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    Determining Genome Targeting Efficiency using T7 Endonuclease I (M0302)

    New England Biolabs

    Published: 2022-02-14 DOI: 10.17504/protocols.io.bfhqjj5w
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    Abstract

    T7 Endonuclease I recognizes and cleaves non-perfectly matched DNA. This protocol describes how to determine genome targeting efficiency by digesting annealed PCR products with T7 Endonuclease I. In the first step PCR products are produced from the genomic DNA of cells whose genomes were targeted using Cas9, TALEN, ZFN etc. In the second step, the PCR products are annealed and digested with T7 Endonuclease I. Fragments are analyzed to determine the efficiency of genome targeting.

    Before start

    Steps

    PCR

    1.

    Set up a 50µL PCR reaction using ~100ng as a template. For each amplicon set up 3 PCR reactions using the following templates:

    • gDNA from targeted cells (e.g. Cas9, or TALEN transfected cells)
    • gDNA from negative control cells (e.g. non-specific DNA transfected cells)
    • water (i.e. no template control) PCR using Q5 High-Fidelity DNA Polymerase
    ABC
    COMPONENT50 µl REACTIONFINAL CONCENTRATION
    Q5® Hot Start High-Fidelity 2X Master Mix (M0494)25 µl1X
    10 µM Forward Primer2.5 µl0.5 µM
    10 µM Reverse Primer2.5 µl0.5 µM
    Template DNAvariable100 ng total
    Nuclease-free waterTo 50 µl
    2.

    Gently mix the reaction.

    3.

    Collect all liquid to the bottom of the tube by a quick spin if necessary.

    4.

    Transfer PCR tubes to a PCR machine and begin thermocycling:

    Cycling Conditions

    ABC
    STEPTEMPERATURETIME
    Initial Denaturation98°C30 seconds
    35 cycles98°C5 seconds
    *50-72°C10 seconds
    72°C20 seconds
    Final Extension72°C2 minutes
    Hold4-10°C

    *Use of the NEB Tm Calculator is highly recommended.

    Note
    Note: Q5 Hot Start High-Fidelity 2X Master Mix does not require a separate activation step. Standard Q5 cycling conditions are recommended.

    5.

    Analyze a small amount of the of the PCR product to verify size and appropriate amplification.

    6.

    Purify the PCR reaction using 90µL following the manufacturer’s recommendations.

    Note
    Other PCR purification systems (e.g. Other PCR purification systems (e.g. Monarch PCR & DNA Clean Up Kit, or Zymo DNA Clean and Concentrator™) are acceptable., or Zymo DNA Clean and Concentrator™) are acceptable.

    7.

    Elute PCR products in 30µL, recovering 25µL.

    8.

    Measure the concentration of the purified PCR products.

    T7 Endonuclease I digestion

    9.

    Assemble reactions as follows:

    AB
    COMPONENT19 µl ANNEALING REACTION
    DNA200 ng
    10X NEBuffer 22 µl
    Nuclease-free WaterTo 19 µl
    10.

    Anneal the PCR products in a thermocycler using the following conditions:

    Hybridization Conditions

    ABCD
    STEPTEMPERATURERAMP RATETIME
    Initial Denaturation95°C5 minutes
    Annealing95-85°C-2°C/second
    85-25°C-0.1°C/second
    Hold4°CHold
    11.

    Add 1 to the annealed PCR products for a final volume of 20µL.

    12.

    Incubate at 37°C for 0h 15m 0s.

    13.

    Stop the reaction by adding 1.5µL.

    14.

    Purify the reaction using 36µL according to the manufacturer’s suggestion.

    Note
    This step is optional since 1 µl of the reaction will not interfere with analysis on an Agilent Bioanalyzer using DNA1000 reagents.

    15.

    Elute the DNA fragments in 20µL, recovering . 15µL.

    Analysis

    16.

    Analyze the fragmented PCR products and determine the percent of nuclease-specific cleavage products (fraction cleaved).

    17.

    Calculate the estimated gene modification using the following formula:

    % gene modification = 100 x (1 – (1- fraction cleaved)1/2)

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