Tetrad analysis

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Tetrad analysis ססססס ססססס/ססס/סססס ססססס ססססס

description

Tetrad analysis. אסקוס. ספורה/נבג/תוצר מיוזה. טטרדה. Replica plating. Replica plating. -URA. -TRP. -ADE. -LYS. YePD. URA3 TRP1 ade2 lys2. URA3 trp1 ade2 lys2. ab X a + b +. A. B. a. b. A. B. A. b. A. B. A. b. a. b. a. B. a. b. a. B. PD. =. NPD. A. B. A. B. - PowerPoint PPT Presentation

Transcript of Tetrad analysis

Page 1: Tetrad analysis

Tetrad analysis

אסקוס

/ מיוזה/ תוצר נבג טטרדהספורה

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Replica plating

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ab X a+b+

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A

a

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PD

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NPD=

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A B

a b

A B

a b

A B

a bA B

a b PD only

A B

a b

X

A B

a b

A b

a B

TT

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Thus RF=1/2TT

הכפולות הרקומבינציות עם מה ?אבל

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מכך ויתרה כפולות רקומבינציות כולל אינו הקודם החישוב כלומרה כי מטעה כפולות TTהוא גם ....כולל

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Assuming that, in our hypothetical cross of a+ b+ × a b, the observed frequencies of the ascus classes are 56 percent PD, 41 percent T, and 3 percent NPD. Using the formula, we find the map distance between the a and b loci to be:

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Let us compare this value with that obtained directly from the RF. Recall that the formula is:

In our example,

This RF value is 6 m.u. less than the estimate we obtained by using the map-distance formula because we could not correct for double crossovers in the RF analysis.

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SummaryPD=NPD - No linkage

PD only high linkage maybe the same gene

PD>TT>NPD -Linkage

RF=1/2(TT+6NPD)

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Repair, and Recombination

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• E. Coli SOS system

Emergency response that allow the insertion of non specific base!

In bacteria its DinB, UmuC and UmuD that encode for pol IV and V, the error prone polymerase that incorporate an arbitrary base across to the damaged base.

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Pol eta/iota

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Direct reversal By photolyase

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Base excision repair

• Start with glycosylase that break the sugar-base bond* and release the altred base and generating apurinic or apyrimidinic sites.

* For example guanine +EMS -> 0-6-ethylgunine (can mispaired with Thymine)

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Nucleotide excision repair (NER) in bacteria

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Nucleotide excision repair (NER) in yeast

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XPD and XPB – helicaseXPG and XPF - endonuclase

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Cockayne syndrome

• Mutation in CSA or CSB causes to retinal degeneration, hearing impairment, ataxia and photosensitivity

• Die very young

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Tricothiodystrophy (TTD)

• Mutations in XPD

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WT

TTD

Human shows photosensetivity, brittle hair, skin defects and short life span.

XPD -/- mice show also wasting, scoliosis, osteophoresis and melanocyte loss.

WT TTD

3m

15m

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Mismatch repair in bacteria

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Mismatch repair (NER) in human

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Spo11

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Aberrant ratio

4:4 6:2 2:6 5:3 3:5

Gene conversion