BISC 219/2009: Mod 3 Structural Evidence for Transgenic Plants

Structural Evidence for Transgenic Plants

PCR Analysis of Transformed Plants
The goal of this procedure is to determine that your kanamycin-resistant plants are transformed by testing directly for the introduced DNA using the polymerase chain reaction (PCR) and gel electrophoresis.

The screening of transformed plants for the presence of an introduced gene used to be a time consuming process that involved the isolation of genomic DNA and Southern blot analysis. The polymerase chain reaction (PCR) however, has made this a relatively simple task that can be completed in an afternoon. In this lab you will use PCR to detect the GUS gene. The gene contains approximately 500 to 600 base pairs.

REDExtract-N-Amp™ Plant PCR kit (Sigma Product # XNAP http://www.sigmaaldrich.com)

Each team should test a control and all the experimental plants that you tested for GUS enzyme assay. Your instructor will amplify by PCR the gusA gene on the pBI121 plasmid to run on one of the gels as a positive control.

For each plant or control to be tested:

1. Collect 1 disk of young leaf tissue from a transgenic plant .by punching it out with the top of a microfuge tube. Wear gloves so that you do not contaminate the tube or the leaf with anything that might contain DNA and DNAase (your hands).
2. Push the leaf disk into the bottom of the microfuge tube using a tip from your P200. It is ok if the tissue tears, but be gentle.
3. Add 100 µl of Extraction Solution to the microfuge tube containing the leaf disk. Please note that this solution is in a microfuge tube in your ice bucket and is NOT the same as the “extraction solution” used for making the leaf extract in the GUS activity assay. DO NOT confuse these two reagents. Check with your instructor if you are not sure which is the correct reagent to use. Make sure the disk is completely covered with solution. Close the tube and vortex briefly.
4. Incubate for 10 minutes at 95 C. If using a water bath, be careful not to burn your fingers when placing tubes into and taking tubes out of the water bath. Use a cap holder to make sure your tubes do not becoming uncapped during the incubation. If you are using the dry bath note that the entire surface is HOT.
5. Remove tube from the incubator. The leaf tissue usually doesn’t appear degraded after this treatment.
6. Add 100µl of Dilution Solution, cap the tube, and vortex to mix.
7. Place the diluted DNA extracts on ice. You do not need to remove the leaf disk.

NOTE: The exact ingredients for the solutions in the kit are proprietary, but the extraction solution probably contains NaOH and the dilution solution used to neutralize the NaOH is probably HCl in a Tris buffer with detergent.