Chapter 39 Presentation-Plant Responses to Internal and External
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Transcript Chapter 39 Presentation-Plant Responses to Internal and External
Chapter 39
Plant Responses to Internal and
External Signals
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Response to Stimuli
Plants are sensitive to a wide range of
stimuli.
They elicit a response.
They use a signal transduction pathway.
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Response to Stimuli
Consider a forgotten
potato in the cupboard.
The eyes of the potato
(axillary buds) sprout
shoots that are suited to
their function. They are
pale and lack broad
green leaves. They lack
elongated roots.
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Etiolation
These adaptations for growing in the
dark are called etiolation.
The “stimulus” for growth is complete
darkness.
The plant uses all energy to elongation
of the stem so the leaves can open after
reaching the surface.
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Etiolation
During etiolation, there is no evaporative
loss of water.
Leaves would be a hindrance to the
shoot passing through the soil.
There’s no need for chlorophyll--there’s
no light.
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De-etiolation
When the shoot hits
the light, de-etiolation
occurs.
Leaves now expand.
Elongation of the
stem slows.
Roots elongate.
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Signal Reception
Signals are detected by receptors.
Proteins change in response to the
stimulus.
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Signal Transduction
Second messengers are small, internally
produced chemicals.
They transfer and amplify signals from the
receptor to the other proteins causing a
response.
One signal receptor protein can give rise to
hundreds of specific enzymes.
In this way, 2nd messenger signal
transduction leads to rapid amplification of the
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signal
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Response
Signal transduction leads to one or more
cellular pathways being regulated.
Usually, this leads to an increase in the
activity of certain enzymes.
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Response: 2 Main Mechanisms
1. Stimulating transcription of mRNA.
2. Activating existing enzyme
molecules.
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1. Stimulating Transcription of
mRNA
This is called transcriptional regulation.
These transcription factors bind directly
to DNA molecules and control the
transcription of specific genes.
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The De-etiolation Response and
Phytochrome
The receptor involved in de-etiolation is
a phytochrome.
The mutant tomato studied has lower
levels of phytochrome.
They green less when exposed to light
than normal tomatoes.
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The De-etiolation Response and
Phytochrome
When the mutants were injected with
phytochrome from other plants they
exhibited a normal de-etiolation
response when exposed to light.
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The De-etiolation Response and
Phytochrome
Small amounts of light can trigger the
de-etiolation response.
In the phytochrome example, small
amounts of light give rise to activated
phytochrome.
This gives rise to hundreds of second
messenger molecules which leads to
hundreds of activated
enzymes.
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The Change in Phytochrome
Light causes the conformation of phytochrome to
change.
This leads to an increase in cGMP (2nd messenger)
and Ca2+ influx.
cGMP activates protein kinases.
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If we inject the mutant tomatoes with
cGMP, we get a partial de-etiolation
response--even without the addition of
phytochrome.
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Protein kinases are activated by cGMP
and Ca2+, and can act to phosphorylate
and activate other enzymes.
These can be used to stimulate or shut
down transcription.
When transcription is affected, the
enzymes can now synthesize proteins
for chlorophyll production and other detravismulthaupt.com
greening proteins.
The mechanism by which a signal
promotes a new developmental course
depends on the activation of positive or
negative control factors.
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Post-translational modification involves
activating existing enzyme molecules.
This is where existing proteins are
modified--usually via phosphorylation.
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Kinases
Often, kinases become activated by
phosphorylation which activates more
kinases, and so on.
Eventually, the cascades link initial
stimuli to responses at the gene level
where they are expressed.
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Signal Pathways
Signal pathways lead to both a turning
on and off of genes.
For example, putting a potato back into
the cupboard activates many
phosphatases which dephosphorylate
specific proteins and switch off certain
pathways.
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The Idea of Signal Pathways
Classic experiments studying grass
uncovered the notion of chemical
messengers.
The movement of a plant shoot toward
or away from a stimulus is called
tropism.
The hormone pathway.
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Signal Pathways and Grass
Seedlings
Phototropism is the process
that directs plants toward
sunlight for photosynthesis.
Grass shoots kept in the
dark will grow straight up.
So will those illuminated
equally on all sides.
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Signal Pathways and Grass
Seedlings
If illuminated from only one side, the plant will grow
toward the stimulus.
This results in differential growth on the opposite side
of the stimulus.
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The Darwins’ Experiments
Observations:
Plants will only bend toward the light
source if the coleoptile is present--no tip, no
curve.
Covering the tip with an opaque cap
prevents curving.
Covering the tip with a transparent cap or
placing a cover below the tip--curving.
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The Darwins’ Experiments
Their conclusions:
The tip of the coleoptile is responsible
for curvature.
Also, the curvature of the plant actually
was the result of differential growth
some distance below the coleoptile.
Some signal must be responsible for
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elongation of the
coleoptile.
Peter Boysen-Jensen
A few decades later:
He separated the tip
of the coleoptile with
a block of gelatin.
The cells still showed
the normal growth
response.
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Peter Boysen-Jensen
Using mica, there
was no response.
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Frits Went
A Dutchman that modified BoysenJensen’s experiment to extract the
chemical messenger.
He removed the coleoptile tip and placed
it on an agar block.
If the messenger could diffuse into the
block, then it could be substituted for the
tip and placed on the decapitated
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coleoptile resulting
in normal growth.
Frits Went
Results:
Decapitated
coleoptile--no
growth.
Decapitated
coleoptile + agar
only--no growth.
Decapitated
coleoptile + agar with
hormones--growth. travismulthaupt.com
Frits Went
Also, placing the block on one side of
the coleoptile or the other caused
unequal growth on the side containing
the block causing curvature in the
opposite direction.
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Frits Went
Conclusions:
The plants curved due to the higher
concentration of growth promoting chemical
on the dark side of the plant.
Went named this hormone auxin.
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Went’s Model
This model doesn’t necessarily occur in
all plants.
There is still an unequal distribution of
auxin in a plant causing curvature.
Some plants show an increase in growth
inhibitors on the light side of the plant.
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Plant Hormones
There are many different classes of plant
hormones.
They all have different effects on plants.
Most are produced in very small
amounts and often have profound
effects on the plant.
The hormones are often amplified and
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acts to alter gene
expression.
3 Common Plant Hormones
Auxin-stimulate growth. Produced in the
embryo, growth tissue, and meristematic
tissue.
Gibberillins--produced in the apical
meristems of buds and roots, young
leaves and embryos.
Ethylene--promotes ripening. Opposes
auxin.
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Light
Light is an important environmental
factor in the growth and development of
plants.
Photomorphogenesis is the effect of light
on plant morphology.
The ability of a plant to perceive light
allows plants to measure the passage of
days and seasons.
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Circadian Rhythms
Common to all eukaryotic life, and is not
governed by an known environmental
factor.
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Photoperiodism
Is the physiological response of plant
due to a change in the lengths of night
and day--a photoperiod.
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Different Types of Plants
There are 3 general varieties of plants
classified according to their light
requirements for flowering:
1. Short-day plants
2. Long-day plants
3. Day-neutral plants.
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Short-Day Plants
Respond the long nights.
A.k.a. long-night plants.
They usually flower in the late summer,
fall, or winter as the light period is
shorter than 14 hours.
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Long-Day Plants
Respond to short nights.
A.k.a. short-night plants.
They flower when the light period is
longer than 14 hours.
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Day-Neutral Plants
These are unaffected by the light period,
and flower when they reach maturity.
Tomatoes, rice, and dandelions.
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Classic Experiments
In the 1940’s scientists began
experimenting with photoperiods.
They looked at the length of the night
and day.
They found that short-day plants flower
when days are 16 hours or shorter
(nights are 8 hours or longer).
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Classic Experiments
In the short-day plants, they looked at
flowering:
They found that if the daytime portion of
photoperiod is broken by a brief period of
darkness, there is no effect.
However, if the nighttime portion of the
photoperiod is interrupted by a short period
of dim light, the plant doesn’t flower.
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Classic Experiments
The opposite is true for long-day plants:
When long day plants are grown in a
photoperiod of a long night, flower doesn’t
occur.
However, if the long night portion of the
experiment is interrupted by a brief period
of dim light, flowering will occur.
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From These Experiments
Red light is most effective at interrupting
the nighttime portion of the photoperiod.
Scientists have demonstrated that
phytochrome is the pigment that
measures the photoperiod.
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Extending the Experiments
Scientists at the USDA conducted these
experiments.
Phytochrome was demonstrated to be
the pigment responsible for seed
germination.
From this, they were able to elucidate
the flowering cycle.
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USDA Flowering Experiments
Seeds were subjected to a variety of
monochromatic light.
Red and far-red light opposed each
other in their germinating ability.
One induced germination, the other
inhibited it.
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USDA Flowering Experiments
It was determined that the two different
forms of light switched the phytochrome
back and forth between two isomeric
forms.
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USDA Flowering Experiments
One form caused seed germination, the
other inhibited the germination response.
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USDA Flowering Experiments
The question: How do plants in nature
illicit a response to light and begin
germination?
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USDA Flowering Experiments
If seeds are kept in the dark, they synthesize
Pr.
When seeds are illuminated with sunlight, they
begin to be converted to Pfr.
The appearance of Pfr is one of the ways
plants detect sunlight.
Adequate sunlight converts Pr to Pfr and
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triggers germination.
USDA Flowering Experiments
In the flowering response, scientists
were able to show the effects of the red
and far red light on the flowering ability
in plants.
Again, the 2 forms of light canceled each
other.
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Other Stimuli
There are also a wide variety of stimuli
other than light that effects plant growth.
Gravity, mechanical stimuli, and
environmental stress also play a role in
plant growth and development.
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