Measuring UV-induced Mutagenesis at the CAN1 Locus in Saccharomyces cerevisiae   

Download PDF How to cite Favorites 1 Q&A Share your feedback

In this protocol

Original research article

A brief version of this protocol appeared in:
PLOS Biology
Jan 2014


There are several methods to measure the capacity of yeast cell to respond to environmental impacts on their genome by mutating it. One frequently used method involves the detection of forward mutations in the CAN1 gene. The CAN1 gene encodes for an arginine permease that is responsible for the uptake of arginine and it can also transport the toxic analog of arginine, canavanine (Whelan et al., 1979). When CAN1 cells are grown on a media containing canavanine but lacking arginine, the cells die because of the uptake of the toxic canavanine. However, if a mutation in the CAN1 gene inactivates the permease, that cell survives and forms a colony on the plate.
The following protocol describes the measurement of UV-induced mutagenesis at the CAN1 locus.

Keywords: Yeast, Mutagenesis, Forward mutations, Canavanine, UV light

Materials and Reagents

  1. Strains that have the wild type CAN1 gene (e.g., BY4741, EMY747)
  2. Yeast nitrogen base [w/o amino acids and w (NH4)2SO4] (Difco)
  3. Adenine (Sigma-Aldrich)
  4. Arginine (Sigma-Aldrich)
  5. Canavanine (Sigma-Aldrich)
  6. Histidine (Sigma-Aldrich)
  7. Isoleucine (Sigma-Aldrich)
  8. Leucine (Sigma-Aldrich)
  9. Lysine (Sigma-Aldrich)
  10. Methionine (Sigma-Aldrich)
  11. Phenylalanine (Sigma-Aldrich)
  12. Tryptophan (Sigma-Aldrich)
  13. Tyrosine (Sigma-Aldrich)
  14. Uracil (Sigma-Aldrich)
  15. Valine (Sigma-Aldrich)
  16. Yeast extract
  17. Pepton
  18. D-glucose
  19. Bacto agar
  20. Yeast extract-pepton-D-glucose (YPD) media (see Recipes) (or other media needed for the strain in use)
  21. Synthetic complete media (SC) plates (see Recipes)
  22. SC-arginine plates containing canavanine (+can) (see Recipes)


  1. 30 °C incubator-shaker (180-200 round per minute)
  2. 30 °C incubator
  3. Glass slide
  4. Centrifuge
  5. Microscope
  6. Vortex
  7. UV-irradiation machine
  8. Box
  9. Spreader
  10. Culture tube
  11. Waterbath sonicator
  12. Hemocytometer (Burker counting chamber)


  1. By inoculating a single colony from a fresh plate, grow up 10 ml overnight cultures in YPD (one reference, or wild type strain, and the strains to be examined).
  2. Put the culture tube into a waterbath sonicator and sonicate the cells at room temperature for 3 min to disrupt clumps (40 Hz). Check for the presence of clumps under the microscope.
  3. Make 200x dilutions of each strain in water (5 µl cell culture into 995 µl water) and put 10 µl onto a Burker-chamber.
  4. Count the cells under the microscope in a big square of the Burker-chamber (bordered by three lines) (Figure 1). One cell in a big square means 1 x 104 cells/ml.
  5. Calculate the density of the original cultures (multiply the counted cell number by 200).
  6. Make 10x serial dilutions of each strain, starting from 108 to 103 cells/ml. If necessary concentrate cells to get 108 cells/ml. When calculating the volume of a given dilution step, take into consideration how many plates you will be plating from that dilution (see steps 8 and 9 below).
  7. Label the SC and the +can plates with the strain names and the UV doses you want to apply. For each UV dose, including zero, label 2 SC and 2 +can plates for each strain. The SC plates will be used to calculate survival at different UV doses, the +can plates will be used to calculate mutagenesis at different UV doses.
  8. Plate 200 µl on the control, 0 J/m2 SC plates from the 103 cells/ml dilution. For wild type, EMY747 or BY4741 cells that are quite resistant to UV showing 20% survival at 80 J/m2, for up to that dose the 103 cells/ml dilution should be used for plating. In case of more sensitive strains the expected survival rate should be taken into consideration when determining which dilution to use for plating for given UV doses.
  9. Plate 200 µl cells on the +can plates from the 108 cells/ml dilutions.
  10. Wait till plates absorb the moisture, then irradiate the plates without lids, with the required UV doses. Make sure the irradiated plates are not exposed to white light after irradiation (work with yellow light on), and they are placed right away in a box that shields them from light and put in the 30 °C incubator.
  11. Incubate the plates until colonies grow to 2-3 mm in diameter. For SC plates it takes usually 2-3 days, for +can plates it takes up to 5 days (check them under yellow light).
  12. Count the colonies on each plate.
  13. Calculate the percentage of survival on SC plates. Divide the average number of colonies of the two 0 J/m2 plates with the number of cells that were plated on one plate and multiply it by 100. That gives the percentage of cells that survived plating.
  14. Calculate the survival at each UV doses. Multiply the average colony number of the two parallel plates with the plating survival percentage calculated from 0 J/m2 plates (see step 13 above), and divide it by the number of cells that was plated. (Take into consideration the actual volumes you plated at different doses: 100 µl, or 200 µl!)
  15. Calculate mutagenesis from +can plates. Multiply with the survival percentage the number of cells plated on a plate at the given UV dose. Calculate the average number of colonies from the two parallel plates of the same UV dose. That gives you the number of mutants/plated cells. Based on that calculate how many mutants would be in 106 cells, because mutagenesis data usually corresponds to 106 cells. (Take into consideration the actual volumes you plated at different doses: 100 µl, or 200 µl!)

    Figure 1. Burker chamber. One cell in one blue area means 1 x 104 cells/ml. (Source:

Representative data

  1. Since the result of this experiment depends on the number of inactivating mutations in the CAN1 gene inflicted upon by UV, the number of mutants can vary. Because of that average numbers should be calculated based on 3-5 experiments.


  1. YPD liquid
    1% yeast extract
    2% pepton
    2% D-glucose
  2. SC plates
    Bacto-agar: 16.6 g/L
    D-glucose: 20 g/L
    12 media mix: 7.2 g/L
    12 media mix
    Yeast nitrogen base [w/o amino acids and w (NH4)2SO4]
    400 g
    1.8 g  
    1.2 g
    1.2 g
    1.8 g
    1.8 g
    1.8 g
    1.2 g
    3.0 g
    1.2 g
    1.8 g
    1.2 g
    9.0 g
  3. SC -arginine plates containing canavanine
    Same as the SC plates, but the media mix contains 3.6 g canavanine instead of arginine


We used this protocol in our work (Daraba et al., 2014). Funding support: Wellcome Trust, 070247/Z/03/A.


  1. Daraba, A., Gali, V. K., Halmai, M., Haracska, L. and Unk, I. (2014). Def1 promotes the degradation of Pol3 for polymerase exchange to occur during DNA-damage--induced mutagenesis in Saccharomyces cerevisiae. PLoS Biol 12(1): e1001771.
  2. Whelan, W. L., Gocke, E. and Manney, T. R. (1979). The CAN1 locus of Saccharomyces cerevisiae: fine-structure analysis and forward mutation rates. Genetics 91(1): 35-51.
Copyright: © 2014 The Authors; exclusive licensee Bio-protocol LLC.
How to cite:  Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
  1. Unk, I. and Daraba, A. (2014). Measuring UV-induced Mutagenesis at the CAN1 Locus in Saccharomyces cerevisiae. Bio-protocol 4(20): e1272. DOI: 10.21769/BioProtoc.1272.
  2. Daraba, A., Gali, V. K., Halmai, M., Haracska, L. and Unk, I. (2014). Def1 promotes the degradation of Pol3 for polymerase exchange to occur during DNA-damage--induced mutagenesis in Saccharomyces cerevisiae. PLoS Biol 12(1): e1001771.

Please login to post your questions/comments. Your questions will be directed to the authors of the protocol. The authors will be requested to answer your questions at their earliest convenience. Once your questions are answered, you will be informed using the email address that you register with bio-protocol.
You are highly recommended to post your data including images for the troubleshooting.

You are highly recommended to post your data (images or even videos) for the troubleshooting. For uploading videos, you may need a Google account because Bio-protocol uses YouTube to host videos.

Ying Wu
University of Maryland College Park

Right now I am trying to doUV mutagenesis for powdery mildew (a biotroph fungi). However, I am not sure what machine and dose I should use. Could you tell me the UV machine you used? I have a UV-crosslinker. The power is 10,000uJ/cm2. Do you think if I can use it for mutagenesis?



5/29/2017 4:53:44 AM Reply
Ildiko Unk
The Institute of Genetics, Biological Research Center of The Hungarian Academy of Sciences, Hungary

The machine was made here at the institute according to my request.
I have never worked with powdery mildew, so you have to search the literature, or try different doses.
In my experience, UV cross linkers do not work well for irradiating fungi on plate, because they can only irradiate with one single dose, but you usually have to apply a broad range of doses to perform an experiment, e.g. a killing curve.
My advice is to look for a lab in/around your institute that already has a machine you need.

8/24/2017 7:07:37 AM