A construct with fluorescent indicators for conditional expression of miRNA
© Qiu et al; licensee BioMed Central Ltd. 2008
Received: 14 February 2008
Accepted: 07 October 2008
Published: 07 October 2008
Transgenic RNAi holds promise as a simple, low-cost, and fast method for reverse genetics in mammals. It may be particularly useful for producing animal models for hypomorphic gene function. Inducible RNAi that permits spatially and temporally controllable gene silencing in vivo will enhance the power of transgenic RNAi approach. Furthermore, because microRNA (miRNA) targeting specific genes can be expressed simultaneously with protein coding genes, incorporation of fluorescent marker proteins can simplify the screening and analysis of transgenic RNAi animals.
We sought to optimally express a miRNA simultaneously with a fluorescent marker. We compared two construct designs. One expressed a red fluorescent protein (RFP) and a miRNA placed in its 3' untranslated region (UTR). The other expressed the same RFP and miRNA, but the precursor miRNA (pre-miRNA) coding sequence was placed in an intron that was inserted into the 3'-UTR. We found that the two constructs expressed comparable levels of miRNA. However, the intron-containing construct expressed a significantly higher level of RFP than the intron-less construct. Further experiments indicate that the 3'-UTR intron enhances RFP expression by its intrinsic gene-expression-enhancing activity and by eliminating the inhibitory effect of the pre-miRNA on the expression of RFP. Based on these findings, we incorporated the intron-embedded pre-miRNA design into a conditional expression construct that employed the Cre-loxP system. This construct initially expressed EGFP gene, which was flanked by loxP sites. After exposure to Cre recombinase, the transgene stopped EGFP expression and began expression of RFP and a miRNA, which silenced the expression of specific cellular genes.
We have designed and tested a conditional miRNA-expression construct and showed that this construct expresses both the marker genes strongly and can silence the target gene efficiently upon Cre-mediated induction of the miRNA expression. This construct can be used to increase the efficiency of making cell lines or transgenic animals that stably express miRNA targeting specific genes.
RNAi is a conserved cellular mechanism that can mediate sequence-specific RNA degradation in eukaryotes  and has recently been harnessed for reverse genetics in mammalian cells and transgenic animals [2–5]. Many shRNA and miRNA transgene constructs have been designed and successfully used. The earliest type was composed of a Pol III promoter and a DNA sequence encoding a shRNA [6–10]. This type of constructs was constitutively active and was relatively inefficient in targeting the endogenous genes when pronuclear injection method was used to insert the transgene into the genome [7, 11]. To overcome this limitation, several groups transfected cultured mouse embryonic stem cells, screened for clones where the transgene was active and then used those clones to produce transgenic mice [7, 8, 10]. Other groups used lentivirus to insert transgenes [12–14] or Pol II-promoter-based miRNA expression constructs, which drive the synthesis of a miRNA [15, 16]. These approaches have achieved silencing of endogenous genes and specific loss-of-function phenotypes in transgenic mice.
To further improve the in vivo reverse genetics approach using RNAi, we need to overcome several shortcomings of the currently used transgene constructs. First, extremely high levels of shRNA expression should be avoided because such high levels of shRNA can induce non-specific toxicity . The commonly used Pol III promoter U6 is a very strong and constitutively active promoter  that can drive shRNA expression to a very high level, which may lead to non-specific suppression of the endogenous miRNA expression [19, 20]. By comparison, pol II promoters drive miRNA expression at lower levels and may be advantageous [4, 21].
Second, although the constitutively active constructs work in cells and transgenic mice, a conditional silencing is more desirable. For example, if a target gene is essential, use of constitutively active constructs often yields no useful transgenic founders. This is because once injected into the embryo, the transgene immediately expresses the shRNA or miRNA, resulting in the silencing of the target gene and the death of the embryo. This problem can be avoided by using conditional constructs, which will not express the shRNA or miRNA when first injected, thus allowing the transgenic founders to be generated. Additionally, there is a need in biomedical research to understand hypomorphic phenotypes of a gene in a specific type of cells or at a specific time. A conditional construct will afford investigators this capability.
Third, coexpression of a reporter gene and a miRNA by one promoter can facilitate identification of miRNA expression in cells and in transgenic animals. One strategy for coexpression is to use a miRNA cassette inserted into the 3'UTR of a reporter gene, which has been explored by previous studies [22, 23]. A shortcoming in this design is that the processing of primary miRNA (pri-miRNA) by Drosha will cause the mRNA to lose their 3' polyadenylation, which destabilizes the mRNA and reduces levels of the reporter gene expression. One solution to this problem is to embed the pre-miRNA in an intron as an intronic miRNA, which is common in many genomes . Lin and colleagues  applied this strategy using an artificial in-frame intron placed within the open reading frame (ORF) of a reporter gene. This strategy is ingenious but relatively difficult to apply widely because one has to find sequences required for splicing (AG/GC with exon-splicing enhancers (ESEs) in its proximity) within the ORF, and this sequence requirement cannot always be met in an ORF.
In this report, we designed a new Pol II-based construct that overcomes these shortcomings. This construct uses a Pol II promoter to drive expression of the EGFP gene that is flanked by loxP sites. This feature will allow convenient screening for cells or transgenic mice where the transgene is active. Downstream to the EGFP gene is the gene encoding red fluorescent protein (RFP). In the 3' UTR of the RFP gene, we inserted an artificial intron containing a DNA sequence encoding a pre-miRNA. We show that this construct expresses EGFP under basal conditions. When induced by Cre recombinase, it drives expression of RFP and the miRNA that silences its target gene. We conclude that this construct may be used as a backbone for conditional gene silencing in transgenic mice.
Finding efficient shRNAs against E1k and E2k subunits of KGDHC
Placing miRNA in an intron does not affect the miRNA expression and target silencing but increases the reporter gene expression
Many natural miRNAs are in introns of protein-encoding genes . To determine whether placing a miRNA in an intron can improve the expression of the miRNA and the marker gene, we constructed an artificial intron and placed the pre-miRNA in this intron (pCAG-RFP-miRint, Figure 2A; also see methods). We placed this intron 10 nt-down stream from the stop codon because introns within the 50 nt downstream from the stop codon are found in some eukaryotic mRNAs and do not cause non-sense mediated decay (NMD) . To test whether this intron can be successfully spliced, we extracted RNA from the cells transfected with pCAG-RFP-miRint and carried out RT-PCR across the splicing junction. We found a single band with the size of 212 bps that was expected from the spliced mRNA (Figure 2B). We did not detect any band with the size of 701 bps that would have been derived from the unspliced mRNA (Figure 2B). We sequenced the 212-bp PCR product and confirmed that the intron splicing occurred exactly as expected (see legend of Figure 2B). Thus, the artificial intron functions as designed. To compare pCAG-RFP-miRint with pCAG-RFP-miR, we transfected both constructs into the NF1 cells and determined their knockdown of target genes. By Northern blots, we detected no difference between these two constructs in their degree of knockdown of E1k and E2k mRNAs (Figure 2C), suggesting that intron placement of pre-miRNA encoding sequence does not increase the miRNA production. To confirm this, the pre-miR-E2-4 and miR-E2-4 levels were measured and the levels did not differ between the pCAG-RFP-miR and pCAG-RFP-miRint (Figure 2D). These results suggest that placing a pre-miRNA in an intron does not increase the miRNA expression.
In order to establish whether the enhancing effect of the intron on RFP expression is a result of elevated mRNA levels, we examined RFP mRNA using Northern blot. Addition of intron increased mRNA levels by ~10% (compare lane 3 with lane 2 in Figure 3C). On the other hand, placing the pre-miRNA in the 3'-UTR of the RFP gene reduced the RFP mRNA by ~10–20% (compare lanes 1, 5 and 7 with lane 2 in Figure 3C) and resulted in a lower band (~1.5 kb, lanes 1, 5 and 7 in Figure 3C) that was consistent in size with the band expected from Drosha cropping. By placing the pre-miRNA in the intron, the decrease of mRNA levels caused by the presence of pre-miRNA in the 3'-UTR was largely prevented, and there was no lower band (lanes 4, 6 and 8 in Figure 3C). Overall, the changes in the mRNA levels caused by the addition of the intron did not fully account for the changes in RFP expression, suggesting that other post-transcriptional mechanisms also contribute to the increased levels of RFP expression.
An inducible construct with fluorescent indicators for expression of miRNA
Finally, to determine whether this construct can knock down the target protein levels, we measured KGDHC activity in cells transfected with pCAG-RFP-miRNAint (Figure 5A). We observed a robust knockdown of the KGDHC activity by targeting either the E1k or the E2k subunit (both p < 0.01) (Figure 5E).
We have designed a conditional expression construct for miRNA expression, pCAG-EGFP/RFP-miRNAint (Figure 5A). This construct initially expresses EGFP. When exposed to Cre recombinase, the loxP-flanked EGFP gene is excised, allowing the CAG promoter to drive the expression of the miRNA and the marker RFP. This construct will be useful for generating conditional silencing in transgenic mice and will have several advantages compared with the currently available transgenic silencing constructs. For example, the constitutive Pol III or Pol II promoter-based constructs are inefficient in generating transgenic animals with high levels of knockdown [7, 11]. Although, by screening for transfected ES cells with high levels of knockdown or using lentiviral delivery, transgenic mice with hypomorphic gene functions have been generated [10, 12, 13], these technologies are more complex and more costly than pronuclear injection. Furthermore, it will be difficult to obtain transgenic lines with a high degree of gene silencing if one targets an essential gene, because founders with high levels of shRNA or miRNA expression cannot survive. While this problem might be partially circumvented by expressing miRNA using a tissue-specific promoter , the conditional approach that we have designed here will be more versatile and a superior solution to this problem. By crossing with different Cre-expression lines, one can induce specific gene silencing in many different tissues from a single line of mice made with this conditional construct. Transgenic silencing mice can be made with conditional constructs using pronuclear injection method [2, 43, 44] or using more complex methods such as ES cell screening or lentiviral delivery. In addition, compared with the inducible transgenic RNAi constructs that have been reported in the literature, our conditional construct has the following advantages: It expresses EGFP before induction of the miRNA, thus affording a convenient screen for transgenic lines with desirable expression pattern. When crossed with a Cre driver transgenic line, the coexpression of RFP and miRNA will provide a convenient and precise indication as to in which cell type gene silencing is occurring.
While developing this construct, we compared the effects of placing the pre-miRNA in an intron with the effects of placing the pre-miRNA directly in the 3' UTR of the RFP gene. Our results indicate that placing the pre-miRNA in an intron does not increase the miRNA expression (Figure 2) but enhances the marker protein RFP expression (Figure 3). This conclusion agrees with a previous report, where a pre-miRNA was placed in a 5' intron in the EGFP gene . Our analysis, however, further revealed that the intron enhances the RFP gene expression by two effects. First, intron can directly enhance the protein gene expression (compare bar h with bar g in Figure 3). Second, the pre-miRNA sequence placed in the 3'-UTR exerts an inhibitory effect on the protein gene expression, and this effect can be removed with the elimination of the pre-miRNA sequence by the intron splicing (Figure 3). These findings justify the inclusion of the intron in our conditional miRNA expression construct.
How the pre-miRNA placed in the 3'-UTR inhibits the RFP gene expression and why intron placement of the pre-miRNA eliminates this inhibition remain unknown. One model, as has been proposed , suggests that cropping of the pre-miRNA from the 3'-UTR by Drosha and DGCR8 complex led to a cleavage in the pri-miRNA, resulting in a separation between the 5'-Cap and 3'-poly A and the degradation of the residue mRNA, thereby reducing the RFP expression. By placing the pre-miRNA in an intron, the cropping of the pre-miRNA might occur in the spliced intron lariat. Alternatively, the cropping of pre-miRNA might occur before splicing, but this might not affect splicing . In either case, the integrity of the mRNA will be protected, thus enhancing the RFP expression.
Changes in the RFP expression are consistent with the above models. When the pre-miRNA was present in the 3'-UTR, the RFP expression was decreased (compare bars a, c and e with bar g in Figure 3B) and this decrease was prevented by inhibition of Drosha (Figure 4); when the pre-miRNA was placed in the intron, the RFP expression was enhanced (compare bars a, c and e with bars b, d, and f, respectively) and inhibition of Drosha did not affect the RFP expression (Figure 4). However, at the mRNA level, the presence of pre-miRNA in the 3'-UTR caused only a slight decrease (compare lanes 1, 5 and 7 with lane 2 in Figure 3C); and placing the pre-miRNA in an intron caused a relatively small increase (compare lanes 1, 5 and 7 with lanes 4, 6 and 8). These changes are not sufficient to account for the changes in the RFP expression, thus suggesting that protection of mRNA from Drosha/DGCR8 processing is not the only mechanism whereby the intron placement of the pre-miRNA increases the RFP expression. From our data, it is clear that most of the enhancing effect of RFP expression is derived from the intrinsic properties of the intron, rather than protecting the mRNA from Drosha/DGCR8 cropping.
Our data also show that the presence of a miRNA in an intron does not interfere with intron splicing because the level of mature mRNA produced from the construct with intron alone was not higher than those from the constructs with intron containing pre-miRNA (Figure 3C, compare lane 3 with lanes 4, 6 and 8). Conversely, intron containing the pre-miRNA does not affect the miRNA processing because constructs with or without an intron produced similar levels of miRNA (Figure 2C). Thus, intron splicing and miRNA processing do not interfere with each other in a miRNA-containing intron. This conclusion agrees with a previous study . However, our data also revealed that some pre-miRNA can dampen the intron-enhanced RFP expression (e.g. compare bar b with bar h in Figure 3B), possibly by interfering with the translation-enhancing effect of the intron. This observation indicates that the levels of the reporter gene expression cannot be used to compare the expression levels of different miRNA because the miRNAs may affect the reporter gene expression differently. Nevertheless, the reporter expression levels may be used as an indicator of the same miRNA expression levels in different cell populations, provided that the miRNA processing machinery is not saturated.
Based on our analysis, several improvements in our construct design is worth noting. First, we use a single promoter to drive both the reporter and the miRNA expression. This is advantageous compared with a commonly used design in Pol III-driven shRNA constructs, which places a reporter expression cassette on the same linear sequence with the shRNA expression cassette [12, 13]. Because the synthesis of the reporter and the shRNA are driven by independent promoters, the reporter expression does not necessarily represent the shRNA expression and the degree of silencing. This is especially worrisome in transgenic animals, where a genomic insertion locus may influence different promoters differently. Our construct will not have this problem because the expression of the reporter and the miRNA is driven by a single promoter. Second, the intron-placement of pre-miRNA enhances the reporter expression, which improves from constructs that place the miRNA directly in the 3' UTR of the reporter [22, 23] (Figure 3). Third, our placement of the intron in the 3' UTR makes our construct easily adaptable if one desires to use other reporters. The RFP in our construct can be easily replaced by any other commonly used reporter. This is advantageous compared with the construct using an in-frame intron within the open reading frame , where the reporter cannot be easily replaced.
We have built a conditional miRNA-expression construct that expresses EGFP initially, and upon induction by Cre recombinase, expresses RFP and a miRNA, which mediates efficient silencing of the target gene. This construct can be used to increase the efficiency of making stable cell lines or transgenic animals that stably express miRNA for silencing specific genes.
The pEGFP-U6 short hairpin expression vector (Figure 1A) was constructed by inserting the U6 promoter derived from BSENU6  into pEGFP-N1 (Clontech) at the EcoO109I site (all restriction enzymes were obtained from New England Biolabs unless indicated otherwise). The U6 promoter fragment was amplified by PCR with introduction of EcoO109I sites at both ends using a pair of PCR primers (Forward: 5'-CAAGGCCCTTTGACGTCAATGGGAGTTTGTTTTGG-3'; Reverse: 5'-TTAGGGCCCGAGCGGATAACAATTTCACACAGGAA-3'). Additionally, the multiple cloning site (MCS) in pEGFP-N1 was modified by deleting the fragment between Hind III and Xma I. A shRNA coding sequence was cloned between the restriction enzyme sites PmeI and EcoRI downstream of the U6 promoter.
shRNAs against the E1k and E2k subunits of KGDHC were designed based on the asymmetry rule  as well as other rules . The shRNA sequences were further screened by RNAfold analysis http://www.tbi.univie.ac.at/~ivo/RNA/RNAfold.html, which predicts minimum energy for secondary structures and pair probabilities, to exclude sequences with Tm of intrastrand folds greater than 55°C and by Blast homology searching to select sequences with minimal similarity with other mouse genes. The loop sequence (TTCAAGAGA) and the terminal poly-thymidines (TTTTT) were used for all shRNAs. The sense and antisense strands of shRNAs contain 23 nt. All the sense strands start with a "G" while the antisense strands complement the target mRNA sequences (Figure 1A). To insert shRNAs into the shRNA expression vector pEGFP-U6, two strands of synthetic DNA oligonucletides were annealed and cloned into the vector using the restriction sites PmeI and EcoRI. For each gene target, a total of eight shRNA plasmids were constructed. All constructs were verified by DNA sequencing. Target sequences for E1k are: shR-E1-1, GATGAGAAGATCTTGCACATCAA; shR-E1-2, GCAAGAACTAGCTTTGACGAGAT; shR-E1-3, GTTTCAACAGATTCGGTGCTATT; shR-E1-4, GCACAACCTAACGTCGACAAACT; shR-E1-5, GATGATGCTCCGGTAACTGTTTC; shR-E1-6, GATCTGGTGTGTTATCGACGAAA; shR-E1-7, GCAATTAGGACGTTTCAACAGAT; and shR-E1-8, GCATCGTATATGAGACCTTCCAT. Target sequences for E2k are: shR-E2-1, GTGCAATGCTGACGACTTTCAAT; shR-E2-2, GCAATGCTGACGACTTTCAATGA; shR-E2-3, GAGGTTGACATGAGTAACATACA; shR-E2-4, GGAAGTGGTGTATAGAGATTATA; shR-E2-5, GATATTGAACGGACCATTAATGA; shR-E2-6, GCAGCAGTAGAAGATCCAAGAGT; shR-E2-7, GAGGTTGACATGAGTAACATACA; and shR-E2-8, GCAGATATTGAACGGACCATTAA. The scrambled sequence is shR-Scr, GCGATGCTCTAAGGTTCTATCAA.
For miRNA expression, vectors based on CAG promoter were constructed. The lacZ and the human placental alkaline phosphatase (AP) genes in the pZ/AP vector  were replaced with EGFP, synthesized by PCR from pEGFP-N1 (Clontech), and RFP, synthesized by PCR from pDsRed2-C1 (Clontech), respectively. One cryptic start codon at the 5'UTR of the original AP gene that was not in frame was eliminated. These modifications produced a conditional vector for miRNA expression, pCAG-EGFP/RFP. A synthetic artificial intron (Figure 2A) was designed to contain typical intron splicing regulatory elements [50–52]. This intron was placed 10 nt-downstream of the stop codon of the RFP gene to avoid NMD . A fragment of ~400 bases surrounding the miRNA insertion site was amplified from the first intron of the vector pUbC-miRNA-EGFP  with primers 5'-GCAATGACGCGATCGCTAATGCGGGAAAGCTCTTATTCGGGT-3' (forward) and 5'-AAGGCATGACGCGTTGTTGCGGCCGCCAGAGGTCCGGCGCCTGT-3' (reverse). The amplified fragment was digested using AsiSI and MluI and inserted into the artificial intron as stuff DNA, which can carry a miRNA (Figure 2A). This generated construct pCAG-EGFP/RFP-miRNAint (Figure 5A). By in vitro Cre-mediated excision, EGFP gene along with its poly A was eliminated to generate pCAG-RFP-miRNAint (Figure 5A), which expressed RFP and the miRNA constitutively.
miRNAs targeting E1k and E2k were derived from the shRNA sequences and were designed based on the pre-miR-30a structure (Figure 2A). Each strand of a miRNA was chemically synthesized. Two strands were annealed and cloned into the vector pUbC-EGFP as previously described . The miRNA and its flanking sequences of about 200 bases at both sides from the vector pUbC-miRNA-EGFP were amplified by PCR and cloned to generate the pCAG-EGFP/RFP-miRNAint or pCAG-RFP-miRNAint vectors as described above.
The intron-less control vector pCAG-RFP-miRNA (Figure 2A) was constructed by amplifying the same miRNA and its flanking sequences from pUbC-miRNA-EGFP plasmid with SanDI site at both ends. After digestion with SanDI (Stratagene), the fragment was inserted directly into the 3'-UTR of the RFP gene at the SanDI site. The vectors U6-shR-Drosha and U6-shR-Scr with a shRNA targeting Drosha and a scrambled shRNA, respectively, were described previously .
Cell culture and transfection
Mouse NF-1 cells were maintained in DMEM supplemented with 10% fetal bovine serum (Gibco). Cells were inoculated the day before transfection, which was performed at ~60% cell confluence using Lipofectamine 2000 (Invitrogen) based on the manufacturer's instructions. For pEGFP-U6-shRNA constructs and the constitutive miRNA expression constructs with CAG promoter, 4 μg DNA was used for each well in a 6-well plate. For the conditional miRNA constructs under the control of CAG promoter, 2 μg pCAG-EGFP/RFP-miRNAint and 6 μg CMV-Cre plasmids were cotransfected. In all experiments where multiple plasmids were used, the total plasmid amount was kept constant by supplementing with the empty vector.
Cell images with fluorescence were taken using Zeiss Axiovert S100 microscope equipped with Axiocam camera and appropriate filters and were processed by Openlab software. For fluorescence quantification, total cell lysates were extracted using 1× reporter lysis buffer (Promega) with sonication and subsequent centrifugation. Protein concentrations were determined with BCA protein assay kit (Pierce) according to the manufacturer's instructions. The fluorescence intensity was determined using Tecan Safire microplate reader with appropriate excitation and emission wavelength for EGFP and DsRed2.
Northern blot for mRNA was described previously  and used to determine the target knockdown. Briefly, two days following transfection, cells were harvested and total RNA was extracted using STAT-60 total RNA isolation reagent (Tel-Test). All mouse cDNA clones (Clone ID for E1K: 6417392; clone ID for E2k: 3583936) for probe preparation were purchased from Open Biosystems. Their cDNA sequences were verified by DNA sequencing. DIG-labeled probes were synthesized using the PCR DIG probe synthesis kit (Roche) according to the protocols of the manufacturer. The probe for RFP mRNA was derived from pDsRed2-C1 by PCR using primers 5'-GCCTCCTCCGAGAACGTCATCAC-3' (forward) and 5'-TAATACGACTCA CTATAGGGTGTAGTCCTCGTTGTGGGAGGT-3' (reverse). The E1k probe was derived from E1k cDNA using primers 5'-CACAGTCCCTGGTGGAAGCACA-3' (forward) and 5'-CCATCCGAGGGTCTGTGGTGAAG-3' (reverse). The E2k probe was derived from E2k cDNA using primers 5'-GACCAGGTTACCCTGACAACAGGA-3' (forward) and 5'-GCTGATGGTGAAGGTACCACCATC-3' (reverse). Dig-labeled RNA size marker was obtained from Roche. Northern images were visualized with the LAS-3000 imaging system and quantified by the Multi-Gauge software (FujiFilm).
For small RNA detection, RNA samples were prepared using mirVANA miRNA Isolation Kit (Ambion). Equal amounts of small RNA (1.5 μg) were resolved by 15% Acrylamide Sequagel (National Diagnostics). The RNA was transferred to a Nylon membrane (Ambion) with a semi-dry electroblotter (Owl Scientific). Dig-labeled RNA probes were synthesized with SP6/T7 Transcription Kit (Roche). Template DNA was derived from pCAG-RFP-miR-E1-1int and pCAG-RFP-miR-E2-4int by PCR with primers 5'-GAT CGCTAATGCGGGAAAGCTCTTATTC-3' (forward) and 5'-TAATACGACTCACTATAG GGAAAAAGAAAGAGGATGAATGGTCAG G-3' (reverse). The probe was approximately 450 bases long and included the miRNA and its flanking sequence. Subsequent detection of the signals was done similar to mRNA Northern blotting with a few modifications. For detection of pre-miRNA, the probe was hybridized with the membrane at 50°C overnight and then washed twice at 50°C for 15 min. For detection of mature miRNA, the membrane was hybridized with the probe at 30°C overnight and then washed twice at 40°C for 15 min.
RT-PCR to detect the spliced junction
Transfection of pCAG-RFP-miRNAint vector into NF-1 cells was done as described above. Twenty-four hours after transfection, the RNA was extracted from the cells. The cDNA was synthesized using the SuperScript III CellsDirect cDNA Synthesis Kit (Invitrogen) according to the instructions provided by the manufacturer using the following primers: 5'-GCTGGACATCACCTCCCACAACG-3' (forward) and 5'-ACAGGAGGTGGGGAGCAGGAGA-3' (reverse). The spliced intron would produce a PCR product of 212 bps while the unspliced intron would produce a PCR product of 701 bps. Platinum Taq DNA polymerase (Invitrogen) was used for PCR. The samples were denatured at 94°C for 2 minutes, followed by 35 cycles of (1) denaturation at 94°C for 30 seconds, (2) annealing at 64°C for 30 seconds and (3) extension at 72°C for 60 seconds. The PCR product was fractionated by electrophoresis on a 2% agarose gel. The amplified fragment was further purified by PCR purification kit (Qiagen) for sequencing analysis with the two primers.
KGDHC activity assay
The activity assay for KGDHC was adapted from Shi et al. . Three days after transfection with pCAG-RFP-miR-E1-1int, pCAG-RFP-miR-E2-4int, or pCAG-RFP-miR-Scrint, NF-1 cells in 6-well plates were washed twice with D-PBS buffer (Gibco). Total cell lysates were obtained after adding 250 μl/well of the lysate buffer followed by sonication and centrifgation. The lysate buffer contains 50 mM Tris-HCl (pH 8.0), 1 mM Dithiothreitol (DTT), 0.2 mM K2EGTA, 0.4% Triton X-100, and 50 μM leupeptin (all chemicals were obtained from Sigma unless indicated otherwise). Forty μl of the supernatant was added to the 160 μl activity assay buffer which consists of 63 mM Tris-HCl (pH8.0), 0.63 mM K2EDTA, 1.25 mM MgCl2, 1.25 mM CaCl2, 0.63 mM dithiothreitol (DTT), 0.4 mM thiamine pyrophosphate (TPP), 3.1 mM nicotinamide adenine dinucleotide (NAD), 0.4 mM coenzyme A, 0.13% Triton X-100, and 0.63 mM 2-ME. After 5 minutes incubation at 30°C, 10 μl of 0.1 M α-ketoglutarate was added to the reaction. The change of absorbance at A340 nm was recorded every minute for 18 minutes at 30°C with Tecan Safire microplate reader and the rates of the change were determined. The percentages of the rate relative to control were calculated.
Results were presented as mean ± SE. Data were analyzed by Student's t-test. Differences were considered statistically significant if p < 0.05.
The authors thank Ms. Yuh-Shin Jiang for the technical assistance, Dr. Andras Nagy at University of Toronto for providing the pZ/AP construct, Dr. Alonzo Ross for sharing equipment and Ms. Emily Lumley for critical reading of the manuscript. This work was supported by grants from the ALS Association, NIH/NINDS (RO1NS048145), NIH/NIA (R21 AG028548) and The Robert Pachard Center for ALS Research at Johns Hopkins to ZX.
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