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Help needed for the Art & Science Day at the Chester Street Elementary school 110 Chester St, Kingston 12- 3:30 on Tuesday, March 22.

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Presentation on theme: "Help needed for the Art & Science Day at the Chester Street Elementary school 110 Chester St, Kingston 12- 3:30 on Tuesday, March 22."— Presentation transcript:

1 Help needed for the Art & Science Day at the Chester Street Elementary school 110 Chester St, Kingston 12- 3:30 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

3 Senescence 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

4 Senescence 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

5 Senescence Induce specific senescence-associated genes ; eg DNAses, proteases, lipases Also seen during xylem formation: when cell wall is complete cell kills itself

6 Senescence 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

7 Senescence 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 -> 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)

22 Light 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

23 Light 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

24 Light 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

25 Light 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

26 Light regulation of growth
Next : color matters! Red light (666 nm) works best for flowering & for germination of many seeds!

27 Light 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!

28 Light 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!

29 Light regulation of growth
But, Darwin showed blue works best for phototropism! Different photoreceptor! Red light (666 nm) promotes germination Far red light (>700 nm) blocks germination

30 Light regulation of growth
But, Darwin showed blue works best for phototropism! Different photoreceptor! Red light (666 nm) promotes germination Far red light (>700 nm) blocks germination

31 Light regulation of growth
Red light (666 nm) promotes germination Far red light (>700 nm) blocks germination After alternate R/FR flashes last flash decides outcome

32 Light regulation of growth
Red light (666 nm) promotes germination Far red light (>700 nm) blocks germination After alternate R/FR flashes last flash decides outcome Seeds don't want to germinate in the shade!

33 Light regulation of growth
Red light (666 nm) promotes germination Far red light (>700 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

34 Light 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! -> helped purify it! Looked for pigment that absorbs first at 666 nm, then 730

35 Phytochrome 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! -> helped purify it! Looked for pigment that absorbs first at 666 nm, then 730

36 Phytochrome 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! -> helped purify it! Looked for pigment that absorbs first at 666 nm, then 730 Made as inactive cytoplasmic Pr that absorbs at 666 nm

37 Phytochrome 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2

44 Types of Phytochrome Responses
Two categories based on speed 3 classes based on fluence (amount of light needed) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 Changes 0.02% of Pr to Pfr

45 Types of Phytochrome Responses
3 classes based on fluence (amount of light needed) VLF:induced by 0.1 nmol/m-2 , 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) VLF:induced by 0.1 nmol/m-2 , 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) VLF:induced by 0.1 nmol/m-2 , 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) VLF:induced by 0.1 nmol/m-2 , 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) VLF:induced by 0.1 nmol/m-2 , 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) VLF:induced by 0.1 nmol/m-2 , 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, 1000 µmol/m-2

51 Types of Phytochrome Responses
3 classes based on fluence (amount of light needed) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, µmol/m-2 Are FR-reversible!

52 Types of Phytochrome Responses
3 classes based on fluence (amount of light needed) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, µmol/m-2 Are FR-reversible! Need > 3% Pfr

53 Types of Phytochrome Responses
3 classes based on fluence (amount of light needed) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, µmol/m-2 Are FR-reversible! Need > 3% Pfr Obey law of reciprocity

54 Types of Phytochrome Responses
3 classes based on fluence (amount of light needed) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, µmol/m-2 Are FR-reversible! Need > 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, µmol/m-2 Are FR-reversible! Need > 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, 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) VLF:induced by 0.1 nmol/m-2 , 50nmol/m-2 2. LF: induced by 1 µmol/m-2, 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"

70 Phytochrome Pr has cis-chromophore

71 Phytochrome Pr has cis-chromophore Red converts it to trans = active shape

72 Phytochrome 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 can’t degrade specific proteins

84 Phytochrome Protein degradation is important for light regulation Cop mutants can’t degrade specific proteins COP1/SPA targets specific transcription factors for degradation

85 Phytochrome Protein degradation is important for light regulation Cop mutants can’t 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 can’t 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 can’t 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 < 1 hour

90 Other Phytochrome Responses
In shade avoidance FR stimulates IAA synthesis from trp! Occurs in < 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

94 Circadian 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-translation 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

104 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 So does blue light

105 Blue Light Responses Circadian Rhythms

106 Blue Light Responses Circadian Rhythms Solar tracking

107 Blue Light Responses Circadian Rhythms Solar tracking Phototropism

108 Blue Light Responses Circadian Rhythms Solar tracking Phototropism Inhibiting stem elongation

109 Blue Light Responses Circadian Rhythms Solar tracking Phototropism Inhibiting stem elongation Chloroplast movement

110 Blue Light Responses Circadian Rhythms Solar tracking Phototropism Inhibiting stem elongation Chloroplast movement Stomatal opening

111 Blue Light Responses Circadian Rhythms Solar tracking Phototropism Inhibiting stem elongation Chloroplast movement Stomatal opening Gene expression

112 Blue Light Responses Circadian Rhythms Solar tracking Phototropism Inhibiting stem elongation Chloroplast movement Stomatal opening Gene expression Flowering in Arabidopsis

113 Blue 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

114 Blue 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

115 Blue Light Responses Responses vary in their fluence requirements & lag time Stomatal opening is reversible by green light; others aren’t

116 Blue Light Responses Responses vary in their fluence requirements & lag time Stomatal opening is reversible by green light; others aren’t Multiple blue receptors with different functions!

117 Blue Light Responses Responses vary in their fluence requirements & lag time Stomatal opening is reversible by green light; others aren’t Multiple blue receptors with different functions! Identified by mutants

118 Blue Light Responses Responses vary in their fluence requirements & lag time Stomatal opening is reversible by green light; others aren’t Multiple blue receptors with different functions! Identified by mutants, then clone the gene and identify the protein

119 Blue Light Responses Responses vary in their fluence requirements & lag time Stomatal opening is reversible by green light; others aren’t Multiple blue receptors with different functions! Identified by mutants, then clone the gene and identify the protein Cryptochromes repress hypocotyl elongation

120 Blue Light Responses Cryptochromes repress hypocotyl elongation Stimulate flowering

121 Blue Light Responses Cryptochromes repress hypocotyl elongation Stimulate flowering Set the circadian clock (in humans, too!)

122 Blue Light Responses Cryptochromes repress hypocotyl elongation Stimulate flowering Set the circadian clock (in humans, too!) Stimulate anthocyanin synthesis

123 Blue Light Responses Cryptochromes repress hypocotyl elongation Stimulate flowering Set the circadian clock (in humans, too!) Stimulate anthocyanin synthesis 3 CRY genes

124 Blue 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)

125 Blue 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

126 Blue 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

127 Blue 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 don’t 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 don’t 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 don’t 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!


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