chapter 18 Flashcards

1
Q

Cells reproduce by _ a process called the _.

A

duplicating their contents and dividing in two in
_
cell cycle

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2
Q

The cell grows continuously during _, which consists of _

A

interphase
_
three phases: G1, S, and G2.

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3
Q

DNA replication is confined to _

A

S phase.

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4
Q

During M phase, the _ divides in a process called mitosis; then
the _ divides, in a process
called cytokinesis.

A

nucleus
cytoplasm

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5
Q

During M phase, the nucleus divides in a process called _; then
the cytoplasm divides, in a process
called _.

A

mitosis
cytokinesis

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6
Q

M phase, for example, is typically much _and G1 much _ .

A

shorter
longer

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7
Q

The cell-cycle control system ensures that key processes in the cycle _

A

occur in the proper sequence.

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8
Q

The control system can transiently halt the cycle at specific transition points—in _— if _.

A

G1, G2, and M phase
_
extracellular or intracellular conditions are unfavorable

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9
Q

checks before entering in MITOSIS

A

Is all DNA replicated? Is all DNA damage repaired?

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10
Q

checks before PULL DUPLICATED CHROMOSOMES APART

A

Are all chromosomes properly attached to the mitotic spindle?

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11
Q

checks before ENTER S PHASE

A

Is environment favorable?

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12
Q

Distinct Cdks associate with different _ to trigger the different events of the cell cycle.

A

cyclins

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13
Q

Distinct _ associate with different cyclins to trigger the different events of the cell cycle.

A

Cdks

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14
Q

cyclins that are specifically active during the G1 phase of the cell cycle:

A

cyclin D

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15
Q

cyclins that help G1 –> S transition:

A

cyclin E

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16
Q

cyclins that are specifically active during the S phase of the cell cycle:

A

cyclin A

17
Q

cyclins that are specifically active during the M phase of the cell cycle:

A

cyclin B

18
Q

The activity of some Cdks is regulated by _

A

cyclin degradation.

19
Q

_ of S or M cyclin by _ marks the protein for destruction in proteasomes. The loss of cyclin renders _

A

Ubiquitylation
_
APC/C
_
its Cdk partner inactive.

20
Q

For M-Cdk to be active, _.

A

inhibitory phosphates must be removed

21
Q

As soon as the M cyclin–Cdk complex is formed, it is _ by an _ called _. This modification keeps M-Cdk in an _ state until these phosphates are removed by an _ called _.
!!!!mechanism specific to M-Cdks!!!!!

A

phosphorylated at two adjacent sites
_
inhibitory protein kinase
_
Wee1
_
inactive
_
activating protein phosphatase
_
Cdc25

22
Q

The activity of a Cdk can be blocked by the _

A

binding of a Cdk inhibitor. eg: inhibitor protein (called p27) binds to an activated cyclin–Cdk complex = prevents the Cdk from phosphorylating target proteins

23
Q

control mechanism when
DNA replication not complete
DNA damage

A

INHIBITION OF ACTIVATING PHOSPHATASE (Cdc25) BLOCKS ENTRY TO MITOSIS

24
Q

control mechanism when chromosomes not properly attached to spindle

A

INHIBITION OF APC/C ACTIVATION DELAYS EXIT FROM MITOSIS

25
Q

control mechanism when
environment not favorable

A

Cdk INHIBITORS BLOCK ENTRY TO S PHASE

26
Q

mitogens :

A

stimulate cell proliferation

27
Q

mitogens inhibit

A

the Rb protein.

28
Q

dephosphorylated Rb protein (active), what do they do?

A

holds specific transcription regulators in an inactive state.

29
Q

Mitogens binding to _ activate _
that lead to the _. These complexes _, and thereby inactivate, the _ protein, releasing the transcription regulators needed to activate the transcription of genes required for entry into S phase.

A

cell-surface receptors
_
intracellular signaling pathways
_
formation and activation of G1-Cdk and G1/S-Cdk complexes
_
phosphorylate
_
Rb

30
Q

DNA damage can arrest the cell cycle in _.

A

G1

31
Q

When DNA is damaged, specific protein kinases respond by both activating the _ and halting _. _ protein thus accumulates and stimulates the _. The p21 protein binds to G1/S-Cdk and S-Cdk and inactivates them, so that the cell cycle arrests in G1.

A

p53 protein
_
its otherwise rapid degradation
_
Activated p53
_
transcription of the gene that encodes the Cdk inhibitor protein p21 (same shape and system as p27)
_

32
Q

explain the initiation of DNA replication (fig 16)

A

During G1, Cdc6 on ORC (origin recognition complex sitting on origin)
_
HELICASE BINDS, Cdc6 DISSOCIATES from ORC
_
At the start of S, S-Cdk triggers the firing of this loaded replication origin
_
S-Cdk also blocks re-replication by phosphorylating Cdc6 and the ORC = both inactive = prevents reassembly of the prereplicative complex until the Cdks are turned off in the next G1.

33
Q

Activated M-Cdk indirectly activates _, creating a _

A

more M-Cdk
positive feedback loop.

34
Q

APC/C triggers _ by _

A

the separation of sister chromatids
_
by promoting the destruction of cohesins.

35
Q

APC/C catalyzes the _ and _ of an _ protein called _, which _ the activation of a proteolytic enzyme called _. When freed from _, _ cleaves the _, allowing the _.

A

ubiquitylation
_
destruction
_
inhibitory
_
securin
_
blocks
_
separase
_
securin
_
separase
_
cohesin complexes
_
mitotic spindle to pull the sister chromatids apart

36
Q

(A) In anaphase A, _ The force driving this movement is generated mainly at the _.

A

the sister chromatids are pulled toward opposite poles as the kinetochore microtubules depolymerize.
_
kinetochore

37
Q

(B) In anaphase B, _ as the result of two separate forces: (1) _, and (2) _
Both forces
are thought to depend on _

A

the two spindle poles move apart
_
the elongation and sliding of the interpolar microtubules past one another pushes the two poles apart
_
Microtubules at the edges (astral microtubules) are pulled toward the cell edges dragging the two poles apart.
_
the action of motor proteins associated with the microtubules.

38
Q

The nuclear envelope
breaks down and re-forms during mitosis. The _ of _ and _ helps trigger the disassembly of the nuclear envelope at _. _ of these proteins at telophase helps reverse the process.

A

phosphorylation
_
nuclear pore proteins
_
lamins
_
prometaphase
_
Dephosphorylation