Materials and reagents

Axygen^® 10 μL microvolume, Gilson-style P2/P10 filter tips (Axygen^®, catalog number: TF-300)
Axygen^® 20 μL universal fit filter tips (Axygen^®, catalog number: TF-20)
Axygen^® 200 μL universal fit filter tips (Axygen^®, catalog number: TF-200)
Axygen^® 1,000 μL universal fit filter tips (Axygen^®, catalog number: TF-1000)
MicroAmp^TM Fast 8-tube strip (Applied Biosystems, catalog number: 4358293)
MicroAmp^TM Optical 8-cap strip (Applied Biosystems, catalog number: 4323032)
0.2 mL 8-strip PCR UltraFlux^® i Tubes, flat cap (SSIbio, catalog number: 3247-00)
MicroAmp^TM Optical 96-well reaction plate (Applied Biosystems, catalog number: N8010560)
Plate septa, 96 well (Applied Biosystems, catalog number: 4315933)
0.2 mL PCR tubes (Fisher Scientific, catalog number: MBP#3412-PK)
1.5 mL MaxyClear Snaplock microcentrifuge tube (Axygen^®, catalog number: MCT-150-C)
0.6 mL MaxyClear Snaplock microcentrifuge tube (Axygen^®, catalog number: MCT-060-C)
15 mL high clarity PP centrifuge tube (Falcon^®, catalog number: 352097)
Water (HPLC) (Sigma-Aldrich, catalog number: 270733-1L)
SYBR^TM Green I nucleic acid gel stain, 10,000× concentrate in DMSO (Invitrogen^TM, catalog number: S7563)
Primers:
1. ATXN1-specific forward primer, SCA1-F (5′-AGCCAGACGCCGGGACAC-3′)
2. Ned-labeled SCA1-F
3. ATXN1-specific TP primer, SCA1-TP (5′-GTTTCGGCGTTACGAGTGGAGTG(CTG)₅-3′)
4. ATXN1-specific reverse primer, SCA1-R (5′-CTGCGGAGAACTGGAAATGTGG-3′)
5. ATXN2-specific forward primer, SCA2-F (5′-GTGCGAGCCGGTGTATGG-3′)
6. Hex-labeled SCA2-F
7. ATXN2-specific TP primer, SCA2-TP (5′-GTTTCGGCGTTACGAGTGGACGG(CTG)₅-3′)
8. ATXN2-specific reverse primer, SCA2-R (5′-CTTGCGGACATTGGCAGCC-3′)
9. ATXN3-specific forward primer, SCA3-F (5′-CTGCTCTTGCATTCTTTTAATACCAGTGAC-3′)
10. Fam-labeled SCA3-F
11. ATXN3-specific TP primer, SCA3-TP (5′-GTTTCGGCGTTACGAGTGGAGTC(CTG)₅-3′)
12. ATXN3-specific reverse primer, SCA3-R (5′-CACATGGATGTGAACTCTGTCCTG-3′)
13. Tail primer (5′-GTTTCGGCGTTACGAGTGGA-3′)
Deoxynucleoside triphosphate set (dNTPs), PCR grade (Roche Applied Science, catalog number: 11969064001)
HotStarTaq DNA Polymerase (Qiagen, catalog number: 203205)
Q-solution (Qiagen, catalog number: 203205)
PCR Buffer (Qiagen, catalog number: 203205)
10 ng/μL genomic DNA
1 pg/μL pATXN1(CAG)_35(14+1+18) and pATXN2(CAG)_25(15+9), 10 pg/μL pATXN3(CAG)₄₁, and 50 ng/μL pATXN1(CAG)_35(14+1+18), pATXN2(CAG)_25(15+9), and pATXN3(CAG)₄₁ plasmid DNA (see sections A and E)
Hi-Di^TM formamide (Applied Biosystems^TM, catalog number: 4311320)
GeneScan^TM 500 ROX^TM dye size standard (Applied Biosystems, catalog number: 401734)
Agarose (1st BASE, catalog number: BIO-1000-500g)
Ethidium bromide solution (Sigma-Aldrich, catalog number: E1510-10ML)
1 kb DNA ladder (New England Biolabs Ltd., catalog number: N3232S)
Zymoclean^TM Gel DNA Recovery kit (Zymo Research, catalog number: D4007)
illustra^TM GFX^TM PCR DNA and Gel Band Purification kit (GE Healthcare Life Sciences, catalog number: G13/28-9034-70)
TOPO^TM TA Cloning^TM kit, Dual Promoter, without competent cells (Invitrogen^TM, catalog number: 450640)
Max efficiency DH5a competent cells (Invitrogen^TM, catalog number: 18258012)
S.O.C medium (Invitrogen^TM, catalog number: 15544034)
Ampicillin ready-made solution (Sigma-Aldrich, catalog number: A5354-10ML)
LB broth (Invitrogen^TM, catalog number: 10855001)
10× Tris-EDTA (TE) buffer, pH 8.0, ultra-pure grade, 1 L (1st BASE, catalog number: BUF-3020-10X1L)
Zyppy^TM Plasmid Miniprep kit (Zymo Research, catalog number: D4019)
BigDye^® Terminator v3.1 Cycle Sequencing kit (Applied Biosystems^TM, catalog number: 4337455)
Absolute ethanol (Fisher Chemical, catalog number: E/0650DF/17)
Sodium acetate solution (3 M), pH 5.2 (Thermo Scientific^TM, catalog number: R1181)
Glycerol (Sigma-Aldrich, catalog number: G5516)
DNA AWAY^TM surface decontaminant (Thermo Scientific^TM, catalog number: 7010)

Equipment

Pipetman P2, 0.2–2 μL (Gilson, model number: F144054M)
Pipetman P10, 1–10 μL (Gilson, model number: F144055M)
Pipetman P20, 2–20 μL (Gilson, model number: F144056M)
Pipetman P200, 20–200 μL (Gilson, model number: F144058M)
Pipetman P1000, 100–1,000 μL (Gilson, model number: F144059M)
microONE Mini Personal Centrifuge (TOMY, model number: Capsulefuge PMC-880)
Genie 2 Vortex Mixers (Scientific Industries, Inc., model number: G-560E)
StepOnePlus^TM Real-Time PCR System (Applied Biosystems, catalog number: 4376600)
GeneAmp^® PCR System 9700 Fast Thermal Cycler (Applied Biosystems, catalog number: 4339386)
Eppendorf tabletop centrifuge (Eppendorf, model number: 5810)
Genetic Analyzer (Applied Biosystems^TM, model number: 3130xl)
SUBCELL GT Horizontal Electrophoresis System (Bio-Rad, catalog number: A2-OK)
NanoDrop^TM 1000 spectrophotometer (Thermo Scientific^TM, model: ND-1000)
Water bath (Memmert, model number: MEM-EW-WB14L4)
Innova 4330 refrigerated incubator shaker (New Brunswick Scientific, model: Innova 4330)
Biofuge Fresco microcentrifuge (Heraeus, catalog number: 75005521)
Shake ‘n’ Stack (Hybaid Limited, catalog number: 50125590)
Scalpel

Software

StepOne^TM Real-Time PCR Software (Applied Biosystems)
GeneMapper^® Software (Applied Biosystems)
Sequencing Analysis Software (Applied Biosystems)
Microsoft Excel (Microsoft)

Procedure

TP-PCR master mix preparation for amplification and melting curve analysis of the ATXN1, ATXN2, and ATXN3 CAG repeat loci

This protocol outlines the steps to perform TP-PCR amplification of the ATXN1, ATXN2, and ATXN3 CAG repeats and melting curve analysis (MCA) of the generated TP-PCR products. Each TP-PCR assay utilizes a plasmid control DNA [pATXN1(CAG)_35(14+1+18), pATXN2(CAG)_25(15+9), and pATXN3(CAG)₄₁ in SCA1, SCA2, and SCA3 TP-PCR MCAs, respectively], to generate threshold melt peak temperature (T_m), which is used to classify test samples as expansion-negative (if T_m is lower than the plasmid control’s T_m) or potentially expansion-positive (if T_m is higher than the plasmid control’s T_m).

Prepare the TP-PCR master mix by dispensing the following reagents into a microcentrifuge tube (volumes stated are for a single reaction):
9.60 μL of HPLC water
7.50 μL of 5× Q-solution
2.50 μL of 10× HotStarTaq PCR buffer
0.25 μL of 10× SYBR^TM Green I Nucleic Acid Gel Stain
1.25 μL of 10 μM ATXN1-specific forward primer (SCA1-F), ATXN2-specific forward primer (SCA2-F), or ATXN3-specific forward primer (SCA3-F)
1.25 μL of 10 μM Tail primer
1.25 μL of 1 μM ATXN1-specific TP primer (SCA1-TP), ATXN2-specific TP primer (SCA2-TP), or ATXN3-specific TP primer (SCA3-TP)
0.20 μL of 25 mM dNTPs
0.20 μL of HotStarTaq DNA polymerase
Vortex to mix and spin the tube briefly.
Aliquot 24 μL of the master mix into the MicroAmp^TM Fast 8-tube strip tubes.
Add 1 μL of test sample genomic DNA (10 ng/μL) or relevant plasmid DNA [1 pg/μL pATXN1(CAG)_35(14+1+18) and pATXN2(CAG)_25(15+9) for SCA1 and SCA2 TP-PCR MCAs, respectively, and 10 pg/μL pATXN3(CAG)₄₁ for SCA3 TP-PCR MCA] into the appropriate tubes. To the non-template control tube, add 1 μL of HPLC water.
Apply the MicroAmp^TM Optical 8-cap strip. Sample labeling can be done on the edge instead of in the middle of the cap to avoid blocking of light to the reaction tubes.
Spin the tubes briefly.

Set the following program on the StepOnePlus^TM system, transfer the tubes into the instrument, and start the amplification and melt curve analysis (melt peaks are automatically generated upon completion of the run by the on-board StepOne^TM software).

Stage	Step	Temperature and duration
Amplification	Hold	95 °C, 15 min
	Cycling (35 cycles)	98 °C, 45 s
		60 °C, 1 min
		72 °C, 2 min
	Hold	72 °C, 5 min
Melt curve	Hold	95 °C, 1 min
	Hold	60 °C, 1 min
	Temperature ramp (at a rate of 0.8% in continuous mode)	60 °C to 95 °C
	Hold	40 °C, 1 min

Generation of TP-PCR melting curve analysis profiles
This protocol outlines the steps to create melt peak plots to identify samples with potential expansion.
1. Open the results in Microsoft Excel.
2. For each sample and plasmid control, plot “Melt Region Derivative Data” (i.e., the -dF/dT values) against “Melt Region Temperature Data” by choosing “X Y (Scatter)” from the Charts option under the Insert Tab, followed by selecting “Scatter with Smooth Lines” to create the melt peak plots.
3. Look for the temperature that gives the highest derivative data to determine the T_m.
4. Observe the melt peak profiles to identify samples that display a higher T_m relative to the plasmid control used.
5. Identify samples with potential expansion for further repeat size verification by capillary electrophoresis.

Extension labeling of TP-PCR products for capillary electrophoresis
This protocol outlines the steps to perform extension fluorescent labeling using an aliquot of the TP-PCR products, followed by capillary electrophoresis for determination of the ATXN1, ATXN2, and ATXN3 CAG repeat sizes in samples with potential expansion.
1. Prepare the extension labeling master mix by dispensing the following reagents into a microcentrifuge tube (volumes stated are for a single reaction):
  8.84 μL of HPLC water
  6.00 μL of 5× Q-solution
  2.00 μL of 10× HotStarTaq PCR buffer
  0.80 μL of 10 μM Ned-labeled SCA1-F, Hex-labeled SCA2-F, or Fam-labeled SCA3-F
  0.16 μL of 25 mM dNTPs
  0.20 μL of HotStarTaq DNA polymerase
2. Vortex to mix and spin the tube briefly.
3. Aliquot 18 μL of the master mix into the PCR strip tubes.
4. Add 2 μL of TP-PCR products into the appropriate tubes.
5. Spin the strip tubes briefly.
6. Set the following program on the thermal cycler, transfer the tubes into the instrument, and start the amplification.
  Stage Step Temperature and duration
  Amplification Hold 95 °C, 15 min
  Cycling (5 cycles) 98 °C, 45 s
  60 °C, 1 min
  72 °C, 2 min
  Hold 72 °C, 5 min
  Hold 4 °C
7. Remove the tubes and spin them briefly.
8. Prepare the capillary electrophoresis master mix by dispensing the following reagents into a microcentrifuge tube (volumes stated are for a single reaction):
  9.00 μL of Hi-Di^TM formamide
  0.50 μL of GeneScan 500 ROX dye size standard
9. Vortex to mix and spin the tube briefly.
10. Aliquot 9.5 μL of the master mix into the MicroAmp^TM Optical 96-well reaction plate.
11. Aliquot 4 μL of the labeled TP-PCR products into the appropriate wells.
12. Seal the plate with a rubber septum and spin the plate briefly.
13. Denature the content at 95 °C for 5 min.
14. Place the plate on ice.
15. Set the injection time and voltage in the Genetic Analyzer to be 15 s and 1 kV, respectively, and the run time to 40 min (the rest of the parameters set at default values) and start the capillary electrophoresis.
16. Analyze the results using the GeneMapper^® software.
17. Examine the electropherograms to assess the ATXN1, ATXN2, and ATXN3 genotypes, repeat counts, and the number and placement of any CGG interruptions.

Flanking PCR master mix preparation and generation of control ATXN1, ATXN2, or ATXN3 plasmids for TP-PCR melting curve analysis
This protocol outlines the steps to prepare ATXN1, ATXN2, or ATXN3 plasmid controls for use in TP-PCR MCA. Briefly, it covers how to set up flanking PCR to amplify across the ATXN1, ATXN2, and ATXN3 CAG repeat sequence, followed by isolation, purification, and cloning of fragments of interest, transformation, colony PCR, and isolation of plasmid DNA.
1. Prepare the flanking PCR master mix by dispensing the following reagents into a microcentrifuge tube (volumes stated are for a single reaction; for each sample, set up 2–3 reactions):
  11.60 μL of HPLC water
  7.50 μL of 5× Q-solution
  2.50 μL of 10× HotStarTaq PCR buffer
  1.00 μL of 10 μM SCA1-F, SCA2-F, or SCA3-F
  1.00 μL of 10 μM SCA1-R, SCA2-R, or SCA3-R
  0.20 μL of 25 mM dNTPs
  0.20 μL of HotStarTaq DNA polymerase
2. Vortex to mix and spin the tube briefly.
3. Aliquot 24 μL of the master mix into the PCR tubes.
4. Add 1 μL of genomic DNA (10 ng/μL) into the appropriate tubes. To the non-template control tube, add 1 μL of HPLC water.
5. Spin the tubes briefly.
6. Set the following program on the thermal cycler, transfer the tubes into the instrument, and start the amplification.
  Stage Step Temperature and duration
  Amplification Hold 95 °C, 15 min
  Cycling (5 cycles) 98 °C, 45 s
  60 °C, 1 min
  72 °C, 2 min
  Hold 72 °C, 5 min
  Hold 4 °C
7. Remove the tubes and spin them briefly.
8. Pool the PCR products of each sample and load them into a 2% agarose gel prepared with ethidium bromide (0.5 μg/mL) alongside with 4 μL of the 1 kb DNA ladder.
9. Electrophorese the gel and visualize the results in an imaging system.
10. Locate and excise the band of interest from the gel using a razor blade, scalpel, or other device.
11. Isolate and purify the fragments of interest using a gel band purification kit such as the Zymoclean^TM Gel DNA Recovery kit or illustra^TM GFX^TM PCR DNA and Gel Band Purification kit, following the manufacturer’s instructions.
12. Quantitate the purified PCR products using NanoDrop.
13. Store the purified PCR products at -20 °C until further use.
14. Thaw the DH5α^TM competent cells on ice, set the water bath to 42 °C, and thaw the S.O.C medium at room temperature.
15. Prepare the ligation reaction by adding 1 μL of salt solution and 1 μL of pCR^®II-TOPO^® TA vector to 4 μL of purified PCR product.
16. Add the ligation reaction to the thawed DH5α^TM competent cells (50 μL per tube).
17. Gently tap the tubes to mix.
18. Incubate the cells on ice for 30 min.
19. Immerse two-thirds of the tubes into the water bath pre-set to 42 °C for 20 s to heat-shock the cells.
20. Place the tubes on ice for 2 min.
21. Add 0.95 mL of the S.O.C medium to each tube.
22. Shake the tubes at 250 rpm for 1 h at 37 °C.
23. Centrifuge the tubes at 16,060× g for 5 min.
24. Remove 800 μL of the supernatant and discard.
25. Resuspend the pellet with the remaining supernatant.
26. Spread the content from each tube on an LB agar plate containing 100 μg/mL ampicillin using a sterilized spreader.
  To prepare LB agar plates containing ampicillin, dissolve agar powder in LB medium following manufacturer’s instructions and autoclave to sterilize. Cool the agar to approximately 50 °C and add 1 mL of 100 mg/mL ampicillin before pouring them into Petri dishes and allowing them to cool and set. Store the prepared LB agar plates at 4 °C.
27. Incubate the plates overnight at 37 °C.
28. Randomly pick 10–20 colonies from each plate using micropipette tips.
29. Suspend each colony into a PCR tube containing 10 μL of 1× TE buffer and mark the colony numbers on the LB plates and the PCR tubes.
30. Perform colony PCR by setting up TP-PCR (see section A; use fluorescently labeled SCA1-F, SCA2-F, or SCA3-F and omit SYBR^TM Green I Nucleic Acid Gel Stain) using 1 μL of the picked colony as the template, followed by capillary electrophoresis (see section C).
31. Examine the electropherograms to identify colonies that have the DNA inserts with expected ATXN1, ATXN2, or ATXN3 CAG repeat size and structure.
32. Create starter culture by inoculating the remaining 9 μL of the colonies of interest into 3–5 mL of LB broth containing 100 μg/mL ampicillin.
33. Shake the tubes at 250 rpm overnight at 37 °C.
34. Expand the culture by transferring the starter culture to 50–100 mL of LB broth containing 100 μg/mL ampicillin.
35. Shake the tubes at 250 rpm overnight at 37 °C.
36. Prepare bacterial glycerol stocks for future use by adding 400 μL of the culture into 400 μL of glycerol and gently pipetting them up and down to mix. Store the bacterial glycerol stocks at -80 °C.
37. Isolate plasmid DNA using kits such as the Zyppy^TM Plasmid Miniprep kit, following the manufacturer’s instructions.
38. Quantitate the extracted plasmid DNAs using NanoDrop and store them at -20 °C.
39. Use 1–10 pg of plasmid DNA as the template for TP-PCR MCA assay.
  The CAG repeat size and structure of the plasmid DNA can also be verified by Sanger sequencing (see section E).

Sanger sequencing for verification of ATXN1, ATXN2, or ATXN3 CAG repeat size and structure of plasmid DNA controls
This protocol outlines the steps to perform Sanger sequencing of the plasmid DNA for verification of the ATXN1, ATXN2, and ATXN3 CAG repeat sizes.
1. Prepare the sequencing reaction master mix by dispensing the following reagents into a microcentrifuge tube (volumes stated are for a single reaction):
  HPLC water (top up to 20 μL per reaction)
  8 μL of 2.5× BigDye^® Terminator Mix v3.1
  3.2 pmol M13 or T7 primers
2. Vortex to mix and spin the tube briefly.
3. Aliquot 16 μL of the master mix into the PCR tubes.
4. Add 4 μL of plasmid DNA (50 ng/μL) into the appropriate tubes.
5. Spin the tubes briefly.
6. Set up the following program on the thermal cycle, transfer the tubes into the instrument, and start the amplification.
  Stage Step Temperature and duration
  Amplification Hold 96 °C, 1 min
  Cycling (25 cycles) 96 °C, 10 s
  60 °C, 5 s
  60 °C, 4 min
  Hold 4 °C
7. Remove the tubes and spin them briefly.
8. Prepare the precipitation reaction master mix by dispensing the following reagents into a microcentrifuge tube (volumes stated are for a single reaction):
  14.50 μL of HPLC water
  3.00 μL of 3M sodium acetate
  62.50 μL of 100% ethanol
9. Vortex to mix and spin the tube briefly.
10. Aliquot 80 μL of the master mix into the 1.5 mL microcentrifuge tube.
11. Transfer all 20 μL of the sequencing products into the appropriate tubes.
12. Vortex to mix and spin the tubes briefly.
13. Leave the tubes at room temperature away from light for 15 min.
14. Spin the tubes at 13,000 rpm for 20 min.
15. Aspirate and discard the supernatant.
16. Add 250 μL of 70% ethanol into each tube.
17. Spin the tubes at 13,000 rpm for 5 min.
18. Aspirate and discard the supernatant.
19. Repeat steps E16–E18.
20. Air dry the tubes.
21. Add 12 μL of Hi-Di^TM formamide into each tube.
22. Vortex the tubes to dislodge and suspend the pellets.
23. Load all 12 μL of the content into the MicroAmp^TM Optical 96-well reaction plate.
24. Seal the plate with a rubber septum and spin the plate briefly.
25. Denature the content at 95 °C for 5 min.
26. Place the plate on ice.
27. Start the capillary electrophoresis run in the Genetic Analyzer using sequencing module and all parameters set at default values.
28. Analyze the results using the Sequencing Analysis software.

Data analysis

The SCA1, SCA2, and SCA3 TP-PCR employs locus-specific flanking and TP primers and a common Tail primer, which together generate multiple products, each differing by one CAG repeat (Lian et al., 2021). The shorter TP-PCR products generated from an allele with smaller CAG repeat size produce melt peaks with lower T_m, whereas the longer TP-PCR products generated from an allele with larger CAG repeat size yield melt peaks with higher T_m. Plasmid control DNA carries repeat size that is sufficiently lower than the upper boundary of the normal repeat size range and is included in each TP-PCR MCA run for generation of threshold T_m to classify samples based on their T_m. The melt peak plots of non-SCA samples, SCA-positive samples, and plasmid DNA controls after SCA1, SCA2, and SCA3 TP-PCR MCAs are shown in Figure 1 (left panel). Non-SCA samples carrying non-expanded (normal) alleles are left-shifted with lower T_m compared with that of the plasmid DNA control and will not be further subjected to capillary electrophoresis sizing. On the other hand, SCA-positive samples are right-shifted relative to the control, due to their higher T_m. Any sample whose T_m is higher than the relevant plasmid’s T_m is potentially expansion-positive and will be further subjected to capillary electrophoresis for repeat size confirmation (Figure 1, right panel). Due to the unique design of the primers, the first peak in the SCA1 and SCA2 TP-PCR electropherogram represents TP-PCR product containing five repeats, while the first peak in the SCA3 TP-PCR electropherogram represents product containing 11 repeats. Each successive peak represents product containing an additional repeat, and the last peak represents the largest TP-PCR product generated. The repeat number in a sample can be determined by counting the number of peaks. In situations where CGG interruptions are present in ATXN1 and ATXN2 alleles, inefficient annealing of the TP primer to the interrupted sequences results in little to no amplification, resulting in a gap between two discrete clusters of peaks.

Figure 1. Example of melt peak profiles (left) and electropherograms (right) of non-spinocerebellar ataxia (SCA) and SCA-positive samples, together with the plasmid control DNA, after SCA1, SCA2, and SCA3 TP-PCR MCAs. In the left panel, non-SCA samples are left-shifted with lower melt peak temperatures compared with that of the relevant plasmid DNA control, while SCA-positive samples are right-shifted relative to the control. -dF/dT is shown on the x-axis and temperature is shown on the y-axis. In the right panel, numbered black arrows indicate the number of CAG repeats in non-expanded (normal) alleles, and numbered red arrows indicate the number of CAG repeats in expanded alleles. Relative fluorescence unit (RFU) is shown on the x-axis and size is shown on the y-axis.

Notes

Clean lab bench before start of experiments with 70% ethanol and DNA AWAY^TM.
Mix reagents before use to ensure that they are uniform and spin them briefly to collect the content at the bottom of the tube.
Use the HotStarTaq PCR buffer and Q-solution provided with the HotStarTaq DNA polymerase.
Use aerosol barrier pipette tips. Change tips after each use.
Open and close all sample tubes carefully. Avoid splashing PCR products.
Note that SYBR Green is light sensitive. Wrap tubes containing SYBR Green with aluminum foil or use amber tubes to avoid direct light exposure.
We recommend that plasmid DNA controls are included in each TP-PCR MCA run to differentiate the melt peaks of samples with repeat expansion from those of expansion-negative samples. The result of the plasmid DNA generated from one run should not be used to differentiate samples used in other runs.
Include at least one positive control (e.g., sample with a known expansion) as well as a negative or non-template control in each assay, to ensure reliable amplification/repeat sizing and absence of amplicon or DNA contaminants in the reagents used, respectively.
We recommend using POP-7^TM polymer.
The genomic DNA and plasmid DNA should be diluted with 1× TE buffer to prevent DNA degradation.

Acknowledgments

This work was supported by internal departmental funds. This protocol was derived from the original research paper (Lian et al., 2021).

Competing interests

A patent application was submitted on June 2, 2021, directed to a method of detecting a repeat expansion sequence. The authors declare that they have no other competing interests.

References

Cagnoli, C., Brussino, A., Mancini, C., Ferrone, M., Orsi, L., Salmin, P., Pappi, P., Giorgio, E., Pozzi, E., Cavalieri, S., et al. (2018). Spinocerebellar Ataxia Tethering PCR: A Rapid Genetic Test for the Diagnosis of Spinocerebellar Ataxia Types 1, 2, 3, 6, and 7 by PCR and Capillary Electrophoresis. J Mol Diagn 20(3): 289-297.
Cagnoli, C., Stevanin, G., Michielotto, C., Gerbino Promis, G., Brussino, A., Pappi, P., Durr, A., Dragone, E., Viemont, M., Gellera, C., et al. (2006). Large pathogenic expansions in the SCA2 and SCA7 genes can be detected by fluorescent repeat-primed polymerase chain reaction assay. J Mol Diagn 8(1): 128-132.
Chung, M. Y., Ranum, L. P., Duvick, L. A., Servadio, A., Zoghbi, H. Y. and Orr, H. T. (1993). Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. Nat Genet 5(3): 254-258.
Dorschner, M. O., Barden, D. and Stephens, K. (2002). Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis. J Mol Diagn 4(2): 108-113.
Hersheson, J., Haworth, A. and Houlden, H. (2012). The inherited ataxias: genetic heterogeneity, mutation databases, and future directions in research and clinical diagnostics. Hum Mutat 33(9): 1324-1332.
Kawaguchi, Y., Okamoto, T., Taniwaki, M., Aizawa, M., Inoue, M., Katayama, S., Kawakami, H., Nakamura, S., Nishimura, M., Akiguchi, I., et al. (1994). CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet 8(3): 221-228.
Klockgether, T., Mariotti, C. and Paulson, H. L. (2019). Spinocerebellar ataxia. Nat Rev Dis Primers 5(1): 24.
Lian, M., Rajan-Babu, I. S., Singh, K., Lee, C. G., Law, H. Y. and Chong, S. S. (2015). Efficient and highly sensitive screen for myotonic dystrophy type 1 using a one-step triplet-primed PCR and melting curve assay. J Mol Diagn 17(2): 128-135.
Lian, M., Zhao, M., Phang, G. P., Soong, Y. T., Yoon, C. S., Lee, C. G., Law, H. Y. and Chong, S. S. (2021). Rapid Molecular Screen of Spinocerebellar Ataxia Types 1, 2, and 3 by Triplet-Primed PCR and Melting Curve Analysis. J Mol Diagn 23(5): 565-576.
Melo, A. R., Ramos, A., Kazachkova, N., Raposo, M., Bettencourt, B. F., Rendeiro, A. R., Kay, T., Vasconcelos, J., Bruges-Armas, J. and Lima, M. (2016). Triplet Repeat Primed PCR (TP-PCR) in Molecular Diagnostic Testing for Spinocerebellar Ataxia Type 3 (SCA3). Mol Diagn Ther 20(6): 617-622.
Orr, H. T., Chung, M. Y., Banfi, S., Kwiatkowski, T. J., Jr., Servadio, A., Beaudet, A. L., McCall, A. E., Duvick, L. A., Ranum, L. P. and Zoghbi, H. Y. (1993). Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat Genet 4(3): 221-226.
Pulst, S. M., Nechiporuk, A., Nechiporuk, T., Gispert, S., Chen, X. N., Lopes-Cendes, I., Pearlman, S., Starkman, S., Orozco-Diaz, G., Lunkes, A., et al. (1996). Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat Genet 14(3): 269-276.
Rajan-Babu, I. S., Law, H. Y., Yoon, C. S., Lee, C. G. and Chong, S. S. (2015). Simplified strategy for rapid first-line screening of fragile X syndrome: closed-tube triplet-primed PCR and amplicon melt peak analysis. Expert Rev Mol Med 17: e7.
Ruano, L., Melo, C., Silva, M. C. and Coutinho, P. (2014). The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies. Neuroepidemiology 42(3): 174-183.
Zhao, M., Cheah, F. S. H., Chen, M., Lee, C. G., Law, H. Y. and Chong, S. S. (2017). Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay. PloS One 12(7): e0180984.