RNase H-dependent PCR
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RNase H-dependent PCR (rhPCR)[1] is a modification of the standard PCR technique. In rhPCR, the primers are designed with a removable amplification block on the 3’ end. Amplification of the blocked primer is dependent on the cleavage activity of a hyperthermophilic archaeal Type II RNase H enzyme during hybridization to the complementary target sequence. This RNase H enzyme possesses several useful characteristics that enhance the PCR. First, it has very little enzymatic activity at low temperature, enabling a “hot start PCR” without modifications to the DNA polymerase. Second, the cleavage efficiency of the enzyme is reduced in the presence of mismatches near the RNA residue. This allows for reduced primer dimer formation,[1] detection of alternative splicing variants,[2][3] ability to perform multiplex PCR with higher numbers of PCR primers, and the ability to detect single-nucleotide polymorphisms.[4]
Principle
rhPCR primers consist of three sections. 1) The 5’ DNA section, equivalent in length and melting temperature (Tm) requirements to a standard PCR primer, is extended after cleavage by the RNase HII enzyme. 2) A single RNA base provides the cleavage site for the RNase HII. 3) A short 3’ extension of four or five bases followed by a blocker (usually a short, non-extendable molecule like a propanediol) prevents extension by a DNA polymerase until removal. A rhPCR reaction begins with the primers and template free in solution (Figure 1). While free in solution, these primers are not deblocked by the RNase HII enzyme, as they must be in an RNA:DNA heteroduplex with the template to be cleaved. Once bound to the template, the rhPCR primers are cleaved by the thermostable RNase HII enzyme. This removes the block, allowing for the DNA polymerase to extend off of the primers. The cycling of the PCR reaction continues the process. rhPCR primers are designed so that after cleavage by the RNase H2 enzyme, the Tm of the primers are still greater than the annealing temperature of PCR reaction. These primers can be used in both 5’ nuclease Taqman and SYBR Green types of quantitative PCR.
Applications
rhPCR can be used for quantitative PCR and medical or environmental laboratories:
See also
- Quantitative PCR
- Taqman
- SYBR Green
- Reverse transcription polymerase chain reaction
- Molecular beacon
- Gene Expression
References
- ^ a b Dobosy JR, Rose SD, Beltz KR, Rupp SM, Powers KM, Behlke MA, Walder JA (August 2011). "RNase H-dependent PCR (rhPCR): improved specificity and single nucleotide polymorphism detection using blocked cleavable primers". BMC Biotechnology. 11: 80. doi:10.1186/1472-6750-11-80. PMC 3224242. PMID 21831278.
{{cite journal}}: CS1 maint: unflagged free DOI (link) - ^ Gordon, Erin D.; Simpson, Laura J.; Rios, Cydney L.; Ringel, Lando; Lachowicz-Scroggins, Marrah E.; Peters, Michael C.; Wesolowska-Andersen, Agata; Gonzalez, Jeanmarie R.; MacLeod, Hannah J.; Christian, Laura S.; Yuan, Shaopeng; Barry, Liam; Woodruff, Prescott G.; Ansel, K. Mark; Nocka, Karl; Seibold, Max A.; Fahy, John V. (2 August 2016). "Alternative splicing of interleukin-33 and type 2 inflammation in asthma". Proceedings of the National Academy of Sciences. 113 (31): 8765–8770. doi:10.1073/pnas.1601914113.
- ^ Boucard, Antony A.; Maxeiner, Stephan; Südhof, Thomas C. (3 January 2014). "Latrophilins Function as Heterophilic Cell-adhesion Molecules by Binding to Teneurins REGULATION BY ALTERNATIVE SPLICING". Journal of Biological Chemistry. 289 (1): 387–402. doi:10.1074/jbc.M113.504779.
- ^ Cahoon, A.; Nauss, John; Stanley, Conner; Qureshi, Ali (20 February 2017). "Deep Transcriptome Sequencing of Two Green Algae, Chara vulgaris and Chlamydomonas reinhardtii, Provides No Evidence of Organellar RNA Editing". Genes. 8 (2): 80. doi:10.3390/genes8020080. PMC 5333069. PMID 28230734.
{{cite journal}}: CS1 maint: unflagged free DOI (link)