页数：72页文件大小：1.79 MB来源： 分子生物学基因Geneppt课件
本课件为《分子生物学》第27章细胞周期与生长调控（Cell cycle and growth regulation），依据 Gene VII 编排，讲解本章核心概念与分子机制，配逐页图示与文字版。
Chapter 27 Cell cycle and growth regulation
Figure 27.1 Over view: interphase is divided into the G1, S, and G2 periods. One cell cycle is separated from the next by mitosis (M). Cells may withdraw from the cycle into G0 or reenter from it.
Figure 27.2 Synthesis of RNA and proteins occurs continuously, but DNA synthesis occurs only in the discrete period of S phase. The units of mass are arbitrary.
Figure 27.1 Over view: interphase is divided into the G1, S, and G2 periods. One cell cycle is separated from the next by mitosis (M). Cells may withdraw from the cycle into G0 or reenter from it.
Figure 27.3 Checkpoints control the ability of the cell to progress through the cycle by determining whether earlier stages have been completed successfully. A horizontal red bar indicates the stage at which a checkpoint blocks the cycle.
Figure 27.4 Cell fusions generate heterokaryons whose nuclei behave in a manner determined by the states of the cells that were fused.
Figure 27.5 The phases of the cell cycle are controlled by discrete events that happen during G1, at S phase, and at mitosis.
MPF(maturation-or M phase-promoting factor) is a dimeric kinase, containing the p34 catalytic subunit and a cyclin regulatory subunit, whose activation triggers the onset of mitosis.
Figure 27.6 MPF induces M phase in early Xenopus development.
Figure 27.5 The phases of the cell cycle are controlled by discrete events that happen during G1, at S phase, and at mitosis.
Figure 27.7 The activity of M phase kinase is regulated by phosphorylation, dephosphorylation, and protein proteolysis. The 3 phosphorylated amino acids are: Thr-14, Tyr-15, Thr-161. The first two are in the ATP-binding site.
Phosphorylation (catalyzed by kinases) and dephosphorylation (catalyzed by phosphatases) are the critical events that regulate the cell cycle. They are used both to control the activities of the regulatory circuit itself and to control the activities of the substrates that execute the dec is ions of the regulatory circuit.
The cell cycle regulatory circuit consists of a series of kinases and phosphatases that respond to external signals and checkpoints by phosphorylating or dephosphorylating the next member of the pathway. The ultimate readout of the circuit is to determine the activity of M phase kinase (or the S phase kinase) by controlling its state of phosphorylation.
Phosphorylation (catalyzed by kinases) and dephosphorylation (catalyzed by phosphatases) are the critical events that regulate the cell cycle. They are used both to control the activities of the regulatory circuit itself and to control the activities of the substrates that execute the dec is ions of the regulatory circuit.
The cell cycle regulatory circuit consists of a series of kinases and phosphatases that respond to external signals and checkpoints by phosphorylating or dephosphorylating the next member of the pathway. The ultimate readout of the circuit is to determine the activity of M phase kinase (or the S phase kinase) by controlling its state of phosphorylation.
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Cyclins are proteins that accumulate continuously throughout the cell cycle and are then destroyed by proteolysis during mitosis. A cyclin is one of the two subunits of the M-phase kinase.
G1 is the period of the eukaryotic cell cycle between the last mitosis and the start of DNA replication.
Figure 27.8 S. pombe lengthens and then divides during a conventional cell cycle, while S. cerevisiaebuds during a cycle in which G2 is absent or very brief, and M occupies the gre a test part.
Figure 27.9 S. pombe cells are stained with calcoflu or to identify the cell wall (surrounding the yeast cell) and the septum (which forms a central division when a cell is dividing). Wild-type cells double in length and then divide in half, but cdc mutants grow much longer, and wee mutants divide at a much smaller size. Photograph kindly provided by Paul Nurse.
Figure 27.10 Haploid yeast cells of either a or a mating type may reproduce by a mitotic cycle. Cells of opposite type may mate to form an a/a diploid. The diploid may sporulate to generate haploid spores of both a and a types.
Figure 27.11 The cell cycle in S. pombe requirescdc genes to pass specific stages, but may be retarded by genes that respond to cell size (wee1). Cells may be diverted into the mating pathway early in G1.
Figure 27.12 The state of the cell cycle in S. pombe is defined by the forms of the Cdc2-cyclin complexes.
Figure 27.16 rum1 inactivates the M phase kinase , preventing it from blocking the initiation of S phase.
Figure 27.13 Cell cycle control in S. pombe involves successive phosphoryl at ions and dephosphoryl at ions of cdc2. Checkpoints operate by influencing the state of the Tyr and Thr residues.
Figure 27.14 DNA damage triggers the G2 checkpoint.
Figure 27.15 cdc18 is required to initiate S phase and is part of a checkpoint for ordering S phase and mitosis. Active M phase kinase inactivates cdc18, generating a reciprocal relationship between mitosis and S phase.
Figure 27.16 Rum1 inactivates the M phase kinase, preventing it from blocking the initiation of Sphase.
Figure 27.17 Checkpoints can arrest the cell cycle at many points in response to intr in sic or extr in sic conditions.
Figure 27.8 S. pombe lengthens and then divides during a conventional cell cycle, while S. cerevisiaebuds during a cycle in which G2 is absent or very brief, and M occupies the gre a test part.27.6 CDC28 acts at both START and mitosis in S. cerevisiae.
Figure 27.18 The cell cycle in S. cerevisiae consists of three cycles that separate after START and join before cytokines is. Cells may be diverted into the mating pathway early in G1.27.6 CDC28 acts at both START and mitosis in S. cerevisiae.
Figure 27.19 Cell cycle control in S. cerevisiae involves association of CDC28 with redundant cyclins at both START and G2/M.27.6 CDC28 acts at both START and mitosis in S. cerevisiae.
Figure 27.20 Similar or overlapping components are used to construct M phase kinase and a G1 counterpart.
Figure 27.20 Similar or overlapping components are used to construct M phase kinase and a G1 counterpart.
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Figure 27.21 Control of mitosis in animal cells requires phosphoryl at ions and dephosphoryl at ions of M phase kinase by enzymes that themselves are under similar control or respond to M phase kinase.
Figure 27.13 Cell cycle control in S. pombe involves successive phosphoryl at ions and dephosphoryl at ions of cdc2. Checkpoints operate by influencing the state of the Tyr and Thr residues.
Figure 27.7 The activity of M phase kinase is regulated by phosphorylation, dephosphorylation, and protein proteolysis. The 3 phosphorylated amino acids are: Thr-14, Tyr-15, Thr-161. The first two are in the ATP-binding site.
Figure 27.22 Several cdk-cyclin complexes are active during G1 and S phase. The shaded arrows show the dur at ion of activity.
Figure 13.34 Licensing factor in the nucleus is inactivated after replication. A new supply of licensing factor can enter only when the nuclear membrane breaks down at mitosis.
Figure 27.23 A block to the cell cycle is released when RB is phosphorylated by cdk-cyclin.
Figure 27.24 p16 binds to cdk4 and cdk6 and to cdk4,6-cyclin dimers. By inhibiting cdk-cyclin D activity, p16 prevents phosphorylation of RB and keeps E2F sequestered so that it is unable to initiate S phase.
Figure 27.25 p21 and p27 inhibit assembly and activity of cdk4,6-cyclin D and cdk2-cyclin E by CAK. They also inhibit cycle progression independent of RB activity. p16 inhibits both assembly and activity of cdk4,6-cyclin D.
Figure 27.26 The SCF is an E3 ligase that targets the inhibitor Sic1.
Figure 8.49 The ubiquitin cycle involves three activities. E1 is linked to ubiquitin. E3 binds to the substrate protein. E2 transfers ubiquitin from E1 to the substrate. Further cycles generate poly ubiquitin.
Figure 27.27 Progress through mitosis requires destruction of cyclins and other targets.
Figure 8.49 The ubiquitin cycle involves three activities. E1 is linked to ubiquitin. E3 binds to the substrate protein. E2 transfers ubiquitin from E1 to the substrate. Further cycles generate poly ubiquitin.
Figure 27.28 Two versions of the APC are required to pass through anaphase.
Figure 27.29 Anaphase progression requires the APC to degrade Pds1p to allow Esp1p to remove Scc1 from sister chromatids.
Figure 27.30 CDC20 is required for both exit from anaphase and exit from mitosis.
Figure 27.31 An unattached kinetochore causes the Mad pathway to inhibit CDC20 activity.
Figure 27.32 Major changes in the cell at mitosis involve the chromosomes, nuclear envelope, nuclear lamina, and microtubules.
Figure 27.33 The centriole consists of nine microtubule triplets, apparent in cross-secti on as the wall of a hollow cylinder. Photograph kindly provided by A. Ross.
Figure 27.34 A centriole reproduces by forming a procentriole on a perpendicular axis; the procentriole is subsequently extended into a mature centriole. Photograph kindly provided by J. B. Rattner and S. G. Phillips.
Apoptosis is the capacity of a cell to undergo programmed cell death; in response to a stimulus, a pathway is triggered that leads to destruction of the cell by a characteristic set of reactions.
Figure 27.35 The nucleus becomes heteropycnotic and the cytoplasm blebs when a cell apoptoses.
Figure 27.36 Cell structure changes during apoptosis. The top panel shows a normal cell. The lower panel shows an apoptosing cell; arrows indicate condensed nuclear fragments. Photographs kindly provided by Shigekazu Nagata.
Figure 27.37 Fragment at ion of DNA occurs ~2 hours after apoptosis is initiated in cells in culture. Photograph kindly provided by Shigekazu Nagata.
Figure 27.38 Apoptosis is triggered by a variety of pathways.
Figure 27.39 The Fas receptor and ligand are both membrane proteins. A target cell bearing Fas receptor apoptoses when it interacts with a cell bearing the Fas ligand.
Figure 27.40 Fas forms trimers that are activated when binding to FasL causes aggreg at ion.
Caspases comprise a family of protease some of whose members are involved in apoptosis (programmed cell death)
Figure 27.41 Apoptosis can be triggered by activating surface receptors. Caspase proteases are activated at two stages in the pathway. Caspase-8 is activated by the receptor. This leads to release of cytochome c from mitochondria. Apoptosis can be blocked at this stage by Bcl-2. Cytochrome c activates a pathway involving more caspases.
Figure 27.42 The TNF-R1 and Fas receptors bind FADD (directly or indirectly). FADD binds caspase-8. Activation of the receptor causes oligomeriz at ion of caspase-8, which activates the caspase.
Figure 27.43 Caspase activation requires dimerization and two cleavages.
Figure 27.44 The mitochondri on plays a central role in apoptosis by releasing cytochrome c. This is activated by BID. It is inactivated by Bcl-2. Cytochrome c binds to Apaf-1 and (pro)-Caspase-9 to form the apop to some. The proteolytic activity of caspase-9 (and other caspases) can be inhibited by IAP proteins. Proteins that antagonize IAPs may be released from the mitochondri on.
Figure 27.45 Cytochrome c causes Apaf-1 to interact with caspase-9, which activates caspase-3, which cleaves targets that cause apoptosis of the cell.
Figure 27.41 Apoptosis can be triggered by activating surface receptors. Caspase proteases are activated at two stages in the pathway. Caspase-8 is activated by the receptor. This leads to release of cytochome c from mitochondria. Apoptosis can be blocked at this stage by Bcl-2. Cytochrome c activates a pathway involving more caspases.
Figure 26.31 JNK is a MAP-like kinase that can be activated by UV light or via Ras.
Figure 27.46 Fas can activate apoptosis by a JNK-mediated pathway.
Figure 27.46 Fas can activate apoptosis by a JNK-mediated pathway.
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1.The cell cycle consists of transitions from one regulatory state to another. 2.The two key control points in the cell cycle are in G1 and at the end of G2. 3.A unifying feature in the cell cycles of yeasts and animals is the existence of an M phase kinase, consisting of two subunits: Cdc2, with serine/threonine protein kinase catalytic activity; and a mitotic cyclin of either the A or B class.4.The activity of the M phase kinase is controlled by the phosphorylation state of the catalytic subunit.5.A comprehensive analysis of genes that affect the cell cycle has identified cdc mutants in both S. pombe and S. cerevisiae.
6.By phosphorylating appropriate substrates, the kinase provides MPF activity, which stimulates mitosis or meiosis (as originally defined in Xenopus oocytes). 7.Transition from G1 into S phase requires a kinase related to the M phase kinase. 8.In mammalian cells, a family of catalytic subunits is provided by the cdk genes, named because they code for the catalytic subunits of cyclin-dependent kinases. 9.Checkpoints control progression of the cell cycle. 10.Apoptosis is achieved by an active pathway that executes a program for cell death.
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