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Lecture 8 Getting into and out of mitosis Outline: Uncovering the cyclin/CDK paradigm G2/M Exiting M-phase Paper: Anaphase regulation in budding yeast 2001 who won the Nobel prize??
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M-phase is induced by a soluble factor 70’s cell fusion experiments Factor in mitotic cell induces premature mitosis in interphase cell
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premature chromosome condensation is a disaster! the cell cycle must be highly coordinated. S M
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What is M-phase inducer? 3 lines of experimental approach: yeast Xenopus eggs invertebrate eggs
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YEAST rapidly growing, divides every 90 min powerful genetics cell cycle progress easy to follow Lee Hartwell S. cerevisiae Paul Nurse S. pombe Advantages:
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Disadvantages: nuclear envelope does not break down in M-phase spindle assembly occurs during DNA replication (budding yeast) little or no chromosome condensation in M-phase Different from higher eukaryotes
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Note on yeast nomenclature S. cerevisiae (budding yeast) wild type or dominantCDC28 mutationscdc28-4 ts, ∆cdc28 proteinCdc28 S. pombe (fission yeast) wild type or dominantcdc2 + cdc2 D mutationscdc2 ts cdc2 - proteinCdc2
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S. pombe = fission yeast
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Approach Identify temperature sensitive mutants that block the cell cycle at a specific stage (size) Fission yeast must reach a critical size to enter mitosis most arrest at random cell cycle states cdc mutant “cell division cycle” asynchronous population
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cdc2(ts) loss of function Cdc2 is the master regulator of cell division essential, no other mutation can rescue loss of cdc2 cdc2 D gain of function “wee” WT always divide at the same size
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Mitosis-inducing activity of Cdc2 is inhibited by Wee1 and stimulated by Cdc25 cdc2 ts WT cdc25 ts wee1 ts cdc25 ts, wee1 ts cdc2 D, wee1 ts mitotic catastrophe
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Cdc2 - protein kinase Cdc25 - protein phosphatase Wee1 - protein kinase 3X wee1 + WT5X cdc25 + 5X cdc2 + can confirm interactions by overexpression:
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Conclusions: Cdc2 is the master regulator of cell division in fission yeast Cdc25 is a positive regulator of Cdc2 Wee1 is a negative regulator of Cdc2 These genes are highly conserved in all eukaryotes S. cerevisiae cdc2 homologue = CDC28 human gene also complements ~ 65% identical
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Invertebrate and Xenopus eggs sea urchin, starfish, clam Advantages: stripped down cell cycle: alternating S- and M-phases no G1 or G2 phases M S synchronous divisions good for biochemistry easy to inject
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somatic cells embryonic cells Eggs divide without growing
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SG1G2M 36901215182124 Hours typical somatic cell cycle 12 embryonic cell cycles Observation: protein synthesis is required for early embryonic divisions
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fertilize eggs synchronous rounds of division incubate with 35 S - methionine take sample every 10 min SDS-PAGE and autoradiography Identification of “cyclins” sea urchin eggs newly synthesized proteins get labeled Tim Hunt, Joan Ruderman
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mitosis interphase cyclin A cyclin B abundance cell cycle state IMIM other proteins
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Conclusion Cyclin synthesis and destruction correlates with progression through the cell cycle cyclins are potential regulators
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Xenopus laevis
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1 mm diameter! diploidhaploid oocyte maturationmeiosisfertilizationcleavage diploid
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Discovery of MPF = Maturation Promoting Factor Masui and Markert 1971
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MPF = M-phase Promoting Factor a more general role..... also present in mitotic somatic cells
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KEY EXPERIMENT - Masui, Lohka and Maller biochemical purification of MPF 1 liter of frog eggs 1 g using oocyte maturation as an assay? no. monitored nuclear envelope breakdown of pronuclei in egg extract MPF has two subunits: p34 p46 complex has kinase activity toward histone H1
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VERY FAMOUS WESTERN BLOT: 1988 p34 = cdc2 antibody to conserved region of cdc2: “PSTAIRE” p46 = cyclin B
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M-phase promoting factor = MPF =cdk1/cyclinB 1) cdk1 cyclin dependent kinase 1 = yeast cdc2 Induces mitosis by phosphorylating specific downstream targets on serine and threonine protein kinase complex, 2 subunits: 2) cyclin B regulatory subunit that activates cdk1 abundance oscillates during the cell cycle
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cell cycle paradigm: transitions are regulated by cdk/cyclin complexes In yeast: single cdk, many cyclins
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Cyclin B protein is synthesized continuously Threshold cyclin B level induces MPF kinase activity Cyclin B disappears suddenly during anaphase
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Experiments to prove that cyclin synthesis drives the embryonic cell cycle in vitro system Marc Kirschner Andrew Murray electric shock simulates fertilization
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cell cycle reconstitution in vitro high MPF high histone H1 kinase activity low MPF low histone H1 kinase activity
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cyclin B synthesis can drive the cell cycle is cyclin B necessary to drive the cell cycle?
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specifically degrade cyclin B mRNA: cyclin B is both necessary and sufficient
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Is cyclin B destruction required to exit mitosis? YES add mRNAs to extract:
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Other post-translational steps control MPF activation Why the lag if enough cyclin B has been synthesized?
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fission yeast - Cdc13 (cyclin B) overexpression does not affect cell cycle: Cdc25 and Wee1 regulate clams and starfish oocyte maturation preMPF MPF, no protein synthesis Drosophila embryo limiting protein is Cdc25, not cyclin B Other evidence for post-translational regulation
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Phosphorylation on different cdk sites can either stimulate or inhibit MPF activity mutational analysis of cdc2 in yeast: Tyrosine 15 (Y-15) phosphorylation inhibits Cdc2 Threonine 161 (T-161) phosphorylation activates Cdc2 e.g. mutate tyrosine-15 to phenylalanine wee phenotype
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Cdc25 Y15 ppase Wee1 Mik1 Y15 kinases
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MPF activity controlled by: 1) cyclin B levels 2) phosphorylation of cdk1 Multiple levels of regulation provide input for “checkpoint control”
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When MPF level reaches threshold irreversible activation High MPF levels trigger cyclin B degradation irreversible inactivation Feedback mechanisms:
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Exit from mitosis Ubiquitin-mediated proteolysis
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E1: activates ubiquitin only 1 gene in yeast E2: acquires ubiquitin through high energy thioester linkage = ubiquitin-carrier or conjugating enzyme 11 genes in yeast E3: catalyzes attachment of ubiquitin to protein substrate = ubiquitin ligase binds E2 and substrate, like a scaffold can be in large regulatory complex many versions, provides specificity rate-limiting step!! Enzymes in ubiquitin pathway
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proteosome
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EM
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E3 ligase for cyclin B = Anaphase Promoting Complex (APC) 8 subunits identified by fractionating egg extracts, yeast genetics degrades other proteins besides cyclin B that are required for anaphase and mitotic exit
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What are the APC targets? Xkid Pds1 - chromosome cohesion regulator ?? mitotic cyclins temporally specific proteolysis: orderly and irreversible sequence of events
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What generates specificity of APC? Accessory factors: recognize destruction box Cdc20 - activates APC earlier targets Pds1, mitotic cyclins Cdh1 - activates APC later targets more cyclins, APC subunits ENTRY INTO INTERPHASE
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