Table 7.
Literature investigating the impact of RT enzyme on cDNA fidelity.
Paper | RT enzymes | Main findings |
---|---|---|
Waugh et al., 2015 | SuperScript II and AMV RT enzymes | RNA concentration during first strand synthesis; effect of RNase H activity and PCR cycling conditions all impact both the yield and fidelity of RT |
Input RNA concentration and PCR cycles might generate a larger viral cDNA population for analysis but are likely to compromise the quality of sequencing data obtained | ||
Yasukawa et al., 2017 | HIV-1 RT, AMV, or MMLV | HIV-1 RT demonstrated lower fidelity than AMV or MMLV |
Okano et al., 2018 | HIV-1 RT, AMV, or MMLV | High concentrations of MgCl2 and dNTP negatively impact RT fidelity |
Zucha et al., 2020 | Maxima H, SuperScript II, Superscript IV, PrimeScript, SensiScript, Accuscript | Performance reproducibility was best for Maxima H and Superscript IV |
Cholet et al., 2020 | SuperScript II, SuperScript IV, Sesniscript, Omnicsript, | Addition of RNA mock communities into environmental RNA (before reverse transcription) can aid interpret sequencing results |