Mitosis and Meiosis - Biology Courses...
Transcript of Mitosis and Meiosis - Biology Courses...
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Lecture # 15 Chapter 7b
Mitosis and Meiosis
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• During fetal development, many cells are programmed to die
Cell Death
• Human cells appear to be programmed to undergo only so many cell divisions– About 50 in cell cultures
• Only cancer cells can divide endlessly Fig. 7.9 Programmed cell death
Fingers and toes form from these paddlelike
hands and feet
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7.5 Controlling the Cell Cycle• The eukaryotic cell cycle is controlled by feedback at
three checkpoints– 1. Cell growth is assessed at the G1 checkpoint– 2. DNA replication is assessed at the G2 checkpoint– 3. Mitosis is assessed at the M checkpoint
Fig. 7.10 Fig. 7.11
G0 is an extended rest period
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7.6 What is Cancer?• Cancer is unrestrained cell growth and division• The result is a cluster of cells termed a tumor
• Benign tumors– Encapsulated and
noninvasive
• Malignant tumors – Not encapsulated
and invasive
• Leave the tumor and spread throughout the body
Fig. 7.13– Can undergo metastasis
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• Most cancers result from mutations in growth-regulating genes
• There are two general classes of these genes– 1. Proto-oncogenes
• Encode proteins that simulate cell division• If mutated, they become oncogenes
– 2. Tumor-suppressor genes• Encode proteins that inhibit cell division
• Cancer can be caused by chemicals, radiation or even some viruses
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7.7 Cancer and Control of the Cell Cycle
• The p53 gene plays a key role in the G1 checkpoint of cell division
• The p53 protein (the gene’s product), monitors the integrity of DNA– If DNA is damaged, the protein halts cell division
and stimulates repair enzymes
• If the p53 gene is mutated– Cancerous cells repeatedly divide – No stopping at the G1 checkpoint
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Fig. 7.14 Cell division and p53 protein
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7.8 New molecular therapies for cancer
Fig. 7.15Receiving the signal to divide
Passing the signal via a relay switch
Amplifying the signal
Releasing the “brake”
Checking that everything is ready
Stepping on the gas
Stopping tumor growth
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7.9 Meiosis produces gametes• Meiosis was first observed by the Belgian cytologist Pierre-
Joseph van Beneden in 1887
• Gametes (eggs and sperm) contain half the complement of chromosomes found in other cells
• The fusion of gametes is called fertilization or syngamy– It creates the zygote, which contains two copies of each
chromosome
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7.10 The Sexual Life Cycle• The life cycles of all sexually-reproducing organisms
follows the same basic pattern– Haploid cells or organisms alternate with diploid cells
or organismsFig. 7.18
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Fig. 7.19 The sexual lifecycle in animals
• Meiosis only occurs in thegonads (ovaries and testes).
• All other cell divisions aremitotic
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7.11 The Stages of Meiosis
• Meiosis consists of two successive divisions, but only one DNA replication
– Meiosis I• Separates the two homologs
– Meiosis II• Separates the two sister chromatids
• Meiosis halves the number of chromosomes
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Prophase I
• Chromosomes condense (coil)
• Nuclear membrane breaks down
• Homologous chromosomes undergo synapsis (Pair up )
• Recombination (cross over) occurs and chromosomes exchange segments
newly forming microtubules
Fig. 7.20
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Metaphase I
• Homologous chromosome pairsline up at random at the equatorial midline
spindle equator
one pair ofhomologouschromosomes
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Anaphase I
• Centromeres do not divide
• Homologsseparate and move to opposite poles
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Telophase I
• Nuclear membrane reforms
• Chromosomes uncoil
After Cytokinesis• Two haploid cells
are produced
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• Meiosis II
– After meiosis I there is a brief interphase• No DNA synthesis occurs
– Meiosis II is similar to mitosis, but with two main differences
• 1. Haploid set of chromosomes
• 2. Sister chromatids are not identicalbecause of cross over
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Prophase IIbegins with haploid cells
• Chromosomes coil
• Spindle forms
• Nuclear membrane breaks down
• Each chromosome is composed of two sister chromatids attached at the centromere
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Metaphase II
• Chromosomes line up on the midline and attach to spindle fibers
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Anaphase II
•Centromeres divide
•Sister chromatidsmove to opposite poles
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Telophase II
• Nuclear membrane reforms
• Chromosomes uncoil
After Cytokinesis• Four unique haploid
cells are produced
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7.12 Meiosis I has two unique features1. Synapsis
• Homologous chromosomes pair all along their lengths in prophase I• While paired homologs cross over
2. Reduction division• Homologs separate in Anaphase I reducing the chromosome number
in 1/2 (2n to 1n)• This produces haploid gametes
Fig. 7.24
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7.13 Evolutionary Consequences of Sex
• Sexual reproduction increases genetic diversity through three key mechanisms
– 1. Crossing over
– 2. Independent assortment
– 3. Random fertilization
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• DNA exchanges between maternal and paternal chromatid pairs
Crossing over
• This adds even more recombination to independent assortment that occurs later
Fig. 7.20
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Fig. 7.26• In humans, a gamete receives one homolog of each of the 23 chromosomes
– Humans have 23 pairs of chromosomes• Independent assortment gives 223 combinations in an egg or sperm
– 8,388,608 possible kinds of gametes• Random fertilization of two independently-produced gametes
– Therefore, the possible combinations in an offspring– 8,388,608 X 8,388,608 = 70,368,744,177,664– More than 70 trillion!
• And this number does not count crossing-over
Independent assortment
Three chromosome pairs23 combinations
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Compare and contrastMitosis and Meiosis*
*guaranteed to be onquiz and exam
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MITOSIS MEIOSIS
PARENT CELL(before chromosome replication)
Site ofcrossing over
MEIOSIS I
PROPHASE ITetrad formedby synapsis of homologous chromosomes
PROPHASE
Duplicatedchromosome(two sister chromatids)
METAPHASE
Chromosomereplication
Chromosomereplication
2n = 4
ANAPHASETELOPHASE
Chromosomes align at the metaphase plate
Tetradsalign at themetaphase plate
METAPHASE I
ANAPHASE ITELOPHASE ISister chromatids
separate duringanaphase
Homologouschromosomesseparateduringanaphase I;sisterchromatids remain together
No further chromosomal replication; sister chromatids separate during anaphase II
2n 2n
Daughter cellsof mitosis
Daughter cells of meiosis II
MEIOSIS II
Daughtercells of
meiosis I
Haploidn = 2
n n n n
See Fig. 7.25