2.2 All cells arise from other cells Flashcards

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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 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 the cell

cycle and mitosis?

A

Cell cycle includes 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
  1. Prophase
  2. Metaphase
  3. Anaphase
  4. 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 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 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

Outline how to prepare a temporary

mount of root tissue.

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° 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 &

proto-oncogenes?

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-oncogenes 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

Estimate the exponential growth of
bacteria within 8 hours. Assume binary
fission occurs once every 20 minutes &
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 & 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.