You Light Up My Life
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Transcript You Light Up My Life
PowerLecture:
Chapter 15
Controls over Genes
Impacts, Issues: Between You
and Eternity
Loss of gene controls can be disastrous
Some gene mutations, either inherited or spontaneously
mutated due to environmental factors, predispose
individuals to develop cancer
ERBB2, a type of membrane receptor, is encoded on
chromosome 17
This gene controls the cell cycle - overexpression or
mutation triggers cancerous transformations
Impacts, Issues: Between You
and Eternity
BRCA1
and BRCA2 are tumor
suppressing proteins that fix damaged
DNA
Breast
cancer cells often contain their
mutated forms
Changes in DNA
Trigger Cancer
Ultraviolet
radiation can
cause breaks
Can
promote
formation of
dimers
Controlling the Cell Cycle
Cycle
has built-in checkpoints
Proteins monitor chromosome structure,
whether conditions favor division, etc.
Proteins are products of checkpoint genes
Kinases
Growth factors
Oncogenes
Have
potential to induce cancer
Mutated
Can
forms of normal genes
form following insertions of viral
DNA into DNA or after carcinogens
change the DNA
Cancer Characteristics
Plasma
membrane and cytoplasm
altered
Cells
grow and divide abnormally
Weakened
Lethal
capacity for adhesion
unless eradicated
Apoptosis
Programmed
Signals
cell death
unleash molecular weapons of
self-destruction
Cancer
cells do not commit suicide on cue
Gene Control
Which genes are expressed in a cell
depends upon:
• Type of cell
• Internal chemical conditions
• External signals
• Built-in control systems
Mechanisms of Gene Control
Controls related to transcription
Transcript-processing controls
Controls over translation
Post-translation controls
Regulatory Proteins
Can exert control over gene
expression through interactions with:
DNA
RNA
New polypeptide chains
Final proteins
Control Mechanisms
Negative
control
Regulatory proteins slow down
or curtail gene activity
Positive
control
Regulatory proteins promote or
enhance gene activities
Control Mechanisms
Promoters
Enhancers
Chemical Modifications
Methylation
of DNA
can inactivate
genes
Acetylation of
histones allows
DNA unpacking
and transcription
Controls in Eukaryotic Cells
Control
Transcript
processing controls
Controls
Controls
of transcription
over translation
following translation
Controls in Eukaryotic Cells
NUCLEUS
DNA
pre-mRNA
transcript
transcription
control
CTYOPLASM
translational
control
mRNA
transport
processing
control
mRNA
mRNA
transport
control
mRNA
degradation
control
inactivated
mRNA
protein
product
protein
product
control
inactivated
protein
Fig. 15-3, p.233
Chromosome Puff
Portion of the
chromosome in which the
DNA has loosened up to
allow transcription
Translation of transcripts
from puffed region
produces protein
components of saliva
X Chromosome Inactivation
One
X inactivated in each cell of female
Creates
a “mosaic” for X chromosomes
Governed
by XIST gene
X Chromosome Inactivation
A
condensed X
chromosome (Barr
body) in the somatic
cell nucleus of a
human female
Fig. 15-4a, p.234
Most Genes Are Turned Off
Cells
of a multicelled organism rarely
use more than 5-10 percent of their
genes at any given time
The
remaining genes are selectively
expressed
Phytochrome
Signaling
molecule in plants
Activated
by red wavelengths,
inactivated by far-red wavelengths
Changes
in phytochrome activity
influence transcription of certain genes
petal
carpel
stamen
sepal
Fig. 15-6, p.235
B
A
1
C
2
3
petals
sepals
4
carpel
stamens
Fig. 15-6, p.235
Fig. 15-6, p.235
Fig. 15-6, p.235
Fig. 15-6, p.235
Fig. 15-6, p.235
Fig. 15-6, p.235
Homeotic Genes
Occur
in all eukaryotes
Master genes that control development of
body parts
Encode homeodomains (regulatory
proteins)
Homeobox sequence can bind to
promoters and enhancers
Knockout Experiments
Prevent a gene’s transcription or translation
Differences between genetically engineered
knockout individuals and wild-type individuals
point to function of knocked out gene
Knockout experiments shed light on genes that
function in Drosophila development
Knockout Experiments
Fig. 15-7c, p.237
A7 A5 A3 A1 T2 T2
A8
A4 A2 T3 T1
T2
T2
Body
Plan
A5
A4
A6
A7
A8
A3
A2
A1
T3
T1 Lb Mx Md
T2
A8
A7
A6
A4
A3 A2
A1 T3
T2
T1
A5 A4
A3 A2
A1 T3
T2
T1
A6
A7
A8
Fig. 15-8a, p.237
Body Plan
Fig. 15-8b, p.237
Body Plan
Fig. 15-8c, p.237
Gene Control in Prokaryotes
No
nucleus separates DNA from
ribosomes in cytoplasm
When
nutrient supply is high,
transcription is fast
Translation
occurs even before
mRNA transcripts are finished
The Lactose Operon
operator
regulatory
gene
transcription,
translation
operator
gene 1
gene 2
gene 3
promoter
lactose operon
repressor protein
Fig.15-10, p. 241
High Lactose
allolactose
lactose
mRNA
operator
promoter
operator
RNA
polymerase
gene 1
Fig.15-10, p. 241
Low Lactose
Repressor
Binding
binds to operator
blocks promoter
Transcription
is blocked
Fig.15-10, p. 241
CAP Exerts Positive Control
CAP
is an activator protein
Adheres
to promoter only when in
complex with cAMP
Level
of cAMP depends on level of
glucose
Positive Control –
High Glucose
There
CAP
is little cAMP
cannot be activated
The
promoter is not good at binding
RNA polymerase
The
lactose-metabolizing genes are
not transcribed very much
Positive Control –
Low Glucose
cAMP
accumulates
CAP-cAMP
Complex
RNA
The
complex forms
binds to promoter
polymerase can now bind
lactose-metabolizing genes are
transcribed rapidly
Hormones
Signaling
molecules
Stimulate
or inhibit activity in target cells
Mechanism
of action varies
May bind to cell surface
May enter cell and bind to regulatory
proteins
May bind with enhancers in DNA
Polytene Chromosomes
Occur
in salivary
glands of midge
larvae
Consist of multiple
DNA molecules
Can produce
multiple copies of
transcripts
Vertebrate Hormones
Some
have widespread effects
Somatotropin (growth hormone)
Others
signal only certain cells at
certain times
Prolactin stimulates milk
production
Fig. 15-11a, p.241
Fig. 15-11b, p.241