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One-Step Ligation on RNA Amplification for the Detection of Point Mutations  Lei Zhang, Jingjing Wang, Mia Coetzer, Stephanie Angione, Rami Kantor, Anubhav.

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Presentation on theme: "One-Step Ligation on RNA Amplification for the Detection of Point Mutations  Lei Zhang, Jingjing Wang, Mia Coetzer, Stephanie Angione, Rami Kantor, Anubhav."— Presentation transcript:

1 One-Step Ligation on RNA Amplification for the Detection of Point Mutations 
Lei Zhang, Jingjing Wang, Mia Coetzer, Stephanie Angione, Rami Kantor, Anubhav Tripathi  The Journal of Molecular Diagnostics  Volume 17, Issue 6, Pages (November 2015) DOI: /j.jmoldx Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

2 Figure 1 A schematic overview of the three stages of ligation on RNA amplification. The temperature cycling during the ligation stage 1 allows for a linear increase of ligated products and off sets the lower hybridization rate of low copies of mutant in high wild-type concentration mixtures. The ligase is heat inactivated, whereas the polymerase becomes activated during stage 2. The polymerase initiates quantitative PCR amplification of the ligated products during stage 3. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

3 Figure 2 The effects of length of ligation probes on the rate and the specificity of ligation on RNA. The right y axis indicates the specificity expressed as rate of reaction on mutant templates divided by the rate of reaction on wild-type templates. The left y axis indicates the efficiency expressed as rate of reaction with the use of different detector probe lengths divided by the optimum rate. Data are expressed as means ± SD. nt, nucleotide. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

4 Figure 3 The effect of a single DP nucleotide mismatch on RNA ligation efficiency and specificity. The right y axis indicates the specificity expressed as rate of reaction on mutant templates divided by the rate of reaction on wild-type templates. The left y axis indicates the efficiency expressed as rate of reaction using different DP lengths divided by the optimum rate. Shown above the graph are the target sequence (top) with wild-type/mutant nucleic acids; the CP sequence (bottom left); and the DP sequence (bottom right) with mismatches (Cs instead of Ts) at positions 2 and 3. Data are expressed as means ± SD. CP, common probe; DP, detector probe; nt, nucleotide. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

5 Figure 4 Chemical modifications used on the CP and the DP. Adenosine monophosphate (navy) modifications used include 1-Thio-AMP (the red denotes the sulfur on the phosphate group). Deoxyribose sugar modifications used include 2-Fluoro analogs (black). Nitrogenous base modifications used include inosine and cytosine (orange). RNA template is in lime, CP is in cyan, and DP is in pink. The 3′-OH group on DP is depicted in yellow. CP, common probe; DP, detector probe. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

6 Figure 5 The effects of chemical modifications of CP and DP on the specificity of LRA. The right y axis indicates the specificity expressed as rate of the reaction on mutant templates divided by the rate of reaction on wild-type templates. The left y axis indicates the efficiency expressed as rate of the reaction using different lengths of the DP divided by the optimum rate. For each modification, the rates of specific and unspecific reactions are determined by their difference in the Cts with that of no modification control. Shown above the graph are the target sequence (top) with wild-type/mutant nucleic acids being differentiated by the A/C nucleotide; the CP sequence (bottom left) with AMP modification (yellow); and the DP sequence (blue) with modifications (bottom right) with various modifications. Data are expressed as means ± SD. CP, common probe; DP, detector probe; LRA, ligation on RNA amplification. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

7 Figure 6 Detection of K103N-containing RNA transcripts in wild-type mixtures by ligation on RNA amplification. A: Quantitative PCR amplification curves of the RNA mixtures. B: Ratios of mutant to wild-type RNA mixtures plotted against their cycle number. The slope of the plot is −3.2. Error bars represent 1 SD. NTC, no template control. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

8 Figure 7 Quantitative PCR amplification curves of the detection of K103N mutant and wild-type RNA with the use of reverse transcription ASPCR. The rate of ASPCR on mutant RNA is 208 times faster than that on wild-type RNA (as determined by the difference in threshold values during quantitative PCR, 2−ΔCt). ASPCR, allele-specific PCR; NTC, no template control. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

9 Figure 8 Detection of concentration of K103N templates diluted into K103 wild-type templates by pyrosequencing. A: Pyrosequencing reads of K103N mutant in wild-type templates. B: Percentage of K103N detected by pyrosequencing compared with the actual percentage of K103N mutant present. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

10 Figure 9 Detection of HIV-1 K103N RNA transcripts with the use of ligation on RNA amplification. The sensitivity of the assay is evaluated by quantitative PCR amplification. A: Amplification curves of different concentrations of the K103N-containing RNA and NTC. The samples were prepared by 10-fold serial dilutions into nuclease-free water, and water is used in the NTC. The limit of detection is determined to be 5 × 102 copies/μL. B: The concentrations of K103N mutant RNA, in log (copy number), plotted against their cycle number. The slope is −3.2. Error bars represent 1 SD. NTC, no template control. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

11 Supplemental Figure S1 The pre-adenylation efficiency of the common probe with the use of ATP and ATP analogs. The pre-adenylation efficiency was evaluated over a period of 1, 2, and 8 hours. Data are expressed as means ± SD. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

12 Supplemental Figure S2 Effects of reaction conditions on rates of the LRA reaction. Rates (y axis) are shown by the relative Ct values normalized to the lowest Ct within each set of conditions (1/2ΔCt). The sets of conditions evaluated are shown on the x axis and include the pH, Mg2+, and the presence of ATP with and without PA. Data are expressed as means ± SD. LRA, ligation on RNA amplification; PA, pre-adenylation. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

13 Supplemental Figure S3 Derivation of relative efficiency and specificity of using cytosine-modified ligation probe for ligation on RNA amplification. The relative efficiency and specificity are calculated from Ct values obtained from quantitative PCR reactions. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

14 Supplemental Figure S4 Illustration of potential undesired production of ligated products for traditional ligation amplification on DNA. A: Besides the desired reaction, side reactions can produce the ligated product. B: The FP can be extended along the CP to produce a complimentary copy of the CP. C: In the event, the CP and the DP are not enzymatically ligated because of a single-nucleotide mismatch on the 3′ end of the DP, extension of the DP can still occur on the DNA target sequence. D: The DP′ and the FP′ on hybridization can dimerize and produce the ligated product. E: The formation of DP dimers. CP, common probe; DP, detector probe; DP′, extended detector probe; FP, forward primer; FP′, extended forward primer. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

15 Supplemental Figure S5 Melting curve analysis of one-step ligation on RNA amplification with the sequence-specific probe replaced with EvaGreen intercalating dye. The graph shows the formation of primer dimers (lower peak) in a nonoptimized NTC reaction, the formation of the specific amplicon with 107 copies of mutant RNA (middle peak), and the formation of DP dimer (higher peak) in a NTC reaction with no CP. Both the specific product and the DP dimer will be detectable when sequence-specific probes are used. CP, common probe; DP, detector probe; NTC, no-template control. The Journal of Molecular Diagnostics  , DOI: ( /j.jmoldx ) Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology Terms and Conditions

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