Mitosis Flashcards

(39 cards)

1
Q

What type of cells are produced by mitosis?

A

Genetically identical daughter cells.

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2
Q

State three biological roles of mitosis in organisms.

A

• Growth of multicellular organisms.
• Repair of damaged tissues.
• Asexual reproduction in some organisms.

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3
Q

What is the cell cycle?

A

The cell cycle is the series of stages that cells go through to grow and divide.

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4
Q

Name the longest phase of the cell cycle and what it involves.

A

The longest phase of the cell cycle is Interphase – Longest phase, involves cell growth & DNA replication.

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5
Q

Describe the events that occur during each stage of interphase.

A

• G₁ (Gap phase 1): Cell grows, makes proteins & organelles.
• S (Synthesis): DNA replication → chromosomes become 2 sister chromatids.
• G₂ (Gap phase 2): Cell grows more, produces proteins for division.

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6
Q

List three key processes that occur during interphase.

A

• DNA unravels & replicates.
• Organelles replicate.
• ATP content increases.

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7
Q

When does mitosis occur in the cell cycle?

A

Mitosis occurs after interphase.

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8
Q

What is the result of mitosis?

A

Results in two genetically identical daughter cells.

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9
Q

Describe the key events in prophase.

A

• Chromosomes condense (shorter, fatter).
• Centrioles move to poles and form spindle fibres.
• Nuclear envelope breaks down.
• Chromosomes lie free in cytoplasm.

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10
Q

What happens during metaphase?

A

• Chromosomes (each with 2 chromatids) align at cell equator.
• Attach to spindle fibres by centromeres.

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11
Q

Explain what happens during anaphase.

A

• Centromeres divide, separating sister chromatids.
• Spindle fibres pull chromatids to opposite poles (centromere first).
• Chromatids look V-shaped.

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12
Q

Describe the events that occur in telophase.

A

• Chromatids uncoil and form chromosomes again.
• New nuclear envelopes reforms around each group of chromosomes .
• Cytoplasm divides (cytokinesis) and 2 identical daughter cells are produced

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13
Q

What information is needed to calculate how long a stage of mitosis lasts?

A

• Number of cells in a stage
• Total cells observed
• Duration of the cell cycle

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14
Q

Write the formula used to calculate the time spent in one stage of mitosis.

A

Time in stage = (cells in stage / total cells) × duration of cell cycle

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15
Q

What regulates mitosis?

A

Mitosis is regulated by genes.

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16
Q

How can cancer form as a result of problems in the cell cycle?

A

Cancer can form due to
•Mutation in these genes resulting to uncontrolled division causing tumours.
•If tumour invades surrounding tissue its is cancer.

17
Q

How do cancer treatments target the cell cycle?

A

Treatments disrupt the cycle that rapidly divides cells (e.g. tumour cells).

18
Q

How do G₁ phase inhibitors work?

A

G₁ phase inhibitors Prevent enzyme synthesis needed for DNA replication therefore cell cannot enter S phase and dies

19
Q

How do S phase inhibitors work?

A

S phase inhibitors Damage DNA which triggers cell death if damage is detected at checkpoints.

20
Q

Why might normal cells also be affected by these treatments?

A

Normal dividing cells can be affected too.

21
Q

Why is the tip of the root used in the mitosis practical?

A

Because the tip of the root is where growth occurs (and so that’s where mitosis takes place).

22
Q

List the full method used to prepare a root tip for viewing mitosis.

A
  1. Cut 1 cm of root tip (onion).
    1. Fix in ethanoic acid (if staining with ethano-orcein).
    2. Place in 1 M HCl at 60°C for 5 mins.
    3. Rinse in cold water & dry.
    4. Cut 2 mm of tip; discard the rest.
    5. Use needle to break open and spread cells.
    6. Add stain (e.g. toluidine blue, orcein, Feulgen).
    7. Add cover slip and squash straight down (don’t smear).
    8. Observe under optical microscope.
23
Q

Describe how to observe prepared cells under a microscope.

A
  1. Clip slide to microscope stage.
    1. Use low-power objective lens.
    2. Use coarse adjustment to bring stage close.
    3. Look through eyepiece, lower stage slowly to focus.
    4. Use fine adjustment to sharpen image.
    5. Switch to high-power lens if needed, refocus.
    6. Label any drawings, state magnification.
24
Q

What is the mitotic index used for?

A

Mitotic index is used to assess the rate of cell growth or detect abnormal tissue (e.g. cancer).

25
Write the formula used to calculate mitotic index.
Mitotic Index = Number of cells in mitosis / Total number of cells observed
26
What does a high mitotic index indicate?
• A high mitotic index is normal in root tips, where active growth occurs. • In other tissues, an abnormally high mitotic index may indicate rapid cell division due to tissue repair or could be a sign of cancerous growth.
27
What safety precautions should be taken during the mitosis root tip practical?
• Wear gloves, goggles, and lab coat. • Handle acid and stains carefully.
28
What is an eyepiece graticule, and what is it used for?
An eyepiece graticule is a transparent ruler fitted into the eyepiece. It has divisions (no units). It is used to measure cells once calibrated.
29
What is a stage micrometer and what is its purpose?
A stage micrometer is a slide with a precise scale and units. It is used to calibrate the eyepiece graticule. Each division typically = 0.1 mm (or 100 μm).
30
Describe the process used to calibrate an eyepiece graticule using a stage micrometer.
Line up graticule and micrometer under the microscope. Suppose 4.5 eyepiece divisions = 1 micrometer division. Each micrometer division = 0.1 mm.
31
Calculate the size of one eyepiece graticule division if 4.5 graticule divisions equal 0.1 mm.
1 eyepiece division = 0.1 mm ÷ 4.5 = 0.022 mm
32
A cell measures 4 eyepiece divisions in length at a calibrated magnification. What is its actual size?
Actual length = 4 × 0.022 = 0.088 mm
33
What must you do to the eyepiece graticule when changing magnification?
Recalibrate the eyepiece graticule at each magnification.
34
State the formula used to calculate actual cell size from a microscope image.
Actual size= size of image/ magnification
35
What are artefacts in microscopy?
Artefacts are objects seen under the microscope that aren’t part of the specimen.
36
Give four examples of common artefacts.
• Dust • Air bubbles • Fingerprints • Squashing or staining errors
37
When are artefacts typically formed?
Artefacts are formed during slide preparation.
38
In which type of microscopy are artefacts especially common, and why?
Artefacts are especially common in electron microscopy due to complex preparations of the slide
39
How can scientists distinguish between artefacts and real organelles?
• Use multiple preparation techniques. • If an object is only visible in one preparation, it is likely an artefact. • If visible across multiple methods, it’s likely a real organelle.