Cell Division in Eukaryotic + Prokaryotic Cells Flashcards

1
Q

Describe cell division in multicellular organisms.

A
  • not all cells retain ability to divide
  • eukaryotic cells that do retain ability to divide show a cell cycle
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2
Q

What are the 3 stages of the eukaryotic cell cycle?

A
  • interphase (G1, S, G2)
  • nuclear division (mitosis or meiosis)
  • cell division (cytokinesis)
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3
Q

What is the movement from 1 stage of the cell cycle to another triggered by?

A
  • chemical signals called cyclins thus making mitosis a controlled process
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4
Q

What are the 3 phases (stages) of interphase?

A
  • G1 (growth 1) phase
  • S (DNA synthesis) phase
  • G2 (growth 2) phase
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5
Q

Describe interphase in the cell cycle.

A
  • during G1 phase, cell makes RNA, enzymes + other proteins needed for growth
  • during S phase, DNA in nucleus replicates
  • during G2 phase, cell continues to grow + new synthesised DNA is checked + any errors repaired
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6
Q

Describe what occurs during nuclear division.

A
  • either a eukaryotic cell divides by mitosis to form 2 identical, diploid daughter cells w identical DNA for growth + repair, during DNA replication
  • or cell divides by meiosis to form 4 genetically diff. haploid cells (gametes)
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7
Q

Why is mitosis important?

A
  • forms 2 genetically identical daughter cells enabling unicellular zygotes to grow into multicellular organisms
  • allows damaged cells to be replaced by genetically identical cells so repairs tissues
  • allows organisms to reproduce asexually + produce genetically identical offspring
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8
Q

What are the 4 key stages of mitosis?

A
  • prophase
  • metaphase
  • anaphase
  • telophase
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9
Q

Describe prophase.

A
  • chromosomes condense + become visible
  • in animal cells, centrioles separate + move to opposite poles of cell + are responsible for creating spindle fibres, released from both poles
  • the nuclear envelope also starts to disintegrate
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10
Q

Describe metaphase.

A
  • chromosomes line up along equator of cell + spindle fibres, released from centrioles at each pole, attach to centromere + chromatid
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11
Q

Describe anaphase.

A
  • spindle fibres start to retract + pull centromere + chromatids towards opposite poles causing centromere to divide in 2 + pull individual chromatids to opposite poles
  • this requires energy from ATP provided by respiration in mitochondria
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12
Q

Describe telophase.

A
  • chromosomes at opposite poles of cell start to decondense, becoming longer + thinner
  • spindle fibres disintegrate + nuclear envelope starts to reform around each set of chromosomes
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13
Q

Describe cell division (cytokinesis).

A
  • cytoplasm splits in 2, forming 2 new genetically identical cells in final stage of cell cycle
  • in animal cells a cleavage furrow forms, separating daughter cells
  • however in plants, a cell plate forms which expands towards cell wall + fuses w it, separating daughter cells
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14
Q

Describe a method for identifying mitotic stages.

A
  • remove tips of garlic roots + place in ethanoic alcohol to prevent mitosis from continuing
  • place root tips in warm dilute HCl to soften + loosen root tissue
  • transfer root tip to a microscope slide + add a stain (so chromosomes r visible) using a pipette
  • place a coverslip on top of root tip + press down to spread out cells so is 1 cell thick meaning light can pass through
  • view cells under a microscope
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15
Q

What is the equation for mitotic index?

A
  • mitotic index = (NO° of cells in mitosis / total NO° of cells) x100
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16
Q

How do you calculate the actual size of root tip cells?

A
  • actual size = size of image / magnification
  • nm (x1000) = μm (x1000) = mm (x1000) = m
17
Q

Explain how tumours + cancer are formed.

A
  • an oncogene (mutation in genes that control cell division + cause cancer), causes cell to divide repeatedly + uncontrollably to form a tumour
  • benign tumours don’t spread or cause cancer
  • malignant tumours spread through body, invading + destroying tissues, + cause cancer
  • if cells break off malignant tumour + travel through blood/lymphatic system they can form secondary cancers (metastasis)
18
Q

What are carcinogens?

A
  • agents that may cause cancer (e.g. UV light, tar in tobacco, smoke + X-rays)
19
Q

How do most cancer treatments/drugs work?

A
  • by controlling rate of cell division (mitosis)
20
Q

Describe binary fission (cell division) of prokaryotic cells.

A
  • circular DNA molecule + any plasmids present undergo DNA replication + move to opposite poles of cell
  • the cytoplasm divides to produce 2 daughter cells each containing a single copy of circular DNA + a variable NO° of plasmids
21
Q

Why don’t viruses undergo cell division?

A
  • bc they’re non-living
22
Q

What is the structure of a virus?

A
  • a nucleic acid core (DNA or RNA)
  • a capsid (protein coat)
  • some have an envelope formed from phospholipids of membrane from cell they were made in
23
Q

Describe viral particle replication.

A
  • attachment proteins on surface of virus binds to complementary receptor proteins on surface of host cell
  • virus injects its nucleic acid (DNA or RNA) into host cell which uses its nucleic acid + ribosomes to produce new viral particles
  • eventually, either host cell bursts open, releasing new viral particles or viral particles leave individually through host cell membrane
  • this damages host cell, causing disease