All cells arise from other cells Flashcards

Cells revisions

1
Q

State what 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 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

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 consists of 2 sister chromatids joined at a centromere

G2: organelles divide

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4
Q

What happens during prophase (1st phase)

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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5
Q

What happens during metaphase (2nd phase)

A

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

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6
Q

What happens during anaphase

A

required 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
  3. Spindle fibres break down
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7
Q

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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8
Q

Explain procedure for root tip squash experiment

A
  1. Prepare a temporary mount of root tissue
  2. Focus an optical microscope on the slide. Count total no. of cells in field of view & no. of cells in a stage of mitosis
  3. Calculate mitotic index (proportion of cells undergoing mitosis)
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9
Q

Explain how to prepare 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 single layer of cells. Avoid tapping air bubbles.
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10
Q

What are tumour suppressor genes?

A

Genes that code for proteins to trigger apoptosis (progammed death of damaged cells)/ slow cell cycle

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11
Q

What are proto-oncogenes?

A

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

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12
Q

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

A
  • Tumour suppressor: no production of a protein needed to slow cell cycle
  • Proto-oncogenes: form permanently - activated oncogenes
  • Disruption to cell cycle -> uncontrolled cell division -> tumour
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13
Q

Suggest how cancer treatments control rate of cell division

A

Disrupt cell cycle

  • prevent DNA replication
  • disrupt spindle formation = inhibit metaphase/ anaphase

(can also damage healthy cells)

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14
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 2 DNA loops
  3. Cell membrane contracts & septum forms
  4. Cell splits into 2 identical progeny cells, each with 1 copy of DNA loop but a variable number of plasmids
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15
Q

Why are viruses classified as non-living?

A

Are acellular: no cytoplasm, no metabolism & cannot self-replicate

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16
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 info to synthesise new viral proteins/ nucleic acid
  4. Components of new viral particle assemble
17
Q

How do new viral particles leave host cell?

A

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

18
Q

Why is it difficult to develop effective treatments against viruses?

A

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