). Transfection of the pGFP-KLF4-3′UTR-B plasmid into HEK 293 cells resulted in a 52.07% reduction in GFP expression, whereas cells expressing pGFP-KLF4-3′UTR-T showed no noticeable difference compared with cells transfected with pGFP plasmid without the 3′UTR insert. These results clearly revealed the ability of miR-2909 to repress KLF4 expression in pediatric ALL B-cell, but not T-cell lineages. Our results thus highlight the molecular differences in miR-2909-mediated differential regulation of KLF4 between B- and T-ALL. Importantly, our results identifying KLF4 as a target of miR-2909 in B-ALL are similar to published reports of miRNA-145-mediated repression of KLF4 in human embryonic stem cells  and miR-10b regulation of KLF4 in human esophageal cancer cell lines . However, these results in pediatric T-ALL provide the first functional demonstration of loss of repression of any target gene as a result of a mutated seed sequence for any miRNA in any disease.
We also explored why elevated KLF4 levels failed to control excessive proliferation in T-ALL patients by amplifying the full-length KLF4 sequences from B- and T-ALL samples. Most patients with B-ALL expressed KLF4 isoform 1, while T-ALL patients expressed isoform 2. However, the precise contributions of each isoform to the overall functions of KLF4 are not well understood and it will be interesting to validate these findings in a larger cohort to improve our understanding of its implications for the pathogeneses of ALL. In addition to identifying the isoforms present in B- and T-ALL, we also discovered nucleotide insertions or deletions in the Zf1 or Zf3 motif in pediatric T-ALL samples, resulting in frameshift mutations and complete alteration of the zinc-finger motif sequence, which could possibly destroy its DNA-binding affinity.
The crystal structure of the zinc-finger domain of KLF4 bound to target DNA was recently reported , and we exploited this structural information to construct homology models and perform docking studies of wild-type and mutant KLF4 with the 10-bp KLF4 target DNA sequence (5′-cgggcggggc-3′). The modeled structure of the Zf3 motif in the mutant KLF4 revealed the replacement of three key residues (C462V, C465M and H482F) involved in coordination with zinc. Moreover, the docking results demonstrated that mutant KLF4 was unable to interact with its 10-bp target sequence in the p21 CIP gene promoter, while wild-type KLF4 displayed cation-π and hydrogen-bonding interactions with its target sequence in controls. These results clearly demonstrate the importance of the Zf3 motif in KLF4-mediated functional regulation of its target gene. These findings are consistent with a previous study demonstrating that KLF4-mediated macrophage differentiation was primarily controlled by the two C-terminal Zf2 and Zf3 motifs, while Zf1 imparted little specificity . More importantly, we provided experimental proof to support the docking studies, showing that mutant KLF4 in T-lymphoblasts was unable to induce p21 CIP promoter activity, while KLF4 in control T-cells increased p21 CIP promoter reporter activity. A similar phenomenon was reported in colorectal cancer cell lines, where KLF4 mutations resulted in reduced p21 CIP promoter activity .
KLF4 acts as cell cycle regulator and functions as a tumor suppressor through its ability to induce p21CIP and suppress SP1 expression . Based on these findings, we studied the expression levels of genes involved in this process in ALL patients. We observed significant reductions in p21 CIP and increases in SP1 in B-ALL as a result of suppressed KLF4 expression. In contrast, elevated levels of mutant KLF4 failed to induce p21 CIP or inhibit SP1 expression in T-ALL, leading to low levels of p21 CIP and high levels of SP1, respectively. Moreover, the increased levels of SP1 were associated with increased transcriptional activity of a reporter construct containing an SP1 response element in both B-and T-ALL subtypes. Earlier work from our laboratory showed that SP1 upregulated AATF and MYC gene in Jurkat cells . Additionally, bioinformatics analysis revealed the presence of an SP1 response element in the promoter regions of AATF, MYC and BCL3 (data not shown). Consistent with these results, we also confirmed that upregulated SP1 levels resulted in increased BCL3, AATF and MYC expression in both B- and T-ALL subtypes. Our results therefore suggest that KLF4-mediated regulation of these genes most likely occurs through SP1 in both B- and T-ALL. The current study also assessed the key role of miR-2909 in the regulation of the above-mentioned genes. Results in B-lymphoblasts transfected with antagomiR-2909 confirmed that miR-2909 regulates these genes through KLF4. Transfection of pediatric B-lymphoblasts with antagomiR-2909 for 48 h resulted in significant upregulation of KLF4 expression. Furthermore, antagomiR-2909-transfected B-lymphoblasts revealed significant repression of the AATF, MYC and BCL3 genes. In contrast, antagomiR-2909-transfection had no such effects in pediatric T-lymphoblasts, as a result of failure of miR-2909 to bind to the mutated 3′UTR of KLF4 and mutated KLF4 protein. We subsequently tested the functional relevance of increased KLF4 in antagomiR-2909-transfected B- and T-lymphoblasts. B-lymphoblasts showed cell cycle arrest at G1/S phase, most likely through increased expression of p21 CIP , and increased apoptosis, possibly resulting from AATF suppression. However, no such changes were seen in antagomiR-2909-transfected pediatric T-lymphoblasts, despite increased levels of KLF4, which was rendered transcriptionally inactive as a result of the altered Zf3 motif, which lacked DNA-binding activity. In addition, antagomiR-2909-transfected B-lymphoblasts also exhibited decreased mRNA expression of MYC and BCL3 mRNA expression levels, which may reduce cell proliferation. These results were similar to other reported studies showing increased expression of p21 CIP and decreased expression of MYC and cyclin D2 in pro/pre-B cells expressing KLF4. Furthermore, miR-2909 overexpression and its ability to target the tumor suppressor KLF4 suggest that it displays oncogenic properties in B-ALL. To prove this, we overexpressed miR-2909 in HeLa cells to silence KLF4 expression. This resulted in significantly increased CCND1 and MYC and decreased p21CIP protein levels. These results are consistent with previous findings, which showed that KLF4- silencing in HeLa cells promoted cell growth and tumor formation .
Collectively, our experimental results suggest the existence of a molecular pathway as depicted in Figure 8G, which summarizes the differential nature of the miR-2909-KLF4 axis in B-ALL and T-ALL. The proposed pathway explains how high mutant KLF4 protein expression in T-ALL subjects is unable to induce p21 CIP , which plays a major role in inhibiting CCND1 expression. Mutant KLF4 protein also failed to repress SP1 expression, a gene known to be downregulated by KLF4, in parallel with upregulation of the oncogenes MYC, BCL3 and the anti-apoptotic AATF, potentially leading to unbridled T-cell transformation. A similar phenomenon is proposed in B-ALL subjects, wherein downregulation of KLF4 protein by miR-2909 overexpression results in B-cell transformation. Significantly, our studies revealed two breakpoints in the miR-2909-KLF4 axis caused by mutation in the 3′UTR-KLF4 and the altered Zf3 motif sequence, leading to loss of miR-2909 binding to the KLF4 3′UTR and loss of KLF4 binding to DNA sequences in target genes in T-cell ALL subjects. Moreover, structural modeling of the zinc-finger motif of KLF4 uncovered the precise molecular basis of loss of DNA binding in T-ALL, associated with alterations of three key amino acid residues involved in zinc coordination. Overall, our findings suggest that KLF4 function is compromised in T-cells derived from patients with pediatric T-ALL because of alteration of the Zf3 motif sequence as a result of a frameshift mutation. Furthermore, its regulation by miR-2909 is impaired because of a mutation in the miR-2909 target sequence present in the 3′UTR of the KLF4 mRNA. In B-ALL subjects, KLF4 function is compromised because of miR-2909-dependent downregulation. KLF4 is therefore unable to act as a tumor suppressor gene in either pediatric B-ALL or T-ALL. These results raise the possibility of the existence of similar KLF4 mutations in other tissues. However it was not possible to investigate the presence of such mutations in other tissues from the study patients because of ethical considerations.
The present study discovered that elevated levels of the novel miR-2909 target the tumor suppressor KLF4, which regulates the cell cycle and apoptosis in pediatric ALL. miR-2909-mediated downregulation resulted in loss of KLF4 activity in B-ALL. In contrast, miR-2909 failed to regulate KLF4 expression in T-ALL because of mutations in the KLF4 3′UTR, which includes the miR-2909 binding site. The molecular defect responsible for loss of KLF4 function in T-ALL despite its elevated level, lies within the Zf3 motif, which is altered as a result of a frameshift mutation. Homology modeling/docking studies and p21 CIP promoter activity confirmed the lack of functional activity of mutant KLF4. Comprehensive sequence analysis of KLF4 identified the predominance of isoform 1 in most patients with pediatric B-ALL, and of isoform 2 in patients with T-ALL. These results demonstrate the existence of a novel miR-2909-KLF4 molecular axis able to differentiate between B- and T-ALL pathogeneses, and which may provide a new diagnostic/prognostic marker to evaluate the pathogenesis of ALL in pediatric subjects. Our results also suggest that screening for these two mutations could be developed as a diagnostic strategy to differentiate between these two ALL subtypes. Overall, this study provides the basis for further research that could lead to a novel therapeutic approach for patients with B-and T-cell ALL.
Materials and methods
The reagents were procured as follows: MiniMACS™ Starting Kit (Miltenyi Biotech, Auburn, CA); miRNeasy mini kit, miScript Reverse transcription kit, miScript SYBR Green kit, Universal primer for amplifying miR-2909, Pfu polymerase (Fermentas, Vilnius, Lithuania); Qiaquick PCR purification kit (Qiagen, Valencia, CA); pBlue TOPO reporter vector, Lipofectamine 2000 and β Gal Assay Kit (Invitrogen,Carlsbad, USA); anti-KLF4 (Abcam), anti-p21CIP, anti-SP1, anti-MYC, anti-CCND1, anti-β actin; Annexin V-FITC apoptosis kit (Sigma-Aldrich, St.Louis, MO, USA); pMIR-GFP Reporter Vector (Cell Biolabs, San Diego, CA, USA); miRCURY LNA™ miR-2909 power inhibitor (EXIQON, Denmark); PMIRH-2909 lentiviral construct (System Biosciences, CA, USA).
The pediatric B-ALL, T-ALL samples and age-matched control samples were obtained from Advanced Pediatric Centre, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India with prior consent from their guardian through ethical approval by the Institutional Review Board of PGIMER. Total samples of B-ALL and T-ALL were 30 and 20 respectively. Age-matched subjects (n = 50) with no manifestations of any haematological malignancy were treated as control. All patients were <14 years of age and flow cytometric immunophenotyping showed mostly cells in the blast/progenitor region (SSC low to moderate, CD45 negative to dim) comprising ~80% of all singlet events acquired. Patients undergoing chemotherapy and cases with mixed phenotype acute leukemia (MPAL) and relapsed cases from pediatric acute lymphoblastic leukaemia (ALL) were excluded in the present study. Diagnosis of pediatric ALL samples into B- and T-cell lineage was evaluated by immunophenotyping using CD19, CD22, CD79a, CD10, CD20, and CD24 for B-ALL and CD7,CD2,CD3,CD5 for T-ALL. Mononuclear cells were isolated using Ficoll-Hypaque density gradient method . B- and T-cells were purified using MiniMACS™ Separator Kit.
RNA Extraction, cDNA synthesis and qRT-PCR
Total RNA including the small RNA was extracted from patient samples using miRNeasy mini kit in accordance with the manufacturer’s instructions. The quality and quantity of extracted RNAs were analyzed using electrophoresis and optical density measurement at 260 nm; cDNA synthesis was performed via miScript Reverse transcription kit as per suppliers’s instructions. For assaying gene expression, miScript SYBR Green Mix and the Real-time PCR (Stratagene, San Diego, CA, USA) were used. The qRT-PCR reaction was performed with a starting temperature of 95°C for 10 min, followed by 35 cycles of 45 s at 94°C, 30 s at 56°C, and 45 s at 72°C. The small non-coding nuclear RNA U6 and β-actin were used as an invariant controls for normalizing the expression of miR-2909 and other genes respectively. The 2-ΔΔCT method was used to calculate the relative expression of target genes.
Total cellular protein was extracted using Laemmli’s buffer  and the protein levels of KLF4, p21 CIP , SP1, MYC and CCND1 was determined through western blotting using appropriate antibodies as described previously . β-actin antibody was used as an internal control. Scion Image Analysis software was used for densitometry analysis and the results were expressed as intensity ratio of target protein to β-actin protein taken as arbitrary unit.
Primer sets were designed to amplify the full coding region and 3′untranslated region of KLF4 in ALL samples using Pfu polymerase. The resultant PCR products were purified using Qiaquick PCR purification kit and sequenced to detect the presence of any genetic aberration(s) in KLF4 in samples from pediatric patients with ALL. The sequence data was analysed using Cluster X 2.0.12 Software (http://www.clustal.org/clustal2) .
Plasmid constructs and reporter assays
Full length 3′UTR of KLF4 in B-ALL was cloned into miRNASelect™ pMIR GFP reporter vector; designated as pGFP-KLF4-3′UTR-B which carried no substitution of nucleotides within miR-2909 target site in KLF4 3′UTR. Mutant 3′UTR of KLF4 present in T-ALL was named as pGFP-KLF4-3′UTR-T with substitution of nucleotides within core binding site in KLF4 3′UTR. The plasmid constructs were transfected in HEK-293 cells. After 48 h, fluoresence microscopy and FACS analysis was performed to quantitate the number of cells expressing GFP. For p21 CIP promoter analysis, promoter sequence of p21 CIP with putative KLF4 binding site was cloned into pBlue TOPO reporter vector with subsequent transfection of β-gal construct into control and T- lymphoblasts. For analysis of SP1 transcriptional activity, B- and T-lymphoblasts with reporter plasmids containing SP1 response elements were transfected. β galactosidase activity was measured 72 h after transfection. To knockdown miR-2909 expression, leukemia cells were transfected with miRCURY LNA™ miR-2909 power inhibitor. To increase miR-2909 expression, HeLa cells were transfected with the PMIRH-2909 expression vector. All the transfections were performed with Lipofectamine 2000 transfection reagent according to the manufacturer’s instructions.
Cell cycle analysis and apoptosis assays by Flow cytometry
Cell cycle analysis and apoptotic assays was done on leukemia cells transfected with antagomiR-2909 (50 nM) and scrambled RNA (50 nM) for 48 h in RPMI 1640 medium supplemented with 10% FBS, 100 U/ml penicillin and 100 μg/ml streptomycin under 5% CO2 at 37°C. For cell cycle experiments, cells were fixed in 70% ethanol and stained with PI. Cells percentage at different phases were analysed with FACSCalibur cytometer and Cell Quest Pro software (Becton Dickinson, NJ, USA). For apoptosis assays, cells were stained with FITC Annexin V coupled with propidium iodide and apoptosis was measured using BD FACS Diva Software (Becton Dickinson, FACS Canto II).
KLF4 structural model & docking with target DNA
The structural models of zinc finger motifs of wild-type and mutant KLF4 were modeled with template PDB ID: 2WBUA. The Homology models were built using MODELLER (9.9) . Model validation was performed using Verify-3D (http://nihserver.mbi.ucla.edu/Verify_3D/)  and PROCHECK . The quality of the final models was evaluated from Ramachandran plot (Additional file 3: Figure S3B). Molecular visualization and structural alignment was done using CHIMERA http://bioinformatics.org/wiki/Chimera and PYMOL http://www.pymol.org/. Target DNA sequence (5′-cgggcggggc-3′) in p21 CIP promoter was modeled into B-FORM using DNA analysis servers . Docking studies were performed using High Ambiguity-Driven bimolecular Docking (HADDOCK) under solvated conditions [44, 45]. Cation-π interactions were analysed with CAPTURE http://capture.caltech.edu/.
Statistical analyses were performed by SPSS Windows version 19. Data was expressed as mean ± S.D of the experiments performed in triplicate. Student’s t test or Mann-Whitney-Wilcoxon test was performed to determine the significance of difference between two groups. Differences were considered significant at p < 0.01 and p < 0.05.
Acute lymphoblastic leukemia
B-cell lineage acute lymphoblastic leukemia
T-cell lineage acute lymphoblastic leukemia
Anti-apoptotic transcription factor
Kruppel like factor transcription factor 4
B-cell lymphoma 3-encoded protein
First zinc finger motif
Second zinc finger motif
Third zinc finger motif
- SP1 :
Specificity protein transcription factor-1
Cluster of differentiation
Green fluorescent protein
We acknowledge Dr. Neelam Varma for her support in the diagnosis of leukemic samples through Immunophenotyping. We thank Dr. Nitin Patel for his invaluable inputs and critical reading of the manuscript. The study was supported by the funds provided by Indian Council of Medical Research (ICMR), New Delhi (India). http://www.icmr.nic.in/ and this funding agency had no role in designing the experiment, sample collections and analysis done or preparation of this manuscript.
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