Synthetic Genetic Arrays


Personal Robotics for Omics with High-Density Yeast Arrays

Charles Boone¹, Amy Tong¹, Pawel Kusan², Harry Singer³, and Carl Singer³

¹Boone Lab, University of Toronto, Toronto, Canada M56 1L6. ²Engineering Services Inc., Toronto, Canada, M5R 2J7. ³Singer Instrument Co. Ltd., Roadwater, Somerset, TA23 ORE, UK.

Summary

Synthetic Genetic Array (SGA) analysis involves the manipulation of high-density yeast arrays to identify synthetic genetic interactions.  In a typical SGA screen, a query strain is systematically crossed to an ordered array of deletion mutants, such that the meiotic progeny harbouring both gene mutations can be assayed for growth defects.  Identifying these interactions allows for the construction of large genetic networks, which reveal functional dependency and pathway redundancy in yeast.

Principles of SGA

SGA offers an approach for the systematic construction of double gene deletion mutants and enables global analysis of genetic interactions [1,2].  Below are the steps involved in a SGA screen [3] :

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  1. MATα strain with a strain background of MFA1pr-HIS3, can1, and lyp1 is used to construct a query deletion mutant linked to a nourseothricin (clonNAT)-resistance marker, natMX.
  2. The query mutant is then crossed to an ordered array of MATa mutants, each carrying a gene deletion linked to the geneticin (G418)-resistance marker, kanMX (Figure 1A).
  3. The resulting heterozygous diploids are selected on a medium that contains clonNAT and G418 (Figure 1B).
  4. Then diploids are transferred to a medium that contains reduced levels of carbon and nitrogen to induce the sporulation of haploid meiotic progeny (Figure 1C).
  5. Spores are then transferred to medium that lacks histidine and contains canavanine and thialysine to select for MATa meiotic progeny (Figure 1D).
  6. MATa meiotic progeny containing both gene deletions is selected on a medium that lacks histidine and contains canavanine, thialysine, clonNAT, and G418. Double mutants that grow on such a medium are then scored for growth fitness (Figure 1E).
double mutant selection using Synthetic Genetic Arrays

The theory behind genetic interactions

If two genes are functionally unrelated, the double mutant containing these two gene mutations would exhibit a phenotype that is approximately the product of the phenotypes of the individual mutants.

However, when mutations in two gene products produce a phenotype that deviates from each gene’s individual effect, these two genes exhibit a genetic interaction.  There are two general categories of genetic interactions: aggravating interactions and alleviating interactions (Figure 2A).

theory of genetic interactions in yeast

An aggravating (or negative) interaction occurs when a double mutant exhibits a phenotype that is more severe than expected from the phenotypes of the individual mutants. This type of interaction indicates that the gene products function in redundant parallel pathways, and highlights the robustness of the molecular network in tolerating genetic variations [4].

An alleviating (or positive) interaction occurs when a double mutant exhibits a phenotype that is less severe than expected from the phenotypes of individual mutants.  This type of interaction indicates that the gene products operate in concert or in series within the same pathway [4].

Genes that function in the same pathway tend to have similar genetic interaction profiles.  Therefore, identifying genetic interactions can reveal functional relationships between genes and biological pathways [4] (Figure 2B).

Synthetic Genetic Array for synthetic leathal selection

Applying SGA to Functional Studies

SGA analysis enables the genome-wide screening of synthetic lethal or synthetic sick interactions, which are examples of aggravating interactions.  Synthetic interactions reveal functional relationships between genes whose products buffer each other or impinge on a common essential pathway.  Therefore, SGA analysis sheds light on the function of genes and permits the identification of novel components of specific pathways [1].

SGA analysis can be applied to the high-resolution mapping of genetic suppressors (Figure 3).  A suppressor is a mutation occurring elsewhere in the genome that alleviates the growth defect of the query mutant.  This application, termed SGAM (SGA mapping), is based on the principle that the frequency of meiotic recombination, which is the basis of creating double mutants in SGA, reduces as chromosomal locations of two genes get closer [5].  Therefore, a set of genes that is closely located, or “linked,” to the suppressor gene would appear synthetic lethal/sick with the query mutation.  Identifying genetic suppressors is useful because alleviating interactions reveals genes whose products function in the same complex or pathway [6].


Suppressor Mapping

Yeast-2-hybrid suppressor mapping

Library Collections

In addition to the deletion collections [7,8], there are many other genome-wide libraries available in the yeast community.  A sample of the available libraries includes arrays of the Tet-promotor [9] and transposon [10] mutants, genes tagged with TAP (tandem affinity purification) [11] and GFP (green fluorescent protein) [12], and strains containing Y2H (yeast 2-hybrid) [13] and GST (glutathione S-transferase) [14] fusion plasmids.

This collection of library arrays extends the applications of the SGA methodology to other forms of interactions, including dosage lethality and higher-order genetic interactions [3], thereby allowing scientists to comprehensively decipher biological networks in yeast.

Working with libraries

High-throughput SGA screening can be done quickly and easily using automated robotics, such as the Singer ROTOR+, which can rapidly pin high-density arrays of yeast as well as facilitate strain mating, sporulation, and selection.  In addition, the ROTOR+ screening robot provides an automated platform to simultaneously produce multiple experimental replicates.

SGA Applications

Use of ROTOR+ for Synthetic Lethality Screens

Dhungel N et al. (Neuron, 2015) Parkinson’s Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein, doi: 10.1016/j.neuron.2014.11.027

Methods

Dhungel et al., (Neuron, 2015) used ROTOR+ to conduct a synthetic genetic array (SGA) (Tong and Boone, 2006) to introduce either the VPS35 or the TIF4631 deletion, by mating, to a collection of ∼4,900 yeast strains harboring single deletions in nonessential genes (Figure S1A available online). After performing the vps35Δ and tif4631Δ synthetic lethal screens independently (each screen replicated three times), they scored each of the double deletions for growth.

References

1. Tong AH, Evangelista M, Parsons AB, Xu H, Bader GD, et al. (2001) Systematic genetic analysis with ordered arrays of yeast deletion mutants. Science 294: 2364-2368.

2. Tong AHY, Lesage G, Bader GD, Ding H, Xu H, et al. (2004) Global mapping of the yeast genetic interaction network. Science (New York, NY) 303: 808-813.

3. Tong AH, Boone C (2006) Synthetic genetic array analysis in Saccharomyces cerevisiae. Methods Mol Biol 313: 171-192.

4. Dixon SJ, Costanzo M, Baryshnikova A, Andrews B, Boone C (2009) Systematic mapping of genetic interaction networks. Annual Review of Genetics 43: 601-625.

5. Costanzo M, Boone C (2009) SGAM: an array-based approach for high-resolution genetic mapping in Saccharomyces cerevisiae. Methods Mol Biol 548: 37-53.

6. Boone C, Bussey H, Andrews BJ (2007) Exploring genetic interactions and networks with yeast. Nat Rev Genet 8: 437-449.

7. Winzeler EA, Shoemaker DD, Astromoff A, Liang H, Anderson K, et al. (1999) Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis. Science (New York, NY) 285: 901-906.

8. Giaever G, Chu AM, Ni L, Connelly C, Riles L, et al. (2002) Functional profiling of the Saccharomyces cerevisiae genome. Nature 418: 387-391.

9. Mnaimneh S, Davierwala AP, Haynes J, Moffat J, Peng W-T, et al. (2004) Exploration of essential gene functions via titratable promoter alleles. Cell 118: 31-44.

10. Ross-Macdonald P, Coelho PS, Roemer T, Agarwal S, Kumar A, et al. (1999) Large-scale analysis of the yeast genome by transposon tagging and gene disruption. Nature 402: 413-418.

11. Gavin A-C, Bösche M, Krause R, Grandi P, Marzioch M, et al. (2002) Functional organization of the yeast proteome by systematic analysis of protein complexes. Nature 415: 141-147.

11. Huh W-K, Falvo JV, Gerke LC, Carroll AS, Howson RW, et al. (2003) Global analysis of protein localization in budding yeast. Nature 425: 686-691.

12. Uetz P, Giot L, Cagney G, Mansfield TA, Judson RS, et al. (2000) A comprehensive analysis of protein-protein interactions in Saccharomyces cerevisiae. Nature 403: 623-627.

13. Zhu H, Bilgin M, Bangham R, Hall D, Casamayor A, et al. (2001) Global analysis of protein activities using proteome chips. Science (New York, NY) 293: 2101-2105.

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