Arabidopsis Experiments

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Arabidopsis Arabidopsis Experiments Experiments Forward Genetic Screen (Ethylene Insensitive Mutants) Forward Genetic Screen (Ethylene Insensitive Mutants) Reverse Genetic Screen / PCR Genotyping (H Reverse Genetic Screen / PCR Genotyping (H + - ATPase Mutants) - ATPase Mutants)

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Arabidopsis Experiments. Forward Genetic Screen (Ethylene Insensitive Mutants) Reverse Genetic Screen / PCR Genotyping (H + - ATPase Mutants). Arabidopsis. - PowerPoint PPT Presentation

Transcript of Arabidopsis Experiments

Page 1: Arabidopsis  Experiments

ArabidopsisArabidopsis Experiments ExperimentsForward Genetic Screen (Ethylene Insensitive Mutants)Forward Genetic Screen (Ethylene Insensitive Mutants)

Reverse Genetic Screen / PCR Genotyping (HReverse Genetic Screen / PCR Genotyping (H++- ATPase Mutants)- ATPase Mutants)

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ArabidopsisArabidopsis

AArabidopsis thalianarabidopsis thaliana is the predominant model organism used by is the predominant model organism used by plant biologists today. Considered a “weed" in nature, this small plant biologists today. Considered a “weed" in nature, this small mustard serves as an experimental subject for everything from root mustard serves as an experimental subject for everything from root growth to flower development in the laboratory. growth to flower development in the laboratory. ArabidopsisArabidopsis has has gained prominence as a model organism for several reasons: gained prominence as a model organism for several reasons: 

Generation timeGeneration time. Seed to seed in about 42 days.. Seed to seed in about 42 days. FecundFecund. One . One ArabidopsisArabidopsis plant yields thousands of seeds. plant yields thousands of seeds. Genome sizeGenome size. 125 . 125 mmegaegabbases. Maize has 5000 mb, tobacco1500 mb.ases. Maize has 5000 mb, tobacco1500 mb. DiploidDiploid. Relatively simple genome.. Relatively simple genome. TractableTractable. Easily worked and amenable to genetic, molecular genetic, . Easily worked and amenable to genetic, molecular genetic,

physiological and biochemical studies.physiological and biochemical studies. Real plantReal plant. Roots, leaves, flowers, seeds, and a full component of . Roots, leaves, flowers, seeds, and a full component of

physiological and biochemical processes. physiological and biochemical processes.

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ArabidopsisArabidopsis HistoryHistory

LinnaeusLinnaeus

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Forward vs. Reverse Forward vs. Reverse GeneticsGenetics

Treat thousands of organisms with a mutagen,Treat thousands of organisms with a mutagen,

- random mutagenesis, - random mutagenesis,

Identify an Identify an individualindividual with a with a phenotypephenotype of interest, of interest,

Identify the gene. Identify the gene.

• Treat thousands of organisms with a mutagen (usually),Treat thousands of organisms with a mutagen (usually),

– random mutagenesis, random mutagenesis,

• Identify an Identify an individualindividual with a with a genotypegenotype of interest, of interest,

• Identify the phenotype. Identify the phenotype.

Forward

Reverse

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EthyleneEthylene“the gaseous “the gaseous

hormone”hormone”

Egyptians gassed figs in Egyptians gassed figs in order to stimulate ripening, order to stimulate ripening,

The ancient Chinese burned The ancient Chinese burned incense in closed rooms to incense in closed rooms to enhance the ripening of enhance the ripening of pears.pears.

In 1864, gas leaks from In 1864, gas leaks from street lights were observed street lights were observed to stunt plant growth, twist to stunt plant growth, twist plants, and abnormally plants, and abnormally thicken stems thicken stems

Dimitry Neljubow (1901) Dimitry Neljubow (1901) showed that the active showed that the active component was ethylene. component was ethylene.

R. Gane (1934) reported R. Gane (1934) reported that plants synthesize that plants synthesize ethylene.ethylene.

HH22C = CHC = CH22

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Receptor Receptor enzyme-linked receptorenzyme-linked receptor

…found first in bacteria, then in plants, now in most eukaryotes, including mammals.

Two-component regulators.Two-component regulators.

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EthyleneEthylene…promotes fruit …promotes fruit

ripening,ripening,

Ethylene signals the Ethylene signals the transition from transition from unripe to ripe fruits,unripe to ripe fruits,

cell wall cell wall components are components are broken down,broken down,

starches and acids starches and acids are broken down are broken down resulting in resulting in “sweetening” and “sweetening” and aromatic aromatic compounds ,compounds ,

pigmentation may pigmentation may also be induced.also be induced.

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ACC: 1-aminocyclopropane-1-carboxylate

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EthyleneEthylene…promotes the “triple …promotes the “triple

response”,response”,

……in etiolated seedlings,in etiolated seedlings,

reduced stem reduced stem elongation,elongation,

thicker stem, thicker stem,

horizontal growth,horizontal growth,

May provide the plant May provide the plant with “behavior” that with “behavior” that will provide escape will provide escape from soil from soil impediments.impediments.

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EthyleneEthylene…mutant analysis,…mutant analysis,

wild typewild type einein

ein ein (ethylene present),(ethylene present),

……eethylene thylene ininsensitive.sensitive.

wild typewild type

ctr ctr (ethylene absent),(ethylene absent),

……cconstitutiveonstitutive t triple riple rresponse.esponse.

ctrctr

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Ethylene Signal Ethylene Signal TransductionTransduction

…negative regulation.…negative regulation.

Tricky Concept(s)Tricky Concept(s)

In the absence of ethylene, the In the absence of ethylene, the enzyme receptor activates enzyme receptor activates CTR1,CTR1,

active CTR1 active CTR1 inhibitsinhibits the triple the triple response, response,

With ethylene present, or the With ethylene present, or the receptor “absent”, or the receptor “absent”, or the CTR1CTR1 or the gene mutated, or the gene mutated,

the triple response is activated.the triple response is activated.

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ein, etr, etc,

…blocks pathway.

ethylene,

…or ctr mutant,

no ethylene

…no triple response.

active

inactive

induces transcription,erf: ethylene response

factor.

?

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Friday’s WorkFriday’s Work

Sterilizing/PlantingSterilizing/Planting GerminatingGerminating

Breaking DormancyBreaking Dormancy  

HH22O/Imbibition, O/Imbibition, 

OO22/Aeration,  /Aeration,  

Cold/Prechilling Cold/Prechilling "stratification” "stratification” 

Inducing GerminationInducing Germination  

LightLight

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Conditional ScreenConditional Screen

Grow on ACC,Grow on ACC,

……in the dark in the dark (etiolated).(etiolated).

Score for mutants,Score for mutants,

Transfer to 0.5X MS Transfer to 0.5X MS (Murisige and (Murisige and Skoog) media (-Skoog) media (-ACC),ACC),

Grow in light.Grow in light.

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What Next?What Next?

Backcross to wild-type,Backcross to wild-type,

what might the F1 and what might the F1 and F2 tell us?F2 tell us?

Complementation Complementation tests?tests?

dominantdominant

recessiverecessive

Thought Experiments…Thought Experiments…

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Proton Pumps Proton Pumps in plantain planta

Stemstransport; sucrose hormones Leaves

stomata (gas exchange)sucrose transport

Antherscell elongation

Pollentip growth

Embryo/SeedsloadingRoots

root hair growthmineral uptake

Arabidopsis

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Adapted from Biochemistry and Molecular Biology of Plants, pp. 115

H+ (protons) ATP synthase

ATP hydrolase (ATPase)

Transporters

- carriers, - channels.

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Arabidopsis Arabidopsis GenomeGenome

~125 Mb (Megabases, million base pairs),~125 Mb (Megabases, million base pairs),

Rice: 420 Mb, Human: 3 Gb,Rice: 420 Mb, Human: 3 Gb,

25,498 genes from 11,000 gene families,25,498 genes from 11,000 gene families, Rice: 32,000 - 50,000, Human: 25,000 - 66,000.Rice: 32,000 - 50,000, Human: 25,000 - 66,000.

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ArabidopsisArabidopsis Experiments ExperimentsForward Genetic Screen (Ethylene Insensitive Mutants)

Reverse Genetic Screen / PCR Genotyping (HReverse Genetic Screen / PCR Genotyping (H++- ATPase Mutants)- ATPase Mutants)

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Proton Pumps Proton Pumps in plantain planta

Stemstransport; sucrose hormones Leaves

stomata (gas exchange)sucrose transport

Antherscell elongation

Pollentip growth

Embryo/SeedsloadingRoots

root hair growthmineral uptake

Arabidopsis

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Gene Location FunctionAHA1 whole plant ?AHA2 root cortex ?AHA3 phloem ?AHA4 root endodermis nutrient uptakeAHA5 whole plant ?AHA6 - ?AHA7 - ?AHA8 - ?AHA9 anthers ?

AHA10 seeds ?AHA11 hypocotyl ?AHA12 - psuedogene

Arabidopsis H+-ATPase

Gene Family

Phylogenetic Family Tree(ClustalW --> Phylip: protdist, fitch)

Baxter et al. , Plant Physiol, 123, (2003)

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Reverse GeneticsReverse GeneticsFunctional GenomicsFunctional Genomics

Gene DNASequence

Gene Disruption PhenotypeAnalysis

Function

MutateDNA Sequence

DevelopmentPhysiology

Cell BiologyGenetically Link

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Agrobacterium

Plant Cells

NatureTi-Plasmid T-DNA

HormonesOpines

Lab

Selectable MarkersReporter Genes

Genes

Out: Ti genes, opine genes,

In: DNA of choice.

T-DNA

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wtwtplantplantchromosomechromosome

Ti PlasmidTi Plasmid(from (from agroagro))

hormone genes (i.e. auxins)hormone genes (i.e. auxins)

opalineopaline

nopalinenopaline

virulencevirulencegenesgenes

virulencevirulencegenesgenes

hormone geneshormone genes

opaline, nopalineopaline, nopaline

neoplastic transformationneoplastic transformation

Agrobacterium tumefaciensAgrobacterium tumefaciensTi Plasmid (Ti Plasmid (TTumor umor iinducing)nducing) Mother NatureMother Nature

AgroAgrofoodfood

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Construct T-DNAConstruct T-DNA

selection genesselection genes

virulencevirulencegenesgenes

infect plant, select for plants with T-DNAinfect plant, select for plants with T-DNA

T-DNA (T-DNA (TTransfer DNA)ransfer DNA)LaboratoryLaboratory

transform, select for transform, select for agroagro with T-DNA with T-DNA

AgrobacteriumAgrobacterium

……if the T-DNA lands in a gene, the gene is disrupted. if the T-DNA lands in a gene, the gene is disrupted.

……can put other genes.can put other genes.

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To DoTo DoGerminationGermination Breaking DormancyBreaking Dormancy  

HH22O/Imbibition, O/Imbibition, 

OO22/Aeration, /Aeration,

Cold/Prechilling Cold/Prechilling "scarification”  "scarification”  

Inducing Inducing GerminationGermination  

LightLight

Surface Sterilize Seeds Surface Sterilize Seeds Plant on Nutrient MediaPlant on Nutrient MediaGerminateGerminate

1. EMS Treated Seeds on 1. EMS Treated Seeds on MS/ACC media.MS/ACC media.

2. 2. aha3-1aha3-1 on MS media. on MS media.

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Probability of Finding an Insert in a Specific Probability of Finding an Insert in a Specific GeneGene

thousands of insertsthousands of inserts

p = 1-(1-f)p = 1-(1-f)nn

p = probability of insertion eventp = probability of insertion event

f = 1-(Genome/Size of Gene)f = 1-(Genome/Size of Gene)

n = number of T-DNA insertsn = number of T-DNA inserts

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KnockologyKnockology

Plants/Pools DNA/Pools

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Set-UpSet-UpDNA PoolingDNA Pooling

Seeds (9)

Seedlings

(225)

DNA (225)

1 2 3 4 5 6 …30SuperPools(2025)

Germinate and grow seeds in liquid culture.

Extract DNA,

Super Pool DNA,

Maintain lines as pools of seed.

PCR Screen

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94o

3’--CGTACGTAATACGATGTAGCTGTAGCTGATCGTGAC--5’

5’--GCATGCATTAGGCTACATCGACATCGACTAGCACTG--3’

5’--GCATGCATTAT

CTGATCGTGAC--5’

Denature Step~30 seconds

~65o

3’--CGTACGTAATACGATGTAGCTGTAGCTGATCGTGAC--5’

5’--GCATGCATTAGGCTACATCGACATCGACTAGCACTG--3’

5’--GCATGCATTAT

CTGATCGTGAC--5’

Annealing Step~30 seconds

72o

3’--CGTACGTAATACGATGTAGCTGTAGCTGATCGTGAC--5’

5’--GCATGCATTAGGCTACATCGACATCGACTAGCACTG--3’

5’--GCATGCATTAT

CTGATCGTGAC--5’

5’--GCATGCATTAGGCTACATCGACATCGACTAGCACTG--3’

3’--GCTACGTAATCCGATGTAGCTGTAGCTGATCGTGAC--5’

5’--GCATGCATTAGGCTACATCGACATCGACTAGCACTG--3’

3’--GCTACGTAATCCGATGTAGCTGTAGCTGATCGTGAC--5’

Synthesis~1 minute/kb

PCR

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PCR StrategyPCR Strategy

5’ 3’

PPolymerase olymerase CChain hain RReaction (PCR),eaction (PCR),

with oligonucleotide primers with homology with oligonucleotide primers with homology to the 5’ and 3’ ends of your gene, amplify to the 5’ and 3’ ends of your gene, amplify the DNA sequence between the primers.the DNA sequence between the primers.

Your geneReaction:

Product:Your gene amplified

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Reverse Genetic PCR StrategyReverse Genetic PCR Strategy

T-DNAReaction:

Product:

Reaction:

Product: none.

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PCR Screens for PCR Screens for MutantsMutants

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PCR StrategyPCR Strategy

T-DNAReaction:

Product:

T-DNAReaction:

Product:

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Find the Find the PlantPlant

You are ~hereYou are ~here

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T-DNA T-DNA MutantsMutants

Genetic Analysis Genetic Analysis

taggedseed line

taggedseed line

isolate homozygous

mutant

isolate homozygous

mutant

backcrossto wildtypebackcrossto wildtype

2x

phenotype analysis

phenotype analysis

tt x TT (wt)

Tt

T-DNASegregation

TT Tt

Tt tt

T t

T

t

F2

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PCR GenotypingPCR Genotyping

L t T

5’ 3’

5’ 3’heterozygote

L t T

5’ 3’

5’ 3’homozygotewt

L t T

5’ 3’

5’ 3’

homozygotemutant

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Genetic AnalysisGenetic AnalysisF2 Segregation F2 Segregation

1 : 2 : 1

TT Tt

Tt tt

T t

T

t

Not Lethal

1 wt : 2 het

TT Tt

Tt tt

T t

T

t

Lethal

1 wt : 1 het

TT Tt

Tt tt

T t

T

t

GametophyteLethal

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MidtermMidterm

Review on Wednesday,Review on Wednesday,

1 hour midterm,1 hour midterm,

Look for Ethylene-Insensitive Mutants.Look for Ethylene-Insensitive Mutants.