Title: Help needed for the Art
1Help needed for the Art Science Day at the
Chester Street Elementary school 110 Chester St,
Kingston 12- 330 on Tuesday, March 22.
2- Plant Growth Development
- 3 stages
- Embryogenesis
- Fertilization to seed
- Plant Growth Development
- 3 stages
- Embryogenesis
- Fertilization to seed
- 2. Vegetative growth
- Juvenile stage
- Germination to adult
- "phase change" marks transition
- 3. Reproductive development
- Make flowers, can
- reproduce sexually
3Senescence Shoot apical meristem now starts
making new organ flowers, with many new
structures cell types Eventually petals, etc
senesce genetically programmed cell death
controlled by specific genes
4Senescence Eventually petals, etc senesce
genetically programmed cell death controlled by
specific genes Also seen in many other cases
deciduous leaves in fall, annual plants, older
trees
5Senescence Induce specific senescence-associated
genes eg DNAses, proteases, lipases Also seen
during xylem formation when cell wall is
complete cell kills itself
6Senescence Also seen during xylem formation when
cell wall is complete cell kills itself Also seen
as wound response hypersensitive response Cells
surrounding the wound kill themselves
7Senescence Also seen during xylem formation when
cell wall is complete cell kills itself Also seen
as wound response hypersensitive response Cells
surrounding the wound kill themselves Some
mutants do this w/o wound -gt is controlled by
genes!
8- Light regulation of Plant Development
- Plants use light as food and information
- Use information to control development
9- Light regulation of Plant Development
- Plants use light as food and information
- Use information to control development
- germination
10- Light regulation of Plant Development
- Plants use light as food and information
- Use information to control development
- Germination
- Photomorphogenesis vs skotomorphogenesis
11- Light regulation of Plant Development
- Plants use light as food and information
- Use information to control development
- Germination
- Photomorphogenesis vs skotomorphogenesis
- Sun/shade shade avoidance
12- Light regulation of Plant Development
- Germination
- Morphogenesis
- Sun/shade shade avoidance
- Flowering
13- Light regulation of Plant Development
- Germination
- Morphogenesis
- Sun/shade shade avoidance
- Flowering
- Senescence
14- Light regulation of growth
- Plants sense
- Light quantity
15- Light regulation of growth
- Plants sense
- Light quantity
- Light quality (colors)
16- Light regulation of growth
- Plants sense
- Light quantity
- Light quality (colors)
- Light duration
17- Light regulation of growth
- Plants sense
- Light quantity
- Light quality (colors)
- Light duration
- Direction it comes from
18- Light regulation of growth
- Plants sense
- Light quantity
- Light quality (colors)
- Light duration
- Direction it comes from
- Have photoreceptors
- that sense specific
- wavelengths
19- Light regulation of growth
- Early work
- Darwins showed
- blue light controls
- phototropism
20- Light regulation of Plant Development
- Early work
- Darwins blue light controls phototropism
- Duration photoperiodism (Garner and
Allard,1920) - Maryland Mammoth tobacco flowers in the S but not
in N
21- Light regulation of Plant Development
- Early work
- Darwins blue light controls phototropism
- Duration photoperiodism (Garner and
Allard,1920) - Maryland Mammoth tobacco flowers in the S but not
in N - short-day plant (SDP)
22Light regulation of Plant Development Duration
photoperiodism (Garner and Allard,1920) Maryland
Mammoth tobacco flowers in the S but not in N
short-day plant (SDP) Measures night! 30" flashes
during night stop flowers
23Light regulation of growth Duration
photoperiodism (Garner and Allard,1920) Maryland
Mammoth tobacco flowers in the S but not in N
short-day plant (SDP) Measures night! 30" flashes
during night stop flowers LDP plants such as
Arabidopsis need long days to flower
24Light regulation of growth Duration
photoperiodism (Garner and Allard,1920) Maryland
Mammoth tobacco flowers in the S but not in N
short-day plant (SDP) Measures night! 30" flashes
during night stop flowers LDP plants such as
Arabidopsis need long days to flower SDP flower
in fall, LDP flower in spring, neutral flower
when ready
25Light regulation of growth Measures night! 30"
flashes during night stop flowers LDP plants such
as Arabidopsis need long days to flower SDP
flower in fall, LDP flower in spring, neutral
flower when ready Next color matters! Red light
works best for flowering
26Light regulation of growth Next color matters!
Red light (666 nm) works best for flowering for
germination of many seeds!
27Light regulation of growth Next color matters!
Red light (666 nm) works best for flowering for
germination of many seeds! But, Darwins showed
blue works best for phototropism!
28Light regulation of growth Next color matters!
Red light (666 nm)works best for flowering for
germination of many seeds! But, Darwin showed
blue works best for phototropism! Different
photoreceptor!
29Light regulation of growth But, Darwin showed
blue works best for phototropism! Different
photoreceptor! Red light (666 nm) promotes
germination Far red light (gt700 nm) blocks
germination
30Light regulation of growth But, Darwin showed
blue works best for phototropism! Different
photoreceptor! Red light (666 nm) promotes
germination Far red light (gt700 nm) blocks
germination
31Light regulation of growth Red light (666 nm)
promotes germination Far red light (gt700 nm)
blocks germination After alternate R/FR flashes
last flash decides outcome
32Light regulation of growth Red light (666 nm)
promotes germination Far red light (gt700 nm)
blocks germination After alternate R/FR flashes
last flash decides outcome Seeds don't want to
germinate in the shade!
33Light regulation of growth Red light (666 nm)
promotes germination Far red light (gt700 nm)
blocks germination After alternate R/FR color of
final flash decides outcome Seeds don't want to
germinate in the shade! Pigment is
photoreversible
34Light regulation of growth Red light (666 nm)
promotes germination Far red light (730 nm)
blocks germination After alternate R/FR color of
final flash decides outcome Pigment is
photoreversible! -gt helped purify it! Looked for
pigment that absorbs first at 666 nm, then 730
35Phytochrome Red light (666 nm) promotes
germination Far red light (730 nm) blocks
germination After alternate R/FR color of final
flash decides outcome Pigment is photoreversible!
-gt helped purify it! Looked for pigment that
absorbs first at 666 nm, then 730
36Phytochrome Red light (666 nm) promotes
germination Far red light (730 nm) blocks
germination After alternate R/FR color of final
flash decides outcome Pigment is photoreversible!
-gt helped purify it! Looked for pigment that
absorbs first at 666 nm, then 730 Made as
inactive cytoplasmic Pr that absorbs at 666 nm
37Phytochrome Made as inactive cytoplasmic Pr that
absorbs at 666 nm or in blue Converts to active
Pfr that absorbs far red (730nm)
38- Types of Phytochrome Responses
- Two categories based on speed
- Rapid biochemical events
- Morphological changes
39- Types of Phytochrome Responses
- Two categories based on speed
- Rapid biochemical events
- Morphological changes
- Lag time also varies from minutes to weeks
40- Types of Phytochrome Responses
- Two categories based on speed
- Rapid biochemical events
- Morphological changes
- Lag time also varies from minutes to weeks
numbers of steps after Pfr vary
41- Types of Phytochrome Responses
- Lag time also varies from minutes to weeks
numbers of steps after Pfr vary - "Escape time" until a response can no longer be
reversed by FR also varies
42- Types of Phytochrome Responses
- Lag time also varies from minutes to weeks
numbers of steps after Pfr vary - "Escape time" until a response can no longer be
reversed by FR also varies time taken for Pfr to
do its job - Conclusions phytochrome acts on many processes
in many ways
43- Types of Phytochrome Responses
- Two categories based on speed
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2
44- Types of Phytochrome Responses
- Two categories based on speed
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
45- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
- Are not FR-reversible!
46- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
- Are not FR-reversible! But action spectrum same
as Pr
47- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
- Are not FR-reversible! But action spectrum same
as Pr - Induced by FR!
48- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
- Are not FR-reversible! But action spectrum same
as Pr - Induced by FR!
- Obey law of reciprocity
- 1 nmol/m-2 x 100 s
- 100 nmol/m-2 x 1 sec
49- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
- Are not FR-reversible! But action spectrum same
as Pr - Induced by FR!
- Obey law of reciprocity
- 1 nmol/m-2 x 100 s
- 100 nmol/m-2 x 1 sec
- Examples Cab gene
- induction, oat
- coleoptile growth
50- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - Changes 0.02 of Pr to Pfr
- Are not FR-reversible! But action spectrum same
as Pr - Induced by FR!
- Obey law of reciprocity
- 1 nmol/m-2 x 100 s
- 100 nmol/m-2 x 1 sec
- Examples Cab gene
- induction, oat
- coleoptile growth
- 2. LF induced by
- 1 µmol/m-2, saturate _at_
- 1000 µmol/m-2
51- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - Are FR-reversible!
52- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - Are FR-reversible! Need gt 3 Pfr
53- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - Are FR-reversible! Need gt 3 Pfr
- Obey law of reciprocity
54- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - Are FR-reversible! Need gt 3 Pfr
- Obey law of reciprocity
- Examples Lettuce seed
- Germination, mustard
- photomorphogenesis,
- inhibits flowering in SDP
55- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - Are FR-reversible! Need gt 3 Pfr
- Obey law of reciprocity
- Examples Lettuce seed
- Germination, mustard
- photomorphogenesis,
- inhibits flowering in SDP
- 3. HIR require prolonged
- exposure to higher fluence
56- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - 3. HIR require prolonged exposure to higher
fluence - Effect is proportional to
- Fluence
57- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - 3. HIR require prolonged exposure to higher
fluence - Effect is proportional to
- Fluence
- Disobey law of reciprocity
- Are not FR-reversible!
58- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - 3. HIR require prolonged exposure to higher
fluence - Effect is proportional to fluence
- Disobey law of reciprocity
- Are not FR-reversible!
- Some are induced by FR!
59- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - 3. HIR require prolonged exposure to higher
fluence - Effect is proportional to fluence
- Disobey law of reciprocity
- Are not FR-reversible!
- Some are induced by FR!
- Examples inhibition of
- hypocotyl elongation in
- many seedlings,
- Anthocyanin synthesis
60- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - 3. HIR require prolonged exposure to higher
fluence - Effect is proportional to fluence
- Disobey law of reciprocity
- Are not FR-reversible!
- Some are induced by FR!
- Examples inhibition of
- hypocotyl elongation in
- many seedlings,
- Anthocyanin synthesis
- Different responses
- Different phytochromes
61- Types of Phytochrome Responses
- 3 classes based on fluence (amount of light
needed) - VLFinduced by 0.1 nmol/m-2 , saturate _at_
50nmol/m-2 - 2. LF induced by 1 µmol/m-2, saturate _at_ 1000
µmol/m-2 - 3. HIR require prolonged exposure to higher
fluence - Different responses Different phytochromes
- 3 in rice, 5 in Arabidopsis
62- Types of Phytochrome Responses
- Different responses Different phytochromes
- 3 in rice, 5 in Arabidopsis
- PHYA mediates VLF and HIR due to FR
63- Types of Phytochrome Responses
- Different responses Different phytochromes
- 3 in rice, 5 in Arabidopsis
- PHYA mediates VLF and HIR due to FR
- Very labile in light
64- Types of Phytochrome Responses
- Different responses Different phytochromes
- 3 in rice, 5 in Arabidopsis
- PHYA mediates VLF and HIR due to FR
- Very labile in light
- 2. PHYB mediates LF and HIR due to R
- Stable in light
65- Types of Phytochrome Responses
- PHYA mediates VLF and HIR due to FR
- Very labile in light
- 2. PHYB mediates LF and HIR due to R
- Stable in light
- 3. Roles of PHYs C, D E not so clear
66- Types of Phytochrome Responses
- PHYA mediates VLF and HIR due to FR
- Very labile in light
- 2. PHYB mediates LF and HIR due to R
- Stable in light
- 3. Roles of PHYs C, D E not so clear
- PHYA PHYB are often antagonistic.
67- Types of Phytochrome Responses
- PHYA PHYB are often antagonistic.
- In sunlight PHYB mainly controls development
68- Types of Phytochrome Responses
- PHYA PHYB are often antagonistic.
- In sunlight PHYB mainly controls development
- In shade PHYA 1st controls development, since FR
is high
69- Types of Phytochrome Responses
- PHYA PHYB are often antagonistic.
- In sunlight PHYB mainly controls development
- In shade PHYA 1st controls development, since FR
is high - But PHYA is light-labile PHYB takes over stem
grows - "shade-avoidance"
70Phytochrome Pr has cis-chromophore
71Phytochrome Pr has cis-chromophore Red
converts it to trans active shape
72Phytochrome Pr has cis-chromophore Red
converts it to trans active shape Far-red
reverts it to cis
73- Phytochrome
- Pfr is a protein kinase acts by kinasing key
proteins - some stays in cytoplasm activates ion pumps
74- Phytochrome
- Pfr is a protein kinase acts by kinasing key
proteins - some stays in cytoplasm activates ion pumps
- Rapid responses are due to changes in ion fluxes
75- Phytochrome
- Pfr is a protein kinase acts by kinasing key
proteins - some stays in cytoplasm activates ion pumps
- Rapid responses are due to changes in ion fluxes
- Increase growth by activating PM H pump
76- Phytochrome
- Pfr is a protein kinase acts by kinasing key
proteins - some stay in cytoplasm activate ion pumps
- Rapid responses are due to changes in ion fluxes
- most enter nucleus and kinase transcription
factors
77- Phytochrome
- some stay in cytoplasm activate ion pumps
- Rapid responses are due to changes in ion fluxes
- most enter nucleus and kinase transcription
factors - Slow responses are due to changes in gene
expression
78- Phytochrome
- most enter nucleus and kinase transcription
factors - Slow responses are due to changes in gene
expression - Many targets of PHY are transcription factors, eg
PIF3
79- Phytochrome
- most enter nucleus and kinase transcription
factors - Slow responses are due to changes in gene
expression - Many targets of PHY are transcription factors, eg
PIF3 - Activate cascades of genes for photomorphogenesis
80- Phytochrome
- Slow responses are due to changes in gene
expression - Many targets of PHY are transcription factors, eg
PIF3 - Activate cascades of genes for light responses
- Some overlap, and some are unique to each phy
81- Phytochrome
- Slow responses are due to changes in gene
expression - Many targets of PHY are transcription factors, eg
PIF3 - Activate cascades of genes for light responses
- Some overlap, and some are unique to each phy
- 20 of genes are light-regulated
82- Phytochrome
- 20 of genes are light-regulated
- Protein degradation is important for light
regulation
83- Phytochrome
- 20 of genes are light-regulated
- Protein degradation is important for light
regulation - Cop mutants cant degrade specific proteins
84- Phytochrome
- Protein degradation is important for light
regulation - Cop mutants cant degrade specific proteins
- COP1/SPA targets specific transcription factors
for degradation
85- Phytochrome
- Protein degradation is important for light
regulation - Cop mutants cant degrade specific proteins
- COP1/SPA targets specific
- TF for degradation
- DDA1/DET1/COP10 target
- other proteins for degradation
86- Phytochrome
- Protein degradation is important for light
regulation - Cop mutants cant degrade specific proteins
- COP1/SPA targets specific
- TF for degradation
- DDA1/DET1/COP10 target
- other proteins for degradation
- Other COPs form part of
- COP9 signalosome
87- Phytochrome
- Protein degradation is important for light
regulation - Cop mutants cant degrade specific proteins
- COP1/SPA targets specific TF for degradation
- DDA1/DET1/COP10 target other proteins
- Other COPs form part of COP9 signalosome
- W/O COPs these TF act in dark
88- Phytochrome
- COPs target specific TF for degradation
- W/O COPs they act in dark
- In light COP1 is exported to cytoplasm so TF can
act - Tags PHYA by itself on the way out!
89- Other Phytochrome Responses
- In shade avoidance FR stimulates IAA synthesis
from trp! - Occurs in lt 1 hour
90- Other Phytochrome Responses
- In shade avoidance FR stimulates IAA synthesis
from trp! - Occurs in lt 1 hour
- Also occurs in response to endogenous ethylene!
91- Other Phytochrome Responses
- Flowering under short days is controlled via
protein deg - COP CUL4 mutants flower early
92- Other Phytochrome Responses
- Flowering under short days is controlled via
protein deg - COP CUL4 mutants flower early
- Accumulate FT (Flowering locus T) mRNA early
- FT mRNA abundance shows strong circadian rhythm
93- Other Phytochrome Responses
- Circadian rhythms
- Many plant responses, some developmental, some
physiological, show circadian rhythms
94Circadian rhythms Many plant responses, some
developmental, some physiological, show circadian
rhythms Leaves move due to circadian ion fluxes
in/out of dorsal ventral motor cells
95- Circadian rhythms
- Many plant responses show circadian rhythms
- Once entrained, continue in constant dark
96- Circadian rhythms
- Many plant responses show circadian rhythms
- Once entrained, continue in constant dark, or
light
97- Circadian rhythms
- Many plant responses show circadian rhythms
- Once entrained, continue in constant dark, or
light! - Gives plant headstart on photosynthesis, other
processes that need gene expression
98- Circadian rhythms
- Many plant responses show circadian rhythms
- Once entrained, continue in constant dark, or
light! - Gives plant headstart on photosynthesis, other
processes that need gene expression - eg elongation at night!
99- Circadian rhythms
- Gives plant headstart on photosynthesis, other
processes that need gene expression - eg elongate at night!
- Endogenous oscillator is temperature-compensated,
so runs at same speed at all times
100- Circadian rhythms
- Endogenous oscillator is temperature-compensated,
so runs at same speed at all times - Is a negative feedback loop of transcription-trans
lation - Light TOC1 activate LHY CCA1 at dawn
101- Circadian rhythms
- Light TOC1 activate LHY CCA1 at dawn
- LHY CCA1 repress TOC1 in day, so they decline
too
102- Circadian rhythms
- Light TOC1 activate LHY CCA1 at dawn
- LHY CCA1 repress TOC1 in day, so they decline
too - At night TOC1 is activated (not enough LHY
CCA1)
103- Circadian rhythms
- Light TOC1 activate LHY CCA1 at dawn
- LHY CCA1 repress TOC1 in day, so they decline
too - At night TOC1 is activated (not enough LHY
CCA1) - Phytochrome entrains the clock
104Circadian rhythms Light TOC1 activate LHY
CCA1 at dawn LHY CCA1 repress TOC1 in day, so
they decline too At night TOC1 is activated (not
enough LHY CCA1) Phytochrome entrains the clock
So does blue light
105- Blue Light Responses
- Circadian Rhythms
106- Blue Light Responses
- Circadian Rhythms
- Solar tracking
107Blue Light Responses Circadian Rhythms Solar
tracking Phototropism
108Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem elongation
109Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem
elongation Chloroplast movement
110Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem
elongation Chloroplast movement Stomatal opening
111Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem
elongation Chloroplast movement Stomatal
opening Gene expression
112Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem
elongation Chloroplast movement Stomatal
opening Gene expression Flowering in Arabidopsis
113Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem
elongation Chloroplast movement Stomatal
opening Gene expression Flowering in
Arabidopsis Responses vary in their fluence
requirements
114Blue Light Responses Circadian Rhythms Solar
tracking Phototropism Inhibiting stem
elongation Chloroplast movement Stomatal
opening Gene expression Flowering in
Arabidopsis Responses vary in their fluence
requirements lag times
115Blue Light Responses Responses vary in their
fluence requirements lag time Stomatal opening
is reversible by green light others arent
116Blue Light Responses Responses vary in their
fluence requirements lag time Stomatal opening
is reversible by green light others
arent Multiple blue receptors with different
functions!
117Blue Light Responses Responses vary in their
fluence requirements lag time Stomatal opening
is reversible by green light others
arent Multiple blue receptors with different
functions! Identified by mutants
118Blue Light Responses Responses vary in their
fluence requirements lag time Stomatal opening
is reversible by green light others
arent Multiple blue receptors with different
functions! Identified by mutants, then clone the
gene and identify the protein
119Blue Light Responses Responses vary in their
fluence requirements lag time Stomatal opening
is reversible by green light others
arent Multiple blue receptors with different
functions! Identified by mutants, then clone the
gene and identify the protein Cryptochromes
repress hypocotyl elongation
120Blue Light Responses Cryptochromes repress
hypocotyl elongation Stimulate flowering
121Blue Light Responses Cryptochromes repress
hypocotyl elongation Stimulate flowering Set the
circadian clock (in humans, too!)
122Blue Light Responses Cryptochromes repress
hypocotyl elongation Stimulate flowering Set the
circadian clock (in humans, too!) Stimulate
anthocyanin synthesis
123Blue Light Responses Cryptochromes repress
hypocotyl elongation Stimulate flowering Set the
circadian clock (in humans, too!) Stimulate
anthocyanin synthesis 3 CRY genes
124Blue Light Responses 3 CRY genes All have same
basic structure Photolyase-like domain binds FAD
and a pterin (MTHF) that absorbs blue transfers
energy to FAD in photolyase (an enzyme that uses
light energy to repair pyr dimers)
125Blue Light Responses 3 CRY genes All have same
basic structure Photolyase-like domain binds FAD
and a pterin (MTHF) that absorbs blue transfers
energy to FAD in photolyase (an enzyme that uses
light energy to repair pyr dimers) DAS binds COP1
has nuclear localization signals
126Blue Light Responses 3 CRY genes All have same
basic structure Photolyase-like domain binds FAD
and a pterin (MTHF) that absorbs blue transfers
energy to FAD in photolyase (an enzyme that uses
light energy to repair pyr dimers) DAS binds COP1
has nuclear localization signals CRY1 CRY2
kinase proteins after absorbing blue
127Blue Light Responses 3 CRY genes CRY1 CRY2
kinase proteins after absorbing blue CRY3 repairs
mt cp DNA!
128- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - Triggers rapid changes in PM potential growth
129- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - Triggers rapid changes in PM potential growth
- Opens anion channels in PM
130- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - Triggers rapid changes in PM potential growth
- Opens anion channels in PM
- Stimulates anthocyanin synthesis
131- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - Triggers rapid changes in PM potential growth
- Opens anion channels in PM
- Stimulates anthocyanin synthesis
- Entrains the circadian clock
132- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - Triggers rapid changes in PM potential growth
- Opens anion channels in PM
- Stimulates anthocyanin synthesis
- Entrains the circadian clock
- Also accumulates in nucleus interacts with PHY
COP1 to regulate photomorphogenesis, probably
by kinasing substrates
133- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - Triggers rapid changes in PM potential growth
- Opens anion channels in PM
- Stimulates anthocyanin synthesis
- Entrains the circadian clock
- Also accumulates in nucleus interacts with PHY
COP1 to regulate photomorphogenesis, probably
by kinasing substrates - 2. CRY2 controls flowering
134- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - 2. CRY2 controls flowering little effect on
other processes - Light-labile
135- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
light-stable - 2. CRY2 controls flowering little effect on
other processes - Light-labile
- 3. CRY3 enters cp mito, where binds repairs
DNA!
136- Blue Light Responses
- 3 CRY genes
- CRY1 regulates blue effects on growth
- 2. CRY2 controls flowering little effect on
other processes - CRY3 enters cp mito, where binds repairs DNA!
- Cryptochromes are not
- involved in phototropism or
- stomatal opening!
137- Blue Light Responses
- Cryptochromes are not involved in phototropism or
- stomatal opening!
- Phototropins are!
138- Blue Light Responses
- Phototropins are involved in phototropism
stomatal opening! - Many names (nph, phot, rpt) since found by
several different mutant screens
139- Phototropins
- Many names (nph, phot, rpt) since found by
several different mutant screens - Mediate blue light-induced growth enhancements
140- Phototropins
- Many names (nph, phot, rpt) since found by
several different mutant screens - Mediate blue light-induced growth enhancement
blue light-dependent activation of the plasma
membrane H-ATPase in guard cells
141- Phototropins
- Many names (nph, phot, rpt) since found by
several different mutant screens - Mediate blue light-induced growth enhancement
blue light-dependent activation of the plasma
membrane H-ATPase in guard cells - Contain light-activated serine-threonine kinase
domain and LOV1 (light-O2-voltage) and LOV2
repeats
142- Phototropins
- Many names (nph, phot, rpt) since found by
several different mutant screens - Mediate blue light-induced growth enhancement
blue light-dependent activation of the plasma
membrane H-ATPase in guard cells - Contain light-activated serine-threonine kinase
domain and LOV1 (light-O2-voltage) and LOV2
repeats - LOV1 LOV2 bind FlavinMonoNucleotide cofactors
143- Phototropins
- Many names (nph, phot, rpt) since found by
several different mutant screens - Mediate blue light-induced growth enhancement
blue light-dependent activation of the plasma
membrane H-ATPase in guard cells - Contain light-activated serine-threonine kinase
domain and LOV1 (light-O2-voltage) and LOV2
repeats - LOV1 LOV2 bind FlavinMonoNucleotide cofactors
- After absorbing blue rapidly autophosphorylate
kinase other proteins
144- Phototropins
- After absorbing blue rapidly autophosphorylate
kinase other proteins - 1 result phototropism
- due to uneven auxin
- transport
145- Phototropins
- After absorbing blue rapidly autophosphorylate
kinase other proteins - 1 result phototropism
- due to uneven auxin
- transport
- Send more to side away
- from light!
146- Phototropins
- After absorbing blue rapidly autophosphorylate
kinase other proteins - 1 result phototropism
- due to uneven auxin
- transport
- Send more to side away
- from light!
- Phot 1 mediates LF
147- Phototropins
- After absorbing blue rapidly autophosphorylate
kinase other proteins - 1 result phototropism
- due to uneven auxin
- transport
- Send more to side away
- from light!
- PHOT 1 mediates LF
- PHOT2 mediates HIR
148- Phototropins
- 2nd result stomatal opening via stimulation of
guard cell PM proton pump - Also requires photosynthesis by guard cells!
149- Phototropins
- 2nd result stomatal opening via stimulation of
guard cell PM proton pump - Also requires photosynthesis by guard cells
signaling from xanthophylls
150- Phototropins
- 2nd result stomatal opening via stimulation of
guard cell PM proton pump - Also requires photosynthesis by guard cells
signaling from xanthophylls - npq mutants dont
- make zeaxanthin
- lack specific blue
- response
151- Phototropins
- 2nd result stomatal opening via stimulation of
guard cell PM proton pump - Also requires photosynthesis by guard cells
signaling from xanthophylls - npq mutants dont
- make zeaxanthin
- lack specific blue
- response
- Basic idea open when pump in K
152- Phototropins
- 2nd result stomatal opening via stimulation of
guard cell PM proton pump - Also requires photosynthesis by guard cells
signaling from xanthophylls - npq mutants dont
- make zeaxanthin
- lack specific blue
- response
- Basic idea open when pump in K
- Close when pump out K
153- Phototropins
- Basic idea open when pump in K
- Close when pump out K
- Control is hideously complicated!
154- Phototropins
- Basic idea open when pump in K
- Close when pump out K
- Control is hideously complicated!
- Mainly controlled by blue light
155- Phototropins
- Basic idea open when pump in K
- Close when pump out K
- Control is hideously complicated!
- Mainly controlled by blue light, but red also
plays role
156- Phototropins
- Basic idea open when pump in K
- Close when pump out K
- Control is hideously complicated!
- Mainly controlled by blue light,
- but red also plays role
- Light intensity is also important
157- Phototropins
- Mainly controlled by blue light, but red also
plays role - Light intensity is also important due to effect
on - photosynthate in guard cells
158- Phototropins
- Mainly controlled by blue light, but red also
plays role - Light intensity is also important due to effect
on - photosynthate in guard cells
- PHOT1 2 also help
159- Phototropins
- Mainly controlled by blue light, but red also
plays role - Light intensity is also important due to effect
on - photosynthate in guard cells
- PHOT1 2 also help
- Main GC blue
- receptor is zeaxanthin!
160- Phototropins
- Mainly controlled by blue light, but red also
plays role - Light intensity is also important due to effect
on - photosynthate in guard cells
- PHOT1 2 also help
- Main GC blue
- receptor is zeaxanthin!
- Reason for green reversal
161- Phototropins
- Mainly controlled by blue light, but red also
plays role - Light intensity is also important due to effect
on - photosynthate in guard cells
- PHOT1 2 also help
- Main GC blue
- receptor is zeaxanthin!
- Reason for green reversal
- water stress overrides light!
162- Phototropins
- water stress overrides light roots make Abscisic
Acid closes stomates blocks opening regardless
of other signals!