Introduction to Cell Cycle Flashcards

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1
Q

Why do cells divide?

A

Reproduction for single-celled organisms

Development for multicellular organisms

Healing of wounds

Replacement of cells lost to normal wear and tear

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2
Q

What is the lifespan of erthryocytes in the human body?

A

120 days

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3
Q

What are the four phases of the cell cycle?

A

G1, S, G2, M

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4
Q

How long does the mammalian cell cycle last?

A

Approximately 24 hours

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5
Q

In mammals, the G1 phase lasts from ___ hours to years, and the S phase lasts from ___ to ___ hours. Meanwhile, G2 phase lasts for ___ to __ hours, and M phase lasts only ___ hour(s).

A

8 hours

10 to 12 hours

1 to a few hours

1 hour

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6
Q

What phases make up interphase?

A

G1, S, G2

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7
Q

To what does G0 phase refer?

A

Cells that have terminally differentiated

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8
Q

At the end of the cell cycle, some cells begin the process of _____________ or _________ ________________, meaning they will become one type of cell and remain as such for the remainder of their lives and they are incapable of returning to the cell cycle.

A

Differentiation

Terminal differentiation

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9
Q

Lee Hartwell studied budding yeast or _______________ _______________, which are small, ovoid cells that can be easily observed in a microscope.

A

Saccharomyces cerevisiae

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10
Q

How do yeast divide?

A

Budding

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11
Q

In yeast, cell division occurs by budding. First, a _____ appears in late ____ and grows continuously through S and ____ phases until it is equal in size to the original cell. After _______, one set of chromosomes enters the bud, and the daughter cell then “pinches” or buds off.

A

Bud

G1

M

Mitosis

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12
Q

What are the advantages of a yeast model?

A

They are single-celled organisms, and yeast can grow and divise as either haploid or diploid, making identification of mutations and mutant genes much easier (i.e., only a single mutation is required for a mutation to occur in a haploid organism)

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13
Q

Hartwell gained experience as an undergraduate studying ____________ mutants in the replication cycle of ________, a bacteriophage. He created mutant strains of yeast that were defective in different aspects of the cell cycle by treating them with __________________, a DNA mutagen. He _____-____ and screened for mutants.

Hartwell found that at higher temperatures some colonies were not present that were at lower temperatures and determined that something was preventing the colonies’ growth. They were _____________ _______________.

A

Conditional

T4

Nitrosoguanidine

Replica-plated

Temperature sensitive

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14
Q

Hartwell’s experiments in yeast led him to identify 35 mutant cell lines that he called ___ mutants for _____ ______ _______.

A

cdc mutants

Cell division cycle mutants

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15
Q

Hartwell’s undergraduate student realized that in yeast ____ ______ correlates with the position in the _____ _______.

A

Bud size

Cell cycle

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16
Q

Ultimately, Hartwell mapped each mutant to specific cell cycle events by monitoring where each mutant stalled in the cycle and could not move further, using this information to determine which proteins were critical to each stage of the cell cycle

A
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17
Q

What cdc mutation did Hartwell find to be crucial for the initiation of cell division?

A

cdc 28

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18
Q

Hartwell identified the _____________ of the cell cycle.

A

Start

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19
Q

There are three major checkpoints within the cell cycle: ______________, _________________________, and __________________.

A

Start transition

G2/M transition

Metaphase-to-anaphase transition

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20
Q

At which transition of the cell cycle does the cell confirm whether the environment is favorable to division?

A

The start transition

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21
Q

At which transition of the cell cycle does the cell confirm all DNA is replicated and the environment is favorable for division?

A

G2/M transition

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22
Q

At which transition of the cell cycle does the cell check to see if the chromosomes are properly attached to their spindles?

A

Metaphase-to-anaphase

23
Q

G0 phase leads to _____________ that may or may not be terminal.

A

Differentiation

24
Q

Through what types of experiments did Hartwell begin to identify the individual genes responsible for mutations in yeast cell cycle division?

A

Complementation experiments

25
Q

Explain the principle behind complementation experiements.

A
  1. Hartwell closed every yeast gene into its own plasmid
  2. He placed each plasmid into mutant yeast cells
    1. The appropriate wild-type gene would “rescue” the mutant
  3. This enabled Hartwell to locate exactly which gene was responsible for each mutation
26
Q

What virus did Rao and Johnson use to induce mammalian cells to fuse at different stages of the cell cycle?

A

Sendai virus

27
Q

What was the ultimate conclusion Rao and Johnson made in their studies of the Sendai virus?

A

Mitotic nuclei release mitosis-promoting factors that affect interphase nuclei

28
Q

How did Rao and Johnson determine that the presence of mitosis-promoting factors were responsible for triggering cell division?

A

Rao and Johnson took nuclei from different stages of the cell cycle and merged them with nuclei from other stages. What they found was that something in the S phase nucleus and mitotic nuclei was released that drove the other nuclei into the S phase or mitosis, respectively

29
Q

Yoshio Masui studied ________________ using North American leopard frog oocytes. Oocytes are arrested in the ____ phase until the hormone ________________________ stimulates their entry into meiosis, where they are again arrested in ________ _____ until fertilization occurs.

A

Oocytes

Arrested in G2 phase

Progesterone

Meiosis II

30
Q

What does MPF stand for?

A

Maturation promoting factor

31
Q

How did Masui discover maturation promoting factor (MPF)?

A

He isolated cytosolic factors from oocytes at different times following progesterone stimulation and then injected them into oocytes that had not been exposed to progesterone; these oocytes were triggered into meiosis, and Masui called these cytoplasmic factors maturation promoting factors (MPFs)

32
Q

Wasserman and Smith discovered ______ activity in North American leopard frogs underwent rapid cycling following fertilization, and similar results were found in the African claw-toed frog. They determined that the more rapid fluctiations, the more rapid rates of _________.

A

MPF

Cleavage

33
Q

Rao synchronized HeLa cells by serum-starvation, isolated cytoplasmic extracts at different time points, and found that cytoplasmic extracts from the late _____ phase cells of frog oocytes stimulated meiosis in a non-mammalian animal.

A

Late G2 phase

34
Q

While Hartwell studied budding yeast, Paul Nurse studied _______ yeast.

A

Fission

35
Q

Schizosaccharomyces pombe or fission yeast are ____-shaped yeast that grow until they are _____ times their original length and then enter ______ followed by cytokinesis.

A

Rod-shaped

Two times

Mitosis

36
Q

Nurse, like Hartwell, did _________________ __________________ and determined that ______ is required for the ___________ transition.

A

Complementation experiments

cdc2

G2/M transition

37
Q

Nurse found that cdc2 from S. pombe or fission yeast rescued cdc28 from S. cerevisiae or budding yeast, leading to the conclusion that there is some functional ____________ between cdc2 and cdc28.

A

Redundancy

38
Q

Tim Hunt studied ______________________ and surf-clam eggs at Cambridge and found that _________________, an inhibitor of protein synthesis, prevented cell division following fertilization. He determined that protein synthesis is required for cell division following fertilization.

A

Sea urchins

Cycloheximide

39
Q

In addition to determining the protein requirment for cell division, Hunt also discovered what?

A

He also discovered that proteins appear and disappear during the cell cycle, and he named them cyclins

40
Q

How did Hunt identify cyclins?

A

He incubated cells with heavy methionine, isolated the newly made proteins, separated them on polyacrylamide gels, and exposed them to film

41
Q

Why did Hunt use 35S-methionine as opposed to another radiolabel?

A

Because only proteins contain sulfur

42
Q

Cyclin ____ levels drop raidly near the end of mitosis.

A

A

43
Q

Cyclins are the ____________________________ factors identifed by Hartwell.

A

Maturation promoting factors

44
Q

cdc genes are very highly ______________ from yeast to humans.

A

Conserved

45
Q

In the 1980s, cdc mutations 28 and 2 were found to be _______________.

A

Kinases

46
Q

In the late 1980s, multiple labs purified the maturation promoting factor (MPF) and determined that it was composed of two polypeptide units, one of which had kinase activity. cdcs are now known as ______ _______ _______.

A

Cyclin dependent kinases

47
Q

Cyclin-dependent kinase 1 (CDK1) is composed of the previously identified cyclin ______________ and yeast mutants ________ and ________.

A

Cyclin B

  • cdc*2
  • cdc*28
48
Q

There are four cyclin-dependent kinase complexes for each stage of the cell cycle: ____, _____, ______, and ______.

A

G1 Cdk

G1/S Cdk

S Cdk

M Cdk

49
Q

The G1-Cdk complex in vertebrates is composed of cyclin ___ and cyclin-dependent kinases ____ and ____. In yeast, this same complex is composed of cyclin (Cln) _____ and cyclin-dependent kinase _____.

A

Cyclin D

Cdk4 &Cdk6

Cln3

Cdk1

50
Q

The G1/S-Cdk complex in verebrates is composed of cyclin ____ and cyclin-dependent kinase _____ while in yeast it is composed of cylcin (Cln) _____ and cyclin-dependent kinase ____.

A

Cyclin E

Cdk2

Cln1, 2

Cdk1

51
Q

The S-Cdk complex is composed of cyclin _____ and Cdk ____ and ____ in vertebrates and cyclin (Clb) ______ and Cdk1 in yeast.

A

Cyclin A

Cdk2 & Cdk1

Clb5, 6

52
Q

In the M-Cdk complex, cyclin _____ and cdk _____ are present in vertebrates and cyclin ________ and cdk ____ in yeast.

A

Cyclin B

Cdk1

Clb 1, 2, 3, 4

Cdk1

53
Q
A