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 the cell cycle does not occur in some cells.

A

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

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3
Q

What is the difference between the cell cycle and mitosis?

A

The cell cycle includes the growth period between divisions; 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 the 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 the stages of mitosis.

A

Prophase
Metaphase
Anaphase
Telophase

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7
Q

Outline what happens during prophase.

A
  1. Chromosomes condense, becoming visible. (X-shaped: 2 sister chromatids joined at centromere).
  2. Centrioles move to opposite poles of a 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 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 the 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 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 the cell cycle.

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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 and proto-oncogenes cause cancer?

A
  • Tumour suppressor: no production of a protein needed to slow the cell cycle.
  • Proto-oncogenes: forms 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

Assume the exponential growth of bacteria within 8 hours. Assume binary fission occurs once every 20 minutes and there is 1 bacterium at the start.

A

8 x 60 = 480 mins
480 / 20 = 24 divisions
2(^24)

21
Q

Why are viruses classified as non-living?

A

They are acellular: no cytoplasm, no metabolism, cannot self replicate.

22
Q

Outline how viruses replicate.

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.
23
Q

How do new viral particles leave the host cell?

A

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

24
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.