Unit 4 - Cell Cycle Episode 2 Flashcards

1
Q

rhythmic fluctuations in the abundance and
activity of cell cycle control molecules pace the
sequential events of the cell cycle

A

The Cell Cycle Clock

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2
Q

these regulatory molecules are mainly proteins of two types:

A

protein kinases and cyclins

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3
Q

re enzymes that activate or inactivate other proteins by phosphorylating them

many of the kinases that drive the cell cycle are actually present at a constant concentration in the growing cell, but much of the time they are in an active form

A

Protein Kinases

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4
Q

to be active, such kinase must be attached to a ________

A

cyclin

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5
Q

a protein that gets its name from cyclically
fluctuating concentration in the cell

A

cyclin

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6
Q

Because of this requirement, these kinases are
called __________________, or Cdks

the activity of a Cdk rises and falls with changes in the concentration of its cyclin partner

A

Cyclin-dependent kinases

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7
Q

the cyclin-Cdk complex, activity correspond to the peaks of cyclin concentration

the cyclin level rises during the S phase and G2 phases and then falls abruptly during M phase

A

Maturation-promoting factor

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8
Q

he initial MPF stands for “maturationpromoting factor”, but we can think of MPF as _________________ because it triggers the cell’s passage into the M phase, past the G2 checkpoint

A

M-phase promoting factor

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9
Q

when ________ that accumulate during G2 associate with __________, the resulting MPF complex phosphorylates a variety of proteins, initiating mitosis

A

cyclins; Cdk molecules

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10
Q

_________ acts both directly as a kinase and indirectly by activating other kinases

A

MPF

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11
Q

during ______, MPF helps switch itself off by initiating a process that leads to the destruction of its own cyclin

A

Anaphase

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12
Q

the noncyclin part of MPF,________, persists in the cell, inactive until it becomes part of MPF again by associating with new cyclin molecules synthesized during the S and G2 phases of the next round of the cycle

A

the CDK

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13
Q

proteins known as _____ (named because their concentration increases and decreases in a regular pattern through the cell) and enzymes known as __________________ are the key components in the regulatory events that occur at checkpoints

A

cyclins; cyclin-dependent kinases (Cdks)

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14
Q

at the ___________________, two different G1 cyclin-Cdk complexes form, resulting in activation of the kinase

A

G1-to-S checkpoint

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15
Q

the kinases catalyze a series of _______________ (additions of phosphate groups) of cell cycle control proteins, affecting the functions of those proteins and leading, therefore, to transition into the S phase

a similar process occurs at the G2-to -M
checkpoint

A

phosphorylations

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16
Q

a cyclin binds to a Cdk to form a _________

A

complex

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17
Q

until the cell is ready to enter ________, phosphorylation of the Cdk by another kinase keeps the Cdk inactive

A

mitosis

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18
Q

at that time, a phosphatase removes the key
phosphate from the Cdk, activating the enzyme

_________________________________ move
the cell into mitosis

A

Phosphorylations of proteins by Cdk

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19
Q

Three important checkpoints are those

A

G1, G2, and M phase

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20
Q

for many cells, the G1 checkpoint-dubbed
the __________________ in mammalian cells -seem
to be the most important

A

“restriction point”

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21
Q

most cells of the human body are actually in
the ____ phase

A

G0

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22
Q

T/F: Mature nerve cells and muscle cells never divide

A

True

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23
Q

other cells, such as ___________, can be “called back” from the G0 phase to the cell cycle by external cues, such as growth factors released during injury

A

liver cells

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24
Q

do not head the normal signals that regulate the cell cycle

in culture, they do not stop dividing when growth factors are depleted

do not need growth factors in their culture medium to grow and divide

A

Cancer Cells

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25
Q

they make a required growth factors themselves, or they may have an abnormality in the signaling pathway that conveys growth factor’s signal to the cell cycle control system even in the absence of that factor

A

Cancer Cells

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26
Q

can go on dividing indefinitely in the culture if they are given a continual supply of nutrients; in essence, they are “immortal”

A

Cancer Cells

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27
Q

a striking example is a cell line that has been reproducing in culture since 1951

A

HeLa Cells

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28
Q

Original source of HeLa Cells

A

a tumor removed from a woman named Henrietta Lacks

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29
Q

by contrast, nearly all normal, nontransformed mammalian cells growing in culture divide only about ________ before they stop dividing, age, and die

A

20 to 50 times

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30
Q

the abnormal cells may remain at the original site if they have too few genetic and cellular changes to survive at another site. In that case, the tumor is called

A

Benign tumor

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31
Q

most of this tumors do not cause serious
problems and can be removed by surgery

A

benign tumor

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32
Q

includes cells whose genetic and cellular changes enable them to spread to new tissues and impair the functions of one or more organs; these cells are also considered transformed cells

A

Malignant tumor

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33
Q

The process by which cancer cells spread to other parts of the body

A

Metastasis

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34
Q

also known as reduction division

A

Meiosis

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35
Q

cell growth, DNA replication, cellular activators

A

Interphase

36
Q

condensation of chromatids

A

Leptolema

37
Q

lining with homologous pairs

A

Zygonema

38
Q

crossing over

A

Pachynema

39
Q

synaptonemal complex begin to move apart

A

Diplonema

40
Q

nuclear envelopes disappear

microtubules enter the nucleus

A

Prometaphase I/II (Meiosis I/II)

41
Q

homologous pairs align in the middle

A

Metaphase I/II (Meiosis I/II)

42
Q

production of two new cells (diploid)

***Cytokinesis for cell division

A

Telophase I/II (Meiosis I/II)

43
Q

Reductional Division

A

Meiosis I

44
Q

Equational Division

A

Meiosis II

45
Q

result in a reduction in the number of chromosomes in each cell from diploid to haploid (reductional division-each resulting pair of attached sister chromatids count as a single chromosome)

A

Meiosis I

46
Q

result in the separation of the sister chromatids

A

Meiosis II

47
Q

Meiosis I, in which the chromosome number is reduced from diploid to haploid, consists of five stages:

A
  • Prophase
  • Prometaphase
  • Metaphase
  • Anaphase
  • Telophase
48
Q

early prophase I,

A

Leptotene Stage

49
Q

the extended chromosomes begin to condense and become visible as long, thin threads

A

Leptonema

50
Q

early to middle prophase I

A

Zygotene Stage

51
Q

the chromosomes continue to condense

the homologous pairs of chromosomes actively find each other and align roughly along their lengths

A

Zygonema

52
Q

the formation along the length of the chromatids of a zipperlike structure called the SYNAPTONEMAL COMPLEX

A

Synapsis

53
Q

aligns the two homologs precisely, base pair for base pair

A

Synaptonemal Complex

54
Q

middle prophase I

A

Pachytene Stage

55
Q

starts when synapsis is completed

because of the replication that occurred earlier, each synapsed set of homologous chromosomes consists of four chromatids and is called a bivalent or a tetrad

A

Pachynema

56
Q

during pachynema, a most significant event
for genetics occurs:

A

Crossing-over

57
Q

the reciprocal physical exchange of chromosome segments at corresponding positions along pairs of homologous chromosomes

A

Crossing-over

58
Q

the physical exchange that occurs in crossing over is facilitated by the alignment of the homologous chromosomes brought about by the

A

Synaptonemal complex

59
Q

a chromosome that emerges from meiosis with a combination with which it started is called

A

Recombinant DNA

60
Q

a mechanism that can give rise to genetic recombination

A

Crossing-over

61
Q

at the end of pachynema, the synaptonemal complex is _______, and the chromosomes have started to elongate

A

disassembled

62
Q

middle to late prophase I

A

Diplotene Stage

63
Q

the synaptonemal complex disassembles and the homologous chromosomes begin to move apart

A

Diplonema

64
Q

the result of crossing-over becomes visible during diplonema as a cross-shaped structured called

A

chiasma (plural, chiasmata)

65
Q

late Prophase I

A

Diakinesis

66
Q

the chromosomes condense even more, making it now possible to see the four members of the tetrads

the chiasmata are clearly visible at this stage

A

Diakinesis

67
Q

the nucleoli disappear, the nuclear envelop breaks down, and the meiotic spindle that has been forming between the separating centriole pairs enters the former nuclear area

A

Prometaphase I

68
Q

the kinetochore microtubules align the tetrads on the metaphase plate

A

Metaphase I

69
Q

importantly, the pairs of homologs (the tetrads) are found at

A

the metaphase plate

70
Q

at this time, homologous chromosomes have segregated from each other, but sister chromatids remain attached at their respective centromeres. In other words, a key difference between meiosis I and mitosis is that sister chromatids remain joined after metaphase in meiosis I, whereas they separate in mitosis

A

Anaphase I

71
Q

the dyads complete their migration to opposite poles of the cell and the spindle assemble

in some species, but not all, new nuclear envelopes form around each haploid grouping

A

Telophase I

72
Q

after __________________, each of the two progeny cells has a nucleus with a haploid set of dyads

A

cytokinesis

73
Q

the chromosomes condense

formation of spindle fibers

A

Prophase II

74
Q

the nuclear envelope breakdown (if formed in telophase) breaks down, and the spindle organizes across the cell

kinetochore microtubules from the opposite poles attach to the kinetochores of each chromosome

A

Prometaphase II

75
Q

the movement of the kinetochore microtubules aligns the chromosomes on the metaphase plate

A

Metaphase II

76
Q

the centromeres separate, and the now-daughter chromosomes are pulled to the opposite poles of the spindle

one sister chromatid of each pair goes to one pole, and the other goes to the opposite pole

the separated chromatids are now considered chromosomes in their own right

A

Anaphase II

77
Q

the chromosomes begin decondensing, a nuclear envelope forms around each set of chromosomes, and cytokinesis takes place

A

Telophase II

78
Q

after __________, the chromosomes continue decondensing eventually becoming invisible under the light microscope

A

telophase II

79
Q

The end products of the two meiotic division
are

A

four haploid cells (gametes in animals) from one original diploid cell

80
Q

reduces the number of chromosomes sets from two (diploid) to one (haploid)

A

Meiosis

81
Q

conserves the number of chromosome sets

A

Mitosis

82
Q

produces cells that differ genetically from their parent cell and from each other

A

Meiosis

83
Q

produces daughter cells that are genetically identical to their parent cell and each other

A

Mitosis

84
Q

Three Events Unique to Meiosis Occur During Meiosis I

A
  1. Synapsis and Crossing-Over
  2. Alignment of homologous pairs at the
    metaphase plate
  3. Separation of homologues
85
Q

during prophase I, duplicated homologs
pair up

normally do not occur during prophase of mitosis

A

Synapsis and Crossing-over

86
Q

chromosomes are positioned at the metaphase plate as pairs of homologs, rather that individual chromosomes, as in metaphase of mitosis

A

Alignment of homologous pairs at the metaphase plate

87
Q

at anaphase I of meiosis, the duplicated chromosomes of each homologous pair move toward opposite poles, but the sister chromatids of each duplicated chromosome remain attached

in anaphase of mitosis, by contrast, sister
chromatids separate

A

Separation of homologues