1 / 35

Training session on Drosophila mating schemes

Training session on Drosophila mating schemes. STEP 1: Remind yourself of the key differences between mitosis and meiosis:. crossing-over / interchromosomal recombination during prophase I ( ➊ ) separation of homologous chromosomes during telophase I ( ➋ )

Télécharger la présentation

Training session on Drosophila mating schemes

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Training session on Drosophila mating schemes

  2. STEP 1: Remind yourself of the key differences between mitosis and meiosis: • crossing-over / interchromosomal recombination during prophase I (➊) • separation of homologous chromosomes during telophase I (➋) • an additional division in meiosis (➌)

  3. Mitosis and meiosis diploid generating sister chromatids for each of the homologous chromosomes separating sister chromatids ➌ ➋ ➊ haploid haploid synapsis - interchromosomal recombination separating homologous chromosomes

  4. STEP2: Remind yourself of the basic rules of Drosophila genetics: • law of segregation • independent assortment of chromosomes • linkage groups and recombination (recombination rule) • balancer chromosomes and marker mutations

  5. Law of segregation / linkage groups Homologous chromosmes are separated during meiosis

  6. Law of segregation / linkage groups 1 • each offspring receives one parental and one maternal chromosome • loci on the same chromsome are passed on jointly (linkage) 2 1

  7. Complication: recombination in females interchromosomal recombination takes place randomly during oogenesis Recombination rule: there is no recombination in males (nor of the 4th chromosome)

  8. Complication: recombination in females wildtype heterozygous homozygous mutant 7 instead of 3 different genotypes

  9. Balancers and stock keeping • remedy for work on mice: genotyping of every new generation through PCR analysis of tail tips - impossible in flies! • lethal mutations are difficult to keep as a stock and will eventually segregate out

  10. Balancers and stock keeping • lethal mutations are difficult to keep as a stock and will eventually segregate out • remedy in Drosophila:balancer chromosomes

  11. Balancers and stock keeping • balancers carry easily identifiable dominant and recessive markers

  12. Balancers and stock keeping • balancers carry easily identifiable dominant and recessive markers • balancers are homozygous lethal or sterile

  13. Balancers and stock keeping only heterozygous flies survive and maintain the stock • balancers carry easily identifiable dominant and recessive markers • balancers are homozygous lethal or sterile • the products of recombination involving balancers are lethal • During mating schemes, balancers can be used to prevent unwanted recombination - providing an additional means to the recombination rule. • You can use balancers and their dominant markers strategically to follow marker-less chromosomes through mating schemes.

  14. Rules to be used here: • 'X' indicates the crossing step; female is shown on the left, male on the right • sister chromosomes are separated by a horizontal line, different chromosomes are separated by a semicolon, the 4th chromosome will be neglected • maternal chromosomes (inherited from mother) are shown above, paternal chromosomes (blue) below separating line • the first chromosome represents the sex chromosome, which is either X or Y - females are X/X, males are X/Y • generations are indicated as P (parental), F1, 2, 3.. (1st, 2nd, 3rd.. filial generation) • to keep it simple: dominant markers start with capital, recessive markers with lower case letters

  15. Now apply your knowledge: • follow a step-by-step explanation of a typical crossing task experienced during routine fly work • you will be prompted to make your choices at each step of the mating scheme; take this opportunity before forwarding to see a solution

  16. Task:To study the potential effect of a 2nd chromsomal recessive lethal mutation m(stock 1) on brain development, you want to analyse certain neurons in the brain of m mutant embryos. These neurons can be specifically labelled with ß-Gal using a 2nd chromosomal P-element insertion P(lacZ,w+) (stock 2). To perform the experiment, you need to recombine m and P(lacZ,w+) onto the same chromosome. Design a suitable mating scheme. Tip:w+ on the P-element gives orange eyes. , Hu Identify the eye colours of these flies

  17. CyO If TM6b, Hu Sb CyO * * * * Task:To study the potential effect of a 2nd chromsomal recessive lethal mutation m(stock 1) on brain development, you want to analyse certain neurons in the brain of m mutant embryos. These neurons can be specifically labelled with ß-Gal using a 2nd chromosomal P-element insertion P(lacZ,w+) (stock 2). To perform the experiment, you need to recombine m and P(lacZ,w+) onto the same chromosome. Design a suitable mating scheme. Tip:w+ on the P-element gives orange eyes. , Hu Identify all other markers of these flies

  18. Task:To study the potential effect of a 2nd chromsomal recessive lethal mutation m(stock 1) on brain development, you want to analyse certain neurons in the brain of m mutant embryos. These neurons can be specifically labelled with ß-Gal using a 2nd chromosomal P-element insertion P(lacZ,w+) (stock 2). To perform the experiment, you need to recombine m and P(lacZ,w+) onto the same chromosome. Design a suitable mating scheme. Tip:w+ on the P-element gives orange eyes. CyO If TM6b, Hu , Hu Sb CyO Identify the balancer chromosomes

  19. cross Task:To study the potential effect of a 2nd chromsomal recessive lethal mutation m(stock 1) on brain development, you want to analyse certain neurons in the brain of m mutant embryos. These neurons can be specifically labelled with ß-Gal using a 2nd chromosomal P-element insertion P(lacZ,w+) (stock 2). To perform the experiment, you need to recombine m and P(lacZ,w+) onto the same chromosome. Design a suitable mating scheme. Tip:w+ on the P-element gives orange eyes. , Hu Define the first cross! Assign ♀ & ♂ to these stocks

  20. first? second? third? m + ; ; Y Task: Recombine P(lacZ,w+) with lethal mutation m Selecting F1 stock 2 stock 1 Now select gender and genotype!

  21. second? third? m + ; ; Y Task: Recombine P(lacZ,w+) with lethal mutation m Selecting F1 stock 2 stock 1 first? • take females(to allow for recombination) • select against curly wings (to have P-element & mutation)

  22. m + + gonad haploid gametes * Remember: recombination occurs at random * * * In the germline of the selected females, recombination takes place P(lacZ,w+) * * no recombination m * each layed egg has its individual recombination history P(lacZ,w+) m recombination * Task: Recombine P(lacZ,w+) with lethal mutation m Designing the F1 cross Challenge: how to select for the F2 flies carrying correctly recombined chromosomes?

  23. choose the stock for the males m + + Stocks available: 1st step: stabilise recombinant chromosomes with a balancer Task: Recombine P(lacZ,w+) with lethal mutation m Designing the F1 cross

  24. m + + w P(lacZ,w+),[m]* Y CyO + + P(lacZ,w+),[m]* TM6b Y If w + [m]* w Sb CyO + [m]* w If [m]*= potentially present Task: Recombine P(lacZ,w+) with lethal mutation m F2 selection first? second? third? F2 ; ; not important here; ignored hereafter

  25. w P(lacZ,w+),[m]* Y CyO + + P(lacZ,w+),[m]* TM6b Y If w + [m]* w Sb CyO + [m]* w If [m]*= potentially present Task: Recombine P(lacZ,w+) with lethal mutation m Identify the eye colours! first second third F2 ; ; not important here; ignored hereafter

  26. w P(lacZ,w+),[m]* Y CyO + + P(lacZ,w+),[m]* TM6b Y If w + [m]* w Sb CyO + [m]* w If select for white back-ground, to see orange eyes select for orange eyes, for Cy, against If [m]*= potentially present Task: Recombine P(lacZ,w+) with lethal mutation m Define your selection criteria for 2nd and 1st chromosomes first second third F2 ; ; not important here; ignored hereafter

  27. F2 w P(lacZ,w+),[m]* ; Y CyO Choose female from available stocks Key strategy: backcross to "m" stock Task: Recombine P(lacZ,w+) with lethal mutation m Selecting recombinants Challenge: determine whether recessive "m" is present

  28. F2 w P(lacZ,w+),[m]* ; Y CyO Problem: Each individual represents a unique recombination event. Solution: perform many(1) parallel single crosses, in each using ONE potentially recombinant male(2) and 3 to 5 females of stock1. (1) If the chromosomal positions of m and P(lacZ,w+) are known, the recombination frequency can be calculated; typically between 20-100 single crosses are required. (2) Males can mate several females. Even if they die early, females store enough sperm to lay eggs for a while. Hence, the likelihood that a single male successfully establishes a large enough daughter generation is considerably higher than a single female. Task: Recombine P(lacZ,w+) with lethal mutation m performing the back cross + m X ; stock 1 + CyO

  29. F2 w P(lacZ,w+),[m]* ; Y CyO F3 2nd? m P(lacZ,w+),[m]* All flies Cy? If yes, the lethal mutation "m" is present on the putatively recombinant chromosome. m CyO To establish the recombinant stock, you need to distinguish these two genotypes, i.e. select for orange eyes. CyO P(lacZ,w+),[m]* CyO CyO Task: Recombine P(lacZ,w+) with lethal mutation m performing the back cross + m X ; stock 1 + CyO Can you spot the recombinants? Define your criteria!

  30. F2 w P(lacZ,w+),[m]* ; Y CyO F3 1st? + w To establish the recombinant stock, you need to distinguish these two genotypes, i.e. select for orange eyes. ; + Y Task: Recombine P(lacZ,w+) with lethal mutation m performing the back cross + m X ; stock 1 + CyO Since you have w+ background, this strategy does not work m P(lacZ,w+),[m]* m CyO CyO P(lacZ,w+),[m]* CyO CyO

  31. F2 w P(lacZ,w+),[m]* ; Y CyO Task: Recombine P(lacZ,w+) with lethal mutation m X Rethink your strategy: • given the complexity of genetic crosses, trial and error is often unavoidable • careful planning is pivotal!

  32. single males! F2 aid 1 stock w P(lacZ,w+),[m]* ; Y CyO to establish stable fly stocks cross single potentially recombinant males to the balancer stock Task: Recombine P(lacZ,w+) with lethal mutation m X Choose female from available stocks • 2 possibilities: • You could use strategy 1, but add a parallel F1 cross between stock 1 and aid 1 to bring m into w mutant background (thus preparing it for the backcross in F2). Try whether it works for you! • Here we will use an alternative strategy, establishing stable stocks and test for lethality.

  33. F2 aid 1 stock w P(lacZ,w+),[m]* ; Y CyO 2nd? If P(lacZ,w+),[m]* • for Cy • for orange eyes • against If • against white eyes w w CyO P(lacZ,w+),[m]* ; If CyO w Y CyO CyO take males & females Task: Recombine P(lacZ,w+) with lethal mutation m establishing stable stocks X F3 1st? select!

  34. w w P(lacZ,w+),[m]* P(lacZ,w+),[m]* ; ; Y Y CyO CyO 2nd? All flies Cy? If yes, the marker "m" is present on the putatively recombinant chromosome. P(lacZ,w+),[m]* P(lacZ,w+),[m]* 1 w w P(lacZ,w+),[m]* CyO 2 ; CyO P(lacZ,w+),[m]* w Y maintain as stock CyO CyO 1 Task: Recombine P(lacZ,w+) with lethal mutation m select stable stocks X F3 F4 1st?

  35. Now continue with independent crossing tasks

More Related