Eukaryotic Gene Control 14-15
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Transcript Eukaryotic Gene Control 14-15
Control of
Eukaryotic Genes
AP Biology
2007-2008
The BIG Questions…
How are genes turned on & off
in eukaryotes?
How do cells with the same genes
differentiate to perform completely
different, specialized functions?
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Development: cellular level
Cell division
Differentiation
cells become specialized in structure & function
if each kind of cell has the same genes,
how can they be so different
shutting off of genes = loss of totipotency
Morphogenesis
“creation of form” = give organism shape
basic body plan
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polarity
one end is different than the other
symmetry
left & right side of body mirror each other
asymmetry
pssst, look at your hand…
Development: step-by-step
Gamete formation
Fertilization
Cleavage (cell division, mitosis)
Gastrulation (morphogensis)
Organ formation (differentiation)
Growth & tissue formation
(differentiation)
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Evolution of gene regulation
Prokaryotes
single-celled
evolved to grow & divide rapidly
must respond quickly to changes in
external environment
exploit transient resources
Gene regulation
turn genes on & off rapidly
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flexibility & reversibility
adjust levels of enzymes
for synthesis & digestion
Cell signaling
Regulating the expression of genes that
affect the developmental fate of the cell
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Gastrulation
zygote blastula gastrula
How you looked
as a blastula…
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Gastrulation
Cells change size & shape: sheets of cells
expand & fold inward & outward
Changes in cell
shape involve
reorganization
of cytoskeleton
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Stem cells
pluripotent cells
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Evolution of gene regulation
Eukaryotes
multicellular
evolved to maintain constant internal
conditions while facing changing
external conditions
homeostasis
regulate body as a whole
growth & development
long term processes
specialization
turn on & off large number of genes
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must coordinate the body as a whole rather
than serve the needs of individual cells
Master control genes
Homeotic genes
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master regulatory
genes
in flies these genes
identify body
segments & then
turn on other
appropriate genes
to control further
development of
those body sections
Homeotic genes
Mutations to homeotic genes produce flies
with such strange traits as legs growing from
the head in place of antennae.
structures characteristic of a particular part of
the animal arise in wrong place
antennapedia flies
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Homeobox DNA
Master control
genes evolved
early
Conserved for
hundreds of
millions of years
Homologous
homeobox genes in
fruit flies &
vertebrates
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kept their
chromosomal
arrangement
Evolutionary Constraints on
Development
Basic body plans of the major animal
groups have not changed due to a limited
number of homeotic genes (master
genes)
These genes have imposed limits
taxonomic / evolutionary
physical
architectural
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Points of control
The control of gene
expression can occur at any
step in the pathway from
gene to functional protein
1. packing/unpacking DNA
2. transcription
3. mRNA processing
4. mRNA transport
5. translation
6. protein processing
7. protein degradation
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1. DNA packing
How do you fit all
that DNA into
nucleus?
DNA coiling &
folding
double helix
nucleosomes
chromatin fiber
looped
domains
chromosome
from DNA double helix to
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condensed
Nucleosomes
8 histone
molecules
“Beads on a string”
1st level of DNA packing
histone proteins
8 protein molecules
positively charged amino acids
bind tightly to negatively charged DNA
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DNA
packing movie
DNA packing as gene control
Degree of packing of DNA regulates transcription
tightly wrapped around histones
no transcription
genes turned off
heterochromatin
darker DNA (H) = tightly packed
euchromatin
lighter DNA (E) = loosely packed
H
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E
DNA methylation
Methylation of DNA blocks transcription factors
no transcription
genes turned off
attachment of methyl groups (–CH3) to cytosine
nearly permanent inactivation of genes
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C = cytosine
ex. inactivated mammalian X chromosome = Barr body
Histone acetylation
Acetylation of histones unwinds DNA
loosely wrapped around histones
attachment of acetyl groups (–COCH3) to histones
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enables transcription
genes turned on
conformational change in histone proteins
transcription factors have easier access to genes
2. Transcription initiation
Control regions on DNA
promoter
nearby control sequence on DNA
binding of RNA polymerase & transcription
factors
“base” rate of transcription
enhancer
distant control
sequences on DNA
binding of activator
proteins
“enhanced” rate (high level)
of transcription
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Control of transcription movie
Model for Enhancer action
Enhancer DNA sequences
Activator proteins
distant control sequences
bind to enhancer sequence
& stimulates transcription
Silencer proteins
bind to enhancer sequence
& block gene transcription
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Turning
on Gene movie
Transcription complex
Activator Proteins
• regulatory proteins bind to DNA at
Enhancer Sites
distant enhancer sites
• increase the rate of transcription
regulatory sites on DNA
distant from gene
Enhancer
Activator
Activator
Activator
Coactivator
A
E
F
B
TFIID
RNA polymerase II
H
Core promoter
and initiation complex
Initiation Complex at Promoter Site binding site of RNA polymerase
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3. Post-transcriptional control
Alternative RNA splicing
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variable processing of exons creates a
family of proteins
4. Regulation of mRNA degradation
Life span of mRNA determines amount
of protein synthesis
mRNA can last from hours to weeks
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RNA
processing movie
RNA interference
Small interfering RNAs (siRNA)
short segments of RNA (21-28 bases)
bind to mRNA
create sections of double-stranded mRNA
“death” tag for mRNA
triggers degradation of mRNA
cause gene “silencing”
post-transcriptional control
turns off gene = no protein produced
siRNA
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Action of siRNA
dicer
enzyme
mRNA for translation
siRNA
double-stranded
miRNA + siRNA
breakdown
enzyme
(RISC)
mRNA degraded
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functionally
turns gene off
RNA interference
RNAi
http://www.pbs.org/wgbh/nov
a/body/rnai.html
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Andrew Fire
Stanford
Craig Mello
U Mass
1990s | 2006
“for their discovery of
RNA interference —
gene silencing by
double-stranded RNA”
5. Control of translation
Block initiation of translation stage
regulatory proteins attach to 5' end of mRNA
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prevent attachment of ribosomal subunits &
initiator tRNA
block translation of mRNA to protein
Control of Translation
http://www.hhmi.org/biointeractive/tran
slation-advanced-detail
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6-7. Protein processing & degradation
Protein processing
folding, cleaving, adding sugar groups,
targeting for transport
Protein degradation
ubiquitin tagging
proteasome degradation
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Protein
processing movie
1980s | 2004
Ubiquitin
“Death tag”
mark unwanted proteins with a label
76 amino acid polypeptide, ubiquitin
labeled proteins are broken down
rapidly in "waste disposers"
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proteasomes
Aaron Ciechanover
Biology Israel
Avram Hershko
Israel
Irwin Rose
UC Riverside
Proteasome
Protein-degrading “machine”
cell’s waste disposer
breaks down any proteins
into 7-9 amino acid fragments
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cellular recycling
6
7
Gene Regulation
protein
processing &
degradation
1 & 2. transcription
- DNA packing
- transcription factors
5
4
initiation of
translation
mRNA
processing
3 & 4. post-transcription
- mRNA processing
- splicing
- 5’ cap & poly-A tail
- breakdown by siRNA
5. translation
- block start of
translation
1 2
initiation of
transcription
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3
6 & 7. post-translation
- protein processing
- protein degradation
4
mRNA
protection
Epigenetics
For more than a decade, scientists
have had access to a reference
human genome. Now, the
equivalent for the epigenome has
been published, in a collection of
papers appearing on 18 February
in Nature and several other
journals.
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Researchers looked for features including chemical tweaks to
DNA that prime genes to be switched on or off, and alterations
to the 'histone' proteins around which DNA is wrapped.
Chemical or structural modifications to histones can affect which
genes the cellular machinery translates into proteins and which
remain silent. Such epigenetic changes can dramatically affect a
cell’s behaviour and function.
The epigenomes also contain hints of how epigenetic changes
could be involved in diseases, including cancer, Alzheimer's
disease and autoimmune diseases.
Taken together, the work demonstrates how a cell’s epigenome
is complex and exquisitely arranged — just like a Beethoven
symphony.
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Epigenome The Symphony in Your
Cells
Nature Video
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http://www.nature.com/news/epigenome
-the-symphony-in-your-cells-1.16955
Gene Control in Eukaryotes
X-Inactivation
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X-inactivation
Female mammals inherit 2 X chromosomes
one X becomes inactivated during
embryonic development
condenses into compact object = Barr body
which X becomes Barr body is random
patchwork trait = “mosaic”
patches of black
XH
XH Xh
tricolor cats
can only be
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female
Xh
patches of orange
Turn your
Question Genes on!
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2007-2008
Gene Regulation in Eukaryotes
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http://www.hhmi.org/biointeractive/regul
ation-eukaryotic-dna-transcription
6
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Gene Regulation
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3 & 4. _________________
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6 & 7. _________________
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Kim Foglia
As always a huge thank you to Kim for
her most most most excellent work
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