Recombinant DNA Technology
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Transcript Recombinant DNA Technology
Genetics of Cancer
Genetic Mutations that Lead
to Uncontrolled Cell Growth
How do we define cancer?
Cancer is a group of disorders that causes
cells to escape normal controls on cell
division
-cancer cells divide more frequently
-cancer cells divide an unlimited number of
times
-cancer cells are not inhibited by contact with
other cells and can form tumors
-cancer cells can invade other tissues, a
process called metastasis
Non-cancerous
cells form sheets.
Cancer cells
grow into tumors.
Cancer cells can
invade other tissues.
Cancer is the result of a series of
mutations in genes already existing within
the cell. Environmental agents cause a
signficant number of these mutations.
Oncogene
Tumor
Suppressor
A series of mutations is responsible for the
development of FAP colon cancer.
Types of Mutations Causing
Cancer
• Dominant Oncogenic Alleles
– Gain of function mutations
– Dominant allele codes for gene product that
stimulates cell proliferation
– Proto-oncogene undergoes mutation or
comes under alternate control to become
an oncogene (may involve viruses)
– Increased cell division provides opportunity
to accumulate mutations in additional
genes
Types of Mutations Causing
Cancer
• Recessive Tumor Suppressor
Alleles
– Loss of function mutations
– Recessive allele codes for gene
product that fails to inhibit cell
proliferation.
Applying Your Knowledge
TRUE: Thumbs Up
FALSE: Thumbs Down
Indicate whether each statement is TRUE or FALSE
• Cancer cells escape the normal controls on cell
division.
• Oncogenes are recessive mutations.
• The growth of a cancer cell is stopped by
contact with another cell.
• Cancer-causing mutations in tumor suppressor
alleles represent a loss of function.
Control of the Cell Cycle
Mechanisms for controlling progress
through the cell cycle
Extracellular Signals
Control the timing of cell division
Transitions
Orderly progression from one stage of cell
cycle to another
Checkpoints
Delay progression to next stage if cell
must repair damage
Extracellular Signals
The normal RAS protein product
is reversibly activated by a signal
from a growth factor and
stimulates cell proliferation when
active.
The RAS oncogene is
always activated, leading
to uncontrolled growth.
Cell Cycle Transitions and Checkpoints
G2M
Transition
Apoptosis
Checkpoint
G2M
Checkpoint
SG2
Transition
P M
G2
assembly of
components
for division
S
A
T
Mitosis
cytokinesis
G1
chromosomes
replicate
DNA Damage
Checkpoint
Spindle
Assembly
Checkpoint
cytoplasm
doubles
G1S
Transition
G1S
Checkpoint
Proteins Controlling Cell Cycle Transitions
• G1S and G2M Transitions are
controlled by CDK-cyclin complexes
– CDK = cyclin-dependent kinase
• Enzyme that activates or inactivates a target
protein by phosphorylation
– Cyclin
• Protein that accumulates at specific stages of cell
cycle to associate with CDK and specify the
target proteins
• Cyclin levels are controlled
by gene regulation and
protein degradation
Phosphorylation of Rb Protein Mediates the
G1 S Transition
Rb = product of the retinoblastoma gene
E2F = transcription factor
How Do Mutations in Rb
Cause Retinal Cancer?
In heterozygotes,
conversion of the
Rb+ allele to Rbby mutation leads
to uncontrolled
growth of retinal cells.
Tumor Suppressor Genes p53 and p21
Control the G1 S Checkpoint
How Do Mutations in p53
Cause Cancer?
In the absence of p53 function,
cells enter S phase despite
breaks in chromosomes. This
can lead to chromosomal
rearrangements.
How Do Mutations in p53
Cause Cancer?
p53 gives an internal
signal for apoptosis
If DNA damage cannot be
repaired, functional p53
protein triggers apoptosis
(programmed cell death).
Mutations in p53 allow
defective cells to proliferate.
Defects in DNA Repair
•BRCA1 is a tumor
suppressor involved
in DNA repair. Faulty
copies of BRCA1
cause inherited breast
cancer.
•The disease Xeroderma
Pigmentosum results
from a defect in
nucleotide excision
repair.
Applying Your Knowledge
1.
2.
3.
4.
Dominant Oncogenic Allele
Recessive Tumor Suppressor Allele
CDK-Cyclin Complex
Growth Factor
Which description best represents the
• Cancer-causing allele for Rb protein?
• Extracellular signal for cell division?
• Cancer-causing RAS allele?
• Component that influences cell cycle
progress through phosphorylation of
molecules?