McClean: Yeast Mating Halo Assay

From OpenWetWare
Revision as of 06:34, 3 November 2011 by Megan N McClean (talk | contribs) (References)
Jump to: navigation, search


This is a template for how to write a new protocol in openwetware for our lab. In your real protocol, a description of what the protocol is and when to use it would go here.


  • Item 1
  • Item 2
  • Stock Solution 1
  • Stock Solution 2

Stock Solutions

Stock Solution 1

  • This is a very simple solution, so we only need a one line description of how to make it.

Stock Solution 2

This is a more involved solution, so we will describe how to make it in several steps:

  1. Step 1
  2. Step 2
  3. Step 3


  1. Step 1
  2. Step 2
  3. Step 3


Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input!

  1. List troubleshooting tips here.
  2. You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
  3. Anecdotal observations that might be of use to others can also be posted here.

Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.


Adapted from Maitreya Dunham's protocol (Dunham Lab Protocols) which was adapted from Katja Schwartz's protocol from the Botstein lab (Botstein Lab Protocols)


or instead, discuss this protocol.

Halo Mating Type Assay Maitreya Dunham July 2004 Protocol derived from Katja Schwartz's protocol. In addition to your strains of interest, streak out: DBY7730 (aka RC634a) MATa ade2 his6 met1 ura1 can1 cyh1 rme sst1-3 DBY7442 (aka XT1-20A) MATalpha leu- ura- ade- sst2 These strains were made in the Thorner lab. See Julius et al (1983) Cell, 32, 839-52 for documentation of DBY7730. DBY7442's exact genotype is unknown. The sst mutations make them super-sensitive to pheromone. When exposed to pheromone of the opposite mating type, the cells arrest. Let streaks grow 2 days 30C. Inoculate overnight YPD cultures of the mating type testers. Dilute the overnights 1:10 with sterile media or water. Spread ~200 μl lawn on YPD plates, one for each mating type. Incubate 30C 30 min. Pin your strains of interest to the lawns, or use a toothpick to make small, well-separated patches on the lawn. Make sure to flame the frogger between each plate, or use a fresh toothpick for each plate. Incubate 30C overnight. Score whether or not the patch has a halo of space around it. If it does, that means that the lawn strain responded to the pheromone emitted by the patch, and thus that they are of opposite mating type. So, if a halo formed around the patched strain on the a tester plate, the strain itself is alpha. The nice thing about having both the a and the alpha tester plates is that you can double-check your scoring by making sure there is a halo on only one tester plate.