Sporulation of Diploids
Overview
Sporulation is how you generate haploid yeast strains from diploid yeast strains. An example of this would be to generate haploid deletion strains from a diploid strain from the het dip (heterozygous diploid) deletion collection.
If this doesn't work, try GNA sporulation, which takes longer but is reported to be more reliable.
Materials
Procedure
Set up and label culture tubes. Label each tube with a piece of tape and tough spot.
Fill each culture tube with 3 mL of YEP + 2% glucose.
Inoculate each tube using a pipette tip (P10 or P20 work well) from a single colony of your diploid strain in question. Circle, initial, and date the colony used. Shake at 30°C overnight.
The next day, add 3ml of Sporulation Media (SPM) to a new culture tube for each strain (be sure to label your new tubes).
Using 1000μL tips and a P1000 pipettor, for each strain, aliquot 300μL of your diploid culture into the new tube containing 3mL of Sporulation Media. Shake at 30°C for 5-7 days before going to
Tetrad Dissection
Notes
Part Numbers