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Suppressor and Enhancer Screens

Suppressor and Enhancer Screens. Suppressor and enhancer screens. 1. General considerations 2. Using suppressors to delineate a signaling pathway: vulval induction in C. elegans 3. Suppressor screens don’t always work pha-1 suppressors

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Suppressor and Enhancer Screens

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  1. Suppressor and Enhancer Screens

  2. Suppressor and enhancer screens 1. General considerations 2. Using suppressors to delineate a signaling pathway: vulval induction in C. elegans 3. Suppressor screens don’t always work pha-1 suppressors 4. Using enhancers to identify new glp-1 interacting genes

  3. Final paper: Developmental Genetic Analysis in Xenopus Due: December 8, 2008 No more problem sets. Read carefully the instructions for the assignment on the web site.

  4. Saturation screens have limitations: • not all phenotypes are amenable to saturation screening • sometimes it is not practical to do enough screening to reach saturation • many genes involved in a process will not appear in the screens because of • a) pleiotropy • b) redundancy • c) bad luck

  5. Suppression: A + suppressor --> less severe “A” phenotype Enhancement: A + enhancer --> more severe “A” phenotype “synthetic” phenotype

  6. Modes of suppression: • compensating mutation • bypass suppressor: • Gain-of-function can suppress mutation in positive regulator • Loss-of-function can suppress mutation in a negative regulator • indirect supressor: • informational suppressors (e.g. tRNA nonsense suppressors, alternative splicing, NMD) • Physiological suppressors (e.g. mutations in collagen suppress glp-1) • intragenic suppressor • second site compensatory mutation • true revertant

  7. Enhancer Weak mutation in A - no phenotype or weak phenotype Mutation in B enhances A phenotype equivalent to synthetic lethal in yeast Can identify genes in a pathway and can identify genes with redundant functions.

  8. Enhancers in a pathway Enhancers due to redundancy gene A Genotype x Activity sufficient; little or no phenotype gene A(null) gene B gene A gene B (null) Activity sufficient; little or no phenotype gene B x gene A x Activity reduced or eliminated; strong phenotype gene A(null); gene B x Herman, R and Yochem J. (September 16, 2005), WormBook, ed. The C. elegans Research Community, WormBook, doi/10.1895/wormbook.1.7.1, http://www.wormbook.org.

  9. Advantages: • Both enhancers and suppressors can identify genes at any point in the pathway. • Is not restricted to proteins that directly interact. • Can identify genes that would not appear in directed phenotype-based screens. • Disadvantages: • Noise: • Intragenic revertants • Indirect suppressors • Suppressors and enhancers may have no phenotype alone. • Cloning suppressors and enhancers with no phenotypes can be difficult.

  10. ac 2° 2° 1° P3.p P4.p P5.p P6.p P7.p P8.p 2° 2° Hyp 7 Question: What is the mechanistic basis for signaling? What are the signals and receptors? What are the molecular targets of the signals? How is signaling regulated?

  11. Suppressors in analysis of Vulval development: Working out the components of the signaling pathway Observation: extensive screens had identified many genes with roles in vulval specification, but many other genes were expected to be undetectable in these screens. (specifically, loci whose null phenotype would be embryonic or larval lethality or sterility.)

  12. How can one identify such genes? One way is luck, the other way is to search for extragenic suppressors.

  13. Identification of one essential locus was by luck Identified by a single allele with a Vul phenotype: n1045 Mapped near a known larval lethal called let-23. n1045 failed to complement lethal alleles of let-23. Cloning of let-23 reveals it is a receptor tyrosine kinase (RTK).

  14. Epistasis relationship of let-23 to lin-15 leads to a suppressor screen let-23(n1045) -- Vul and Egl lin-15 (n309) -- Muv (Egl+) n309; n1045 -- Vul and Egl n1045 is epistatic to n309 but…. another way to look at this is that a mutation in a Vul gene suppresses the Muv phenotype of lin-15(n309) Aroian, R. V., and Sternberg, P. W. (1991). Multiple functions of let-23 a Caenorhabditis elegans receptor tyrosine kinase gene required for vulval induction. Genetics 128, 251-268.

  15. Screen for suppressors of lin-15 (Two screens in different labs: Sternberg, Horvitz) Mutagenize lin-15 (n309) worms (n765ts) Screen in F2 for nonMuv, Vul animals 100,000 gametes screened (38,000) 10 extragenic suppressors 2 are recessive new let-23 Vul mutations (as predicted) 1 is a recessive mutation in a new gene (later) 7 dominant suppressors mapped to a single locus (5 recessive and 2 dominant suppressors in this locus among others) Han, M., Aroian, R. V., and Sternberg, P. W. (1990). Genetics 126, 899-913. Beitel,G.J., Clark, S.G., and Horvitz, H.R. (1990) Nature 348:503.

  16. Digression: The two new let-23 alleles made it possible to screen for additional loss-of-function alleles by a noncomplementation screen. let-23(sy1)/Df = viable Vul Therefore screening for new mutations that fail to complement the Vul phenotype of sy1 will identify putative null alleles. (much more difficult to screen for new lethal alleles of let-23.)

  17. How to analyze the new suppressors: Map them map near genes defined by two existing mutations: lin-34 (single Muv allele) and let-60, a larval lethal. What is the nature of the suppressor mutations and what is their relationship to one another? 2 1 Vul x (self) Muv x (self) Vul ; Muv only Muv 2 1 Suppressor (Vul) x (self) Suppressor is dominant; recessive lethal

  18. Suppressor (Vul) x (self) Vul x (self) Muv x (self) s/+; lin-15+; lin-15 Vul ; Muv only Muv 2 1 s/+; lin-15+; lin-15 Dead 1 s/s; lin-15

  19. Additional properties of the suppressors: s/+; + still dominant Vul, recessive lethal 2) failed to complement the let-60 recessive lethals What is the nature of the dominant suppressor mutation? How to test? Make deletion heterozygote: Df(let-60)/+ --> not dominant Vul Therefore, must be gain of function

  20. What is the loss-of-function phenotype of the suppressor locus? Can isolate loss-of-function mutations by reverting the gain-of-function allele. dominant gof x x x wild type F1 screen x recessive lof x x x

  21. Method 1: revert the dominant Vul let-60 + dpy-20+ + /+ let-65 + unc-22 (balanced lethal) Only Vul hets survive, screen for rare nonVul animals by looking for eggs. Result: 1 cis-revertant Method 2: suppress the suppressor! unc-24 let-60/dpy-20 let-3; lin-15/lin-15 Mutagenize and score for Muv animals in the F1 Result: 2 suppressors of suppressor (one cis- one trans)

  22. Both cis-mutations mapped to let-60 region, failed to complement recessive let-60 alleles and are wild type as heterozygotes. (come back to trans mutation in a bit) Conclusion: dominant Vul mutations are in the let-60 locus, and loss-of-function phenotype is lethal. What is the role of let-60 in vulval development? How to assess? Loss of function animals die before vulva forms!

  23. “The biology of a given gene is often revealed using non-null mutations, a valuable point to stress as we approach a post-genomic sequencing project era. Classical forward genetics will be as useful as ever for isolating such special alleles because genetic screens can select out relatively rare, but informative, mutations. Of course, rare alleles can also be misleading and need to be interpreted in the context of a complete genetic analysis, including knowledge of null phenotype.” Sternberg and Han (1998) Trends in Genetics 14: 466.

  24. Solution: use weak lof allele that allows some survival. let-60(s1124lf)/let-60(s1124lf) rare survivors fail to induce vulva. Conclusion: lof phenotype is Vul. Because the dominant mutations produce a phenotype identical to the recessive mutations they are called “dominant negative” (Muller’s antimorph)

  25. One suppressor of the let-60 suppressor of lin-15 was unusual It mapped to the let-60 region and it functioned as a trans-dominant suppressor That is: let-60(dn)/sup; lin-15 = Muv sup/+ ---> Muv (10%) sup/sup --> Muv (90%) This phenotype was similar to that described for lin-34, a mutation closely linked to let-60. lin-34/let-60(dn) = weak Muv (i.e. lin-34 suppresses let-60(dn) lin-34/let-60(lf) ---> rescues the lethality; some let-60/let-60 progeny survive

  26. Conclusion: lin-34 mutations are gain of function (hypermorph) mutations in let-60. (G13E) If excess let-60 is provided in trans it can counteract the effect of the dominant negative And maternal expression can rescue the complete loss of zygotic let-60. (even let-60(lf)/let-60(lf) homozygotes from lin-34/let-60 hets can survive.)

  27. Summary of let-60 story: let-60 can mutate in three ways 1) lof – Vul 2) dn - Vul 3) gof - Muv Therefore let-60 plays a pivotal role in vulval induction.

  28. What is let-60?? Han and Sternberg cloned let-60 and found that it was a member of the Ras family of small GTPases. Compare to the fly eye. RTK Ras Sev Ras1 LET-23 LET-60 RAS

  29. There was one other new gene identified as a lin-15 suppressor. lin-45 Larval lethal, few survivors are Vul, phenotypes are similar to other genes in the Vul pathway.

  30. Summary of suppressor screen: two new let-23 alleles identified let-60 as having an essential role in vulval development. identified an additional new gene, lin-45

  31. SO WHAT ????? let-23 cloned: receptor tyrosine kinase let-60 cloned: ras lin-45 cloned: raf Epistasis showed relationships between these genes and other existing lin mutants lin-3 let-23 let-60 lin-45 lin-1 vulval fate lin-15 AND The let-60(gof) mutations provided a new starting point for additional suppressor screens

  32. Suppression of the dominant ras mutation let-60(n1046gf) = Muv Look for non-Muv let-60(n1046); +/* or */* in F2 after mutagenesis Any gene required downstream of ras will show a non-Muv phenotype. sur-1 one of 50 or so sur mutants Null mutation is larval lethal Epistasis puts it downstream of raf but upstream of lin-1 = map kinase = mpk-1 Wu Y, Han M. (1994) Suppression of activated Let-60 ras protein defines a role of Caenorhabditis elegans Sur-1 MAP kinase in vulval differentiation.Genes Dev. 8:147-59.

  33. Not all suppressors screens are productive: The story of pha-1 suppressors pha-1 (pharynx abnormal) - poor differentiation of pharynx Schnabel, H., Bauer, G., and Schnabel, R. (1991). Suppressors of the organ-specific differentiation gene pha-1 ofCaenorhabditis elegans. Genetics 129, 69-78.

  34. Screen for suppressors of pha-1 EMS pha-1 (ts) x (self) 15° 15° F1 pha-1; */+ 25° (restrictive temp) F2 All die, except pha-1 suppressors pha-1/pha-1; */+ or */*

  35. Results: 360,000 genomes 220 suppressors! All recessive Three complementation groups, sup-35, 36, 37 Suppress most but not all pha-1 alleles Have no phenotype on their own. Published in 1991 - no follow-up

  36. Enhancers

  37. Enhancers. • The basic idea is similar to finding suppressors. • the process in question involves the combined action of many proteins. • the successful execution of the process requires sufficient levels of all the components. • If levels of two components are lowered simultaneously, that can result in strong phenotypes not seen when only one component is lowered.

  38. Enhancers of sevenless: Hypersensitive background F1 screen Enhancers in essential genes can be recovered Enhancing mutations are likely to have recessive phenotypes and can include null alleles Provided a means to identify Ras1 as a component of R7 fate specification in photoreceptor development.

  39. Screen for enhancers of glp-1 glp-1 (germline proliferation) Suppressor screens to identify interacting genes failed: only intragenic revertants and Indirect suppressors (collagen mutants??!!)

  40. glp-1 enhancer screen Sensitized background: glp-1 (ts): 15° nearly wild-type 25° sterile But 20° fertile (but 50% maternal effect lethal) At 21° start to see sterility Qiao, L., Lissemore, J., Shu, P., Smardon, A., Gelber, M. B., and Maine, E. M. (1995). Enhancers of glp-1, a gene required for cell-signaling in Caenorhabditis elegans, define a set of genes required for germline development. Genetics 141, 551-569.

  41. EMS glp-1(ts) x (self) 15° glp-1(ts) ; */+ x (self) 20° All should be fertile except enhancers recessive zygotic steriles that have nothing to do with glp-1

  42. To eliminate zygotic steriles: keep only those with Glp-looking germline b) keep only those that require glp-1 for the phenotype.

  43. Results: Mutations are all recessive and define seven complementation groups. 1) five alleles of lag-1 (known to function downstream of glp-1.) 2) one allele of glp-4 (similar phenotype to glp-1) 3) Five ego genes four have phenotypes on their own

  44. ego-1 - produces abnormal oocytes ego-2 - no phenotype on its own. ego-3 - complex defects in germ line: abberant transition from mitosis to meiosis ego-4 & 5- these have defects in germ line proliferation and oogenesis, oocytes that are produced and fertilized always die as embryos.

  45. Conclusions: all of the genes affect multiple aspects of development (like glp-1 itself) the screen can identify genes in the glp-1 pathway (e.g. lag-1) the phenotypes of the ego genes are consistent with a role in the glp-1 pathway. ego-1 and ego-3 are epistatic to a glp-1(gf) allele Overall, enhancement is a way to recover lof mutations identifying new players in a common process. 5. ego-1 encodes an RNA-dependent RNA polymerase that has a role in germline RNAi. 6. ego-2 encodes a Bro1 domain protein facilitates ligand production or action. Role in secretory pathway?

  46. Summary: Suppressor and enhancer screens can help to identify genes acting in a particular process, but which also have essential roles in other processes.

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