Lecture 23: Cell Cycle Flashcards

1
Q

Each living cells undergoes growth and cell division resulting in the formation of ___________________ each of which contains the same genetic information

A

Two daughter cells

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2
Q

The cell cycle is a balance of _____________ and ______________

A

cell division and cell death

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3
Q

What are the stage of the cell cycle, which are the __________________, _____________, ______________ and _____________

A

G1, S, G2, and M phase

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4
Q

What occurs during interphase

A

G1, S, and G2

it is the longest phase

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5
Q

___________________ lasts for hours to several days, cell grows and proteins are synthesized, restoring daughter cells to normal volume and size, cells preparing for S phase

A

G1 phase

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6
Q

_________ no cell division occurs

A

G0

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7
Q

_________ RNA and protein synthesis, cell growth

A

G1 phase

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8
Q

_____________- DNA replication, Histone synthesis, centrosome formed, chromosome duplication

A

S phase

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9
Q

_________ preparation for mitosis

A

G2 phase

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10
Q

______ mitosis, prophase, metaphase, anaphase, telophase, cytokinesis. Chromosome seperation, cell division

A

cytokinesis

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11
Q

____________ also known as quiescence, temporarily suspend in non dividing rest cells, cells are in a stable state, cellular processes in the cell are continuing as usual, cells may reenter the cycle to begin to divide again through growth factors or can be made to enter through other means

A

Go Phase (Gap outside phase)

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12
Q

_____________ DNA replication occurs, histone and non histone protein synthesis occurs, duplication of chromosomes, at the end of the S phase, chromosome consist of two double strands, cohesion applied to hold sister chromatids tightly together

A

S phase

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13
Q

_____________________ several proteins regulated the cohesion complex interaction and chromatin. The roles of cohesion:
1. regulates sister chromatic cohesion during meiosis and mitosis
2. Regulates DNA replication
3. Regulates DNA repair
4. Regulates transcription

A

Cohesion complex

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14
Q

________________ abnormalities in these genes are associated with multi system developmental disorders which are termed

A

Cohesionpathies

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15
Q

____________ lasts 2-4 hours, extends to M phase, cells prepare for mitosis, second growth phase, high rate of cellular activity, energy required for the complete of mitosis is accumulated. RNA proteins and tubules for spindle apparatus are synthesized

A

G2 phase

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16
Q

___________________ chromosomes begin to condense
Centrosomes made of two centrioles at tight angles, move to oppose pose of cell beginning formation of the spinal apparatus, nuclear membrane begins to break down

A

Prophase

16
Q

______________ nuclear membrane completely broken down, chromosomes continue to condense, centromere attach to spindle fibers and chromosomes move toward midway point between spindle poles

A

Prometaphase

17
Q

________________. chromosomes become fully condensed by end of this phase, chromosomes align on fibers of spindle apparatus at midway point, specialized proteins called kinetochores bind to centromeres and attach to chromosomes to spindle fibers

A

metaphase

18
Q

_______________ sister chromatids separate and move to opposite poles of spindle apparatus

A

Anaphase

19
Q

______________ chromosome begin to decondense, two nuclear membranes to form

A

Telophase

20
Q

____________ formation of two new daughter cells by division of cytoplasmic contents

A

Cytokinesis

21
Q

__________________ both sister chromatids go to same pole, it produces both trisomic and monosomic cells aneuploidy

A

Non disjunction

22
Q

__________________
separated sister chromatid “lags” behind and is not included within new nuclear membrane, micronucleus with lone chromosomes forms in cytoplasm, eventually lost from cell, results in monosomic cells,

A

anaphase lag

23
Q

________________is a ubiquitin ligase that
controls the levels of the M-phase
cyclins as well as other regulators of
mitosis. One important function of
APC is to control the initiation of
sister chromatid separation which
begins at the metaphase-anaphase
transition. The attachment of the
sister chromatids to the opposite
poles of the mitotic spindles occurs
early during mitosis. The ability of
the sister chromatids to be pulled
apart is initially inhibited because
they are bound together by a protein
complex termed cohesin complex.

A

The anaphase-promoting complex
(APC)

24
Q

____________________
*Initiate/induce cell progression through the
cell cycle
*Progression can be STOPED by various
checkpoints
* Accuracy of cellular events is monitored.
_____________________ key player
for cell cycle regulation
____________________for their
activity

A

Cyclins and Cyline dependent kinases
*Cyclin-dependent kinsase (Cdk)

25
Q

What are some checkpoints in G1 phase

A

*Cyclins D & E bind to their
respective Cdk’s
*Cyclin D: helps the passage
of cells through restriction
point in late G1 phase.
*Cyclin E: helps the cells at
the end of G1 phase to
commit to DNA replication
and enter S phase.
*Enable cell to enter/advance
to S phase

26
Q

What are some checkpoints are in the G1 and S phase

A

*Replication of DNA is monitored
*If errors are detected, the cell
cycle cannot continue until errors
corrected
*G1 DNA damage checkpoint
*S DNA damage checkpoint

27
Q

What are some checkpoints in the S phase

A

*Cyclin A binds to its CDK
*Cyclin A: enables cell to
leave S phase and enter G2
phase
Necessary for the initiation
of DNA synthesis
*Cyclin B is manufactured.

28
Q

What are some checkpoints at the G2 phase

A

*Replication of DNA is monitored
*If errors are detected, the cell cycle
cannot continue until errors corrected
*Unreplicated DNA checkpoint:
DNA that hasn’t been replicated can
not pass. Making sure S phase
occurred.
*G2 DNA damage checkpoint:
prevents the continuation of the G2
phase if errors are present in the
replicated DNA
*Cyclin B binds to its CDK
*Cyclin B: induces the cell
to leave the G2 phase and
enter the M phase
*Cyclin B is manufactured.

29
Q

Checkpoints at the M phase

A

Spindle Assembly Checkpoint:
*When: Beginning of the M phase
*Monitored: Spindle apparatus
If Spindle apparatus is faulty cell cannot leave
the M phase.
Chromosome Segregation Checkpoint
*When: End of the M phase
*Monitored: condition of chromosomes
if any of the chromosomes are sticking to each
other, cell is not permitted to leave M phase

30
Q

Tumor suppressor _______________ normally halts
cells in the G1 phase of the cell cycle.
In normal, resting cells, the RB
protein is unphosphorylated
RB prevents a cell’s entry into S
phase by binding to transcription
factor E2F and its binding partner
DP1/2, which are critical for the
G1/S transition
RB normally prevents progression
out of early G1 and into S phase in a
resting cell.

A

RB

31
Q

*The retinoblastoma protein (pRb or RB or
RB1)
*tumor suppressor
*important role in regulating the progression of
proliferating cells through the cell cycle
*the exit of differentiating cells from the cell
cycle.
* This protein affects these two functions by
sequestration of other transcription factors
and by promoting deacetylation of histones,
a chromatin modification associated with
gene silencing.
*Pathogenic variants cause ______________

A

Retinoblastoma

32
Q

Activation of mitotic ____________involves the addition of inhibiting and
activating phosphate groups
* Followed by removal of the inhibiting phosphate groups by a phosphatase.
* Once removal of the inhibiting phosphate groups has begun, a positive
feedback loop is set up:
* The activated Cdk-cyclin complex generated by this reaction stimulates the
phosphatase, thereby causing the activation process to proceed more
rapidly

A

Cdk-cyclin

33
Q

What two produces produce a response to damage to DNA

A

-ATM
-ATR

34
Q

ATM and ATR leads to the activation of p53 which in turn stimulates transcription of p21, which binds Cdks in G1 and S preventing progression of the cell cycle until ______________

A

damage DNA is repaired

35
Q

If DNA is too damaged p53 _________________

A

initiates apoptosis

36
Q

transcription factor p53
responds to diverse cellular
stresses to regulate target genes
that induce cell cycle arrest,
apoptosis, senescence, DNA
repair, or changes in metabolism
*p53 appears to induce apoptosis
through nontranscriptional
cytoplasmic processes
*Pathogenic variants cause ________________

A

Li Fraumeni syndrome