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α-synuclein (α-SYN) is a major pathologic contributor to Parkinson’s disease (PD). Multiplication of α-SYN encoding gene (SNCA) is correlated with early onset of the disease underlining the significance of its transcriptional regulation. Thus, monitoring endogenous transcription of SNCA is of utmost importance to understand PD pathology. We developed a stable cell line expressing α-SYN endogenously tagged with NanoLuc luciferase reporter using CRISPR/Cas9-mediated genome editing. This allows efficient measurement of transcriptional activity of α-SYN in its native epigenetic landscape which is not achievable using exogenous transfection-based luciferase reporter assays. The NanoLuc activity faithfully monitored the transcriptional regulation of SNCA following treatment with different drugs known to regulate α-SYN expression; while exogenous promoter-reporter assays failed to reproduce the similar outcomes. To our knowledge, this is the first report showing endogenous monitoring of α-SYN transcription, thus making it an efficient drug screening tool that can be used for therapeutic intervention in PD.
α-synuclein (α-SYN) is a key protein involved in the progression and pathogenesis of Parkinson’s disease (PD)1. Familial PD studies have revealed that multiple copies of the gene encoding α-SYN (SNCA) cause severe early onset PD, highlighting the importance of its tight transcriptional control2,3,4,5. However, little is known about the transcriptional dysregulation of SNCA. Recently, Gründemann et al. confirmed significant increase in SNCA mRNA levels in individual dopamine neuron from idiopathic PD brains using laser capture microdissection, implying a significant transcriptional de-regulation in pathologic conditions6. Moreover, recent progress in research on epigenetic influences on SNCA transcription revealed that hypomethylation of SNCA regulatory region play a significant role towards its higher expression in idiopathic PD7,8,9.
Advances in genome mapping and the completion of ENCODE project (Encyclopedia of DNA Elements) highlighted the importance of epigenetic architecture governing transcriptional regulation of a gene10,11. In light of these discoveries, complete understanding of SNCA expression in pathologic conditions may require a molecular tool/system that can detect changes in transcription and also account for changes brought about by endogenous epigenetic modulation of the gene. Currently, the most widely used tool for understanding transcriptional activity of a gene is by using luciferase reporter fused to the promotor of a gene of interest12. However, the plasmid-based exogenous reporter systems largely ignore the comprehensive aspect of gene expression regulation by complex interaction between different epigenetic factors, transcription factors and various cis elements by artificially limiting investigation on a putative promoter region. To overcome this limitation of exogenous reporter system, we developed a novel tool where a reporter construct is tagged at the 3′end of SNCA endogenously, allowing us to monitor transcriptional activity of the gene keeping its epigenetic architecture unperturbed. The NanoLuc luciferase reporter used in this study is 150-fold brighter and significantly smaller in size than firefly or Renilla luciferase, thus making it an ideal tag for even low expressing genes13,14. Recent breakthrough in genome editing techniques like CRISPR/Cas9 (clustered regularly interspaced short palindromic repeats) have made specific genome editing simple and scalable15. Tagging SNCA endogenously with the NanoLuc using CRISPR/Cas9 method allows sensitive and real-time measurement of changes in transcriptional activity under various conditions of stimuli. This strategy can help to shed light on the transcriptional regulation of SNCA, and may serve as a very strong tool for screening of drugs to limit the progression of PD.
To introduce the NanoLuc reporter at the 3′end of the SNCA, a double-strand DNA break (DSB) was introduced on the reverse strand with the –NGG protospacer adjacent motif sequence (PAM) directly abutting the stop codon located in the exon 6. This was achieved in human embryonic kidney cell line (HEK293T) by transient transfection with the pSpCas9 (BB)-2A-Puro vector16. Along with the CRISPR/Cas9 construct, a donor vector containing the NanoLuc sequence was co-transfected to take advantage of the cell’s homology-directed repair (HDR)17. This donor construct contained two flanking homology domains each of about 800 base pairs, corresponding to the upstream and downstream of the DSB target site (Fig. 1a). The NanoLuc sequence was cloned between these two domains to precisely introduce this reporter construct right before the stop codon of SNCA. Potential positive clones were identified by PCR amplification of the genomic DNA using the NanoLuc forward and reverse primers (Table 1) (Fig. 1b; Supplementary Fig. 1). To confirm NanoLuc insertion at the target location in the SNCA gene, a second PCR using “Insertion Confirmation Primers” (Table 1) was performed and later sequenced (Supplementary Fig. 1). The wild-type (WT) allele generated a 280 base pair (bp) PCR amplicon while the NanoLuc-tagged allele generated a 805bp band, indicating a heterozygous insertion of the reporter construct (Fig. 1c). To overcome the PCR amplification bias towards the shorter allele, a separate amplification for NanoLuc-tagged allele was performed using a forward primer (NanoLuc Internal Forward Primer) on the NanoLuc insert in combination with the same reverse primer (cDNA sequencing Reverse Primer) on the 3′UTR, generated a comparable amplification of 356bp product for NanoLuc insert (Fig. 1c, lane 2). The PCR using NanoLuc internal forward primer failed to amplify any band in wild type HEK293T cells (Fig. 1c, lane 4). A second potential positive clone was found to have an incomplete insertion of the NanoLuc reporter tag (colony 14, Fig. 1b), and thus not used any further. To confirm the expression of NanoLuc-tagged SNCA allele tagged with the NanoLuc in the cell line, hereafter referred to as 293T-SNCA-3′NL, RT-PCR was conducted using primers encompassing the entire coding region of the gene and the 3′ UTR. The amplicon was then sequence verified to confirm the presence of NanoLuc insertion (Fig. 1d, Supplementary Fig. 2).
Following confirmation of the NanoLuc insertion in the SNCA genomic region and the presence of mature mRNA, we sought to confirm protein expression and functional activity of the NanoLuc. Western blot analysis of cell lysates with a polyclonal anti α-SYN antibody confirmed the presence of both wild type α-SYN (~15KDa) and a NanoLuc-tagged protein (~34KDa) matching α-SYN fused with the NanoLuc (19.1KDa) (Fig. 2a, Supplementary Fig. 3). We performed luciferase activity assay on 293T-SNCA-3′NL cells by measuring luminescence after addition of substrate furimazine. 293T-SNCA-3′NL cells produced a considerably high signal distinguishable from cells without the NanoLuc incorporation or 293T-SNCA-3′NL cells without furimazine (Fig. 2b). Titration of cell counts from 2,500 to 50,000 produced a linear increase in luminescence activity (R2=0.95), indicating that the luminescence of the SNCA-tagged NanoLuc reporter is internally consistent (Fig. 2c).
Taken together, these results show that SNCA was successfully tagged with the NanoLuc construct at the 3′end, and that expression of the NanoLuc-tagged allele leads to generation of a fusion protein.
To validate whether this system would be able to monitor changes in endogenous SNCA transcription, 293T-SNCA-3′NL cells were treated with known epigenetic modulators like DNA methyltransferase 1(DNMT1) inhibitor (5-AzadC), histone deacetylase (HDAC) inhibitors (sodium butyrate) and also dopamine which may have a toxic effect beyond a certain threshold concentration 18. SNCA harbors CpG islands at the regulatory regions encompassing the promoter and intron18,9. The CpG island in the intron1of SNCA in HEK293T remains completely methylated which upon demethylation can increase gene expression9. We treated the 293T-SNCA-3′NL cells with 5-AzadC for 72hours to allow more than one round of cell division. A significant increase in the NanoLuc activity was observed in cells treated with 5-AzadC as compared to vehicle treated ones (3.68 times increase; p≤0.0001) (Fig. 3a). SNCA transcript level from sister cultures correlated well with the observed increase in the NanoLuc activity (Fig. 3a). Changes in methylation of the SNCA-intron1 CpG island were detected using bisulfite sequencing as done by Jowaed et al.8. Ten clones from each sample were analyzed and a significant reduction in mean intron 1 methylation by 31.7% (p<0.05) was observed (Fig. 3b). The reduction of cytosine methylation in the intron1 positively correlated with increase in SNCA transcript, as we saw with the increased NanoLuc activity.
It has already been reported that dopamine at 100μM concentration can enhance SNCA transcription in HEK293T cells without inducing subsequent toxicity9,18. Likewise, we treated 293T-SNCA-3′NL cells with 100μM dopamine for 48hours and a significant 1.31 times increase in the NanoLuc activity was observed as compared to the controls (p<0.0001) (Fig. 3c). Again this increase in the NanoLuc luciferase activity complied with an increasing trend in α-SYN/Nanoluc mRNA and protein expression after dopamine treatment as seen by RT-PCR and western blot analyses (Fig. 3c, Supplementary Fig. 4). Hyper-acetylation of histone is expected to unwind underlying DNA, which in turn favors transcription19,20. To test whether HDAC inhibition in 293T-SNCA-3′NL cells would faithfully monitor transcription in response to histone hyper-acetylation, cells were treated with sodium butyrate (class I and IIa inhibitor of HDAC) at concentrations 2.5mM and 5.0mM for 24hours19. This treatment paradigm significantly increased the NanoLuc activity by 1.5 and 2.35 times respectively as compared to the controls (p<0.001) (Fig. 3d). α-SYN/NanoLuc transcript levels also corroborated well with the activity measurement and showed a dose-dependent increase (Fig. 3d).
Firefly luciferase-based promoter assay is considered a gold standard for assessing promoter activity of a target gene, which in turn reflects the transcriptional activity of the gene21. We compared the reporter activity of SNCA transcription between transient transfection-based luciferase system and the endogenous NanoLuc system that we designed. HEK293T cells were co-transfected with pGL3 basic plasmid containing SNCA promoter-intron1 region cloned upstream of luciferase coding sequence and CMV-Renilla (transfection control). Twenty-four hours later, transfected cells were treated exactly with the same modulators of SNCA expression as described in the previous result. We observed a significant decrease in normalized reporter activity upon 5-AzadC treatment post 72hrs (p<0.0001) (Fig. 4a) contrary to the increased NanoLuc activity and transcript expression (Fig. 3a). The CMV promoter-driven Renilla luciferase activity which was used as an internal control significantly varied upon 5-AzadC treatment, while the SNCA promoter-intron1 driven firefly luciferase activity remained largely unaffected, thereby leading to reduction in the normalized reporter activity (firefly/Renilla) (Fig. 4a). Next, to compare the effect of dopamine on the exogenous luciferase activity driven by SNCA promoter-intron1 and the endogenous SNCA behavior, the transfected cells were treated with 100μM dopamine for 48hrs, exactly following paradigm followed for the 293T-SNCA-3′NL cells. Interestingly, we did not observe any significant change in the normalized luciferase activity (p=0.22) (Fig. 4b). In this treatment, no significant change was observed for either firefly luciferase (p=0.15) or Renilla luciferase activity (p=0.16) (Fig. 4b), although an increasing trend could be seen for both. This data again failed to demonstrate the endogenous state of regulation upon dopamine treatment (Fig. 3c).
We also investigated the effect of HDAC inhibition (for 24hrs) on the SNCA promoter-intron1 driven luciferase activity. Similar to 5-AzadC treatment, normalized firefly activity showed a significant decrease from control (p<0.0001) (Fig. 4c). This time we saw a significant increase in the firefly luciferase activity (p<0.05), along with a significant increase in the Renilla activity (p<0.001) thereby causing an artefactual reduction in SNCA promoter activity after normalization (p<0.0001). This observation is again opposite to what we found with the NanoLuc-based endogenous system after addition of HDAC inhibitor (Fig. 3d). Together, these observations showed that the exogenous luciferase-based reporter system largely failed to demonstrate original state of endogenous transcriptional activity of SNCA.
In the present study, we have successfully incorporated the NanoLuc reporter construct at the 3′end of SNCA in HEK293T cells using CRISPR/Cas9 technology and monitored changes in expression induced by two epigenetic modulators and dopamine which are known to deregulate the gene’s expression. The newly emerging endogenous reporter system represents a significant paradigm shift in the study of gene regulation and may provide new and exciting opportunities for both basic and translational research. Such strategies allow to insert a reporter directly into the targeted genome, enabling us to investigate endogenous gene regulation while keeping the epigenetic structure intact.
This particular feature is extremely relevant in studying SNCA expression, as this gene has been shown to get extensively regulated by its epigenetic structure7,8,9. Moreover, α-SYN is a molecule whose level of expression is directly correlated with the severity of the PD pathogenesis, thus making this tool very helpful for developing potential therapeutic options2,3,4,6. Recent studies have demonstrated that epigenetic regulation by 5-AzadC increases SNCA expression in SK-SN-SH and SH-SY5Y cells8,22. This cytidine analogue passively demethylates by irreversibly trapping DNA methyltransferase I (DNMTI), which positively correlates with higher expression of various genes23. SNCA harbors CpG islands at the regulatory regions encompassing the promoter and intron18,9. It has been shown that hypomethylation of the intron1 CpG island but not the promoter CpG island is strongly associated with PD8. So, we sought to check the methylation status of the 23 CpG sites8 in the SNCA-intron1 by bisulfite sequencing. As expected, a decrease in methylation of intron1 CpG correlated with an increase in transcript levels as measured by the NanoLuc activity. Conventionally, to study the effect of methylation on the promoter’s transcriptional efficiency, that promoter-reporter construct is fully methylated in vitro and the reporter activity is then compared with the unmethylated one8,24. Consistent with our observation for endogenous α-SYN with nanoluc activity, Jowaed et al. showed that in-vitro methylation of regulatory promoter-reporter construct of α-SYN reduces transcription of α-SYN. Studying gene expression this way could lead to different outcome than actual transcriptional state of the target gene as the regulatory region of that gene might exist as partially methylated condition endogenously, which cannot be replicated using the exogenous system. Moreover, comprehensive regulation of the target gene promoter with inputs coming from other local epigenetic modifications such as histone post translational modifications (PTMs)25 and trans factors which are usually present endogenously, might not be able to regulate the exogenously introduced promoter of the same gene.
During genetic typing, we saw that the intensity of the NanoLuc-tagged allele after PCR is relatively weaker when compared to the wild-type PCR product for both the genomic DNA and cDNA (Fig. 1c and Supplementary Fig. 2a). This may be a result of PCR bias towards the amplification of the shorter allele over the longer ones involving reaction in a single tube26. This problem of preferential amplification was overcome by using separate primer set to amplify only the NanoLuc-tagged allele (not encompassing the wild-type allele, Fig. 1c and Supplementary Fig. 4a,b) which could amplify the NanoLuc-tagged allele very efficiently and comparably to the wild-type allele (Fig. 1c and Supplementary Fig. 4b). In addition to using separate set of primers, we used equal number of cycles (30 cycles) to ensure that the PCR products are not saturated, which is indicated by the increase in expression after dopamine treatment. However, the western blot shown in the Fig. 2a indicated that the NanoLuc-tagged α-SYN protein (band shown at ~34KDa) is higher in intensity than the wild type protein (band at ~15KDa) when probed with α-SYN specific antibody. This unequal distribution of protein bands between wild type (low) and NanoLuc-tagged allele (high) may indicate that either that the Nanoluc luciferase has been targeted to α-SYN in more than one allele of the locus, or it is also possible that fusion of a highly stable NanoLuc luciferase protein with α-SYN may affect the stability of the target protein positively. HEK293T cells are not typically diploid, and are instead complex hypo-triploid in nature, containing less than three times the number of chromosomes of a normal diploid human cell27. Our results show that the nanoluc reporter construct is precisely targeted to the end of SNCA and faithfully reports the transcriptional changes of α-SYN.
The advantage of using an endogenous reporter system to study regulation of transcription by epigenetic environment of the gene was highlighted by the data obtained from conventional reporter assays after treatment with different drugs such as 5-AzadC, dopamine and sodium butyrate.
As 5-AzadC inhibits DNA methylation in dividing cells therefore we previously observed that the drug reduced endogenous SNCA-intron1 methylation and increased transcription or nanoluc activity in our endogenous reporter system. However, we did not observe such increase in exogenous SNCA-promoter/intron1 firefly reporter activity upon drug treatment, may be due to lack of DNA methylation in the exogenous plasmid (Fig. 4a first panel). Surprisingly, we observed a significant increase in Renilla luciferase activity upon 5-AzadC treatment (Fig. 4a second panel) and a significant decrease in normalized reporter activity (Fig. 4a third panel). However, the observed decrease in reporter activity can be attributed to CMV-Renilla luciferase activity which, although equally transfected, significantly varied upon 5-AzadC treatment. The mechanism of this apparent variation in Renilla luciferase activity is yet unknown. However, it is known that Renilla luciferase activity can vary significantly upon treatment paradigm depending on the promoter driving its activity. This could lead to erroneous interpretation of the observed data after normalization to Renilla as is a standard protocol for these type of assays28. Therefore it was suggested to use different or multiple endogenous controls in case of employing exogenous reporter systems28.
It was also shown that dopamine can enhance α-SYN transcription in HEK293 cells9. Similarly, we also observed a significant increase in the NanoLuc activity upon dopamine treatment to 293T-SNCA-3′NL cells (Fig. 3b) unlike exogenous promoter-reporter assay (Fig. 4b), which further fortifies the reliability of our endogenous tagging system. This apparent discrepancy between the outcome coming from endogenous and exogenous systems may be attributed to either lack of appropriate crosstalk between cis/trans elements in exogenous reporter system or due to lack of methylation structure in the SNCA promoter-intron1 construct in the plasmid-based luciferase system. Since, the aim of our study was to design a tool that can faithfully monitor changes in endogenous α-SYN transcription at physiological level, the question that we seek to address was whether this NanoLuc-tagged α-SYN reflected accurately the change in transcription of wild-type α-SYN (although present in higher copy) after treatment with dopamine. The comparable increasing trend of mRNA and protein of both the wild-type and the tagged α-SYN after treatment with dopamine (Supplementary Fig. 4b,c) indicated that the engineered cell line could efficiently replicate transcriptional changes of endogenous wild-type α-SYN.
Next we investigated how HDAC inhibitor, sodium butyrate can regulate transcription of SNCA. As the dynamics between histone acetylation or chromatin relaxation and histone deacetylation or chromatin condensation play an important role in regulation of gene transcription29,30, it can be envisaged that the application of HDAC inhibitor would result in hyper-acetylated condition in the gene promoter, which in turn might favor induction in transcription. As expected, we observed a significant increase in the NanoLuc activity in response to sodium butyrate (p<0.001) (Fig. 3d). However, a significant opposite observation was noticed using exogenous reporter system (Fig. 4c). This prominent decrease in the normalized reporter activity can again be attributed to the significant increase of Renilla luciferase activity following sodium butyrate treatment. Interestingly, it has been shown that this HDAC inhibitor can change the overall chromatin structure of the cell and functions through the butyrate response elements on the gene regulatory regions that encompass Sp1/Sp3 binding sites31. Since, SNCA regulatory region contains multiple Sp1/Sp3 binding sites, it is reasonable to assume that recruitment of acetylated Sp1/Sp3 can enhance SNCA expression. Analysis of CMV promoter sequence revealed that it harbors around 5 cognate sequences for Sp1/Sp3 binding, suggesting a possible mechanism for sodium butyrate mediated significant increase in the Renilla luciferase activity. Since, Renilla luciferase plasmid is usually used as endogenous control for this kind of conventional luciferase assay, it is very important to interpret the reporter assay results with caution using this type of transfection controls28.
Transcriptional upregulation of SNCA has long been a concern in PD pathogenesis. Most intellectual effort has been focused on aggregation behavior, resulting in a lacuna of information on transcriptional regulation of this gene despite its immense importance. In this study we developed a novel screening tool that can efficiently monitor SNCA transcript levels under different treatment conditions known to up-regulate transcription. This tool can provide a new diagnostic platform for drug development and testing of compounds believed to regulate SNCA in the cell in an inexpensive and precise way. As the epigenetic environment for this gene regulation is kept unchanged, the effects of treatments would more closely mimic the state seen in the cells than has previously been available. It is also worth mentioning that the stability and sensitivity of this nanoluc luciferase reporter makes it suitable to monitor very low expressing genes which is unlikely to be achievable by any other conventional reporter systems. At this juncture it is also important to mention that our study highlights the importance of using endogenous reporter system over exogenous reporter system particularly for studying comprehensive epigenetic regulation of gene transcription. Specifically this SNCA-NL reporter system is very useful to study the effects of drugs or agents that are known to modulate gene’s chromatin structure or any other epigenetic environment. Therefore previous studies which used exogenous firefly/Renilla-based reporter system to demonstrate the important cis elements of the SNCA promoter or novel transcription factors and pathways for the gene are still useful32,33,34,35.
HEK293T LVX cells were maintained in DMEM (Dulbecco’s Modified Eagle Medium) supplemented with heat-inactivated 10% fetal bovine serum and 1% Penicillin/Streptomycin (Gibco, 10000U/mL). Cells were maintained at 37°C in humidified incubators with 5% CO2 and passaged following trypsinaization with 0.25% Trypsin/0.53mM EDTA (ThermoFisher Scientific).
The vector for cloning of the sgRNA pSpCas9 (BB)-2A-Puro (PX459) was a gift from Feng Zhang Lab (Addgene plasmid # 48139)16. The sgRNA targeting the stop codon area of the SNCA gene was ligated into the pSpCas9(BB)-2A-Puro vector as previously described with minor modifications16 (Table 1). Briefly, sgRNA oligos corresponding to 20 base pairs immediately upstream of –AGG PAM sequence located on the reverse strand at the SNCA stop codon were ligated into pSpCas9(BB)-2A-Puro vector using Fast-Digest BbsI (ThermoFisher Scientific) and T7 ligase (New England Biolabs) by cycling between 37°C and 21°C 10 times for 6 minutes. Ligation reaction was treated with Plasmid-Safe ATP-Dependent DNase (Epicentre) and transformed into CaCl2 competent cells DH5α E. coli by heat shock (42°, 50sec). Plasmid was purified using Gene-Jet plasmid Miniprep Kit (ThermoFisher Scientific) according to manufacturer’s protocol and successful insertion of the sgRNA was confirmed by sequencing.
Primers used for amplification, addition of restriction sites and insert confirmation are listed in Table 1. Approximately 800bp-length homology domains were amplified from HEK293T genomic DNA using Q5-Polymerase (New England Biolabs). Upstream homology arm (Chromosome 4, 89,727,231–89,728,021, reverse strand GRCh38:CM000666) was modified to include a 5′ NotI restriction site and a 3′ SacI restriction site (Fig. 1). Downstream homology arm (Chromosome 4, 89,726,457–89,727,235, reverse strand GRCh38:CM000666) was modified to include a 5′ HindIII cut site and 3′ NotI/AatII cut site. The NanoLuc luciferase sequence was amplified from pNL1.1 vector (a gift from Promega Corporation). To allow for sequential plasmid ligation, NanoLuc coding sequence was modified to include terminal 5′ SacI and 3′ HindIII/AatII restriction enzyme sites. Upstream homology arm and the NanoLuc were ligated together and cloned into NotI and AatII digested pGEM -T Easy vector (Promega Corporation; cat no. A137A) and transformed into competent DH5α cells. Plasmid was purified using Gene-Jet Plasmid Miniprep Kit according to manufacturer’s protocol (ThermoFisher Scientific). Downstream homology arm was then cloned into AatII-digested vector. Completed homology sequence was digested with NotI to release sequence from pGEM -T Easy vector and delete AatII sequence, then ligated into NotI digested pAAV-IRES-hrGFP backbone (2,846bp) and transformed into chemically competent DH5α cells. Presence of insert was confirmed by sequencing.
Vector constructs were transfected into HEK293T LVX (CloneTech) cells using X-Fect Polymer (CloneTech) according to manufacturer’s protocol. Briefly, HEK293T LVX cells were seeded in a 6-well plate with 1×106 and allowed to grow to 80% confluency. X-Fect Polymer was mixed with 1.25μg pSpCas9 (BB)-2A-Puro with SNCA sgRNA and 1.25μg NanoLuc-homology arm donor vector and incubated with cells for 4hours, followed by a change with fresh media. After 48hours, cells were subjected to 5μg/mL puromycin (ThermoFisher Scientific, cat no. AC227420100) selection for 48hours. Surviving puromycin resistant cells were diluted to a single cell level and plated in 96 well plate then allowed to propagate for approximately two weeks. 15 pure colonies were recovered and grown to 50% confluency before passaging them to 1:2 in a 24 well plate.
Genomic DNA of the puromycin resistant colonies was extracted by 16hours incubation in lysis buffer (10mM Tris-HCl pH 7.6, 0.5mM EDTA, 0.67% SDS, 132μg/ml Proteinase-K) at 55°C, followed by precipitation in 100% ethanol with 150mM NaCl. Presence of the NanoLuc insert was confirmed by PCR using NanoLuc forward and reverse cloning primers and identity of insert was confirmed by gene specific confirmation primers in intron 5′ and the 3′ UTR of SNCA using PCR master mix (GenDepot, P0311-200). The details of the “Insert Confirmation primers” are listed in Table 1. Individual bands were excised and sequenced to confirm the sequence to ensure introduction of any mutations and location of insert in the genomic DNA and cDNA (Macrogen USA).
For Western blotting, protein was extracted using RIPA (Radio Immuno Precipitation buffer) buffer (PBS, 1% NP-40, 0.5% Sodium deoxycholate, 0.1% PMSF, 100ng/ml protease inhibitor, dH2O) and 40μg protein were ran on 10% denaturing SDS gel and transferred to PVDF membrane (Millipore cat no. IPFL00010). Following the transfer process, the membrane was fixed in 0.4% PFA in PBS as suggested by Lee et al.36. The membrane was then blocked with Odyssey Blocking Buffer (LI-COR cat no. 927-50000) mixed 1:1 with TBS. Specific protein bands were detected using rabbit anti-α-SYN antibodies (Santa Cruz Biotechnology, cat no. SC-7011R, 1:1000 dilution) overnight and followed by goat anti-rabbit secondary antibodies for fluorescent detection at 680nm (LI-COR, cat no. 926-68020). Western blotting for the experiments related to 48hour dopamine treatment, proteins were extracted as before and transferred to PVDF membrane. Membrane was blocked with 5% milk in TBS-T. Specific protein bands were detected using mouse anti-α-SYN antibodies (BD Transduction Laboratories, cat no. 610786) at 1:250 dilution, followed by goat anti-mouse HRP secondary antibodies for chemiluminescent detection (Jackson Immuno Research laboratories Inc. cat no. 115-035-146).
To measure the NanoLuc luciferase activity, 200,000 cells were seeded per well of a 24 well plate. After 24hours, appropriate treatments were done and incubated for designated periods of time in duplicate. Cells were detached by trypsinization and two wells were combined in a 1.5mL microcentrifuge tube and pelleted at 2,000×g for 3minutes. Cell pellets were resuspended in 500μL colorless DMEM and counted using an automated cell counter (BIORAD, USA) three times and then luciferase activity was monitored in technical triplicate using the Nano-Glo Luciferase Assay System according to manufacturer’s protocol with minor modifications (Promega corporation, cat no. N1110). Briefly, 5,000 cells in 30μL colorless DMEM were assayed using 30μL of assay buffer mixed 1:100 with NanoGlo substrate. Plates were incubated for 5minutes and then luminescence was recorded in triplicate on a multi-plate reader (EnVision, PerkinElmer). This experiment was performed three times independently.
To generate the SNCA promoter luciferase construct, SNCA promoter-intron1 region (−2,200 to +118bp; with respect to ATG) was amplified from HEK293T genomic DNA and cloned into XhoI/HindIII sites of promoter less pGl3 basic vector (Promega, USA, cat no. E1751). The presence of insert was validated by sequencing. For the promoter-reporter assays, 200,000 HEK293T LVX cells were co-transfected with SNCA-pGL3 and CMV-pRL (as a transfection control) vectors in a 24 well plate format. Each well were co-transfected with 500ng of SNCA-pGL3 and 10ng of CMV-pRL plasmids using X-Fect polymer as described above and incubated 24hours before proceeding to any chemical/drug treatments. Following the drug treatments for appropriate time HEK293T LVX cells were collected for lysis. Briefly, cell pellet was lysed in 100μL of Lysis Buffer (25mM Tris-Phosphate Buffer pH 8.0, 4mM EGTA, 2mM DTT, 20% Glycerol & 1% Triton X-100) for 10minutes at room temperature with occasional shaking, then centrifuged at 16,000×g for 5minutes and the lysate was collected in a separate tube. 10μL of this lysate was assayed with 140μL of luciferase assay buffer (25mM Tris-Phosphate Buffer pH 8.0, 4mM EGTA, 20mM MgSO4, 1mM DTT, and 2mM ATP). Firefly luciferase activity (0.75mM luciferin, 10mM DTT) and Renilla luciferase activity (1.5μM Coelenterazine, 100mM NaCl, 25mM Tris pH 7.5) were measured in triplicate using a multi-plate reader (EnVision, PerkinElmer). Relative luciferase activity was measured by normalizing the firefly luciferase activity to Renilla luciferase activity (F/R).
All the treatments were performed in duplicate wells. Compounds used in the study are as follows: Sodium butyrate (Alfa Aeser; cat no. A11079), (5-AzadC) (Sigma, cat no. A3656) and Dopamine hydrochloride (Sigma, cat no. H8502). Sodium butyrate stock was prepared in distilled water at a concentration of 500mM and cells were treated with sodium butyrate for 24hours at 2.5mM and 5.0mM. 5-AzadC stock of 5mM was prepared in 50% acetic acid and immediately aliquoted and frozen. Cells were treated with 10μM 5-AzadC for 72hours, refreshed every 8–12hours8. Dopamine stock was prepared in distilled water at a concentration of 10mM. Cells were treated with 100μM dopamine for 48hours, refreshed every 24hours9. Control wells were treated with respective vehicles for indicated times and no visible cellular toxicity was noticed under aforementioned treatment paradigms.
Genomic DNA from 293T-SNCA-3′NL cells following 5-AzadC treatment was extracted as mentioned above. Approximately, 500ng high quality DNA (260/280>1.8) was used for bisulfite conversion using EZ DNA Methylation-Direct Kit (Zymo Research cat no. D5020) then used as template for PCR amplification of SNCA intron1 region using specific primers designed for bisulfite modified DNA as described in article by Jowaed et al.8. EpiMark Hot Start Taq DNA Polymerase (NEB Inc; cat No. M0490S) was used for PCR and the amplicon was cloned into pGEM -T Easy vector (Promega Corporation). 10 positive colonies were selected for sequencing analysis using T7 universal primer. The sequenced products were analyzed for degree of methylation using BISMA and QUMA software37,38.
RNA was extracted using TRIzol Reagent according to manufacturer protocols (Life Technologies Inc.; cat no. 15596-026). Complementary DNA (cDNA) was generated by conversion of 1μg total RNA using amfiRivert cDNA Synthesis Platinum Master Mix according to manufacturer’s protocol (GenDEPOT; cat no. R5600-50). The cDNA was diluted 1:1 with nuclease free water before PCR. To check the expression of SNCA, amplification was done using primers against the NanoLuc sequence and normalized by the amplification of an endogenous control gene, β-actin. The scheme of the differential amplification of NanoLuc-tagged allele and wild type SNCA alleles are shown in Supplementary Fig. 4a. Details of all the primers are listed in the Table 1.
Statistical analysis was performed using GraphPad Prism 5 (GraphPad Software Inc.). Data are presented as mean±SEM. To get statistically meaningful data, all experiments were performed in technical triplicates. The times change in the NanoLuc luciferase activities in treated groups were calculated by normalizing the value with respective control for each experiment. All the experiments were independently repeated three separate times using separate batches of cells and the means of each experimental set were analyzed. In case of exogenous luciferase reporter assays, minimum of four independent repeats were performed. Statistical significance was determined by comparing means of different groups and conditions using unpaired 2-tailed Student’s t test, and one-way ANOVA. Multiple corrections were made using post-hoc Tukey test, Bonferroni test and Scheffe’s test whenever it was required. Significance was assessed at 95% level.
How to cite this article: Basu, S. et al. A novel tool for monitoring endogenous alpha-synuclein transcription by NanoLuciferase tag insertion at the 3′end using CRISPR-Cas9 genome editing technique. Sci. Rep. 7, 45883; doi: 10.1038/srep45883 (2017).
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The study is supported by the financial support from National Institute of Health vide grant number 5R21NS088923-02 awarded to Y.S.K. S.B. is supported from University of Central Florida’s Graduate Dean’s Dissertation Completion Fellowship. L.A. is recipient of University of Central Florida’s Trustees Doctoral Fellowship. All the financial supports are gratefully acknowledged.
The authors declare no competing financial interests.
Author Contributions S.G. and Y.S.K. conceived the idea and planned the project. S.G. supervised the project. L.A. and S.B. jointly created the 293T-SNCA-3′NL cell line. L.A., S.G. and S.B. jointly performed experiments related to the NanoLuc assays after treatments with dopamine and epigenetic modulators. S.G. did experiments related to assessment of DNA methylation and made the SNCA promoter-intron1 reporter construct. L.A. and S.B. designed the vectors for stable cell line generation. L.A. performed all cloning and also did validation experiments for the NanoLuc assays. S.B. made single cell isogenic colonies, and L.A. validated the presence of NanoLuc. L.A., S.G. and S.B. jointly performed experiments related to luciferase-reporter assays. S.G. and S.B. wrote the manuscript. L.A. prepared all the figures. L.A., S.B., S.G., and Y.S.K. contributed equally in careful reading and editing the manuscript.