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שיטות מיפוי נוספות תדירות רקומבינציה מהכלאה עצמית

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Presentation on theme: "שיטות מיפוי נוספות תדירות רקומבינציה מהכלאה עצמית"— Presentation transcript:

1 שיטות מיפוי נוספות תדירות רקומבינציה מהכלאה עצמית
שימוש בכרומוזום Y כ-'בוחן' "הגבול" בין תאחיזה להפרדה עצמית – 2 C התחשבות בשיחלופים שלא רואים – "mapping function” טטרדות – מיוזות בודדות, ומיפוי בין גן לצנטרומר

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4 =Budding Yeast =Bakers Yeast
The yeast Saccharomyces cerevisiae is commonly used as a model system =Budding Yeast =Bakers Yeast

5 The yeast Saccharomyces cerevisiae is clearly the most ideal
eukaryotic microorganism for biological studies. The "awesome power of yeast genetics" has become legendary and is the envy of those who work with higher eukaryotes. The complete sequence of its genome has proved to be extremely useful as a reference towards the sequences of human and other higher eukaryotic genes. Furthermore, the ease of genetic manipulation of yeast allows its use for conveniently analyzing and functionally dissecting gene products from other eukaryotes. --Fred Sherman

6 Major characteristic of the budding yeast
Unicellular Eukaryote Grows by budding 16 linear chromosomes Generation Time: ~100 min Can exist as stable diploid or haploid

7 Major advantages of the budding yeast as a genetic system
Grows fast Cheap Compact genome, fully sequenced since 1996. Easy to handle Superb Genetics, Biochemistry, Molecular Biology Easy to transform, high efficiency of gene targeting

8 Yeast: A model eukaryote
Lee Hartwaell Paul Nurse Tim Hunt "for their discoveries of key regulators of the cell cycle" The Nobel Prize in Physiology or Medicine 2001 Yeasts – the ultimate model eukaryote for unicellular issues and some basic cell-cell interactions Yeast studies have broken new ground in: Cytoskeleton functions transcription mechanisms** cell cycle** transcriptional regulation organelle biogenesis chromatin modification secretion* signal transduction protein targeting mechanisms protein degradation* chromosome replication DNA repair genome dynamics retroviral packaging prions recombination mechanisms ageing function of new genes metabolism protein modification *Lasker Award **Nobel Prize The Nobel Prize in Physiology or Medicine 2016 Yoshinori Ohsumi The Nobel Prize in Physiology or Medicine 2016 was awarded to Yoshinori Ohsumi "for his discoveries of mechanisms for autophagy". The Nobel Prize in Physiology or Medicine 2013 for their discoveries of machinery regulating vesicle traffic, a major transport system in our cells James E. Rothman Thomas C. Südhof Randy W. Schekman

9 What is yeast? Yeast - a fungus that divides to yield individual separated cells (as opposed to molds- mycelium) Saccharomyces cerevisiae (budding yeast) baker’s yeast closely related to brewer’s yeasts grows on rotting fruits Schizosaccharomyces pombe (fission yeast) African brewer’s yeast Saccharomyces relatives (S. bayanus, S. paradoxus, etc.) Candida albicans Cryptococcus neoformans

10 Yeast life cycle

11 Yeast cell cycle (mitosis)
Major control point is at G1/S morphology reflects cell cycle position same in haploids and diploids major control point is ‘start’-- cells can choose mitosis, meiosis or mating depends on ploidy, env. & presence of partner Morphology + nuclear localization and MT localization indicates the precise stage of the cell cycle

12 ura3- Diploid Meiosis ura3- ura3- ura3- strain WT strain Mating URA3+

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14 Mendel’s rules are relevant for organisms that sexually reproduce: diploid/haploid
Plants, Animals, many More… Those that ‘do’ meiosis

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16 Diploid Mitosis Haploid Mitosis

17 Of diploid 1n 2 1 Of haploid

18 Centromere mapping

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21 Centromere mapping Nonsister chromatids do not cross over First-division segregation pattern or MI pattern

22 Centromere mapping Nonsister chromatids cross over Second-division segregation pattern or MII pattern

23 Second-division MII segregation

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32 1. The loci are on separate chromosomes
2. The loci are on opposite sides of the centromere on the same chromosome 3. The loci are on the same side of the centromere

33 Unordered tetrads BA ba Ba bA BA Ba ba bA NPD PDT TT B B b b B B b b a
Mating b A b A Heterozygous diploid Tetrad B a Meiosis B a b A b A BA ba Ba bA BA Ba ba bA Tetrad Dissection NPD PDT TT

34 Yeast tetrad analysis (classic method)
Step1: separate spores by micromanipulation with a glass needle tetrad Step2: place the four spores from each tetrad in a row on an agar plate Step3: let the spores grow into colonies

35 Classical approach (tetrad dissection)
BA ba Ba bA BA Ba ba bA Tetrad Dissection NPD PDT TT Tetrad bni1∆ bnr1∆

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37 Map distance=50(T+6NPD) m.u
MESSAGE Linear and unordered tetrads can be used to calculate the frequencies of single and double crossovers, which can be used to calculate accurate map distances. Perkin formula Map distance=50(T+6NPD) m.u

38 BA ba Ba bA BA Ba ba bA NPD PDT TT
What PD, NPD and T values are expected when dealing with unlinked genes? B b B Mating b a a a A a a a A Tetrad Meiosis B a a B a a b a A b A Heterozygous diploid BA ba Ba bA BA Ba ba bA Tetrad Dissection NPD PDT TT

39 BA ba Ba bA BA Ba ba bA NPD PDT TT
What PD, NPD and T values are expected when dealing with unlinked genes? The sizes of the PD and NPD classes will be equal as a result of independent assortment. The T class can be produced only form a crossover between the specific loci and their respective centromeres B b B Mating b a a a A a a a A Tetrad B a a Meiosis B a a b A b A Heterozygous diploid BA ba Ba bA BA Ba ba bA Tetrad Dissection NPD PDT TT

40 שיטות מיפוי נוספות תדירות רקומבינציה מהכלאה עצמית
שימוש בכרומוזום Y כ-'בוחן' "הגבול" בין תאחיזה להפרדה עצמית – 2 C התחשבות בשיחלופים שלא רואים – "mapping function” טטרדות – מיוזות בודדות, ומיפוי בין גן לצנטרומר

41 A formula that relates RF values to the “real” physical distance
Haldane’s mapping function A formula that relates RF values to the “real” physical distance

42 Any number of crossovers produces a frequency of 50%
Haldane’s mapping function Any number of crossovers produces a frequency of 50% Recombinants within those meiosis The true determinant of RF is the relative sizes of the classes with no crossovers, versus classes with any nonzero number of cross overs

43 The larger m get e-m tends to 0
התחשבות בשיחלופים שלא רואים – "mapping function” The larger m get e-m tends to 0 and RF tends to 1/2 , or 50m.u A formula that relates RF values to “real” physical distance m-is the mean number of cross overs that occur in a segment per meiosis

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46 התחשבות בשיחלופים שלא רואים – "mapping function”

47 of map distance can be circumvented by the use of map function
MESSAGE The inherent tendency of multiple crossovers to lead to an underestimate of map distance can be circumvented by the use of map function (in any organism), and by the Perkin formula (in tetrad-producing organisms such as fungi)


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