Lecture 11 The Cell Cycle and Mitosis



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Transcription:

Lecture 11 The Cell Cycle and Mitosis

In this lecture Cell division Chromosomes The cell cycle Mitosis PPMAT Apoptosis

What is cell division? Cells divide in order to reproduce themselves

The cell cycle Cells go through a predictable cycle controlled by cell signaling

Two stages of the cell cycle Interphase Most cell growth growth and development takes place Mitotic phase Cell division takes place

Interphase Interphase (about 90% of the cell cycle) can be divided into subphases G 1 phase ( first gap ) S phase ( synthesis ) G 2 phase ( second gap ) The cell grows during all three phases, but chromosomes are duplicated only during the S phase

Which portion of the cell cycle do you think is most energy intensive and why?

G 0 phase Some cells exit the cell cycle and go quiescent This is a resting phase where no active cell growth or division takes place, only maintenance Cells can enter G 0 and stay there for years, and many will never go back into the regular cycle Neurons are usually in G 0

Controlling the cell cycle The sequential events of the cell cycle are directed by a distinct cell cycle control system, which is similar to a clock The cell cycle control system is regulated by both internal and external controls The clock has specific checkpoints where the cell cycle stops until a go-ahead signal is received

The cell cycle control system Two main components of the cell cycle control system: Cyclins Control the overall flow of the cell cycle Checkpoints Ensure that certain requirements are met at certain points Cyclins are the traffic flow on the freeway, checkpoints are the traffic on surface streets

Cyclins in the cell cycle Two types of regulatory proteins are involved in cell cycle control: cyclins and cyclindependent kinases (Cdks) A cyclin is a regulatory protein involved in the cell cycle Its concentration varies with the cell cycle The Nobel Prize in medicine was awarded in 2001 for the discovery of cyclins

Different cyclins control different parts of the cell cycle

Cyclins and Cdks Cyclins control cyclin-dependent kinases (Cdks) by binding to them When cyclins bind cdk, they become MPF, maturation-promoting factor MPF triggers a cell s passage past the G 2 checkpoint into the M phase MPF activates other proteins through phosphorylation These proteins are responsible for microtubule formation and chromatin condensing

Cyclin + Cdk = MPF

Checkpoints in the cell cycle Each checkpoint serves as a stoplight for the cell The cell must pass the requirements of that checkpoint before it can proceed Cells respond to both internal and external checkpoint signals

Internal and external checkpoint signals Internal signal example: centromeres not properly aligned send a molecular signal that delays mitosis Some external signals are growth factors, proteins released by certain cells that stimulate other cells to divide For example, platelet-derived growth factor (PDGF) stimulates the division of human fibroblast cells in culture PDGF is also released near the sites of wounds, causing cells nearby to divide and close the wound

PDGF is important in culturing stem cells PDGF sends a signal that tells stem cells to divide in an artificial culture

More external checkpoints A clear example of external signals is densitydependent inhibition, in which crowded cells stop dividing Most animal cells also exhibit anchorage dependence, in which they must be attached to a substratum in order to divide Cancer cells exhibit neither density-dependent inhibition nor anchorage dependence

The frequency of cell division varies with the type of cell These differences result from regulation at the molecular level Cancer cells manage to escape the usual controls on the cell cycle

Cell division and cancer All cancers are caused by the deregulation of cell division In order to become cancerous, two types of regulatory genes must be affected: Oncogenes, which promote cell division Tumor-suppressor genes, which inhibit cell division Usually, many different changes in many different genes are required for cancer The Dark Arts Cancers," said Snape, "are many, varied, ever-changing, and eternal. Fighting them is like fighting a many-headed monster, which, each time a neck is severed, sprouts a head even fiercer and cleverer than before. You are fighting that which is unfixed, mutating, indestructible."

P53 and cancer P53 is a major tumor-suppressor protein Nicknamed the guardian of the genome It recognizes and repairs DNA damage It can stop cell growth after it recognizes DNA damage It can initiate cell suicide if the DNA damage is too severe P53 also activates p21, which binds to and inhibits MPF If p53 is inactivated, you suddenly have lots a main weapon in your anti-cancer arsenal

Cancer and aging Why not just add extra p53 to a person who has/is at risk for cancer? P53 causes aging! Many other genes/proteins that cancer uses to become cancerous are related to embryonic development Evolved for Cancer?

Ras and p53 Ras is the most common oncogene found in cancer Ras is a GPCR that, once activated cannot be unactivated This constantly stimulates cell division P53 is the most common tumorsuppressor gene found in cancer http://www.youtube.com/watch?v=hm03 rcuodqg&nr=1&feature=fvwp

Describe how p53 prevents cancer both through its tumor suppressor capabilities and its apoptosis-inducing capabilities

Somates and Gametes A somatic cell is a normal body cell Muscle cells, neurons, epithelial cells In humans, each somatic cell contains two copies of our genome 2n, diploid A gamete/germline cell is a reproductive cell Sperm and eggs Contains 1 copy of our genome N, haploid

Mitosis and Meiosis In general, when a somatic cell divides it produces two identical daughter cells Same genetic information, 2n Same cell types Somatic cell division is called mitosis Gamete division is called meiosis

Some DNA stuff Genome all of the DNA in a cell DNA molecules in a cell are packaged into chromosomes composed of chromatin Chromosome the X-shaped structure composed of a single molecule of DNA Humans have 23 chromosomes Chromatin a complex of DNA and protein that condenses during cell division

A genome can consist of a single DNA molecule (common in prokaryotic cells) or a number of DNA molecules (common in eukaryotic cells)

How chromatin makes up chromosomes

Anatomy of a chromosome Each chromosome has two sister chromatids The sister chromatids are identical copies of each other The two chromatids are linked together by a centromere The centromere is a series of repetitive DNA sequences that have a high affinity for kinetochore proteins Sister chromatids Centromere 0.5 m

Keeping your terms straight Chromosome The X made of DNA. 23 in humans Chromatid One leg of a chromosome, composed of chromatin. 46 in humans Chromatin DNA wound around protein

Karyotype the organized numbering and appearance of the full set of an organism s chromosomes Karyotypes

Karyotyping and disease diagnosis Down syndrome is caused by the abnormal presence of an extra chromosome 21

Chromosomes during cell replication During cell division, the two sister chromatids of each duplicated chromosome separate and move into two nuclei Once separate, the chromatids are called chromosomes

Chromosomes during cell replication

Chromosomes during cell replication

Chromosomes during cell replication

Mitosis: an overview Mitosis is the process of cell division, and focuses mainly on the chromosomes Chromosomes are evenly divided into two daughter cells Five stages of mitosis: Prophase Prometaphase Metaphase Anaphase Telophase PPMAT Cytokinesis is the division of the cytoplasm, and overlaps anaphase and telophase

10 m Figure 12.7 Mitosis: an overview G 2 of Interphase Prophase Prometaphase Metaphase Anaphase Telophase and Cytokinesis Centrosomes Chromatin (with centriole pairs) (duplicated) Early mitotic spindle Aster Centromere Fragments of nuclear envelope Nonkinetochore microtubules Metaphase plate Cleavage furrow Nucleolus forming Nucleolus Nuclear envelope Plasma membrane Chromosome, consisting of two sister chromatids Kinetochore Kinetochore microtubule Spindle Centrosome at one spindle pole Daughter chromosomes Nuclear envelope forming Mitosis is truly a continuous process there appear to be distinct stages, but really, it s all one big mashup

New terms Spindle Composed of centrosome and the microtubules that extend from it Aster The smaller microtubules that extend from the centrosome Metaphase plate the imaginary plate chromosomes line up against in metaphase Kinetochore a protein complex in the centromere of the chromosome that attaches to the spindle Centrosome the microtubule-organizing center of the cell

Before prophase Unorganized chromatin (2n) One centrosome Nuclear envelope intact and nucleolus visible Normal cell activities taking place

Prophase Chromatin (duplicated in S) begins to condense into chromosomes Centrosomes duplicate Nuclear envelope begins to dissolve Spindle begins to form

Prometaphase Chromosomes completely condense Centromeres build up kinetochores Microtubules begin to attach to kinetochores Nonkinetochore microtubules begin to extend

Metaphase Centrosomes localize to opposite ends of the cell Chromosomes line up on the metaphase plate Microtubules finish attaching to kinetochores

Anaphase Chromosomes break apart and the halves begin moving toward opposite ends The cell elongates as nonkinetochore microtubules lengthen The shortest stage lasts only a few minutes

Telophase Nuclei and nuclear envelopes reform Chromosomes decondense Spindles are depolymerized Nucleoli reappear Cytokinesis overlaps with telophase

Cytokinesis

A closer look at kinetochores

The role of microtubules Microtubules both push and pull during mitosis Some microtubules attach to kinetochores and pull apart chromosomes Others span the length of the cell, and lengthen during cytokinesis to push apart the daughter cells

Another look at mitosis (in plants) http://www.youtube.com/watch?v=0 ojzdkdperu&feature=related http://www.youtube.com/wat ch?v=dd3iqkncedc

Comparing cell division in other organisms

Apoptosis Programmed cell suicide Many causes for apoptosis, but a big one is a cell repeatedly failing checkpoints Your body can also induce apoptosis in your damaged, infected, or cancerous cells P53 can force cells into apoptosis when their DNA is too damaged http://www.youtube.com/watch?v=xdlpp dou2nc

What would happen to animal cells that did not undergo cytokinesis?

Polyploidy Some cells undergo S phase DNA replication, but not mitosis They have many duplicate copies of their genome Plants can tolerate this very well seedless grapes and watermelons arise from polyploid gametes Not humans, except in rare examples

Genome Chromosomes Vocabulary Cyclin, MPF Mitosis Chromatin Prophase, Somatic cell, gamete prometaphase, Karyotyping metaphase, anaphase, telophase Oncogene, tumorsuppressor gene Cytokinesis P53 Microtubules Apoptosis

Suggested Links Khan Academy http://www.khanacademy.org/video/phases -of-mitosis?topic=biology

Questions?