Cell Cycle Control and Cell Division Part 2 Flashcards

1
Q

G1/S checkpoint (1)

A

is the environment favorable?

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2
Q

pass G1/S checkpoint…

A

enter cell cycle and proceed to S phase

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3
Q

G2M checkpoint (2)

A

is the DNA replicated?

is the environment favorable?

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4
Q

pass G2/M checkpoint…

A

enter mitosis

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5
Q

metaphase to anaphase transition

A

are all chromosomes attached to the spindle?

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6
Q

pass metaphase to anaphase transition…

A

trigger anaphase and proceed to cytokinesis

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7
Q

checkpoint controls (4)

A

late G1 or start checkpoint
G2/M checkpoint
metaphase to anaphase transition
G0

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8
Q

the system is designed to — — through each of the checkpoints if problems are sensed

A

block progression

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9
Q

what is the G0 checkpoint associated with

A

dREAM complex

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10
Q

passage through the start checkpoint in late G1 launches

A

DNA replication and the S phase of the cell cycle

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11
Q

DNA replication occurs at specific sites or

A

origins of replications (AT rich regions)

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12
Q

what two steps is the initiation phase of DNA replication divided into?

A

late mitosis-early G1: prereplication complex assembles at the origins of replication
onset of S phase when prereplication complex nucleates the formation of the preinitiation complex

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13
Q

the G2/M checkpoint ensures that

A

all of the DNA has been properly replicated

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14
Q

abrupt increases in M-cdk activity at the G2/M checkpoint drives (2)

A

entry into mitosis and the events of early mitosis

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15
Q

M-cdk induces (4)

A

assembly of the mitotic spindle
chromosome condensation
promotes breakdown of the nuclear envelope
rearrangements of the actin cytoskeleton and the goggle apparatus

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16
Q

each of the above events is triggered by — mediated — of specific proteins in conjugation with two other families of protein kinases

A

m-cdk

phosphorylation

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17
Q

how long does mitosis take to occur

A

1 hour

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18
Q

phases of mitosis

A
prophase
prometaphase
metaphase
anaphase
telophase
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19
Q

at prophase, the replicated chromosomes, each consisting of two closely associated sister chromatids, —-

A

condense

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20
Q

outside the nucleus the mitotic spindle assembles between the two centrosomes, which are (2)

A

replicated and moved apart

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21
Q

what is at the center of sister chromatids

A

kinetochore

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22
Q

pro metaphase starts abruptly with

A

the breakdown of the nuclear envelope

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23
Q

chromosomes can now

A

attach to spindle MT via their kinetochores and undergo active movement

24
Q

what allows the chromosomes to line up and move apart?

A

kinetochore MT

25
Q

chromosome painting

A

Ab to specific regions of chromosome associated with fluorescent dye
paint the chromosome with dye
can see chromosome rearrangement in metaphase

26
Q

at metaphase, the chromosomes are

A

aligned at the equator of the spindle, midway between the spindle poles

27
Q

the kinetochore MT attach sister chromatids to

A

opposite poles of the spindle

28
Q

at anaphase, the sister chromatids

A

synchronously separate tot form two daughter chromosomes

29
Q

each is pulled slowly toward the

A

spindle pole it faces

30
Q

what contributes to chromosome segregation? (2)

A

the kinetochore microtiniles get shorter, and the spindle poles move apart

31
Q

during telophase, the two sets of daughter chromosomes arrive at the poles of the spindle and

A

decondense

32
Q

a new nuclear envelope reassekhpes around each set, completing the formation of

A

two nuclei and marking the end of mitosis

33
Q

the division of the cytoplasm begins with

A

contraction of the contractile ring (cleavage furrow)

34
Q

during cytokinesis. the cytoplasm is divided in to by

A

a contractile ring of actin and myosin filaments, which pinches the cell into two to create two daughter cells, each with one nucleus

35
Q

Roberts syndrome

A

Prenatal growth retardation (mild to severe), craniofacial
abnormalities such as microcephaly and cleft lip/palate and
limb malformations (usually limbs are short and the arms
are more severely affected than legs).

36
Q

roberts syndrome is a homozygous mutation of —, which encodes an
— important for the formation of the
cohesion complex that binds to chromosomes and creates
cohesion between sister chromatids.

A

ESCO2

acetyltransferase

37
Q

Closely related to Cornelia de Lange Syndrome (mutations in

Smc1, Smc3, NIPBL), collectively referred to as

A

Cohesionopathies

38
Q

Studies suggest that the ESCO2 mutations lead to decreased
— transcription and subsequent — biogenesis
and the observed defects in nucleolar morphology. This
leads to decreased — —

A

rDNA
ribosomal
protein synthesis

39
Q

extracellular signals controlling cell division (3)

A

mitogens
growth factors
survival factors

40
Q

mitogens

A

stimulate cell division mainly by stimulating the G1/S-cdk activity that inhibits intracellular negative controls that block progression through the cell cycle

41
Q

growth factors

A

stimulate cell growth (increase in cell mass) by stimulating protein synthesis and inhibiting protein degradation

42
Q

survival factors

A

suppress programmed cell death (apoptosis)

43
Q

with growth factors, the cells get bigger but may or may not

A

divide

44
Q

mitogens interact with cell surface receptors to trigger multiple

A

intracellular signaling pathways

45
Q

one major pathway involves the small — — signaling proteins

A

GTPase ras

46
Q

was leads to activation of a

A

MAP kinase cascade

47
Q

MAP kinase cascade leads to

A

activation of immediate early gene expression (genes that are tuned on very early or almost immediately after a mitogen binds to its receptor)

48
Q

example of immediate early gene

A

Myc

49
Q

what does Myc promote

A

cell cycle entry

50
Q

how does Myc promote cell cycle entry?

A

by increasing the expression of the genes encoding the G1 cyclins (D cyclins) which results in increased G1-cdk (cyclin D-cdk4) activity

51
Q

One of the key functions of G1-Cdk is to

A

activate the E2F proteins that are themselves gene regulatory factors

52
Q

Normally the E2F proteins are inhibited by an

interaction between

A

E2F and the retinoblastoma protein (Rb) family

53
Q

G1-Cdk phosphorylates the — protein, rendering it inactive and reducing its binding to

A

Rb

E2F

54
Q

phosphorylation of Rb protein …

A

frees E2F to activate expression of its target genes

55
Q

extracellular factors can lead to (2)

A

cell growth then cell division

simultaneous cell growth and cell division

56
Q

growth factors lead to

A

cell growth

57
Q

mitogens lead to

A

cell division