Identifying essential genes in phage. Screens for essential genes To identify essential genes, you can screen for what types of mutations?

Slides:



Advertisements
Similar presentations
Genetika Molekuler (5) Sutarno. Lecture #4 Notes (Yeast Genetics) LECTURE 4: CLONING AND MANIPULATING GENES IN YEAST Basically, we use the same techniques.
Advertisements

LECTURE 23: DISSECTION OF GENE FUNCTION I: GENETIC FINE STRUCTURE
Chapter 15 - Genetics of Bacteria and Bacteriophages: Mapping bacteria, 3 different methods: Conjugation Transformation Transduction Bacteriophage mapping:
Presented By: NUPUR GUPTA
Mutations and defects in chromosomal structure January 2009
Isolate Mutations Continued. HW 2 Due Next Tue Tue Lecture: Suppression.
Bacterial conjugation is the transfer of genetic material (conjugative plasmid) between bacteria through direct cell to cell contact, or through a bridge-like.
Microbial Genetics (Micr340)
Microbial Genetics (Micr340) Lecture 6 Genetic Analysis.
Quantitative Traits. Quantitative Traits Distribution of Corn Ear Lengths.
Microbial Genetics (Micr340) Lecture 10 Lytic Bacteriophages (II)
General Microbiology (Micr300) Lecture 10 Microbial Genetics (Text Chapter: ; )
Detecting Mutagens and Carcinogens. introduction - Increased number of chemicals used and present as environmental contaminats, testes for the mutagenicity.
CHAPTER 10 Bacterial Genetics.
Gene Mutations.
Outline Zen of Screen vs Selection Mutation Rate
Microbial Genetics Mutation Genetic Recombination Model organism
Chapter 9 Genetics of Bacteria and Their Viruses Jones and Bartlett Publishers © 2005.
Topic 6 Growth & Reproduction of Bacteria
Gene Transfer in Bacteria and Bacteriophage
Section H Cloning Vectors.
Ensuring DNA Integrity Redundancy inherent in structureRedundancy inherent in structure DNA repair enzymologyDNA repair enzymology High precision in ReplicationHigh.
Chapter 7 The Genetics of Bacteria and Their Viruses
1 Genetic Information in Bacterial Cells. 2 Bacterial Reproduction: Binary Fission Bacterial chromosome and Plasmids to each.
Arabidopsis Experiments: I.Forward Genetic Screen (Ethylene Insensitive Mutants): requires thinking. requires thinking. II. Reverse Genetic Screen / PCR.
This Week Score Conjugation Plates, Start High Frequency of Recombination (HFR) experiment, Continue Nasonia experiment.
Recombination Recombination 1.Overview of Recombination 2.Requirements of Recombination 3.Functions of Recombination 4.Mechanism.
Genetic Fine Structure Nature of the Gene at the Molecular Level.
BIO 351 PREPARATION AND PLAQUE ASSAY OF A PHAGE STOCK 2007 Özlem Yalçın Sunay Usluer Sunay Usluer M. Aslı Kayserili Taliha Paşaoğlu.
Chap. 5 Problem 1 Recessive mutations must be present in two copies (homozygous) in diploid organisms to show a phenotype (Fig. 5.2). These mutations show.
Yeast geneticists frequently invoke:
Isolation of Bacteriophages
Chapter 9 Genetics of Bacteria and Their Viruses: Transduction and phage genetics Jones and Bartlett Publishers © 2005.
Erwin Schrodinger What is Life? 1944 Nobel Prize in Physics 1933 Atomic Theory.
This Week, Nov 10th Tuesday: no class Thursday: Bacteria, Conjugation
Virology 1.5-Genetics Some terminology from the last part of Chapter 3.
Add 20uL Opsonization Buffer (OB) to shaded wells 1.
Susceptibility (Sensitivity) Testing: Results Pharmaceutical Microbiology – Practical Course Semester One_ Sensitivity Results & MIC Broth Dilution/
Genetics and Genomics Forward genetics Reverse genetics
Microbiology B.E Pruitt & Jane J. Stein AN INTRODUCTION EIGHTH EDITION TORTORA FUNKE CASE Chapter 8, part C Microbial Genetics.
BIS Office hours/review sessions for Midterm I No calculators or cell phones during test, use pen if you want the possibility to request a regrade.
Announcements Ms. Laina Long from the UCLA Bridges Program will give a brief presentation today at 10:40 in this room. She will give you an overview of.
Mutations to Aid in Gene Study By: Yvette Medina Cell Phys
Chromosomal Basis of Inheritance Linked Genes Sex-linked Genes.
Chapter 7 The Genetics of Bacteria and Their Viruses
GENETIC VARIATION OF VIRUSES Part 2 Lecture 3 1. Types of Viral Mutation A. Point Mutations Point mutations occur when a single nucleotide is changed.
BACTERIAL GENETICS Dr. Waleed Khalid Lec. : 3.
Reading for lectures Chp 8: from 258 (Nonoverlapping...) to 261 (…Cracking) & from 285 (8.6) to 293 (end of "essential concepts) Chp 14: Using deletions.
Transformation of Escherichia coli
BISC 220 Lab—Series 2 Protein Transport through the Secretory Pathway
BIOL 2416 Chapter 15: Gene Mapping in Bacteria and Viruses
Bacterial and viral genetic systems
Viral Genetics.
Chapter 15 - Genetics of Bacteria and Bacteriophages:
Genetic Fine Structure
Transduction.
Bacterial Genome & Variations
Chapter 8, part C Microbial Genetics.
Genetic Analysis and Mapping in Bacteria and Bacteriophages
This Week Start High Frequency of Recombination (HFR) experiment (Weds.), work to do Thursday, Friday and next week, Start Bacteria Mutagenesis experiment.
Relationship between Genotype and Phenotype
Figure: Title: Bacterial Population Growth Curve Caption:
Office hours: Monday 5-6pm (door 5:15p) Friday 4-5 pm 11 Koshland Hall.
Cancer therapeutics in yeast
Interplay between Nonsense-Mediated mRNA Decay and DNA Damage Response Pathways Reveals that Stn1 and Ten1 Are the Key CST Telomere-Cap Components  Eva-Maria.
A Suppressor of Two Essential Checkpoint Genes Identifies a Novel Protein that Negatively Affects dNTP Pools  Xiaolan Zhao, Eric G.D Muller, Rodney Rothstein 
The basis for a genetic screen for budding-yeast cell-cycle mutants.
Relationship between Genotype and Phenotype
Primary GBM cells support productive HCMV replication in vitro.
Presentation transcript:

Identifying essential genes in phage

Screens for essential genes To identify essential genes, you can screen for what types of mutations?

Screens for essential genes To identify essential genes, you can screen for what types of mutations? conditional lethal mutations

Screens for essential genes To identify essential genes, you can screen for what types of mutations? conditional lethal mutations What are the two types of conditional lethal screens that you can do in phage?

Screens for essential genes To identify essential genes, you can screen for what types of mutations? conditional lethal mutations. What are the two types of conditional lethal screens that you can do in phage? Temperature sensitivity Nonsense suppression

Screens for essential genes To identify essential genes, you can screen for what types of mutations? conditional lethal mutations. What are the two types of conditional lethal screens that you can do in phage? Temperature sensitivity Nonsense suppression

Screens for essential genes To identify essential genes, you can screen for what types of mutations? conditional lethal mutations. What are the two types of conditional lethal screens that you can do in phage? Temperature sensitivity Nonsense suppression What is the observable phenotype in screens for essential genes?

Screens for essential genes To identify essential genes, you can screen for what types of mutations? conditional lethal mutations. What are the two types of conditional lethal screens that you can do in phage? Temperature sensitivity Nonsense suppression What is the observable phenotype in screens for essential genes? Dead (don’t form plaques) at non-permissive conditions

Screens for essential genes STEPS of temperature sensitivity screen: 1.Mutagenize phage particles phage

Screens for essential genes STEPS of temperature sensitivity screen: 2. Add mutagenized phage to E. coli at a low MOI E.coli phage

Screens for essential genes STEPS of temperature sensitivity screen: 3.Plate and incubate overnight at permissive temperature Mutagen- ized phage E.coli Mutagenized phage

Screens for essential genes STEPS of temperature sensitivity screen: 3.Plate and incubate overnight at permissive temperature Why first incubate at permissive temperature? Mutagen- ized phage E.coli Mutagenized phage

Screens for essential genes STEPS of temperature sensitivity screen: 3.Plate and incubate overnight at permissive temperature Why first incubate at permissive temperature? To allow all phage to replicate Mutagen- ized phage E.coli Mutagenized phage

Screens for essential genes STEPS of temperature sensitivity screen: 3.Plate and incubate overnight at permissive temperature Why first incubate at permissive temperature? To allow all phage to replicate Mutagen- ized phage E.coli Wild type phage E.coli Mutagenized phageControl: Wild type phage

Screens for essential genes STEPS of temperature sensitivity screen: 3.Plate and incubate overnight at permissive temperature Why first incubate at permissive temperature? To allow all phage to replicate Mutagen- ized phage E.coli Wild type phage E.coli Mutagenized phageControl: Wild type phage What is the reason for wild type control?

Screens for essential genes STEPS of temperature sensitivity screen: 3.Plate and incubate overnight at permissive temperature Why first incubate at permissive temperature? To allow all phage to replicate Mutagen- ized phage E.coli Wild type phage E.coli Mutagenized phageControl: Wild type phage What is the reason for wild type control? to ensure that the temperature change is not lethal to all phage

Screens for essential genes STEPS of temperature sensitivity screen: 4.Transfer plaques to duplicate plates and incubate overnight: Mutagenized phage At permissive temperature At non-permissive temperature Permissive temp Non-Permissive temp mutagenized

Screens for essential genes STEPS of temperature sensitivity screen: 4.Transfer plaques to duplicate plates and incubate overnight: Mutagenized phage At permissive temperature At non-permissive temperature Control: Wild type phage At permissive temperature At non-permissive temperature Permissive temp Non-Permissive temp Permissive tempNon-Permissive temp mutagenized Wild type

Screens for essential genes STEPS of temperature sensitivity screen: 5. Mutagenized phage that form plaques at permissive temp but not at non-permissive temp are temperature-sensitive mutants Mutagenized phage At permissive temperature At non-permissive temperature Control: Wild type phage At permissive temperature At non-permissive temperature Permissive temp Non-Permissive temp Permissive tempNon-Permissive temp mutagenized Wild type Temperature- sensitive mutant

Screens for essential genes STEPS of nonsense-suppressor screen: 1.Mutagenize a known concentration of phage particles phage

Screens for essential genes STEPS of nonsense-suppressor screen: 2.Add mutagenized phage to a suppressor E. coli strain at a low MOI; plate and incubate overnight mutagenized phage suppressor E.Coli strain

Screens for essential genes STEPS of nonsense-suppressor screen: 2.Add mutagenized phage to a suppressor E. coli strain at a low MOI; plate and incubate overnight Why incubate first on suppressor strain? mutagenized phage suppressor E.Coli strain

Screens for essential genes STEPS of nonsense-suppressor screen: 2.Add mutagenized phage to a suppressor E. coli strain at a low MOI; plate and incubate overnight Why incubate first on suppressor strain? to allow all phage to replicate and form plaques mutagenized phage suppressor E.Coli strain

Screens for essential genes STEPS of nonsense-suppressor screen: 3.Transfer plaques to duplicate plates and incubate overnight: On a lawn of suppressor E.coli strain On a lawn of wild type E.coli Suppressor E.coli Wild type E.coli

Screens for essential genes STEPS of nonsense-suppressor screen: 4.Those phage that are nonsense mutants produce a plaque on the suppressor E.coli strain but not on the wild type E.coli strain Suppressor E.coli Wild type E.coli Nonsense mutant

Complementation test Complementation tests allow you to determine whether your isolated mutations affect the same gene.

Complementation test STEPS 1.Infect wild type strain with two of your isolated mutants at high MOI for 1 hour (to allow one round of infection) am1 - am2 - Wild type E.Coli strain

Complementation test STEPS 1.Infect wild type strain with two of your isolated mutants at high MOI for 1 hour (to allow one round of infection) Why at high MOI? am1 - am2 - Wild type E.Coli strain

Complementation test STEPS 1.Infect wild type strain with two of your isolated mutants at high MOI for 1 hour (to allow one round of infection) Why at high MOI? So each cell can be infected by both mutants am1 - am2 - Wild type E.Coli strain

Complementation test STEPS 2.To determine whether the mutations complemented each other, you must determine the amount of phage that was successfully replicated in the co-infected wild type E. coli strain: Perform a plaque assay of the phage supernatant, this time on a suppressor E.coli strain. am1 - + am2 - + suppressor E.coli

Complementation test STEPS 2.To determine whether the mutations complemented each other, you must determine the amount of phage that was successfully replicated in the co-infected wild type E. coli strain: Perform a plaque assay of the phage supernatant, this time on a suppressor E.coli strain. Positive control: wild type phage in suppressor E.coli strain am1 - + am2 - + suppressor E.coli wt phage + suppressor E.coli

Complementation test STEPS 2.To determine whether the mutations complemented each other, you must determine the amount of phage that was successfully replicated in the co-infected wild type E. coli strain: Perform a plaque assay of the phage supernatant, this time on a suppressor E.coli strain. Positive control: wild type phage in suppressor E.coli strain Negative control: each single mutant phage in suppressor E.coli strain am1 - + am2 - + suppressor E.coli wt phage + suppressor E.coli am1 - + suppressor E.coli am2 - + suppressor E.coli

Complementation test STEPS 3.If plaques are formed in the plaque assay involving am1 - + am2 - + suppressor E.coli, the mutations complement each other and are likely mutations in two different genes. am1 - + am2 - + suppressor E.coli am1 - + suppressor E.coli am2 - + suppressor E.coli wt phage + suppressor E.coli

Complementation test STEPS 3.If plaques are not formed in the plaque assay involving am1 - + am2 - + suppressor E.coli, the mutations do not complement each other and are likely mutations in the same gene. am1 - + am2 - + suppressor E.coli am1 - + suppressor E.coli am2 - + suppressor E.coli wt phage + suppressor E.coli

Complementation test STEPS 3.If plaques are not formed in the plaque assay involving am1 - + am2 - + suppressor E.coli, the mutations do not complement each other and are likely mutations in the same gene. Why are plaques are not formed? am1 - + am2 - + suppressor E.coli am1 - + suppressor E.coli am2 - + suppressor E.coli wt phage + suppressor E.coli

Complementation test STEPS 3.If plaques are not formed in the plaque assay involving am1 - + am2 - + suppressor E.coli, the mutations do not complement each other and are likely mutations in the same gene. Why are plaques are not formed? The phage produced are unable to infect further cells. am1 - + am2 - + suppressor E.coli am1 - + suppressor E.coli am2 - + suppressor E.coli wt phage + suppressor E.coli

Mapping Once you determine that two mutations complement each other and thus are mutations in different genes, you can map the genes to determine the physical distance between them.

Mapping STEPS 1. Infect suppressor strain with your two different mutants at high MOI am1 - am2 - Suppressor E.Coli strain

Mapping STEPS 2. Allow infected cells to produce phage (1 hour) Suppressor E.Coli strain 1 hour

Mapping STEPS: 3.Perform a plaque assay to determine total number of phage and number of recombinants: - Serial dilutions of phage - Plate on suppressor strain AND wild-type strain Wild type E.coli 100 phage Suppressor E.coli phage buffer ~1000 phage

Mapping STEPS: 4. Count the # of plaques formed on the suppressor strain and on the wild type strain. Wild type E.coli Suppressor E.coli

Mapping STEPS: 5. Calculate the frequency of recombination: Frequency of recombination = total recombinants/total phage Wild type E.coli Suppressor E.coli

Mapping What is the genotype of the plaques formed on the wild type E.coli strain? Wild type E.coli Suppressor E.coli

Mapping What is the genotype of the plaques formed on the wild type E.coli strain? Wild type E.coli Suppressor E.coli am1+, am2+

Mapping Recalling that we are dealing with essential genes, do the total recombinants = # of plaques formed on the wild type E.coli strain? Wild type E.coli Suppressor E.coli

Mapping Recalling that we are dealing with essential genes, do the total recombinants = # of plaques formed on the wild type E.coli strain? No Wild type E.coli Suppressor E.coli

Mapping Recalling that we are dealing with essential genes, do the total recombinants = # of plaques formed on the wild type E.coli strain? No What do the actual # of total recombinants equal? Wild type E.coli Suppressor E.coli

Mapping Recalling that we are dealing with essential genes, do the total recombinants = # of plaques formed on the wild type E.coli strain? No What do the actual # of total recombinants equal? 2 X # of plaques formed on wild type E.coli Wild type E.coli Suppressor E.coli

Mapping Why multiply by 2? Wild type E.coli Suppressor E.coli

Mapping Why multiply by 2? To account for the recombinants that cannot grow on wild type E.coli: am1-, am2- Wild type E.coli Suppressor E.coli

Mapping The farther the genes are from each other, the higher the frequency of recombination is between them. Wild type E.coli Suppressor E.coli