eISSN: 2221-6197 DOI: 10.31301/2221-6197

Structure of the products of classical PCR and the reasons for the plateau of the reaction

Year: 2024

Pages: 18-32

Number: Volume 16, issue 1

Type: scientific article

Summary:

Classical PCR with two primers usually produces one amplicon. However, despite the apparent simplicity of this reaction, additional products of different lengths and structures are inevitably synthesized, even when ideal primers are used. These minor products are not given enough attention, but in some cases they can significantly affect the efficiency of PCR, and also contribute to an earlier plateau of the reaction, due to several reasons. The main one is a decrease in the efficiency of primer annealing on the chains of the target amplicon due to an increase in its quantity during PCR and, therefore, an increase in the probability of reassociation of its chains. To describe the processes occurring during PCR, it is proposed to operate with a conventional reaction cell with a volume of 1 zeptoliter (1000 nm3), containing quaternary complexes “DNA/primer/DNA polymerase/dNTP”. The number of ingredient molecules required for PCR to occur per such reaction cell was calculated. 

Keywords:

PCR, amplicon, DNA polymerase, primer, plateau, thermal convection, zeptoliter

References:

1. Chemeris A.V., Aminev F.G., Garafutdinov R.R., Anisimov V.A., Sagitov A.M., Khusnutdinova E.K., Sakhabutdinova A.R., Chemeris D.A., Mikhailenko K.I. DNA forensics. M.: Nauka, 2022. 466 p. (In Russian)

2. Chemeris D.A., Garafutdinov R.R., Sakhabutdinova A.R., Maleev G.V., Chemeris A.V. Convection PCR in different types of convective cells. Biomics. 2018. V. 10(4). P. 410-443. DOI: 10.31301/2221-6197.bmcs.2018-52 (In Russian)

3. Chemeris D.A., Kiryanova O.Yu., Gubaydullin I.M., Chemeris A.V. Design of primers for polymerase chain reaction (Brief review of software and databases). Biomics. 2016. V. 8(3). P.215-238. (In Russian)

4. Chemeris D.A., Magdanov E.G., Mashkov O.I., Garafutdinov R.R., Chemeris A.V. Hot start or timerelease PCR. Biomics. 2011. V.2(1). P.1-8. (In Russian)

5. Cho Y, Lee HS, Kim YJ, Kang SG, Kim SJ, Lee JH. Characterization of a dUTPase from the hyperthermophilic archaeon Thermococcus onnurineus NA1 and its application in polymerase chain reaction amplification. Mar Biotechnol. 2007. V.9(4). P.450-458. doi: 10.1007/s10126-007-9002-8

6. Clark JM. Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases. Nucleic Acids Res. 1988. V.16(20). P.9677-9686. doi: 10.1093/nar/16.20.9677

7. Dabrowski S, Kiaer Ahring B. Cloning, expression, and purification of the His6-tagged hyper-thermostable
dUTPase from Pyrococcus woesei in Escherichia coli: application in PCR. Protein Expr Purif. 2003. V.31(1).
P.72-78. doi: 10.1016/s1046-5928(03)00108-6

8. Dimitrov DS, Apostolova MA. The limit of PCR amplification. J Theor Biol. 1996. V.178(4). P.425-426. doi: 10.1006/jtbi.1996.0041

9. Doronin S.V., Nevinsky G.A., Malygina T.O., Podust V.N., Khomov V.V., Lavrik O.I. The efficiency of interaction of deoxyribonucleoside-5'-mono-, di- and triphosphates with the active center of E. coli DNA polymerase I Klenow fragment // FEBS Lett. 1989. V. 259. P. 83-85. doi: 10.1016/0014-5793(89)81500-5

10. Douglas A, Atchison B. Degradation of DNA during the denaturation step of PCR. PCR Methods Appl. 1993. V.3(2). P.133-134. doi: 10.1101/gr.3.2.133

11. Garafutdinov R.R., Baymiev An.Kh., Maleev G.V., Alexeyev Ya.I., Zubov V.V., Chemeris D.A., Kiryanova
J.Yu., Gubaydullin I.M., Matniyazov R.T., Sakhabutdinova A.R., Nikonorov Yu.M., Kuluev B.R., Baymiev Al.Kh., Chemeris A.V. Diversity of PCR primers and principles of their design. Biomics. 2019. V.11(1). P. 23 – 70. DOI: 10.31301/2221-6197.bmcs.2019-04 (In Russian)

12. Garafutdinov R.R., Chemeris D.A., Mavzyutov A.R., Akhmetzyanova L.U., Davletkulov T.M., Gubaydullin I.M., Chemeris A.V. LAMP amplification of nucleic acids. I. Two decades of development and improvement. Biomics. 2021. V.13(2). P. 176-226. DOI: 10.31301/2221-6197.bmcs.2021-14 (In Russian)

13. Garafutdinov R.R., Chemeris D.A., Sakhabutdinova A.R., Kiryanova O.Y., Mikhaylenko C.I., Chemeris A.V. Encoding of non-biological information for its long-term storage in DNA. Biosystems. 2022. V.215-216. 104664. doi: 10.1016/j.biosystems.2022.104664

14. Garafutdinov R.R., Galimova A.A., Sakhabutdinova A.R. The influence of quality of primers on the formation of primer dimers in PCR. Nucleos. Nucleot. Nucleic Acids. 2020. V. 39(9). P. 1251-1269. doi: 10.1080/15257770.2020.1803354

15. Garafutdinov RR, Chemeris DA, Sakhabutdinova AR, Moiseev KV, Urmancheev SF, Mikhaylenko CI, Privalov LY, Chemeris AV. Convective polymerase chain reaction in standard microtubes. Anal Biochem. 2022a. V.641. 114565. doi: 10.1016/j.ab.2022.114565

16. Hogrefe HH, Hansen CJ, Scott BR, Nielson KB. Archaeal dUTPase enhances PCR amplifications with archaeal DNA polymerases by preventing dUTP incorporation. Proc Natl Acad Sci USA. 2002. V.99(2). P.596-601. doi: 10.1073/pnas.012372799

17. Jansson L, Hedman J. Challenging the proposed causes of the PCR plateau phase. Biomol Detect Quantif. 2019. V.17. 100082. doi: 10.1016/j.bdq.2019.100082

18. Kainz P. The PCR plateau phase - towards an understanding of its limitations. Biochim Biophys Acta. 2000. V.1494(1-2). P.23-27. doi: 10.1016/s0167-4781(00)00200-1

19. Lyamichev V, Brow MA, Dahlberg JE. Structurespecific endonucleolytic cleavage of nucleic acids by eubacterial DNA polymerases. Science. 1993. V.260(5109). P.778-783. doi: 10.1126/science.7683443 20. Lyamichev V, Brow MA, Varvel VE, Dahlberg JE. Comparison of the 5' nuclease activities of taq DNA polymerase and its isolated nuclease domain. Proc Natl Acad Sci USA. 1999. V.96(11). P.6143-6148. doi: 10.1073/pnas.96.11.6143

21. Mori Y, Kitao M, Tomita N, Notomi T. Real-time turbidimetry of LAMP reaction for quantifying template DNA. J Biochem Biophys Methods. 2004. V.59(2). P.145-157. doi: 10.1016/j.jbbm.2003.12.005

22. Morrison C, Gannon F. The impact of the PCR plateau phase on quantitative PCR. Biochim Biophys Acta. 1994. V.1219(2). P.493-498. doi: 10.1016/0167-4781(94)90076-0

23. Mullis KB, Faloona FA. Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction. Methods Enzymol. 1987. V.155. P.335-350. doi: 10.1016/0076-6879(87)55023-6

24. Mullis KB. The polymerase chain reaction in an anemic mode: how to avoid cold oligodeoxyribonuclear
fusion. PCR Methods Appl. 1991. V.1(1). P.1-4. doi: 10.1101/gr.1.1.1

25. Saiki RK, Scharf S, Faloona F, Mullis KB, Horn GT, Erlich HA, Arnheim N. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. Science. 1985. V.230(4732). P.1350-1354. doi: 10.1126/science.2999980

26. Sakhabutdinova A.R., Chemeris D.A., Chemeris A.V., Garafutdinov R.R. PCR enhancers. I. General information. Biomics. 2023. Т.15(3). С. 218-223. DOI: 10.31301/2221-6197.bmcs.2023-20 (In Russian)

27. Sikorsky JA, Primerano DA, Fenger TW, Denvir J. DNA damage reduces Taq DNA polymerase fidelity and PCR amplification efficiency. Biochem Biophys Res Commun. 2007. V.355(2). P.431-437. doi:  10.1016/j.bbrc.2007.01.169

28. Sikorsky JA, Primerano DA, Fenger TW, Denvir J. Effect of DNA damage on PCR amplification efficiency with the relative threshold cycle method. Biochem Biophys Res Commun. 2004. V.323(3). P.823-830. doi: 10.1016/j.bbrc.2004.08.168

29. Spaete RR, Frenkel N. The herpes simplex virus amplicon: a new eucaryotic defective-virus cloningamplifying vector. Cell. 1982. V.30(1). P.295-304. doi: 10.1016/0092-8674(82)90035-6.

Download pdf
up
eISSN: 2221-6197 DOI: 10.31301/2221-6197