YEAST CELL CYCLE + START + G0 + MATING/SPORULATION

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Last updated 2:42 PM on 1/10/26
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64 Terms

1
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Which CDK drives the entire S. cerevisiae cell cycle?

Cdc28

2
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How does one CDK control different stages in yeast?

By binding different cyclins at different times

3
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Which cyclins function at START?

Cln1

4
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Which cyclins drive DNA replication?

Clb5 and Clb6

5
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Which cyclins drive G2/M and mitosis?

Clb1

6
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What is START?

A decision point in late G1 where cells commit to division

7
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Where does START occur?

In yeast G1 phase

8
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Is START a single moment or a window?

A series of diminishing choices rather than a single point

9
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What major event is decided at START?

Whether the cell has sufficient nutrients and signals to divide

10
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What happens if conditions are unfavourable at START?

Cell enters G0 instead of progressing

11
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What is G0 in yeast?

A quiescent state where cells are metabolically quiet and do not divide

12
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Why do yeast enter G0?

Nutrient limitation or environmental stress

13
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What happens to haploid yeast in G0?

They arrest and can mate with cells of opposite mating type

14
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What happens to diploid yeast in G0?

They may undergo meiosis and form spores

15
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Why does yeast mating occur?

To combine genetic material when growth conditions are poor

16
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What do diploids produce during meiosis?

Spores

17
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What is required for mating to occur?

Haploid cells of opposite mating type and pheromone signalling

18
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What decides whether diploid cells sporulate?

Starvation

19
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What role does Cdc28 play in G0 entry?

Temperature-sensitive cdc28(ts) mutants allow G0 entry even though G1 cannot proceed

20
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What happens in cdc7(ts) mutants?

Cells cannot enter G0 and cannot mate/sporulate appropriately

21
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Why does cdc7(ts) block G0 entry?

cdc7 functions downstream of START

22
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How does the cdc7(ts) mutant behave in haploids?

Cells lack mating factors and cannot enter G0

23
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How does the cdc28(ts) mutant behave in diploids?

Meiosis and sporulation can still occur despite G1 arrest

24
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What happens in cdc7(ts) diploids?

Cells cannot enter G0 but meiosis can occur

25
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What do these mutant behaviours demonstrate?

START is upstream of the decision to arrest or differentiate

26
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What is the major checkpoint equivalent to START in mammals?

The Restriction Point (R point)

27
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What is the key environmental cue for START?

Nutrient availability

28
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How do cells detect nutrient conditions?

Through signalling pathways that regulate G1 cyclin transcription

29
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Why do multiple cyclins exist at START?

They allow graded activation of Cdc28 activity

30
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Which cyclins appear first at START?

Cln3 followed by Cln1/Cln2

31
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What does Cln3 do?

Initiates the first activation of Cdc28 to trigger START gene expression

32
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Which cyclins amplify Cdc28 activity?

Cln1 and Cln2

33
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What transcriptional programme is triggered at START?

Genes required for budding

34
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Why is START irreversible?

It triggers CDK activity that commits cells to replication

35
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Can a cell reverse START?

No — once past START

36
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What happens to cells lacking Cln1

2

37
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Which phase do cells arrest if START is not passed?

G1 phase

38
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Why must budding occur before S phase?

Morphogenesis and cell wall expansion need to precede DNA replication

39
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Which cyclins support budding?

G1 cyclins Cln1/2

40
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Which cyclins support spindle formation?

Clb1–4

41
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How does START relate to DNA replication licensing?

Cdc28–Clb cyclins promote replication origin firing

42
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How do yeast prevent relicensing?

High CDK activity prevents new origin loading until mitotic exit

43
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Why is Cdc28 essential?

Without it

44
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What is the impact of nutrient starvation on cell cycle?

Cells downregulate CDK activity

45
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Is yeast G0 permanent?

No — cells can re-enter the cycle when nutrients return

46
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Why can haploid cells mate while diploids cannot?

Diploids express both mating alleles and cannot respond to pheromone in the same way

47
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What determines fate after G0?

Ploidy and environmental triggers (mating vs sporulation)

48
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What is sporulation?

Meiosis producing four spores enclosed in an ascus

49
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Why is sporulation beneficial?

Increases survival during adverse conditions

50
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What causes spores to germinate?

Return of nutrients

51
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What cellular structures change during G0?

Ribosome production declines and metabolism slows

52
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Why is G0 important in nature?

Helps yeast survive feast–famine environments

53
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What happens to cdc28(ts) if restrictive temperature is removed?

Cell cycle resumes — mutant is reversible

54
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Why are temperature-sensitive mutants useful?

They allow synchronised arrest at a chosen stage

55
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Why is synchronisation important experimentally?

Permits study of fluctuations in CDK and cyclin levels

56
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What does the START decision integrate?

Internal cell mass and external environment

57
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How is START controlled genetically?

Cdc28 activity and cyclin accumulation

58
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Why must cells reach critical size?

To ensure sufficient resources for genome duplication and division

59
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What causes small daughter cells to delay START?

Lower cyclin accumulation rates than mother cells

60
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Why do fast-growing cells pass START earlier?

Rapid nutrient uptake accelerates cyclin transcription

61
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What is the connection between START and mating pheromones?

Pheromone signalling arrests cells before START

62
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What happens to signalling pathways at START?

They trigger transcription of over 200 G1/S genes

63
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64
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Why are START decisions layered?

Later steps lock in commitment while earlier choices remain reversible