The cell cycle Flashcards

1
Q

Define ‘the cell cycle’

A

The fundamental mechanism of all living organisms to reproduce themselves and to pass down their genetic material to the next generation.

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2
Q

Describe the cell cycle

A

o Duplication of cell contents -> DNA, organelles, cytoplasm
o Division into new progeny cells.
• Unicellular organisms such as bacteria or yeast: - each cell cycle gives rise to 2 new organisms.
• Multicellular organisms, such as humans:
o Single fertilised egg (zygote) must undergo many rounds of the cell cycle to make a new fully-grown organism.
o Must also constantly replace any cells that die during the lifetime of the organism.

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3
Q

Describe the phases in the cell cycle

A

• G1 = Gap 1 phase: growth and preparation for S phase.
• S = Synthesis phase: chromosome duplication, DNA synthesis.
• G2 = Gap 2 phase: growth and preparation for M phase.
• Interphase = G1 + S + G2
• M = Mitotic phase: mitosis + cytokinesis (cell division).
• Between S and M two phases G1 and G2 cells prepare for next stage, G0 non-dividing stage.
• Many cells in our body are in G0 and not all can re-enter the cell cycle
o Cell cycle re-entry not possible (e.g. nerve cells)
o Maintained in Go unless stimulated to divide (e.g. hepatocytes-liver cells).
o Constantly in the cell cycle (e.g. epithelial cells of the gut, haematopoietic cells [blood forming cells- stem cells that continue to replicate as fresh blood is needed continuously] in the bone marrow).

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4
Q

Describe mitosis

A
  • Prophase - Chromosomes condense, centrosomes move to opposite poles, mitotic spindle forms.
  • Prometaphase - Breakdown of nuclear envelope, chromosomes attach to mitotic spindle.
  • Metaphase - Centrosome are at opposite poles, chromosomes are at their most condensed and line up at the equator of the mitotic spindle.
  • Anaphase - Sister chromatids separate synchronously, each new daughter chromosome moving to the opposite spindle pole.
  • Telophase - Chromosome arrives at the spindle poles, chromosomes decondense, nuclear envelope reforms.
  • Cytokinesis: cytoplasmic division - At the position of the metaphase plane. Contractile ring of actin and myosin II constrict the cell into two daughter cells.
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5
Q

Describe the mitotic spindle

A

“Bipolar” array of microtubules – they have a plus (growing) end and a minus end (shrinking).
• Start to assemble during prophase from the centrosomes at each pole.
• Attach to the chromosomes via the kinetochore (a large protein structure assembled on the centromere).
• Pull apart the sister chromatids.
• 3 types of spindle microtubules:
• Astral microtubules
• Kinetochore microtubules
• Interpolar microtubules

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6
Q

Define Kinetochore, Centromere and Chromatids

A
  • Kinetochore: a protein structure formed on a chromatid, where the spindle fibers attach to pull the chromatids apart during cell division.
  • Centromere: a part of the chromosome connected to the spindle fibre.
  • Chromatids: the two chromosomes that have been replicated and linked through the centromere.
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7
Q

Describe the centrosome cycle

A
  • Microtubule-organising centre in somatic animal cells.
  • Centrosome consists of a pair of centrioles surrounded by pericentriolar matrix (a cloud of amorphous material (doesn’t have a fixed form).
  • Duplicated during interphase.
  • Migrate to opposite poles in preparation for M phase.
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8
Q

Describe cytokinesis

A

Cytokinesis
• Final step in the cell cycle.
• Divides the cytoplasm into two daughter cells.
• Contractile ring
• Cytoskeletal structure composed of actin and myosin bundles.
• Accumulates between the poles of the mitotic spindle beneath the plasma membrane.
• Ring contracts and forms an indentation or cleavage furrow, dividing the cell in two.

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9
Q

Describe cell organelle division

A
  • All cell organelles must be redistributed between the 2 new daughter cells.
  • Cell organelles cannot spontaneously regenerate so must be already present in the new daughter cells.
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10
Q

Compare and contrast Meiosis and Mitosis

A

As shown on table

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11
Q

Describe Meiosis

A

• Meiosis is a specialised cell division that starts with one diploid cells and ends with 4 haploid cells.
• Purpose is to produce gametes: sperm and egg (sex cells).
• One round of DNA replication during S phase and two rounds of cell division.
o Meiosis I: homologous chromosomes line up on the spindle and separate to opposite spindle poles.
o Meiosis II: sister chromatids line up on the spindle and separate to opposite spindle pole.
• Recombination occurs between homologous chromosomes.
• Nondisjunction- failure of homologous chromosomes to separate from one another, either at meiotic division I or meiotic division II.
• Autosomes- usually fatal, exceptions are:
o Trisomy 21 (Down’s Syndrome)
o Trisomy 18 (Edward’s syndrome)
o Trisomy 13 (Patau Syndrome)
• No viable autosomal monosomies – cells with 1 autosome bottom right pic will not survive.
• Sex chromosomes:
o XO (Turner’s syndrome)
o XXX (Triple X syndrome)
o XXY (Klinefelter’s syndrome)

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12
Q

Describe the regulation of the cell cycle

A
  • Entry into the cell cycle must be strictly controlled.
  • Each phase must occur only once per cell cycle.
  • Phases must be in the correct order: G1-S-G2-M
  • Phases must be nonoverlapping.
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13
Q

Describe the checkpoints in the cell cycle

A

On image

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14
Q

Describe cell cycle regulators

A

These include CDK and cyclins

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15
Q

Describe cell cycle control in yeast

A

On image

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16
Q

Describe cell cycle control in humans

A

A,B,D,E cyclins

17
Q

Describe the basic principles of cell cycle control

A
  • Cdk levels fairly stable throughout the cell cycle.
  • Cyclin levels vary as part of the cell cycle.
  • Cdk bound to cyclin is active and can phosphorylate “target protein”.
  • Cdk activation triggers the next step in the cell cycle such as entry into S phase or M phase.
  • Cyclin degradation terminates Cdk activity.
18
Q

Describe DNA damage repair

A
  • Normally p53 degraded quickly, unstable and maintained at very low levels.
  • Phosphorylated (active) p53 is not degraded.
  • Active p53 promotes transcription of genes that induce cell cycle arrest, it binds to promoter region of p21 gene and stimulates p21 expression.
  • p21 binds and inhibits G1/S-Cdk complexes.
  • Cell arrests in G1 (allowing time to repair the damaged DNA).
  • If DNA repair is not possible→ cells undergo apoptosis
19
Q

Describe CDK inhibitors

A
  • Two families of CKIs
  • Inhibitor of Kinase 4 family (INK4): specifically inhibit G1 CDKs (e.g. CDK4)
  • CDK Inhibitory Protein/Kinase Inhibitory Protein (CIP/KIP) family: inhibit all other CDK-cyclin complexes (late G1, G2 & M) gradually sequestered by G1 CDKs thus allowing activation of later CDKs
20
Q

Describe the cell cycle and cancer

A
  • Neoplasia - The presence or formation of new, abnormal growth of tissue.
  • Mis-regulation of cell cycle causes cancer.
  • Cells escape normal cell cycle checkpoint -> uncontrolled progression through the cell cycle.
  • Many genes that regulate cell cycle (e.g. p53 and pRB) are often mutated in human cancers.