2.2- All cells arise from other cells Flashcards

1
Q

State what the cell cycle is and outline its stages

A

cycle of division with intermediate growth periods
1. interphase
2. mitosis or meiosis (nuclear division)
3. cytokinesis (cytoplasmic division)

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2
Q

Explain why cell cycle doesn’t occur in some cells

A

After differentiation, some types of cell in multicellular organisms (e.g. neurons) no longer have the ability to divide

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3
Q

What is the difference between cell cycle and mitosis?

A

Cell cycle includes growth period between division; mitosis is only 10% of the cycle & refers only to nuclear division

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4
Q

Outline what happens during interphase

A

G1: cell synthesises proteins for replication e.g. tubulin for spindle fibres & cell size doubles
S: DNA replicates= chromosomes consist of 2 sister chromatids joined at a centromere
G2: organelles divide

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5
Q

State purpose of mitosis

A

Produces 2 genetically identical daughter cells for:
- Growth
- Cell replacement/ tissue repair
- Asexual reproduction

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6
Q

Name stages of mitosis

A
  1. Prophase
  2. Metaphase
  3. Anaphase
  4. Telophase
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7
Q

Outline what happens during prophase

A
  1. Chromosomes condense, become visible. (X-shaped: 2 sister chromatids joined at centromere)
  2. Centrioles move to opposite poles of cell (animal cells) & mitotic spindle fibres form
  3. Nuclear envelope & nucleolus break down= chromosomes free in cytoplasm
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8
Q

Outline what happens during metaphase

A

Sister chromatids line up at cell equator, attached to the mitotic spindle by their centromeres

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9
Q

Outline what happens during anaphase

A

Requires energy from ATP hydrolysis
1. Spindle fibres contract = centromeres divide
2. Sister chromatids separate into 2 distinct chromosomes & are pulled to opposite poles of cell (looks like ‘V’ shapes facing each other)
3. Spindle fibres break down

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10
Q

Outline what happens during telophase

A
  1. Chromosomes decondense, becoming invisible again
  2. New nuclear envelopes form around each set of chromosomes= 2 new nuclei, each with 1 copy of each chromosome
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11
Q

Explain procedure for a root tip squash experiment

A
  1. Prepare a temporary mount of root tissue
  2. Focus an optical microscope on the slide. Count total number of cells in the field of view and number of cells in a stage of mitosis
  3. Calculate mitotic index (proportion of cells undergoing mitosis)
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12
Q

Explain how to prepare a temporary root tip mount

A
  1. Place root tip in hydrochloric acid to halt cell division & hydrolyse middle lamella
  2. Stain root tip with a dye that binds to chromosomes
  3. Macerate tissue in water using mounted needle
  4. Use mounted needle at 45 degrees to press down coverslip & obtain a single layer of cells. Avoid trapping air bubbles.
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13
Q

Name 2 dyes that bind to chromosomes

A
  • toluidine blue (blue)
  • acetic orcein (purple-red)
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14
Q

Why is only the root tip used when calculating a mitotic index?

A
  • Meristematic cells at root tip are actively undergoing mitosis
  • Cells further from root tip are elongating rather than dividing
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15
Q

What are tumour suppressor genes?

A

Genes that code for proteins to trigger apoptosis (programmed death of damaged cells)/ slow cell cycle (e.g. p53 acts between G1 & S in interphase so damaged DNA cannot replicate)

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16
Q

What are proto-oncogenes?

A

Genes that code for proteins to stimulate cell cycle to progress from one stage to the next

17
Q

How can mutation to tumour suppressor genes & proto-oncognes cause cancer?

A
  • Tumour suppressor: no production of a protein needed to slow the cell cycle
  • Proto-oncogenes: form permanently-activated oncogenes
  • Disruption to cell cycle -> uncontrolled cell division -> tumour
18
Q

Suggest how cancer treatments control the rate of cell division

A

Disrupt the cell cycle:
- prevent DNA replication
- disrupt spindle formation= inhibit metaphase/ anaphase

NB: can also damage healthy cells

19
Q

How do prokaryotic cells replicate?

A

Binary fission:
1. DNA loop replicates. Both copies stay attached to cell membrane. Plasmids replicate in cytoplasm
2. Cell elongates, separating the 2 DNA loops
3. Cell membrane contracts & septum forms
4. Cell splits into 2 identical progeny cells, each with 1 copy of the DNA loop but a variable number of plasmids

20
Q

Why are viruses classed as non-living?

A

They are acellular: no cytoplasm, no metabolism & cannot self-replicate

21
Q

Outline how viruses repliate

A
  1. Attachment proteins attach to receptors on host cell membrane
  2. Enveloped viruses fuse with cell membrane or move in via endocytosis & release DNA/RNA into cytoplasm OR viruses inject DNA/ RNA
  3. Host cell uses viral genetic information to synthesise new viral proteins/ nucleic acid
  4. Components of new viral particle assemble
22
Q

How do new viral particles leave the host cell?

A

a) Bud off & use cell membrane to form envelope
b) Cause lysis of host cell

23
Q

Why is it so difficult to develop effective treatments against viruses?

A

Replicate inside living cells= difficult to kill them without killing host cells