Unit 5

103
1 Unit 5 Cell Communication and Division

description

Unit 5. Cell Communication and Division.  factor. Receptor. a. . Exchange of mating factors. 1. Fig. 11-2. a factor. Yeast cell, mating type a. Yeast cell, mating type . a. . Mating. 2. a/. New a/  cell. 3. Cell Communication. Types of communication - PowerPoint PPT Presentation

Transcript of Unit 5

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Unit 5

Cell Communication and Division

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Fig. 11-2

Receptor factor

a factor

a

a

Exchangeof matingfactors

Yeast cell,mating type a

Yeast cell,mating type

Mating

New a/cell

a/

1

2

3

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Cell Communication

• Types of communication

- Local signaling

- Hormonal signaling

- Direct contact b/w cells

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Types of Local Signaling

• Paracrine signaling – transmitting cell secretes molecules to influence neighbors

- ie. Growth factors

• Synaptic signaling – one cell produces a neurotransmitter (chemical signal) that crosses the synapses (space b/w nerve cells)

• Fig 11.3

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Hormonal Signaling (long distance)

• Cells release chemical into blood

• Chemical travels to target cell

• Target cell not in neighborhood

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Direct Contact Between Cells

• Animal Cells

gap junctions

cell surface mol’s

• Plant Cells

plasmodesmata

• Fig. 11.4

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Stages of Signaling

• Fig. 11.6

• Reception -- detects first message

• Transduction – relays message

signal transduction pathway

• Response

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Reception

• Signal molecules bind to receptor proteins that recognize the specific signal.

• Ligand – term for a small molecule that specifically binds to a larger one.

• Ligand binding causes a receptor protein to undergo a shape change.

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Reception

• 3 types of reception

1. G protein linked -- fig. 11.7

– receptor on membrane - switch

- signal mol’s turn it on or off

– on causes change in shape which triggers G protein change which causes enzyme to be activated

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Reception cont’d

• 2. Tyrosine – Kinase receptors fig. 11.8

- located on memb.

- catalyse the transfer of P from ATP to

tyrosine

- this causes polypeptide to aggregate and phosphorylation of receptor which causes activation of relay proteins

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• 3. Ion – Channel receptors

gated channels that are protein pores in memb.

• Ligand-gated ion channel

• Act as gates

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Tyrosine - Kinase

• Tyrosine – Kinase advantage: a single ligand-binding event can trigger many pathways

• Abnormal tyrosine - kinase receptors that aggregate without ligand causes some cancers

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Vocabulary

• Protein kinase

- Enzyme that transfers phosphate groups from ATP to a protein

• Protein phosphatase

- Enzyme that can rapidly remove phosphate groups from proteins (dephosphorylation)

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Transduction

• Relays message

• Usually proteins

• Protein phosphorylation and second messengers

i.e.. Cyclic AMP in mitosis fig. 11.10

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Response

• Respond to messages

• Regulation of activities

• Regulation of synthesis

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Apoptosis

• Program of controlled cell suicide• 2 genes control cell death (Ced-3 and ced-4)• They produce proteins Ced-3 and Ced-4 which are

continually present but inactive.• The death signal molecule triggers proteases

(capsases) that cut up proteins and DNA • C. elegans (a nematode) is the organism of

research for this.

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Fig. 11-19

2 µm

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Fig. 11-20

Ced-9protein (active)inhibits Ced-4activity

Mitochondrion

Receptorfor death-signalingmolecule

Ced-4 Ced-3

Inactive proteins

(a) No death signal

Ced-9(inactive)

Cellformsblebs

Death-signalingmolecule

Otherproteases

ActiveCed-4

ActiveCed-3

NucleasesActivationcascade

(b) Death signal

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Fig. 11-20a

Ced-9protein (active)inhibits Ced-4activity

Mitochondrion

Ced-4 Ced-3Receptorfor death-signalingmolecule

Inactive proteins

(a) No death signal

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Fig. 11-20b

(b) Death signal

Death-signalingmolecule

Ced-9(inactive)

Cellformsblebs

ActiveCed-4

ActiveCed-3

Activationcascade

Otherproteases

Nucleases

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Fig. 11-21

Interdigital tissue 1 mm

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Cell Division

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Why Cell Division

1. Reproduction

2. Growth & development

3. Tissue renewal

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3 Types of Cell Division

1. Binary fission

2. Mitosis

3. Meiosis

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1. Binary Fission

• Prokaryotes do this - have one circular chromosome

- Hypothesis on significance of membrane

- Divides into 2 new cells

- Simplest form of cell division

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Fig. 12-11-1

Origin ofreplication

Two copiesof origin

E. coli cellBacterialchromosome

Plasmamembrane

Cell wall

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Fig. 12-11-2

Origin ofreplication

Two copiesof origin

E. coli cellBacterialchromosome

Plasmamembrane

Cell wall

Origin Origin

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Fig. 12-11-3

Origin ofreplication

Two copiesof origin

E. coli cellBacterialchromosome

Plasmamembrane

Cell wall

Origin Origin

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Fig. 12-11-4

Origin ofreplication

Two copiesof origin

E. coli cellBacterialchromosome

Plasmamembrane

Cell wall

Origin Origin

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2. Mitosis

• Eukaryotes do this - have many linear chromosomes

• Cell divides after duplication and organization of DNA

• See fig. 12.12 for intermediary types of cell division

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Fig. 12-12

(a) Bacteria

Bacterialchromosome

Chromosomes

Microtubules

Intact nuclearenvelope

(b) Dinoflagellates

Kinetochoremicrotubule

Intact nuclearenvelope

(c) Diatoms and yeasts

Kinetochoremicrotubule

Fragments ofnuclear envelope

d. Most eukaryotes

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3. Meiosis

• Division of cells to form gametes (egg & sperm cells)

• Results in cells having ½ the original # of chromosomes

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Eukaryotic Cells

• Life Cycle of Eukaryotic Cell pg. 217

- Interphase

- Mitosis

- Cytokinesis

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Fig. 12-5

S(DNA synthesis)

MITOTIC(M) PHASE

Mito

sis

Cytokinesis

G1

G2

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Interphase

• G1 - cell growth & development - organelles begin to double• S - synthesis DNA replicates• G2 - growth continues - organelles complete duplication

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Phases of Mitosis

• Prophase

• Prometaphase

• Metaphase

• Anaphase

• Telophase & cytokinesis

• Pg. 232-233

• See fig. 12.6

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Plant Vs. Animal Mitosis

Plant• Forms cell plate• No centrioles • Spindle fibers from

cytoskeleton

Animal• Cleavage of cell

membrane• Centrioles w/ aster

rays form spindle

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Fig. 12-6d

Metaphase Anaphase Telophase and Cytokinesis

Nucleolusforming

Metaphaseplate

Centrosome atone spindle pole

SpindleDaughterchromosomes

Nuclearenvelopeforming

A CB

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Regulation of the Cell Cycle

• Molecular control system

• Internal & external signals

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Molecular Control

• Checkpoints at G1, G2, & M

• G1 checkpoint most important

- Decision

Go or don’t go

Continues Enters G0 phase

cell cycle

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Molecular control continued

• The cell cycle clock

- See fig. 12.17

- Levels of cyclin, cdks & MPF control the onset of mitosis

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Fig. 12-16

Pro

tein

kin

as

e a

cti

vit

y (

– )

% o

f d

ivid

ing

ce

lls (

– )

Time (min)300200 400100

0

1

2

3

4

5 30

500

0

20

10

RESULTS

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Fig. 12-17

M G1S G2

M G1S G2

M G1

MPF activity

Cyclinconcentration

Time(a) Fluctuation of MPF activity and cyclin concentration during the cell cycle

Degradedcyclin

Cdk

G 1S

G 2

M

CdkG2

checkpointCyclin isdegraded

CyclinMPF

(b) Molecular mechanisms that help regulate the cell cycle

Cy

clin

ac

cu

mu

latio

n

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Fig. 12-17a

Time(a) Fluctuation of MPF activity and cyclin concentration during the cell cycle

Cyclinconcentration

MPF activity

M M MSSG1 G1 G1G2 G2

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Fig. 12-17b

Cyclin isdegraded

Cdk

MPF

Cdk

MS

G 1G2

checkpoint

Degradedcyclin

Cyclin

(b) Molecular mechanisms that help regulate the cell cycle

G2

Cyclin

accum

ulatio

n

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External Signals

1. Density dependent inhibition

Crowding inhibits division

Insufficient growth regulators

fig. 12.18

2. Requirement for adhesion

Cells stop dividing if they lose their anchorage

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Internal Signals

• Separation of sister chromatids does not occur until all chromosomes are properly attached to the spindle fibers.

• APC -- anaphase promoting complex will be activated

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Apoptosis

• Programmed cell death

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Cancer

Abnormal cell division

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Characteristics of a cancer cell

1. Do not respond to controls thus form a tumor.

- Tumor can be:

benign – not invading other tissue

malignant – spreading into surrounding tissue

fig. 12.17

2. Division can stop at any stage or divide indefinitely

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Characteristics continued

3. May have unusual # of chromosomes

4. Deranged metabolism

5. Surface can’t attach to “normal neighbors”

6. Cells are loose & free so can spread quickly (metastasize)

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What triggers a cell to become cancerous?

1. Genetic alterations due to carcinogens i.e. Asbestos, nicotine

2. Oncogenes -- genes that stimulate cancer cell

-- switch is in “off” position but can switch “on”

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Meiosis

Division of cells to form haploid gametes

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Terms

• Gamete – egg or sperm• Somatic cell – all cells of the body except gametes• Zygote – fertilized egg• Diploid – 2 sets of chromosomes (2N)• Haploid – one set of chromosomes (N)• Homologous chromosomes – chromosomes that

make a pair. One from each parent. See diagram

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Terms continued

• Tetrad – complex of 4 chromatids. Present during prophase I of meiosis

• Crossing over – exchange of piece of chromosomes. Occurs while tetrad is present.

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a tetrad of the grasshopper Chorthippus parallelus shows 5 chiasmata courtesy of Prof. Bernard John

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Meiosis

• Pgs. 240 – 241

• Spermatogenesis – produces four haploid sperm

• Oogenesis – produces 1 egg an 3 polar bodies

• MEIOSIS

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Differences & Similarities

• Name 3 differences b/w mitosis & meiosis

• Name 3 similarities b/w mitosis & meiosis

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The life cycle of Sordaria fimicola is shown in Figure 1.

                                      

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• http://dragonnet.hkis.edu.hk/hs/science/Biology/apbio/images/Sordaria%20Tetrad%20Pics/3sordaria.jpg

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Nondisjunction

• Chromosomes fail to separate• Aneuploidy – gamete with abnormal # of chromosomes• If this gamete is fertilized it results in Monosomy or

Trisomy• Monosomy – missing a chromosome• Trisomy – extra chromosome

- Down Syndrome- Turners- Klienfelters

• Karyotype will show this

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2. Fix cells

1. Allow cells to grow

2. Add distilled H2O – cells swell

3. Add chemical to stop cell functions w/o exploding cell

4. Add dye to stain chrom.

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3. Karyotype chromosomes

• Cut out and arrange chromosomes by size

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The life cycle of Sordaria fimicola is shown in Figure 1.