* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Problem set 8 answers
History of genetic engineering wikipedia , lookup
Gene nomenclature wikipedia , lookup
Genomic imprinting wikipedia , lookup
Cancer epigenetics wikipedia , lookup
Epigenetics of neurodegenerative diseases wikipedia , lookup
Therapeutic gene modulation wikipedia , lookup
Saethre–Chotzen syndrome wikipedia , lookup
Genetic engineering wikipedia , lookup
Vectors in gene therapy wikipedia , lookup
Neuronal ceroid lipofuscinosis wikipedia , lookup
Genome evolution wikipedia , lookup
No-SCAR (Scarless Cas9 Assisted Recombineering) Genome Editing wikipedia , lookup
Population genetics wikipedia , lookup
Epigenetics of human development wikipedia , lookup
X-inactivation wikipedia , lookup
Gene expression programming wikipedia , lookup
Koinophilia wikipedia , lookup
Gene expression profiling wikipedia , lookup
Polycomb Group Proteins and Cancer wikipedia , lookup
Dominance (genetics) wikipedia , lookup
Gene therapy of the human retina wikipedia , lookup
Designer baby wikipedia , lookup
Artificial gene synthesis wikipedia , lookup
Genome (book) wikipedia , lookup
Frameshift mutation wikipedia , lookup
Oncogenomics wikipedia , lookup
Site-specific recombinase technology wikipedia , lookup
Problem set 8 answers 1. Integrins are alpha/beta heterodimeric receptors that bind to molecules in the extracellular matrix. A primary role of integrins is in adhesion, ensuring that cells attach to the matrix, and cell biologists have identified several proteins that link the intracellular tail of the beta integrin to the actin cytoskeletin. During the development of the Drosophila wing, cells on the dorsal and ventral surfaces adhere to the matrix. Mutations in the beta integrin gene lethal(1)myospheroid lead to recessive lethality, but hypomorphic mutations lead to wing blisters where the portions of the dorsal and ventral surfaces separate. From what you now know about integrins, propose a model for how integrins function in wing development. Integrins are the receptors than mediate adhesion between the dorsal and ventral surfaces of the wing. You screen for mutations that lead to wing blisters using FLP/FRT induced recombination. Describe which genetic tools you will need to conduct the screen. You will need an enhancer to drive FLP expression in the wing and chromosomes with FRT near the centromeres. A cell autonomous marker will also help define which cells are mutant. 2. To study DNA repair mechanisms, geneticists isolated yeast mutants that were sensitive to various types of radiation; for example, mutants that were more sensitive to UV light. Ten haploid mutants were isolated. a. How would you do the complementation tests for these mutants? A complementation test would be done by crossing the haploid strains and scoring the phenotype in the diploids. b. Based on the complementation chart below, how many genes are defined by these mutations? + indicates complementation, - failure to complement. 1 2 3 4 5 6 1 - 2 - 3 + + - 4 + - 5 + + + - 6 + + + + + - Three genes: 1, 2, and 4 are in one gene, 3 and 5 in another, and 6 in a third gene. c. The gene defined by mutation 1 was cloned. Overexpression of the wildtype gene reduces the UV sensitivity of either mutant 3 or mutant 6. Describe two models to explain the genetic interactions. The gene could be in the same pathway. In this case the gene defined by mutation 1 would be downstream of the genes defined by mutations 3 and 6 since its overexpression can bypass the UV sensitivity of the other mutations. Alternatively, the gene defined by mutation 1 could be in a parallel pathway and its overexpression can bypass the requirement for the pathway(s) defined by the mutations 3 and 6. 3. The sup-7 mutation of C. elegans is an amber suppressor tRNA that inserts tryptophan at UAG amber codons. You isolate 20 mutations in the unc-22 gene, which lead to a recessive phenotype causing worms to be uncoordinated in their movement. Three of the mutations are suppressed by the sup-7 mutation, but when you clone the gene and sequence the mutant alleles, eight mutations resulted in amber stop codons. Why do you suppose that the sup-7 suppressor didn't suppress some of these mutations? Placing a tryptophan in those positions did not yield a functional protein. 4. Animals homozygous for the sup-7 mutation die at 15o C. In 1981, Bob Waterston mutagenized sup-7/sup-7 hermaphodites, grew them at 25o C, and shifted the F2s to 15o C. Several strains were isolated that now could grow at 15o C. The suppressors of the sup-7 lethality were inseparable by recombination from the sup-7 mutation. Strains carrying sup-7 and the tightly linked suppressor (suppressor of a suppressor) no longer suppressed amber alleles of genes that were suppressed by the original sup-7. Animals homozygous for the sup-7 suppressor chromosome appear wild type. From what you know about nonsense suppressors explain these results. (Note: these suppressors were too frequently isolated to be explained by the reverting the mutant nucleotide in sup-7 back to the wildtype nucleotide, which should be a rare event.) The suppressor eliminates the function of the sup-7 gene, and thus it is no longer an amber suppressor. The animals homozygous for this mutation are wild type because there are other tRNATRP genes that can function in its absence. 5. You are working with a pure breeding stock of white-eyed flies and notice a spontaneous red-eyed male. You generate a pure breeding stock of the revertant in additional crosses. Design a crossing scheme to distinguish between two possible explanations for the mutation leading to the red-eyed male: an intragenic suppressor that restores the function of white gene and an autosomal extragenic dominant suppressor. Assume that if the suppressor is in a second gene that the recessive phenotype of the suppressor in the absence of the original white mutation leads to red eyes. We are trying to distinguish between a suppressor mutation that is intragenic from one that is extragenic. There are several ways to do this. One simple way is to cross the suppressed red-eyed males to white-eyed females. If the suppressor mutation is intragenic, all the F1 males will have a mutant white allele from their mother and have white eyes. If the suppressor mutation is on an autosome, all the F1 males will have a mutant white allele from their mother, but will also inherit the dominant suppressor from their father and have red eyes. 6. The C. elegans lin-14 gene controls the timing of development in C. elegans. LIN-14 protein is high early in development and gradually decreases as development proceeds. lin-14 is defined by both dominant and recessive mutant alleles. Animals that are homozygous for recessive alleles develop precociously (developmental events occur much earlier than normal) because LIN-14 protein levels are lowered or eliminated, similar to the levels seen later in development. Animals that contain dominant alleles are retarded in development (developmental events occur much earlier than normal) because LIN-14 levels are higher than they should be late in development. You are given three lin-14 mutants. Animals that are homozygous for loss-of-function alleles of the lin-4 gene are retarded in development. The lin-4 RNA is thought to bind to the lin-14 mRNA and inhibit translation of the LIN-14 protein. What genetic epistasis result would be consistent with lin-4 functioning as a negative regulator of lin-14. The lin-4(lf); lin-14(lf) double mutant should develop precociously. 7. Kin1p and Kin2p are protein kinases that act sequentially in a "kinase cascade.” Kin1p places a phosphate group on Kin2p, and this increases the activity of Kin2p so that it may, in turn, place a phosphate group on its target. Two kin1 mutants are isolated. One suppressor of each kin1 mutant is then isolated. Both map to the KIN2 gene. One kin2sup mutant shows allele specificity, only suppressing the kin1 allele that it was originally selected to suppress. a) Propose a model to account for these observations. What is the nature of the original kin1 mutations and how can the kin2 mutants be allelespecific suppressors of these mutants? The original mutation disrupts the ability of the Kin1 and Kin2 proteins to interact, and the suppressor restores their ability to interact. b) The other kin1 suppressor suppresses all kin1 alleles. How do you think that this suppressor acts? The mutant Kin-2 protein is active in the absence of functional Kin-1 protein. 8. The supply of nitrogen regulates yeast genes affecting nitrogen catabolism (Remember the prion lectures). The Ure2 protein of S. cerevisiae is a negative regulator of nitrogen catabolism that inhibits the Gln3 protein, a positive transcriptional regulator of genes involved in nitrogen assimilation. For example, the Gln3 protein activates the transcription of DAL5, which encodes allantoate permease, a cell surface molecule that transports this alternate nitrogen source under poor nitrogen conditions. In the presence of a good nitrogen source like ammonia, Ure2 protein is active and inhibits Gln3 activity, whereas in a poor nitrogen source such as allantoate, Ure2 is not active and Gln3 is active. Overproduction of the Mks1 protein allows DAL5 expression on ammonia, and lack of Mks1 protein prevents DAL5 expression on allantoate. In addition, an mks1 ure2 double mutant (both are null mutations) expresses DAL5 on either ammonia or allantoate. Describe a linear genetic pathway for the function of GLN3, MKS1, URE2 and DAL5, and describe which genes are active or inactive in ammonia and in allantoate. 9. The yeast SUP35 and SUP45 genes encode proteins that are involved in translational termination at stop codons. Mutations in these genes result in low levels of readthrough at stop codons, and were isolated as suppressor mutations. Do you think that the sup35 and sup45 mutations are gene specific or nonspecific? allele specific or nonspecific? Explain your reasoning. Gene nonspecific because sup35 and sup45 should suppress nonsense mutations in other genes. Allele specific because sup35 and sup45 should not suppress mutations other than nonsense mutations, like missense and frameshift alleles. 10. Sexual development in C. elegans is controlled by the X:autosome ratio. In XX animals the ratio is 1.0, resulting in hermaphrodite development; in X0 animals the ratio is 0.5, resulting in male development. Amorphic or null mutations in the genes tra-1 and tra-2 result in the transformation of XX animals into phenotypic males. Gain-of-function mutations in tra-1 result in the opposite transformation: XO animals are transformed into phenotypic hermaphrodites. Double mutant combinations between tra2(lf) and tra-1(gf) mutations have placed tra-1 downstream of tra-2. Recessive mutations in the fem-1 gene result in the transformation of XO animals into phenotypic females. Remember that C. elegans hermaphrodites are females that produce sperm for a short term. The fact that fem-1 XO animals are transformed into females and not hermaphrodites has you puzzled. You think that perhaps the mutations are hypomorphic mutations and null alleles would result in transformation of XO animals into hermaphrodites. a. You perform a genetic test to determine whether the mutations are hypomorphic or amorphic. Describe the genetic experiments and the results that would suggest that the fem-1 mutations are amorphic and not hypomorphic. Compare fem-1/fem-1 XO animals to fem-1/Df XO animals. The phenotypes should be the same. In this case, both types of XO animals will be transformed into females. b. fem-1 acts between the two tra genes in the sex determination pathway. Propose a genetic pathway for these three genes and define the activity states (ON/OFF) of the genes in XX and XO animals. Describe the fem-1; tra double mutant combinations that you would use to demonstrate this pathway, and describe the karyotypes and the phenotypes of the double mutants that support the proposed pathway. fem-1; tra-2(lf) XO animals will be females. fem-1; tra-1(lf) XX animals will be males. 11. A deletion in the p53 gene causes a dominantly inherited form of cancer. Normal cells of an individual with cancer contain both the normal and deleted forms of the p53 gene, but the cancer cells contain only the deleted version. Explain these observations. p53 is a tumor suppressor gene. While the cancer trait is inherited in a dominant fashion, all p53 function must be lost for cells to become cancerous. The loss of heterozygosity is caused either by mitotic recombination, loss of the normal chromosome or a spontaneous mutation in the wild-type p53 gene. 12. Utpal Banerjee's lab isolated a dominant mutation in Sos (SosJC2) on chromosome 2 as a suppressor of a hypomorphic sev allele known as sevE4. a. The investigators conducted a series of dosage experiments to determine the nature of their dominant suppressor. The data are below. Genotype sevE4 / sevE4 ; Sos+ / Sos+ sevE4 / sevE4 ; SosJC2 / SosJC2 sevE4 / sevE4 ; SosJC2 / Sos+ sevE4 / sevE4 ; SosJC2 / Df Level of suppression 0% 36.0% 16.4% 4.0% What type of mutant allele is the SosJC2 allele? Be as specific as possible, and explain your reasoning. Hypermorphic, because the suppression of sev enhanced by adding a wild-type allele (sev E4 E4 / sev / sev E4 E4 ; Sos ; Sos JC2 JC2 / Df is + / Sos ). b. Mosaic analysis of loss-of-function alleles of Sos isn't informative because these alleles result in a cell lethal phenotype (there are no mutant clones of Sos cells because the cells die). The SosJC2 allele, however, is not cell lethal. Animals of the genotype w sevE4 / w sevE4 ; SosJC2 P[w+] / Sos+ were irradiated with X-rays, and mosaic ommatidia scored. Below are the results. Cell R1 R2 R3 R4 R5 R6 R7 R8 wild type for w 57 39 42 46 46 57 69 41 mutant for w 12 30 27 23 23 12 0 28 These are the results for 69 mosaic ommatidia scored that had R7. Each number represents the number of cells that are mutant or wild type for white (w). In the 69 ommatidia analyzed, for example, 57 of the R1 cells were wild type for white and 12 were mutant. Describe a strategy that could have been used to insert the P[w+] transgene into chromosome 2? Be specific and use crosses if necessary. Inject white embryos (w/w or w/Y) with w+ cloned between P element inverted repeats and with a plasmid that contains the trasposase gene. The injected animals are crossed to white mutants, and the F1 progeny screened for animals with red eyes. These should have w+ inserted into the chromosomes at random positions. One of the w+ insertions that mapped to chromosome 2 was used here. What is the purpose of the P[w+] transgene? The P[w+] transgene is used to mark the mutant chromosome so that cells that are homozygous for Sos+ can be identified by their white phenotype. What is (are) the genotype(s) of the w+ clones. E4 w sev E4 / w sev ; Sos JC2 + + P[w ] / Sos E4 or w sev E4 / w sev ; Sos JC2 + JC2 P[w ] / Sos + P[w ] What is (are) the genotype(s) of the w clones. E4 w sev E4 / w sev + + ; Sos / Sos Do you think that Sos is acting cell autonomously or nonautonomously? Explain your reasoning. Cell autonomously. None of the mosaic ommatidia with R7 were JC2 homozygous for wild-type Sos, indicating that the Sos mutant needs to be present in R7 for R7 to be generated. 13. In FLP/FRT mosaic screens for mutants with white eye clones that had expanded and overgrown at the expense of red eye tissue to generate unusually large eyes, several tumor suppressor genes were identified on chromosome 3. As we discussed in class, these genes were interesting because they normally inhibit cell division and promote apoptosis. In these same screens the investigators also identified a second class of mutants. In these mutant animals, the eyes were unusually large because there were too many cell divisions just like the mutants that we discussed. The difference is that the red eye tissue is also overgrown in this second class of mutants. Expression of the Unpaired secreted ligand is increased in the mutant cells. Unpaired is a signal in a conserved pathway that regulates the transcription factor STAT. Loss of one copy of the STAT gene can suppress the overproliferation phenotype caused by the loss of this second class of tumor suppressor genes. a. Describe four genetic elements/mutations present on the chromosomes (not including the induced mutations) that are used to generate and detect the mosaic eyes and define which cells are homozygous for the mutagenized chromosome in these screens. white mutation FRT sites FLP driven by the eyeless promoter P[white+] transgene The white cells are homozygous for the mutagenized chromosome. b. In the original screen, what are the genotypes of the white cells and the red cells of the mosaic females that have the second type of tumor suppressor gene mutation? The white cells are eyeless-FLP w/w; FRT TS/FRT TS where TS is the tumor suppressor mutation. The red cells are either eyeless-FLP w/w; FRT TS/FRT P[w+] or eyelessFLP w/w; FRT P[w+]/FRT P[w+] c. Describe a model that can explain the overgrowth phenotype of this second class of tumor suppressor that incorporates the tumor suppressor, Unpaired and STAT, defining in which cells the genes act and how they might regulate one another. No molecular details are necessary. TS inhibits Unpaired expression, and Unpaired activates STAT. TS and Unpaired act in the same cells to send a signal to surrounding cells. STAT acts in the responding cells.