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Plant defense responses Hypersensitive response

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Presentation on theme: "Plant defense responses Hypersensitive response"— Presentation transcript:

1 Plant defense responses Hypersensitive response
Prepare a 10’ talk for Friday March 22 on plant defenses or describe interactions between plants & pathogens, pests or symbionts Plant defense responses Hypersensitive response Systemic acquired resistance Innate immunity Phytoalexins Defensins Oxidative burst Some possible pests Nematodes Rootworms Aphids Thrips Gypsy moths hemlock woolly adelgid Some possible pathogens Agrobacterium tumefaciens Agrobacterium rhizogenes Pseudomonas syringeae Pseudomonas aeruginosa Viroids DNA viruses RNA viruses Fungi Oomycetes Some possible symbionts N-fixing bacteria N-fixing cyanobacteria Endomycorrhizae Ectomycorrhizae Burkholderia ambifaria

2 Light regulation of Plant Development
Plants use light as food and information Use information to control development

3 Light regulation of growth
Plants sense Light quantity Light quality (colors) Light duration Direction it comes from Have photoreceptors that sense specific wavelengths

4 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

5 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

6 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"

7 Phytochrome Pr has cis-chromophore Red converts it to trans = active shape Far-red reverts it to cis

8 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

9 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

10 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

11 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

12 Circadian rhythms Many plant responses show circadian rhythms Once entrained, continue in constant dark

13 Circadian rhythms Many plant responses show circadian rhythms Once entrained, continue in constant dark, or constant light

14 Circadian rhythms Many plant responses show circadian rhythms Once entrained, continue in constant dark, or constant light! Gives plant headstart on photosynthesis, other processes that need gene expression

15 Circadian rhythms Many plant responses show circadian rhythms Once entrained, continue in constant dark, or constant light! Gives plant headstart on photosynthesis, other processes that need gene expression eg elongation at night!

16 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

17 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

18 Circadian rhythms Light & TOC1 activate LHY & CCA1 at dawn LHY & CCA1 repress TOC1 in day, so they decline too

19 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)

20 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

21 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

22 Blue Light Responses Circadian Rhythms

23 Blue Light Responses Circadian Rhythms Solar tracking

24 Blue Light Responses Circadian Rhythms Solar tracking Phototropism

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

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

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

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

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

30 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

31 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

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

33 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!

34 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

35 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

36 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

37 Blue Light Responses Cryptochromes repress hypocotyl elongation Stimulate flowering

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

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

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

41 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)

42 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

43 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

44 Blue Light Responses 3 CRY genes CRY1 & CRY2 kinase proteins after absorbing blue CRY3 repairs mt & cp DNA!

45 Blue Light Responses 3 CRY genes CRY1 regulates blue effects on growth: light-stable Triggers rapid changes in PM potential & growth

46 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

47 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


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