Method Article

Using In Vitro and In-cell SHAPE to Investigate Small Molecule Induced Pre-mRNA Structural Changes

DOI:

10.3791/59021

⸱

January 30th, 2019

 ,  , 
1Calibr, The Scripps Research Institute, 2Department of Integrative Structural and Computational Biology, The Scripps Research Institute

In This Article

Summary

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Detailed protocols for both in vitro and in-cell selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) experiments to determine the secondary structure of pre-mRNA sequences of interest in the presence of an RNA-targeting small molecule are presented in this article.

Abstract

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In the process of drug development of RNA-targeting small molecules, elucidating the structural changes upon their interactions with target RNA sequences is desired. We herein provide a detailed in vitro and in-cell selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) protocol to study the RNA structural change in the presence of an experimental drug for spinal muscular atrophy (SMA), survival of motor neuron (SMN)-C2, and in exon 7 of the pre-mRNA of the SMN2 gene. In in vitro SHAPE, an RNA sequence of 140 nucleotides containing SMN2 exon 7 is transcribed by T7 RNA polymerase, folded in the presence of SMN-C2, and subsequently modified by a mild 2'-OH acylation reagent, 2-methylnicotinic acid imidazolide (NAI). This 2'-OH-NAI adduct is further probed by a 32P-labeled primer extension and resolved by polyacrylamide gel electrophoresis (PAGE). Conversely, 2'-OH acylation in in-cell SHAPE takes place in situ with SMN-C2 bound cellular RNA in living cells. The pre-mRNA sequence of exon 7 in the SMN2 gene, along with SHAPE-induced mutations in the primer extension, was then amplified by PCR and subject to next-generation sequencing. Comparing the two methodologies, in vitro SHAPE is a more cost-effective method and does not require computational power to visualize results. However, the in vitro SHAPE-derived RNA model sometimes deviates from the secondary structure in a cellular context, likely due to the loss of all interactions with RNA-binding proteins. In-cell SHAPE does not need a radioactive material workplace and yields a more accurate RNA secondary structure in the cellular context. Furthermore, in-cell SHAPE is usually applicable for a larger range of RNA sequences (~1,000 nucleotides) by utilizing next-generation sequencing, compared to in vitro SHAPE (~200 nucleotides) that usually relies on PAGE analysis. In case of exon 7 in SMN2 pre-mRNA, the in vitro and in-cell SHAPE derived RNA models are similar to each other.

Introduction

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Selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) is a method of measuring the kinetics of each nucleotide in an RNA sequence of interest and elucidating the secondary structure at single-nucleotide resolution1. SHAPE methodologies, both in in vitro conditions2,3,4 (purified RNA in a defined buffer system) and in living mammalian cells5,6, have been developed to investigate the secondary structure of medium length RNA sequences (typically <1,000 nucleotides for in-cell SHAPE and <200 nucleotides for in vitro SHAPE). It is particularly useful to evaluate structural changes in receptor RNA upon binding to RNA-interacting small molecule metabolites2,4,7,8 and to study mechanistic actions of RNA-targeting molecules during drug development9,10.

RNA-targeting drug discovery has recently drawn attention in academic laboratories and the pharmaceutical industry11,12 via different approaches and strategies13,14,15,16. Recent examples of RNA-targeting small molecules for clinical use include two structurally distinct experimental drugs, LMI-07017 and RG-791618,19, for spinal muscular atrophy (SMA), which showed promising results in phase II clinical trials20. Both molecules were demonstrated to target survival of motor neuron (SMN) 2 pre-mRNA and regulate the splicing process of the SMN2 gene6,17,21. We previously demonstrated the application of in vitro and in-cell SHAPE in an examination of the target RNA structural changes in the presence of an analog of RG-7916 known as SMN-C26.

In principle, SHAPE measures the 2'-OH acylation rate of each nucleotide of an RNA sequence in the presence of excess amounts of a self-quenching acylation reagent in an unbiased manner. The acylation reagent is not stable in water, with a short half-life of (e.g., T1/2 = 17 s for 1-methyl-7-nitroisatoic anhydride; or 1M7, ~20 min for 2-methylnicotinic acid imidazolide, or NAI)22 and insensitivity to the identity of the bases23. This results in a more favorable acylation of the 2'-OH groups of flexible bases, which can be transformed into an accurate assessment of the dynamics of each nucleotide. Specifically, a nucleotide in a base-pair is usually less reactive than an unpaired one to a 2'-OH modifying reagent, such as NAI and 1M7.

Looking at the source of the RNA template and where 2'-OH acylation takes place, SHAPE can generally be categorized into in vitro and in-cell SHAPE. In vitro SHAPE uses purified T7 transcribed RNA and lacks a cellular context in experimental designs. In in-cell SHAPE, both the RNA template transcription and 2'-OH acylation occur within living cells; therefore, the results can recapitulate the RNA structural model in a cellular context. In-cell SHAPE has been referred to as in vivo SHAPE for the SHAPE carried in living cells in the literature24. Since this experiment is not performed in an animal, we termed this experiment as in-cell SHAPE for accuracy.

The strategies for the primer extension stage of in vitro and in-cell SHAPE are also different. In in vitro SHAPE, reverse transcription stops at the 2'-OH acylation position in the presence of Mg2+. A 32P-labled primer extension therefore appears as a band in polyacrylamide gel electrophoresis (PAGE) and the intensity of the band is proportional to the acylation rate1. In in-cell SHAPE, reverse transcription generates random mutations at the 2'-OH adduct position in the presence of Mn2+. The mutational rate of each nucleotide can be captured by in depth next-generation sequencing, and the SHAPE reactivity at single-nucleotide resolution can then be calculated.

A potential problem for in-cell SHAPE is the low signal-to-noise ratio (i.e., a majority of the 2'-OH groups is unmodified, while the unmodified sequences occupy most of the read in next-generation sequencing). Recently, a method to enrich the 2'-OH modified RNA, referred to as in vivo click SHAPE (icSHAPE), was developed by the Chang laboratory25. This enrichment method may be advantageous in studying weak small molecules such as RNA interactions, especially in a transcriptome-wide interrogation.

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Protocol

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1. In Vitro SHAPE

NOTE: The protocol is modified from the published protocol1.

  1. Preparing the RNA template
    NOTE: The template for T7 transcription was ordered as a synthetic double-stranded DNA (dsDNA) and amplified by either insertion into an E. coli vector that carries a unique pair of EcoRI/BamHI restriction endonuclease sites, such as pET28a, or by PCR. The protocol for PCR amplification is illustrated below.
    1. Mix the following material: 50 μL of PCR master mix (see Table of Materials), 2 μL for each primer in 10 μM (see Table 1 for sequences), 200 ng of dsDNA template in 2 μL and 3 μL of dimethyl sulfoxide (DMSO), and 41 μL of H2O. Aliquot into two PCR tubes (each tube contains 50 μL of reaction mixture).
    2. Set up the thermal cycler as follows: stage 1) 95 °C for 30 s; stage 2) 95 °C for 20 s; stage 3) 56 °C for 20 s; stage 4) 72 °C for 20 s; stage 5) loop back to stage 2 for 30 cycles; stage 6) 72 °C for 3 min; and stage 7) infinite holding at 4 °C until the following step.
    3. Purify the PCR amplicon by extraction of gel slices (see Table of Materials and use the manufacturer’s protocol). Elute the product DNA with 35 μL of Tris-EDTA (TE) buffer, containing 10 mM Tris (pH 8.0) and 1 mM EDTA, to yield a 0.1–0.5 μg/μL template. Normalize the purified DNA template into 0.10 μg/μL.
      NOTE: Optionally, the quality of the template may be analyzed on a 1.8% agarose gel electrophoresis with 0.10 μg of DNA. A single band of desired template DNA is expected on the gel.
    4. Set up the T7 transcription reaction (total volume 40 μL) by adding the following materials into a PCR tube: 4 μL of 10x reaction buffer, 4 μL of ATP, 4 μL of CTP, 4 μL of GTP, 4 μL of UTP, 4 μL of T7 enzyme (see Table of Materials), 4 μL of purified PCR amplicon from step 1.1.3 (0.4 μg), and 12 μL of diethyl pyrocarbonate (DEPC)-treated water. Mix by pipetting up and down 4x. Incubate at 37 °C for 4–16 h in a thermal cycler or in a 37 °C incubator.
      NOTE: Start to set up step 1.1.6 while the reaction in step 1.1.4 is ongoing.
    5. Add 2 μL of DNase, mix by pipetting up and down 4x, and incubate at 37 °C for 15 min. Mix with equal volume of 2x Tris-borate-EDTA (TBE)-urea sample buffer (see Table of Materials). Heat at 70 °C for 3 min to inactivate.
    6. In an RNase-free bottle, mix 75 mL of 40% acrylamide/bisacrylamide solution (29:1, see Table of Materials), 180.2 g of urea, and 50 mL of 10x TBE buffer (RNase-free, see Table of Materials). Put the bottle on an orbital shaker (250 rpm) until all crystals of urea are dissolved (may take up to 2 h). Adjust the volume to 500 mL with DEPC-treated water. Filter the solution with a 0.2 μm membrane (see Table of Materials).
      NOTE: In this process, avoid using specular and stir-bar to prevent RNase contamination. The solution can be stored at 4 °C for up to 1 year.
    7. Clean two electrophoresis glass plates of a proper size (16.5 cm x 24 cm) with deionized water and 70% EtOH using a piece of wiping paper. Align the plates with a pair of 2.0 mm spacers (the plate with a siliconized surface is facing inward) and seal the edge of the plates with tape. Double-tape the corner of the plate to prevent leaking.
    8. In a beaker, mix 200 mL of acrylamide solution from step 1.1.6, 2.0 mL of 10% ammonium persulfate solution, and 100 μL of tetramethylethylenediamine (TEMED) with an RNase-free pipette tip by stirring rapidly for 30 s. Tilt the plates on a piece of benchtop cover and pour the solution from the gap of the plates. Tap the plate to lift any bubbles and lay the plate flat on the benchtop cover. Immediately insert the comb and let the gel polymerize for at least 1 h.
      NOTE: If the gel is to be used within the next day, cover the top of the gel with a piece of wet paper towel and wrap up with a larger piece of plastic wrap. Place it lying flat at 4 °C.
    9. Remove the tape and clamp the plate in an electrophoresis stand. Remove the comb and add adequate 1x TBE buffer at the top and bottom of the reservoir. Pre-run the gel for 30 min at 20 W.
      NOTE: Optionally, if the content of the desired RNA is ~90% or more, a mini-gel can be used in substitution of a preparative gel.
    10. Wash each of the loading wells by pipetting up and down twice with the liquid in the reservoir. Add crude RNA from step 1.1.5 into the wells. Run the gel at 20 W until the xylene cyanol FF dye (light blue) passes about two-thirds of the gel’s length (~60 min).
      NOTE: Ensure to load no more than one-third of the height of the well (use multiple wells if necessary).
    11. Immerse the gel in 1x TBE buffer with 1:10,000 dilution of the safe dye (see Table of Materials) in a container large enough for the gel. Put the container on an orbital shaker for 5 min at 80 rpm.
    12. Under UV light, identify the desired RNA band and swiftly cut a thin band of the gel using a clean razor blade. Place 1–2 gel slices in a 1.7 mL tube.
    13. Recover the RNA from the gel slice by passive elution. Add adequate elution/precipitation mix (~0.3 mL per slice) to each tube: 0.3 M NaOAc (pH 5.2), 2.5 M LiCl, 1 mM EDTA, 0.1% sodium dodecyl sulfate (SDS) in DEPC-treated water. Rotate the tube that contains the gel splice(s) at 4 °C for 16 h.
      NOTE: A typical recovery rate is ~75% in this step. To increase the yield, remove and collect the eluent and add the same volume of elution buffer, then repeat this step.
    14. Combine the eluent in a new 1.7 mL tube. Add 2.5x ice-cold EtOH, invert the tubes six times to mix the liquid, and place the tubes at -80 °C for at least 1 h.
    15. Centrifuge for 10 min at 10,000 x g and 4 °C. Carefully remove the supernatant by pipetting. Wash the RNA pellet by adding 80% EtOH (1 mL per tube), vortex for 15 s, and centrifuge for 10 min at 10,000 x g and 4 °C.
    16. Remove the supernatant and air-dry the RNA pellet for 5 min. Add 50 μL of RNase-free water and mix by pipetting up and down 10 times. Normalize the RNA concentration to 0.10 μg/μL. Store the purified RNA at -80 °C.
      NOTE: Do not over-dry the RNA pellet.
    17. Optionally, to analyze the quality of the RNA, dilute 1 μL (100 ng) of RNA from step 1.1.16 in 5 μL of water and mix with 5 μL of 2x TBE-urea sample buffer. Then, heat at 70 °C for 3 min and load on a 6% TBE-urea mini-gel.
      1. Run the gel at 180 V for 1 h. Perform the staining as done in step 1.1.11. Visualize the gel with UV in an imaging system. A single band is expected at the desired length.
  2. Preparing the 32P-labeled primer
    1. Set up the reaction by mixing the following materials: 10 μL of γ-32P-ATP (~1.5 mCi, ~25 μM, see Table of Materials), 2 μL of reverse transcription (RT) primer (100 μM, for sequence see Table 1), 2 μL of 10x T4 polynucleotide kinase (PNK) reaction buffer, 1 μL of T4 PNK (see Table of Materials), and 5 μL of RNase-free water. Incubate at 37 °C for 1 h.
      CAUTION: Proper protection is need for steps 1.2-1.5 in an authorized workplace for radioactive materials. 
    2. Heat-inactivate for 20 min at 65 °C. Add the samples onto a desalting column and centrifuge at 1,000x g for 1 min. Mix the eluent with 25 μL of 2x TBE-urea sample buffer. .
      NOTE: Store the labeled crude product at -20 °C if it is not to be immediately purified.
    3. Run a 10% acrylamide gel at 20 W for 1 h.
      CAUTION: Load the 32P-labeled primer from step 1.2.1 onto the gel and avoid bleeding the radioactivity into the top reservoir. Do not load more than one-third of the height of the well to ensure a thin band on the gel (use multiple wells if necessary). The liquid in the bottom reservoir can be highly radioactive.
    4. Remove the glass plates of the gel cassette and lay the gel on a piece of plastic wrap. Fold the plastic wrap to cover the top of the gel to make an air-tight sandwich. Place the gel sandwich on a calcium tungstate phosphor screen and expose with an imaging instrument. Image the gel again with regular light to know where the edges of the gel are.
    5. Use an image processing software to overlay the two images. Align the gel on to the printed image. Use a fresh razor blade to cut the desired bands out of the gel . Place 1 to 2 gel slices in a 1.7 mL tube.
      NOTE: Make sure the printed image has the same size as the actual gel. Double check the alignment by imaging the leftover gel again after cutting out the gel slice.
    6. Recover the 32P-labeled primer by following steps 1.1.13 to 1.1.16. Take 1.0 μL of solution into a 0.4 mL tube and dilute the primer with 1x TE buffer to obtain the radioactivity of 1.0 μL at ~100,000 cpm. Store the purified 32P-labeled primer at -80 °C until RNA 2’-OH modification reaction but for no longer than 4 weeks.
  3. Small molecule binding and RNA 2’-OH modification
    1. To prepare four samples, add 8 pmol RNA in 32 μL of 0.5x TE buffer to a 1.7 mL tube, heat at 80 °C for 2 min, and snap-cool on ice for at least 1 min.
      NOTE: Use the following equation to calculate the approximate molecular weight of RNA: MW = (# of bases) x 340 Da.
    2. Add 8 μL of 5x folding mix containing 500 mM HEPES (pH 8.0), 20 mM MgCl2, and 500 mM NaCl. Aliquot 9 μL of the RNA mixture into each of the four PCR tubes and label them #1-#4. Add 1 μL of 10% DMSO into the #1 tube, 1 μL of concentrated small molecule solution (10% DMSO) into #2, 1 μL of diluted small molecule solution (10% DMSO) into #3, and 1 μL of water into #4.
    3. Incubate the PCR tubes at 37 °C in a thermal cycler for 30 min.
    4. Right before the 2’-OH modification reaction, dilute 1 μL of NAI stock solution (2 M) with 3 μL of DEPC-treated water to yield a 0.5 M working solution. Without delay, add 1 μL of NAI working solution into tubes #1, #2, and #3, and 1 μL of 25% DMSO into #4. Incubate at 37 °C in a thermal cycler for 15 min.
    5. Add 100 μL of elution/precipitation mix (see step 1.1.13 for recipe), 2 μL of glycogen (15 mg/mL), and transfer all the liquid in each PCR tube into a 1.7 mL tube. Add 0.34 mL of ice-cold 200-proof EtOH (3x volume) into each tube. Mix by vortexing for 5 s and place the tubes in a -80 °C freezer for at least 1 h.
      NOTE: During this period, start setting up the sequencing gel to be used in step 1.5.1.
    6. Centrifuge for 15 min at 14,000 x g and 4 °C. Remove the supernatant without disturbing the RNA pellet. Wash the RNA pellet by adding 80% EtOH (0.5 mL per tube), vortex for 15 s, and centrifuge for 15 min at 20,000 x g and 4 °C. Remove the supernatant again.
      NOTE: Optionally, use a Geiger counter to ensure the radioactive pellet retaining in the tube.
    7. Air-dry the RNA pellet for 5 min. Add 9 μL of RNase-free water and mix by pipetting up and down 10 times.
      NOTE: Do not over-dry the RNA pellet. All precipitation is expected to be dissolved at the end of this step.
  4. Marker preparation and primer extension
    1. Transfer the modified RNA into 4 new PCR tubes and label them #1-#4 as previously. Add 2 pmol control RNA in 7 μL of DEPC-treated water to 4 additional PCR tubes and label them #5–#8. Add 2 μL of radiolabeled primer (step 1.2.6) in all eight tubes. Heat to anneal at 65 °C for 5 min, then immediately cool down to 4 °C in the thermal cycler.
    2. Add 4 μL of 5x RT buffer (see Table of Materials), 1 μL of dithiothreitol (DTT, 0.1 M), and 1 μL of dNTP mix (10 mM each) to each of the eight PCR tubes.
    3. Add 2 μL of DEPC-treated H2O to tubes #1–#4. Add 4 μL of ddATP (5 mM), 4 μL of ddTTP (5 mM), and 4 μL of ddCTP (5 mM) into tubes #5–#7, respectively. Add 1 μL of ddGTP (5 mM) and 3 μL of DEPC-treated water to tube #8. Pipette four times to mix.
    4. Heat at 52 °C for 1 min in the thermal cycler. Add 1 μL of reverse transcriptase (see Table of Materials), then mix by pipetting up and down four times. Incubate the reaction at 52 °C for 20 min.
    5. Add 1 μL of 5 M NaOH into each of the tubes to hydrolyze the RNA. Heat the tubes at 95 °C for 5 min.
    6. Add 5 μL of 1 M HCl and repeat the ethanol precipitation (steps 1.3.5 and 1.3.6), except omit the glycogen and liquid transfer.
      NOTE: Omitting step 1.4.6 results in a blurring region in the middle of the gel known as the “salt front”.
    7. Air-dry the DNA pellet for 5 min. Add 10 μL of H2O and 10 μL of 2x TBE-urea sample loading buffer and pipette up and down 10 times to redissolve. Heat at 70 °C for 5 min. Place the tubes on ice before loading onto the gel.
  5. PAGE analysis
    1. To prepare an 8% polyacrylamide sequencing gel, follow steps 1.1.6 to 1.1.10 with the following modifications: use 100 mL of 40% acrylamide/bisacrylamide solution (29:1) to prepare an 8% acrylamide solution, and use sequencing gel glass plates (e.g., 46 x 57 cm) with a 0.4 mm spacer.
    2. Load 10 μL of the sample from step 1.4.7. Run the gel at 65 W for 2 h or until the bottom dye reaches 3/4 of the gel.
      NOTE: Store the rest of the samples at -80 °C for repeating if needed.
    3. Remove the top siliconized glass plate by removing the spacer and gently inserting a spatula. Place a piece of large filter paper to cover the gel and press gently to allow the gel to adhere to the filter paper. Starting from the bottom end, lift the filter paper and remove the gel from the glass plate together.
    4. Place the gel together with the filter paper on a piece of plastic wrap that is large enough to cover the whole gel (filter paper facing up). Transfer the filter paper/gel/plastic wrap sandwich to a gel drier with the filter paper side facing down.
      CAUTION: To avoid radioactive material contamination, use 3 to 4 more pieces of large filter paper between the gel sandwich and gel drier.
    5. Dry the gel at 70 °C for 1 h with a vacuum. Transfer the gel sandwich onto a photo-bleached phosphor storage screen cassette. Expose the radioactivity of the gel to the screen for 4–16 h.
    6. Place the phosphor storage screen on an imaging device and scan with medium resolution (~30 min).
      NOTE: If a smile-like artifact is present on the gel image, use correcting software (e.g., SAFA) to process the image to a publishable quality. Keep in mind that the standard marker lane is 1 nucleotide longer than the 2’-OH modification lanes.

2. In-cell SHAPE

  1. Primer design
    NOTE: Unlike in vitro SHAPE, in-cell SHAPE does not need to design an expression cassette. However, an optimal primer set should be used and must be evaluated before SHAPE experiment.
    1. Generate at least three unique primer pairs by a BLAST-based primer design tool (e.g., Primer-BLAST). To study pre-mRNA in human cells, select the human genome (not transcriptome) as a reference database in Primer Pair Specificity Checking Parameters. Pick the size of amplicon in the range of 200–1,000 base-pair (bp).
    2. Extract the genomic DNA from ~106 cells of interest with a spin column-based method with the treatment of RNase A and protease K (see Table of Materials and use the manufacturer’s protocol). Normalize the purified genomic DNA in 0.1 μg/μL TE buffer.
    3. Test PCR with the protocol performed in steps 1.1.1 and 1.1.2.
      NOTE: The desired primer set should yield a single band on a 1.8% agarose gel.
  2. Cell preparation and 2’-OH modification
    NOTE: To increase the abundance of the pre-mRNA of interest, a minigene with the correct sequence under cytomegalovirus (CMV) promoter for constitutive expression is transfected into the host cells.
    1. Pre-warm the culture medium containing 10% fetal bovine serum (FBS) and 1x antibiotic mixture in Dulbecco's Modified Eagle Medium (DMEM) at 37 °C. Seed 293T cells at 50% confluency 24 h prior to the transfection in culture medium. Change the medium into 2% FBS in DMEM without antibiotics ~1 h prior to the transfection.
    2. Add 10 μg of minigene plasmid into 100 μL of reduced serum media (see Table of Materials) in 1 well of a 96-well plate. Pipette the solution up and down four times to mix.
    3. Add 40 μL of transfection reagent (see Table of Materials) into 100 μL of reduced serum media in another well of the plate. Pipette up and down four times to mix. Incubate at room temperature for 5 min.
    4. Add the entire plasmid solution to the transfection reagent suspension. Pipette up and down four times to mix. Incubate at room temperature for 30 min.
    5. Add the entire DNA/ transfection reagent mixture dropwise on the surface of the medium throughout the dish. Incubate at 37 °C for 6–12 h.
    6. Aspirate the medium and gently wash once with 5 mL of phosphate-buffered saline (PBS, pH 7.4, without CaCl2 and MgCl2, see Table of Materials). Trypsinize the cells with 3 mL of trypsin solution. Incubate at room temperature for 5 min.
    7. Knock the dish gently to dissociate the cells from the bottom of the dish. Neutralize trypsin with 6 mL of culture medium. Centrifuge at 300 x g for 4 min and remove the medium.
    8. Resuspend the ~106 cells for each sample in 199 μL of reaction medium (1% FBS in DMEM) and transfer the cell suspension into a 96-well plate. Incubate the cells with 1 μL of compound working solution or 1 μL of DMSO in all three controls for 30 min at 37 °C.
      NOTE: Three control samples should be included: DMSO control with NAI, denatured RNA with NAI, and NAI negative control.
    9. Add 10 μL of 2 M NAI to each sample, except for the denaturing control (DC) RNA and NAI negative controls. Pipette up and down four times to mix. Incubate at 37 °C for 15 min. Gently shake the plates to re-suspend the cells every 5 min.
    10. Transfer the cells into 1.7 mL tubes and centrifuge at 400 x g for 2 min without delay. Remove the supernatant without disturbing the cell pellet.
    11. Add 0.4 mL of guanidinium thiocyanate (see Table of Materials). Vortex for 15 s to homogenize. Incubate the samples at room temperature for 5 min.
      NOTE: The samples can be stored at -20 °C until proceeding to the next step.
  3. RNA extraction
    1. Add 0.2 mL of chloroform to each of the guanidinium thiocyanate homogenized samples. Vortex for 15 s. Incubate at room temperature for 2 min.
    2. Centrifuge for 5 min at 12,000 x g and 4 °C. The top colorless aqueous layer contains RNA. Transfer ~380 μL of aqueous solution into a new 1.7 mL tube.
      CAUTION: Do not disturb the interphase to avoid contamination.
    3. Add 1.5x volume of EtOH (~570 μL). Vortex for 15 s to mix.
    4. Transfer 600 μL of RNA mixture into an RNA isolation spin-column (see Table of Materials). Centrifuge at 12,000 x g for 15 s. Discard the eluent. Repeat this step to pass through all liquid into the same spin column.
    5. Wash the column with 0.35 mL of RW1 buffer (see Table of Materials) by spinning for 15 s. Add 80 μL of RNase-free DNase I in RDD buffer (see Table of Materials). Incubate at room temperature for 20 min.
      NOTE: It is critical to remove all DNA contamination.
    6. Subsequently wash the column with 0.35 mL of RW1 buffer and 0.6 mL of 2x RPE buffer (see Table of Materials) by spinning for 15 s at each step. Dry the column by centrifuging the spin column with an empty collection tube at 12,000 x g for 1 min.
    7. Add 32 μL of RNase-free water to the center of the column. Incubate for 1 min. Centrifuge at 12,000 x g for 30 s to obtain ~30 μL of purified RNA solution. Put the samples at -20 °C while processing the denatured sample.
  4. Denatured RNA control preparation
    1. Place 30 µL RNA sample for DC in a 1.7 mL plastic tube on ice. Add 50 μL of formamide and 15 μL of DC buffer containing 300 mM HEPES (pH 8.0) and 25 mM EDTA into the tube.
    2. Heat to denature the RNA at 95 °C for 1 min. Quickly add 5 μL of NAI stock solution (2 M), then flick twice to mix and put the tube back on to the heating block. Incubate at 95 °C for an additional 1 min then immediately put the tube on ice.
    3. Add 0.4 mL of guanidinium thiocyanate. Repeat steps 2.3.1–2.3.4.
    4. Wash the column with 0.6 mL of 2x RPE buffer (see Table of Materials) by spinning for 15 s at each step. Dry the column by centrifuging the spin column with an empty collection tube at 12,000 x g for 1 min.
    5. Add 32 μL of RNase-free water to the center of the column. Incubate for 1 min. Centrifuge at 12,000 x g for 30 s to obtain ~30 μL of recovered DC RNA solution.
  5. Primer extension
    1. Normalize the RNA solution from 2.3.7 and 2.4.5 into 0.5 μg/μL with RNase-free water. Freshly prepare 30 mM MnCl2 solution from MnCl2∙4H2O powder.
    2. Transfer 9 μL of RNA solution for each sample into a PCR strip. Add 1 μL of 10 mM dNTP and 1 μL of 2 μM gene-specific primer (GSP) in each tube. Pipette up and down four times to mix. Incubate at 65 °C for 5 min in a thermal cycler and put on ice for >1 min.
      NOTE: Alternatively, 1 μL of a random nonamer can be used in substitution of GSP.
    3. In each PCR tube, add a mixture of 2 μL of 10x RT buffer (see Table of Materials), 4 μL of 30 mM MnCl2, and 2 μL of 100 mM DTT. Pipette up and down 4x to mix. Incubate at 42 °C for 2 min.
    4. Add 1 μL of reverse transcriptase (see Table of Materials). Pipette up and down 4x to mix. Incubate at 42 °C in a thermal cycler for 3 h.
  6. Library preparation and next-generation sequencing
    1. Set up a PCR reaction by adding 1 μL of DNA polymerase, 5 μL of 10x DNA polymerase buffer (see Table of Materials), 2 μL of DMSO, 1.5 μL for each of the primers (10 μM), 34 μL of H2O, and 5 μL of cDNA from step 2.5.4.
    2. Set up the thermal cycler as follows: stage 1) 95 °C for 2 min; stage 2) 95 °C for 30 s; stage 3) 60 °C for 30 s; stage 4) 68 °C for 30 s; stage 5) loop back to stage 2 for 30 cycles; stage 6) 68 °C for 3 min; and stage 7) infinite holding at 4 °C until the following step.
    3. Purify the amplicon by using 1.8% agarose gel.
      NOTE: The PCR band should appear as a single band on the gel.
    4. Construct the library by using standard fragmentation and ligation methods established in the literature6,26.
    5. Sequence on a next-generation sequencing equipment using 1 x 75 single-end reads to generate approximately 10 million reads per sample.
    6. Analyze the results using ShapeMapper and SuperFold software packages developed by the Weeks group26.

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Results

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We previously demonstrated that an RNA splicing modulator, SMN-C2, interacts with AGGAAG motif on exon 7 of the SMN2 gene's pre-mRNA, and used SHAPE to assess the RNA structural changes in the presence of SMN-C26. The binding site of SMN-C2 is distinct from the FDA-approved antisense oligonucleotide (ASO) for SMA, nusinersen, which binds and blocks the intronic splicing silencer (ISS) on intron 727,28 (

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Discussion

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In in vitro SHAPE, it is critical to use high quality homogeneous RNA template. T7 transcription, however, often yields heterogeneous sequences36. Especially, sequences with ±1 nucleotide at the 3'-terminus with non-negligible yields36 are usually difficult to be removed by polyacrylamide gel purification. Heterogeneous RNA template can result in more than one set of the signal in the sequencing gel profiling of the primer extension product, which sometimes makes i...

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Disclosures

$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

The authors declare no conflict of interest.

Acknowledgements

$$\rightleftharpoonup{xx}$$ $$\longleftharp{xx}$$, $$\longrightharp{xx}$$,

This work was made possible by the NIH R01 grant (NS094721, K.A.J.). 

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
DNA oligonucleotideIDTgBlock for >200 bp DNA synthesis
Phusion Green Hot Start II High-Fidelity PCR Master MixThermo FisherF566S
NucleoSpin gel and PCR clean-up kitTakara740609.50
MegaScript T7 transcription kitThermo FisherAM1333Contains 10x reaction buffer, T7 enzyme, NTP and Turbo DNase
DEPC-treated waterThermo Fisher750023
2x TBE-urea sample bufferThermo FisherLC6876
40% acrylamide/ bisacrylamide solution (29:1)Bio-Rad1610146
10x TBE bufferThermo Fisher15581044
Nalgene Rapid-Flow™ Filter UnitThermo Fisher166-0045
KimwipeKimberly-Clark34133
TEMEDThermo Fisher17919
SYBR-Safe dyeThermo FisherS33102
6% TBE-urea mini-gelThermo FisherEC6865BOX
ChemiDocBio-Rad
T4 PNKNEBM0201S
γ-32P-ATPPerkin ElmerNEG035C005MC
Hyperscreen™ Intensifying ScreenGE HealthcareRPN1669calcium tungstate phosphor screen
phosphor storage screenMolecular DynamicsBAS-IP MS 3543 E
Amersham TyphoonGE Healthcare
NAI (2M)EMD Millipore03-310
GlycoBlueThermo FisherAM9515
SuperScript IV Reverse TranscriptaseThermo Fisher18090010Contains 5x RT buffer, SuperScript IV
dNTP mix (10 mM)Thermo FisherR0192
ddNTP set (5 mM)SigmaGE27-2045-01
large filter paperWhatman1001-917
Gel dryerHoeferGD 2000
QIAamp DNA Blood Mini KitQiagen51104Also contains RNase A and protease K
SMN2 minigene34Addgene72287
Heat inactivated FBSThermo Fisher10438026
Pen-StrepThermo Fisher15140122
Opti-MEM IThermo Fisher31985062
FuGene HDPromegaE2311
TrpLEThermo Fisher12605010
DPBS without Ca/MgThermo Fisher14190250
TRIzolThermo Fisher15596018
RNeasy mini columnQiagen74104Also contains RW1, RPE buffer
RNase-Free DNase SetQiagen79254Contains DNase I and RDD buffer
Deionized formamideThermo FisherAM9342
MnCl2•4H2OSigma-AldrichM3634
random nonamerSigma-AldrichR7647
SuperScript First-Strand Synthesis SystemThermo Fisher11904-018Contains 10x RT buffer, SuperScript II reverse transcriptase
AccuPrime pfx DNA polymerseThermo Fisher12344024
NextSeq500Illumina
NucAway columnThermo FisherAM10070for desalting purpose

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Tags

In Vitro SHAPEIn cell SHAPEPre mRNARNA Structural ChangesSmall MoleculeRNA TargetingSecondary StructureNucleotide DynamicsRadio Label Reverse TranscriptionPolynucleotide KinaseDesalting ColumnAcrylamide GelPhosphor Screen ImagingImage processing SoftwareElution Precipitation MixCentrifugation