PCR-based Assay for Genome Integrity after Methyl Methanesulfonate Damage in Physcomitrella patens

Materials and Reagents

1. 90 mm plastic Petri dish
   
2. 50 ml tube
   
3. 1.5 ml tube
   
4. Physcomitrella patens protonemal cells (cultivated for 4 days)
   
5. BCDAT medium (Nishiyama et al., 2000)
   
6. Methyl methanesulfonate (MMS) (Sigma-Aldrich, catalog number: 129925 )
   
7. Chloroform (Sigma-Aldrich, catalog number: V800117 )
   
8. Ethanol (Sigma-Aldrich, catalog number: 09-0770 )
   
9. RNase A
   
10. LA Taq (TAKARA BIO, catalog number: RR002A )
    
11. Agarose powder (Promega, catalog number: V3125 )
    
12. 0.7% agarose gel
    
13. Ethidium bromide (EtBr)
    
14. Power SYBR^® green PCR master mix (Thermo Fisher Scientific, Applied Biosystems^TM, catalog number: 4367659 )
    
15. Hexadecyltrimethylammonium bromide (CTAB) (Sigma-Aldrich, catalog number: H-5882 )
    
16. Sodium chloride (NaCl) (Sigma-Aldrich, catalog number: 28-2270 )
    
17. Tris-HCl, pH 8.0 (Wako Pure Chemical Industries, catalog number: 206-07884 )
    
18. Ethylenediamine-N,N,N’,N’-tetraacetic acid, disodium salt, dihydrate (EDTA) (DOJINDO, catalog number: 345-01865 )
    
19. PEG8000 (MP Biomedicals, catalog number: 02194839 )
    
20. Oligonucleotide DNA primers for long amplicon quantitative PCR:
    Nuclear DNA (5′-GTGGAAGTGAGATGCAGTTTGG-3′ and 5'-GTGGCTCTGGACAGTGAAATTG-3′)
    Chloroplast DNA (5′-AATTGGAGTCGGTCCTTCCATA-3′ and 5′-TGGCAAATACAATGGCAAAAAG-3′)
    Mitochondrial DNA (5′-GACTGCCCTCACTAGGATGCTT-3′ and 5′-TGGGTGATTTACTCCATTGACG-3′)
    
21. Oligonucleotide DNA primers for short amplicon quantitative PCR:
    Nuclear DNA (5′-CAACCGTCTTCTGTGTCTAGGTC-3′ and 5′-GAAACCGGCCTGCATTACATG-3′)
    Chloroplast DNA (5′-AGTAATCCCATCGCGTGACAT-3′ and 5′-AGGTATGGAAAAAATCGCTGAAAA-3′)
    Mitochondrial DNA (5′-CGTGCTAAAAATCCAGTCCATTC-3′ and 5′-AGCAAAGAAGTCAAGACCTAACAAAAC-3′)
    
22. 2x CTAB buffer (see Recipes)
    
23. 10% CTAB (see Recipes)
    
24. CTAB ppt buffer (see Recipes)
    
25. NaCl-TE (see Recipes)
    
26. TE buffer (see Recipes)
    
27. PEG solution (see Recipes)
    

Equipment

1. Forceps
   
2. Multi-beads shocker (Yasui Kikai)
   
3. Vacuum pump (Tokyo Rikakikai, catalog number: AS-3 )
   
4. Bench top centrifuge for 1.5 ml tubes
   
5. Heat block for 1.5 ml tubes (TAITEC, catalog number: DTU-2CN )
   
6. Standard thermal cycler (Bio-Rad Laboratories, catalog number: 170-8720JA )
   
7. Real-time PCR thermal cycler (Thermo Fisher Scientific, Applied Biosystems^TM, model: Applied Biosystems^® 7500 Fast Real-Time PCR Systems )
   

Software

1. ImageJ (https://imagej.nih.gov/ij/)
   
2. Excel (Microsoft)

Procedure

1. MMS treatment of plants
   1. Cultivate P. patens protonemal cells on four BCDAT agar plates for each strain under continuous light at 25 °C.
      
   2. Immerse P. patens protonemal cells in 12 ml BCDAT liquid medium containing 20 mM MMS in 90 mm plastic Petri dishes under vacuum for 1 h. Note that undamaged control samples are harvested prior to the MMS treatment. These should include three biological replicates.
      Note: MMS is a carcinogen.
      
   3. After washing with BCDAT liquid medium (twice with 15 ml BCDAT liquid medium in 50 ml tubes), cultivating the protonemal cells under continuous light at 25 °C.
      
   4. Using forceps, harvest the cells at 0, 6, 24 and 48 h after washing.
      
      
2. Extraction of total genomic DNA
   1. Grind frozen protonemal cells using a homogenizer (Multi-beads shocker: 1,500 rpm, 10 sec, thrice). Alternatively, mortar and pestle can be used.
      
   2. Add an equal volume (approximately 300 µl in a 1.5 ml tube) of 2x CTAB buffer to the powdered protonemal cells. Mix and then incubate at 60 °C for 1 h.
      
   3. Mix with an equal volume of chloroform and centrifuge at 4,500 x g for 20 min. Recover aqueous phase (approximately 500 µl).
      
   4. Add 1/10 volume of 10% CTAB.
      
   5. Extract DNA with an equal volume of chloroform and recover the aqueous phase. Repeat this step twice.
      
   6. Add an equal volume of CTAB ppt buffer and mix well by inverting.
      
   7. Centrifuge at 4,500 x g for 20 min. Discard the supernatant.
      
   8. Dissolve the pellet in 400 µl of NaCl-TE. Incubate at 60 °C for 30 min.
      
   9. Add two volumes of ethanol.
      
   10. Centrifuge at 14,000 x g for 10 min. Discard the supernatant.
       
   11. Dissolve the pellet in 100 µl of TE. The pellet may be insoluble at this step, but will dissolve in the next step.
       
   12. Add 2 µl of RNase A (1 mg/ml) and incubate at 37 °C for 1 h.
       
   13. Add an equal volume of PEG solution.
       
   14. Centrifuge at 14,000 x g at 4 °C for 10 min.
       
   15. After removing the supernatant, rinse the pellet with 70% ethanol.
       
   16. Dissolve the pellet in 100 µl of TE.
       
       
3. Long amplicon quantitative PCR
   Long amplicon PCR is performed to quantify the amount of undamaged DNA template.
   
   1. Design primers to generate 8-10 kb PCR amplicons from the nuclear, chloroplast, and mitochondrial genomes.
      Note: Long amplicons efficiently detect DNA damage; however, amplification efficiency is poor.
      
   2. Prepare a dilution series (20, 10, 5, 2.5, 1.25 and 0.625 ng/µl by diluting with TE buffer) of undamaged DNA, spanning the range from the lowest to the highest amount of PCR product in the damaged samples, to use as standard. Diluted samples to 10 ng/µl by adding TE buffer, and use 1 µl for each PCR reaction.
      
   3. Perform a 2-step PCR (first step, 98 °C for 10 sec; second step, 68 °C for 10 min) using a Taq DNA polymerase optimized for long amplicon (LA-Taq). Subject all samples and control dilutions to a single PCR reaction. Use the number of PCR cycles at which the resulting DNA amplicon is exponentially amplified. Thus, the resulting amount/yield of the PCR amplicon reflects the amount of DNA template used in the reaction. Use 17, 20 and 27 cycles for amplifying the chloroplast, mitochondria and nuclear DNA, respectively.
      
   4. Electrophorese on 0.7% agarose gels stained with EtBr to resolve the PCR products (Figure 1). Load a suitable fraction of the PCR product on the gel.
      
      
      Figure 1. Electrophoresis of long PCR amplicons on agarose gel. An example of agarose gel electrophoresis of long PCR products from nuclear actin locus. No MMS damage control (no) and MMS-damaged samples (0, 6, 24 and 48 h after washing) were analyzed with serially diluted standard samples. RECA2-KO is shown as an example of a mutant (Odahara et al., 2015).
      
      
4. Short amplicon quantitative PCR
   Short amplicon PCR allows copy number quantification of the nuclear, chloroplast and mitochondrial DNA. Both standard and real-time PCRs are applicable for this short amplicon quantitative PCR, but the latter provides more accurate values.
   
   1. Design primers to amplify approximately 100 bp of the nuclear, chloroplast and mitochondrial loci, based on the standard protocol for quantitative real-time PCR assay using intercalating dyes, such as SYBR Green I.
      
   2. Prepare a dilution series to use as standard controls, including all sample concentrations. It is important to use the 10 ng/µl sample DNA prepared in the long amplicon PCR.
      
   3. Perform real-time PCR using DNA polymerase mixture optimized for real-time PCR (Power SYBR^® Green PCR Master Mix) and thermal cycler real-time PCR system with a PCR program (first step, 95 °C for 15 sec; second step, 60 °C for 1 min). Calculate the relative copy number of the nuclear, chloroplast, and mitochondrial DNA of each sample using standard curves prepared using the standard samples.
      

Data analysis

1. Measure the volume of each band in the electrophoresis gel with ImageJ using the “measure” tool, and calculate the relative amount of long PCR products from all samples by fitting them to the standard curve prepared using those from the serially diluted standard samples.
   
2. Divide the relative amount of long amplicon PCR products by the relative copy number of the nuclear, chloroplast and mitochondrial DNA calculated from short amplicon PCR products to obtain the relative copy number of undamaged DNA.
   
3. Relative recovery is calculated by dividing the amount of undamaged DNA in damaged samples by that of undamaged controls. Use t-test for statistical analysis of data from three biological replicates and Excel.
   

Recipes

1. 2x CTAB buffer
   2% CTAB
   1.4 M NaCl
   100 mM Tris-HCl, pH 8.0
   20 mM EDTA
   Store at room temperature (RT).
   
2. 10% CTAB
   10% CTAB
   0.7 M NaCl
   Store at RT.
   
3. CTAB ppt buffer
   1% CTAB
   50 mM Tris-HCl, pH 8.0
   10 mM EDTA
   Store at RT.
   
4. NaCl-TE
   1 M NaCl
   10 mM Tris-HCl, pH 8.0
   1 mM EDTA
   Store at RT.
   
5. TE buffer
   10 mM Tris-HCl, pH 8.0
   1 mM EDTA
   Store at RT.
   
6. PEG solution
   2 M NaCl
   20% PEG8000
   Store at RT.
   

Acknowledgments

The long amplicon PCR assay is based on Hunter et al. (2010) with slight modifications. The genomic DNA extraction protocol is based on PHYSCObase (http://moss.nibb.ac.jp/). This work was supported by the Strategic Research Foundation Grant-aided Project for Private Universities from the Ministry of Education, Culture, Sports, Science and Technology, Japan, and the Funding Program for Next-Generation World-Leading Researchers (NEXT Program).

References

1. Hunter, S. E., Jung, D., Di Giulio, R. T. and Meyer, J. N. (2010). The QPCR assay for analysis of mitochondrial DNA damage, repair, and relative copy number. Methods 51(4): 444-451.
   
2. Nishiyama, T., Hiwatashi, Y., Sakakibara, I., Kato, M. and Hasebe, M. (2000). Tagged mutagenesis and gene-trap in the moss, Physcomitrella patens by shuttle mutagenesis. DNA Res 7(1): 9-17.
   
3. Odahara, M., Inouye, T., Nishimura, Y. and Sekine, Y. (2015). RECA plays a dual role in the maintenance of chloroplast genome stability in Physcomitrella patens. Plant J 84(3): 516-526.