prof. fahd m. nasr · 2019. 3. 14. · •under nitrogen starvation diploid cells meiosis and...
TRANSCRIPT
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Prof. Fahd M. Nasr
Lebanese universityFaculty of sciences
https://yeastwonderfulworld.wordpress.com/
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Mighty Yeasts
Yeast sexual lifeMating type switch by gene
conversion
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• Under nitrogen starvation diploid cells meiosis and sporulation an ascus with four haploid spores
• Although unicellular distinguish different cell types with different genetic programmes– Haploid MATa versus MATa– Haploid versus Diploid (MATa/a)– Spores– Mothers and daughters
Yeast has a sexual life!
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• Pheromone response signal transduction pathway sexual communication
• Controls the response of yeast cells to a- or a-factor• Specific pheromone receptor binds a- or a-factor• Pheromone binding
– Stimulates reorientation of the cell towards the source of the pheromone (the mating partners)
– Stimulates a signalling cascade MAP kinase pathway– This signalling pathway causes cell cycle arrest
• The pathway controls expression of genes important for mating
Yeast with a sexual life
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MAPK cascades in Yeast• Gpa1 Gα subunit plays three roles
– No pheromone signalingGpa1 binds to the Ste4-Ste18 Gßγ dimer prevent activation of the MAPK pathway
– Upon activation Gpa1 binds the Fus3 MAPK to positively regulate cell growth and cellular fusion
– Positive role in signaling via an interaction with Scp160
– RGS protein Sst2 accelerates Gpa1 GTPase activity and desensitize the cells to the pheromone present in the growth environment
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MAPK cascades in Yeast
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Signal Transduction Pathways• Overlap and integration of signal transduction pathways
Yeast Pheromone Signaling Pathway
Humans : MAPK signaling pathway : growth control -> tumor developmenthttp://www.bio.davidson.edu/courses/Immunology/Flash/MAPK.html
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Cell attachment, cell fusion and nuclear fusion in an electron micrograph
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Yeast mating type chromosome diagram
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Structure of MATa and MATalpha alleles
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Mating type
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Model for the STE2 gene regulation
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Mating Type Switching in Yeast
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Mating Type Switching in Yeast
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Haploids and dipoids in nature and laboratory
• Several reasons– Spores are hardy and survive very harsh
conditions– Sporulation is a way to "clean" the genome
from accumulated mutations– Meiosis is a way to generate new combinations
of alleles – New allele combinations with a partner from a
different tetrad
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Mating Type Conversion: heterothallic strains of yeast switch sex each generation!
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a/a
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So what regulates HO expression?
• Transcription of HO– in the late G1 phase of the cell cycle– is determined by binding of cell- cycle box
factor CCBF to the cell-cycle box – CCBF = Swi4p and Swi6p– Cell-cycle box sequences 12bp sequence
motif that is repeated 10 times in URS2– CCBF is active only during G1
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Two regulators HO gene
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Transcriptional Regulation
SWI/SNF
SWI5
RNA Pol IITATA BPGENERAL TFs
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Ash1p: a negative regulator of HO expression in daughter cells
• Found in 3 different mutant screening strategies– Bobola et al. (1996) also looked for mutations that
restore HO expression in a she1 mutant background– SHE1 (Swi5p-dependent HO expression) is essential for
HO expression in mother cells– but encodes an unconventional myosin– therefore may be involved in localization of negative
regulator (repressor) of HO expression– Then loss of negative regulator would restore HO
expression in she1 mutants
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Recombination enhancer structure
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Mating type switching is initiated by a ds-break in the recipient site (MAT). The break point is a 24 bp sequence recognized by HO endonuclease.
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3 4
1 23'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
A B
a b
C D
C Dc d
c d
A Ba bDouble-strand
break model for recombination
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3 4
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
3'5'
3'5'
5'3'
5'3'
1 23'5'
3'5'
5'3'
5'3'
1 + 2
3 + 4
1 + 4
2 + 3
Resolution of theheteroduplex with twoHolliday junctions
A B
a b
C D
c DC D
C d
A Ba b
A B
a b
C d
C Dc D
C D
A Ba b
A b
a B
C D
c DC D
C d
A ba B
a B
A b
C D
c DC D
C d
a BA b
(H1)
(H2)
(H3)
(H4)
(H3 and H4) CO(H1 and H2) no CO
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a Bc D
C Da B
A b
C D
C d
A b
A B
a b
C D
C D
c d
c d
A B
a b
Cen
trom
ere
a BC D
C Da B
A B
a b
C D
C D
c d
c d
A B
a b
A b
C D
C D
A b
Sister chromatids
Cen
trom
ere
Cen
trom
ere
Cen
trom
ere
Sister chromatids
Non-sister chromatids
Gene conversion leads to unusual ratiosof 3C:1c or 3D:1d during meiosis
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Gene conversion occurs during HR
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HO endonuclease is
transcriptionally regulated
via three different systems
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Cellular Polarity and Morphogenesis
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Cellular Polarity(Protein Dynamics)
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Cellular Polarity
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Cellular Polarity
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Cellular PolaritymRNA Localization & Maternal
Effect
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Why yeast as genetics model
• Basic cellular mechanisms conserved• Unicellular• Grow on readily controlled, defined media• Ideal life cycle• Very compact genome• Quick to map a phenotype producing gene• Single gene deletion mutants• One third of the genes have counterparts in
human
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Yeast chromosomes
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The S. cerevisiae genome of 12.1 Mb has 6000 genes, almost all uninterrupted
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Yeast Genetic InformationInheritance Mendelian Non-Mendelian
Nucleic acid Double-stranded DNA Double-stranded RNA
Location Nucleus Cytoplasm
Genetic determinant
Chrs 2-mm plasmid
Mito. DNA RNA viruses
L-A M L-BC T W
Relative amount
85% 5% 10% 80% 10% 9% 0.5% 0.5%
Nb of copies 2 sets of 16 60-100 ~50 (8-130) 103 170 150 10 10
Size (kb) 12,100 6.318 70-76 4.576
1.8 4.6 2.7 2.25
Deficiencies in mutants
All kinds None Cytochromes a.a3 and b
Killer toxin None
Wild type YFG1 cir+ r+ KIL-k1
Mutant of variant
yfg1-1 cir0 r- KIL-o
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Function of ARS and Centromere Sequences
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Identification of Telomeres
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The end