Abstract
Downregulation of microRNA-31 has been linked with enhanced stress resistance, while its overexpression leads to cell death. In this study, we found mediatory role of microRNA-31 in γ-radiation-induced apoptosis in a model insect cell line Sf9 carrying well-conserved apoptotic machinery. Mature microRNA-31 is perfectly conserved amongst insects; hence we used biotinylated probes designed from Bombyx mori sequence for its successful detection in Sf9 cells. Target identification using Bombyx mori 3′UTRs predicted miR-31′s potential role in Lepidopteran apoptosis, which prompted us to investigate alterations in its expression during radiation-induced cell death. We found significant overexpression of Sf-miR-31 following lethal dose (1,000Gy–3,000Gy) irradiation. Its mediatory role was finally confirmed as antisense-microRNA-31 could successfully inhibit radiation-induced cytochrome-c release, caspase-3 activation and apoptosis. While Bax/Bcl-2 expression remained unchanged, lethal radiation doses induced Bim overexpression and direct Bim-Bax interaction (co-immunoprecipitation) which is not yet unequivocally demonstrated during apoptosis. Quite important, these events were found to be dependent on radiation-induced miR-31 overexpression, as antisense-miR-31 inhibited both the responses and resulted in significant inhibition of cell death. Pro-apoptotic role of miR-31 was further confirmed when miR-31 mimic induced apoptosis involving similar Bim/Bax alterations. Therefore, our study reveals an important mediatory role of miR-31 in radiation-induced cell death.
MicroRNAs (miRNAs) are evolutionarily conserved 20–22 nucleotide long non-translating RNAs that are transcribed by RNA polymerase-II and comprise about 1–3% of the genome1,2,3. Biogenesis of miRNAs involves multistage processing spread over nuclear as well as cytoplasmic compartments, and culminates in inclusion of 20–22 nucleotide long single strands in a protein complex known as RNA-induced silencing complex (RISC) mainly comprising of Argonaute-2 (AGO2). This miRNA-induced silencing complex (miRISC) finally mediates translational repression and/or increased degradation of its mRNA targets4 by binding to 3′ UTR’s. A single miRNA may be able to repress multiple different transcripts and hence regulate multiple pathways and responses by altering protein expression. Therefore, miRNA’s are now recognized as important cell fate determinants in response to cellular environment as well as exposure to chemical agents or radiation.
Radiation-induced alterations in the expression level of certain miRNAs have been demonstrated in various cell types5,6,7. Increased expression of some miRNAs like miR-1285, miR-151-5p, Let-7i may enhance radioresistance while Let-7 upregulation has been shown to increase radiosensitivity in various cancer cell lines following clinical dose (~2Gy X-Rays) irradiation8. However, limited studies have so far been conducted on the role of miRNAs in cellular radiosensitivity, and many miRNAs remain to be investigated. Out of various miRNAs now known for regulating cellular functions, we aimed to study miRNAs that carry substantially high specificity while having good pleiotropic activity. One such miRNA is miR-31, which is known to regulate a variety of cellular functions. Interestingly, miR-31 is the only known miRNA that is present in vertebrates as well as in Drosophila and carries an eight nucleotide motif (seed region) that squarely enhances its targeting specificity to a level unmatched by most other miRNA’s9. It has been found significantly downregulated in many cancerous cells10,11,12 while its upregulation is linked with metastatic regression and increased cell death13,14. It has also been shown to target genes involved in apoptosis regulation including E2F615, Receptor tyrosine kinase MET16, Protein kinase-C epsilon14, NF-κB inducing kinase (NIK)17, fibroblast growth factor 3 (FGF3)18, and pathways like Akt-dependent signaling as well as Bim induction13. In an isolated study, down-regulation of miR-31 was shown to be associated with increased radioresistance19, although underlying mechanism is not yet known. Therefore, miR-31 is an important candidate for studying its role in cellular radioresistance/radiosensitivity.
In the present study, we investigated whether altering the miR-31 level can modify cellular radioresistance, using a cell system that efficiently expresses this specific miRNA. We chose a model cell system (Sf9 ovarian cell line derived from Spodoptera frugiperda; class Insecta, order Lepidoptera) that shows unusual radioresistance (~100–200 times higher than human/mammalian cells20) marked by excessive resistance against radiation-induced apoptosis20,21. Due to such level of resistance achieved despite extensive structural/functional homologies with mammalian cells, it is considered an important higher eukaryotic model system to study molecular radiation responses. High radioresistance of Sf9 cells allows choice of fairly distant sub-lethal versus lethal doses for delineating the molecular pathways elicited during cell death. Factors involved in radioresistance of these cells include unusually low induction of DNA damage and oxidative stress22, efficient DNA repair23,24 absence of nitrosative stress25, and higher resilience to death-inducing signals21,26. Very little is however known about the miRNA-mediated regulation of apoptosis in these cells27. In the present study, we not only detected the existence of miR-31 in Sf9 cells, but also found its significant contribution in mediating radiation-induced cell death through a novel molecular pathway. Our study also suggests that downregulation of miR-31 could contribute to cellular radioresistance, and hence adds significantly to the understanding of cellular radiation responses.
Results
Identification of Sf-miR-31 and predicting its putative physiological role
Fully annotated nucleic acid sequences or microRNA database for Spodoptera are not available. Therefore, we extracted pre-miRNA-31 sequences from different orders of class Insecta using the microRNAs database (miRbase.org). ClustalW analysis of these pre-microRNA-31 sequences showed near–complete conservation within the mature microRNA-31 (miR-31) region across various orders including Lepidoptera (Fig. 1a). It was thus apparent that this conservation in the mature microRNA region should be definite within the same order. To test this, we used Bombyx mori miR-31 (order Lepidoptera) as a reference sequence for generating biotinylated probes for Sf9 (Fig. 1b). Hybridization of biotinylated probes with the miRNA pool isolated from Sf9 cells followed by RNase protection assay showed an integral single band (Fig. 1b), confirming complete homology of mature miRNA-31 between the two Lepidopteran species, viz., Bombyx mori and Spodoptera frugiperda as suggested previously by Mehrabadi, M. et al.28.
Target prediction for miR-31 using PITA executable software showed many important genes that are important for stress signaling, cell death, cellular and organelle development as well as cellular communication (Supplementary Table 1). Gene Ontology (GO) term clustering of Bmo-/Sf-miR-31 using Panther and Cytoscape (Bingo) tools suggested involvement of Sf-miR-31 in diverse cellular processes (Fig. 1c,d). Cell death/apoptosis regulation and stress signaling are among the important predicted target pathways of Sf-miR-31. These in-silico predictions hence strongly suggest Sf-miR-31 as a regulator of cell death/apoptosis.
Radiation-induced caspase-3 dependent cell death coincides with Sf-miR-31
We have earlier shown that doses up to 200Gy fail to induce significant apoptosis in Sf9 cells20. In this study as well, Sf9 cells irradiated with 200Gy and 500Gy of γ-radiation did not undergo caspase-3 activation or apoptosis (Fig. 2). Interestingly, the Sf-miR-31 expression was significantly downregulated at these sub-lethal doses (p < 0.05). On the other hand, a dose-dependent increase in caspase-3 activation and cell death marked by typical apoptotic bodies (Fig. 2a,b) was evident by 24 h following irradiation at higher doses (1,000Gy–3,000 Gy), which was associated with a concomitant increase in the expression of Sf-miR-31 (p < 0.002; Fig. 2c).
Suppression of Sf-miR-31 inhibits radiation-induced cell death
In order to confirm whether overexpression of Sf-miR-31 has a functional role in the induction of radiation-induced Sf9 cell death, its expression was suppressed using antisense RNA prior to irradiation, and alteration in cell death induction was studied using morphological scoring (necrotic/apoptotic cells), flow cytometry (sub-G1 population) as well as by caspase-3 activity. Quite important, radiation-induced overexpression of Sf-miR-31 at doses >1,000Gy resulted in significant inhibition (p < 0.05) of cell death when it was inhibited/compromised using antisense miR-31 (AS-miR-31) (Fig. 3).
Radiation induced Bax translocation in the absence of Bax/Bcl-2 alterations is mediated by miR-31 overexpression
Recent study from our laboratory has established that radiation induces cell death in Sf9 cells in a primarily Bax-dependent manner21. In the present study, we further observed that expression of pro-apoptotic protein Bax or anti-apoptotic protein Bcl-2 is not altered by radiation doses (1,000Gy–3,000Gy) inducing apoptosis (Fig. 4a). Pre-treatment with AS-miR-31 also failed to alter Bax and Bcl-2 expression/ratio (Fig. 4b). Despite unchanged protein expression, we found clear evidence of translocation of Bax to mitochondria following irradiation at 1,000Gy–3,000Gy, using immunofluorescence microscopy (Fig. 5a) as well as by immunoblotting of mitochondrial and cytosolic fractions (Fig. 5b). Inhibition of Sf-miR-31 using antisense significantly inhibited Bax translocation induced by high doses, which implied an apparently indirect regulation of Bax-mediated processes by miR-31 (Fig. 5c,a). Lethal doses also caused release of cytochrome-c from mitochondria into cytosol following irradiation at 1,000Gy–3,000Gy and inhibiting Sf-miR-31 resulted in its partial but significant reduction (Fig. 5c). These results thus show that Bax translocation and consequent cytochrome-c release/cell death are partly regulated by Sf-miR-31.
Radiation-induced miR-31 overexpression enhances Bim expression as well as its interaction with Bax
We further explored potential regulators of radiation-induced Bax translocation to mitochondria. Bim (and its BH3-only peptide) has been earlier shown to interact with Bax29,30, although consequent effect on Bax functioning was not clearly shown. We investigated whether Bax translocation to mitochondria involves Bim-Bax interaction following lethal dose irradiation. Western immunoblotting confirmed a dose-dependent increase in Bim expression especially at doses >1,000Gy (Fig. 6a). Co-immunoprecipitation experiments further revealed direct interaction of Bim and Bax that was considerably increased at lethal radiation doses inducing mitochondrial translocation of Bax (Fig. 6b). In these experiments, we performed immunoprecipitation (IP) of either proteins (IP and reverse IP) followed by detection of the interacting protein.
Since AS-miR-31 was able to significantly inhibit the induction of Bax translocation as well as apoptosis, we tested if radiation-induced Bim overexpression is also altered in this condition. As shown in Fig. 6c,d, treatment with AS-miR-31 indeed caused inhibition of radiation-induced Bim overexpression and Bim/Bax interaction, confirming miR-31’s role in regulating Bim-Bax pathway.
Ectopic overexpression of miR-31 induces apoptosis in Sf9 cells and confirms its mediatory role in cell death
Since radiation induced significant overexpression of miR-31 which in turn mediated Bim-Bax pathway, we further confirmed the pro-apoptotic role of miR-31 by ectopically enhancing its expression in the unirradiated cells. Mere transfection of Sf9 cells with the miR-31 mimic sequence oligos could induced apoptotic cell death. Approximately four-fold increase in miR-31 level (using real-time PCR) following transfection with miR-31 mimics resulted in ~20% increase in cell death (Fig. 7a), which was associated with increase in caspase-3 activity (Fig. 7b) as well as significant mitochondrial Bax translocation and cytochrome-c release(*,#P < 0.02) (Fig. 7c,d). Importantly, miR-31 mimic-induced apoptosis also involved the upregulation of Bim expression (Fig. 7e).
Discussion
This study presents significant evidence to demonstrate that microRNA-31, which has been recently reported to regulate tumour radiosensitivity19, is a prominent mediator of radiation-induced cell death in higher eukaryotes. Even more important, the study demonstrates that radiation-induced miR-31 alters Bim-mediated regulation of Bax translocation that in turn results in the post-irradiation mitochondrial cytochrome-c release and apoptosis. We used a model cell system that offers very high radioresistance and thereby allows choice of fairly distant sub-lethal versus lethal doses. These cells also carry a well conserved apoptotic mechanism that is highly homologous to the human system. In fact, we had recently reported that Sf9 cells undergo Bax-dependent apoptosis that is similar to the mitochondria-mediated intrinsic pathway known in human/mammalian cells21. Since miR-31 is also known to be highly conserved from insects to mammals and regulates many cellular responses/functions, the present study provides a valuable insight into the potential role of this microRNA in the cellular radiosensitivity of higher eukaryotes.
We detected miR-31 in Sf9 cells using in silico and experimental steps that involved in vitro transcription and generation of biotinylated probe, despite the fact that complete transcriptome database was not available for the organism Spodoptera including the miRNA sequences. Since our in silico analysis showed that mature miR-31 sequence is perfectly conserved between as well as within different insect orders (Fig. 1a), we used the Bombyx mori sequence for designing these biotinylated probes (as detailed in the methods section) for detecting miR-31 in the RNA pool of Sf9 cells. Functional annotation analysis further predicted participation of Sf-miR-31 in various cellular functions including the regulation of apoptosis (Fig. 1c,d; Supplementary Fig. 3 and Supplementary table 1). Following this, our results showing upregulation of miR-31 in cells irradiated at lethal doses indeed indicated its mediatory role in apoptosis, which was consequently confirmed by significant alteration (inhibition) of cell death by the ectopically administered AS-miR-31(*P < 0.05, **P < 0.02) (Fig. 3). Pro-apoptotic role of miR-31 is further clear from the fact that at sub-lethal doses (<500Gy), its expression was significantly downregulated (Fig. 2c). Together, our results confirm the existence of miR-31 as well as its mediatory role in radiation-induced cell death in the radioresistant Sf9 cells.
While our recent study indicated obligatory involvement of Bax in the radiation-induced apoptosis in Sf9 cells21, the present findings further show translocation of cytosolic Bax to mitochondria as a critical step. Studies in mammalian/human cells have generally shown that Bax/Bcl-2 ratio is increased significantly during mitochondria-mediated apoptosis31,32,33 largely as a result of induced Bax overexpression32,34,35,36, even as some contradictory reports suggest lack of Bax overexpression during apoptosis involving its translocation37,38,39. In our study, Bcl-2 or Bax expression (thereby Bcl-2/Bax ratio) failed to show any alteration at any of the lethal radiation doses used (Fig. 4a), even as Bax translocation was quite evident (Fig. 5a,b). This prompted us to further investigate the possible mechanism underlying Bax translocation at these high radiation doses. In a recent study29, binding of Bax with the BH3-only peptide of Bim was shown. Although Bim has not been directly implicated in the mitochondrial translocation of Bax, this remote observation encouraged us to investigate whether Bim-Bax interaction occurs constitutively or following irradiation. Our co-immunoprecipitation results (Fig. 6b) indeed show direct Bim-Bax interaction that is enhanced by lethal radiation doses involving Bax translocation. We further found that this radiation-induced Bim-Bax interaction is effectively inhibited by AS-miR-31, and so is the radiation-induced Bim overexpression (Fig. 6c,d). An isolated report has earlier shown upregulation of Bim by miR-31 albeit in unirradiated cells13. Therefore, Bim upregulation may be consequently induced through miR-31 overexpression in different stress responses.
Since microRNAs invariably seem to suppress the expression of their putative targets, miR-31 may target an unknown transcript which in turn negatively regulates the expression of Bim under constitutive condition. This indirect relationship between miR-31 and Bim was further corroborated when we treated Sf9 cells with the mimic sequences of miR-31. A nearly four-fold increase in miR-31 expression was sufficient to cause ~20% increase in apoptotic cell death, which was essentially mediated through Bim overexpression, Bax translocation and cytochrome-c release into cytosol (Fig. 7). Therefore, our study confirms beyond doubt that miR-31 overexpression mediates Bax-dependent cell death through indirect induction of Bim overexpression by suppressing an intermediate gene/protein. We are presently looking for these putative targets of miR-31 that could be regulating Bim expression. In silico predictions indicate few proteins (e.g., BG4, LKb1, MKK4, EGFR and Jafrac1) that seem important in the regulation of apoptosis (Supplementary Fig. 3 and table 1). However, the possibility of missing some additional proteins cannot be ruled out as all the predicted 3′UTR targets cannot be traced to specific genes due to lack of completely annotated B. mori genome sequence. Further, administering AS-miR-31 could inhibit radiation-induced cell death significantly but partially (Fig. 3). Therefore, it cannot be an exclusive cell death pathway and additional mechanisms also seem to contribute in the radiation-induced cell death.
To summarize, our study reveals a hitherto unknown cell death regulation mechanism involving two significant features. Firstly, the well-known Bax translocation to mitochondria induced by lethal radiation doses was regulated by Bim overexpression as well as direct Bim-Bax interaction in the absence of alterations in Bax or Bcl-2 expression. Secondly, these radiation-induced alterations in Bim-Bax ultimately leading to Bax translocation were dependent on miR-31 upregulation through yet unknown mediators. Interestingly, this study also implies that miR-31 downregulation could result in enhanced cellular radioresistance, since sub-lethal radiation doses were associated with considerable reduction in its expression level. Even as further investigations may be needed to thoroughly elucidate the mechanisms, our study demonstrates definite role of miR-31 in radiation-induced cell death.
Materials and Methods
Cell line and irradiation
Sf9 cell line, originally established from the ovaries of Spodoptera frugiperda (obtained from National Institute of Immunology, New Delhi, India), was maintained as semi-adherent monolayer in the 25 cm2 culture flasks (Falcon, BD Biosciences, Cat. No. 353108) at 28 °C in Grace’s insect cell medium (Sigma, Cat. No. G9771) supplemented with 3.33 g/l lactalbumin hydrolysate (Sigma, Cat. No. V196623), 3.33 g/l yeastolate (BD Biosciences, Cat. No. 255772), 0.35 g/l NaHCO3 and antibiotics (Penicillin sodium salt 50,000 units/l, streptomycin sulfate 50,000 μ g/l, Nystatin 2000 μ g/l from 500,000 USP Units/mg; Sigma). Growth medium (pH 6.2) was prepared by adding 10% heat inactivated fetal bovine serum (FBS) (Sigma, Cat. No.10082-147). Cells were subcultured twice a week in the exponential phase by seeding at a density of 35,000–40,000 cells/cm2 as described earlier20. Irradiation was performed in the exponential phase of cell growth at a dose rate of 19.16 Gy/min (Gamma Chamber 5000, Board of Radiation and Isotope Technology, Department of Atomic Energy, Mumbai, India) and cells were kept at 28 °C till harvesting.
In vitro probe construction and microRNA identification
Construction of probe for the Sf-miR-31 identification was done using Bombyx mori mature miR-31 as a template for in vitro transcription. Mature miR-31 oligonucleotides (oligos) were synthesized in DNA format along with T7 promoter sequence (GGACAGAG) added at the 3′ end, which is complementary to the T7 promoter primer and facilitated hybridization of the two of DNA oligos so that the fill-in reaction produced a double-strand transcription template containing the T7 promoter site. Probes were constructed using miRNA probe construction kit (Ambion, Cat. No. AM1550) as per manufacturer’s protocol with some modifications, by adding 2 μl of T7 promoter primers, 6 μl of DNA hybridization buffer and 2 μl of oligonucleotide template and heating at 70 °C for 5 minutes followed by 5 minutes incubation at room temperature. Further, 2 μl of 10X Klenow reaction buffer, 2 μl of 10X dNTP mix, 4 μl of nuclease free water and 2 μl of Exo-klenow buffer were added and incubated at 37 °C for 45 min. Then 2 μl of this reaction was used for in vitro transcription by adding 2 μl of 10X transcription buffer, 1 μl each of ATP, CTP, GTP, biotin-labeled UTP, 2 μl of T7 RNA polymerase and RNase free water to make final volume to 20 μl. The reaction mix was kept at 37 °C for 30 min at RT, and DNase treatment was given to remove double stranded template. Thus formed biotin-labeled probe was used for the RNase protection assay. miRNA pool was isolated from Sf9 cells using miRVana miRNA isolation kit (Ambion, Cat. No. AM1561), and mature miRNAs (<40bp) were screened using flash PAGE fractionators (Ambion, Cat. No. 13100) for hybridization with the biotinylated probes at 37 °C for 2 h. RNase protection assay was performed using miRVana miRNA Detection Kit (Ambion, Cat. No. AM1552) as per manufacturer’s protocol. RNase-protected miRNAs/probe hybrids were then separated by 15% Urea-PAGE (8M Urea) and after transfer on to nylon membrane, detected with streptavidin-HRP.
Western immunoblotting, sub-cellular fractionation and immunoprecipitation
For protein expression analysis, western immunoblotting was performed at different time intervals after treatment, as detailed earlier25. Sub-cellular fractionation was performed to observe the Bax translocation from cytosol to mitochondria using immunoblotting of both fractions. Both the fractions were separated using protocol as discussed in previous study26. Purity of cytosolic and mitochondrial fractions was confirmed using anti-VDAC and anti- GAPDH antibodies (Santa Cruz Biotechnology, Dallas, Texas, USA), respectively. For Bim-Bax interaction analysis, immunoprecipitation (IP) assay was done using anti-Bax antibody (Calbiochem, Sandiego, CA, USA). Reverse immunoprecipitation was also performed using anti –Bim antibody (Calbiochem, Sandiego, CA, USA) and detection by anti-Bax antibody. Cells were irradiated with and without previous transfection with AS-miR-31 and harvested 18 h post-irradiation. Cells were lysed using native lysis buffer (150 mM NaCl, 10 mM HEPES [pH 7.4], 1% CHAPS, 10% Protease inhibitor cocktail) and 250 μg of whole cell lysate was used for immunoprecipitation using Catch and Release kit (Millipore Cat. No. 17-500) as per manufacturer’s protocol. Eluted proteins were then separated by 15% PAGE and following transfer onto PVDF membrane, detected with anti-Bax and anti-Bim antibody (Calbiochem) and Enhanced Chemiluminescence (ECL) reagent (Pierce, Cat. No. 34087).
Cell death/Apoptosis analysis
Cell death was assessed by observing cells under DIC microscope (Axiovert-200 Zeiss inverted DIC microscope, Carl Zeiss, Germany). Cell morphology assay40 and measurement of sub-G1 population by flow cytometry were used for determining dead cell population. In brief, cells were harvested 24h following irradiation with or without transfection with AS-miR-31. Direct cell suspension was used for embedding on agarose-laden slides and fluorescence staining with FITC-PI for assessing morphological changes. For flow cytometry, Cells were washed with PBS and fixed in 70% ethanol and kept for overnight incubation at −20 °C. Propidium iodide (20μg/ml) was used for nuclear staining following RNase treatment for 30 min at 37 °C. Relative DNA content and cell cycle distribution were analysed with the help of FACSCalibur flow cytometer (Becton- Dickinson & Co., New Jersey, USA) using the CellQuest software (v.3.0.1) for acquisition and ModFit LT software (v.2.0; Verity Software House, Inc., Maine, USA) for cell cycle analysis (Supplementary Fig. 1a). Again for more precise measurement of cell death, Sub-G1 cell population was gated and 5000 cells were counted in gated region irrespective of the total numbers of cells. Dead cells were then calculated by normalizing gated cells (5000 fixed number) against the total cell count (Supplementary Fig. 1b).
Quantitative Real Time PCR and transfection
Radiation-induced changes in the expression of Sf-miR-31 were observed with real time PCR. miRNA isolation was performed using miRVana microRNA isolation kit and mature miRNAs were screened using Flash PAGE Fractionators (Ambion). 1 μg of total miRNA was used for cDNA preparation in a 20 μl reaction using miScript Reverse Transcription Kit as per manufacturer’s protocol (Qiagen, Cat. No. 218061). 2 μl of cDNA was used to analyze the Sf-miR-31 expression using Sf-miR-31 specific forward primer in Real Time Thermocycler (Stratagene, MX3005P). Single peak of dissociation curve from the amplified produced was considered as specific amplification. For transfection of AS-miR-31 and mimic miR-31, 0.50 μg of each was used with RNAiFect (Qiagen, Cat No. 301605) in 1:5 ratio (w/v). The expression of miR-31 after antisense and mimic miR-31 was quantified using Real Time PCR (Supplementary Fig. 2). All the transfections were carried out in exponential phase of cell growth.
Immunofluorescence microscopy and caspase activity assay
To study Bax translocation using immunofluorescence microscopy, cells were grown on cover slips in a 35 mm culture dish 24 h prior to transfection (with AS-miR-31 or MM-miR-31) and/or irradiation. Irradiated/treated cells were first incubated with mitotracker red (Life Technologies, Cat No. M-7512) for 30 min at 37 °C and washed twice with wash buffer containing PBS and Tween-20 (0.1% v/v). Cell fixation was done by incubating cells in chilled acetone for 10 min at 4 °C followed by permeabilization (0.05% TritonX-100 in PBS) for 5 min. Blocking was performed with 1% FBS in PBS for 30 min at RT to reduce nonspecific signals. Anti-Bax antibody was diluted in wash buffer at 1:100 dilution and incubated for 1 h at RT. After washing twice with wash buffer, cells were incubated with secondary antibody conjugated with FITC for 45 min, washed and mounted with 50% glycerol in PBS and images were captured using Leica SP8 spectral confocal microscope (Courtesy Leica Microsystems India). Caspase-3 activity was assessed 24h post-irradiation using caspase-3 activation assay kit (Sigma, Cat. No. CASP3F) according to manufacturer’s recommendation. The mean fluorescence values of triplicates were plotted to determine variation in caspase-3 activation.
Target prediction/Gene Ontology term clustering
For target gene prediction of miR-31, we extracted 3′ UTRs of the Bombyx mori (silkworm, Dazao strain) from NCBI UniGene database (http://www.ncbi.nlm.nih.gov/sites/entrezdbunigene). These 3′ UTRs were then queried against Bombyx mori miR-31 (Bmo-miR-31) for target accessibility and interaction using PITA executable program41. We determined only those potential targets which had a score ΔΔG ≤ −15 kcal/mol (Supplementary Table 1). The locations of these screened UTR’s (nscaf) were then searched for the associated gene in the silkworm database. The reference sequence IDs (nucleic acid, protein) of those genes were then searched for the Drosophila homologs and converted to Flybase ID using DAVID Bioinformatics Resource, gene ID conversion tool42. As miRNA functions could be evolutionarily conserved between species such as B. mori and D. melanogaster43, we used Flybase IDs of identified targets for the GO term clustering using Panther and Cytoscape44 (Bingo) tools for the functional analysis of Sf-miR-31. Cytoscape (GeneMANIA) tool was used for the prediction of targets involved in stress signaling/cell death (Supplementary Fig. 3).
Statistical Analysis
Differences between the mean values were analyzed for significance using the paired two tailed student’s ‘t’ test for independent samples using Microsoft Excel, with p value ≤ 0.05 considered as statistically significant.
Additional Information
How to cite this article: Kumar, A. et al. Evidence for microRNA-31 dependent Bim-Bax interaction preceding mitochondrial Bax translocation during radiation-induced apoptosis. Sci. Rep. 5, 15923; doi: 10.1038/srep15923 (2015).
Supplementary Material
Acknowledgments
This work was supported by DRDO project INM-311.1.5 funded by the Defence Research and Development Organisation, Ministry of Defence, India. Senior research fellowship was received by Soma Ghosh and Ashish Kumar from the University Grants Commission, India during the course of this study.
Footnotes
Author Contributions A.K. and S.C. conceived the idea and designed the experiments, A.K. performed the experiments, S.G. helped in co-immunoprecipitation and immuno- fluorescence experiments, A.K. and S.C. analyzed the data and wrote the paper.
References
- Lee Y., Jeon K., Lee J. T., Kim S. & Kim V. N. MicroRNA maturation: stepwise processing and subcellular localization. EMBO J 21, 4663–4670 (2002). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson S. M., Lin S. Y. & Slack F. J. The time of appearance of the C. elegans let-7 microRNA is transcriptionally controlled utilizing a temporal regulatory element in its promoter. Dev Biol 259, 364–379 (2003). [DOI] [PubMed] [Google Scholar]
- Cai X., Hagedorn C. H. & Cullen B. R. Human microRNAs are processed from capped, polyadenylated transcripts that can also function as mRNAs. RNA 10, 1957–1966 (2004). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fabian M. R. & Sonenberg N. The mechanics of miRNA-mediated gene silencing: a look under the hood of miRISC. Nat Struct Mol Biol 19, 586–593 (2012). [DOI] [PubMed] [Google Scholar]
- Weidhaas J. B. et al. MicroRNAs as potential agents to alter resistance to cytotoxic anticancer therapy. Cancer Res 67, 11111–11116 (2007). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kato M. et al. The mir-34 microRNA is required for the DNA damage response in vivo in C. elegans and in vitro in human breast cancer cells. Oncogene 28, 2419–2424 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ilnytskyy Y., Koturbash I. & Kovalchuk O. Radiation-induced bystander effects in vivo are epigenetically regulated in a tissue-specific manner. Environ Mol Mutagen 50, 105–113 (2009). [DOI] [PubMed] [Google Scholar]
- Niemoeller O. M. et al. MicroRNA expression profiles in human cancer cells after ionizing radiation. Radiat Oncol 6, 29 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grimson A. et al. MicroRNA targeting specificity in mammals: determinants beyond seed pairing. Mol Cell 27, 91–105 (2007). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Valastyan S. et al. A pleiotropically acting microRNA, miR-31, inhibits breast cancer metastasis. Cell 137, 1032–1046 (2009). [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
- Liu X. et al. MicroRNA-31 functions as an oncogenic microRNA in mouse and human lung cancer cells by repressing specific tumor suppressors. J Clin Invest 120, 1298–1309 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Augoff K. et al. miR-31 is a broad regulator of beta1-integrin expression and function in cancer cells. Mol Cancer Res 9, 1500–1508 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Valastyan S., Chang A., Benaich N., Reinhardt F. & Weinberg R. A. Activation of miR-31 function in already-established metastases elicits metastatic regression. Genes Dev 25, 646–659 (2011). [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
- Korner C. et al. MicroRNA-31 sensitizes human breast cells to apoptosis by direct targeting of protein kinase C epsilon (PKCepsilon). J Biol Chem 288, 8750–8761 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bhatnagar N. et al. Downregulation of miR-205 and miR-31 confers resistance to chemotherapy-induced apoptosis in prostate cancer cells. Cell Death Dis 1, e105 (2010). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mitamura T. et al. Downregulation of miRNA-31 induces taxane resistance in ovarian cancer cells through increase of receptor tyrosine kinase MET. Oncogenesis 2, e40 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yamagishi M. et al. Polycomb-mediated loss of miR-31 activates NIK-dependent NF-kappaB pathway in adult T cell leukemia and other cancers. Cancer Cell 21, 121–135 (2012). [DOI] [PubMed] [Google Scholar]
- Xiao W. et al. Upregulation of miR-31* is negatively associated with recurrent/newly formed oral leukoplakia. PLoS One 7, e38648 (2012). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lynam-Lennon N. et al. MicroRNA-31 modulates tumour sensitivity to radiation in oesophageal adenocarcinoma. J Mol Med (Berl) 90, 1449–1458 (2012). [DOI] [PubMed] [Google Scholar]
- Chandna S. et al. Radiation responses of Sf9, a highly radioresistant lepidopteran insect cell line. Int J Radiat Biol 80, 301–315 (2004). [DOI] [PubMed] [Google Scholar]
- Chandna S. et al. Radioresistant Sf9 insect cells undergo an atypical form of Bax-dependent apoptosis at very high doses of gamma-radiation. Int J Radiat Biol 89, 1017–1027 (2013). [DOI] [PubMed] [Google Scholar]
- Chandna S. RE: Multiple factors conferring high radioresistance in insect Sf9 cells. (Mutagenesis, 24, 259-269, 2009). Mutagenesis 25, 431–432 (2010). [DOI] [PubMed] [Google Scholar]
- Koval T. M., Hart R. W., Myser W. C. & Hink W. F. DNA single-strand break repair in cultured insect and mammalian cells after X-irradiation. Int J Radiat Biol Relat Stud Phys Chem Med 35, 183–188 (1979). [DOI] [PubMed] [Google Scholar]
- Koval T. M. & Kazmar E. R. DNA double-strand break repair in eukaryotic cell lines having radically different radiosensitivities. Radiat Res 113, 268–277 (1988). [PubMed] [Google Scholar]
- Suman S., Seth R. K. & Chandna S. A calcium-insensitive attenuated nitrosative stress response contributes significantly in the radioresistance of Sf9 insect cells. Int J Biochem Cell Biol 43, 1340–1353 (2011). [DOI] [PubMed] [Google Scholar]
- Kumarswamy R., Seth R. K., Dwarakanath B. S. & Chandna S. Mitochondrial regulation of insect cell apoptosis: evidence for permeability transition pore-independent cytochrome-c release in the Lepidopteran Sf9 cells. Int J Biochem Cell Biol 41, 1430–1440 (2009). [DOI] [PubMed] [Google Scholar]
- Kumarswamy R. & Chandna S. Inhibition of microRNA-14 contributes to actinomycin-D-induced apoptosis in the Sf9 insect cell line. Cell Biol Int 34, 851–857 (2010). [DOI] [PubMed] [Google Scholar]
- Mehrabadi M., Hussain M. & Asgari S. MicroRNAome of Spodoptera frugiperda cells (Sf9) and its alteration following baculovirus infection. J Gen Virol 94, 1385–1397 (2013). [DOI] [PubMed] [Google Scholar]
- Sarosiek K. A. et al. BID preferentially activates BAK while BIM preferentially activates BAX, affecting chemotherapy response. Mol Cell 51, 751–765 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marani M., Tenev T., Hancock D., Downward J. & Lemoine N. R. Identification of novel isoforms of the BH3 domain protein Bim which directly activate Bax to trigger apoptosis. Mol Cell Biol 22, 3577–3589 (2002). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pastorino J. G., Chen S. T., Tafani M., Snyder J. W. & Farber J. L. The overexpression of Bax produces cell death upon induction of the mitochondrial permeability transition. J Biol Chem 273, 7770–7775 (1998). [DOI] [PubMed] [Google Scholar]
- Pawlowski J. & Kraft A. S. Bax-induced apoptotic cell death. Proc Natl Acad Sci USA 97, 529–531 (2000). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Raisova M. et al. The Bax/Bcl-2 ratio determines the susceptibility of human melanoma cells to CD95/Fas-mediated apoptosis. J Invest Dermatol 117, 333–340 (2001). [DOI] [PubMed] [Google Scholar]
- Deng Y. & Wu X. Peg3/Pw1 promotes p53-mediated apoptosis by inducing Bax translocation from cytosol to mitochondria. Proc Natl Acad Sci USA 97, 12050–12055 (2000). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hsu Y. T., Wolter K. G. & Youle R. J. Cytosol-to-membrane redistribution of Bax and Bcl-X(L) during apoptosis. Proc Natl Acad Sci USA 94, 3668–3672 (1997). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rosse T. et al. Bcl-2 prolongs cell survival after Bax-induced release of cytochrome c. Nature 391, 496–499 (1998). [DOI] [PubMed] [Google Scholar]
- Jia L. et al. Bax translocation is crucial for the sensitivity of leukaemic cells to etoposide-induced apoptosis. Oncogene 20, 4817–4826 (2001). [DOI] [PubMed] [Google Scholar]
- Park M. T. et al. Phytosphingosine induces apoptotic cell death via caspase 8 activation and Bax translocation in human cancer cells. Clin Cancer Res 9, 878–885 (2003). [PubMed] [Google Scholar]
- Cai Z. et al. Apoptotic response to homoharringtonine in human wt p53 leukemic cells is independent of reactive oxygen species generation and implicates Bax translocation, mitochondrial cytochrome c release and caspase activation. Leukemia 15, 567–574 (2001). [DOI] [PubMed] [Google Scholar]
- Hambarde S., Singh V. & Chandna S. Evidence for involvement of cytosolic thioredoxin peroxidase in the excessive resistance of Sf9 Lepidopteran insect cells against radiation-induced apoptosis. PLoS One 8, e58261 (2013). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kertesz M., Iovino N., Unnerstall U., Gaul U. & Segal E. The role of site accessibility in microRNA target recognition. Nat Genet 39, 1278–1284 (2007). [DOI] [PubMed] [Google Scholar]
- Huang da W., Sherman B. T. & Lempicki R. A. Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources. Nat Protoc 4, 44–57 (2009). [DOI] [PubMed] [Google Scholar]
- Grun D., Wang Y. L., Langenberger D., Gunsalus K. C. & Rajewsky N. microRNA target predictions across seven Drosophila species and comparison to mammalian targets. PLoS Comput Biol 1, e13 (2005). [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cline M. S. et al. Integration of biological networks and gene expression data using Cytoscape. Nat Protoc 2, 2366–2382 (2007). [DOI] [PMC free article] [PubMed] [Google Scholar]
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