1. Reference: Science 240, 1439-1443 (1988). Methods in Enzymology 194, 3-77 (1991). Science 274, 546-567 (1996). Yeast molecular biology-yeast vectors, expression of proteins in Yeast

2. Saccharomyces cerevisiae (budding yeast, bakers yeast) Schizosaccharomyces pombe (fission yeast, brewers yeast) Two commonly used yeast in molecular genetics:

4. non-pathogenic, edible contain all the advantage of bacterial genetics a monocellular eukaryotic cell with essentially all the organelles a genetically manipulable life cycle well established molecular biology tools well studied biochemical pathway the sequences of S. cerevisiae genome had been determined What ‘s special about yeast:

5. Nomenclature in yeast YFG1: locus or dominant allele (mostly wild type), capital, italic yfg1-119: a specific recessive mutant of YFG1, -119 is the name of allele yfg1::LEU2: YFG1 is integrated by LEU2 yfg1  1: a deletion mutant of YFG1 Yfg1p: gene product of YFG1, a protein

6. Genome of diploid Saccharomyce cerevisiae cell CharacteristicChromosomes2-  m plasmidMitochondiral Relative amount (%)85510 Number of copies2 x 1660-100~50 (8-130) Size (kbp)14,000 6.31870-76 MutantsAll kindsnoneCyt a.a 3, b Yeast genome

7. Yeast life cycle

8. Sporulation and tetrad dissection

9. Tetrad dissection

10. Analysis of spore products Complement medium Selection medium

11. Yeast Molecular Genetics vectors cloning Making mutants Gene expression

12. Yeast vectors Plasmids Yeast artificial chromosome Origin of replication Selection markers Yeast strains

13. Need an autonomous replication sequence (ARS) for plasmid to replicate. CEN: contain a chromosomal centromere, YCp (yeast centromeric plasmid) 2  m: YEp (yeast episomal plasmid) origin-less: YIp (yeast integrating plasmid) cannot replicate in yeast, integrate into yeast chromosome Plasmids Origin of replication: Origincopy numberstability (%) # ARS1-5 ARS -CEN1-290-99 ARS -2  m  origin-less1100 # stability of plasmid is determined as the percentage of plasmid bearing colonies after overnight culture (~10 cell divisions) in the absence of selection.

14. Plasmids Nutrition dependence: uracil (URA3), adenine (ADE2, ADE3), leucine (LEU2), tryptophan (TRP1), lysine (LYS2) Selection marker: Diploid vs. halploid Mating type: a or  Genotype: yeast strains should have genotypes that can accommodate plasmids with various selection markers. MATa ade2-1 lys2-1 his3-  200 leu2-  1 trp1-  63 ura3-52 Strain

15. URA3: The gene product of URA3 (orotidine-5’-phosphate decarboxylase) converts 5-FOA (5-fluoroorotic acid) to a toxic product that kills the URA3 cells. LYS2: The LYS2 gene encodes  -aminoadipate reductase, an enzyme required for lysine biosynthesis. Yeast cells with wild-type LYS2 activity will not grow on media containing  -aminoadipate (  -AA) as a primary nitrogen source. CAN1: The CAN1 gene encodes an arginine permease. In the absence of arginine, canavanine (arginine analog) is readily incorporated into proteins with lethal consequences; therefore, CAN1 cells are sensitive to canavanine. CYH2: The CYH2 gene encodes the L29 protein of the yeast ribosome. Cycloheximide blocks translation elongation by interacting with L29. Yeast negative selection systems:

16. A typical yeast plasmid

17. High cloning capacity, ~300 kbp. centromere, telomere, selection markers. Linear plasmids (YLp) Yeast artificial chromosome (YAC)

18. Transformation in yeast Li-acetate method Up to 2.2 x 10 7 transformants/  g DNA; simple, easy, and cheap. Spheroplast method ~1-5 x 10 4 transformants/  g DNA; need to digest yeast cells with zymolyase, technically difficult and time consuming Electroporation Transformation efficiency can be ~4 x 10 5 transformants /  g DNA. Need a gene pulser, usually expensive.

19. Unlike the well established plasmid purification methods in E. coli, no easy plasmid purification method is developed in yeast. Plasmids are purified along with chromosomal DNA. Most yeast plasmids are “shuttle vectors”, i. e., can propagate in both yeast and E. coli. To recover yeast plasmid DNA, total yeast DNA is purified and transformed into E. coli. Yeast plasmid DNA is then isolated from E. coli. Isolation of yeast DNA Budding yeast has thick walls, to break the cell walls, two methods are used: Mechanical force: use glass beads to break the cell walls. Enzymatic digestion: zymolyase or glusulase are used to digest apart the cell walls.

20. Cloning by mail Complementation of recessive alleles Cloning dominant alleles High-copy suppression Isolating regulated promoters Isolating specific genes from other organisms Yeast genomic and cDNA libraries Cloning in yeast

22. Plasmidinsert size (kbp)selection markeroriginreference YRp75-20 TRP1no1 YEp135-7LEU22  m YEp247-10URA32  m2 YCp5010-20URA3CEN43 pRS3146-8TRP1CEN6 pRS4246-8TRP12  m pRS4256-8LEU22  m YEPFAT106-8TRP1 leu2-d2  m pMAC561cDNATRP12  m4 pRS316GALcDNAURA3CEN5 ________________________________________________________ Nasmyth & Reed PNAS 77, 2119-2123, 1980. Carlson and Botstein Cell 28, 145-154, 1982. Rose et al. Gene 60, 237-243, 1987. McKnight & McConaughy PNAS 80, 4412-4416, 1983. Liu et al. Genetics 132, 665-673, 1992 Yeast genomic and cDNA libraries

23. Gene expression in yeast Copy number Promoter Protease problem

24. Copy number alternate the copy number of DNA alternate the expression of genes. Plasmid copy number: cryptic allele of leu2-d promoter increases the plasmid copy number up to several hundred copies per cell. Ty transposition vector insert semi-randomly into yeast genome

25. Promoter Constitutive: ADH1 (alcohol dehydrogenase I) and PGK (3- phosphoglycerate kinase), produce about 1% each of total yeast mRNA. Inducible: GAL1, GAL10 (repressed by glucose, induced by galactose), PHO5 (induced by inorganic phosphate), upon induction the level of gene expression increase from 10-30 folds.

26. Protease problem Growth stage Protease deficient strain: there are protease-deficient mutants available that can be used for gene expression purposes. For example: BJ2168 (MATa leu2 trp1 ura3-52 prb1-1122 prc1-407 pep4-3 prc1-407 gal2) Yeast contains a large number of proteases that are located in various compartments of the cell.

27. Chemicals: ethylmethane sulfonate (EMS), N-methyl-N’-nitro- N-nitrosoguanidine (MNNG), produce transitions at G-C sites. UV: usually occur in runs of pyrimidines and include both transitions and transversions. Frame-shift mutations are also observed. Making mutants Classical mutagenesis techniques: The highest proportion of mutants per treated cell is usually found at doses giving 10 to 50% survival. Gene targeting: In the absence of ARS sequences, DNA transformed into yeast cells integrated into the genome exclusively by homologous recombination.

28. Gene targeting scheme: